Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5500 |
| ensemblid | ENSG00000213639.11 |
| hgncid | 9282 |
| symbol | PPP1CB |
| name | protein phosphatase 1 catalytic subunit beta |
| refseq_nuc | NM_002709.3 |
| refseq_prot | NP_002700.1 |
| ensembl_nuc | ENST00000395366.3 |
| ensembl_prot | ENSP00000378769.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 28751830 |
| end | 28802940 |
| strand | + |
| ver | v1.2 |
| region | chr2:28751830-28802940 |
| region5000 | chr2:28746830-28807940 |
| regionname0 | PPP1CB_chr2_28751830_28802940 |
| regionname5000 | PPP1CB_chr2_28746830_28807940 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 981 | 207 | 37 | 40 | 103 | 8 | 18 | PPP1CB_chr2_28746830_28807940 | PPP1CB | ATGGC others(976): Show |
chr2 | 28746830 | 28807940 | ||
| a0001c0002 | 0/1 | 981 | 159 | 49 | 34 | 49 | 10 | 16 | PPP1CB_chr2_28746830_28807940 | PPP1CB | ATGGC others(976): Show |
chr2 | 28746830 | 28807940 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4917 | 143 | 16 | 32 | 77 | 6 | 12 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0004 | 1/0 | 4916 | 18 | 3 | 6 | 7 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4911): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0005 | 0/0 | 4915 | 12 | 0 | 0 | 12 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0006 | 0/0 | 4918 | 10 | 1 | 0 | 4 | 1 | 4 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4913): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0012 | 0/0 | 4917 | 5 | 4 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0013 | 0/0 | 4910 | 4 | 4 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4905): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0016 | 0/0 | 4917 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0017 | 0/0 | 4917 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0018 | 0/0 | 4915 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0023 | 0/0 | 4917 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0026 | 0/0 | 4915 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0027 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4911): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0028 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4911): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0029 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4911): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0030 | 0/0 | 4917 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0032 | 0/0 | 4918 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4913): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0035 | 0/0 | 4917 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0036 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4909): Show |
chr2 | 28746830 | 28807940 |
| a0001c0001t0038 | 0/0 | 4913 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4908): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0001 | 0/0 | 4917 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0002 | 0/1 | 4915 | 62 | 14 | 19 | 12 | 7 | 9 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0003 | 0/0 | 4915 | 42 | 8 | 5 | 24 | 2 | 3 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0004 | 0/0 | 4916 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4911): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0007 | 0/0 | 4915 | 9 | 9 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0008 | 0/0 | 4915 | 8 | 6 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0009 | 0/0 | 4914 | 6 | 0 | 3 | 1 | 1 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4909): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0010 | 0/0 | 4916 | 6 | 0 | 0 | 5 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4911): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0011 | 0/0 | 4915 | 5 | 4 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0014 | 0/0 | 4916 | 3 | 0 | 1 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4911): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0015 | 0/0 | 4914 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4909): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0019 | 0/0 | 4915 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0020 | 0/0 | 4915 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0021 | 0/0 | 4915 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0022 | 0/0 | 4916 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4911): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0024 | 0/0 | 4915 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0025 | 0/0 | 4915 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0031 | 0/0 | 4917 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0033 | 0/0 | 4918 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4913): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0034 | 0/0 | 4917 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4912): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0037 | 0/0 | 4918 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4913): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0039 | 0/0 | 4914 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4909): Show |
chr2 | 28746830 | 28807940 |
| a0001c0002t0040 | 0/0 | 4915 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | GCGGA others(4910): Show |
chr2 | 28746830 | 28807940 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 2 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0239 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0004g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0006g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0012g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0012g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0012g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0012g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0012g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0013g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0016g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0016g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0017g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0017g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0018g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0023g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0026g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0027g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0028g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0029g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0030g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0032g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0035g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0036g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0001t0038g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0002 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0007g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0007g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0008g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0008g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0008g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0009g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0009g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0009g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0009g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0009g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0010g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0010g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0010g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0010g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0011g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0014g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0014g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0014g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0015g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0015g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0019g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0020g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0021g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0022g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0024g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0025g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0031g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0033g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0034g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0037g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0039g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| a0001c0002t0040g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0054 | EUR | GBR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | GBR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0064 | EUR | GBR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00280 | hp2 | a0001 | c0002 | t0002 | g0096 | EUR | FIN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0080 | EUR | FIN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0004 | EUR | FIN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00438 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0236 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00609 | hp2 | a0001 | c0002 | t0015 | g0195 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00673 | hp1 | a0001 | c0002 | t0010 | g0061 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | CHS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0043 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00738 | hp1 | a0001 | c0002 | t0019 | g0208 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0095 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0327 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0074 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01070 | hp2 | a0001 | c0002 | t0009 | g0046 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01074 | hp1 | a0001 | c0002 | t0008 | g0159 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01074 | hp2 | a0001 | c0002 | t0015 | g0207 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0194 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01099 | hp2 | a0001 | c0002 | t0014 | g0212 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01106 | hp2 | a0001 | c0002 | t0008 | g0170 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01109 | hp1 | a0001 | c0001 | t0030 | g0223 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01243 | hp2 | a0001 | c0002 | t0011 | g0021 | AMR | PUR | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0168 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01256 | hp1 | a0001 | c0002 | t0009 | g0161 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01256 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01346 | hp1 | a0001 | c0001 | t0012 | g0296 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0020 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01433 | hp2 | a0001 | c0002 | t0009 | g0007 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0198 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | CLM | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0067 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0131 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01517 | hp1 | a0001 | c0002 | t0009 | g0002 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01884 | hp1 | a0001 | c0001 | t0027 | g0271 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01884 | hp2 | a0001 | c0001 | t0013 | g0033 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01891 | hp1 | a0001 | c0002 | t0033 | g0213 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01934 | hp1 | a0001 | c0002 | t0037 | g0330 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0200 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01993 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG01993 | hp2 | a0001 | c0001 | t0004 | g0117 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0190 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0272 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0273 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0044 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0063 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0209 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0079 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02280 | hp1 | a0001 | c0002 | t0011 | g0021 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0240 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02451 | hp1 | a0001 | c0002 | t0007 | g0176 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02451 | hp2 | a0001 | c0001 | t0013 | g0003 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0078 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02572 | hp2 | a0001 | c0001 | t0023 | g0275 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0180 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02615 | hp2 | a0001 | c0002 | t0002 | g0171 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02630 | hp1 | a0001 | c0001 | t0017 | g0297 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02647 | hp1 | a0001 | c0002 | t0007 | g0014 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02647 | hp2 | a0001 | c0001 | t0017 | g0315 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0185 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02723 | hp2 | a0001 | c0001 | t0038 | g0034 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0017 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02735 | hp2 | a0001 | c0002 | t0009 | g0076 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02809 | hp1 | a0001 | c0001 | t0012 | g0318 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02818 | hp2 | a0001 | c0002 | t0008 | g0037 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0049 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0015 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02922 | hp2 | a0001 | c0001 | t0028 | g0024 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0204 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0025 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02970 | hp1 | a0001 | c0002 | t0022 | g0174 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02970 | hp2 | a0001 | c0002 | t0008 | g0036 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03098 | hp1 | a0001 | c0002 | t0007 | g0175 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03098 | hp2 | a0001 | c0002 | t0008 | g0038 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0025 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03139 | hp2 | a0001 | c0002 | t0007 | g0013 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03195 | hp1 | a0001 | c0002 | t0007 | g0014 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03195 | hp2 | a0001 | c0001 | t0026 | g0241 | AFR | ESN | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0321 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0316 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03453 | hp1 | a0001 | c0002 | t0011 | g0215 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03453 | hp2 | a0001 | c0001 | t0029 | g0298 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0160 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03486 | hp2 | a0001 | c0002 | t0039 | g0090 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03491 | hp1 | a0001 | c0001 | t0016 | g0141 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03492 | hp2 | a0001 | c0001 | t0016 | g0150 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03540 | hp1 | a0001 | c0002 | t0011 | g0214 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03579 | hp1 | a0001 | c0002 | t0011 | g0216 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0314 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0051 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03688 | hp1 | a0001 | c0002 | t0002 | g0053 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03704 | hp1 | a0001 | c0002 | t0024 | g0066 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0097 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03710 | hp1 | a0001 | c0002 | t0010 | g0167 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03831 | hp1 | a0001 | c0002 | t0003 | g0181 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03831 | hp2 | a0001 | c0001 | t0006 | g0325 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0164 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0165 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0087 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0166 | SAS | BEB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG04199 | hp1 | a0001 | c0001 | t0006 | g0146 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0233 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0324 | SAS | STU | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18522 | hp1 | a0001 | c0001 | t0036 | g0032 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0003 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18906 | hp1 | a0001 | c0002 | t0007 | g0177 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0173 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18942 | hp1 | a0001 | c0002 | t0003 | g0205 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0196 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0238 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18947 | hp2 | a0001 | c0002 | t0003 | g0193 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18948 | hp2 | a0001 | c0002 | t0003 | g0201 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18951 | hp1 | a0001 | c0001 | t0032 | g0152 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18954 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18954 | hp2 | a0001 | c0002 | t0025 | g0094 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18959 | hp1 | a0001 | c0002 | t0010 | g0093 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0101 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18962 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18963 | hp2 | a0001 | c0001 | t0005 | g0237 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18973 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0235 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18977 | hp2 | a0001 | c0002 | t0034 | g0058 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18978 | hp1 | a0001 | c0002 | t0003 | g0192 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18979 | hp2 | a0001 | c0002 | t0003 | g0206 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18982 | hp1 | a0001 | c0002 | t0009 | g0068 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18990 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18991 | hp2 | a0001 | c0002 | t0014 | g0183 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18993 | hp1 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18993 | hp2 | a0001 | c0002 | t0014 | g0018 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0191 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0303 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19001 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19010 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19012 | hp1 | a0001 | c0002 | t0010 | g0059 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0203 | AFR | LWK | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19030 | hp2 | a0001 | c0002 | t0007 | g0013 | AFR | LWK | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19043 | hp1 | a0001 | c0002 | t0031 | g0331 | AFR | LWK | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19043 | hp2 | a0001 | c0002 | t0007 | g0179 | AFR | LWK | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19056 | hp1 | a0001 | c0002 | t0010 | g0060 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19058 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19060 | hp1 | a0001 | c0001 | t0035 | g0280 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19062 | hp1 | a0001 | c0001 | t0018 | g0221 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19065 | hp2 | a0001 | c0002 | t0021 | g0187 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19070 | hp1 | a0001 | c0001 | t0006 | g0156 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19075 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19080 | hp1 | a0001 | c0002 | t0020 | g0052 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19080 | hp2 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19081 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19083 | hp1 | a0001 | c0002 | t0010 | g0062 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19088 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19090 | hp2 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0199 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | YRI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | ASW | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20129 | hp2 | a0001 | c0002 | t0007 | g0178 | AFR | ASW | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20752 | hp1 | a0001 | c0002 | t0003 | g0211 | EUR | TSI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20805 | hp2 | a0001 | c0002 | t0003 | g0188 | EUR | TSI | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | GIH | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02109 | hp1 | a0001 | c0002 | t0008 | g0039 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0091 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG02559 | hp2 | a0001 | c0002 | t0008 | g0035 | AFR | ACB | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0184 | AFR | MSL | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0172 | AFR | USA | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0003 | AFR | USA | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18955 | hp1 | a0001 | c0002 | t0002 | g0008 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20300 | hp1 | a0001 | c0002 | t0040 | g0089 | AFR | USA | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0329 | AFR | USA | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0042 | REF | REF | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0239 | REF | REF | PPP1CB_chr2_28746830_28807940 | PPP1CB | chr2 | 28746830 | 28807940 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28778825 | A | G | 1 | a0001c0002 | 158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
