Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4148 |
| ensemblid | ENSG00000132031.13 |
| hgncid | 6909 |
| symbol | MATN3 |
| name | matrilin 3 |
| refseq_nuc | NM_002381.5 |
| refseq_prot | NP_002372.1 |
| ensembl_nuc | ENST00000407540.8 |
| ensembl_prot | ENSP00000383894.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 19992052 |
| end | 20012668 |
| strand | - |
| ver | v1.2 |
| region | chr2:19992052-20012668 |
| region5000 | chr2:19987052-20017668 |
| regionname0 | MATN3_chr2_19992052_20012668 |
| regionname5000 | MATN3_chr2_19987052_20017668 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 486 | 415 | 92 | 76 | 188 | 15 | 42 | 146 | MATN3_chr2_19987052_20017668 | MATN3 | MPRPA others(481): Show |
chr2 | 19987052 | 20017668 |
| a0002 | 0/0 | 486 | 6 | 3 | 1 | 1 | 0 | 1 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | MPRPA others(481): Show |
chr2 | 19987052 | 20017668 |
| a0003 | 0/0 | 486 | 5 | 0 | 2 | 0 | 2 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | MPRPA others(481): Show |
chr2 | 19987052 | 20017668 |
| a0004 | 0/0 | 486 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MATN3_chr2_19987052_20017668 | MATN3 | MPRPA others(481): Show |
chr2 | 19987052 | 20017668 |
| a0005 | 0/0 | 486 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | MPRPA others(481): Show |
chr2 | 19987052 | 20017668 |
| a0006 | 0/0 | 486 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | MPRPA others(481): Show |
chr2 | 19987052 | 20017668 |
| a0007 | 0/0 | 486 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | MPRPA others(481): Show |
chr2 | 19987052 | 20017668 |
| a0008 | 0/0 | 486 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | MPRPA others(481): Show |
chr2 | 19987052 | 20017668 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1458 | 198 | 34 | 25 | 121 | 4 | 14 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0001c0002 | 1/1 | 1458 | 158 | 43 | 33 | 55 | 6 | 19 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0001c0003 | 0/0 | 1458 | 57 | 14 | 18 | 12 | 5 | 8 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0001c0010 | 0/0 | 1458 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0001c0012 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0002c0004 | 0/0 | 1458 | 5 | 2 | 1 | 1 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0002c0007 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0003c0005 | 0/0 | 1458 | 5 | 0 | 2 | 0 | 2 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0004c0006 | 0/0 | 1458 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0005c0008 | 0/0 | 1458 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0006c0009 | 0/0 | 1458 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0007c0013 | 0/0 | 1458 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 | ||
| a0008c0011 | 0/0 | 1458 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | ATGCC others(1453): Show |
chr2 | 19987052 | 20017668 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2557 | 190 | 26 | 25 | 121 | 4 | 14 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0001c0001t0002 | 0/0 | 2557 | 8 | 8 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0001c0002t0001 | 0/0 | 2557 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0001c0002t0002 | 1/1 | 2557 | 156 | 41 | 33 | 55 | 6 | 19 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0001c0002t0004 | 0/0 | 2557 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0001c0003t0001 | 0/0 | 2557 | 54 | 11 | 18 | 12 | 5 | 8 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0001c0003t0002 | 0/0 | 2557 | 3 | 3 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0001c0010t0001 | 0/0 | 2557 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0001c0012t0001 | 0/0 | 2557 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0002c0004t0001 | 0/0 | 2557 | 5 | 2 | 1 | 1 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0002c0007t0005 | 0/0 | 2557 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0003c0005t0001 | 0/0 | 2557 | 5 | 0 | 2 | 0 | 2 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0004c0006t0001 | 0/0 | 2557 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0005c0008t0003 | 0/0 | 2557 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0006c0009t0002 | 0/0 | 2557 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0007c0013t0002 | 0/0 | 2557 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| a0008c0011t0001 | 0/0 | 2557 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | GCCCC others(2552): Show |
chr2 | 19987052 | 20017668 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 15 | 0 | 3 | 12 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0059 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0001 | 0/0 | 22 | 4 | 6 | 8 | 1 | 3 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0003 | 0/0 | 9 | 0 | 1 | 7 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0009 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 0 | 1 | 4 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0013 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0048 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0060 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0117 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0002t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0022 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0054 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0003t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0010t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0001c0012t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0002c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0002c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0002c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0002c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0002c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0002c0007t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0003c0005t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0003c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0003c0005t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0004c0006t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0004c0006t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0005c0008t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0006c0009t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0007c0013t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| a0008c0011t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0104 | EUR | GBR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0121 | EUR | GBR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0143 | EUR | GBR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00140 | hp2 | a0003 | c0005 | t0001 | g0131 | EUR | GBR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00280 | hp1 | a0003 | c0005 | t0001 | g0044 | EUR | FIN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0257 | EUR | FIN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0010 | EUR | FIN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00438 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00609 | hp1 | a0001 | c0003 | t0001 | g0274 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00639 | hp1 | a0001 | c0003 | t0001 | g0055 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0282 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0113 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0230 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0122 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0255 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01106 | hp1 | a0003 | c0005 | t0001 | g0165 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01106 | hp2 | a0001 | c0003 | t0001 | g0054 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01109 | hp1 | a0001 | c0003 | t0001 | g0120 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01109 | hp2 | a0001 | c0002 | t0002 | g0100 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0283 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0055 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0053 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01192 | hp2 | a0003 | c0005 | t0001 | g0044 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01243 | hp1 | a0005 | c0008 | t0003 | g0065 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01255 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0253 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0266 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01261 | hp1 | a0002 | c0004 | t0001 | g0063 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0053 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01346 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0273 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0215 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0097 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0265 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0031 | EUR | IBS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0214 | EUR | IBS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0261 | EUR | IBS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0262 | EUR | IBS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | IBS | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0069 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01943 | hp2 | a0001 | c0002 | t0002 | g0013 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01952 | hp1 | a0001 | c0002 | t0002 | g0219 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0205 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01975 | hp1 | a0001 | c0003 | t0001 | g0184 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0109 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01993 | hp2 | a0001 | c0003 | t0001 | g0260 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0185 