Variant report

Variant	rs8030804
Chromosome Location	chr15:60664076-60664077
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:60661349..60669397-chr15:60674958..60683269,11	MCF-7	breast:
2	chr15:60660685..60664137-chr15:60687847..60691351,5	K562	blood:
3	chr15:60649414..60651159-chr15:60662340..60664090,2	MCF-7	breast:
4	chr15:60662032..60669365-chr15:60683457..60694611,25	MCF-7	breast:
5	chr15:60652874..60655330-chr15:60662617..60664818,3	K562	blood:
6	chr15:60661044..60665019-chr15:60767961..60772025,5	K562	blood:
7	chr15:60663405..60665055-chr15:60665417..60667717,2	MCF-7	breast:
8	chr15:60659971..60669409-chr15:60678563..60693961,40	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000128915	Chromatin interaction
ENSG00000245534	Chromatin interaction
ENSG00000240163	Chromatin interaction
ENSG00000182718	Chromatin interaction

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1033028	0.85[AMR][1000 genomes]
rs10851677	0.89[AMR][1000 genomes]
rs11071522	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12900365	0.86[AMR][1000 genomes]
rs1463329	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2136554	0.85[AMR][1000 genomes]
rs28437402	0.89[AMR][1000 genomes]
rs28508289	0.88[AMR][1000 genomes]
rs28642929	0.86[AMR][1000 genomes]
rs28676840	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4775260	0.89[AMR][1000 genomes]
rs4775261	0.89[AMR][1000 genomes]
rs7163836	0.88[AMR][1000 genomes]
rs7165285	0.82[AMR][1000 genomes]
rs8030787	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:60647400-60669000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:60647800-60666400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr15:60648000-60681000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
4	chr15:60649200-60681000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr15:60649400-60668600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:60649400-60681000	Weak transcription	Primary T cells from cord blood	blood
7	chr15:60649600-60666600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr15:60651800-60667600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr15:60652800-60666800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr15:60656000-60668000	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr15:60656600-60664200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr15:60656800-60664400	Weak transcription	Pancreas	Pancrea
13	chr15:60656800-60665400	Weak transcription	Gastric	stomach
14	chr15:60656800-60667000	Weak transcription	Primary B cells from cord blood	blood
15	chr15:60656800-60667200	Weak transcription	Fetal Kidney	kidney
16	chr15:60656800-60667400	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr15:60656800-60667800	Weak transcription	Primary B cells from peripheral blood	blood
18	chr15:60656800-60682600	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr15:60657000-60665800	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr15:60657000-60668800	Weak transcription	Liver	Liver
21	chr15:60660600-60667000	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr15:60660600-60671000	Transcr. at gene 5' and 3'	A549	lung
23	chr15:60660600-60678400	Strong transcription	Primary monocytes fromperipheralblood	blood
24	chr15:60660600-60678400	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr15:60660600-60680000	Genic enhancers	NHDF-Ad	bronchial
26	chr15:60660800-60666000	Strong transcription	HUES6 Cell Line	embryonic stem cell
27	chr15:60660800-60671000	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr15:60661200-60666200	Genic enhancers	NHEK	skin
29	chr15:60661200-60669200	Enhancers	Right Atrium	heart
30	chr15:60661200-60669400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr15:60661200-60670800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr15:60661200-60681200	Genic enhancers	Osteobl	bone
33	chr15:60661400-60664600	Genic enhancers	Fetal Intestine Small	intestine
34	chr15:60661400-60664600	Strong transcription	Rectal Mucosa Donor 29	rectum
35	chr15:60661400-60670800	Genic enhancers	Adipose Nuclei	Adipose
36	chr15:60661800-60664600	Strong transcription	Esophagus	oesophagus
37	chr15:60661800-60664800	Genic enhancers	Duodenum Mucosa	Duodenum
38	chr15:60661800-60669400	Strong transcription	K562	blood
39	chr15:60662000-60676000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr15:60662000-60677200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr15:60662000-60681600	Genic enhancers	HMEC	breast
42	chr15:60662200-60667000	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr15:60662200-60667000	Genic enhancers	HepG2	liver
44	chr15:60662200-60668400	Enhancers	Right Ventricle	heart
45	chr15:60662200-60669400	Genic enhancers	Placenta Amnion	Placenta Amnion
46	chr15:60662200-60670600	Genic enhancers	NHLF	lung
47	chr15:60662400-60665200	Strong transcription	Fetal Lung	lung
48	chr15:60662400-60665400	Enhancers	Small Intestine	intestine
49	chr15:60662400-60668000	Strong transcription	Colonic Mucosa	Colon
50	chr15:60662400-60670200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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