Variant report

Variant	rs11187165
Chromosome Location	chr10:94515985-94515986
allele	C/T
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:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:94511052..94514419-chr10:94514793..94517097,3	K562	blood:
2	chr10:94515977..94518036-chr10:94533263..94535173,2	K562	blood:
3	chr10:94506528..94510913-chr10:94515438..94518140,4	K562	blood:
4	chr10:94350476..94356035-chr10:94515020..94520020,6	K562	blood:
5	chr10:94454513..94457218-chr10:94513369..94516034,3	K562	blood:
6	chr10:94459361..94461445-chr10:94514300..94516299,2	K562	blood:
7	chr10:94515716..94518429-chr10:94608106..94610155,2	K562	blood:
8	chr10:94514784..94516606-chr10:94517572..94519517,2	K562	blood:
9	chr10:94448814..94452346-chr10:94514330..94519117,6	K562	blood:
10	chr10:94448776..94451564-chr10:94514826..94518516,6	K562	blood:
11	chr10:94515128..94517989-chr10:94586362..94588868,2	K562	blood:
12	chr10:94515342..94517333-chr10:94557588..94560376,2	K562	blood:
13	chr10:94515577..94518061-chr10:94639001..94640568,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000138190	Chromatin interaction
ENSG00000138160	Chromatin interaction
ENSG00000152804	Chromatin interaction

Extended variants
information (count: 7 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11187171	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2488056	0.89[EUR][1000 genomes]
rs35235479	0.82[EUR][1000 genomes]
rs4933239	0.89[ASN][1000 genomes]
rs7091916	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs882136	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	esv3446249	chr10:94374508-94549394	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94511200-94516400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr10:94511400-94516200	Weak transcription	Osteobl	bone
3	chr10:94511400-94516400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr10:94512200-94516600	Enhancers	Primary B cells from peripheral blood	blood
5	chr10:94513000-94516000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr10:94513400-94517200	Enhancers	Primary monocytes fromperipheralblood	blood
7	chr10:94514000-94516000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr10:94514600-94518000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr10:94514800-94518200	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr10:94515200-94518000	Enhancers	Placenta	Placenta
11	chr10:94515400-94518000	Enhancers	Fetal Thymus	thymus
12	chr10:94515600-94516000	Enhancers	Duodenum Mucosa	Duodenum
13	chr10:94515600-94516000	Flanking Active TSS	K562	blood
14	chr10:94515600-94516200	Enhancers	Hela-S3	cervix
15	chr10:94515600-94516400	Enhancers	Colon Smooth Muscle	Colon
16	chr10:94515600-94516600	Weak transcription	Fetal Muscle Trunk	muscle
17	chr10:94515600-94516600	Weak transcription	Small Intestine	intestine
18	chr10:94515600-94516800	Enhancers	Skeletal Muscle Male	skeletal muscle
19	chr10:94515600-94517200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr10:94515600-94517200	Enhancers	Dnd41	blood
21	chr10:94515600-94517200	Flanking Active TSS	HepG2	liver
22	chr10:94515600-94517400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr10:94515600-94517400	Flanking Active TSS	Primary hematopoietic stem cells	blood
24	chr10:94515600-94517600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr10:94515600-94517600	Weak transcription	Liver	Liver
26	chr10:94515600-94517600	Enhancers	Fetal Lung	lung
27	chr10:94515600-94517600	Flanking Active TSS	HUVEC	blood vessel
28	chr10:94515600-94517800	Enhancers	Fetal Muscle Leg	muscle
29	chr10:94515600-94518000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
30	chr10:94515600-94518000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr10:94515600-94518000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr10:94515600-94518000	Enhancers	Adipose Nuclei	Adipose
33	chr10:94515600-94518000	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr10:94515600-94518000	Enhancers	Fetal Stomach	stomach
35	chr10:94515600-94518000	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr10:94515600-94518400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr10:94515600-94518600	Flanking Active TSS	GM12878-XiMat	blood
38	chr10:94515800-94516600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr10:94515800-94517200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr10:94515800-94517200	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr10:94515800-94517400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr10:94515800-94517400	Enhancers	Fetal Heart	heart
43	chr10:94515800-94518000	Flanking Active TSS	Primary B cells from cord blood	blood
44	chr10:94515800-94519600	Enhancers	A549	lung

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