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02040 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0102 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0240 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0229 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CDX | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | CDX | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | CDX | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0105 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02258 | hp2 | a0006 | c0009 | t0002 | g0107 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0206 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0101 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0233 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02300 | hp1 | a0001 | c0003 | t0001 | g0258 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02451 | hp2 | a0002 | c0007 | t0005 | g0064 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02572 | hp2 | a0002 | c0004 | t0001 | g0062 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0103 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0238 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0270 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0023 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0288 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02698 | hp1 | a0002 | c0004 | t0001 | g0067 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0221 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0204 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0243 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02818 | hp2 | a0001 | c0002 | t0002 | g0227 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0169 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0247 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02922 | hp1 | a0001 | c0012 | t0001 | g0071 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02970 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0096 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0052 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0051 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0226 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0021 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0050 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0008 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0095 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0252 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0208 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0008 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0051 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0015 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0271 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03490 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03491 | hp1 | a0001 | c0003 | t0001 | g0242 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0202 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03492 | hp1 | a0001 | c0003 | t0001 | g0244 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ESN | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03540 | hp1 | a0001 | c0003 | t0002 | g0023 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0248 | AFR | GWD | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0049 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03688 | hp1 | a0001 | c0010 | t0001 | g0228 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03688 | hp2 | a0001 | c0002 | t0002 | g0211 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03704 | hp2 | a0001 | c0003 | t0001 | g0264 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03710 | hp1 | a0003 | c0005 | t0001 | g0166 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0013 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0054 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03942 | hp2 | a0001 | c0002 | t0002 | g0010 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04115 | hp1 | a0001 | c0003 | t0001 | g0245 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0217 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0267 | SAS | BEB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04199 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0010 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0001 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0108 | SAS | STU | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0130 | AFR | YRI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18522 | hp2 | a0001 | c0003 | t0001 | g0086 | AFR | YRI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0239 | AFR | YRI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | YRI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18940 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18943 | hp2 | a0002 | c0004 | t0001 | g0066 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18944 | hp1 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18946 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0212 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18950 | hp2 | a0001 | c0003 | t0001 | g0032 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18953 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18956 | hp2 | a0004 | c0006 | t0001 | g0194 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18970 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18971 | hp1 | a0007 | c0013 | t0002 | g0163 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18975 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0259 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18979 | hp1 | a0001 | c0003 | t0001 | g0269 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0256 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18984 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18997 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19007 | hp1 | a0001 | c0003 | t0001 | g0249 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0116 | AFR | LWK | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19054 | hp2 | a0004 | c0006 | t0001 | g0183 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0162 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0060 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19081 | hp1 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19084 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19086 | hp1 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19089 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0272 | AFR | YRI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | YRI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA20129 | hp2 | a0001 | c0003 | t0002 | g0023 | AFR | ASW | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0218 | EUR | TSI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA20805 | hp2 | a0008 | c0011 | t0001 | g0155 | EUR | TSI | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0246 | AFR | ACB | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | USA | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | USA | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | USA | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0263 | AFR | USA | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA21309 | hp1 | a0002 | c0004 | t0001 | g0061 | AFR | LWK | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0099 | AFR | LWK | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0114 | REF | REF | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0117 | REF | REF | MATN3_chr2_19987052_20017668 | MATN3 | chr2 | 19987052 | 20017668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:19997257 | G | A | 1 | a0006 | 1 | HG02258.hp2 | missense_variant&splice_region_variant | MODERATE | c.1171C>T | p.Arg391Cys | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/8 | 1208/2557 | 1171/1461 | 391/486 | chr2 | 19997257 | |||
| chr2:20003169 | G | A | 1 | a0008 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.908C>T | p.Thr303Met | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/8 | 945/2557 | 908/1461 | 303/486 | chr2 | 20003169 | |||
| chr2:20005780 | C | T | 1 | a0003 | 5 | HG00140.hp2 HG00280.hp1 HG01106.hp1 others(2): Show |
missense_variant | MODERATE | c.754G>A | p.Glu252Lys | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/8 | 791/2557 | 754/1461 | 252/486 | chr2 | 20005780 | |||
| chr2:20005851 | G | A | 1 | a0005 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.683C>T | p.Ala228Val | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/8 | 720/2557 | 683/1461 | 228/486 | chr2 | 20005851 | |||
| chr2:20005875 | A | G | 1 | a0004 | 2 | NA18956.hp2 NA19054.hp2 |
missense_variant | MODERATE | c.659T>C | p.Val220Ala | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/8 | 696/2557 | 659/1461 | 220/486 | chr2 | 20005875 | |||
| chr2:20006235 | G | A | 1 | a0007 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.299C>T | p.Thr100Ile | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/8 | 336/2557 | 299/1461 | 100/486 | chr2 | 20006235 | |||
| chr2:20012445 | A | C | 2 | a0002 a0005 |
7 | HG01243.hp1 HG01261.hp1 HG02451.hp2 others(4): Show |
missense_variant | MODERATE | c.187T>G | p.Ser63Ala | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/8 | 224/2557 | 187/1461 | 63/486 | chr2 | 20012445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:20003168 | C | T | 4 | a0001c0003 a0002c0007 a0004c0006 others(1): Show |
61 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(58): Show |
synonymous_variant | LOW | c.909G>A | p.Thr303Thr | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/8 | 946/2557 | 909/1461 | 303/486 | chr2 | 20003168 | |||
| chr2:20003180 | G | A | 1 | a0001c0012 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.897C>T | p.Ala299Ala | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/8 | 934/2557 | 897/1461 | 299/486 | chr2 | 20003180 | |||
