Variant report

Variant	rs7129173
Chromosome Location	chr11:17541798-17541799
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:17538690..17542408-chr11:17546927..17550590,3	MCF-7	breast:
2	chr11:17537309..17539675-chr11:17540315..17542082,2	K562	blood:

Variant related genes	Relation type
ENSG00000006611	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11024318	1.00[CHB][hapmap]
rs12271449	1.00[CHB][hapmap]
rs12271589	1.00[CHB][hapmap]
rs16934329	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv469895	chr11:17368270-17584220	Weak transcription Bivalent Enhancer Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv33415	chr11:17532596-17549436	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 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	chr11:17516800-17553000	Weak transcription	Stomach Mucosa	stomach
2	chr11:17527600-17549200	Strong transcription	Duodenum Mucosa	Duodenum
3	chr11:17528800-17544000	Weak transcription	Gastric	stomach
4	chr11:17529800-17548600	Strong transcription	Rectal Mucosa Donor 29	rectum
5	chr11:17531600-17547200	Strong transcription	Fetal Intestine Large	intestine
6	chr11:17531800-17552400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr11:17532200-17547200	Strong transcription	Fetal Intestine Small	intestine
8	chr11:17533600-17541800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr11:17535400-17542400	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr11:17536200-17542600	Enhancers	Brain Angular Gyrus	brain
11	chr11:17536800-17542400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr11:17537200-17542000	Enhancers	Brain Cingulate Gyrus	brain
13	chr11:17537400-17544800	Weak transcription	Rectal Smooth Muscle	rectum
14	chr11:17537400-17546800	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr11:17538000-17542600	Enhancers	Brain Substantia Nigra	brain
16	chr11:17538400-17562200	Weak transcription	Small Intestine	intestine
17	chr11:17539600-17550000	Weak transcription	Spleen	Spleen
18	chr11:17540000-17542000	Enhancers	Brain Hippocampus Middle	brain
19	chr11:17540800-17552400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:17541000-17552600	Strong transcription	Rectal Mucosa Donor 31	rectum
21	chr11:17541200-17542000	Strong transcription	Colonic Mucosa	Colon
22	chr11:17541200-17542400	ZNF genes & repeats	Fetal Stomach	stomach
23	chr11:17541400-17548000	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr11:17541400-17552400	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr11:17541600-17549600	Weak transcription	Brain Anterior Caudate	brain
26	chr11:17541600-17550000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr11:17541600-17551600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr11:17541600-17555800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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