Variant report

Variant	rs4584997
Chromosome Location	chr2:172129983-172129984
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10490605	0.94[ASN][1000 genomes]
rs10754977	0.98[ASN][1000 genomes]
rs10803858	0.98[ASN][1000 genomes]
rs10803859	0.94[ASN][1000 genomes]
rs10930464	0.81[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs11903215	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12474103	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13007471	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34931272	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6717184	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6727785	0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs6743965	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs888272	0.85[JPT][hapmap]

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	esv3382346	chr2:172062677-172363892	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:172127600-172130000	Enhancers	HMEC	breast
2	chr2:172127600-172130400	Enhancers	Colon Smooth Muscle	Colon
3	chr2:172127800-172134000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:172128000-172130000	Enhancers	Stomach Smooth Muscle	stomach
5	chr2:172128600-172134200	Weak transcription	HSMMtube	muscle
6	chr2:172129000-172138800	Weak transcription	Rectal Smooth Muscle	rectum
7	chr2:172129200-172136000	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr2:172129800-172130000	Enhancers	Fetal Brain Female	brain

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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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