Variant report

Variant	rs2793855
Chromosome Location	chr1:158938644-158938645
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs1102001	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856073	0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856081	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856083	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs856086	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]

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	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

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	chr1:158931600-158939600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:158932400-158942400	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr1:158933400-158941200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr1:158933400-158943000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr1:158933400-158949400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr1:158935200-158941400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:158937000-158944000	Weak transcription	Primary T cells from cord blood	blood
10	chr1:158938200-158938800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr1:158938400-158939600	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr1:158938600-158940400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:158938600-158940400	Enhancers	NHEK	skin

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

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