Variant report

Variant	rs327100
Chromosome Location	chr4:187639786-187639787
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:187619254..187623290-chr4:187636723..187640845,3	MCF-7	breast:
2	chr4:187639395..187641125-chr4:187652205..187654706,2	K562	blood:
3	chr4:187638279..187640138-chr4:187642183..187644541,2	K562	blood:

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs17077740	0.84[EUR][1000 genomes]
rs189008	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs327093	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs327095	0.98[ASN][1000 genomes]
rs327096	1.00[ASN][1000 genomes]
rs327097	0.99[ASN][1000 genomes]
rs327098	0.99[ASN][1000 genomes]
rs327099	1.00[ASN][1000 genomes]
rs327101	1.00[ASN][1000 genomes]
rs327102	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3733409	0.84[EUR][1000 genomes]
rs3733415	0.84[EUR][1000 genomes]
rs455219	0.92[ASN][1000 genomes]
rs73015641	0.90[ASN][1000 genomes]
rs73015656	0.84[EUR][1000 genomes]
rs73015660	0.84[EUR][1000 genomes]
rs73015670	0.81[EUR][1000 genomes]
rs907988	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025088	chr4:187407683-187674585	Genic enhancers Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats 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	13 gene(s)	inside rSNPs	diseases
2	nsv1025244	chr4:187419770-188284813	Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv1034212	chr4:187437895-188030805	Weak transcription Active TSS Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv537438	chr4:187437895-188030805	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv532745	chr4:187471692-188205443	Bivalent/Poised TSS Weak transcription Genic enhancers Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv1022262	chr4:187475862-187848284	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
7	nsv1024705	chr4:187534005-187849091	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
8	nsv1026970	chr4:187537418-187913351	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
9	nsv596440	chr4:187538133-187848075	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1031603	chr4:187636716-188020741	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr4:187626400-187643600	Weak transcription	Stomach Mucosa	stomach
2	chr4:187630400-187643600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:187630600-187641600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr4:187631000-187640000	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr4:187631000-187641200	Weak transcription	Fetal Kidney	kidney
6	chr4:187631000-187643600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr4:187633800-187640000	Weak transcription	NHDF-Ad	bronchial
8	chr4:187634800-187640000	Weak transcription	HSMM	muscle
9	chr4:187634800-187644200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr4:187635400-187644200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:187635600-187640800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr4:187635600-187643200	Weak transcription	Right Ventricle	heart
13	chr4:187635800-187639800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr4:187635800-187643800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr4:187636200-187640200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr4:187637000-187641600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:187637200-187640000	Weak transcription	Fetal Lung	lung
18	chr4:187637400-187640800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr4:187637400-187641200	Weak transcription	Osteobl	bone
20	chr4:187637400-187641600	Weak transcription	NH-A	brain
21	chr4:187637400-187643000	Weak transcription	Aorta	Aorta
22	chr4:187637600-187640000	ZNF genes & repeats	Fetal Intestine Small	intestine
23	chr4:187637600-187643400	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:187637800-187641400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr4:187638200-187640000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:187638200-187641800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr4:187638200-187644200	Weak transcription	Pancreas	Pancrea
28	chr4:187638800-187639800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr4:187638800-187640000	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr4:187639000-187640000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr4:187639000-187640000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr4:187639000-187640200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr4:187639200-187639800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:187639200-187640000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr4:187639200-187640200	Enhancers	HMEC	breast
36	chr4:187639200-187641400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:187639200-187642600	Weak transcription	Colon Smooth Muscle	Colon
38	chr4:187639400-187639800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:187639400-187640200	Weak transcription	Fetal Heart	heart
40	chr4:187639400-187643400	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr4:187639600-187640200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr4:187639600-187642600	Genic enhancers	NHEK	skin

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