Variant report

Variant	rs992698
Chromosome Location	chr11:17023880-17023881
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	chr11:16993487..16995936-chr11:17022091..17024047,2	MCF-7	breast:
2	chr11:17018572..17027460-chr11:17032241..17037685,12	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166689	Chromatin interaction
ENSG00000184669	Chromatin interaction

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10741719	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10741720	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10741721	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10741722	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10766370	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10766371	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10766372	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832713	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10832715	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10832716	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832717	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832718	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832720	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10832721	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11024111	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11605426	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12288625	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12365483	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12418132	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12808675	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1468489	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34437677	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34502475	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34819854	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4351794	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4562807	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4756881	0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4756882	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4756883	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757466	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4757467	0.98[EUR][1000 genomes]
rs4757479	0.93[EUR][1000 genomes]
rs4757482	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4757484	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4757485	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757486	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757487	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757488	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757489	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757490	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757491	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757492	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4757493	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61881287	0.84[EUR][1000 genomes]
rs61881311	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6486332	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6486335	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6486336	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6486337	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6486339	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6486340	0.82[EUR][1000 genomes]
rs6486341	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6486342	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6486343	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6486344	0.84[EUR][1000 genomes]
rs7101679	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7117262	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71484746	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7481059	0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7926143	0.81[EUR][1000 genomes]
rs7928955	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7929923	0.80[EUR][1000 genomes]
rs7930890	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7931025	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7933984	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7937479	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7940499	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7947297	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7947897	0.83[EUR][1000 genomes]
rs973323	0.92[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832077	chr11:16834545-17059176	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17004800-17034200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:17006400-17034000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr11:17009400-17032600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr11:17009800-17030000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr11:17009800-17032600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr11:17009800-17032600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr11:17012400-17024200	Enhancers	Stomach Mucosa	stomach
8	chr11:17013400-17033800	Weak transcription	Brain Substantia Nigra	brain
9	chr11:17014000-17025000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:17015000-17024800	Enhancers	Gastric	stomach
11	chr11:17016400-17034600	Weak transcription	Aorta	Aorta
12	chr11:17016600-17030800	Weak transcription	Fetal Kidney	kidney
13	chr11:17018000-17028000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr11:17018000-17029400	Weak transcription	Brain Anterior Caudate	brain
15	chr11:17018800-17032000	Weak transcription	Fetal Muscle Leg	muscle
16	chr11:17019000-17032600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr11:17019200-17025600	Weak transcription	A549	lung
18	chr11:17019400-17034800	Weak transcription	Lung	lung
19	chr11:17019800-17024800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:17019800-17034600	Weak transcription	Right Ventricle	heart
21	chr11:17020000-17025000	Weak transcription	Duodenum Mucosa	Duodenum
22	chr11:17020400-17024600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr11:17021000-17025200	Weak transcription	HepG2	liver
24	chr11:17021000-17034000	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr11:17021000-17034200	Weak transcription	Colonic Mucosa	Colon
26	chr11:17021200-17034600	Weak transcription	Right Atrium	heart
27	chr11:17021400-17030400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr11:17022000-17034600	Weak transcription	Brain Angular Gyrus	brain
29	chr11:17022200-17027200	Weak transcription	Adipose Nuclei	Adipose
30	chr11:17022400-17025000	Strong transcription	Fetal Intestine Small	intestine
31	chr11:17022800-17024800	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr11:17022800-17026000	Genic enhancers	Fetal Intestine Large	intestine
33	chr11:17023000-17025000	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr11:17023200-17026600	Weak transcription	Esophagus	oesophagus
35	chr11:17023200-17028600	Weak transcription	Left Ventricle	heart
36	chr11:17023200-17032600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr11:17023200-17033600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr11:17023400-17024000	Genic enhancers	Fetal Stomach	stomach
39	chr11:17023800-17024000	Enhancers	Pancreas	Pancrea
40	chr11:17023800-17026400	Weak transcription	Liver	Liver
41	chr11:17023800-17028400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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