synonymous_variant | LOW | c.201A>G | p.Gln67Gln | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/8 | 496/4916 | 201/984 | 67/327 | chr2 | 28778825 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28751922 | T | C | 1 | a0001c0001t0018 | 1 | NA19062.hp1 | 5_prime_UTR_variant | MODIFIER | c.-203T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/8 | 203 | chr2 | 28751922 | ||||||
| chr2:28751924 | C | T | 1 | a0001c0001t0018 | 1 | NA19062.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-201C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/8 | chr2 | 28751924 | |||||||
| chr2:28751986 | C | T | 2 | a0001c0002t0002 a0001c0002t0009 |
2 | HG01516.hp1 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-139C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/8 | 139 | chr2 | 28751986 | ||||||
| chr2:28799389 | A | G | 2 | a0001c0002t0039 a0001c0002t0040 |
2 | HG03486.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*86A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 86 | chr2 | 28799389 | ||||||
| chr2:28799416 | TTTAAC | T | 2 | a0001c0001t0013 a0001c0001t0038 |
5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*118_*122delCTTAA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 118 | INFO_REALIGN_3_PRIME | chr2 | 28799416 | |||||
| chr2:28799983 | T | A | 1 | a0001c0002t0019 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*680T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 680 | chr2 | 28799983 | ||||||
| chr2:28800093 | T | C | 9 | a0001c0002t0003 a0001c0002t0007 a0001c0002t0011 others(6): Show |
65 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*790T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 790 | chr2 | 28800093 | ||||||
| chr2:28800198 | G | A | 1 | a0001c0001t0023 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*895G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 895 | chr2 | 28800198 | ||||||
| chr2:28800226 | C | CT | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(12): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
3_prime_UTR_variant | MODIFIER | c.*946dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 947 | INFO_REALIGN_3_PRIME | chr2 | 28800226 | |||||
| chr2:28800226 | C | CTT | 2 | a0001c0001t0006 a0001c0002t0037 |
11 | HG01516.hp2 HG01934.hp1 HG03540.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*945_*946dupTT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 947 | INFO_REALIGN_3_PRIME | chr2 | 28800226 | |||||
| chr2:28800226 | CT | C | 12 | a0001c0001t0026 a0001c0002t0002 a0001c0002t0003 others(9): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*946delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 946 | INFO_REALIGN_3_PRIME | chr2 | 28800226 | |||||
| chr2:28800226 | CTT | C | 3 | a0001c0002t0009 a0001c0002t0015 a0001c0002t0039 |
9 | HG00609.hp2 HG01070.hp2 HG01074.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*945_*946delTT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 945 | INFO_REALIGN_3_PRIME | chr2 | 28800226 | |||||
| chr2:28800234 | T | C | 1 | a0001c0002t0024 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*931T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 931 | chr2 | 28800234 | ||||||
| chr2:28800251 | AGTT | A | 2 | a0001c0001t0013 a0001c0001t0036 |
5 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*955_*957delGTT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 955 | INFO_REALIGN_3_PRIME | chr2 | 28800251 | |||||
| chr2:28800270 | A | G | 1 | a0001c0001t0035 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*967A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 967 | chr2 | 28800270 | ||||||
| chr2:28800321 | G | A | 1 | a0001c0002t0025 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1018 | chr2 | 28800321 | ||||||
| chr2:28800634 | G | T | 1 | a0001c0002t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1331 | chr2 | 28800634 | ||||||
| chr2:28800883 | A | G | 8 | a0001c0002t0002 a0001c0002t0009 a0001c0002t0010 others(5): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1580A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1580 | chr2 | 28800883 | ||||||
| chr2:28801071 | G | T | 1 | a0001c0001t0017 | 2 | HG02630.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1768G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1768 | chr2 | 28801071 | ||||||
| chr2:28801255 | A | G | 1 | a0001c0002t0021 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1952A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 1952 | chr2 | 28801255 | ||||||
| chr2:28801403 | A | C | 1 | a0001c0002t0020 | 1 | NA19080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2100A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2100 | chr2 | 28801403 | ||||||
| chr2:28801432 | C | CT | 6 | a0001c0001t0013 a0001c0001t0030 a0001c0001t0032 others(3): Show |
9 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2143dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2144 | INFO_REALIGN_3_PRIME | chr2 | 28801432 | |||||
| chr2:28801570 | T | C | 1 | a0001c0002t0021 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2267T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2267 | chr2 | 28801570 | ||||||
| chr2:28801678 | A | G | 1 | a0001c0001t0030 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2375A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2375 | chr2 | 28801678 | ||||||
| chr2:28801729 | A | G | 3 | a0001c0001t0013 a0001c0001t0038 a0001c0002t0037 |
6 | HG01884.hp2 HG01934.hp1 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2426A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2426 | chr2 | 28801729 | ||||||
| chr2:28801746 | T | G | 1 | a0001c0001t0027 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2443T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2443 | chr2 | 28801746 | ||||||
| chr2:28801816 | A | T | 1 | a0001c0001t0016 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2513A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2513 | chr2 | 28801816 | ||||||
| chr2:28801997 | C | T | 1 | a0001c0002t0033 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2694C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2694 | chr2 | 28801997 | ||||||
| chr2:28802277 | T | C | 1 | a0001c0002t0031 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2974T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 2974 | chr2 | 28802277 | ||||||
| chr2:28802368 | G | C | 1 | a0001c0002t0011 | 5 | HG01243.hp2 HG02280.hp1 HG03453.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3065G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3065 | chr2 | 28802368 | ||||||
| chr2:28802613 | A | G | 15 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0008 others(12): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*3310A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3310 | chr2 | 28802613 | ||||||
| chr2:28802668 | T | C | 1 | a0001c0001t0028 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3365T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3365 | chr2 | 28802668 | ||||||
| chr2:28802675 | C | G | 3 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0029 |
8 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3372C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3372 | chr2 | 28802675 | ||||||
| chr2:28802852 | A | G | 1 | a0001c0001t0030 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3549A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3549 | chr2 | 28802852 | ||||||
| chr2:28802867 | TAA | T | 2 | a0001c0001t0005 a0001c0001t0018 |
13 | HG00544.hp2 HG00673.hp2 HG02027.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3565_*3566delAA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 8/8 | 3565 | chr2 | 28802867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:28752191 | G | T | 4 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0031g0331 others(1): Show |
5 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+15G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752191 | |||||||
| chr2:28752241 | G | C | 222 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(219): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.52+65G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752241 | |||||||
| chr2:28752246 | C | T | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52+70C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752246 | |||||||
| chr2:28752396 | C | T | 1 | a0001c0002t0002g0220 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52+220C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752396 | |||||||
| chr2:28752430 | G | C | 1 | a0001c0001t0018g0221 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.52+254G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752430 | |||||||
| chr2:28752432 | C | G | 1 | a0001c0001t0018g0221 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.52+256C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752432 | |||||||
| chr2:28752458 | G | A | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+282G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752458 | |||||||
| chr2:28752540 | C | G | 1 | a0001c0001t0018g0221 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.52+364C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752540 | |||||||
| chr2:28752632 | A | T | 1 | a0001c0001t0001g0219 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.52+456A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752632 | |||||||
| chr2:28752669 | A | T | 2 | a0001c0002t0002g0217 a0001c0002t0002g0218 |
2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.52+493A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752669 | |||||||
| chr2:28752681 | C | T | 4 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0031g0331 others(1): Show |
5 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+505C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752681 | |||||||
| chr2:28752787 | T | A | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+611T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752787 | |||||||
| chr2:28752824 | C | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(210): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.52+648C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752824 | |||||||
| chr2:28752875 | A | G | 1 | a0001c0002t0002g0220 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52+699A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752875 | |||||||
| chr2:28752950 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.52+774A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28752950 | |||||||
| chr2:28753032 | A | G | 4 | a0001c0002t0011g0021 a0001c0002t0011g0214 a0001c0002t0011g0215 others(1): Show |
5 | HG01243.hp2 HG02280.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+856A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753032 | |||||||
| chr2:28753064 | A | G | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+888A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753064 | |||||||
| chr2:28753065 | G | A | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+889G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753065 | |||||||
| chr2:28753100 | A | C | 1 | a0001c0001t0004g0327 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52+924A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753100 | |||||||
| chr2:28753177 | A | G | 5 | a0001c0001t0004g0031 a0001c0001t0013g0003 a0001c0001t0013g0033 others(2): Show |
7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+1001A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753177 | |||||||
| chr2:28753215 | T | TC | 153 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(150): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.52+1040dupC | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28753215 | ||||||
| chr2:28753363 | A | T | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+1187A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753363 | |||||||
| chr2:28753502 | T | C | 1 | a0001c0002t0003g0173 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.52+1326T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753502 | |||||||
| chr2:28753537 | A | G | 153 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(150): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.52+1361A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753537 | |||||||
| chr2:28753945 | C | T | 1 | a0001c0001t0005g0326 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.52+1769C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753945 | |||||||
| chr2:28753948 | G | C | 5 | a0001c0002t0008g0035 a0001c0002t0008g0036 a0001c0002t0008g0037 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+1772G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28753948 | |||||||
| chr2:28754031 | C | T | 2 | a0001c0002t0002g0171 a0001c0002t0002g0172 |
2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.52+1855C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754031 | |||||||
| chr2:28754099 | A | C | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+1923A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754099 | |||||||
| chr2:28754107 | T | C | 2 | a0001c0001t0004g0031 a0001c0001t0036g0032 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.52+1931T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754107 | |||||||
| chr2:28754169 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.52+1993T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754169 | |||||||
| chr2:28754196 | T | C | 1 | a0001c0001t0001g0219 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.52+2020T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754196 | |||||||
| chr2:28754200 | A | G | 1 | a0001c0002t0008g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.52+2024A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754200 | |||||||
| chr2:28754225 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.52+2049G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754225 | |||||||
| chr2:28754311 | G | T | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+2135G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754311 | |||||||
| chr2:28754338 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.52+2162G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754338 | |||||||
| chr2:28754345 | CG | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0022 others(120): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.52+2179delG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28754345 | ||||||
| chr2:28754345 | CGG | C | 150 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(147): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.52+2178_52+2179del others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28754345 | ||||||
| chr2:28754350 | G | C | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+2174G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754350 | |||||||
| chr2:28754357 | G | A | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.52+2181G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754357 | |||||||
| chr2:28754378 | T | C | 209 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(206): Show |
230 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.52+2202T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754378 | |||||||
| chr2:28754408 | A | G | 191 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(188): Show |
207 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.52+2232A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754408 | |||||||
| chr2:28754443 | C | T | 4 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(1): Show |
4 | HG03710.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+2267C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754443 | |||||||
| chr2:28754454 | A | G | 1 | a0001c0002t0002g0163 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.52+2278A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754454 | |||||||
| chr2:28754470 | C | G | 1 | a0001c0002t0003g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.52+2294C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754470 | |||||||
| chr2:28754574 | A | G | 2 | a0001c0002t0002g0162 a0001c0002t0009g0161 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.52+2398A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754574 | |||||||
| chr2:28754580 | A | G | 1 | a0001c0002t0003g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.52+2404A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754580 | |||||||
| chr2:28754855 | A | G | 1 | a0001c0002t0019g0208 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.52+2679A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754855 | |||||||
| chr2:28754928 | T | C | 2 | a0001c0002t0002g0047 a0001c0002t0002g0048 |