| chr2:20005829 | A | G | 1 | a0001c0010 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.705T>C | p.Ser235Ser | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/8 | 742/2557 | 705/1461 | 235/486 | chr2 | 20005829 | |||
| chr2:20005919 | C | T | 10 | a0001c0001 a0001c0003 a0001c0010 others(7): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
synonymous_variant | LOW | c.615G>A | p.Glu205Glu | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/8 | 652/2557 | 615/1461 | 205/486 | chr2 | 20005919 | |||
| chr2:20006087 | G | A | 10 | a0001c0001 a0001c0003 a0001c0010 others(7): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
synonymous_variant | LOW | c.447C>T | p.Ala149Ala | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/8 | 484/2557 | 447/1461 | 149/486 | chr2 | 20006087 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:19992861 | A | G | 1 | a0001c0002t0004 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*250T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 8/8 | 250 | chr2 | 19992861 | ||||||
| chr2:19992862 | T | C | 1 | a0002c0007t0005 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 8/8 | 249 | chr2 | 19992862 | ||||||
| chr2:19992935 | G | A | 12 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0004 others(9): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
3_prime_UTR_variant | MODIFIER | c.*176C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 8/8 | 176 | chr2 | 19992935 | ||||||
| chr2:19993052 | A | G | 1 | a0005c0008t0003 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*59T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 8/8 | 59 | chr2 | 19993052 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:19993170 | G | A | 89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(86): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
splice_region_variant&intron_variant | LOW | c.1406-4C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19993170 | |||||||
| chr2:19993442 | C | T | 1 | a0001c0001t0001g0028 | 2 | NA18964.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1406-276G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19993442 | |||||||
| chr2:19993673 | C | A | 2 | a0001c0002t0002g0008 a0006c0009t0002g0107 |
6 | HG02258.hp2 HG02451.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406-507G>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19993673 | |||||||
| chr2:19993791 | C | G | 1 | a0001c0001t0001g0196 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1405+508G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19993791 | |||||||
| chr2:19993888 | C | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0038 others(6): Show |
16 | HG01243.hp1 HG01346.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1405+411G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19993888 | |||||||
| chr2:19994065 | A | G | 61 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0028 others(58): Show |
73 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1405+234T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19994065 | |||||||
| chr2:19994161 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1405+138T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19994161 | |||||||
| chr2:19994186 | A | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
7 | HG00609.hp2 HG02135.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1405+113T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19994186 | |||||||
| chr2:19994275 | G | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1405+24C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 7/7 | chr2 | 19994275 | |||||||
| chr2:19994837 | C | T | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1295-428G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19994837 | |||||||
| chr2:19994904 | C | T | 1 | a0001c0002t0002g0030 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1295-495G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19994904 | |||||||
| chr2:19995145 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0125 |
4 | NA18953.hp1 NA18962.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1295-736A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995145 | |||||||
| chr2:19995314 | G | A | 2 | a0001c0001t0001g0098 a0001c0002t0004g0226 |
2 | HG02818.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1295-905C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995314 | |||||||
| chr2:19995322 | C | A | 194 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(191): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.1295-913G>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995322 | |||||||
| chr2:19995447 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1295-1038G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995447 | |||||||
| chr2:19995448 | G | A | 4 | a0001c0003t0001g0270 a0001c0003t0001g0271 a0001c0003t0001g0272 others(1): Show |
4 | HG01167.hp2 HG02615.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1295-1039C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995448 | |||||||
| chr2:19995571 | G | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0070 others(2): Show |
11 | HG01346.hp2 HG01934.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1295-1162C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995571 | |||||||
| chr2:19995677 | T | C | 2 | a0001c0002t0002g0205 a0001c0002t0002g0216 |
2 | HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1295-1268A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995677 | |||||||
| chr2:19995743 | A | G | 5 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0070 others(2): Show |
11 | HG01346.hp2 HG01934.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1295-1334T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995743 | |||||||
| chr2:19995857 | T | G | 2 | a0001c0002t0002g0205 a0001c0002t0002g0216 |
2 | HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1294+1277A>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19995857 | |||||||
| chr2:19996033 | T | A | 1 | a0002c0004t0001g0066 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1294+1101A>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996033 | |||||||
| chr2:19996345 | A | T | 60 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0028 others(57): Show |
72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1294+789T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996345 | |||||||
| chr2:19996350 | A | T | 65 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(62): Show |
83 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1294+784T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996350 | |||||||
| chr2:19996355 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1294+779A>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996355 | |||||||
| chr2:19996470 | C | T | 1 | a0002c0004t0001g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1294+664G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996470 | |||||||
| chr2:19996650 | T | C | 3 | a0002c0004t0001g0061 a0002c0004t0001g0062 a0002c0004t0001g0063 |
3 | HG01261.hp1 HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1294+484A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996650 | |||||||
| chr2:19996662 | A | C | 1 | a0001c0003t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1294+472T>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996662 | |||||||
| chr2:19996733 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG02135.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1294+401C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996733 | |||||||
| chr2:19996923 | A | G | 1 | a0001c0003t0001g0185 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1294+211T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19996923 | |||||||
| chr2:19997006 | C | T | 1 | a0001c0003t0001g0129 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1294+128G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19997006 | |||||||
| chr2:19997038 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1294+96C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 6/7 | chr2 | 19997038 | |||||||
| chr2:19997266 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19055.hp2 | splice_region_variant&intron_variant | LOW | c.1169-7C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19997266 | |||||||
| chr2:19997269 | C | T | 1 | a0001c0002t0002g0215 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1169-10G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19997269 | |||||||
| chr2:19997566 | C | T | 1 | a0001c0002t0002g0267 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1169-307G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19997566 | |||||||
| chr2:19997615 | T | G | 60 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0028 others(57): Show |
72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1169-356A>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19997615 | |||||||
| chr2:19997770 | G | GCA | 162 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1169-513_1169-512d others(4): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19997770 | |||||||
| chr2:19997770 | G | GCACA | 3 | a0001c0001t0001g0027 a0002c0004t0001g0066 a0002c0004t0001g0067 |
4 | HG02698.hp1 NA18942.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169-515_1169-512d others(6): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19997770 | |||||||
| chr2:19997799 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1169-540C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19997799 | |||||||
| chr2:19998090 | A | T | 34 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(31): Show |
64 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1169-831T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998090 | |||||||
