Variant report
Variant | rs12155078 |
---|---|
Chromosome Location | chr7:4081125-4081126 |
allele | A/T |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10226642 | 0.86[CEU][hapmap];0.82[CHB][hapmap] |
rs10228678 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10229207 | 0.82[CEU][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10231929 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs10234405 | 0.81[CEU][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10235315 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10236620 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10237319 | 0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10237488 | 0.82[CEU][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10237838 | 0.82[CEU][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10237842 | 0.81[CEU][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10237956 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10244597 | 0.80[ASN][1000 genomes] |
rs10253213 | 0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10253393 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10254902 | 0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10255116 | 0.88[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10259751 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10259896 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10262417 | 0.88[CEU][hapmap] |
rs10265219 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10265937 | 0.87[CEU][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10266101 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10270404 | 0.87[CEU][hapmap];0.82[CHB][hapmap] |
rs10278187 | 0.81[CEU][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs10485860 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11974413 | 1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11975100 | 0.88[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs11975109 | 0.83[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs12155028 | 0.87[CEU][hapmap];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs12155314 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12155317 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs12155501 | 0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12386617 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes] |
rs12701363 | 1.00[ASN][1000 genomes] |
rs12701386 | 0.93[ASN][1000 genomes] |
rs12701399 | 1.00[CHB][hapmap] |
rs13226987 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1443647 | 0.87[CEU][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs1562005 | 0.80[ASN][1000 genomes] |
rs1562006 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs17134196 | 0.87[CEU][hapmap];0.83[EUR][1000 genomes] |
rs17134197 | 0.82[EUR][1000 genomes] |
rs17134314 | 0.92[CEU][hapmap] |
rs17265128 | 0.82[CHB][hapmap] |
rs17330921 | 0.82[CHB][hapmap] |
rs2342489 | 0.93[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2342490 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2342491 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2342492 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2342493 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2342494 | 1.00[CHB][hapmap];0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2342496 | 0.86[AMR][1000 genomes] |
rs2342497 | 0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2342498 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs28372090 | 0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28458813 | 0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28591614 | 0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28634483 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs28692591 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2880371 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs2880372 | 0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28828193 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs28839269 | 0.93[ASN][1000 genomes] |
rs34241728 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs34786362 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs35018186 | 1.00[ASN][1000 genomes] |
rs35261707 | 0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35303581 | 0.88[AMR][1000 genomes];1.00[ASN][1000 genomes] |
rs35750587 | 0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs35914968 | 0.92[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4295561 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs4442012 | 0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4526263 | 0.93[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs56249161 | 0.84[ASN][1000 genomes] |
rs56958588 | 1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs57171458 | 1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes] |
rs57367972 | 0.84[EUR][1000 genomes] |
rs60163833 | 0.81[ASN][1000 genomes] |
rs60562202 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6462534 | 0.82[CHB][hapmap] |
rs6462541 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462542 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462543 | 0.93[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462544 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6462545 | 0.88[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462546 | 0.88[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462547 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6462548 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462549 | 0.86[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462550 | 0.88[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462551 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6462558 | 0.93[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6462562 | 1.00[CEU][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6462570 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs6462575 | 0.84[AMR][1000 genomes] |
rs6462576 | 0.85[CEU][hapmap];0.82[CHB][hapmap];0.84[AMR][1000 genomes] |
rs66493879 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs66731402 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs66813989 | 0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs67819387 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs67820803 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs68189920 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6943539 | 0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6946871 | 0.81[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6950754 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6953114 | 0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6953284 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6953630 | 0.82[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6954175 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs6957994 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6958682 | 0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6961232 | 0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes] |
rs6962042 | 0.95[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6970189 | 0.85[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.93[ASN][1000 genomes] |
rs6970334 | 1.00[JPT][hapmap] |
rs6971090 | 0.86[CEU][hapmap] |
rs6972327 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6974248 | 1.00[CHB][hapmap] |
rs6976151 | 1.00[ASN][1000 genomes] |
rs6977480 | 0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6977489 | 0.80[ASN][1000 genomes] |
rs71527466 | 0.80[EUR][1000 genomes] |
rs71527467 | 0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs71527468 | 0.89[ASN][1000 genomes] |