2 | HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.52+2752T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28754928 | |||||||
| chr2:28755025 | G | A | 6 | a0001c0001t0004g0028 a0001c0001t0004g0031 a0001c0001t0013g0003 others(3): Show |
8 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+2849G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755025 | |||||||
| chr2:28755028 | C | T | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG01106.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.52+2852C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755028 | |||||||
| chr2:28755037 | G | A | 2 | a0001c0001t0013g0003 a0001c0001t0013g0033 |
4 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+2861G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755037 | |||||||
| chr2:28755041 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+2865A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755041 | |||||||
| chr2:28755081 | G | A | 3 | a0001c0002t0003g0180 a0001c0002t0003g0211 a0001c0002t0014g0212 |
3 | HG01099.hp2 HG02602.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.52+2905G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755081 | |||||||
| chr2:28755208 | C | T | 195 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(192): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.52+3032C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755208 | |||||||
| chr2:28755258 | C | T | 4 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0002g0166 others(1): Show |
4 | HG03710.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+3082C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755258 | |||||||
| chr2:28755292 | G | A | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.52+3116G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755292 | |||||||
| chr2:28755313 | T | G | 5 | a0001c0002t0008g0035 a0001c0002t0008g0036 a0001c0002t0008g0037 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+3137T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755313 | |||||||
| chr2:28755329 | C | T | 3 | a0001c0002t0008g0159 a0001c0002t0008g0160 a0001c0002t0008g0170 |
3 | HG01074.hp1 HG01106.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.52+3153C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755329 | |||||||
| chr2:28755532 | T | G | 14 | a0001c0001t0001g0029 a0001c0001t0001g0224 a0001c0001t0001g0225 others(11): Show |
14 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.52+3356T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755532 | |||||||
| chr2:28755613 | T | G | 5 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(2): Show |
5 | HG00544.hp2 NA18944.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+3437T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755613 | |||||||
| chr2:28755853 | A | T | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+3677A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755853 | |||||||
| chr2:28755875 | T | C | 17 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0007g0013 others(14): Show |
21 | HG01243.hp2 HG01891.hp1 HG01934.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+3699T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28755875 | |||||||
| chr2:28756030 | A | G | 1 | a0001c0002t0015g0207 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.52+3854A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756030 | |||||||
| chr2:28756107 | T | C | 3 | a0001c0001t0013g0003 a0001c0001t0013g0033 a0001c0001t0038g0034 |
5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+3931T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756107 | |||||||
| chr2:28756210 | T | C | 3 | a0001c0001t0013g0003 a0001c0001t0013g0033 a0001c0001t0038g0034 |
5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+4034T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756210 | |||||||
| chr2:28756312 | T | C | 1 | a0001c0002t0003g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.52+4136T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756312 | |||||||
| chr2:28756323 | T | C | 1 | a0001c0002t0002g0049 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.52+4147T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756323 | |||||||
| chr2:28756330 | C | T | 2 | a0001c0002t0002g0217 a0001c0002t0002g0218 |
2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.52+4154C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756330 | |||||||
| chr2:28756499 | T | G | 54 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(51): Show |
64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.52+4323T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756499 | |||||||
| chr2:28756578 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.52+4402G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756578 | |||||||
| chr2:28756808 | TA | T | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.52+4640delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28756808 | ||||||
| chr2:28756856 | A | G | 1 | a0001c0001t0012g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.52+4680A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756856 | |||||||
| chr2:28756970 | A | G | 2 | a0001c0002t0003g0205 a0001c0002t0003g0206 |
2 | NA18942.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.52+4794A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28756970 | |||||||
| chr2:28757012 | C | A | 1 | a0001c0001t0001g0224 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.52+4836C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757012 | |||||||
| chr2:28757282 | A | G | 2 | a0001c0002t0008g0159 a0001c0002t0008g0160 |
2 | HG01074.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.52+5106A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757282 | |||||||
| chr2:28757376 | A | G | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+5200A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757376 | |||||||
| chr2:28757380 | C | T | 1 | a0001c0002t0003g0204 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+5204C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757380 | |||||||
| chr2:28757381 | G | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0242 a0001c0001t0001g0243 others(16): Show |
23 | HG00280.hp1 HG01106.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.52+5205G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757381 | |||||||
| chr2:28757525 | G | C | 2 | a0001c0002t0003g0211 a0001c0002t0014g0212 |
2 | HG01099.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.52+5349G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757525 | |||||||
| chr2:28757571 | G | A | 1 | a0001c0002t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.52+5395G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757571 | |||||||
| chr2:28757763 | G | C | 9 | a0001c0001t0001g0257 a0001c0001t0001g0259 a0001c0001t0001g0261 others(6): Show |
9 | HG00544.hp1 NA18948.hp1 NA18960.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+5587G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757763 | |||||||
| chr2:28757820 | G | A | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+5644G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28757820 | |||||||
| chr2:28758034 | AT | A | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.52+5866delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28758034 | ||||||
| chr2:28758048 | A | AT | 6 | a0001c0001t0001g0158 a0001c0001t0001g0234 a0001c0001t0001g0319 others(3): Show |
6 | HG02083.hp1 HG02698.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+5886dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28758048 | ||||||
| chr2:28758048 | A | T | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+5872A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758048 | |||||||
| chr2:28758049 | T | A | 1 | a0001c0002t0003g0027 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.52+5873T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758049 | |||||||
| chr2:28758322 | A | G | 1 | a0001c0002t0003g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.52+6146A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758322 | |||||||
| chr2:28758355 | C | G | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52+6179C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758355 | |||||||
| chr2:28758586 | A | G | 2 | a0001c0002t0002g0096 a0001c0002t0002g0097 |
2 | HG00280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.52+6410A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758586 | |||||||
| chr2:28758610 | C | T | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.52+6434C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758610 | |||||||
| chr2:28758650 | A | C | 1 | a0001c0002t0002g0095 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52+6474A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758650 | |||||||
| chr2:28758663 | T | C | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.52+6487T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758663 | |||||||
| chr2:28758755 | G | A | 1 | a0001c0002t0020g0052 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.52+6579G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758755 | |||||||
| chr2:28758788 | C | G | 1 | a0001c0002t0002g0095 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52+6612C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28758788 | |||||||
| chr2:28759117 | G | A | 124 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(121): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.52+6941G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759117 | |||||||
| chr2:28759164 | A | G | 124 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(121): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.52+6988A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759164 | |||||||
| chr2:28759192 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.52+7016G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759192 | |||||||
| chr2:28759239 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG02083.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.52+7063C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759239 | |||||||
| chr2:28759350 | T | C | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52+7174T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759350 | |||||||
| chr2:28759484 | C | T | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+7308C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759484 | |||||||
| chr2:28759492 | C | G | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+7316C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759492 | |||||||
| chr2:28759520 | C | CA | 86 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0022 others(83): Show |
91 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.52+7370dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759520 | ||||||
| chr2:28759520 | C | CAA | 7 | a0001c0001t0001g0225 a0001c0001t0001g0242 a0001c0001t0001g0243 others(4): Show |
7 | HG01106.hp1 HG02074.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+7369_52+7370dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759520 | ||||||
| chr2:28759520 | CAAAAAAA others(3): Show |
C | 135 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(132): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.52+7361_52+7370del others(10): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759520 | ||||||
| chr2:28759520 | CAAAAAAA others(5): Show |
C | 2 | a0001c0002t0031g0331 a0001c0002t0037g0330 |
2 | HG01934.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.52+7359_52+7370del others(12): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759520 | ||||||
| chr2:28759547 | G | C | 2 | a0001c0001t0001g0257 a0001c0001t0005g0258 |
2 | NA19001.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.52+7371G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759547 | |||||||
| chr2:28759557 | A | G | 3 | a0001c0001t0013g0003 a0001c0001t0013g0033 a0001c0001t0038g0034 |
5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+7381A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759557 | |||||||
| chr2:28759643 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.52+7467G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759643 | |||||||
| chr2:28759662 | G | T | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.52+7486G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759662 | |||||||
| chr2:28759684 | C | T | 1 | a0001c0001t0006g0156 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.52+7508C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759684 | |||||||
| chr2:28759713 | G | A | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+7537G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759713 | |||||||
| chr2:28759763 | G | A | 124 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(121): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.52+7587G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759763 | |||||||
| chr2:28759786 | T | C | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52+7610T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759786 | |||||||
| chr2:28759862 | G | A | 1 | a0001c0002t0022g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.52+7686G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759862 | |||||||
| chr2:28759882 | G | C | 1 | a0001c0002t0002g0095 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.52+7706G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759882 | |||||||
| chr2:28759948 | G | GTTAAC | 145 | a0001c0001t0004g0028 a0001c0001t0004g0031 a0001c0001t0013g0003 others(142): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.52+7776_52+7777ins others(5): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28759948 | ||||||
| chr2:28759961 | C | G | 59 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(56): Show |
70 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.52+7785C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28759961 | |||||||
| chr2:28760108 | C | T | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.52+7932C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760108 | |||||||
| chr2:28760300 | T | C | 124 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(121): Show |
136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.52+8124T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760300 | |||||||
| chr2:28760524 | A | G | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.52+8348A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760524 | |||||||
| chr2:28760605 | A | G | 1 | a0001c0001t0004g0327 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.52+8429A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760605 | |||||||
| chr2:28760679 | A | G | 1 | a0001c0001t0012g0318 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.52+8503A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760679 | |||||||
| chr2:28760844 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.52+8668G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760844 | |||||||
| chr2:28760918 | C | T | 1 | a0001c0002t0037g0330 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.52+8742C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760918 | |||||||
| chr2:28760945 | G | C | 1 | a0001c0001t0029g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.52+8769G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760945 | |||||||
| chr2:28760974 | C | T | 1 | a0001c0001t0036g0032 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.52+8798C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760974 | |||||||
| chr2:28760986 | C | G | 1 | a0001c0001t0001g0317 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.52+8810C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28760986 | |||||||
| chr2:28761043 | G | A | 1 | a0001c0001t0027g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.52+8867G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761043 | |||||||
| chr2:28761125 | T | C | 176 | a0001c0001t0001g0030 a0001c0001t0001g0274 a0001c0001t0001g0277 others(173): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.52+8949T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761125 | |||||||
| chr2:28761189 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+9013C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761189 | |||||||
| chr2:28761387 | G | T | 5 | a0001c0002t0003g0020 a0001c0002t0003g0200 a0001c0002t0003g0201 others(2): Show |
6 | HG01074.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+9211G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761387 | |||||||
| chr2:28761552 | C | A | 59 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(56): Show |
70 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.52+9376C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761552 | |||||||
| chr2:28761634 | G | C | 1 | a0001c0001t0004g0244 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.52+9458G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761634 | |||||||
| chr2:28761716 | C | A | 5 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0031g0331 others(2): Show |
6 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+9540C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761716 | |||||||
| chr2:28761831 | C | T | 7 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0176 others(4): Show |
9 | HG02451.hp1 HG02647.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.52+9655C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761831 | |||||||
| chr2:28761864 | A | G | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+9688A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761864 | |||||||
| chr2:28761920 | G | C | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+9744G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28761920 | |||||||
| chr2:28762284 | CTAAA | C | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.52+10123_52+10126d others(6): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28762284 | ||||||
| chr2:28762300 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.52+10124A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762300 | |||||||
| chr2:28762353 | G | A | 5 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0031g0331 others(2): Show |
6 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+10177G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762353 | |||||||
| chr2:28762549 | G | A | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52+10373G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762549 | |||||||
| chr2:28762635 | T | G | 1 | a0001c0002t0003g0173 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.52+10459T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762635 | |||||||
| chr2:28762650 | T | C | 1 | a0001c0001t0004g0117 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.52+10474T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762650 | |||||||
| chr2:28762693 | C | T | 1 | a0001c0001t0038g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.52+10517C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762693 | |||||||
| chr2:28762754 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.52+10578A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762754 | |||||||
| chr2:28762808 | C | G | 155 | a0001c0001t0001g0029 a0001c0001t0001g0224 a0001c0001t0001g0225 others(152): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.52+10632C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28762808 | |||||||
| chr2:28763016 | C | T | 3 | a0001c0002t0008g0159 a0001c0002t0008g0160 a0001c0002t0008g0170 |
