Variant report

Variant	rs369370415
Chromosome Location	chr11:71861610-71861611
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530623	chr11:71088949-72020418	Enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	nsv1054858	chr11:71847797-71880291	Enhancers Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv3493111	chr11:71850822-71893073	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv3493112	chr11:71850822-71893073	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv435918	chr11:71851427-71890983	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	esv5948	chr11:71851479-71890582	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	esv3359634	chr11:71851533-71892403	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	esv2513904	chr11:71852934-71892793	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	esv3446490	chr11:71860854-71862952	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv3404835	chr11:71861404-71862452	Active TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	esv1935888	chr11:71861439-71862108	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	esv6146	chr11:71861440-71862195	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
13	esv3462452	chr11:71861474-71862013	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
14	esv3518401	chr11:71861504-71862027	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
15	esv3518405	chr11:71861514-71862009	Weak transcription Active TSS Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
16	esv3518406	chr11:71861521-71861965	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3518403	chr11:71861523-71861965	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3462441	chr11:71861539-71861979	Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3518402	chr11:71861541-71861964	Weak transcription	n/a	n/a	inside rSNPs	diseases
20	esv3462419	chr11:71861543-71861940	Weak transcription	n/a	n/a	inside rSNPs	diseases
21	esv5256	chr11:71861560-71862101	Weak transcription Flanking Active TSS Active TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
22	esv3428090	chr11:71861561-71861934	Weak transcription	n/a	n/a	inside rSNPs	diseases
23	esv3518404	chr11:71861563-71861968	Weak transcription	n/a	n/a	inside rSNPs	diseases
24	esv3462430	chr11:71861584-71861917	Weak transcription	n/a	n/a	inside rSNPs	diseases
25	esv3346629	chr11:71861597-71861913	Weak transcription	n/a	n/a	inside rSNPs	diseases
26	esv3462463	chr11:71861598-71861925	Weak transcription	n/a	n/a	inside rSNPs	diseases
27	esv3518408	chr11:71861598-71861925	Weak transcription	n/a	n/a	inside rSNPs	diseases
28	esv2469473	chr11:71861608-71861922	Weak transcription	n/a	n/a	inside rSNPs	diseases
29	esv1412330	chr11:71861609-71861924	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71857000-71863600	Weak transcription	Placenta	Placenta
2	chr11:71857800-71862200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr11:71861000-71862000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr11:71861000-71862000	Weak transcription	NHEK	skin

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