Variant report

Variant	rs57712206
Chromosome Location	chr7:5782263-5782264
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:5779441..5783030-chr7:5818852..5821920,4	MCF-7	breast:
2	chr7:5601361..5603179-chr7:5781654..5783256,2	K562	blood:

Variant related genes	Relation type
ENSG00000011275	Chromatin interaction
ENSG00000075624	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10229675	1.00[AMR][1000 genomes]
rs10252738	1.00[AMR][1000 genomes]
rs11977543	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11980653	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11981617	0.86[AFR][1000 genomes]
rs11984261	1.00[AMR][1000 genomes]
rs28590038	1.00[AMR][1000 genomes]
rs6959488	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73341666	1.00[AMR][1000 genomes]
rs73341668	1.00[AMR][1000 genomes]
rs7784998	1.00[AMR][1000 genomes]
rs7795701	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7805039	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869165	chr7:4889618-5799719	Weak transcription Genic enhancers Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	352 gene(s)	inside rSNPs	diseases
2	nsv530979	chr7:5101631-5864814	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription 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 miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
3	nsv530981	chr7:5157150-5920006	Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	348 gene(s)	inside rSNPs	diseases
4	nsv530983	chr7:5370746-6070852	Active TSS Strong transcription Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	368 gene(s)	inside rSNPs	diseases
5	nsv916391	chr7:5417945-5889565	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	336 gene(s)	inside rSNPs	diseases
6	nsv533108	chr7:5488018-6316581	Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	390 gene(s)	inside rSNPs	diseases
7	nsv1033556	chr7:5565080-6186815	Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
8	nsv538710	chr7:5565080-6186815	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	357 gene(s)	inside rSNPs	diseases
9	nsv530467	chr7:5617816-5815082	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
10	nsv1017612	chr7:5629728-5819144	Genic enhancers Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
11	nsv1021989	chr7:5629728-6186815	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	126 gene(s)	inside rSNPs	diseases
12	nsv887419	chr7:5703669-5820383	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
13	nsv830891	chr7:5726301-5895460	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
14	nsv1028601	chr7:5748982-5919098	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
15	nsv1034215	chr7:5748982-6056619	Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
16	nsv1016690	chr7:5749222-6056619	Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	46 gene(s)	inside rSNPs	diseases
17	nsv1027679	chr7:5760731-6056619	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
18	nsv464293	chr7:5778796-5891221	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
19	nsv464294	chr7:5778796-5891221	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
20	nsv605987	chr7:5778796-5891221	Weak transcription Active TSS Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5753200-5794400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:5761600-5785600	Weak transcription	Fetal Brain Male	brain
3	chr7:5761800-5783000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:5762000-5820400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:5762800-5786000	Weak transcription	Fetal Kidney	kidney
6	chr7:5762800-5790200	Weak transcription	Small Intestine	intestine
7	chr7:5765200-5790400	Weak transcription	Psoas Muscle	Psoas
8	chr7:5768800-5798200	Weak transcription	Colonic Mucosa	Colon
9	chr7:5769000-5783800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:5769000-5785600	Weak transcription	Brain Angular Gyrus	brain
11	chr7:5769200-5785000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr7:5769200-5790200	Weak transcription	Pancreas	Pancrea
13	chr7:5769600-5783400	Weak transcription	Fetal Lung	lung
14	chr7:5774200-5783800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr7:5774200-5800600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr7:5775400-5782600	Strong transcription	Fetal Intestine Small	intestine
17	chr7:5775800-5782800	Strong transcription	Fetal Stomach	stomach
18	chr7:5776600-5783200	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr7:5776800-5783400	Strong transcription	Fetal Muscle Trunk	muscle
20	chr7:5776800-5786600	Strong transcription	Fetal Thymus	thymus
21	chr7:5777200-5783400	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr7:5777400-5783000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr7:5777800-5783000	Strong transcription	Cortex derived primary cultured neurospheres	brain
24	chr7:5778800-5782600	Weak transcription	Rectal Smooth Muscle	rectum
25	chr7:5779000-5783400	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr7:5779200-5783200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr7:5779200-5783400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr7:5779200-5783400	Weak transcription	Fetal Heart	heart
29	chr7:5779200-5783400	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr7:5779200-5785800	Weak transcription	NH-A	brain
31	chr7:5779200-5788000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr7:5779400-5783200	Weak transcription	GM12878-XiMat	blood
33	chr7:5779400-5784600	Weak transcription	HUVEC	blood vessel
34	chr7:5779400-5789400	Weak transcription	HMEC	breast
35	chr7:5779600-5783000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
36	chr7:5779600-5783200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr7:5780400-5783200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
38	chr7:5780600-5783400	Weak transcription	Brain Substantia Nigra	brain
39	chr7:5780600-5783600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:5780800-5783600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr7:5781000-5782400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:5781000-5783400	Weak transcription	Fetal Brain Female	brain
43	chr7:5781000-5785200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr7:5781000-5785600	Weak transcription	Aorta	Aorta
45	chr7:5781200-5782800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr7:5781200-5782800	Weak transcription	Brain Germinal Matrix	brain
47	chr7:5781200-5783000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr7:5781200-5783000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr7:5781200-5783200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr7:5781200-5783200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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