Variant report

Variant	rs704702
Chromosome Location	chr11:33765897-33765898
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:33757828..33761273-chr11:33765808..33770040,4	K562	blood:
2	chr11:33756213..33759924-chr11:33763049..33766673,5	MCF-7	breast:
3	chr11:33756685..33760340-chr11:33762544..33766325,4	MCF-7	breast:
4	chr11:33763093..33766098-chr11:33769315..33772187,4	K562	blood:

Variant related genes	Relation type
ENSG00000085063	Chromatin interaction
ENSG00000110429	Chromatin interaction

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10836108	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1096558	0.87[ASN][1000 genomes]
rs1096559	0.87[ASN][1000 genomes]
rs1096563	0.87[ASN][1000 genomes]
rs11032363	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs11032366	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11032374	0.87[EUR][1000 genomes]
rs11032380	0.82[CEU][hapmap]
rs1112840	0.88[EUR][1000 genomes]
rs12146621	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12282096	0.82[CEU][hapmap];0.84[AMR][1000 genomes]
rs12361553	0.82[CEU][hapmap]
rs1402953	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs1402957	0.81[EUR][1000 genomes]
rs1464484	0.85[AMR][1000 genomes]
rs1464486	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1464487	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1522087	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1578986	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1738547	0.87[ASN][1000 genomes]
rs1738548	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2056396	0.83[CEU][hapmap];0.82[AMR][1000 genomes]
rs2140066	0.84[AMR][1000 genomes]
rs2272065	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2901376	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3181274	0.96[CEU][hapmap];0.90[EUR][1000 genomes]
rs34944910	0.88[EUR][1000 genomes]
rs35162575	0.88[EUR][1000 genomes]
rs704703	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7125621	0.82[CEU][hapmap];0.82[AMR][1000 genomes]
rs7927218	0.83[CEU][hapmap];0.84[AMR][1000 genomes]
rs831594	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs831596	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs831603	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs953871	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[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	nsv832113	chr11:33609202-33767781	Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:115 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33758000-33770200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr11:33758200-33766400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr11:33758600-33767800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr11:33758600-33770200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr11:33758800-33768000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
6	chr11:33758800-33768400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr11:33758800-33770000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:33758800-33770800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr11:33758800-33771800	Weak transcription	Brain Angular Gyrus	brain
10	chr11:33758800-33774600	Weak transcription	Esophagus	oesophagus
11	chr11:33758800-33795000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:33759000-33767800	Weak transcription	Brain Hippocampus Middle	brain
13	chr11:33759000-33768200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr11:33759000-33769200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr11:33759000-33770200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr11:33759000-33771800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr11:33759000-33773400	Weak transcription	Lung	lung
18	chr11:33759000-33774600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr11:33759000-33778400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr11:33759000-33780800	Weak transcription	Psoas Muscle	Psoas
21	chr11:33759000-33781000	Weak transcription	Fetal Brain Male	brain
22	chr11:33759000-33795200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr11:33759200-33770200	Weak transcription	GM12878-XiMat	blood
24	chr11:33759200-33771000	Weak transcription	Brain Anterior Caudate	brain
25	chr11:33759200-33771200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr11:33759200-33774600	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr11:33759400-33767800	Weak transcription	Brain Germinal Matrix	brain
28	chr11:33759400-33768200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr11:33759400-33770600	Weak transcription	NH-A	brain
30	chr11:33759400-33773400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr11:33759400-33778200	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr11:33759600-33767800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr11:33759600-33768200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr11:33759600-33768400	Weak transcription	Fetal Kidney	kidney
35	chr11:33759600-33774600	Weak transcription	HSMMtube	muscle
36	chr11:33759800-33769400	Weak transcription	Osteobl	bone
37	chr11:33760000-33766000	Weak transcription	HepG2	liver
38	chr11:33760000-33767600	Weak transcription	HMEC	breast
39	chr11:33760000-33774400	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr11:33760200-33774600	Weak transcription	Hela-S3	cervix
41	chr11:33760400-33769200	Weak transcription	NHLF	lung
42	chr11:33760400-33770600	Weak transcription	NHDF-Ad	bronchial
43	chr11:33760400-33774600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr11:33760400-33785200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr11:33760800-33767600	Weak transcription	K562	blood
46	chr11:33761800-33767400	Weak transcription	NHEK	skin
47	chr11:33763200-33792200	Strong transcription	Fetal Thymus	thymus
48	chr11:33763200-33792400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr11:33763800-33766000	Strong transcription	Fetal Intestine Large	intestine
50	chr11:33763800-33766000	Weak transcription	A549	lung

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