Variant report

Variant	rs12947305
Chromosome Location	chr17:38775400-38775401
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:38772991..38776371-chr17:38950027..38953549,4	MCF-7	breast:
2	chr17:38711199..38713464-chr17:38773822..38775935,2	MCF-7	breast:
3	chr17:38773571..38776015-chr17:38974880..38976971,2	MCF-7	breast:
4	chr17:38771673..38774769-chr17:38774806..38776457,3	K562	blood:
5	chr17:38732131..38732809-chr17:38775272..38776029,4	MCF-7	breast:
6	chr17:38773127..38778716-chr17:38801405..38806004,8	MCF-7	breast:
7	chr17:38722952..38724580-chr17:38773813..38776403,2	MCF-7	breast:
8	chr17:38773408..38778160-chr17:38801455..38807561,11	MCF-7	breast:
9	chr17:38774901..38776948-chr17:38802211..38805004,2	K562	blood:
10	chr17:38732692..38734383-chr17:38772868..38775729,2	MCF-7	breast:
11	chr17:38774850..38777114-chr17:38779652..38781340,2	MCF-7	breast:
12	chr17:38707503..38711120-chr17:38769935..38775644,8	MCF-7	breast:
13	chr17:38772124..38774636-chr17:38774789..38776541,3	MCF-7	breast:
14	chr17:38705642..38709928-chr17:38772338..38775854,5	MCF-7	breast:
15	chr17:38602265..38605118-chr17:38774156..38776452,3	MCF-7	breast:
16	chr17:38775118..38777132-chr17:38858165..38860352,2	MCF-7	breast:
17	chr17:38733163..38735894-chr17:38771819..38775610,4	MCF-7	breast:
18	chr17:38470862..38473621-chr17:38773618..38775413,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000167920	Chromatin interaction
ENSG00000073584	Chromatin interaction
ENSG00000167916	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10305311	1.00[MEX][hapmap]
rs12943070	1.00[MEX][hapmap];1.00[AMR][1000 genomes]
rs12948594	1.00[MEX][hapmap]
rs12952605	1.00[AMR][1000 genomes]
rs16966114	1.00[AMR][1000 genomes]
rs16966124	1.00[MEX][hapmap]
rs35695383	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71371437	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9895118	1.00[MEX][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	nsv574994	chr17:38719799-38824636	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	esv2758454	chr17:38748300-38850104	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	esv2758689	chr17:38748300-38850104	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv431626	chr17:38770965-38999722	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:38763400-38775600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr17:38769600-38784200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr17:38770800-38776200	Enhancers	Placenta	Placenta
4	chr17:38772000-38776400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr17:38772000-38784600	Weak transcription	Gastric	stomach
6	chr17:38772000-38785000	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr17:38772200-38775800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr17:38772200-38776200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr17:38772400-38775400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
10	chr17:38772400-38775400	Weak transcription	A549	lung
11	chr17:38772400-38776200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr17:38772400-38778800	Weak transcription	Spleen	Spleen
13	chr17:38772400-38783600	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr17:38772600-38775400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
15	chr17:38772600-38775600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr17:38772600-38775800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr17:38772600-38785000	Weak transcription	Ovary	ovary
18	chr17:38772800-38775400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr17:38772800-38775400	Weak transcription	Fetal Thymus	thymus
20	chr17:38772800-38776000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr17:38773000-38784400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr17:38773000-38786800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr17:38773200-38775800	Weak transcription	Primary T cells from cord blood	blood
24	chr17:38773400-38775600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr17:38773600-38775400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr17:38773600-38775600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr17:38773600-38776000	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr17:38773800-38775800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr17:38773800-38776600	Enhancers	Fetal Intestine Small	intestine
30	chr17:38774000-38775400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr17:38774000-38775400	Weak transcription	Primary T helper cells fromperipheralblood	blood
32	chr17:38774000-38775400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr17:38774200-38775400	Weak transcription	Primary B cells from cord blood	blood
34	chr17:38774200-38775400	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr17:38774200-38775400	Weak transcription	Colonic Mucosa	Colon
36	chr17:38774200-38776200	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr17:38774200-38776600	Enhancers	Fetal Intestine Large	intestine
38	chr17:38774200-38784600	Weak transcription	Esophagus	oesophagus
39	chr17:38774400-38775400	Weak transcription	Primary B cells from peripheral blood	blood
40	chr17:38774400-38776200	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr17:38774400-38785000	Weak transcription	Lung	lung
42	chr17:38774400-38786200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr17:38774400-38789200	Weak transcription	Right Atrium	heart
44	chr17:38774600-38775800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr17:38775000-38776000	Flanking Active TSS	HepG2	liver
46	chr17:38775000-38776400	Enhancers	Liver	Liver
47	chr17:38775200-38775400	Enhancers	Fetal Kidney	kidney
48	chr17:38775200-38775600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr17:38775200-38776000	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr17:38775200-38776800	Enhancers	Rectal Mucosa Donor 29	rectum

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