Variant report

Variant	rs9462994
Chromosome Location	chr6:44493719-44493720
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs7768974	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs7774489	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9472290	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9472294	0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44492400-44496600	Enhancers	Fetal Thymus	thymus
2	chr6:44492400-44509800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:44493000-44494600	Weak transcription	Thymus	Thymus
4	chr6:44493200-44494400	Weak transcription	Dnd41	blood
5	chr6:44493200-44498000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:44493400-44494800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:44493600-44493800	Enhancers	H9 Cell Line	embryonic stem cell
8	chr6:44493600-44495600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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