Variant report

Variant	rs3775885
Chromosome Location	chr4:8595887-8595888
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:8595618..8598948-chr4:8601035..8605983,4	MCF-7	breast:
2	chr4:8595691..8598338-chr4:8600228..8602977,2	MCF-7	breast:
3	chr4:8470170..8471110-chr4:8595421..8596838,7	MCF-7	breast:
4	chr4:8595503..8598248-chr4:8607204..8609791,3	MCF-7	breast:
5	chr4:8507896..8508408-chr4:8595816..8596778,2	MCF-7	breast:
6	chr4:8470225..8471528-chr4:8595848..8597093,11	K562	blood:

Variant related genes	Relation type
ENSG00000109625	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs2302582	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3756181	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3775884	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3775886	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3796737	0.96[ASN][1000 genomes]
rs3796738	0.80[ASN][1000 genomes]
rs3796739	0.96[ASN][1000 genomes]
rs4696855	0.81[ASN][1000 genomes]
rs6820571	0.81[ASN][1000 genomes]
rs73213354	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73213364	0.99[ASN][1000 genomes]
rs7683057	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878604	chr4:8315938-8618916	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1002680	chr4:8357163-8721214	Active TSS Flanking Active TSS Strong transcription Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv878612	chr4:8534283-8618916	Bivalent Enhancer Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	esv1832730	chr4:8541086-9514568	Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
5	esv1843578	chr4:8541086-9514568	Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	65 gene(s)	inside rSNPs	diseases
6	nsv878613	chr4:8554894-8618916	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv878614	chr4:8554894-8669619	Strong transcription Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv878615	chr4:8566758-8625245	Genic enhancers Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv878616	chr4:8566758-8669619	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv878617	chr4:8566758-9371116	ZNF genes & repeats Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
11	nsv1014219	chr4:8578779-8724531	Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
12	nsv878618	chr4:8579758-8641696	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
13	nsv878619	chr4:8579758-8669619	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
14	nsv878620	chr4:8584879-8674871	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv470015	chr4:8584879-8729638	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
16	nsv878621	chr4:8584879-9371116	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:8573400-8609400	Weak transcription	Right Atrium	heart
2	chr4:8594000-8596200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
3	chr4:8594200-8596000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
4	chr4:8594200-8596400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
5	chr4:8594400-8596000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:8594600-8596000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:8594600-8596000	Flanking Bivalent TSS/Enh	Placenta	Placenta
8	chr4:8594800-8596200	Flanking Bivalent TSS/Enh	Osteobl	bone
9	chr4:8595000-8596000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:8595000-8596200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:8595000-8596200	Bivalent Enhancer	HepG2	liver
12	chr4:8595000-8596400	Enhancers	K562	blood
13	chr4:8595200-8596200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr4:8595200-8596400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
15	chr4:8595400-8596000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
16	chr4:8595400-8596000	Flanking Bivalent TSS/Enh	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr4:8595400-8596000	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
18	chr4:8595400-8596200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr4:8595400-8596200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:8595400-8596200	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
21	chr4:8595600-8596000	Transcr. at gene 5' and 3'	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:8595600-8596000	Active TSS	H9 Cell Line	embryonic stem cell
23	chr4:8595600-8596000	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr4:8595600-8596000	Bivalent Enhancer	Adipose Nuclei	Adipose
25	chr4:8595600-8596000	Flanking Bivalent TSS/Enh	NHDF-Ad	bronchial
26	chr4:8595600-8596000	Bivalent/Poised TSS	NHLF	lung
27	chr4:8595600-8596200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr4:8595600-8596200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr4:8595600-8596200	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr4:8595600-8596200	Flanking Active TSS	Ovary	ovary
31	chr4:8595600-8596200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr4:8595600-8596200	Flanking Active TSS	HSMMtube	muscle
33	chr4:8595800-8596000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
34	chr4:8595800-8596000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
35	chr4:8595800-8596000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
36	chr4:8595800-8596000	Bivalent Enhancer	Esophagus	oesophagus
37	chr4:8595800-8596000	Bivalent Enhancer	Fetal Kidney	kidney
38	chr4:8595800-8596000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
39	chr4:8595800-8596200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
40	chr4:8595800-8596200	Enhancers	H1 Cell Line	embryonic stem cell
41	chr4:8595800-8596200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:8595800-8596200	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr4:8595800-8596200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:8595800-8596200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr4:8595800-8596200	Flanking Active TSS	HSMM	muscle
46	chr4:8595800-8596400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links