Variant report

Variant	rs61520366
Chromosome Location	chr7:100744777-100744778
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:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100742551..100745856-chr7:100780456..100782799,3	MCF-7	breast:
2	chr7:100742716..100745205-chr7:100768993..100771932,2	K562	blood:
3	chr7:100742030..100745253-chr7:100746544..100749068,3	MCF-7	breast:
4	chr7:100744401..100746537-chr7:100796518..100798853,2	K562	blood:
5	chr7:100743492..100745258-chr7:100823374..100825550,2	K562	blood:
6	chr7:100744207..100746658-chr7:100768104..100769613,2	MCF-7	breast:
7	chr7:100743340..100745183-chr7:100770158..100771716,2	MCF-7	breast:
8	chr7:100743845..100746782-chr7:100757454..100760117,2	K562	blood:
9	chr7:100743340..100745457-chr7:100777578..100780413,3	MCF-7	breast:
10	chr7:100743987..100745634-chr7:100746718..100749324,4	MCF-7	breast:
11	chr7:100744152..100746979-chr7:100806016..100808822,2	K562	blood:
12	chr7:100741837..100746865-chr7:100749791..100753773,5	MCF-7	breast:
13	chr7:100743496..100745503-chr7:100745542..100749053,3	K562	blood:
14	chr7:100744230..100748590-chr7:100780366..100783718,4	K562	blood:
15	chr7:100738210..100739761-chr7:100744164..100746838,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000106367	Chromatin interaction
ENSG00000128564	Chromatin interaction
ENSG00000106366	Chromatin interaction
ENSG00000167011	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10230363	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10233905	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10238656	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11546152	1.00[ASN][1000 genomes]
rs2227666	1.00[ASN][1000 genomes]
rs28693845	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56158981	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56275099	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61730716	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61730718	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7241	1.00[ASN][1000 genomes]
rs73712063	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73712067	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1832517	chr7:100355490-100749246	Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	esv2758125	chr7:100355490-100749246	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Active TSS ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
3	esv2759547	chr7:100355490-100749246	Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	esv1826021	chr7:100525848-100749246	Flanking Active TSS Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	esv1846644	chr7:100525848-100749246	Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	esv1822460	chr7:100606044-100749246	Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
7	nsv427796	chr7:100606044-100749246	Strong transcription Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
8	nsv428181	chr7:100606044-100749246	Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
9	nsv831074	chr7:100606051-100745532	Bivalent Enhancer Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
10	nsv1031942	chr7:100606734-100788660	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
11	esv1833777	chr7:100632790-100800131	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
12	nsv1033081	chr7:100669629-100771824	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
13	nsv831075	chr7:100692297-100917018	Bivalent/Poised TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
14	nsv933653	chr7:100701931-101515782	Active TSS ZNF genes & repeats Bivalent Enhancer Enhancers Genic enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	107 gene(s)	inside rSNPs	diseases
15	nsv1030604	chr7:100717732-101223465	Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
16	nsv464649	chr7:100739682-100810983	Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
17	nsv607972	chr7:100739682-100810983	Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
18	esv2422376	chr7:100743485-101016471	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	63 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100733600-100755400	Weak transcription	Aorta	Aorta
2	chr7:100736200-100745000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr7:100738000-100745600	Enhancers	NHDF-Ad	bronchial
4	chr7:100741600-100748600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:100742200-100745200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr7:100742200-100745200	Enhancers	HMEC	breast
7	chr7:100742200-100746200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr7:100742400-100745600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:100742400-100745600	Enhancers	HUVEC	blood vessel
10	chr7:100742400-100745600	Enhancers	NH-A	brain
11	chr7:100742400-100745600	Enhancers	NHLF	lung
12	chr7:100742400-100749200	Enhancers	Placenta	Placenta
13	chr7:100742600-100745200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr7:100742600-100745400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:100742600-100745600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:100742600-100745600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr7:100742600-100745600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:100742800-100745600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr7:100743600-100745400	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr7:100743600-100745600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:100743600-100745600	Enhancers	Placenta Amnion	Placenta Amnion
22	chr7:100743800-100745000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr7:100743800-100745200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:100743800-100745600	Enhancers	H9 Cell Line	embryonic stem cell
25	chr7:100743800-100745600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr7:100744000-100745200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr7:100744000-100746600	Weak transcription	Colonic Mucosa	Colon
28	chr7:100744000-100746600	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr7:100744000-100746600	Enhancers	HepG2	liver
30	chr7:100744000-100746800	Weak transcription	Small Intestine	intestine
31	chr7:100744000-100748200	Weak transcription	Gastric	stomach
32	chr7:100744000-100751000	Weak transcription	Esophagus	oesophagus
33	chr7:100744000-100751800	Weak transcription	Left Ventricle	heart
34	chr7:100744200-100745200	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr7:100744200-100745400	Enhancers	NHEK	skin
36	chr7:100744200-100745400	Enhancers	Osteobl	bone
37	chr7:100744200-100745800	Enhancers	HSMMtube	muscle
38	chr7:100744200-100745800	Enhancers	K562	blood
39	chr7:100744200-100746000	Weak transcription	Liver	Liver
40	chr7:100744200-100746200	Weak transcription	Lung	lung
41	chr7:100744200-100746600	Enhancers	Hela-S3	cervix
42	chr7:100744200-100747600	Weak transcription	Adipose Nuclei	Adipose
43	chr7:100744200-100747600	Weak transcription	Spleen	Spleen
44	chr7:100744200-100748400	Weak transcription	Right Atrium	heart
45	chr7:100744200-100751000	Weak transcription	Brain Hippocampus Middle	brain
46	chr7:100744400-100744800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr7:100744400-100744800	Enhancers	A549	lung
48	chr7:100744400-100745600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr7:100744400-100746600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr7:100744400-100746800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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