Variant report

Variant	rs7298598
Chromosome Location	chr12:106677445-106677446
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]
rs7298823	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73388513	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73388516	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73388519	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73388522	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73388524	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:106666200-106680800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr12:106676200-106678200	Weak transcription	NHEK	skin
3	chr12:106676200-106679200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr12:106676600-106681000	Weak transcription	Stomach Mucosa	stomach
5	chr12:106677000-106681400	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr12:106677200-106677600	Weak transcription	Fetal Heart	heart
7	chr12:106677200-106678600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr12:106677200-106682200	Weak transcription	Fetal Intestine Large	intestine
9	chr12:106677200-106683600	Enhancers	HepG2	liver

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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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