Variant report

Variant	rs831595
Chromosome Location	chr11:33765257-33765258
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:33756213..33759924-chr11:33763049..33766673,5	MCF-7	breast:
2	chr11:33763274..33765772-chr11:33766877..33769018,2	MCF-7	breast:
3	chr11:33756685..33760340-chr11:33762544..33766325,4	MCF-7	breast:
4	chr11:33759115..33761231-chr11:33763394..33765544,2	K562	blood:
5	chr11:33763093..33766098-chr11:33769315..33772187,4	K562	blood:

Variant related genes	Relation type
ENSG00000085063	Chromatin interaction
ENSG00000110429	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10768025	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836107	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10836110	0.87[CEU][hapmap]
rs1096561	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11032367	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11032372	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11032373	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1112841	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12224154	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12806824	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1522084	0.86[CEU][hapmap]
rs1522085	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1718067	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2252927	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2272064	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2686245	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2746601	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2746602	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4348870	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4756002	0.86[CEU][hapmap]
rs6484665	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7116243	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7938603	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs831592	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];0.99[ASN][1000 genomes]
rs831629	0.86[CHB][hapmap];0.80[JPT][hapmap]
rs831633	0.81[CHB][hapmap]
rs861256	1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs884710	0.86[CEU][hapmap]
rs953142	0.86[CEU][hapmap]
rs999479	0.81[CEU][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	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

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs831595	CD59	cis	Nerve Tibial	GTEx
rs831595	CD59	Cis_1M	lymphoblastoid	RTeQTL
rs831595	CD59	cis	Artery Tibial	GTEx
rs831595	CD59	cis	Esophagus Muscularis	GTEx

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	chr11:33758600-33765800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr11:33758600-33767800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr11:33758600-33770200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr11:33758800-33768000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr11:33758800-33768400	Weak transcription	Fetal Muscle Trunk	muscle
8	chr11:33758800-33770000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr11:33758800-33770800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr11:33758800-33771800	Weak transcription	Brain Angular Gyrus	brain
11	chr11:33758800-33774600	Weak transcription	Esophagus	oesophagus
12	chr11:33758800-33795000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr11:33759000-33767800	Weak transcription	Brain Hippocampus Middle	brain
14	chr11:33759000-33768200	Weak transcription	Primary hematopoietic stem cells	blood
15	chr11:33759000-33769200	Weak transcription	Rectal Smooth Muscle	rectum
16	chr11:33759000-33770200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:33759000-33771800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:33759000-33773400	Weak transcription	Lung	lung
19	chr11:33759000-33774600	Weak transcription	Brain Cingulate Gyrus	brain
20	chr11:33759000-33778400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr11:33759000-33780800	Weak transcription	Psoas Muscle	Psoas
22	chr11:33759000-33781000	Weak transcription	Fetal Brain Male	brain
23	chr11:33759000-33795200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:33759200-33770200	Weak transcription	GM12878-XiMat	blood
25	chr11:33759200-33771000	Weak transcription	Brain Anterior Caudate	brain
26	chr11:33759200-33771200	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr11:33759200-33774600	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr11:33759400-33767800	Weak transcription	Brain Germinal Matrix	brain
29	chr11:33759400-33768200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:33759400-33770600	Weak transcription	NH-A	brain
31	chr11:33759400-33773400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr11:33759400-33778200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr11:33759600-33767800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr11:33759600-33768200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr11:33759600-33768400	Weak transcription	Fetal Kidney	kidney
36	chr11:33759600-33774600	Weak transcription	HSMMtube	muscle
37	chr11:33759800-33769400	Weak transcription	Osteobl	bone
38	chr11:33760000-33766000	Weak transcription	HepG2	liver
39	chr11:33760000-33767600	Weak transcription	HMEC	breast
40	chr11:33760000-33774400	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr11:33760200-33774600	Weak transcription	Hela-S3	cervix
42	chr11:33760400-33769200	Weak transcription	NHLF	lung
43	chr11:33760400-33770600	Weak transcription	NHDF-Ad	bronchial
44	chr11:33760400-33774600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:33760400-33785200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr11:33760800-33767600	Weak transcription	K562	blood
47	chr11:33761800-33767400	Weak transcription	NHEK	skin
48	chr11:33763200-33765400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:33763200-33765400	Strong transcription	Liver	Liver
50	chr11:33763200-33792200	Strong transcription	Fetal Thymus	thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links