| chr2:19998194 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0040 a0001c0001t0001g0135 |
5 | HG02074.hp1 NA18950.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169-935C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998194 | |||||||
| chr2:19998223 | A | AT | 7 | a0001c0002t0002g0020 a0001c0002t0002g0046 a0001c0002t0002g0050 others(4): Show |
11 | HG01255.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1169-965dupA | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998223 | |||||||
| chr2:19998305 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.1169-1046C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998305 | |||||||
| chr2:19998340 | T | C | 61 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0028 others(58): Show |
73 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.1169-1081A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998340 | |||||||
| chr2:19998438 | T | C | 1 | a0001c0002t0002g0247 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1169-1179A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998438 | |||||||
| chr2:19998709 | T | A | 1 | a0001c0001t0001g0038 | 2 | HG01884.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.1169-1450A>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998709 | |||||||
| chr2:19998741 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1169-1482T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998741 | |||||||
| chr2:19998767 | G | GA | 49 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0070 others(46): Show |
73 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1169-1509dupT | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998767 | |||||||
| chr2:19998767 | G | GAA | 40 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(37): Show |
55 | HG00597.hp1 HG01255.hp2 HG01261.hp1 others(52): Show |
intron_variant | MODIFIER | c.1169-1510_1169-150 others(6): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998767 | |||||||
| chr2:19998775 | A | AAAT | 5 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0002t0002g0015 others(2): Show |
7 | HG02055.hp2 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1169-1517_1169-151 others(7): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998775 | |||||||
| chr2:19998775 | A | AAT | 13 | a0001c0001t0001g0147 a0001c0002t0002g0020 a0001c0002t0002g0050 others(10): Show |
17 | HG00099.hp2 HG01256.hp2 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1169-1518_1169-151 others(6): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998775 | |||||||
| chr2:19998775 | A | AT | 94 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0017 others(91): Show |
118 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1169-1517_1169-151 others(5): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998775 | |||||||
| chr2:19998775 | A | T | 2 | a0001c0002t0002g0238 a0001c0003t0001g0243 |
2 | HG02615.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1169-1516T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998775 | |||||||
| chr2:19998776 | AT | A | 2 | a0001c0002t0002g0060 a0001c0002t0002g0113 |
3 | HG00642.hp1 NA19062.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1169-1518delA | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998776 | |||||||
| chr2:19998777 | T | A | 57 | a0001c0001t0001g0038 a0001c0001t0001g0153 a0001c0001t0001g0161 others(54): Show |
117 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.1169-1518A>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19998777 | |||||||
| chr2:19999093 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1168+1348G>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999093 | |||||||
| chr2:19999121 | G | GT | 6 | a0001c0001t0001g0098 a0001c0001t0001g0134 a0001c0003t0001g0086 others(3): Show |
8 | HG02647.hp1 HG02818.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1168+1319dupA | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999121 | |||||||
| chr2:19999131 | A | T | 4 | a0001c0001t0001g0027 a0001c0002t0002g0246 a0001c0002t0002g0247 others(1): Show |
5 | HG02486.hp2 HG02896.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1168+1310T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999131 | |||||||
| chr2:19999328 | A | G | 60 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0028 others(57): Show |
72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1168+1113T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999328 | |||||||
| chr2:19999353 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(13): Show |
40 | HG00408.hp2 HG01243.hp2 HG01928.hp2 others(37): Show |
intron_variant | MODIFIER | c.1168+1088G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999353 | |||||||
| chr2:19999602 | G | A | 1 | a0001c0003t0001g0271 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1168+839C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999602 | |||||||
| chr2:19999626 | T | TA | 57 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0028 others(54): Show |
68 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1168+814dupT | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999626 | |||||||
| chr2:19999626 | TA | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(83): Show |
142 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.1168+814delT | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999626 | |||||||
| chr2:19999626 | TAA | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0083 a0001c0001t0001g0091 others(10): Show |
14 | HG01169.hp2 HG02698.hp1 NA18747.hp1 others(11): Show |
intron_variant | MODIFIER | c.1168+813_1168+814d others(4): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999626 | |||||||
| chr2:19999626 | TAAAAA | T | 7 | a0001c0003t0001g0022 a0001c0003t0001g0218 a0001c0003t0001g0253 others(4): Show |
9 | HG01255.hp1 HG01256.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1168+810_1168+814d others(7): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999626 | |||||||
| chr2:19999626 | TAAAAAA | T | 33 | a0001c0003t0001g0032 a0001c0003t0001g0051 a0001c0003t0001g0053 others(30): Show |
38 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1168+809_1168+814d others(8): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999626 | |||||||
| chr2:19999714 | G | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0289 |
2 | NA18968.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1168+727C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999714 | |||||||
| chr2:19999909 | T | G | 2 | a0001c0001t0001g0027 a0002c0004t0001g0066 |
3 | NA18942.hp1 NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1168+532A>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999909 | |||||||
| chr2:19999926 | G | A | 1 | a0001c0002t0002g0118 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1168+515C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 19999926 | |||||||
| chr2:20000008 | C | A | 1 | a0002c0004t0001g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1168+433G>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 20000008 | |||||||
| chr2:20000186 | A | G | 3 | a0001c0002t0002g0015 a0001c0002t0002g0101 a0001c0002t0002g0102 |
5 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1168+255T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 5/7 | chr2 | 20000186 | |||||||
| chr2:20000664 | A | G | 1 | a0001c0002t0002g0082 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1043-98T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 4/7 | chr2 | 20000664 | |||||||
| chr2:20000790 | A | G | 1 | a0001c0002t0002g0213 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1043-224T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 4/7 | chr2 | 20000790 | |||||||
| chr2:20000904 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1043-338G>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 4/7 | chr2 | 20000904 | |||||||
| chr2:20001094 | T | C | 1 | a0001c0002t0002g0223 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1043-528A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 4/7 | chr2 | 20001094 | |||||||
| chr2:20001323 | T | C | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0156 |
3 | NA18942.hp2 NA19062.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1042+632A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 4/7 | chr2 | 20001323 | |||||||
| chr2:20001461 | A | G | 7 | a0001c0002t0002g0020 a0001c0002t0002g0046 a0001c0002t0002g0050 others(4): Show |
11 | HG01255.hp2 HG01891.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1042+494T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 4/7 | chr2 | 20001461 | |||||||
| chr2:20001521 | A | T | 1 | a0001c0003t0001g0253 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1042+434T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 4/7 | chr2 | 20001521 | |||||||
| chr2:20001697 | G | A | 30 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0013 others(27): Show |
52 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.1042+258C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 4/7 | chr2 | 20001697 | |||||||
| chr2:20002159 | T | TACAC | 32 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(29): Show |
61 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.917-80_917-79insGT others(2): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002159 | |||||||
| chr2:20002159 | T | TACACAC | 6 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0125 others(3): Show |
8 | HG00733.hp2 HG01168.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.917-80_917-79insGT others(4): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002159 | |||||||
| chr2:20002159 | T | TACACACA others(3): Show |
3 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0002g0023 |
5 | HG02647.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.917-80_917-79insGT others(8): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002159 | |||||||
