Variant report

Variant	rs652944
Chromosome Location	chr12:10096792-10096793
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11053533	0.85[JPT][hapmap];0.82[ASN][1000 genomes]
rs11053536	1.00[JPT][hapmap]
rs11053538	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs11053548	0.93[JPT][hapmap]
rs11615825	0.83[ASN][1000 genomes]
rs2273987	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs3818343	0.87[CHB][hapmap];1.00[JPT][hapmap]
rs673173	0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs676397	0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][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	nsv1044587	chr12:10029514-10123414	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv523050	chr12:10031880-10124373	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv898755	chr12:10069302-10186284	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10095600-10097200	Enhancers	Primary B cells from peripheral blood	blood
2	chr12:10095800-10096800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr12:10096000-10097800	Enhancers	Primary B cells from cord blood	blood
4	chr12:10096200-10096800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr12:10096200-10101400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:10096400-10096800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr12:10096400-10097000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr12:10096400-10097200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr12:10096400-10097400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr12:10096400-10097400	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr12:10096400-10097400	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr12:10096400-10100800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr12:10096400-10102200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr12:10096400-10104800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr12:10096600-10097400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr12:10096600-10097600	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr12:10096600-10097600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr12:10096600-10097800	Enhancers	Primary T cells from cord blood	blood
19	chr12:10096600-10097800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr12:10096600-10097800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr12:10096600-10098200	Enhancers	Primary hematopoietic stem cells	blood

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