Variant report

Variant	rs9910270
Chromosome Location	chr17:17315717-17315718
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:17291681..17293275-chr17:17315308..17316852,2	MCF-7	breast:

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs28469179	0.82[AFR][1000 genomes]
rs28605635	0.80[AFR][1000 genomes]
rs73288419	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1058849	chr17:17308009-17348548	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1058804	chr17:17308984-17348548	Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1062207	chr17:17310099-17344599	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv543234	chr17:17310099-17344599	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv574523	chr17:17310886-17347995	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1056137	chr17:17311017-17348939	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv543235	chr17:17311017-17348939	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv482648	chr17:17315268-17455442	Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17302000-17318800	Weak transcription	Right Atrium	heart
2	chr17:17307200-17316600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr17:17308000-17322200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr17:17308200-17316600	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr17:17310400-17317200	Weak transcription	Lung	lung
6	chr17:17311000-17317800	Weak transcription	Fetal Brain Female	brain
7	chr17:17312200-17315800	Weak transcription	Adipose Nuclei	Adipose
8	chr17:17312400-17315800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr17:17312400-17317200	Weak transcription	NHLF	lung
10	chr17:17312400-17318800	Weak transcription	HepG2	liver
11	chr17:17313200-17319400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr17:17313400-17317200	Weak transcription	Pancreas	Pancrea
13	chr17:17313600-17319200	Weak transcription	K562	blood
14	chr17:17313800-17317200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr17:17313800-17317400	Weak transcription	Fetal Brain Male	brain
16	chr17:17314000-17317200	Weak transcription	Thymus	Thymus
17	chr17:17314200-17316400	Weak transcription	Brain Germinal Matrix	brain
18	chr17:17314800-17317000	Enhancers	Muscle Satellite Cultured Cells	--
19	chr17:17314800-17317000	Enhancers	Hela-S3	cervix
20	chr17:17315000-17317000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr17:17315000-17317200	Enhancers	Osteobl	bone
22	chr17:17315000-17317400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr17:17315200-17316000	Enhancers	NHEK	skin
24	chr17:17315200-17316400	Enhancers	HMEC	breast
25	chr17:17315200-17316600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr17:17315200-17317000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr17:17315200-17317000	Enhancers	HUVEC	blood vessel
28	chr17:17315200-17317400	Enhancers	NHDF-Ad	bronchial
29	chr17:17315200-17320600	Enhancers	Dnd41	blood
30	chr17:17315400-17316000	Enhancers	Placenta	Placenta
31	chr17:17315400-17316400	Enhancers	Primary hematopoietic stem cells	blood
32	chr17:17315400-17316600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr17:17315400-17316800	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr17:17315400-17317000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr17:17315400-17317200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr17:17315400-17317200	Enhancers	NH-A	brain
37	chr17:17315400-17319600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr17:17315400-17322800	Enhancers	Fetal Thymus	thymus
39	chr17:17315600-17317200	Weak transcription	HSMM	muscle
40	chr17:17315600-17319600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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