| chr2:20002161 | T | C | 44 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0016 others(41): Show |
77 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.917-81A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002161 | |||||||
| chr2:20002161 | T | TAC | 12 | a0001c0001t0002g0132 a0001c0002t0002g0009 a0001c0002t0002g0015 others(9): Show |
20 | HG00544.hp1 HG01255.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.917-83_917-82dupGT | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002161 | |||||||
| chr2:20002161 | T | TACAC | 18 | a0001c0001t0002g0133 a0001c0002t0002g0020 a0001c0002t0002g0050 others(15): Show |
22 | HG01891.hp2 HG02145.hp1 HG02486.hp2 others(19): Show |
intron_variant | MODIFIER | c.917-85_917-82dupGT others(2): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002161 | |||||||
| chr2:20002161 | T | TACACACA others(1): Show |
3 | a0001c0001t0002g0123 a0001c0002t0002g0288 a0002c0004t0001g0062 |
3 | HG02257.hp1 HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.917-89_917-82dupGT others(6): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002161 | |||||||
| chr2:20002161 | T | TACACACA others(3): Show |
8 | a0001c0001t0001g0026 a0001c0001t0001g0090 a0001c0001t0001g0231 others(5): Show |
12 | HG01261.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.917-91_917-82dupGT others(8): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002161 | |||||||
| chr2:20002161 | T | TACACACA others(5): Show |
23 | a0001c0001t0001g0005 a0001c0001t0001g0035 a0001c0001t0001g0072 others(20): Show |
29 | HG00323.hp1 HG00597.hp1 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.917-93_917-82dupGT others(10): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002161 | |||||||
| chr2:20002161 | T | TACACACA others(7): Show |
7 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0081 others(4): Show |
11 | HG02080.hp1 NA18939.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.917-95_917-82dupGT others(12): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002161 | |||||||
| chr2:20002161 | T | TACACACA others(9): Show |
1 | a0001c0001t0001g0232 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.917-97_917-82dupGT others(14): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002161 | |||||||
| chr2:20002191 | C | CACACACA others(15): Show |
3 | a0001c0001t0001g0192 a0001c0003t0001g0272 a0001c0010t0001g0228 |
3 | HG03688.hp1 NA18989.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.917-112_917-111ins others(22): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(13): Show |
5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0180 others(2): Show |
5 | HG03654.hp2 NA18612.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.917-112_917-111ins others(20): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(11): Show |
20 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0045 others(17): Show |
25 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(22): Show |
intron_variant | MODIFIER | c.917-112_917-111ins others(18): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(9): Show |
7 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0170 others(4): Show |
7 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(4): Show |
intron_variant | MODIFIER | c.917-112_917-111ins others(16): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(7): Show |
15 | a0001c0001t0001g0151 a0001c0001t0001g0186 a0001c0001t0001g0187 others(12): Show |
16 | HG00408.hp1 HG00609.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.917-112_917-111ins others(14): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(9): Show |
1 | a0001c0003t0001g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.917-112_917-111ins others(16): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(5): Show |
39 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0036 others(36): Show |
49 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.917-112_917-111ins others(12): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(3): Show |
1 | a0001c0003t0001g0263 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.917-112_917-111ins others(10): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(5): Show |
4 | a0001c0003t0001g0053 a0001c0003t0001g0055 a0001c0003t0001g0261 others(1): Show |
6 | HG00639.hp1 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.917-112_917-111ins others(12): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACACACA others(1): Show |
5 | a0001c0001t0001g0280 a0001c0003t0001g0032 a0001c0003t0001g0128 others(2): Show |
6 | NA18944.hp1 NA18950.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.917-112_917-111ins others(8): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CACAG | 7 | a0001c0001t0001g0004 a0001c0001t0001g0070 a0001c0001t0001g0201 others(4): Show |
12 | HG01243.hp1 HG01934.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.917-112_917-111ins others(4): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002191 | C | CATACACA others(5): Show |
3 | a0001c0003t0001g0249 a0001c0003t0001g0251 a0001c0003t0001g0269 |
3 | NA18979.hp1 NA19007.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.917-112_917-111ins others(12): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002191 | |||||||
| chr2:20002253 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.917-173G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002253 | |||||||
| chr2:20002499 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.917-419G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002499 | |||||||
| chr2:20002713 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(218): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.916+448A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002713 | |||||||
| chr2:20002763 | C | CT | 30 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0045 others(27): Show |
35 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.916+397dupA | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002763 | |||||||
| chr2:20002773 | TA | T | 4 | a0001c0001t0001g0139 a0002c0004t0001g0061 a0002c0004t0001g0062 others(1): Show |
4 | HG01261.hp1 HG02572.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.916+387delT | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002773 | |||||||
| chr2:20002774 | A | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(280): Show |
426 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(423): Show |
intron_variant | MODIFIER | c.916+387T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002774 | |||||||
| chr2:20002803 | C | T | 1 | a0002c0007t0005g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.916+358G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002803 | |||||||
| chr2:20002813 | G | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(38): Show |
53 | HG00323.hp1 HG00597.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.916+348C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002813 | |||||||
| chr2:20002882 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.916+279T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002882 | |||||||
| chr2:20002977 | T | C | 60 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0028 others(57): Show |
72 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.916+184A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20002977 | |||||||
| chr2:20003032 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.916+129T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20003032 | |||||||
| chr2:20003050 | A | G | 44 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0032 others(41): Show |
53 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.916+111T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 3/7 | chr2 | 20003050 | |||||||
| chr2:20003345 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.791-59A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20003345 | |||||||
| chr2:20003351 | A | G | 2 | a0001c0001t0001g0027 a0002c0004t0001g0066 |
3 | NA18942.hp1 NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.791-65T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20003351 | |||||||
| chr2:20003439 | T | C | 7 | a0001c0001t0001g0098 a0001c0001t0001g0134 a0001c0001t0002g0115 others(4): Show |
9 | HG02647.hp1 HG02818.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.791-153A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20003439 | |||||||
| chr2:20003531 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.791-245A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20003531 | |||||||
| chr2:20003614 | A | G | 1 | a0001c0003t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.791-328T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20003614 | |||||||
| chr2:20003775 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.791-489C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20003775 | |||||||
| chr2:20004137 | C | T | 7 | a0001c0002t0002g0056 a0001c0002t0002g0265 a0001c0002t0002g0266 others(4): Show |
8 | HG01256.hp2 HG01258.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.791-851G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004137 | |||||||
| chr2:20004293 | C | T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(137): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.791-1007G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004293 | |||||||
| chr2:20004509 | C | G | 2 | a0001c0001t0002g0119 a0001c0001t0002g0123 |
2 | HG02109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.791-1223G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004509 | |||||||
| chr2:20004523 | C | T | 1 | a0001c0003t0001g0252 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.790+1221G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004523 | |||||||
| chr2:20004667 | A | G | 1 | a0001c0002t0002g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.790+1077T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004667 | |||||||
