Variant report

Variant	rs4624890
Chromosome Location	chr6:144446497-144446498
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11155344	0.85[JPT][hapmap];1.00[YRI][hapmap];0.87[ASN][1000 genomes]
rs2179409	0.88[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.87[ASN][1000 genomes]
rs4896698	0.80[ASN][1000 genomes]
rs6570604	1.00[YRI][hapmap];0.87[ASN][1000 genomes]
rs6570605	0.84[JPT][hapmap];1.00[YRI][hapmap];0.87[ASN][1000 genomes]
rs7747271	0.81[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.87[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144445600-144446600	Enhancers	K562	blood
2	chr6:144445600-144448200	Weak transcription	GM12878-XiMat	blood
3	chr6:144445600-144450600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr6:144446000-144450200	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr6:144446000-144450400	Weak transcription	Primary monocytes fromperipheralblood	blood
6	chr6:144446400-144450600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

Quick Search:

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

what's new

Quick links