Variant report

Variant	rs2453097
Chromosome Location	chr15:57904351-57904352
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:57851773..57853797-chr15:57903678..57905009,17	MCF-7	breast:
2	chr15:57897591..57899946-chr15:57902419..57904652,2	MCF-7	breast:
3	chr15:57850660..57853481-chr15:57902440..57904405,2	MCF-7	breast:
4	chr15:57852740..57853861-chr15:57903786..57904809,7	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11071340	1.00[CEU][hapmap]
rs11071342	1.00[CEU][hapmap]
rs11855136	1.00[JPT][hapmap]
rs12440250	1.00[CEU][hapmap]
rs1346120	1.00[CEU][hapmap]
rs1593439	1.00[CEU][hapmap]
rs1666582	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1690330	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1690332	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2081515	1.00[CEU][hapmap]
rs2414516	1.00[CEU][hapmap]
rs2442072	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2442077	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2451181	1.00[CEU][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];0.91[MKK][hapmap];0.80[YRI][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2451188	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2451189	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2453095	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2453096	1.00[ASW][hapmap];1.00[CEU][hapmap];0.89[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2453098	0.85[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.87[LWK][hapmap];0.94[MKK][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2635379	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2641572	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2641573	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2899603	1.00[CEU][hapmap]
rs2934430	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934432	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2934433	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4564513	1.00[CEU][hapmap]
rs4774279	1.00[CEU][hapmap]
rs4774280	1.00[CEU][hapmap]
rs57014962	1.00[EUR][1000 genomes]
rs6493941	1.00[CEU][hapmap]
rs6493942	1.00[CEU][hapmap]
rs7173197	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs724785	1.00[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8023855	1.00[CEU][hapmap]
rs8024008	1.00[CEU][hapmap]
rs8024736	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8025907	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs935547	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9921015	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045611	chr15:57350965-58070807	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1054547	chr15:57600488-57977659	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv904255	chr15:57790436-57907574	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57890200-57904400	Weak transcription	Fetal Lung	lung
2	chr15:57892000-57908800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:57894400-57938200	Weak transcription	Primary B cells from peripheral blood	blood
4	chr15:57897000-57909200	Weak transcription	Psoas Muscle	Psoas
5	chr15:57899000-57905000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr15:57899200-57905000	Enhancers	Duodenum Mucosa	Duodenum
7	chr15:57899200-57905200	Enhancers	Fetal Heart	heart
8	chr15:57900200-57904800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:57900400-57904400	Enhancers	Stomach Mucosa	stomach
10	chr15:57900600-57905200	Enhancers	Fetal Intestine Large	intestine
11	chr15:57900600-57911800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr15:57900600-57941600	Weak transcription	Colonic Mucosa	Colon
13	chr15:57901200-57905000	Enhancers	Colon Smooth Muscle	Colon
14	chr15:57901600-57905000	Enhancers	Fetal Intestine Small	intestine
15	chr15:57901800-57912000	Weak transcription	Spleen	Spleen
16	chr15:57902000-57904600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:57902200-57904800	Enhancers	NHEK	skin
18	chr15:57902600-57904600	Enhancers	Pancreas	Pancrea
19	chr15:57902600-57904800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr15:57902600-57907800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr15:57902800-57904400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr15:57902800-57904400	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr15:57902800-57904800	Enhancers	Stomach Smooth Muscle	stomach
24	chr15:57903000-57904400	Enhancers	Rectal Smooth Muscle	rectum
25	chr15:57903000-57904400	Weak transcription	Sigmoid Colon	Sigmoid Colon
26	chr15:57903000-57904600	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr15:57903000-57904800	Enhancers	A549	lung
28	chr15:57903000-57907600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr15:57903000-57907800	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr15:57903200-57904400	Weak transcription	Right Atrium	heart
31	chr15:57903200-57904800	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr15:57903200-57905000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr15:57903200-57907600	Weak transcription	Esophagus	oesophagus
34	chr15:57903400-57904600	Enhancers	Adipose Nuclei	Adipose
35	chr15:57903400-57905000	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr15:57903600-57904600	Enhancers	Right Ventricle	heart
37	chr15:57903600-57905000	Enhancers	HMEC	breast
38	chr15:57903800-57904600	Enhancers	Left Ventricle	heart
39	chr15:57903800-57904800	Enhancers	HUVEC	blood vessel
40	chr15:57904000-57904400	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr15:57904000-57904400	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr15:57904000-57904600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr15:57904000-57904600	Enhancers	Fetal Muscle Leg	muscle
44	chr15:57904000-57904600	Enhancers	Placenta	Placenta
45	chr15:57904000-57904600	Enhancers	Lung	lung
46	chr15:57904000-57904600	Enhancers	Ovary	ovary
47	chr15:57904200-57904400	Enhancers	Osteobl	bone
48	chr15:57904200-57904600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr15:57904200-57904600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr15:57904200-57904600	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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