rs71535248 | 0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs73673280 | 0.92[ASN][1000 genomes] |
rs7779616 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.97[AFR][1000 genomes];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7781059 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs7783519 | 0.88[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7784114 | 0.82[CHB][hapmap] |
rs7784928 | 0.84[AMR][1000 genomes] |
rs7790866 | 0.87[CEU][hapmap];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7790918 | 1.00[CHB][hapmap];0.93[ASN][1000 genomes] |
rs7791013 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7791029 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7791174 | 0.86[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7791801 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7794939 | 0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7797081 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7797437 | 0.86[CEU][hapmap];0.84[AMR][1000 genomes] |
rs7799331 | 0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes] |
rs7801816 | 0.86[CEU][hapmap];0.84[AMR][1000 genomes] |
rs7801843 | 0.86[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.89[ASN][1000 genomes] |
rs7801852 | 0.87[CEU][hapmap] |
rs7801978 | 0.84[AMR][1000 genomes] |
rs7802663 | 0.86[CEU][hapmap];0.84[AMR][1000 genomes] |
rs7803030 | 0.87[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7803897 | 0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7804112 | 0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7805933 | 0.88[CEU][hapmap];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes] |
rs7807487 | 0.84[ASN][1000 genomes] |
rs7810233 | 0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7810949 | 0.87[CEU][hapmap];0.80[ASN][1000 genomes] |
rs894776 | 1.00[CHB][hapmap] |
rs963255 | 1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9691924 | 0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs9692219 | 1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1021650 | chr7:3665232-4577439 | Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 4 gene(s) | inside rSNPs | diseases |
2 | nsv1029406 | chr7:3860894-4477095 | Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
3 | nsv538685 | chr7:3860894-4477095 | Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
4 | nsv1026410 | chr7:3869104-4383606 | Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
5 | nsv1025497 | chr7:3905444-4176032 | Enhancers Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | nsv538686 | chr7:3905444-4176032 | Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
7 | nsv464274 | chr7:3955516-4613607 | Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
8 | nsv464275 | chr7:3955516-4613607 | Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
9 | nsv464276 | chr7:3955516-4613607 | Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
10 | nsv464277 | chr7:3955516-4613607 | Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
11 | nsv464278 | chr7:3955516-4613607 | Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
12 | nsv605939 | chr7:3955516-4613607 | Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 5 gene(s) | inside rSNPs | diseases |
13 | nsv1019305 | chr7:3991646-4276004 | Enhancers Weak transcription Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
14 | nsv1033687 | chr7:4006020-4267871 | Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
15 | nsv538688 | chr7:4006020-4267871 | Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
16 | nsv917252 | chr7:4017819-4374090 | Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
17 | nsv527624 | chr7:4027536-4424054 | Enhancers ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
18 | nsv523815 | chr7:4054773-4088876 | Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
19 | nsv887338 | chr7:4054773-4105705 | Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer | Chromatin interactive region | n/a | inside rSNPs | diseases |
20 | nsv1022794 | chr7:4063874-4137968 | Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
21 | nsv538689 | chr7:4063874-4137968 | Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
22 | nsv869540 | chr7:4063875-4302040 | Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
23 | nsv1034582 | chr7:4067574-4084716 | Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
24 | nsv1023893 | chr7:4069711-4084716 | Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
25 | nsv1022507 | chr7:4069711-4085475 | Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
26 | esv18100 | chr7:4073333-4082299 | Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
27 | esv1807485 | chr7:4073998-4088555 | Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
28 | nsv1028689 | chr7:4078345-4166552 | Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
29 | nsv538690 | chr7:4078345-4166552 | Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
30 | esv3526869 | chr7:4079319-4083656 | Enhancers Flanking Active TSS Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
31 | esv3419590 | chr7:4079826-4084024 | Enhancers Flanking Active TSS Weak transcription Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
32 | esv3526864 | chr7:4080026-4083424 | Enhancers Active TSS Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
33 | esv14962 | chr7:4080568-4082559 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
34 | esv3526866 | chr7:4080576-4083274 | Enhancers Weak transcription Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
35 | esv2567177 | chr7:4080778-4083144 | Weak transcription Enhancers Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
36 | esv3475533 | chr7:4080837-4082619 | Weak transcription Enhancers | Chromatin interactive region | n/a | inside rSNPs | diseases |
37 | esv2303183 | chr7:4081066-4082477 | Enhancers Weak transcription | Chromatin interactive region | n/a | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr7:4059000-4091200 | Weak transcription | H1 Derived Mesenchymal Stem Cells | ES cell derived |
2 | chr7:4066800-4082000 | Weak transcription | H9 Derived Neuron Cultured Cells | ES cell derived |
3 | chr7:4066800-4087200 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
4 | chr7:4066800-4091200 | Weak transcription | Pancreas | Pancrea |
5 | chr7:4077800-4087800 | Weak transcription | Spleen | Spleen |
6 | chr7:4078000-4091200 | Weak transcription | Aorta | Aorta |
7 | chr7:4078400-4081200 | Weak transcription | Fetal Muscle Leg | muscle |
8 | chr7:4079600-4081400 | Enhancers | ES-UCSF4 Cell Line | embryonic stem cell |
9 | chr7:4079600-4083800 | Enhancers | HUES6 Cell Line | embryonic stem cell |
10 | chr7:4080200-4081200 | Weak transcription | HUES64 Cell Line | embryonic stem cell |
11 | chr7:4080200-4081600 | Enhancers | H1 Cell Line | embryonic stem cell |
12 | chr7:4080200-4082000 | Weak transcription | iPS DF 19.11 Cell Line | embryonic stem cell |
13 | chr7:4080200-4083800 | Weak transcription | ES-WA7 Cell Line | embryonic stem cell |
14 | chr7:4080200-4083800 | Enhancers | iPS-15b Cell Line | embryonic stem cell |
15 | chr7:4080200-4083800 | Enhancers | iPS-18 Cell Line | embryonic stem cell |
16 | chr7:4080600-4081200 | Enhancers | ES-I3 Cell Line | embryonic stem cell |
17 | chr7:4080600-4084000 | Enhancers | H9 Cell Line | embryonic stem cell |
18 | chr7:4080800-4081400 | Enhancers | iPS DF 6.9 Cell Line | embryonic stem cell |
19 | chr7:4080800-4082200 | Weak transcription | HUES48 Cell Line | embryonic stem cell |
20 | chr7:4080800-4083200 | Enhancers | iPS-20b Cell Line | embryonic stem cell |