Variant report

Variant	rs1800006
Chromosome Location	chr11:73717254-73717255
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:73715121..73717630-chr11:73768007..73770046,2	MCF-7	breast:
2	chr11:73693159..73695424-chr11:73716966..73719233,2	MCF-7	breast:
3	chr11:73709291..73711416-chr11:73716050..73718311,2	K562	blood:

Variant related genes	Relation type
ENSG00000175567	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10501415	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs10898955	0.90[CHB][hapmap]
rs10898957	0.89[CHB][hapmap]
rs10898960	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs10898961	0.90[CHB][hapmap];0.83[JPT][hapmap]
rs10898962	0.89[CHB][hapmap]
rs10898963	0.90[CHB][hapmap];0.83[JPT][hapmap]
rs11235965	0.88[JPT][hapmap]
rs11235971	0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs11235972	0.93[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11235994	0.89[CHB][hapmap]
rs11235995	0.89[CHB][hapmap]
rs11235996	0.90[CHB][hapmap]
rs11235999	0.84[CHB][hapmap]
rs11236000	0.89[CHB][hapmap]
rs11236003	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs11236027	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs11236029	0.89[CHB][hapmap]
rs11600314	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs11602451	0.89[CHB][hapmap];0.82[JPT][hapmap]
rs11604125	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs11604713	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs11606804	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs11607335	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs11608147	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs12223320	0.89[CHB][hapmap]
rs12574038	0.89[CHB][hapmap]
rs12574039	0.90[CHB][hapmap]
rs12574047	0.89[CHB][hapmap]
rs12574556	0.90[CHB][hapmap]
rs12575211	0.90[CHB][hapmap]
rs1527302	0.84[CHB][hapmap];0.89[JPT][hapmap]
rs1565125	0.80[ASN][1000 genomes]
rs1685333	1.00[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17132715	0.90[CHB][hapmap]
rs1800849	0.93[CEU][hapmap];0.95[CHB][hapmap];0.94[JPT][hapmap];0.93[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2075576	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2178000	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs3741135	0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs3814724	0.90[CHB][hapmap];0.83[JPT][hapmap]
rs4019299	0.90[CHB][hapmap];0.89[JPT][hapmap]
rs4539349	0.89[CHB][hapmap];0.83[JPT][hapmap]
rs4565925	0.89[CHB][hapmap]
rs7110734	0.89[CHB][hapmap];0.89[JPT][hapmap]
rs7115407	0.82[CHB][hapmap];0.88[JPT][hapmap]
rs7125032	0.89[CHB][hapmap]
rs7930460	0.88[JPT][hapmap];0.80[ASN][1000 genomes]
rs826044	0.95[CHB][hapmap];0.89[JPT][hapmap]

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	nsv492091	chr11:73285970-73844424	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73703000-73719400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr11:73707400-73719800	Weak transcription	Dnd41	blood
3	chr11:73708000-73717600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:73708800-73729400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:73709000-73724200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr11:73710200-73728400	Weak transcription	Colon Smooth Muscle	Colon
7	chr11:73710600-73741800	Weak transcription	Fetal Kidney	kidney
8	chr11:73710600-73748800	Weak transcription	Fetal Brain Male	brain
9	chr11:73710800-73717800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr11:73710800-73722400	Weak transcription	NHDF-Ad	bronchial
11	chr11:73711000-73718400	Strong transcription	Fetal Brain Female	brain
12	chr11:73711000-73721200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr11:73711000-73729200	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr11:73711200-73718200	Strong transcription	Brain Germinal Matrix	brain
15	chr11:73711400-73717400	Strong transcription	Right Ventricle	heart
16	chr11:73711800-73718200	Strong transcription	Lung	lung
17	chr11:73711800-73718200	Strong transcription	Spleen	Spleen
18	chr11:73711800-73720200	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr11:73711800-73729200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr11:73712000-73721200	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr11:73712200-73721200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr11:73712200-73726800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr11:73712200-73743600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr11:73712200-73743800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr11:73712400-73721800	Weak transcription	Colonic Mucosa	Colon
26	chr11:73712600-73722400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr11:73712800-73743400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr11:73713600-73725000	Weak transcription	A549	lung
29	chr11:73714000-73726000	Weak transcription	Esophagus	oesophagus
30	chr11:73714200-73729800	Weak transcription	Hela-S3	cervix
31	chr11:73714600-73717600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:73714600-73727200	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr11:73714800-73717400	Enhancers	Primary hematopoietic stem cells	blood
34	chr11:73714800-73717800	Weak transcription	Pancreas	Pancrea
35	chr11:73714800-73718400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr11:73714800-73719200	Weak transcription	Fetal Heart	heart
37	chr11:73714800-73721400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr11:73714800-73721600	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr11:73714800-73724000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr11:73715000-73722200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr11:73715000-73729800	Weak transcription	Ovary	ovary
42	chr11:73715200-73717400	Weak transcription	Liver	Liver
43	chr11:73715200-73718000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
44	chr11:73715200-73721000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr11:73715200-73722000	Weak transcription	Primary neutrophils fromperipheralblood	blood
46	chr11:73715200-73722600	Weak transcription	NHLF	lung
47	chr11:73715200-73722800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr11:73715200-73727200	Weak transcription	Fetal Lung	lung
49	chr11:73715200-73727400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr11:73715400-73717400	Genic enhancers	Fetal Intestine Small	intestine

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