| chr2:20004693 | T | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0154 others(1): Show |
6 | HG01168.hp2 HG01169.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.790+1051A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004693 | |||||||
| chr2:20004771 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.790+973G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004771 | |||||||
| chr2:20004911 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.790+833T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004911 | |||||||
| chr2:20004929 | A | C | 45 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0032 others(42): Show |
54 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.790+815T>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004929 | |||||||
| chr2:20004993 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0087 |
3 | HG00323.hp1 NA18946.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.790+751C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20004993 | |||||||
| chr2:20005221 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.790+523A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005221 | |||||||
| chr2:20005289 | C | T | 45 | a0001c0003t0001g0021 a0001c0003t0001g0022 a0001c0003t0001g0032 others(42): Show |
54 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.790+455G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005289 | |||||||
| chr2:20005309 | A | T | 3 | a0001c0002t0002g0052 a0001c0002t0002g0241 a0001c0002t0002g0250 |
4 | HG02630.hp1 HG02717.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.790+435T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005309 | |||||||
| chr2:20005436 | C | A | 30 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0013 others(27): Show |
52 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.790+308G>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005436 | |||||||
| chr2:20005506 | A | G | 1 | a0001c0003t0001g0021 | 3 | HG01496.hp1 HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.790+238T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005506 | |||||||
| chr2:20005591 | C | T | 2 | a0001c0001t0001g0027 a0002c0004t0001g0066 |
3 | NA18942.hp1 NA18943.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.790+153G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005591 | |||||||
| chr2:20005594 | G | A | 6 | a0001c0002t0002g0007 a0001c0002t0002g0014 a0001c0002t0002g0162 others(3): Show |
14 | HG00438.hp1 HG02074.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.790+150C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005594 | |||||||
| chr2:20005595 | C | T | 1 | a0001c0002t0002g0106 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.790+149G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005595 | |||||||
| chr2:20005662 | A | AAAAG | 208 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(205): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.790+81_790+82insCT others(2): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 2/7 | chr2 | 20005662 | |||||||
| chr2:20006654 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(195): Show |
270 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.224-344A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20006654 | |||||||
| chr2:20006710 | T | TG | 38 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(35): Show |
55 | HG00323.hp1 HG01261.hp1 HG01346.hp2 others(52): Show |
intron_variant | MODIFIER | c.224-401dupC | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20006710 | |||||||
| chr2:20006781 | C | T | 29 | a0001c0002t0002g0003 a0001c0002t0002g0007 a0001c0002t0002g0013 others(26): Show |
51 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.224-471G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20006781 | |||||||
| chr2:20006845 | C | T | 2 | a0001c0003t0001g0254 a0001c0003t0001g0259 |
2 | NA18977.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.224-535G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20006845 | |||||||
| chr2:20006928 | T | A | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
417 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(414): Show |
intron_variant | MODIFIER | c.224-618A>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20006928 | |||||||
| chr2:20006955 | T | C | 7 | a0001c0001t0001g0158 a0001c0001t0001g0178 a0001c0001t0001g0179 others(4): Show |
7 | HG02698.hp2 HG03669.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.224-645A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20006955 | |||||||
| chr2:20006963 | A | G | 1 | a0001c0002t0002g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.224-653T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20006963 | |||||||
| chr2:20007035 | C | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(217): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.224-725G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007035 | |||||||
| chr2:20007064 | C | T | 2 | a0001c0002t0002g0046 a0001c0002t0002g0227 |
3 | HG01255.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.224-754G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007064 | |||||||
| chr2:20007080 | T | C | 5 | a0001c0001t0001g0090 a0001c0001t0001g0127 a0001c0001t0001g0137 others(2): Show |
5 | HG00642.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-770A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007080 | |||||||
| chr2:20007088 | T | G | 4 | a0001c0003t0001g0270 a0001c0003t0001g0271 a0001c0003t0001g0272 others(1): Show |
4 | HG01167.hp2 HG02615.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-778A>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007088 | |||||||
| chr2:20007138 | A | G | 275 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(272): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.224-828T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007138 | |||||||
| chr2:20007223 | A | C | 1 | a0001c0002t0002g0211 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224-913T>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007223 | |||||||
| chr2:20007224 | A | C | 1 | a0001c0003t0001g0269 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.224-914T>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007224 | |||||||
| chr2:20007250 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0161 |
3 | HG01884.hp1 HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.224-940C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007250 | |||||||
| chr2:20007292 | G | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(31): Show |
45 | HG00323.hp1 HG02080.hp1 HG02132.hp1 others(42): Show |
intron_variant | MODIFIER | c.224-982C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007292 | |||||||
| chr2:20007444 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.224-1134C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007444 | |||||||
| chr2:20007515 | G | GC | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.224-1206dupG | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007515 | |||||||
| chr2:20007638 | C | T | 1 | a0002c0004t0001g0061 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.224-1328G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007638 | |||||||
| chr2:20007858 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
353 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.224-1548C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20007858 | |||||||
| chr2:20008011 | G | C | 1 | a0001c0003t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.224-1701C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008011 | |||||||
| chr2:20008026 | A | C | 5 | a0001c0002t0001g0239 a0001c0002t0002g0020 a0001c0002t0002g0050 others(2): Show |
8 | HG01891.hp2 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.224-1716T>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008026 | |||||||
| chr2:20008080 | AG | A | 6 | a0001c0002t0002g0007 a0001c0002t0002g0014 a0001c0002t0002g0162 others(3): Show |
14 | HG00438.hp1 HG02074.hp2 HG02080.hp2 others(11): Show |
intron_variant | MODIFIER | c.224-1771delC | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008080 | |||||||
| chr2:20008082 | C | G | 1 | a0001c0002t0004g0226 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.224-1772G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008082 | |||||||
| chr2:20008163 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.224-1853T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008163 | |||||||
| chr2:20008250 | A | G | 1 | a0001c0002t0002g0104 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.224-1940T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008250 | |||||||
| chr2:20008260 | G | A | 1 | a0001c0003t0001g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.224-1950C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008260 | |||||||
| chr2:20008306 | C | T | 1 | a0001c0002t0002g0265 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.224-1996G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008306 | |||||||
| chr2:20008492 | G | A | 5 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0003t0001g0095 others(2): Show |
7 | HG02486.hp1 HG02647.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-2182C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008492 | |||||||
| chr2:20008551 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.224-2241C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008551 | |||||||
| chr2:20008651 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(138): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.224-2341C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008651 | |||||||
| chr2:20008695 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0164 |
3 | HG02135.hp2 NA18971.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.224-2385C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008695 | |||||||
