Variant report

Variant	rs6729936
Chromosome Location	chr2:144535837-144535838
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11680647	0.81[GIH][hapmap]
rs2890738	0.81[GIH][hapmap]
rs6729239	1.00[ASW][hapmap];0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.97[LWK][hapmap];0.87[MEX][hapmap];0.98[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:144532600-144536200	Enhancers	Fetal Lung	lung
2	chr2:144534000-144536000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr2:144534000-144536400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr2:144535600-144537400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:144535800-144536200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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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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