Variant report

Variant	rs190112255
Chromosome Location	chr8:63035165-63035166
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv890955	chr8:62919691-63062581	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3490106	chr8:63033798-63041596	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	inside rSNPs	diseases
3	esv3490111	chr8:63034248-63041446	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
4	esv3490107	chr8:63034802-63040502	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
5	esv3479350	chr8:63034841-63040500	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
6	esv3490109	chr8:63034866-63040463	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3479353	chr8:63034870-63040468	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3479349	chr8:63034886-63040439	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3490112	chr8:63034896-63040463	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3490110	chr8:63034896-63040464	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
11	esv3479351	chr8:63034933-63040397	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
12	esv3479354	chr8:63034947-63040399	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	nsv611428	chr8:63034992-63038096	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	nsv611429	chr8:63034992-63038398	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	nsv611430	chr8:63034992-63038700	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
16	nsv611431	chr8:63034992-63039018	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
17	nsv611432	chr8:63034992-63039350	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
18	nsv611433	chr8:63034992-63039587	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
19	nsv611434	chr8:63034992-63039751	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
20	nsv611435	chr8:63034992-63039968	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
21	nsv611436	chr8:63034992-63040410	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
22	esv12888	chr8:63034999-63040375	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63034000-63038200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:63034200-63036200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:63034600-63037400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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