Variant report

Variant	rs10791867
Chromosome Location	chr11:66081211-66081212
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:66080669..66083117-chr11:66127699..66129564,2	MCF-7	breast:
2	chr11:66055291..66058281-chr11:66079576..66082924,5	MCF-7	breast:
3	chr11:66077296..66081246-chr11:66109722..66112526,4	K562	blood:
4	chr11:66077376..66081785-chr11:66101114..66107038,7	MCF-7	breast:
5	chr11:66050790..66053564-chr11:66079260..66081695,2	MCF-7	breast:
6	chr11:66054404..66057808-chr11:66078165..66081775,4	MCF-7	breast:
7	chr11:66079011..66083261-chr11:66109999..66114385,7	MCF-7	breast:
8	chr11:66078877..66081854-chr11:66383426..66384938,2	K562	blood:
9	chr11:66078878..66081845-chr11:66137612..66139742,3	K562	blood:
10	chr11:66054488..66057665-chr11:66080176..66082833,4	K562	blood:
11	chr11:66079398..66082242-chr11:66082522..66086120,5	K562	blood:
12	chr11:66078412..66081908-chr11:66138198..66140974,6	K562	blood:
13	chr11:66077239..66082197-chr11:66111995..66115447,5	MCF-7	breast:
14	chr11:66080788..66082813-chr11:66088055..66089641,2	K562	blood:
15	chr11:65656399..65658937-chr11:66080213..66082790,2	K562	blood:
16	chr11:66053947..66059144-chr11:66077550..66083439,18	K562	blood:

No data

Variant related genes	Relation type
ENSG00000174669	Chromatin interaction
ENSG00000239306	Chromatin interaction
ENSG00000248643	Chromatin interaction
ENSG00000254756	Chromatin interaction
ENSG00000174807	Chromatin interaction
ENSG00000255468	Chromatin interaction
ENSG00000174791	Chromatin interaction
ENSG00000174744	Chromatin interaction
ENSG00000175602	Chromatin interaction
ENSG00000174684	Chromatin interaction
ENSG00000174851	Chromatin interaction

Extended variants
information (count: 11 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs10219183	1.00[CEU][hapmap];0.89[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.92[MEX][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10444359	0.86[EUR][1000 genomes]
rs10791866	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10896110	0.86[EUR][1000 genomes]
rs580241	0.81[ASN][1000 genomes]
rs7924580	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.92[MEX][hapmap];1.00[MKK][hapmap];0.97[TSI][hapmap];0.94[YRI][hapmap];0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[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	esv3335923	chr11:65741698-66175759	Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
2	esv3407551	chr11:65794503-66158322	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	103 gene(s)	inside rSNPs	diseases
3	esv3392427	chr11:65981489-66273695	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
4	nsv897771	chr11:66011280-66362997	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	124 gene(s)	inside rSNPs	diseases
5	nsv897772	chr11:66018155-66254085	Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs10791867	ASRGL1	cis	parietal	SCAN
rs10791867	SCYL1	cis	lymphoblastoid	seeQTL
rs10791867	B3GNT1	cis	parietal	SCAN
rs10791867	ESRRA	cis	cerebellum	SCAN
rs10791867	MACROD1	cis	parietal	SCAN

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66079200-66081400	Active TSS	ES-I3 Cell Line	embryonic stem cell
2	chr11:66079200-66081600	Active TSS	Brain Anterior Caudate	brain
3	chr11:66079200-66081600	Bivalent/Poised TSS	Fetal Brain Female	brain
4	chr11:66079400-66081400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr11:66079400-66081400	Active TSS	Fetal Stomach	stomach
6	chr11:66079400-66081400	Active TSS	Placenta Amnion	Placenta Amnion
7	chr11:66079400-66081600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr11:66079400-66081600	Active TSS	Fetal Lung	lung
9	chr11:66079400-66081800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr11:66079400-66082400	Active TSS	NHDF-Ad	bronchial
11	chr11:66079400-66083000	Active TSS	Rectal Smooth Muscle	rectum
12	chr11:66079400-66083200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
13	chr11:66079400-66083400	Active TSS	Esophagus	oesophagus
14	chr11:66079400-66083600	Active TSS	Psoas Muscle	Psoas
15	chr11:66079400-66085000	Active TSS	Fetal Kidney	kidney
16	chr11:66079400-66085000	Active TSS	Right Atrium	heart
17	chr11:66079800-66082000	Active TSS	NHLF	lung
18	chr11:66080200-66081800	Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr11:66080200-66082200	Enhancers	Primary hematopoietic stem cells	blood
20	chr11:66080400-66081400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr11:66080400-66081600	Enhancers	Gastric	stomach
22	chr11:66080400-66081600	Enhancers	Lung	lung
23	chr11:66080400-66082000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr11:66080400-66082200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
25	chr11:66080400-66083600	Flanking Active TSS	Fetal Thymus	thymus
26	chr11:66080600-66081400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr11:66080600-66081400	Flanking Active TSS	Right Ventricle	heart
28	chr11:66080600-66081600	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr11:66080600-66081800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr11:66080600-66082000	Flanking Active TSS	Fetal Intestine Small	intestine
31	chr11:66080600-66082000	Flanking Active TSS	Fetal Muscle Leg	muscle
32	chr11:66080600-66082000	Flanking Active TSS	Thymus	Thymus
33	chr11:66080600-66082000	Flanking Active TSS	NH-A	brain
34	chr11:66080600-66082200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
35	chr11:66080600-66082200	Flanking Active TSS	Fetal Intestine Large	intestine
36	chr11:66080600-66082400	Enhancers	Spleen	Spleen
37	chr11:66080600-66082600	Flanking Active TSS	Colonic Mucosa	Colon
38	chr11:66080600-66084000	Weak transcription	Aorta	Aorta
39	chr11:66080600-66084400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:66080600-66084600	Flanking Active TSS	Adipose Nuclei	Adipose
41	chr11:66080800-66081400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr11:66080800-66081400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr11:66080800-66081400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr11:66080800-66081400	Enhancers	Fetal Heart	heart
45	chr11:66080800-66081400	Enhancers	GM12878-XiMat	blood
46	chr11:66080800-66081400	Enhancers	K562	blood
47	chr11:66080800-66081600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr11:66080800-66081800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr11:66080800-66081800	Enhancers	Primary B cells from peripheral blood	blood
50	chr11:66080800-66081800	Enhancers	Fetal Brain Male	brain

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