Variant report

Variant	rs11692537
Chromosome Location	chr2:48670171-48670172
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NR2F2	chr2:48669842-48670197	K562	blood:	n/a	n/a
2	POLR2A	chr2:48667222-48671944	GM12891	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:48668357..48671385-chr2:48673634..48677025,4	K562	blood:
2	chr2:48132531..48135272-chr2:48667743..48670607,2	K562	blood:
3	chr2:47401201..47404315-chr2:48668410..48671549,3	K562	blood:

Variant related genes	Relation type
ENSG00000272663	TF binding region
ENSG00000143933	Chromatin interaction
ENSG00000233230	Chromatin interaction
ENSG00000138081	Chromatin interaction

Extended variants
information (count: 37 )
Associated
traits (count: 3 )

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

rs_ID	r²[population]
rs10182093	0.92[EUR][1000 genomes]
rs10191938	0.92[EUR][1000 genomes]
rs10195717	0.86[CEU][hapmap];0.93[EUR][1000 genomes]
rs10197359	0.93[EUR][1000 genomes]
rs11674217	1.00[CEU][hapmap];0.91[YRI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11676078	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11677205	0.88[CEU][hapmap];0.85[TSI][hapmap]
rs11677234	0.83[YRI][hapmap]
rs11678825	0.83[EUR][1000 genomes]
rs11678934	1.00[CEU][hapmap];0.92[TSI][hapmap];0.90[EUR][1000 genomes]
rs11679685	0.91[EUR][1000 genomes]
rs11681187	0.87[AFR][1000 genomes]
rs11682008	0.87[CEU][hapmap]
rs11682838	0.82[EUR][1000 genomes]
rs11683202	0.88[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[YRI][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11686769	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11687461	0.88[CEU][hapmap]
rs11687771	1.00[CEU][hapmap]
rs11689285	1.00[CEU][hapmap]
rs11690526	1.00[CEU][hapmap];1.00[GIH][hapmap];0.86[MEX][hapmap];0.85[TSI][hapmap]
rs11691302	0.83[EUR][1000 genomes]
rs11691407	0.83[EUR][1000 genomes]
rs11694094	0.83[EUR][1000 genomes]
rs11694955	0.90[EUR][1000 genomes]
rs13398456	0.88[CEU][hapmap];0.93[EUR][1000 genomes]
rs17325698	0.87[CEU][hapmap]
rs17397449	0.88[CEU][hapmap];0.92[TSI][hapmap];0.84[EUR][1000 genomes]
rs17397707	0.87[CEU][hapmap]
rs28505584	0.83[EUR][1000 genomes]
rs2937	1.00[CEU][hapmap]
rs4364065	0.91[EUR][1000 genomes]
rs6747738	0.88[CEU][hapmap]
rs72889641	0.93[EUR][1000 genomes]
rs7573281	0.83[EUR][1000 genomes]
rs7584796	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762252	chr2:48554150-48741093	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv581775	chr2:48619869-48714938	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs11692537	KLRAQ1	cis	parietal	SCAN
rs11692537	CCDC128	Cis_1M	lymphoblastoid	RTeQTL
rs11692537	STON1-GTF2A1L	cis	cerebellum	SCAN

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48668600-48682000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:48668800-48670200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chr2:48668800-48670400	Weak transcription	Gastric	stomach
4	chr2:48668800-48671200	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr2:48668800-48671600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr2:48668800-48672200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr2:48668800-48672600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:48668800-48672600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:48668800-48672600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr2:48668800-48672600	Weak transcription	Esophagus	oesophagus
11	chr2:48668800-48672800	Weak transcription	Left Ventricle	heart
12	chr2:48668800-48673000	Enhancers	Primary B cells from peripheral blood	blood
13	chr2:48668800-48673600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr2:48668800-48674200	Weak transcription	Small Intestine	intestine
15	chr2:48668800-48675200	Weak transcription	HSMM	muscle
16	chr2:48668800-48675800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr2:48668800-48675800	Weak transcription	Psoas Muscle	Psoas
18	chr2:48668800-48678800	Weak transcription	Fetal Muscle Trunk	muscle
19	chr2:48668800-48679600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
20	chr2:48668800-48682400	Weak transcription	Lung	lung
21	chr2:48669000-48670200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr2:48669000-48670200	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chr2:48669000-48670200	Weak transcription	Aorta	Aorta
24	chr2:48669000-48670400	Enhancers	Ovary	ovary
25	chr2:48669000-48671000	Enhancers	Primary T helper naive cells from peripheral blood	blood
26	chr2:48669000-48671200	Enhancers	Primary neutrophils fromperipheralblood	blood
27	chr2:48669000-48672600	Weak transcription	Placenta	Placenta
28	chr2:48669000-48672600	Weak transcription	Right Atrium	heart
29	chr2:48669000-48672800	Enhancers	Liver	Liver
30	chr2:48669000-48673200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr2:48669000-48673200	Flanking Active TSS	GM12878-XiMat	blood
32	chr2:48669000-48673600	Enhancers	Brain Substantia Nigra	brain
33	chr2:48669000-48675200	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr2:48669000-48678400	Weak transcription	Colonic Mucosa	Colon
35	chr2:48669000-48678800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
36	chr2:48669000-48679000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:48669000-48680000	Weak transcription	Fetal Stomach	stomach
38	chr2:48669000-48681800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr2:48669000-48683400	Weak transcription	Right Ventricle	heart
40	chr2:48669200-48670400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr2:48669200-48670400	Enhancers	Fetal Kidney	kidney
42	chr2:48669200-48670600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
43	chr2:48669200-48671800	Enhancers	K562	blood
44	chr2:48669200-48673600	Enhancers	Primary T helper cells PMA-I stimulated	--
45	chr2:48669200-48673600	Enhancers	HepG2	liver
46	chr2:48669200-48674400	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr2:48669200-48675600	Weak transcription	Adipose Nuclei	Adipose
48	chr2:48669200-48678400	Weak transcription	HUVEC	blood vessel
49	chr2:48669200-48698200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
50	chr2:48669400-48670200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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