Variant report

Variant	rs2248752
Chromosome Location	chr6:30076106-30076107
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
TRIM31	TF binding region
ENSG00000204616	Chromatin interaction
ENSG00000066379	Chromatin interaction
ENSG00000231226	Chromatin interaction
ENSG00000204623	Chromatin interaction

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs2256146	0.82[EUR][1000 genomes]
rs2523980	0.89[AFR][1000 genomes]
rs356965	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs356970	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61758092	0.89[AFR][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	nsv432866	chr6:30026321-30080921	Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30071600-30079200	Weak transcription	Gastric	stomach
2	chr6:30072200-30078000	Weak transcription	Colonic Mucosa	Colon
3	chr6:30074400-30076600	Weak transcription	Stomach Mucosa	stomach
4	chr6:30075800-30076600	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr6:30075800-30078000	Weak transcription	Fetal Intestine Small	intestine
6	chr6:30076000-30079400	Weak transcription	Hela-S3	cervix

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

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