3 | HG01074.hp1 HG01106.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.52+10840C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763016 | |||||||
| chr2:28763451 | G | GA | 110 | a0001c0001t0001g0099 a0001c0001t0001g0274 a0001c0001t0001g0277 others(107): Show |
116 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.52+11286dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28763451 | ||||||
| chr2:28763701 | A | G | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+11525A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763701 | |||||||
| chr2:28763702 | CGTTA | C | 83 | a0001c0001t0036g0032 a0001c0002t0002g0002 a0001c0002t0002g0006 others(80): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.52+11531_52+11534d others(6): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28763702 | ||||||
| chr2:28763741 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.52+11565G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763741 | |||||||
| chr2:28763743 | C | T | 4 | a0001c0001t0001g0277 a0001c0001t0001g0307 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+11567C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763743 | |||||||
| chr2:28763928 | A | ACAC | 151 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(148): Show |
161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.52+11753_52+11754i others(5): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28763928 | ||||||
| chr2:28763944 | G | A | 5 | a0001c0002t0011g0021 a0001c0002t0011g0214 a0001c0002t0011g0215 others(2): Show |
6 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+11768G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763944 | |||||||
| chr2:28763981 | A | G | 3 | a0001c0001t0012g0321 a0001c0002t0004g0025 a0001c0002t0004g0329 |
4 | HG02965.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+11805A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28763981 | |||||||
| chr2:28764064 | T | G | 1 | a0001c0002t0021g0187 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.52+11888T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764064 | |||||||
| chr2:28764080 | G | A | 1 | a0001c0002t0008g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.52+11904G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764080 | |||||||
| chr2:28764105 | A | G | 1 | a0001c0002t0025g0094 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.52+11929A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764105 | |||||||
| chr2:28764295 | CT | C | 6 | a0001c0001t0004g0028 a0001c0001t0004g0031 a0001c0001t0013g0003 others(3): Show |
8 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+12121delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28764295 | ||||||
| chr2:28764297 | T | A | 6 | a0001c0001t0004g0028 a0001c0001t0004g0031 a0001c0001t0013g0003 others(3): Show |
8 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+12121T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764297 | |||||||
| chr2:28764337 | A | G | 5 | a0001c0002t0003g0020 a0001c0002t0003g0200 a0001c0002t0003g0201 others(2): Show |
6 | HG01074.hp2 HG01346.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+12161A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764337 | |||||||
| chr2:28764384 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0006g0026 |
2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.52+12208C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764384 | |||||||
| chr2:28764411 | G | A | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.52+12235G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764411 | |||||||
| chr2:28764459 | C | CA | 12 | a0001c0001t0004g0028 a0001c0001t0004g0031 a0001c0001t0013g0003 others(9): Show |
15 | HG01074.hp2 HG01346.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+12298dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28764459 | ||||||
| chr2:28764459 | CA | C | 17 | a0001c0001t0001g0115 a0001c0001t0001g0255 a0001c0001t0001g0295 others(14): Show |
20 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(17): Show |
intron_variant | MODIFIER | c.52+12298delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28764459 | ||||||
| chr2:28764569 | C | G | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-12282C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764569 | |||||||
| chr2:28764701 | G | A | 5 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0031g0331 others(2): Show |
6 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-12150G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764701 | |||||||
| chr2:28764723 | C | T | 1 | a0001c0002t0002g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.53-12128C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764723 | |||||||
| chr2:28764814 | A | G | 1 | a0001c0002t0002g0163 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.53-12037A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764814 | |||||||
| chr2:28764824 | G | C | 1 | a0001c0002t0002g0006 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.53-12027G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764824 | |||||||
| chr2:28764826 | T | C | 2 | a0001c0001t0004g0031 a0001c0001t0036g0032 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-12025T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764826 | |||||||
| chr2:28764918 | C | CA | 119 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(116): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.53-11921dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28764918 | ||||||
| chr2:28764944 | G | A | 6 | a0001c0001t0004g0028 a0001c0001t0004g0031 a0001c0001t0013g0003 others(3): Show |
8 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-11907G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764944 | |||||||
| chr2:28764982 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.53-11869C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28764982 | |||||||
| chr2:28765006 | A | G | 1 | a0001c0002t0002g0092 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.53-11845A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765006 | |||||||
| chr2:28765033 | G | A | 1 | a0001c0002t0002g0049 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.53-11818G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765033 | |||||||
| chr2:28765069 | A | G | 1 | a0001c0001t0001g0294 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.53-11782A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765069 | |||||||
| chr2:28765085 | T | C | 2 | a0001c0001t0001g0225 a0001c0001t0006g0233 |
2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.53-11766T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765085 | |||||||
| chr2:28765217 | T | C | 195 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(192): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.53-11634T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765217 | |||||||
| chr2:28765276 | A | G | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-11575A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765276 | |||||||
| chr2:28765308 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.53-11543T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28765308 | |||||||
| chr2:28766195 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-10656G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766195 | |||||||
| chr2:28766281 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.53-10570T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766281 | |||||||
| chr2:28766474 | A | G | 1 | a0001c0002t0007g0179 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.53-10377A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766474 | |||||||
| chr2:28766801 | A | G | 141 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(138): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.53-10050A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766801 | |||||||
| chr2:28766824 | G | A | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-10027G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766824 | |||||||
| chr2:28766941 | C | T | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-9910C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766941 | |||||||
| chr2:28766949 | C | T | 4 | a0001c0002t0011g0021 a0001c0002t0011g0214 a0001c0002t0011g0215 others(1): Show |
5 | HG01243.hp2 HG02280.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-9902C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766949 | |||||||
| chr2:28766950 | G | A | 2 | a0001c0001t0027g0271 a0001c0002t0008g0159 |
2 | HG01074.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.53-9901G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28766950 | |||||||
| chr2:28767021 | C | T | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.53-9830C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767021 | |||||||
| chr2:28767080 | CA | C | 83 | a0001c0001t0001g0243 a0001c0002t0002g0002 a0001c0002t0002g0006 others(80): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.53-9757delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28767080 | ||||||
| chr2:28767109 | A | G | 143 | a0001c0001t0030g0223 a0001c0002t0001g0228 a0001c0002t0002g0002 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.53-9742A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767109 | |||||||
| chr2:28767111 | A | C | 143 | a0001c0001t0030g0223 a0001c0002t0001g0228 a0001c0002t0002g0002 others(140): Show |
159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.53-9740A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767111 | |||||||
| chr2:28767336 | C | G | 59 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(56): Show |
70 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.53-9515C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767336 | |||||||
| chr2:28767359 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.53-9492G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767359 | |||||||
| chr2:28767446 | AAC | A | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-9401_53-9400del others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28767446 | ||||||
| chr2:28767524 | A | T | 22 | a0001c0001t0001g0274 a0001c0001t0001g0277 a0001c0001t0001g0302 others(19): Show |
22 | HG00544.hp2 HG00673.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.53-9327A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767524 | |||||||
| chr2:28767554 | C | G | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-9297C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767554 | |||||||
| chr2:28767652 | C | A | 1 | a0001c0002t0020g0052 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.53-9199C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767652 | |||||||
| chr2:28767668 | A | G | 5 | a0001c0002t0008g0035 a0001c0002t0008g0036 a0001c0002t0008g0037 others(2): Show |
5 | HG02109.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-9183A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767668 | |||||||
| chr2:28767702 | A | T | 1 | a0001c0001t0038g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-9149A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767702 | |||||||
| chr2:28767713 | T | C | 1 | a0001c0002t0003g0188 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53-9138T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767713 | |||||||
| chr2:28767814 | A | G | 1 | a0001c0002t0003g0188 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.53-9037A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767814 | |||||||
| chr2:28767879 | T | C | 6 | a0001c0001t0001g0024 a0001c0001t0001g0278 a0001c0001t0001g0311 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-8972T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767879 | |||||||
| chr2:28767953 | C | G | 4 | a0001c0002t0002g0041 a0001c0002t0002g0047 a0001c0002t0002g0048 others(1): Show |
4 | HG02257.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-8898C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767953 | |||||||
| chr2:28767980 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.53-8871A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28767980 | |||||||
| chr2:28768188 | G | A | 2 | a0001c0001t0004g0031 a0001c0001t0036g0032 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-8663G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768188 | |||||||
| chr2:28768394 | C | T | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-8457C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768394 | |||||||
| chr2:28768405 | A | G | 2 | a0001c0001t0001g0300 a0001c0001t0004g0301 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.53-8446A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768405 | |||||||
| chr2:28768422 | T | G | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-8429T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768422 | |||||||
| chr2:28768432 | A | G | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-8419A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768432 | |||||||
| chr2:28768490 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.53-8361C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768490 | |||||||
| chr2:28768501 | G | A | 1 | a0001c0001t0027g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.53-8350G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768501 | |||||||
| chr2:28768661 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53-8190G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768661 | |||||||
| chr2:28768856 | A | G | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.53-7995A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28768856 | |||||||
| chr2:28769134 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53-7717A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769134 | |||||||
| chr2:28769138 | T | C | 142 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.53-7713T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769138 | |||||||
| chr2:28769154 | T | G | 125 | a0001c0001t0001g0030 a0001c0002t0002g0002 a0001c0002t0002g0006 others(122): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.53-7697T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769154 | |||||||
| chr2:28769169 | T | C | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-7682T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769169 | |||||||
| chr2:28769248 | A | G | 1 | a0001c0002t0007g0175 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.53-7603A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769248 | |||||||
| chr2:28769255 | G | A | 1 | a0001c0002t0002g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.53-7596G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769255 | |||||||
| chr2:28769298 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.53-7553G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769298 | |||||||
| chr2:28769329 | C | T | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.53-7522C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769329 | |||||||
| chr2:28769395 | C | G | 3 | a0001c0001t0013g0003 a0001c0001t0013g0033 a0001c0001t0038g0034 |
5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-7456C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769395 | |||||||
| chr2:28769415 | T | C | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-7436T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769415 | |||||||
| chr2:28769427 | G | A | 67 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(64): Show |
72 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.53-7424G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769427 | |||||||
| chr2:28769539 | A | G | 142 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.53-7312A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769539 | |||||||
| chr2:28769741 | C | G | 142 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.53-7110C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769741 | |||||||
| chr2:28769749 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.53-7102A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769749 | |||||||
| chr2:28769880 | A | G | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-6971A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28769880 | |||||||
| chr2:28770023 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.53-6828C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770023 | |||||||
| chr2:28770122 | G | T | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-6729G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770122 | |||||||
| chr2:28770148 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.53-6703A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770148 | |||||||
| chr2:28770160 | G | T | 1 | a0001c0002t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.53-6691G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770160 | |||||||
| chr2:28770178 | G | A | 38 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(35): Show |
45 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.53-6673G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770178 | |||||||
| chr2:28770239 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-6612G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770239 | |||||||
| chr2:28770371 | A | G | 1 | a0001c0002t0002g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.53-6480A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770371 | |||||||
| chr2:28770380 | AAGG | A | 4 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0168 others(1): Show |
4 | HG01070.hp2 HG01255.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-6470_53-6468del others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770380 | |||||||
| chr2:28770381 | A | AG | 47 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(44): Show |
52 | HG00558.hp1 HG00733.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.53-6460dupG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770381 | ||||||
| chr2:28770381 | A | AGG | 147 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(144): Show |
157 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.53-6461_53-6460dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770381 | ||||||
| chr2:28770381 | A | AGGG | 28 | a0001c0001t0001g0105 a0001c0001t0001g0110 a0001c0001t0001g0114 others(25): Show |
28 | HG00544.hp1 HG00544.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.53-6462_53-6460dup others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770381 | ||||||
| chr2:28770381 | A | G | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-6470A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770381 | |||||||
| chr2:28770381 | AG | A | 62 | a0001c0001t0038g0034 a0001c0002t0002g0002 a0001c0002t0002g0006 others(59): Show |
66 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(63): Show |
intron_variant | MODIFIER | c.53-6460delG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770381 | ||||||
| chr2:28770382 | G | A | 1 | a0001c0002t0037g0330 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.53-6469G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770382 | |||||||
| chr2:28770392 | A | G | 7 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(4): Show |
7 | HG00597.hp2 HG01192.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-6459A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770392 | |||||||
| chr2:28770464 | G | GA | 54 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(51): Show |
64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53-6382dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770464 | ||||||
