Variant report

Variant	rs17156356
Chromosome Location	chr10:6516880-6516881
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:6506742..6509620-chr10:6514468..6518206,3	K562	blood:
2	chr10:6505761..6513673-chr10:6513705..6518581,11	K562	blood:
3	chr10:6515152..6516947-chr10:6622919..6625201,2	K562	blood:
4	chr10:6515689..6518540-chr10:6536895..6539799,2	K562	blood:

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11819303	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12254757	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12269156	0.86[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45567348	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7075155	0.86[JPT][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7895774	1.00[YRI][hapmap]

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	nsv1042286	chr10:5795129-6578445	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	nsv1053440	chr10:6354798-6669469	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
3	nsv1047309	chr10:6495583-6714060	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:6496600-6539200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr10:6498400-6537000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr10:6498600-6518800	Weak transcription	Fetal Stomach	stomach
4	chr10:6499000-6527800	Weak transcription	Pancreas	Pancrea
5	chr10:6499200-6562000	Weak transcription	Brain Anterior Caudate	brain
6	chr10:6501600-6527200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr10:6501800-6557000	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr10:6502200-6518800	Weak transcription	Fetal Muscle Trunk	muscle
9	chr10:6503000-6533000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr10:6504200-6517200	Weak transcription	Brain Hippocampus Middle	brain
11	chr10:6504400-6518200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr10:6504600-6524200	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr10:6506200-6520400	Weak transcription	Fetal Muscle Leg	muscle
14	chr10:6509200-6541200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr10:6509800-6517600	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr10:6509800-6533000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr10:6510000-6572000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr10:6513200-6517600	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr10:6513400-6517600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr10:6514000-6540000	Weak transcription	Psoas Muscle	Psoas
21	chr10:6514400-6518200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr10:6515000-6518800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr10:6515200-6517400	Flanking Active TSS	Dnd41	blood
24	chr10:6515400-6517000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr10:6515400-6517000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
26	chr10:6515400-6518200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr10:6515400-6520000	Enhancers	NHEK	skin
28	chr10:6516000-6517400	Enhancers	Brain Angular Gyrus	brain
29	chr10:6516000-6517400	Enhancers	Brain Substantia Nigra	brain
30	chr10:6516000-6517600	Enhancers	Fetal Kidney	kidney
31	chr10:6516000-6518200	Enhancers	Fetal Intestine Small	intestine
32	chr10:6516200-6517000	Weak transcription	Fetal Intestine Large	intestine
33	chr10:6516200-6517400	Enhancers	Brain Cingulate Gyrus	brain
34	chr10:6516200-6518000	Enhancers	K562	blood
35	chr10:6516400-6517000	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr10:6516400-6517000	Enhancers	Primary T cells fromperipheralblood	blood
37	chr10:6516400-6517000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
38	chr10:6516400-6517000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
39	chr10:6516400-6517200	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr10:6516400-6517200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr10:6516400-6517200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr10:6516400-6517200	Enhancers	Fetal Thymus	thymus
43	chr10:6516400-6517400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr10:6516400-6517400	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr10:6516400-6517800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
46	chr10:6516400-6517800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr10:6516400-6517800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr10:6516400-6518000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr10:6516400-6518600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr10:6516400-6518600	Weak transcription	HMEC	breast

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