Variant report

Variant	rs7740741
Chromosome Location	chr6:30100733-30100734
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs17180528	1.00[EUR][1000 genomes]
rs17186951	1.00[EUR][1000 genomes]
rs17187553	1.00[EUR][1000 genomes]
rs17187658	1.00[EUR][1000 genomes]
rs17187826	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17187847	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17194258	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4713289	1.00[EUR][1000 genomes]
rs4959042	1.00[EUR][1000 genomes]
rs56908820	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60471614	1.00[ASN][1000 genomes]
rs6906435	1.00[ASN][1000 genomes]
rs6917420	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6926097	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:30099000-30103600	Weak transcription	A549	lung
2	chr6:30099400-30101800	Enhancers	HepG2	liver
3	chr6:30099400-30103200	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr6:30099400-30103400	Weak transcription	Hela-S3	cervix
5	chr6:30100400-30101400	Weak transcription	Fetal Intestine Small	intestine
6	chr6:30100400-30101800	Weak transcription	Fetal Intestine Large	intestine

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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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