| chr2:20008746 | T | C | 1 | a0002c0007t0005g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.224-2436A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008746 | |||||||
| chr2:20008892 | G | A | 1 | a0001c0001t0001g0043 | 2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.224-2582C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20008892 | |||||||
| chr2:20009016 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.224-2706C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009016 | |||||||
| chr2:20009245 | A | C | 33 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0203 others(30): Show |
43 | HG00438.hp2 HG01255.hp2 HG01256.hp2 others(40): Show |
intron_variant | MODIFIER | c.224-2935T>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009245 | |||||||
| chr2:20009247 | G | C | 1 | a0002c0004t0001g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.224-2937C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009247 | |||||||
| chr2:20009270 | T | TA | 6 | a0001c0001t0002g0115 a0001c0002t0002g0208 a0001c0002t0002g0224 others(3): Show |
6 | HG02451.hp2 HG02723.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.224-2961dupT | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009270 | |||||||
| chr2:20009270 | T | TAA | 7 | a0001c0001t0001g0074 a0001c0001t0001g0088 a0001c0001t0001g0134 others(4): Show |
7 | HG01167.hp1 HG02717.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-2962_224-2961d others(4): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009270 | |||||||
| chr2:20009270 | T | TAAA | 127 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(124): Show |
183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.224-2963_224-2961d others(5): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009270 | |||||||
| chr2:20009270 | TA | T | 35 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0203 others(32): Show |
45 | HG00438.hp2 HG01255.hp2 HG01256.hp2 others(42): Show |
intron_variant | MODIFIER | c.224-2961delT | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009270 | |||||||
| chr2:20009334 | A | G | 22 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0203 others(19): Show |
26 | HG00438.hp2 HG01256.hp2 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.224-3024T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009334 | |||||||
| chr2:20009857 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
185 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.223+2552A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009857 | |||||||
| chr2:20009959 | A | G | 1 | a0001c0002t0002g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.223+2450T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009959 | |||||||
| chr2:20009964 | C | T | 2 | a0001c0002t0002g0246 a0001c0002t0002g0247 |
2 | HG02486.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.223+2445G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20009964 | |||||||
| chr2:20010012 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.223+2397A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010012 | |||||||
| chr2:20010021 | G | A | 1 | a0001c0002t0002g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223+2388C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010021 | |||||||
| chr2:20010064 | T | TCCAAAAA others(18): Show |
1 | a0001c0002t0002g0056 | 2 | HG01256.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.223+2344_223+2345i others(27): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010064 | |||||||
| chr2:20010064 | T | TCCAAAAA others(19): Show |
3 | a0001c0002t0002g0265 a0001c0002t0002g0266 a0001c0002t0002g0267 |
3 | HG01258.hp1 HG01433.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.223+2344_223+2345i others(28): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010064 | |||||||
| chr2:20010064 | T | TCCAAAAA others(20): Show |
1 | a0001c0002t0002g0273 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.223+2344_223+2345i others(29): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010064 | |||||||
| chr2:20010066 | C | A | 5 | a0001c0002t0002g0056 a0001c0002t0002g0265 a0001c0002t0002g0266 others(2): Show |
6 | HG01256.hp2 HG01258.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+2343G>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010066 | |||||||
| chr2:20010066 | C | CAAAAAAA others(16): Show |
1 | a0001c0003t0001g0260 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.223+2342_223+2343i others(25): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010066 | |||||||
| chr2:20010066 | C | CAAAAAAA others(20): Show |
1 | a0001c0003t0001g0274 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.223+2342_223+2343i others(29): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010066 | |||||||
| chr2:20010067 | T | A | 7 | a0001c0002t0002g0056 a0001c0002t0002g0265 a0001c0002t0002g0266 others(4): Show |
8 | HG00609.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.223+2342A>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAA | 10 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0070 others(7): Show |
16 | HG01169.hp1 HG01934.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.223+2338_223+2341d others(6): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAA | 75 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(72): Show |
113 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.223+2337_223+2341d others(7): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAA | 32 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0041 others(29): Show |
41 | HG00621.hp1 HG00621.hp2 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.223+2336_223+2341d others(8): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA | 16 | a0001c0001t0001g0017 a0001c0001t0001g0045 a0001c0001t0001g0068 others(13): Show |
20 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.223+2335_223+2341d others(9): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(1): Show |
10 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0001g0197 others(7): Show |
10 | HG01123.hp2 HG02027.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.223+2334_223+2341d others(10): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(3): Show |
1 | a0001c0002t0002g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.223+2332_223+2341d others(12): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(4): Show |
7 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0002t0002g0013 others(4): Show |
10 | HG01081.hp2 HG01943.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.223+2331_223+2341d others(13): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(5): Show |
25 | a0001c0001t0001g0018 a0001c0001t0001g0209 a0001c0001t0001g0210 others(22): Show |
43 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.223+2330_223+2341d others(14): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(6): Show |
12 | a0001c0001t0001g0019 a0001c0001t0001g0231 a0001c0001t0001g0232 others(9): Show |
20 | HG00735.hp2 HG02055.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+2329_223+2341d others(15): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(7): Show |
5 | a0001c0001t0001g0236 a0001c0002t0002g0233 a0001c0002t0002g0234 others(2): Show |
5 | HG02280.hp2 NA18970.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+2328_223+2341d others(16): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(8): Show |
2 | a0001c0002t0002g0050 a0001c0002t0002g0238 |
3 | HG02615.hp1 HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.223+2327_223+2341d others(17): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(9): Show |
2 | a0001c0002t0002g0020 a0002c0004t0001g0066 |
4 | HG01891.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+2326_223+2341d others(18): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(10): Show |
5 | a0001c0002t0001g0239 a0001c0002t0002g0240 a0001c0002t0002g0241 others(2): Show |
7 | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+2325_223+2341d others(19): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(11): Show |
2 | a0001c0003t0001g0051 a0001c0003t0001g0243 |
3 | HG02735.hp2 HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.223+2324_223+2341d others(20): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(12): Show |
2 | a0001c0002t0002g0099 a0001c0003t0001g0244 |
2 | HG03492.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.223+2323_223+2341d others(21): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(13): Show |
2 | a0001c0002t0002g0052 a0001c0003t0001g0245 |
3 | HG02895.hp2 HG02976.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.223+2322_223+2341d others(22): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(14): Show |
3 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0002g0248 |
3 | HG02486.hp2 HG02896.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.223+2321_223+2341d others(23): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(15): Show |
1 | a0001c0002t0002g0250 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.223+2320_223+2341d others(24): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(16): Show |
2 | a0001c0003t0001g0252 a0001c0003t0001g0253 |
2 | HG01256.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223+2319_223+2341d others(25): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(17): Show |
9 | a0001c0003t0001g0022 a0001c0003t0001g0053 a0001c0003t0001g0054 others(6): Show |
13 | HG00280.hp2 HG01099.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+2341_223+2342i others(26): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(18): Show |
4 | a0001c0003t0001g0261 a0001c0003t0001g0262 a0001c0003t0001g0263 others(1): Show |
4 | HG01516.hp2 HG01517.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+2341_223+2342i others(27): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(19): Show |
