Variant report

Variant	rs10791894
Chromosome Location	chr11:66679738-66679739
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:66677241..66680010-chr11:66694798..66696500,2	MCF-7	breast:
2	chr11:66661363..66663276-chr11:66678554..66680606,2	MCF-7	breast:
3	chr11:66679281..66682230-chr11:66683799..66685977,2	MCF-7	breast:
4	chr11:66678730..66681297-chr11:66687110..66688715,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000239099	Chromatin interaction

Extended variants
information (count: 29 )
Associated
traits (count: 11 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs1077256	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10791896	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11227624	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11227625	0.85[CEU][hapmap];0.91[CHB][hapmap];0.86[CHD][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.91[ASN][1000 genomes]
rs11227628	0.82[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs11227630	0.86[ASN][1000 genomes]
rs1530891	0.96[CEU][hapmap];0.82[CHB][hapmap];0.92[GIH][hapmap];0.87[JPT][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1901376	0.91[ASN][1000 genomes]
rs34482178	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4483596	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4930393	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4930394	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6591226	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67156018	0.89[ASN][1000 genomes]
rs7107498	0.87[CHB][hapmap];0.87[CHD][hapmap];0.95[JPT][hapmap];0.84[MEX][hapmap];0.82[ASN][1000 genomes]
rs7110302	0.87[CHB][hapmap];0.82[GIH][hapmap];0.91[JPT][hapmap]
rs7119682	0.82[CEU][hapmap];0.87[CHB][hapmap];0.87[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.83[ASN][1000 genomes]
rs746018	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs746019	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7935749	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7936290	0.86[ASN][1000 genomes]
rs7944999	0.85[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.91[ASN][1000 genomes]
rs7952017	0.91[ASN][1000 genomes]
rs966021	0.85[CEU][hapmap];0.91[CHB][hapmap];0.89[CHD][hapmap];0.80[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897794	chr11:66579572-66744119	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv555226	chr11:66579572-66845362	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
3	nsv428574	chr11:66619002-66804133	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv832194	chr11:66634462-66805980	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	33 gene(s)	inside rSNPs	diseases
5	nsv531397	chr11:66653381-67465721	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases

mRNA abundance (count:11)

SNP	Gene	Cis/trans	Tissue	Source
rs10791894	CCS	cis	multi-tissue	Pritchard
rs10791894	PC	cis	cerebellum	SCAN
rs10791894	EHBP1L1	cis	cerebellum	SCAN
rs10791894	CDC42BPG	cis	cerebellum	SCAN
rs10791894	ACTN3	cis	Muscle Skeletal	GTEx
rs10791894	LRFN4	cis	multi-tissue	Pritchard
rs10791894	SUV420H1	cis	cerebellum	SCAN
rs10791894	CTD-3074O7.2	cis	Muscle Skeletal	GTEx
rs10791894	B3GNT1	cis	parietal	SCAN
rs10791894	SLC25A45	cis	parietal	SCAN
rs10791894	FGF4	cis	parietal	SCAN

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66672200-66684000	Enhancers	Brain Inferior Temporal Lobe	brain
2	chr11:66672600-66680000	Weak transcription	HUVEC	blood vessel
3	chr11:66672600-66683000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr11:66674000-66687000	Weak transcription	HSMMtube	muscle
5	chr11:66674200-66680000	Weak transcription	Brain Germinal Matrix	brain
6	chr11:66674400-66679800	Weak transcription	Brain Anterior Caudate	brain
7	chr11:66674400-66689600	Weak transcription	NHLF	lung
8	chr11:66674600-66679800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr11:66674600-66680000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:66674600-66680400	Weak transcription	Right Ventricle	heart
11	chr11:66674600-66684800	Weak transcription	Fetal Stomach	stomach
12	chr11:66674600-66696400	Weak transcription	NHEK	skin
13	chr11:66674800-66679800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:66674800-66680200	Weak transcription	Fetal Muscle Leg	muscle
15	chr11:66675000-66696200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr11:66675400-66679800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr11:66675400-66680000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr11:66675400-66681400	Weak transcription	Fetal Intestine Large	intestine
19	chr11:66675600-66682000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr11:66675600-66683000	Weak transcription	A549	lung
21	chr11:66675600-66687000	Weak transcription	Osteobl	bone
22	chr11:66675600-66699800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr11:66675800-66680000	Weak transcription	Fetal Muscle Trunk	muscle
24	chr11:66675800-66680400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr11:66675800-66682200	Weak transcription	Fetal Intestine Small	intestine
26	chr11:66676000-66679800	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr11:66676000-66679800	Weak transcription	Brain Angular Gyrus	brain
28	chr11:66676000-66680000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr11:66676000-66680000	Weak transcription	Stomach Mucosa	stomach
30	chr11:66676200-66682000	Weak transcription	K562	blood
31	chr11:66676200-66682400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr11:66676200-66688600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr11:66676400-66682600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr11:66676800-66682400	Weak transcription	Gastric	stomach
35	chr11:66676800-66683800	Weak transcription	Fetal Brain Female	brain
36	chr11:66676800-66696400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr11:66677000-66683000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr11:66677200-66682400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr11:66677200-66683400	Weak transcription	Liver	Liver
40	chr11:66677200-66692000	Weak transcription	Pancreas	Pancrea
41	chr11:66678000-66680000	Weak transcription	Adipose Nuclei	Adipose
42	chr11:66678000-66682800	Enhancers	Brain Hippocampus Middle	brain
43	chr11:66678000-66688600	Weak transcription	Skeletal Muscle Male	skeletal muscle
44	chr11:66678400-66679800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr11:66678400-66683600	Weak transcription	Hela-S3	cervix
46	chr11:66678600-66679800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr11:66678600-66679800	Weak transcription	Stomach Smooth Muscle	stomach
48	chr11:66678800-66682800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:66679400-66680200	Enhancers	Brain Substantia Nigra	brain
50	chr11:66679400-66680200	Enhancers	HepG2	liver

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