Variant report

Variant	rs11014317
Chromosome Location	chr10:18745595-18745596
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10508561	0.86[ASN][1000 genomes]
rs10741073	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10828704	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10828726	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11014256	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11014261	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11014266	0.86[ASN][1000 genomes]
rs11014284	0.87[ASN][1000 genomes]
rs11014299	0.80[ASN][1000 genomes]
rs11014302	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11014337	0.84[ASN][1000 genomes]
rs12220716	0.86[ASN][1000 genomes]
rs17692465	0.84[ASN][1000 genomes]
rs55761512	0.82[ASN][1000 genomes]
rs7090956	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7091297	0.84[ASN][1000 genomes]
rs7091299	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7099509	0.86[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv550042	chr10:18683267-18994583	ZNF genes & repeats Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18732400-18801600	Weak transcription	Pancreas	Pancrea
2	chr10:18739000-18752600	Weak transcription	Right Atrium	heart
3	chr10:18739000-18761000	Weak transcription	Colon Smooth Muscle	Colon
4	chr10:18741600-18763200	Weak transcription	Fetal Stomach	stomach
5	chr10:18743400-18746200	Enhancers	Dnd41	blood
6	chr10:18744400-18761800	Weak transcription	Ovary	ovary
7	chr10:18744600-18746400	Enhancers	Fetal Heart	heart
8	chr10:18744800-18745600	Enhancers	Primary B cells from cord blood	blood
9	chr10:18745000-18745800	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr10:18745200-18746600	Enhancers	Primary B cells from peripheral blood	blood
11	chr10:18745200-18750800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr10:18745400-18746200	Genic enhancers	Left Ventricle	heart
13	chr10:18745400-18763200	Weak transcription	Right Ventricle	heart

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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