1 | a0001c0003t0001g0055 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.223+2341_223+2342i others(28): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(21): Show |
5 | a0001c0002t0002g0268 a0001c0003t0001g0269 a0001c0003t0001g0270 others(2): Show |
5 | HG02615.hp2 HG03486.hp2 NA18940.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+2341_223+2342i others(30): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(22): Show |
4 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0002t0002g0057 others(1): Show |
5 | HG00438.hp2 HG02083.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+2341_223+2342i others(31): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(23): Show |
7 | a0001c0001t0001g0058 a0001c0001t0001g0279 a0001c0001t0001g0280 others(4): Show |
8 | HG00639.hp2 HG01167.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+2341_223+2342i others(32): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(24): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0284 |
3 | HG01978.hp2 HG02148.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.223+2341_223+2342i others(33): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAAAAAAA others(25): Show |
2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | NA18974.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.223+2341_223+2342i others(34): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAGAAAAA others(16): Show |
1 | a0001c0003t0001g0249 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.223+2341_223+2342i others(25): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | T | TAGAAAAA others(17): Show |
1 | a0001c0003t0001g0251 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.223+2341_223+2342i others(26): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010067 | TAAAA | T | 22 | a0001c0001t0001g0029 a0001c0001t0001g0111 a0001c0001t0001g0289 others(19): Show |
63 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.223+2338_223+2341d others(6): Show |
MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010067 | |||||||
| chr2:20010270 | A | C | 3 | a0001c0002t0002g0015 a0001c0002t0002g0101 a0001c0002t0002g0102 |
5 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+2139T>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010270 | |||||||
| chr2:20010272 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.223+2137A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010272 | |||||||
| chr2:20010315 | G | A | 1 | a0002c0004t0001g0067 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.223+2094C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010315 | |||||||
| chr2:20010353 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG00733.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.223+2056G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010353 | |||||||
| chr2:20010362 | T | C | 3 | a0001c0003t0001g0095 a0001c0003t0001g0096 a0001c0003t0002g0023 |
5 | HG02647.hp1 HG02970.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+2047A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010362 | |||||||
| chr2:20010396 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.223+2013C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010396 | |||||||
| chr2:20010420 | C | G | 1 | a0001c0002t0002g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223+1989G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010420 | |||||||
| chr2:20010525 | T | C | 1 | a0001c0002t0002g0288 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.223+1884A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010525 | |||||||
| chr2:20010690 | C | T | 1 | a0001c0002t0002g0099 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.223+1719G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010690 | |||||||
| chr2:20010989 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.223+1420G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20010989 | |||||||
| chr2:20011416 | A | T | 1 | a0001c0002t0002g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.223+993T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20011416 | |||||||
| chr2:20011431 | AC | A | 3 | a0001c0001t0001g0289 a0001c0002t0002g0011 a0001c0002t0002g0060 |
8 | NA18952.hp1 NA18968.hp1 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.223+977delG | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20011431 | |||||||
| chr2:20011493 | A | G | 2 | a0001c0003t0001g0095 a0001c0003t0001g0096 |
2 | HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.223+916T>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20011493 | |||||||
| chr2:20011532 | G | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0024 others(29): Show |
47 | HG00323.hp1 HG01934.hp1 HG02109.hp2 others(44): Show |
intron_variant | MODIFIER | c.223+877C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20011532 | |||||||
| chr2:20011605 | C | T | 2 | a0002c0004t0001g0061 a0002c0004t0001g0062 |
2 | HG02572.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.223+804G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20011605 | |||||||
| chr2:20012103 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+306C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012103 | |||||||
| chr2:20012104 | G | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+305C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012104 | |||||||
| chr2:20012105 | G | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+304C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012105 | |||||||
| chr2:20012107 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+302G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012107 | |||||||
| chr2:20012108 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+301C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012108 | |||||||
| chr2:20012109 | G | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+300C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012109 | |||||||
| chr2:20012112 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+297G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012112 | |||||||
| chr2:20012113 | T | G | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+296A>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012113 | |||||||
| chr2:20012122 | G | A | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+287C>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012122 | |||||||
| chr2:20012125 | G | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+284C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012125 | |||||||
| chr2:20012126 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+283G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012126 | |||||||
| chr2:20012132 | A | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+277T>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012132 | |||||||
| chr2:20012133 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+276C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012133 | |||||||
| chr2:20012134 | C | G | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+275G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012134 | |||||||
| chr2:20012137 | C | A | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+272G>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012137 | |||||||
| chr2:20012139 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+270G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012139 | |||||||
| chr2:20012144 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+265C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012144 | |||||||
| chr2:20012145 | C | G | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+264G>C | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012145 | |||||||
| chr2:20012150 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+259G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012150 | |||||||
| chr2:20012153 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+256G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012153 | |||||||
| chr2:20012155 | G | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+254C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012155 | |||||||
| chr2:20012156 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+253G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012156 | |||||||
| chr2:20012158 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+251G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012158 | |||||||
| chr2:20012161 | T | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+248A>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012161 | |||||||
| chr2:20012162 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+247C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012162 | |||||||
| chr2:20012167 | T | A | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+242A>T | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012167 | |||||||
| chr2:20012168 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+241C>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012168 | |||||||
| chr2:20012169 | G | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+240C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012169 | |||||||
| chr2:20012170 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+239G>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012170 | |||||||
| chr2:20012172 | G | C | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+237C>G | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012172 | |||||||
| chr2:20012177 | A | T | 1 | a0001c0002t0002g0069 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.223+232T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012177 | |||||||
| chr2:20012222 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.223+187T>A | MATN3 | ENSG00000132031.13 | transcript | ENST00000407540.8 | protein_coding | 1/7 | chr2 | 20012222 |