Variant report

Variant	rs11805576
Chromosome Location	chr1:85687693-85687694
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:85665362..85671529-chr1:85685487..85692910,10	MCF-7	breast:
2	chr1:85665411..85671906-chr1:85683759..85698338,27	MCF-7	breast:
3	chr1:85666946..85668694-chr1:85686380..85689036,2	K562	blood:

Variant related genes	Relation type
ENSG00000097096	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17123230	1.00[AMR][1000 genomes]
rs17125247	1.00[AMR][1000 genomes]
rs2790912	1.00[AMR][1000 genomes]
rs709784	1.00[AMR][1000 genomes]
rs817402	1.00[AMR][1000 genomes]
rs817405	1.00[AMR][1000 genomes]
rs817408	1.00[AMR][1000 genomes]
rs817412	1.00[AMR][1000 genomes]
rs817442	1.00[AMR][1000 genomes]
rs817443	1.00[AMR][1000 genomes]
rs817444	1.00[AMR][1000 genomes]
rs817448	1.00[AMR][1000 genomes]
rs817450	1.00[AMR][1000 genomes]
rs817454	1.00[AMR][1000 genomes]
rs817455	1.00[AMR][1000 genomes]
rs817459	1.00[AMR][1000 genomes]
rs817460	1.00[AMR][1000 genomes]
rs817461	1.00[AMR][1000 genomes]

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	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv34165	chr1:85542040-85846249	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv830459	chr1:85589585-85786311	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:28 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85668000-85689000	Weak transcription	Gastric	stomach
2	chr1:85673800-85690400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:85681400-85690400	Weak transcription	Stomach Smooth Muscle	stomach
4	chr1:85684400-85688200	Enhancers	Rectal Smooth Muscle	rectum
5	chr1:85684600-85689200	Enhancers	Fetal Stomach	stomach
6	chr1:85685400-85690000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:85685600-85688400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr1:85685600-85690400	Enhancers	Fetal Lung	lung
9	chr1:85685800-85690800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr1:85686400-85690000	Weak transcription	Fetal Intestine Large	intestine
11	chr1:85686400-85690400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:85686400-85690400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr1:85686600-85690000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr1:85686600-85690000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr1:85686600-85690400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr1:85686600-85690400	Weak transcription	H9 Cell Line	embryonic stem cell
17	chr1:85686600-85690800	Weak transcription	Esophagus	oesophagus
18	chr1:85686800-85687800	Enhancers	K562	blood
19	chr1:85686800-85689600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr1:85686800-85690000	Weak transcription	Fetal Kidney	kidney
21	chr1:85686800-85690800	Weak transcription	Right Atrium	heart
22	chr1:85687000-85688200	Weak transcription	Colon Smooth Muscle	Colon
23	chr1:85687000-85689200	Weak transcription	Stomach Mucosa	stomach
24	chr1:85687000-85690000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr1:85687000-85709600	Weak transcription	Aorta	Aorta
26	chr1:85687400-85690400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr1:85687600-85688200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:85687600-85689000	Weak transcription	Fetal Heart	heart

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