| chr2:28770627 | G | C | 1 | a0001c0002t0002g0044 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-6224G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770627 | |||||||
| chr2:28770740 | G | A | 2 | a0001c0002t0008g0035 a0001c0002t0008g0036 |
2 | HG02559.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.53-6111G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770740 | |||||||
| chr2:28770744 | A | G | 1 | a0001c0002t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.53-6107A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770744 | |||||||
| chr2:28770786 | CA | C | 130 | a0001c0001t0001g0030 a0001c0001t0032g0152 a0001c0002t0001g0228 others(127): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.53-6061delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28770786 | ||||||
| chr2:28770979 | T | C | 8 | a0001c0001t0001g0100 a0001c0002t0002g0057 a0001c0002t0010g0059 others(5): Show |
8 | HG00673.hp1 NA18959.hp1 NA18977.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-5872T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28770979 | |||||||
| chr2:28771034 | C | T | 2 | a0001c0002t0004g0329 a0001c0002t0037g0330 |
2 | HG01934.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-5817C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771034 | |||||||
| chr2:28771037 | T | C | 156 | a0001c0001t0001g0030 a0001c0001t0004g0028 a0001c0001t0004g0031 others(153): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.53-5814T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771037 | |||||||
| chr2:28771040 | T | TC | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(69): Show |
79 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.53-5800dupC | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771040 | ||||||
| chr2:28771040 | T | TCC | 43 | a0001c0001t0001g0012 a0001c0001t0001g0098 a0001c0001t0001g0107 others(40): Show |
44 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.53-5801_53-5800dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771040 | ||||||
| chr2:28771040 | TC | T | 15 | a0001c0001t0001g0157 a0001c0001t0006g0026 a0001c0001t0012g0314 others(12): Show |
16 | HG00609.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-5800delC | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771040 | ||||||
| chr2:28771043 | C | A | 1 | a0001c0002t0003g0189 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.53-5808C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771043 | |||||||
| chr2:28771049 | C | G | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.53-5802C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771049 | |||||||
| chr2:28771050 | C | A | 10 | a0001c0002t0002g0063 a0001c0002t0002g0064 a0001c0002t0002g0065 others(7): Show |
11 | HG00140.hp1 HG00558.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-5801C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771050 | |||||||
| chr2:28771051 | C | A | 100 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(97): Show |
113 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.53-5800C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771051 | |||||||
| chr2:28771051 | CA | C | 10 | a0001c0002t0002g0063 a0001c0002t0002g0064 a0001c0002t0002g0065 others(7): Show |
11 | HG00140.hp1 HG00558.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-5799delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771051 | |||||||
| chr2:28771052 | A | C | 101 | a0001c0001t0001g0030 a0001c0002t0001g0228 a0001c0002t0002g0002 others(98): Show |
114 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.53-5799A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771052 | |||||||
| chr2:28771053 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-5798C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771053 | |||||||
| chr2:28771055 | C | CT | 27 | a0001c0001t0001g0104 a0001c0001t0001g0116 a0001c0001t0001g0129 others(24): Show |
28 | HG00438.hp2 HG00673.hp1 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.53-5781dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771055 | ||||||
| chr2:28771055 | C | CTT | 10 | a0001c0002t0002g0048 a0001c0002t0002g0086 a0001c0002t0002g0218 others(7): Show |
10 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-5782_53-5781dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771055 | ||||||
| chr2:28771055 | C | T | 110 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(107): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.53-5796C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771055 | |||||||
| chr2:28771056 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-5795T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771056 | |||||||
| chr2:28771109 | A | G | 42 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(39): Show |
49 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.53-5742A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771109 | |||||||
| chr2:28771226 | G | C | 4 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0033g0213 others(1): Show |
5 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-5625G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771226 | |||||||
| chr2:28771243 | G | T | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.53-5608G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771243 | |||||||
| chr2:28771298 | A | G | 214 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(211): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.53-5553A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771298 | |||||||
| chr2:28771310 | C | G | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5541C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771310 | |||||||
| chr2:28771338 | A | G | 1 | a0001c0002t0002g0006 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.53-5513A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771338 | |||||||
| chr2:28771347 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.53-5504G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771347 | |||||||
| chr2:28771416 | C | CAT | 126 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(123): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.53-5434_53-5433dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771416 | ||||||
| chr2:28771478 | C | T | 1 | a0001c0001t0001g0151 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.53-5373C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771478 | |||||||
| chr2:28771604 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0278 a0001c0001t0001g0311 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-5247A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771604 | |||||||
| chr2:28771671 | G | T | 58 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(55): Show |
69 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.53-5180G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28771671 | |||||||
| chr2:28771975 | C | CA | 62 | a0001c0001t0001g0107 a0001c0001t0001g0277 a0001c0001t0001g0307 others(59): Show |
72 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.53-4861dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771975 | ||||||
| chr2:28771975 | CA | C | 85 | a0001c0001t0001g0128 a0001c0002t0001g0228 a0001c0002t0002g0002 others(82): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.53-4861delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28771975 | ||||||
| chr2:28772055 | G | A | 1 | a0001c0001t0005g0258 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.53-4796G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772055 | |||||||
| chr2:28772081 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-4770C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772081 | |||||||
| chr2:28772114 | C | T | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-4737C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772114 | |||||||
| chr2:28772115 | G | A | 5 | a0001c0001t0004g0031 a0001c0001t0013g0003 a0001c0001t0013g0033 others(2): Show |
7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-4736G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772115 | |||||||
| chr2:28772190 | C | T | 2 | a0001c0001t0013g0003 a0001c0001t0013g0033 |
4 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-4661C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772190 | |||||||
| chr2:28772286 | G | A | 1 | a0001c0002t0024g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.53-4565G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772286 | |||||||
| chr2:28772311 | A | T | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.53-4540A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772311 | |||||||
| chr2:28772360 | A | G | 83 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(80): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.53-4491A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772360 | |||||||
| chr2:28772566 | C | T | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-4285C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772566 | |||||||
| chr2:28772594 | G | A | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-4257G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772594 | |||||||
| chr2:28772657 | A | C | 54 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(51): Show |
64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53-4194A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772657 | |||||||
| chr2:28772680 | C | T | 3 | a0001c0002t0003g0015 a0001c0002t0003g0184 a0001c0002t0003g0185 |
4 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-4171C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772680 | |||||||
| chr2:28772746 | T | C | 2 | a0001c0002t0002g0162 a0001c0002t0009g0161 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.53-4105T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772746 | |||||||
| chr2:28772959 | C | G | 2 | a0001c0001t0016g0141 a0001c0001t0016g0150 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53-3892C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28772959 | |||||||
| chr2:28773083 | G | A | 4 | a0001c0002t0002g0054 a0001c0002t0002g0087 a0001c0002t0002g0096 others(1): Show |
4 | HG00099.hp1 HG00280.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-3768G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773083 | |||||||
| chr2:28773088 | A | G | 1 | a0001c0002t0037g0330 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.53-3763A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773088 | |||||||
| chr2:28773131 | A | G | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-3720A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773131 | |||||||
| chr2:28773159 | A | G | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-3692A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773159 | |||||||
| chr2:28773229 | T | C | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.53-3622T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773229 | |||||||
| chr2:28773429 | G | A | 195 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(192): Show |
212 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.53-3422G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773429 | |||||||
| chr2:28773525 | G | C | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.53-3326G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773525 | |||||||
| chr2:28773589 | A | G | 2 | a0001c0002t0002g0217 a0001c0002t0002g0218 |
2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.53-3262A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773589 | |||||||
| chr2:28773670 | CT | C | 213 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(210): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.53-3174delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28773670 | ||||||
| chr2:28773703 | A | T | 1 | a0001c0002t0010g0060 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.53-3148A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773703 | |||||||
| chr2:28773757 | T | C | 1 | a0001c0001t0005g0272 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.53-3094T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773757 | |||||||
| chr2:28773795 | A | G | 1 | a0001c0002t0003g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.53-3056A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773795 | |||||||
| chr2:28773802 | T | C | 1 | a0001c0001t0004g0244 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.53-3049T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773802 | |||||||
| chr2:28773964 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0310 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2887A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28773964 | |||||||
| chr2:28774133 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0006g0026 |
2 | HG02145.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-2718G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774133 | |||||||
| chr2:28774135 | G | C | 213 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(210): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.53-2716G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774135 | |||||||
| chr2:28774143 | T | C | 1 | a0001c0002t0002g0095 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.53-2708T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774143 | |||||||
| chr2:28774262 | A | G | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2589A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774262 | |||||||
| chr2:28774274 | G | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(150): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.53-2577G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774274 | |||||||
| chr2:28774307 | A | G | 1 | a0001c0002t0002g0055 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.53-2544A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774307 | |||||||
| chr2:28774316 | A | G | 2 | a0001c0001t0004g0031 a0001c0001t0036g0032 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-2535A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774316 | |||||||
| chr2:28774435 | T | C | 1 | a0001c0002t0002g0067 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.53-2416T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774435 | |||||||
| chr2:28774575 | G | A | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0310 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2276G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774575 | |||||||
| chr2:28774674 | C | T | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-2177C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774674 | |||||||
| chr2:28774931 | A | C | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.53-1920A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774931 | |||||||
| chr2:28774969 | C | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(150): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.53-1882C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28774969 | |||||||
| chr2:28775070 | A | G | 54 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(51): Show |
64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.53-1781A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775070 | |||||||
| chr2:28775211 | G | C | 141 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(138): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.53-1640G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775211 | |||||||
| chr2:28775271 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.53-1580C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775271 | |||||||
| chr2:28775322 | C | T | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.53-1529C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775322 | |||||||
| chr2:28775553 | C | T | 1 | a0001c0001t0001g0287 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.53-1298C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775553 | |||||||
| chr2:28775580 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.53-1271C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775580 | |||||||
| chr2:28775765 | G | A | 1 | a0001c0001t0038g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.53-1086G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775765 | |||||||
| chr2:28775879 | C | T | 1 | a0001c0002t0014g0212 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.53-972C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775879 | |||||||
| chr2:28775880 | T | G | 1 | a0001c0001t0012g0321 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.53-971T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775880 | |||||||
| chr2:28775977 | T | G | 7 | a0001c0002t0002g0091 a0001c0002t0002g0171 a0001c0002t0002g0172 others(4): Show |
7 | HG01496.hp2 HG02559.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-874T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28775977 | |||||||
| chr2:28776237 | TTTG | T | 5 | a0001c0001t0004g0031 a0001c0001t0013g0003 a0001c0001t0013g0033 others(2): Show |
7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-605_53-603delGT others(1): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 28776237 | ||||||
| chr2:28776266 | T | G | 1 | a0001c0002t0002g0095 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.53-585T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776266 | |||||||
| chr2:28776269 | T | G | 2 | a0001c0001t0001g0050 a0001c0001t0001g0120 |
2 | HG00558.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.53-582T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776269 | |||||||
| chr2:28776292 | C | T | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.53-559C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776292 | |||||||
| chr2:28776318 | A | C | 1 | a0001c0002t0002g0067 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.53-533A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776318 | |||||||
| chr2:28776319 | A | G | 2 | a0001c0002t0002g0054 a0001c0002t0002g0087 |
2 | HG00099.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.53-532A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776319 | |||||||
| chr2:28776411 | G | A | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.53-440G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776411 | |||||||
| chr2:28776419 | A | G | 326 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(323): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.53-432A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776419 | |||||||
| chr2:28776470 | A | G | 213 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(210): Show |
234 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.53-381A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 1/7 | chr2 | 28776470 | |||||||
| chr2:28777077 | A | G | 2 | a0001c0002t0002g0084 a0001c0002t0002g0085 |
2 | HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.184+95A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777077 | |||||||
| chr2:28777127 | CTT | C | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+146_184+147del others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777127 | |||||||
| chr2:28777269 | G | A | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.184+287G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777269 | |||||||
| chr2:28777309 | G | A | 1 | a0001c0002t0003g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.184+327G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777309 | |||||||
| chr2:28777312 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.184+330A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777312 | |||||||
