Variant report

Variant	rs6917628
Chromosome Location	chr6:37204383-37204384
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs262923	0.81[YRI][hapmap]
rs262925	0.84[YRI][hapmap]
rs2842618	0.81[YRI][hapmap]
rs55740797	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56222403	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60947036	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73417837	1.00[AMR][1000 genomes]
rs73417847	1.00[AMR][1000 genomes]
rs73417851	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73417853	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73417868	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7753853	0.83[ASW][hapmap];0.81[LWK][hapmap];0.91[MKK][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9918398	0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9918399	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9918429	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9918482	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:37191400-37207400	Weak transcription	Dnd41	blood
2	chr6:37191400-37207600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr6:37200400-37206200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr6:37203200-37206400	Enhancers	K562	blood
5	chr6:37203600-37204400	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr6:37204000-37204800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:37204000-37206400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:37204200-37205400	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:37204200-37206400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:37204200-37206400	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr6:37204200-37206400	Enhancers	HUVEC	blood vessel

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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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