Variant report

Variant	rs17562958
Chromosome Location	chr12:60089308-60089309
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1795885	0.94[ASN][1000 genomes]
rs73111880	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869425	chr12:59746898-60479741	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
2	nsv899131	chr12:59942122-60124089	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv3365928	chr12:60042531-60343212	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	esv2829972	chr12:60079404-60111653	Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv899132	chr12:60087572-60211476	Strong transcription ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:60045800-60099800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr12:60050800-60098600	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr12:60069600-60131400	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr12:60071600-60098600	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr12:60072200-60098600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr12:60072800-60098000	Weak transcription	Primary B cells from peripheral blood	blood
7	chr12:60084400-60090800	Weak transcription	Fetal Heart	heart
8	chr12:60085200-60098600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr12:60086000-60102400	Weak transcription	Primary T cells from cord blood	blood
10	chr12:60086200-60098400	Weak transcription	Primary B cells from cord blood	blood
11	chr12:60086200-60105200	Weak transcription	Aorta	Aorta
12	chr12:60086200-60106400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr12:60087600-60108000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr12:60088200-60093600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr12:60088400-60093400	Enhancers	NHDF-Ad	bronchial
16	chr12:60088800-60089800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr12:60089000-60089400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr12:60089000-60089400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr12:60089000-60089400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr12:60089000-60089400	Enhancers	Left Ventricle	heart
21	chr12:60089000-60089400	Enhancers	HSMM	muscle
22	chr12:60089000-60089400	Enhancers	NHLF	lung
23	chr12:60089000-60089600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr12:60089000-60089600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr12:60089000-60089600	Enhancers	Muscle Satellite Cultured Cells	--
26	chr12:60089000-60089600	Enhancers	Right Atrium	heart
27	chr12:60089000-60089600	Enhancers	NHEK	skin
28	chr12:60089000-60089600	Enhancers	Osteobl	bone
29	chr12:60089200-60089600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr12:60089200-60089600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr12:60089200-60089600	Enhancers	HMEC	breast

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