Variant report

Variant	rs72785665
Chromosome Location	chr2:7346041-7346042
allele	A/C
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:16)

rs_ID	r²[population]
rs1525493	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1525497	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17628624	0.84[EUR][1000 genomes]
rs55947224	0.81[EUR][1000 genomes]
rs56083950	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56094154	0.81[EUR][1000 genomes]
rs56151241	0.84[EUR][1000 genomes]
rs56253063	0.81[EUR][1000 genomes]
rs72770010	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72770034	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs72770043	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72770047	0.84[EUR][1000 genomes]
rs72770054	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72770062	0.84[EUR][1000 genomes]
rs72785663	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7574754	0.83[EUR][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	nsv915888	chr2:7197783-7461967	Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1000136	chr2:7337270-7379211	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
3	nsv833337	chr2:7337273-7521146	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:7342400-7349600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr2:7343200-7348800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr2:7343200-7349200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr2:7343600-7348200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr2:7344400-7347400	Weak transcription	Fetal Brain Male	brain
6	chr2:7345200-7349800	Weak transcription	Lung	lung
7	chr2:7345600-7346200	Enhancers	Spleen	Spleen
8	chr2:7345600-7347000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr2:7345600-7347200	Enhancers	Primary neutrophils fromperipheralblood	blood
10	chr2:7345600-7347200	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr2:7345800-7346600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood

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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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