| chr2:28777421 | C | T | 79 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(76): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.184+439C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777421 | |||||||
| chr2:28777652 | T | G | 5 | a0001c0001t0004g0240 a0001c0001t0026g0241 a0001c0002t0004g0025 others(2): Show |
6 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+670T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777652 | |||||||
| chr2:28777792 | A | G | 8 | a0001c0002t0008g0035 a0001c0002t0008g0036 a0001c0002t0008g0037 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+810A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777792 | |||||||
| chr2:28777874 | G | A | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.184+892G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777874 | |||||||
| chr2:28777924 | G | A | 4 | a0001c0001t0001g0277 a0001c0001t0001g0307 a0001c0001t0001g0308 others(1): Show |
4 | HG02055.hp1 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-885G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28777924 | |||||||
| chr2:28778596 | G | T | 1 | a0001c0001t0027g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.185-213G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28778596 | |||||||
| chr2:28778649 | C | T | 2 | a0001c0002t0002g0096 a0001c0002t0002g0097 |
2 | HG00280.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.185-160C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28778649 | |||||||
| chr2:28778665 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.185-144C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 2/7 | chr2 | 28778665 | |||||||
| chr2:28779125 | A | C | 4 | a0001c0002t0002g0054 a0001c0002t0002g0087 a0001c0002t0002g0096 others(1): Show |
4 | HG00099.hp1 HG00280.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.415+86A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779125 | |||||||
| chr2:28779295 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.415+256A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779295 | |||||||
| chr2:28779346 | T | G | 5 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0031g0331 others(2): Show |
6 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+307T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779346 | |||||||
| chr2:28779367 | G | T | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.415+328G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779367 | |||||||
| chr2:28779635 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.415+596A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779635 | |||||||
| chr2:28779834 | A | G | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.415+795A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779834 | |||||||
| chr2:28779838 | G | T | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.415+799G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28779838 | |||||||
| chr2:28780034 | A | G | 2 | a0001c0001t0001g0309 a0001c0002t0001g0228 |
2 | HG02615.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.415+995A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780034 | |||||||
| chr2:28780052 | CTTTCTTT | C | 8 | a0001c0001t0012g0296 a0001c0001t0012g0314 a0001c0001t0012g0316 others(5): Show |
8 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.415+1029_415+1035d others(9): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780052 | ||||||
| chr2:28780084 | C | CT | 84 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(81): Show |
92 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.415+1066dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | ||||||
| chr2:28780084 | C | CTT | 6 | a0001c0001t0001g0050 a0001c0001t0001g0125 a0001c0001t0001g0126 others(3): Show |
6 | HG01109.hp2 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+1065_415+1066d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | ||||||
| chr2:28780084 | CT | C | 11 | a0001c0001t0001g0250 a0001c0001t0001g0255 a0001c0001t0001g0259 others(8): Show |
11 | HG01515.hp2 HG01928.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.415+1066delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | ||||||
| chr2:28780084 | CTTTTTTT others(3): Show |
C | 58 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(55): Show |
69 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.415+1057_415+1066d others(12): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | ||||||
| chr2:28780084 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0035g0280 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.415+1056_415+1066d others(13): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780084 | ||||||
| chr2:28780087 | T | TC | 3 | a0001c0002t0002g0083 a0001c0002t0002g0087 a0001c0002t0002g0163 |
3 | HG01069.hp1 HG01361.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.415+1048_415+1049i others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780087 | |||||||
| chr2:28780088 | T | C | 79 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(76): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.415+1049T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780088 | |||||||
| chr2:28780089 | T | C | 2 | a0001c0002t0002g0067 a0001c0002t0002g0088 |
2 | HG01515.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.415+1050T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780089 | |||||||
| chr2:28780174 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0138 |
2 | NA18959.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.415+1135C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780174 | |||||||
| chr2:28780348 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.415+1309C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780348 | |||||||
| chr2:28780487 | A | T | 1 | a0001c0002t0003g0185 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.416-1251A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780487 | |||||||
| chr2:28780585 | G | A | 25 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(22): Show |
30 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.416-1153G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780585 | |||||||
| chr2:28780598 | TG | T | 3 | a0001c0002t0003g0015 a0001c0002t0003g0184 a0001c0002t0003g0185 |
4 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-1136delG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780598 | ||||||
| chr2:28780601 | G | T | 3 | a0001c0002t0003g0015 a0001c0002t0003g0184 a0001c0002t0003g0185 |
4 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-1137G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780601 | |||||||
| chr2:28780712 | G | A | 1 | a0001c0002t0002g0074 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.416-1026G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780712 | |||||||
| chr2:28780847 | A | G | 1 | a0001c0001t0005g0272 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.416-891A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780847 | |||||||
| chr2:28780892 | T | C | 58 | a0001c0001t0001g0010 a0001c0001t0001g0145 a0001c0001t0001g0151 others(55): Show |
69 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.416-846T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28780892 | |||||||
| chr2:28780921 | CTAGT | C | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.416-814_416-811del others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 28780921 | ||||||
| chr2:28781071 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0145 a0001c0001t0001g0151 others(2): Show |
6 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-667C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781071 | |||||||
| chr2:28781154 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.416-584G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781154 | |||||||
| chr2:28781180 | C | T | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.416-558C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781180 | |||||||
| chr2:28781302 | G | C | 1 | a0001c0001t0005g0326 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.416-436G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781302 | |||||||
| chr2:28781348 | A | G | 2 | a0001c0001t0004g0031 a0001c0001t0036g0032 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.416-390A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781348 | |||||||
| chr2:28781433 | T | C | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.416-305T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781433 | |||||||
| chr2:28781583 | G | A | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.416-155G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781583 | |||||||
| chr2:28781718 | T | A | 1 | a0001c0002t0007g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.416-20T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781718 | |||||||
| chr2:28781721 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.416-17A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 3/7 | chr2 | 28781721 | |||||||
| chr2:28782032 | T | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0278 a0001c0001t0001g0311 others(3): Show |
6 | HG01891.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.520+190T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782032 | |||||||
| chr2:28782057 | G | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(330): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.520+215G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782057 | |||||||
| chr2:28782061 | T | A | 1 | a0001c0002t0003g0190 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.520+219T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782061 | |||||||
| chr2:28782360 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.520+518G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782360 | |||||||
| chr2:28782479 | T | C | 4 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0031g0331 others(1): Show |
5 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.520+637T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782479 | |||||||
| chr2:28782491 | T | A | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.520+649T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782491 | |||||||
| chr2:28782624 | A | C | 5 | a0001c0002t0002g0057 a0001c0002t0010g0059 a0001c0002t0010g0062 others(2): Show |
5 | NA18959.hp1 NA18977.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.520+782A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782624 | |||||||
| chr2:28782650 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.520+808G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782650 | |||||||
| chr2:28782665 | G | A | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.520+823G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782665 | |||||||
| chr2:28782734 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.520+892C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782734 | |||||||
| chr2:28782736 | G | A | 150 | a0001c0001t0001g0030 a0001c0001t0004g0028 a0001c0001t0004g0031 others(147): Show |
168 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.520+894G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28782736 | |||||||
| chr2:28783004 | C | T | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.521-903C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783004 | |||||||
| chr2:28783496 | G | A | 2 | a0001c0001t0004g0031 a0001c0001t0036g0032 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.521-411G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783496 | |||||||
| chr2:28783572 | A | G | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.521-335A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783572 | |||||||
| chr2:28783629 | C | A | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.521-278C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783629 | |||||||
| chr2:28783650 | G | A | 19 | a0001c0001t0001g0274 a0001c0001t0001g0299 a0001c0001t0001g0300 others(16): Show |
20 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.521-257G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783650 | |||||||
| chr2:28783714 | G | A | 3 | a0001c0002t0008g0037 a0001c0002t0008g0038 a0001c0002t0008g0039 |
3 | HG02109.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.521-193G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783714 | |||||||
| chr2:28783725 | G | C | 142 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.521-182G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | chr2 | 28783725 | |||||||
| chr2:28783757 | G | GA | 58 | a0001c0002t0001g0228 a0001c0002t0003g0005 a0001c0002t0003g0015 others(55): Show |
69 | HG00438.hp2 HG00609.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.521-138dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 28783757 | ||||||
| chr2:28784096 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.592+118C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784096 | |||||||
| chr2:28784117 | C | T | 5 | a0001c0001t0004g0031 a0001c0001t0013g0003 a0001c0001t0013g0033 others(2): Show |
7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+139C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784117 | |||||||
| chr2:28784168 | C | T | 5 | a0001c0001t0004g0031 a0001c0001t0013g0003 a0001c0001t0013g0033 others(2): Show |
7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+190C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784168 | |||||||
| chr2:28784169 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.592+191G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784169 | |||||||
| chr2:28784402 | C | T | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.592+424C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784402 | |||||||
| chr2:28784472 | C | T | 4 | a0001c0002t0002g0054 a0001c0002t0002g0087 a0001c0002t0002g0096 others(1): Show |
4 | HG00099.hp1 HG00280.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+494C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784472 | |||||||
| chr2:28784483 | T | C | 142 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.592+505T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784483 | |||||||
| chr2:28784509 | C | T | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.592+531C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784509 | |||||||
| chr2:28784709 | G | A | 9 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(6): Show |
11 | HG01884.hp2 HG02055.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.592+731G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784709 | |||||||
| chr2:28784779 | G | A | 1 | a0001c0002t0002g0084 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.592+801G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784779 | |||||||
| chr2:28784917 | C | CA | 93 | a0001c0001t0001g0222 a0001c0001t0001g0274 a0001c0001t0001g0299 others(90): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.592+956dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784917 | ||||||
| chr2:28784917 | C | CAA | 12 | a0001c0001t0001g0030 a0001c0001t0013g0033 a0001c0002t0002g0043 others(9): Show |
13 | HG00733.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.592+955_592+956dup others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784917 | ||||||
| chr2:28784917 | C | CAAA | 42 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(39): Show |
50 | HG00438.hp2 HG00558.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.592+954_592+956dup others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784917 | ||||||
| chr2:28784917 | C | CAAAA | 11 | a0001c0002t0003g0184 a0001c0002t0003g0191 a0001c0002t0003g0192 others(8): Show |
13 | HG01243.hp2 HG01978.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.592+953_592+956dup others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784917 | ||||||
| chr2:28784930 | A | G | 2 | a0001c0002t0001g0228 a0001c0002t0008g0038 |
2 | HG03098.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.592+952A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784930 | |||||||
| chr2:28784942 | GA | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(172): Show |
185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.592+967delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28784942 | ||||||
| chr2:28784989 | C | G | 83 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(80): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.592+1011C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28784989 | |||||||
| chr2:28785065 | C | CT | 63 | a0001c0001t0001g0011 a0001c0001t0001g0050 a0001c0001t0001g0098 others(60): Show |
64 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.592+1115dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTT | 15 | a0001c0001t0001g0104 a0001c0001t0001g0129 a0001c0001t0001g0149 others(12): Show |
15 | HG01109.hp1 HG01346.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.592+1114_592+1115d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0008g0170 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.592+1106_592+1115d others(12): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(4): Show |
7 | a0001c0001t0001g0030 a0001c0002t0002g0057 a0001c0002t0002g0087 others(4): Show |
7 | HG00673.hp1 HG02145.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.592+1105_592+1115d others(13): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(5): Show |
4 | a0001c0002t0002g0217 a0001c0002t0002g0218 a0001c0002t0010g0062 others(1): Show |
4 | HG01496.hp2 HG03209.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+1104_592+1115d others(14): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(6): Show |
3 | a0001c0002t0002g0096 a0001c0002t0008g0160 a0001c0002t0010g0059 |
3 | HG00280.hp2 HG03486.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.592+1103_592+1115d others(15): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(7): Show |
1 | a0001c0002t0008g0035 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.592+1102_592+1115d others(16): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(8): Show |
3 | a0001c0002t0002g0049 a0001c0002t0002g0078 a0001c0002t0008g0036 |
3 | HG02572.hp1 HG02897.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.592+1101_592+1115d others(17): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(9): Show |
5 | a0001c0002t0002g0164 a0001c0002t0002g0165 a0001c0002t0008g0038 others(2): Show |
5 | HG02109.hp1 HG03098.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.592+1100_592+1115d others(18): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(10): Show |
3 | a0001c0002t0002g0008 a0001c0002t0002g0084 a0001c0002t0009g0068 |
4 | HG01081.hp2 NA18955.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+1099_592+1115d others(19): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(11): Show |
3 | a0001c0002t0002g0069 a0001c0002t0002g0070 a0001c0002t0002g0085 |
3 | HG00735.hp2 NA18953.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.592+1098_592+1115d others(20): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(12): Show |
2 | a0001c0002t0002g0086 a0001c0002t0020g0052 |
2 | NA19000.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.592+1097_592+1115d others(21): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(13): Show |
1 | a0001c0002t0002g0071 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.592+1096_592+1115d others(22): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(14): Show |
2 | a0001c0002t0002g0067 a0001c0002t0002g0095 |
2 | HG00738.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.592+1095_592+1115d others(23): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(15): Show |
