Variant report

Variant	rs10141597
Chromosome Location	chr14:32864360-32864361
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10149930	1.00[YRI][hapmap]
rs17098967	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17098983	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1805261	0.83[GIH][hapmap]
rs28452279	1.00[AMR][1000 genomes]
rs28547895	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs3784179	1.00[CEU][hapmap];0.82[JPT][hapmap];0.85[TSI][hapmap]
rs72666177	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72666181	0.81[ASN][1000 genomes]
rs8015220	0.90[AFR][1000 genomes];0.81[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	esv2758352	chr14:32858480-33016442	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	esv2759978	chr14:32858480-33016442	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv976820	chr14:32860301-32873799	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32849000-32867400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:32854200-32866600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:32860200-32865600	Weak transcription	Left Ventricle	heart
4	chr14:32860600-32865600	Weak transcription	Brain Hippocampus Middle	brain
5	chr14:32860800-32865600	Weak transcription	Brain Substantia Nigra	brain
6	chr14:32862000-32867000	Weak transcription	Brain Germinal Matrix	brain
7	chr14:32862400-32864400	Enhancers	Brain Anterior Caudate	brain
8	chr14:32863600-32865400	Weak transcription	Brain Angular Gyrus	brain
9	chr14:32863800-32864400	Enhancers	Fetal Heart	heart
10	chr14:32863800-32865000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr14:32863800-32865400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr14:32864000-32865400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr14:32864200-32864400	Enhancers	Psoas Muscle	Psoas

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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