Variant report

Variant	rs374414091
Chromosome Location	chr1:158945027-158945028
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002401	chr1:158712627-158972031	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv3376764	chr1:158761947-158998617	Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	esv3369957	chr1:158915589-159003393	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
4	nsv947329	chr1:158944939-158948344	Enhancers Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv2512967	chr1:158945026-158945027	Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv153388	chr1:158945026-158945027	Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	esv2219584	chr1:158945026-158945028	Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv1658743	chr1:158945028-158945030	Strong transcription Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:158920600-158950600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr1:158923000-158949600	Weak transcription	Primary B cells from cord blood	blood
3	chr1:158933400-158949400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr1:158939600-158946000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr1:158940600-158953000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr1:158941200-158952200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr1:158941400-158948400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr1:158942400-158948600	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr1:158942800-158947400	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr1:158943000-158949200	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr1:158943600-158945400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr1:158944000-158947400	Strong transcription	Primary T cells from cord blood	blood
13	chr1:158944400-158945800	Weak transcription	Primary T cells effector/memory enriched 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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