Variant report

Variant	rs2245379
Chromosome Location	chr10:50208799-50208800
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs1913528	0.92[ASN][1000 genomes]
rs2090126	0.92[ASN][1000 genomes]
rs2090127	0.91[ASN][1000 genomes]
rs2245392	0.95[ASN][1000 genomes]
rs2249429	0.87[ASN][1000 genomes]
rs2252811	0.80[ASN][1000 genomes]
rs2264553	0.92[ASN][1000 genomes]
rs2264843	0.92[ASN][1000 genomes]
rs2458671	0.87[ASN][1000 genomes]
rs2458675	0.85[ASN][1000 genomes]
rs4838433	0.80[ASN][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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831866	chr10:50165180-50335276	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
3	nsv6620	chr10:50197344-50224635	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2245379	FAM170B	cis	brain	BrainEAC

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50206200-50210400	Enhancers	Duodenum Mucosa	Duodenum
2	chr10:50206200-50211200	Enhancers	Fetal Intestine Small	intestine
3	chr10:50206600-50211000	Enhancers	Fetal Intestine Large	intestine
4	chr10:50206800-50209800	Enhancers	Stomach Mucosa	stomach
5	chr10:50208200-50209600	Weak transcription	Gastric	stomach
6	chr10:50208600-50210200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:50208600-50210600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr10:50208600-50210800	Enhancers	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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