2 | a0001c0002t0002g0055 a0001c0002t0002g0088 |
2 | NA18971.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.592+1094_592+1115d others(24): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(16): Show |
2 | a0001c0002t0002g0065 a0001c0002t0009g0161 |
2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.592+1093_592+1115d others(25): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(17): Show |
3 | a0001c0002t0002g0079 a0001c0002t0002g0162 a0001c0002t0008g0037 |
3 | HG01258.hp1 HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.592+1092_592+1115d others(26): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(18): Show |
2 | a0001c0002t0002g0051 a0001c0002t0002g0171 |
2 | HG02615.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.592+1091_592+1115d others(27): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(19): Show |
3 | a0001c0002t0002g0047 a0001c0002t0002g0048 a0001c0002t0002g0080 |
3 | HG00323.hp1 HG02257.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.592+1090_592+1115d others(28): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(20): Show |
1 | a0001c0002t0002g0220 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.592+1089_592+1115d others(29): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(22): Show |
1 | a0001c0002t0002g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(31): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(23): Show |
1 | a0001c0002t0002g0081 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.592+1115_592+1116i others(32): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(26): Show |
2 | a0001c0002t0002g0006 a0001c0002t0002g0082 |
3 | HG01069.hp2 HG01071.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.592+1115_592+1116i others(35): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(28): Show |
1 | a0001c0001t0004g0031 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(37): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(29): Show |
2 | a0001c0002t0002g0072 a0001c0002t0002g0163 |
2 | HG01361.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.592+1115_592+1116i others(38): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(30): Show |
1 | a0001c0002t0002g0172 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(39): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(32): Show |
1 | a0001c0002t0024g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(41): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(33): Show |
1 | a0001c0002t0002g0166 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.592+1115_592+1116i others(42): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(35): Show |
2 | a0001c0002t0002g0041 a0001c0002t0002g0073 |
2 | HG03130.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.592+1115_592+1116i others(44): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(38): Show |
1 | a0001c0002t0008g0159 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.592+1115_592+1116i others(47): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | C | CTTTTTTT others(42): Show |
1 | a0001c0002t0002g0043 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.592+1115_592+1116i others(51): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | CT | C | 31 | a0001c0001t0001g0040 a0001c0001t0001g0246 a0001c0001t0001g0309 others(28): Show |
38 | HG00558.hp2 HG01074.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.592+1115delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | CTT | C | 6 | a0001c0002t0002g0044 a0001c0002t0002g0056 a0001c0002t0002g0063 others(3): Show |
6 | HG01175.hp2 HG02145.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.592+1114_592+1115d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0004g0028 a0001c0002t0002g0075 |
2 | HG00639.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.592+1106_592+1115d others(12): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0001g0029 a0001c0001t0013g0003 a0001c0001t0013g0033 others(3): Show |
9 | HG00099.hp2 HG01884.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.592+1105_592+1115d others(13): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785065 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0108 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.592+1098_592+1115d others(20): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785065 | ||||||
| chr2:28785220 | G | A | 1 | a0001c0002t0003g0209 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.592+1242G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785220 | |||||||
| chr2:28785223 | C | T | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.592+1245C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785223 | |||||||
| chr2:28785309 | T | C | 151 | a0001c0001t0001g0030 a0001c0001t0004g0028 a0001c0001t0004g0031 others(148): Show |
169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.592+1331T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785309 | |||||||
| chr2:28785354 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(15): Show |
21 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.592+1376G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785354 | |||||||
| chr2:28785451 | G | T | 1 | a0001c0001t0038g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.592+1473G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785451 | |||||||
| chr2:28785534 | T | C | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.592+1556T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785534 | |||||||
| chr2:28785559 | T | A | 88 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(85): Show |
94 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.592+1581T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785559 | |||||||
| chr2:28785657 | A | AT | 7 | a0001c0001t0001g0125 a0001c0002t0001g0228 a0001c0002t0003g0017 others(4): Show |
8 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.592+1690dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785657 | ||||||
| chr2:28785668 | T | A | 49 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(46): Show |
58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.592+1690T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785668 | |||||||
| chr2:28785693 | C | T | 2 | a0001c0002t0003g0200 a0001c0002t0037g0330 |
2 | HG01934.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.592+1715C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28785693 | |||||||
| chr2:28785801 | CCT | C | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.592+1828_592+1829d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28785801 | ||||||
| chr2:28786132 | A | C | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.592+2154A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786132 | |||||||
| chr2:28786183 | G | A | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.592+2205G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786183 | |||||||
| chr2:28786223 | C | A | 87 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(84): Show |
93 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.592+2245C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786223 | |||||||
| chr2:28786314 | A | G | 37 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(34): Show |
43 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.592+2336A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786314 | |||||||
| chr2:28786554 | T | C | 1 | a0001c0001t0001g0283 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.593-2104T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786554 | |||||||
| chr2:28786769 | C | T | 5 | a0001c0001t0001g0281 a0001c0001t0001g0282 a0001c0001t0001g0283 others(2): Show |
5 | NA18940.hp1 NA18951.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1889C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786769 | |||||||
| chr2:28786774 | C | CA | 23 | a0001c0001t0001g0274 a0001c0001t0001g0302 a0001c0001t0001g0306 others(20): Show |
27 | HG01243.hp2 HG01934.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.593-1863dupA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | ||||||
| chr2:28786774 | C | CAAA | 26 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0018 others(23): Show |
31 | HG00438.hp2 HG00609.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.593-1865_593-1863d others(5): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | ||||||
| chr2:28786774 | C | CAAAA | 17 | a0001c0001t0001g0128 a0001c0001t0001g0230 a0001c0001t0001g0247 others(14): Show |
18 | HG00558.hp2 HG01169.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.593-1866_593-1863d others(6): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | ||||||
| chr2:28786774 | C | CAAAAA | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(106): Show |
118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.593-1867_593-1863d others(7): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | ||||||
| chr2:28786774 | C | CAAAAAA | 28 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0102 others(25): Show |
28 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.593-1868_593-1863d others(8): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | ||||||
| chr2:28786774 | CA | C | 8 | a0001c0001t0001g0125 a0001c0001t0006g0156 a0001c0002t0002g0053 others(5): Show |
8 | HG00099.hp1 HG00280.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.593-1863delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | ||||||
| chr2:28786774 | CAA | C | 82 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(79): Show |
88 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.593-1864_593-1863d others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28786774 | ||||||
| chr2:28786797 | A | G | 1 | a0001c0002t0009g0046 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.593-1861A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786797 | |||||||
| chr2:28786934 | A | G | 1 | a0001c0002t0008g0039 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.593-1724A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786934 | |||||||
| chr2:28786974 | A | T | 142 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.593-1684A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28786974 | |||||||
| chr2:28787157 | C | T | 3 | a0001c0001t0013g0003 a0001c0001t0013g0033 a0001c0001t0038g0034 |
5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1501C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787157 | |||||||
| chr2:28787188 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.593-1470G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787188 | |||||||
| chr2:28787200 | T | C | 142 | a0001c0002t0001g0228 a0001c0002t0002g0002 a0001c0002t0002g0006 others(139): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.593-1458T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787200 | |||||||
| chr2:28787226 | G | A | 2 | a0001c0002t0002g0162 a0001c0002t0009g0161 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.593-1432G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787226 | |||||||
| chr2:28787230 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.593-1428C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787230 | |||||||
| chr2:28787320 | G | A | 1 | a0001c0002t0002g0220 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.593-1338G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787320 | |||||||
| chr2:28787351 | C | G | 4 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0033g0213 others(1): Show |
5 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.593-1307C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787351 | |||||||
| chr2:28787445 | C | T | 1 | a0001c0002t0002g0045 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.593-1213C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787445 | |||||||
| chr2:28787473 | G | A | 141 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(138): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.593-1185G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787473 | |||||||
| chr2:28787487 | C | T | 1 | a0001c0001t0038g0034 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.593-1171C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787487 | |||||||
| chr2:28787516 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.593-1142C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787516 | |||||||
| chr2:28787651 | A | G | 83 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(80): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.593-1007A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787651 | |||||||
| chr2:28787709 | A | G | 2 | a0001c0002t0039g0090 a0001c0002t0040g0089 |
2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.593-949A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787709 | |||||||
| chr2:28787711 | G | A | 1 | a0001c0001t0006g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.593-947G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787711 | |||||||
| chr2:28787825 | T | C | 1 | a0001c0001t0004g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.593-833T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787825 | |||||||
| chr2:28787844 | A | G | 8 | a0001c0001t0012g0296 a0001c0001t0012g0314 a0001c0001t0012g0316 others(5): Show |
8 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.593-814A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787844 | |||||||
| chr2:28787951 | A | G | 1 | a0001c0002t0002g0045 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.593-707A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787951 | |||||||
| chr2:28787960 | A | G | 49 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(46): Show |
58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.593-698A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787960 | |||||||
| chr2:28787989 | A | T | 2 | a0001c0002t0003g0205 a0001c0002t0003g0206 |
2 | NA18942.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.593-669A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28787989 | |||||||
| chr2:28788022 | T | C | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.593-636T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788022 | |||||||
| chr2:28788072 | C | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0129 |
2 | NA18974.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.593-586C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788072 | |||||||
| chr2:28788221 | G | A | 49 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(46): Show |
58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.593-437G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788221 | |||||||
| chr2:28788275 | GAAA | G | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.593-382_593-380del others(3): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788275 | |||||||
| chr2:28788404 | T | C | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.593-254T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | chr2 | 28788404 | |||||||
| chr2:28788471 | TTGTA | T | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.593-184_593-181del others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 28788471 | ||||||
| chr2:28788869 | G | A | 1 | a0001c0002t0002g0057 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.744+60G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788869 | |||||||
| chr2:28788914 | A | G | 1 | a0001c0001t0004g0103 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.744+105A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788914 | |||||||
| chr2:28788922 | A | G | 1 | a0001c0001t0004g0031 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.744+113A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788922 | |||||||
| chr2:28788980 | C | T | 2 | a0001c0001t0004g0031 a0001c0001t0036g0032 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.744+171C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788980 | |||||||
| chr2:28788985 | G | A | 1 | a0001c0002t0002g0054 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.744+176G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788985 | |||||||
| chr2:28788987 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.744+178A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28788987 | |||||||
| chr2:28789031 | A | C | 1 | a0001c0002t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.744+222A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789031 | |||||||
| chr2:28789179 | T | C | 1 | a0001c0002t0003g0193 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.744+370T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789179 | |||||||
| chr2:28789335 | C | T | 5 | a0001c0002t0003g0017 a0001c0002t0003g0194 a0001c0002t0003g0198 others(2): Show |
6 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+526C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789335 | |||||||
| chr2:28789400 | G | A | 2 | a0001c0001t0001g0292 a0001c0001t0001g0293 |
2 | HG00621.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.744+591G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789400 | |||||||
| chr2:28789510 | A | G | 1 | a0001c0002t0034g0058 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.744+701A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789510 | |||||||
| chr2:28789565 | T | G | 6 | a0001c0002t0003g0017 a0001c0002t0003g0194 a0001c0002t0003g0198 others(3): Show |
7 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+756T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789565 | |||||||
| chr2:28789588 | T | C | 5 | a0001c0002t0003g0017 a0001c0002t0003g0194 a0001c0002t0003g0198 others(2): Show |
6 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+779T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789588 | |||||||
| chr2:28789593 | A | AT | 11 | a0001c0001t0001g0106 a0001c0001t0001g0113 a0001c0001t0001g0114 others(8): Show |
11 | HG00544.hp1 HG00621.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.744+807dupT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28789593 | ||||||
| chr2:28789593 | AT | A | 89 | a0001c0001t0001g0030 a0001c0001t0001g0247 a0001c0001t0001g0281 others(86): Show |
97 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.744+807delT | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28789593 | ||||||
| chr2:28789593 | ATTTTT | A | 49 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(46): Show |
58 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.744+803_744+807del others(5): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28789593 | ||||||
| chr2:28789619 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.744+810G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789619 | |||||||
| chr2:28789708 | T | C | 149 | a0001c0001t0001g0030 a0001c0001t0004g0028 a0001c0001t0004g0031 others(146): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.744+899T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789708 | |||||||
| chr2:28789711 | G | C | 6 | a0001c0001t0012g0296 a0001c0001t0012g0314 a0001c0001t0012g0318 others(3): Show |
6 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+902G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789711 | |||||||
| chr2:28789791 | G | T | 5 | a0001c0002t0003g0017 a0001c0002t0003g0194 a0001c0002t0003g0198 others(2): Show |
6 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.744+982G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789791 | |||||||
| chr2:28789909 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.744+1100T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789909 | |||||||
| chr2:28789957 | C | A | 2 | a0001c0001t0001g0225 a0001c0001t0006g0233 |
