Variant report

Variant	rs7795672
Chromosome Location	chr7:4019887-4019888
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:4019163..4020923-chr7:4023693..4025732,2	MCF-7	breast:
2	chr7:4017263..4020114-chr7:4033436..4035311,2	MCF-7	breast:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10244444	1.00[EUR][1000 genomes]
rs10441085	1.00[EUR][1000 genomes]
rs11972137	1.00[EUR][1000 genomes]
rs58205148	1.00[EUR][1000 genomes]
rs61080392	1.00[EUR][1000 genomes]
rs6462388	1.00[EUR][1000 genomes]
rs73673203	1.00[EUR][1000 genomes]
rs73673204	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7794993	1.00[EUR][1000 genomes]
rs7805865	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021650	chr7:3665232-4577439	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats 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	4 gene(s)	inside rSNPs	diseases
2	nsv1029406	chr7:3860894-4477095	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv538685	chr7:3860894-4477095	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1026410	chr7:3869104-4383606	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1025497	chr7:3905444-4176032	Enhancers Strong transcription ZNF genes & repeats Genic enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv538686	chr7:3905444-4176032	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv433014	chr7:3910039-4054769	Strong transcription Enhancers Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv464274	chr7:3955516-4613607	Weak transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv464275	chr7:3955516-4613607	Enhancers Active TSS Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv464276	chr7:3955516-4613607	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv464277	chr7:3955516-4613607	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv464278	chr7:3955516-4613607	Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv605939	chr7:3955516-4613607	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	nsv1019086	chr7:3968656-4044519	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv538687	chr7:3968656-4044519	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv1019305	chr7:3991646-4276004	Enhancers Weak transcription Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv1033687	chr7:4006020-4267871	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv538688	chr7:4006020-4267871	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
19	nsv917252	chr7:4017819-4374090	Weak transcription Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3988600-4032600	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr7:3989400-4031000	Weak transcription	Right Ventricle	heart
3	chr7:3989800-4020800	Weak transcription	Colon Smooth Muscle	Colon
4	chr7:3996400-4037600	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr7:3998000-4020800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr7:3998400-4045600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr7:4000200-4032600	Weak transcription	Adipose Nuclei	Adipose
8	chr7:4007800-4027200	Weak transcription	Spleen	Spleen
9	chr7:4008000-4020600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr7:4008000-4021600	Weak transcription	Stomach Smooth Muscle	stomach
11	chr7:4008000-4030400	Weak transcription	Gastric	stomach
12	chr7:4008200-4020800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr7:4013400-4021800	Weak transcription	Fetal Lung	lung
14	chr7:4015400-4031000	Weak transcription	HSMMtube	muscle
15	chr7:4015600-4028800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr7:4015600-4036200	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr7:4017400-4027200	Weak transcription	Pancreas	Pancrea
18	chr7:4017600-4023800	Weak transcription	Fetal Stomach	stomach
19	chr7:4017600-4027200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:4018800-4023800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr7:4019000-4020200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr7:4019000-4020400	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr7:4019000-4020400	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr7:4019000-4020800	Weak transcription	Aorta	Aorta
25	chr7:4019200-4020000	Enhancers	HUES48 Cell Line	embryonic stem cell
26	chr7:4019200-4020200	Enhancers	H1 Cell Line	embryonic stem cell
27	chr7:4019200-4020400	Enhancers	NHEK	skin
28	chr7:4019200-4020800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr7:4019200-4045800	Weak transcription	Fetal Brain Female	brain
30	chr7:4019400-4020000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr7:4019400-4020200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr7:4019400-4020200	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr7:4019400-4020200	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr7:4019400-4020400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr7:4019400-4020800	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr7:4019400-4031800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:4019600-4020000	Flanking Active TSS	HUVEC	blood vessel
38	chr7:4019600-4020600	Weak transcription	Fetal Heart	heart
39	chr7:4019800-4020000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr7:4019800-4020200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr7:4019800-4021000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr7:4019800-4021400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links