Variant report

Variant	rs2038309
Chromosome Location	chr14:37600567-37600568
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:37528200..37530680-chr14:37600178..37602513,2	K562	blood:
2	chr14:37593615..37596516-chr14:37600074..37602839,3	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs1012198	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10134406	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10141752	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs10220604	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs1057564	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs1404	1.00[EUR][1000 genomes]
rs17091939	1.00[CEU][hapmap]
rs17106209	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs17106216	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs17106493	1.00[GIH][hapmap];0.95[EUR][1000 genomes]
rs17106509	1.00[CEU][hapmap]
rs17106512	1.00[CEU][hapmap]
rs17106525	1.00[CEU][hapmap]
rs17178484	1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[EUR][1000 genomes]
rs17178639	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17178764	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17767749	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs17767929	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs17841015	1.00[CEU][hapmap]
rs1884775	1.00[CEU][hapmap]
rs1950372	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[EUR][1000 genomes]
rs1950814	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs1955758	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1956423	1.00[CEU][hapmap]
rs1956424	1.00[CEU][hapmap]
rs2144318	0.83[EUR][1000 genomes]
rs2415373	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs2415379	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs2415380	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs2415386	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs35576618	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs4356385	0.83[EUR][1000 genomes]
rs56666059	0.95[EUR][1000 genomes]
rs57235322	1.00[EUR][1000 genomes]
rs6571781	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs6571783	1.00[CEU][hapmap];1.00[GIH][hapmap];0.95[EUR][1000 genomes]
rs6571785	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs6571786	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs6571787	1.00[EUR][1000 genomes]
rs6571788	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7142723	0.95[EUR][1000 genomes]
rs7151524	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs7159967	0.95[EUR][1000 genomes]
rs725243	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs8009630	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs8012664	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs8014610	0.95[EUR][1000 genomes]
rs8017826	1.00[GIH][hapmap]
rs8019489	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs976171	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 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	nsv564348	chr14:37584981-37608459	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv530038	chr14:37590543-38336191	Weak transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:37582400-37602800	Weak transcription	K562	blood
2	chr14:37598400-37610000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr14:37599800-37600800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr14:37599800-37601000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:37599800-37601400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr14:37599800-37601400	Enhancers	Brain Substantia Nigra	brain
7	chr14:37600400-37601200	Enhancers	Fetal Heart	heart

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