2 | HG03688.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.744+1148C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28789957 | |||||||
| chr2:28789998 | TG | T | 6 | a0001c0002t0003g0017 a0001c0002t0003g0194 a0001c0002t0003g0198 others(3): Show |
7 | HG01099.hp1 HG01099.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.744+1191delG | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28789998 | ||||||
| chr2:28790139 | A | G | 59 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(56): Show |
70 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.744+1330A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790139 | |||||||
| chr2:28790368 | C | G | 2 | a0001c0002t0004g0025 a0001c0002t0004g0329 |
3 | HG02965.hp2 HG03130.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.744+1559C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790368 | |||||||
| chr2:28790411 | C | T | 4 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0033g0213 others(1): Show |
5 | HG01891.hp1 HG01934.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.744+1602C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790411 | |||||||
| chr2:28790525 | A | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0012 others(16): Show |
22 | HG00323.hp2 HG00639.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.744+1716A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790525 | |||||||
| chr2:28790546 | G | C | 53 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(50): Show |
63 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.744+1737G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790546 | |||||||
| chr2:28790741 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0310 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.744+1932A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790741 | |||||||
| chr2:28790911 | A | G | 1 | a0001c0002t0003g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.744+2102A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28790911 | |||||||
| chr2:28791177 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.744+2368C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791177 | |||||||
| chr2:28791325 | G | T | 332 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(329): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.744+2516G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791325 | |||||||
| chr2:28791328 | G | T | 2 | a0001c0002t0033g0213 a0001c0002t0037g0330 |
2 | HG01891.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.744+2519G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791328 | |||||||
| chr2:28791354 | A | G | 1 | a0001c0002t0002g0075 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.745-2509A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791354 | |||||||
| chr2:28791386 | A | G | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.745-2477A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791386 | |||||||
| chr2:28791487 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0133 a0001c0001t0001g0149 |
3 | HG02698.hp1 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.745-2376G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791487 | |||||||
| chr2:28791593 | G | C | 1 | a0001c0002t0002g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.745-2270G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791593 | |||||||
| chr2:28791606 | G | A | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.745-2257G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791606 | |||||||
| chr2:28791880 | C | T | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.745-1983C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28791880 | |||||||
| chr2:28792079 | G | T | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.745-1784G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792079 | |||||||
| chr2:28792167 | C | A | 3 | a0001c0001t0013g0003 a0001c0001t0013g0033 a0001c0001t0038g0034 |
5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.745-1696C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792167 | |||||||
| chr2:28792255 | G | A | 1 | a0001c0002t0010g0059 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.745-1608G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792255 | |||||||
| chr2:28792288 | C | T | 1 | a0001c0002t0007g0178 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.745-1575C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792288 | |||||||
| chr2:28792294 | C | T | 1 | a0001c0001t0006g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.745-1569C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792294 | |||||||
| chr2:28792371 | A | G | 1 | a0001c0001t0001g0274 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.745-1492A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792371 | |||||||
| chr2:28792508 | C | T | 2 | a0001c0001t0004g0031 a0001c0001t0036g0032 |
2 | HG02886.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.745-1355C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792508 | |||||||
| chr2:28792647 | A | G | 2 | a0001c0001t0013g0003 a0001c0001t0013g0033 |
4 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-1216A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792647 | |||||||
| chr2:28792648 | T | A | 55 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0222 others(52): Show |
59 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.745-1215T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792648 | |||||||
| chr2:28792685 | G | A | 4 | a0001c0002t0002g0044 a0001c0002t0002g0045 a0001c0002t0002g0168 others(1): Show |
4 | HG01070.hp2 HG01255.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.745-1178G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792685 | |||||||
| chr2:28792798 | T | C | 1 | a0001c0001t0030g0223 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.745-1065T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792798 | |||||||
| chr2:28792832 | A | G | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.745-1031A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28792832 | |||||||
| chr2:28793079 | G | A | 2 | a0001c0001t0005g0235 a0001c0001t0005g0237 |
2 | NA18963.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.745-784G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793079 | |||||||
| chr2:28793116 | G | C | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.745-747G>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793116 | |||||||
| chr2:28793153 | C | T | 74 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(71): Show |
79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.745-710C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793153 | |||||||
| chr2:28793237 | C | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.745-626C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793237 | |||||||
| chr2:28793367 | A | C | 54 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(51): Show |
64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.745-496A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793367 | |||||||
| chr2:28793396 | TTGTC | T | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.745-464_745-461del others(4): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 28793396 | ||||||
| chr2:28793616 | T | A | 3 | a0001c0002t0003g0199 a0001c0002t0003g0203 a0001c0002t0003g0209 |
3 | HG02258.hp1 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.745-247T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 6/7 | chr2 | 28793616 | |||||||
| chr2:28794083 | G | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0279 others(3): Show |
6 | HG00438.hp1 HG00597.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+86G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794083 | |||||||
| chr2:28794123 | C | T | 8 | a0001c0002t0008g0035 a0001c0002t0008g0036 a0001c0002t0008g0037 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.879+126C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794123 | |||||||
| chr2:28794418 | C | T | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+421C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794418 | |||||||
| chr2:28794419 | G | A | 12 | a0001c0002t0007g0013 a0001c0002t0007g0014 a0001c0002t0007g0175 others(9): Show |
15 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.879+422G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794419 | |||||||
| chr2:28794492 | C | T | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.879+495C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794492 | |||||||
| chr2:28794608 | G | A | 82 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(79): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.879+611G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794608 | |||||||
| chr2:28794615 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.879+618C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794615 | |||||||
| chr2:28794692 | A | C | 12 | a0001c0001t0001g0110 a0001c0001t0001g0114 a0001c0001t0001g0136 others(9): Show |
14 | HG00438.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+695A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794692 | |||||||
| chr2:28794776 | A | T | 8 | a0001c0001t0012g0296 a0001c0001t0012g0314 a0001c0001t0012g0316 others(5): Show |
8 | HG01346.hp1 HG02630.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.879+779A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794776 | |||||||
| chr2:28794815 | G | T | 1 | a0001c0001t0004g0143 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.879+818G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794815 | |||||||
| chr2:28794881 | T | G | 326 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(323): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.879+884T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28794881 | |||||||
| chr2:28795004 | C | T | 54 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(51): Show |
64 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.879+1007C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795004 | |||||||
| chr2:28795025 | A | G | 2 | a0001c0001t0013g0003 a0001c0001t0013g0033 |
4 | HG01884.hp2 HG02451.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+1028A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795025 | |||||||
| chr2:28795176 | T | G | 3 | a0001c0002t0004g0025 a0001c0002t0004g0329 a0001c0002t0037g0330 |
4 | HG01934.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+1179T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795176 | |||||||
| chr2:28795237 | A | T | 2 | a0001c0002t0002g0171 a0001c0002t0002g0172 |
2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.879+1240A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795237 | |||||||
| chr2:28795293 | G | A | 2 | a0001c0001t0001g0257 a0001c0001t0005g0258 |
2 | NA19001.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.879+1296G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795293 | |||||||
| chr2:28795403 | T | C | 2 | a0001c0002t0002g0217 a0001c0002t0002g0218 |
2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.879+1406T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795403 | |||||||
| chr2:28795483 | A | G | 3 | a0001c0001t0004g0028 a0001c0002t0002g0063 a0001c0002t0002g0077 |
3 | HG01257.hp2 HG02055.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.879+1486A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795483 | |||||||
| chr2:28795581 | A | G | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.879+1584A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795581 | |||||||
| chr2:28795860 | T | G | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.879+1863T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28795860 | |||||||
| chr2:28796023 | T | C | 141 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(138): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.879+2026T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796023 | |||||||
| chr2:28796056 | C | T | 1 | a0001c0001t0005g0237 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.879+2059C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796056 | |||||||
| chr2:28796060 | T | C | 5 | a0001c0001t0004g0031 a0001c0001t0013g0003 a0001c0001t0013g0033 others(2): Show |
7 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+2063T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796060 | |||||||
| chr2:28796074 | G | A | 1 | a0001c0002t0002g0064 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.879+2077G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796074 | |||||||
| chr2:28796172 | A | G | 1 | a0001c0002t0022g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.879+2175A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796172 | |||||||
| chr2:28796190 | TA | T | 141 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(138): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.879+2195delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 28796190 | ||||||
| chr2:28796270 | C | T | 1 | a0001c0002t0037g0330 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.879+2273C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796270 | |||||||
| chr2:28796385 | A | G | 1 | a0001c0002t0003g0180 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.879+2388A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796385 | |||||||
| chr2:28796514 | G | T | 3 | a0001c0001t0013g0003 a0001c0001t0013g0033 a0001c0001t0038g0034 |
5 | HG01884.hp2 HG02451.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.879+2517G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796514 | |||||||
| chr2:28796518 | T | A | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.879+2521T>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796518 | |||||||
| chr2:28796700 | T | C | 1 | a0001c0002t0007g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.880-2499T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796700 | |||||||
| chr2:28796723 | A | G | 1 | a0001c0002t0003g0197 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.880-2476A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796723 | |||||||
| chr2:28796775 | T | C | 1 | a0001c0002t0003g0194 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.880-2424T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796775 | |||||||
| chr2:28796854 | A | C | 1 | a0001c0001t0004g0327 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.880-2345A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28796854 | |||||||
| chr2:28797120 | C | A | 1 | a0001c0001t0012g0316 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.880-2079C>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797120 | |||||||
| chr2:28797127 | T | C | 4 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0310 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-2072T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797127 | |||||||
| chr2:28797136 | T | G | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.880-2063T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797136 | |||||||
| chr2:28797186 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.880-2013C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797186 | |||||||
| chr2:28797187 | G | A | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.880-2012G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797187 | |||||||
| chr2:28797305 | C | T | 1 | a0001c0002t0033g0213 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.880-1894C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797305 | |||||||
| chr2:28797413 | A | G | 18 | a0001c0002t0002g0054 a0001c0002t0002g0056 a0001c0002t0002g0057 others(15): Show |
18 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.880-1786A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797413 | |||||||
| chr2:28797436 | A | C | 6 | a0001c0001t0001g0268 a0001c0001t0001g0270 a0001c0001t0001g0279 others(3): Show |
6 | HG00438.hp1 HG00597.hp1 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-1763A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797436 | |||||||
| chr2:28797494 | C | G | 60 | a0001c0002t0003g0005 a0001c0002t0003g0015 a0001c0002t0003g0016 others(57): Show |
71 | HG00438.hp2 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.880-1705C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797494 | |||||||
| chr2:28797514 | A | G | 1 | a0001c0002t0011g0215 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.880-1685A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797514 | |||||||
| chr2:28797725 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.880-1474T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797725 | |||||||
| chr2:28797892 | A | G | 5 | a0001c0001t0005g0235 a0001c0001t0005g0236 a0001c0001t0005g0237 others(2): Show |
5 | HG00544.hp2 NA18944.hp1 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-1307A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797892 | |||||||
| chr2:28797931 | C | T | 1 | a0001c0002t0025g0094 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.880-1268C>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28797931 | |||||||
| chr2:28798292 | C | G | 1 | a0001c0002t0002g0047 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.880-907C>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798292 | |||||||
| chr2:28798365 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0134 |
2 | NA18942.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.880-834A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798365 | |||||||
| chr2:28798645 | GAC | G | 140 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(137): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.880-550_880-549del others(2): Show |
PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 28798645 | ||||||
| chr2:28798664 | G | T | 3 | a0001c0002t0003g0015 a0001c0002t0003g0184 a0001c0002t0003g0185 |
4 | HG02622.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-535G>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798664 | |||||||
| chr2:28798789 | A | C | 1 | a0001c0001t0004g0122 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.880-410A>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798789 | |||||||
| chr2:28798844 | G | A | 1 | a0001c0001t0006g0156 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.880-355G>A | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798844 | |||||||
| chr2:28798948 | CA | C | 140 | a0001c0002t0002g0002 a0001c0002t0002g0006 a0001c0002t0002g0007 others(137): Show |
156 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.880-246delA | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 28798948 | ||||||
| chr2:28798971 | A | G | 12 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0001g0252 others(9): Show |
12 | HG01928.hp1 HG01934.hp2 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.880-228A>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798971 | |||||||
| chr2:28798980 | A | T | 1 | a0001c0002t0031g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.880-219A>T | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28798980 | |||||||
| chr2:28799143 | T | G | 8 | a0001c0002t0008g0035 a0001c0002t0008g0036 a0001c0002t0008g0037 others(5): Show |
8 | HG01074.hp1 HG01106.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-56T>G | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28799143 | |||||||
| chr2:28799195 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02886.hp2 | splice_region_variant&intron_variant | LOW | c.880-4T>C | PPP1CB | ENSG00000213639.11 | transcript | ENST00000395366.3 | protein_coding | 7/7 | chr2 | 28799195 |