Variant report

Variant	rs11207337
Chromosome Location	chr1:59409834-59409835
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:59246467..59248452-chr1:59407731..59410394,2	K562	blood:
2	chr1:59405293..59407465-chr1:59409123..59412417,3	K562	blood:
3	chr1:59400259..59402007-chr1:59409507..59412349,2	MCF-7	breast:
4	chr1:59246952..59251848-chr1:59405165..59409884,6	K562	blood:
5	chr1:59279690..59282444-chr1:59408342..59410197,2	K562	blood:

Variant related genes	Relation type
ENSG00000177606	Chromatin interaction
ENSG00000234807	Chromatin interaction

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10889124	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11207335	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11207336	0.93[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11207338	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11207341	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11207342	0.87[AFR][1000 genomes]
rs11207343	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12060581	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12070905	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12082896	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12091374	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12092950	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12098063	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005354	chr1:59283572-59535812	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv829959	chr1:59340330-59503085	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv546316	chr1:59368947-59457815	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:59405400-59410800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:59406600-59410600	Enhancers	Primary B cells from peripheral blood	blood
3	chr1:59406600-59410800	Enhancers	Fetal Thymus	thymus
4	chr1:59407000-59410400	Enhancers	Pancreas	Pancrea
5	chr1:59407200-59410000	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr1:59407400-59410200	Weak transcription	Colonic Mucosa	Colon
7	chr1:59407400-59410600	Enhancers	Stomach Mucosa	stomach
8	chr1:59407800-59410800	Enhancers	Primary T cells fromperipheralblood	blood
9	chr1:59407800-59411000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr1:59408000-59410000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:59408000-59410000	Weak transcription	Spleen	Spleen
12	chr1:59408000-59412000	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr1:59408000-59412000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr1:59408200-59410000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:59408200-59410000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:59408200-59410000	Enhancers	Fetal Intestine Small	intestine
17	chr1:59408200-59410000	Enhancers	NHEK	skin
18	chr1:59408200-59410800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr1:59408200-59411000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr1:59408200-59412200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr1:59408400-59411000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr1:59408400-59411000	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr1:59408600-59411000	Enhancers	Primary T helper naive cells from peripheral blood	blood
24	chr1:59408600-59412000	Enhancers	Primary T cells from cord blood	blood
25	chr1:59408600-59412000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chr1:59408800-59410400	Enhancers	Esophagus	oesophagus
27	chr1:59408800-59410600	Enhancers	Gastric	stomach
28	chr1:59409000-59410000	Weak transcription	Dnd41	blood
29	chr1:59409200-59410200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr1:59409200-59410200	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr1:59409400-59410200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:59409400-59410400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr1:59409400-59410600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr1:59409600-59414000	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr1:59409800-59410400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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