Variant report

Variant	rs56952904
Chromosome Location	chr7:138011050-138011051
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]
rs17169585	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1963350	0.83[AMR][1000 genomes]
rs57888677	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58361740	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59324490	0.82[AFR][1000 genomes]
rs6467762	1.00[EUR][1000 genomes]
rs6958707	1.00[EUR][1000 genomes]
rs6969445	1.00[EUR][1000 genomes]
rs73458566	1.00[EUR][1000 genomes]
rs73458571	1.00[EUR][1000 genomes]
rs73462471	0.84[AFR][1000 genomes]
rs73465869	1.00[EUR][1000 genomes]
rs7787745	1.00[EUR][1000 genomes]
rs7793617	0.83[AMR][1000 genomes]
rs7808973	1.00[EUR][1000 genomes]
rs9885985	1.00[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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831152	chr7:137884311-138033117	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv5967	chr7:137988239-138015844	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137995200-138012000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:138006200-138012400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:138010000-138012400	Weak transcription	Fetal Heart	heart
4	chr7:138010000-138012400	Weak transcription	Placenta	Placenta
5	chr7:138010400-138012400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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