Variant report

Variant	rs367545997
Chromosome Location	chr2:99370540-99370541
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011278	chr2:99280928-99638376	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv535835	chr2:99280928-99638376	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv520854	chr2:99369757-99373720	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:99359600-99374000	Weak transcription	Aorta	Aorta
2	chr2:99361400-99374000	Weak transcription	Pancreas	Pancrea
3	chr2:99362400-99372800	Weak transcription	Primary T cells from cord blood	blood
4	chr2:99364800-99371200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr2:99365200-99372200	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr2:99365400-99371600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr2:99365400-99372400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr2:99365600-99373600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr2:99365800-99374400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr2:99366200-99372200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr2:99366600-99373200	Weak transcription	Primary T cells fromperipheralblood	blood
12	chr2:99367400-99374000	Weak transcription	Esophagus	oesophagus
13	chr2:99369600-99373600	Weak transcription	HUVEC	blood vessel
14	chr2:99369800-99371200	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr2:99370000-99371200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr2:99370200-99370800	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr2:99370200-99371000	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr2:99370400-99371400	Weak transcription	Primary T helper naive cells fromperipheralblood	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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