Variant report

Variant	rs28729913
Chromosome Location	chr14:31725079-31725080
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10135068	0.81[AFR][1000 genomes]
rs10135482	0.87[AFR][1000 genomes]
rs10146567	0.81[AFR][1000 genomes]
rs10148704	0.97[AFR][1000 genomes]
rs10151215	0.81[AFR][1000 genomes]
rs28460801	0.87[AFR][1000 genomes]
rs28548120	0.81[AFR][1000 genomes]
rs28623024	0.81[AFR][1000 genomes]
rs28793570	0.97[AFR][1000 genomes]
rs58291808	0.81[AFR][1000 genomes]
rs58631398	0.97[AFR][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	nsv901587	chr14:31501505-31752664	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1050054	chr14:31501703-31733642	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats 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	26 gene(s)	inside rSNPs	diseases
3	esv2830427	chr14:31639110-32000034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
4	nsv1050597	chr14:31711248-31904761	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 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	chr14:31707800-31730800	Weak transcription	Pancreas	Pancrea
2	chr14:31721000-31726400	Weak transcription	Fetal Intestine Small	intestine
3	chr14:31721000-31726400	Weak transcription	Gastric	stomach
4	chr14:31721200-31726400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr14:31721200-31731000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr14:31721200-31731000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr14:31721400-31726800	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr14:31722600-31726200	Weak transcription	Stomach Mucosa	stomach
9	chr14:31722600-31726400	Weak transcription	Liver	Liver
10	chr14:31724800-31727600	Enhancers	HepG2	liver

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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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