Variant report

Variant	rs368480932
Chromosome Location	chr1:94851607-94851608
allele	-/AATCTG/AGAATCTG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428510	chr1:94709575-94866655	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv871097	chr1:94850443-94941890	Weak transcription Active TSS Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv3370830	chr1:94851566-94851612	Weak transcription Flanking Active TSS Enhancers Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	esv2570640	chr1:94851586-94851613	Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv159243	chr1:94851605-94851632	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	esv1442299	chr1:94851608-94851632	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:94846200-94854400	Enhancers	Fetal Intestine Small	intestine
2	chr1:94847400-94851800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr1:94849600-94851800	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr1:94849600-94852200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr1:94850000-94854000	Enhancers	Fetal Intestine Large	intestine
6	chr1:94850800-94851800	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr1:94851200-94851800	Enhancers	Rectal Mucosa Donor 31	rectum
8	chr1:94851200-94852000	Enhancers	Stomach Mucosa	stomach
9	chr1:94851200-94852200	Enhancers	Dnd41	blood
10	chr1:94851400-94853000	Weak transcription	Duodenum Mucosa	Duodenum
11	chr1:94851400-94853400	Enhancers	Fetal Thymus	thymus
12	chr1:94851400-94854200	Enhancers	HepG2	liver
13	chr1:94851600-94851800	Flanking Active TSS	Thymus	Thymus
14	chr1:94851600-94854800	Weak transcription	Primary T cells from cord blood	blood

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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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