Variant report
Variant | rs17203028 |
---|---|
Chromosome Location | chr4:127660619-127660620 |
allele | A/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:6)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:6 , 50 per page) page:
1
No. | Distal block | Cell Line | Cell type | Cell Stage |
---|---|---|---|---|
1 | chr4:127655542..127661109-chr4:127874426..127880524,8 | K562 | blood: | |
2 | chr4:127657779..127661019-chr4:127875846..127879215,3 | K562 | blood: | |
3 | chr4:127645103..127647916-chr4:127657804..127660806,3 | K562 | blood: | |
4 | chr4:127659055..127662834-chr4:127664504..127669791,5 | K562 | blood: | |
5 | chr4:127654180..127661020-chr4:127693803..127700410,12 | K562 | blood: | |
6 | chr4:127649446..127654981-chr4:127658045..127662615,6 | K562 | blood: |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs1014773 | 0.87[ASN][1000 genomes] |
rs10461207 | 1.00[ASN][1000 genomes] |
rs10857117 | 0.87[ASN][1000 genomes] |
rs11098891 | 1.00[CHB][hapmap];0.87[ASN][1000 genomes] |
rs11098892 | 0.87[ASN][1000 genomes] |
rs11098893 | 0.87[ASN][1000 genomes] |
rs11098896 | 1.00[ASN][1000 genomes] |
rs11098898 | 1.00[ASN][1000 genomes] |
rs1157308 | 0.87[ASN][1000 genomes] |
rs1167190 | 1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11935382 | 1.00[ASN][1000 genomes] |
rs11940501 | 0.87[ASN][1000 genomes] |
rs11941222 | 0.91[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs12163770 | 0.87[ASN][1000 genomes] |
rs12503440 | 0.87[ASN][1000 genomes] |
rs12504330 | 1.00[ASN][1000 genomes] |
rs12507115 | 1.00[ASN][1000 genomes] |
rs12647109 | 0.87[ASN][1000 genomes] |
rs12650177 | 0.87[ASN][1000 genomes] |
rs13111309 | 1.00[ASN][1000 genomes] |
rs13112652 | 0.87[ASN][1000 genomes] |
rs13143010 | 0.87[ASN][1000 genomes] |
rs13148138 | 0.87[ASN][1000 genomes] |
rs13152826 | 0.87[ASN][1000 genomes] |
rs1393991 | 1.00[CHB][hapmap];1.00[ASN][1000 genomes] |
rs1393993 | 0.87[ASN][1000 genomes] |
rs1503604 | 0.87[ASN][1000 genomes] |
rs1503605 | 1.00[ASN][1000 genomes] |
rs1503606 | 1.00[ASN][1000 genomes] |
rs1503608 | 1.00[ASN][1000 genomes] |
rs1503610 | 0.87[ASN][1000 genomes] |
rs1503611 | 1.00[ASN][1000 genomes] |
rs1503614 | 1.00[ASN][1000 genomes] |
rs1503631 | 0.87[ASN][1000 genomes] |
rs1532768 | 1.00[ASN][1000 genomes] |
rs1604719 | 0.87[ASN][1000 genomes] |
rs1604724 | 1.00[ASN][1000 genomes] |
rs17011528 | 0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs1875740 | 0.87[ASN][1000 genomes] |
rs1948827 | 1.00[ASN][1000 genomes] |
rs1955281 | 0.87[ASN][1000 genomes] |
rs1976483 | 1.00[ASN][1000 genomes] |
rs2013778 | 1.00[CHB][hapmap];0.87[ASN][1000 genomes] |
rs2013864 | 1.00[ASN][1000 genomes] |
rs2089061 | 1.00[ASN][1000 genomes] |
rs2134641 | 0.87[ASN][1000 genomes] |
rs2134645 | 0.87[ASN][1000 genomes] |
rs2174184 | 0.87[ASN][1000 genomes] |
rs2391099 | 1.00[CHB][hapmap] |
rs28666008 | 1.00[ASN][1000 genomes] |
rs28742896 | 0.97[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28811377 | 0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs28876486 | 0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs2893192 | 0.87[ASN][1000 genomes] |
rs4834142 | 0.87[ASN][1000 genomes] |
rs55791209 | 0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62324217 | 0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs62324218 | 0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes] |
rs6534583 | 1.00[ASN][1000 genomes] |
rs6812442 | 0.87[ASN][1000 genomes] |
rs6829454 | 1.00[ASN][1000 genomes] |
rs6830097 | 0.87[ASN][1000 genomes] |
rs6848985 | 1.00[ASN][1000 genomes] |
rs6856064 | 1.00[ASN][1000 genomes] |
rs7654869 | 0.87[ASN][1000 genomes] |
rs7672155 | 1.00[ASN][1000 genomes] |
rs7676848 | 0.87[ASN][1000 genomes] |
rs7681140 | 1.00[ASN][1000 genomes] |
rs7686181 | 1.00[ASN][1000 genomes] |
rs7691822 | 0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7694861 | 1.00[ASN][1000 genomes] |
rs7696445 | 1.00[ASN][1000 genomes] |
rs7696767 | 1.00[ASN][1000 genomes] |
rs969315 | 1.00[ASN][1000 genomes] |
rs986907 | 1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1012833 | chr4:127468474-127760933 | Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
2 | nsv537242 | chr4:127468474-127760933 | Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
3 | nsv524850 | chr4:127470903-127768849 | Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 3 gene(s) | inside rSNPs | diseases |
4 | nsv1013854 | chr4:127508969-127663216 | Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
5 | nsv1007477 | chr4:127561735-127726291 | Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
6 | nsv537244 | chr4:127561735-127726291 | Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Genic enhancers | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
7 | esv2752024 | chr4:127584697-127671942 | Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS | Chromatin interactive region | n/a | inside rSNPs | diseases |
8 | nsv595386 | chr4:127597069-127668828 | Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' | Chromatin interactive region | n/a | inside rSNPs | diseases |
9 | nsv1028609 | chr4:127597319-127664629 | Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats | Chromatin interactive region | n/a | inside rSNPs | diseases |
10 | nsv879907 | chr4:127646765-127709859 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
11 | nsv879908 | chr4:127646765-127749390 | Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | n/a |
12 | nsv879909 | chr4:127646765-127792639 | Enhancers Weak transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
13 | nsv879910 | chr4:127646765-127805466 | ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
14 | nsv879911 | chr4:127646765-127835677 | Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer | Chromatin interactive region | 1 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:127659600-127660800 | Enhancers | Adipose Derived Mesenchymal Stem Cell Cultured Cells | ES cell derived |
2 | chr4:127660000-127660800 | Enhancers | NHDF-Ad | bronchial |
3 | chr4:127660400-127661600 | Enhancers | K562 | blood |
4 | chr4:127660600-127666800 | Weak transcription | Breast variant Human Mammary Epithelial Cells (vHMEC) | Breast |