Variant report

Variant	rs11501747
Chromosome Location	chr11:74751268-74751269
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12293048	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57538714	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6592597	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7112525	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7129614	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7929665	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7941838	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7950413	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74743000-74751800	Weak transcription	Right Atrium	heart
2	chr11:74747400-74751400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:74750800-74751400	Enhancers	Fetal Intestine Small	intestine
4	chr11:74750800-74751800	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:74750800-74751800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:74751200-74751600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr11:74751200-74751600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr11:74751200-74751600	Enhancers	K562	blood
9	chr11:74751200-74752600	Enhancers	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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