Variant report

Variant	rs10015544
Chromosome Location	chr4:87915801-87915802
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:87912671..87915829-chr4:87926237..87929506,4	MCF-7	breast:
2	chr4:87913434..87916324-chr4:87927780..87929757,3	MCF-7	breast:
3	chr4:87892847..87896142-chr4:87913687..87916404,3	K562	blood:

Variant related genes	Relation type
ENSG00000172493	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10003331	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10022825	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10032200	1.00[ASN][1000 genomes]
rs10050309	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1037813	1.00[ASN][1000 genomes]
rs12508231	1.00[ASN][1000 genomes]
rs13103234	1.00[ASN][1000 genomes]
rs13108043	1.00[ASN][1000 genomes]
rs13134084	1.00[ASN][1000 genomes]
rs17012304	1.00[ASN][1000 genomes]
rs17030453	1.00[ASN][1000 genomes]
rs17604937	1.00[ASN][1000 genomes]
rs17668731	1.00[ASN][1000 genomes]
rs17668952	1.00[ASN][1000 genomes]
rs17703261	1.00[ASN][1000 genomes]
rs2230858	1.00[ASN][1000 genomes]
rs28495374	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28667805	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28791499	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35658582	1.00[ASN][1000 genomes]
rs366327	1.00[ASN][1000 genomes]
rs56656813	1.00[ASN][1000 genomes]
rs58478399	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62306540	1.00[ASN][1000 genomes]
rs71607404	1.00[ASN][1000 genomes]
rs72877916	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72877918	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009937	chr4:87795314-88008345	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
2	nsv999176	chr4:87869996-88098136	Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv998335	chr4:87869996-88104414	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
4	nsv1001017	chr4:87872160-88087003	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv537166	chr4:87872160-88087003	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv999098	chr4:87899091-88016048	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
7	nsv537167	chr4:87899091-88016048	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:87872600-87926200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr4:87882600-87920200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr4:87892400-87920600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr4:87894600-87921000	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr4:87895400-87920000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr4:87896200-87916000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr4:87896200-87919200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr4:87896800-87918800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:87899000-87920600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr4:87899000-87921200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr4:87899200-87920800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr4:87899200-87922800	Weak transcription	Osteobl	bone
13	chr4:87899200-87925800	Weak transcription	Hela-S3	cervix
14	chr4:87899200-87926600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:87900000-87924400	Weak transcription	NHEK	skin
16	chr4:87900200-87920800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:87903200-87918800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr4:87903200-87926200	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr4:87903600-87919800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr4:87903600-87921000	Weak transcription	Primary T cells from cord blood	blood
21	chr4:87903800-87919800	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr4:87903800-87920000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr4:87904200-87926200	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr4:87904400-87920000	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr4:87904600-87917800	Weak transcription	Primary B cells from cord blood	blood
26	chr4:87904600-87921000	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr4:87905800-87920200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr4:87907600-87920000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr4:87910000-87919000	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr4:87910000-87921200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr4:87912800-87920600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr4:87913000-87916200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr4:87913000-87919400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr4:87913200-87916400	Enhancers	Liver	Liver
35	chr4:87913200-87916400	Enhancers	HepG2	liver
36	chr4:87913600-87916400	Genic enhancers	Placenta	Placenta
37	chr4:87913800-87919400	Weak transcription	Right Ventricle	heart
38	chr4:87914200-87916000	Enhancers	Stomach Mucosa	stomach
39	chr4:87914200-87916200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:87914200-87927400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr4:87915000-87916200	Enhancers	Fetal Intestine Small	intestine
42	chr4:87915200-87916400	Enhancers	Fetal Intestine Large	intestine
43	chr4:87915200-87916400	Enhancers	Fetal Thymus	thymus
44	chr4:87915200-87916400	Enhancers	K562	blood
45	chr4:87915400-87916000	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr4:87915400-87916000	Enhancers	Fetal Heart	heart
47	chr4:87915400-87916000	Enhancers	Ovary	ovary
48	chr4:87915400-87916000	ZNF genes & repeats	GM12878-XiMat	blood
49	chr4:87915400-87916200	Enhancers	Thymus	Thymus
50	chr4:87915400-87916200	Strong transcription	Dnd41	blood

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