Variant report

Variant	rs17106291
Chromosome Location	chr14:37559401-37559402
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:37558524..37560785-chr14:37561161..37564362,3	K562	blood:
2	chr14:37559384..37561307-chr14:37642361..37644125,2	K562	blood:
3	chr14:37548599..37550986-chr14:37557970..37560958,2	K562	blood:
4	chr14:37546643..37550099-chr14:37558000..37561401,3	K562	blood:

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs1012199	1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs10129152	0.81[ASN][1000 genomes]
rs10132328	1.00[ASN][1000 genomes]
rs10133673	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10136238	0.91[ASN][1000 genomes]
rs10141752	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs10142021	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10151092	1.00[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs10220281	0.98[ASN][1000 genomes]
rs10220604	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10459480	1.00[CHB][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs10483485	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs12050169	1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12050463	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12889634	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17091939	0.93[CHB][hapmap]
rs17105957	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs17106031	0.93[CHB][hapmap];1.00[JPT][hapmap]
rs17106189	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17106209	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17106216	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17106275	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17106290	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17106309	1.00[CHB][hapmap];0.92[JPT][hapmap]
rs17106333	0.93[CHB][hapmap];0.92[JPT][hapmap];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17106393	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs17106396	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs17106404	1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs17106433	1.00[CHB][hapmap];0.93[JPT][hapmap];0.82[ASN][1000 genomes]
rs17106509	0.93[CHB][hapmap]
rs17106512	1.00[CHB][hapmap]
rs17106525	0.86[CHB][hapmap]
rs17841015	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs17841017	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1884220	1.00[ASN][1000 genomes]
rs1884221	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1884775	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1884777	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1950374	0.81[ASN][1000 genomes]
rs1950375	0.81[ASN][1000 genomes]
rs1950376	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1950814	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1955760	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1955761	1.00[CHB][hapmap];0.92[JPT][hapmap];0.82[ASN][1000 genomes]
rs1955762	0.82[ASN][1000 genomes]
rs1955763	1.00[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs1956423	0.86[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1956424	0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs1971451	0.81[ASN][1000 genomes]
rs1998121	0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2057171	1.00[ASN][1000 genomes]
rs2078246	1.00[CHB][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs2415379	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2415380	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2415388	1.00[CHB][hapmap];0.81[ASN][1000 genomes]
rs28517624	0.91[ASN][1000 genomes]
rs28593311	0.85[ASN][1000 genomes]
rs4356385	0.95[ASN][1000 genomes]
rs61293305	0.81[ASN][1000 genomes]
rs7140991	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7151524	1.00[CHB][hapmap];0.93[JPT][hapmap]
rs7160129	1.00[CHB][hapmap];0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs74045463	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs74045478	1.00[ASN][1000 genomes]
rs8008478	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8014186	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs8019489	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs8020153	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534288	chr14:37254539-37697745	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1050174	chr14:37556357-37664143	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1043410	chr14:37556357-37671059	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv564347	chr14:37558794-37590164	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37553400-37562600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr14:37557800-37559600	Enhancers	Fetal Stomach	stomach
3	chr14:37558800-37559600	Flanking Active TSS	K562	blood
4	chr14:37559000-37559600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr14:37559200-37559600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr14:37559400-37559600	Enhancers	Lung	lung
7	chr14:37559400-37559600	Enhancers	Pancreas	Pancrea
8	chr14:37559400-37559800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr14:37559400-37559800	Enhancers	Esophagus	oesophagus
10	chr14:37559400-37559800	Flanking Active TSS	NHDF-Ad	bronchial

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