Variant report

Variant	rs12131917
Chromosome Location	chr1:160824044-160824045
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs2295615	1.00[CHB][hapmap]
rs978763	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1822379	chr1:160545332-160831143	Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv464161	chr1:160747615-160852046	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv548057	chr1:160747615-160852046	Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv946456	chr1:160812650-160824679	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:160811800-160824600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr1:160812800-160824200	Weak transcription	Thymus	Thymus
3	chr1:160817800-160825400	Genic enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr1:160821000-160828200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr1:160821000-160830800	Weak transcription	Spleen	Spleen
6	chr1:160821200-160825200	Weak transcription	Fetal Intestine Small	intestine
7	chr1:160821600-160828000	Weak transcription	Fetal Intestine Large	intestine
8	chr1:160822400-160825400	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr1:160822400-160825800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr1:160823000-160829000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
11	chr1:160823200-160824600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:160823200-160824800	Enhancers	Primary hematopoietic stem cells	blood
13	chr1:160823200-160825000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:160823400-160824800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr1:160823400-160826200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr1:160823600-160826200	Enhancers	Fetal Thymus	thymus
17	chr1:160824000-160826400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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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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