Variant report

Variant	rs10488740
Chromosome Location	chr11:34648615-34648616
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:34647092..34649318-chr11:34661381..34664170,2	MCF-7	breast:
2	chr11:34642302..34644592-chr11:34647851..34649607,2	K562	blood:
3	chr11:34646456..34649204-chr11:34658693..34661498,2	K562	blood:

Variant related genes	Relation type
ENSG00000135373	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10768084	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10836266	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs11032789	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12286877	0.86[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs12286924	0.86[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs1377496	0.86[JPT][hapmap]
rs1466209	0.89[YRI][hapmap]
rs17358030	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2123650	0.85[EUR][1000 genomes]
rs35556136	0.86[EUR][1000 genomes]
rs7481024	0.83[AFR][1000 genomes]
rs7945208	0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832116	chr11:34539536-34673900	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv832117	chr11:34639008-34831199	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1045130	chr11:34641598-34777725	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv1052192	chr11:34641598-34781288	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv1051492	chr11:34641598-34789331	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1052008	chr11:34641598-34794024	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
7	nsv467788	chr11:34642493-34770494	Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
8	nsv553998	chr11:34642493-34770494	Enhancers Strong transcription Active TSS ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
9	nsv518807	chr11:34642493-34780936	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
10	nsv519718	chr11:34642493-34780936	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
11	nsv467789	chr11:34642493-34780936	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
12	nsv467790	chr11:34642493-34780936	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
13	nsv553999	chr11:34642493-34780936	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
14	nsv554000	chr11:34643780-34780936	Genic enhancers Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
15	nsv869812	chr11:34648088-34810956	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34637800-34649200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:34639800-34653800	Weak transcription	Right Atrium	heart
3	chr11:34644000-34650200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr11:34644000-34650200	Weak transcription	Brain Substantia Nigra	brain
5	chr11:34644000-34650200	Weak transcription	A549	lung
6	chr11:34644000-34651200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:34644200-34650800	Weak transcription	Brain Anterior Caudate	brain
8	chr11:34644200-34652000	Weak transcription	Brain Hippocampus Middle	brain
9	chr11:34645800-34651200	Weak transcription	Fetal Intestine Small	intestine
10	chr11:34646200-34653400	Weak transcription	HSMMtube	muscle
11	chr11:34646600-34649000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
12	chr11:34646600-34656000	Weak transcription	Lung	lung
13	chr11:34647000-34653000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr11:34647200-34648800	Active TSS	Esophagus	oesophagus
15	chr11:34647200-34649000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:34647200-34650000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr11:34647200-34652800	Enhancers	Stomach Mucosa	stomach
18	chr11:34647200-34657200	Weak transcription	Gastric	stomach
19	chr11:34647400-34649600	Enhancers	HMEC	breast
20	chr11:34647600-34649200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr11:34647800-34653200	Weak transcription	HepG2	liver
22	chr11:34648000-34649600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr11:34648200-34648800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr11:34648200-34649000	Enhancers	Pancreas	Pancrea
25	chr11:34648200-34649200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr11:34648200-34649200	Flanking Active TSS	NHEK	skin
27	chr11:34648200-34650800	Weak transcription	Colonic Mucosa	Colon
28	chr11:34648400-34649200	Enhancers	Small Intestine	intestine
29	chr11:34648400-34650600	Enhancers	Duodenum Mucosa	Duodenum
30	chr11:34648600-34650000	Weak transcription	Rectal Mucosa Donor 29	rectum

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