Variant report

Variant	rs6950757
Chromosome Location	chr7:5738315-5738316
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:5734503..5737746-chr7:5737831..5742522,7	MCF-7	breast:
2	chr7:5736261..5739455-chr7:5742456..5746657,4	MCF-7	breast:
3	chr7:5569883..5572115-chr7:5735560..5738502,2	MCF-7	breast:
4	chr7:5729527..5732207-chr7:5738007..5741204,4	K562	blood:
5	chr7:5726904..5729292-chr7:5737755..5739393,2	K562	blood:

Variant related genes	Relation type
ENSG00000075624	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10230002	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10242141	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10276132	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10280662	0.91[AFR][1000 genomes]
rs10441129	0.82[AFR][1000 genomes]
rs28411680	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28418908	1.00[AMR][1000 genomes]
rs28446539	1.00[AMR][1000 genomes]
rs28578361	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28588522	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28720074	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58469547	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6964579	0.83[AFR][1000 genomes]
rs6968103	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73338077	0.89[AFR][1000 genomes]
rs73338095	0.89[AFR][1000 genomes]
rs73338096	1.00[AMR][1000 genomes]
rs73341621	1.00[AMR][1000 genomes]
rs73341623	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73341624	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 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	nsv482449	chr7:5557585-5743673	Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	294 gene(s)	inside rSNPs	diseases
8	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
9	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
10	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
11	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
12	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
13	nsv887417	chr7:5667645-5760860	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
14	nsv887418	chr7:5675305-5772551	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
15	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
16	nsv1028652	chr7:5706207-5769489	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
17	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

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5720200-5741400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr7:5723000-5740800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:5723400-5740600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:5723400-5766400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr7:5723600-5740600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr7:5730000-5740400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr7:5731400-5740800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr7:5732000-5740600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr7:5732000-5741000	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr7:5732600-5747600	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr7:5733400-5740800	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr7:5733800-5740400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:5734200-5739400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr7:5734200-5743400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr7:5734400-5740400	Weak transcription	Gastric	stomach
16	chr7:5735000-5738400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:5735200-5738400	Genic enhancers	Fetal Intestine Small	intestine
18	chr7:5735200-5738600	Enhancers	Right Atrium	heart
19	chr7:5735200-5739400	Strong transcription	HepG2	liver
20	chr7:5735200-5739800	Strong transcription	NHEK	skin
21	chr7:5735400-5741000	Enhancers	Brain Cingulate Gyrus	brain
22	chr7:5735400-5741800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr7:5735600-5738800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr7:5735600-5740000	Enhancers	Stomach Mucosa	stomach
25	chr7:5735600-5740800	Genic enhancers	Fetal Stomach	stomach
26	chr7:5735600-5742000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
27	chr7:5735600-5742000	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr7:5735600-5742000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr7:5735800-5738400	Enhancers	Adipose Nuclei	Adipose
30	chr7:5735800-5739000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr7:5735800-5739200	Enhancers	Brain Hippocampus Middle	brain
32	chr7:5735800-5739200	Enhancers	NHDF-Ad	bronchial
33	chr7:5735800-5739400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:5735800-5739600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr7:5735800-5739800	Enhancers	Fetal Kidney	kidney
36	chr7:5735800-5740400	Enhancers	Primary T helper cells PMA-I stimulated	--
37	chr7:5735800-5741400	Genic enhancers	Fetal Thymus	thymus
38	chr7:5735800-5741800	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chr7:5735800-5742000	Enhancers	Primary T cells fromperipheralblood	blood
40	chr7:5735800-5744200	Enhancers	Brain Angular Gyrus	brain
41	chr7:5735800-5744200	Enhancers	Brain Anterior Caudate	brain
42	chr7:5735800-5746000	Weak transcription	HUVEC	blood vessel
43	chr7:5736000-5739200	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr7:5736000-5739200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr7:5736000-5739200	Enhancers	Fetal Heart	heart
46	chr7:5736000-5739200	Weak transcription	A549	lung
47	chr7:5736000-5739400	Weak transcription	Brain Germinal Matrix	brain
48	chr7:5736000-5740400	Weak transcription	Fetal Brain Female	brain
49	chr7:5736000-5740600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr7:5736000-5740800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood

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