Variant report

Variant	rs535455080
Chromosome Location	chr10:26355007-26355008
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1792417	chr10:26263695-26395038	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv1798878	chr10:26339336-26355576	Weak transcription ZNF genes & repeats Enhancers Strong transcription	n/a	n/a	inside rSNPs	diseases
3	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	esv13963	chr10:26345494-26361303	Weak transcription Strong transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv3340579	chr10:26354071-26356094	Strong transcription Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2568953	chr10:26354124-26355620	Weak transcription	n/a	n/a	inside rSNPs	diseases
7	esv2215082	chr10:26354575-26355175	Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3482840	chr10:26354639-26355174	Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv1988727	chr10:26354654-26355262	Weak transcription	n/a	n/a	inside rSNPs	diseases
10	esv3516478	chr10:26354657-26355173	Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3516477	chr10:26354658-26355190	Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3713	chr10:26354666-26355127	Weak transcription	n/a	n/a	inside rSNPs	diseases
13	esv3482951	chr10:26354686-26355143	Weak transcription	n/a	n/a	inside rSNPs	diseases
14	esv3482729	chr10:26354689-26355139	Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3324503	chr10:26354693-26355118	Weak transcription	n/a	n/a	inside rSNPs	diseases
16	esv3482618	chr10:26354701-26355092	Weak transcription	n/a	n/a	inside rSNPs	diseases
17	esv3483062	chr10:26354701-26355092	Weak transcription	n/a	n/a	inside rSNPs	diseases
18	esv3516476	chr10:26354708-26355120	Weak transcription	n/a	n/a	inside rSNPs	diseases
19	esv3516479	chr10:26354756-26355074	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26344200-26355800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr10:26352800-26358400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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