Variant report

Variant	rs737421
Chromosome Location	chr11:119757242-119757243
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17123428	0.86[AFR][1000 genomes]
rs737441	0.86[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051526	chr11:119750335-119775811	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119746000-119762400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr11:119747200-119758600	Weak transcription	Right Ventricle	heart
3	chr11:119747200-119768200	Weak transcription	Fetal Intestine Small	intestine
4	chr11:119747600-119762400	Weak transcription	Esophagus	oesophagus
5	chr11:119749600-119760000	Enhancers	Fetal Heart	heart
6	chr11:119753600-119758400	Weak transcription	Left Ventricle	heart
7	chr11:119755200-119760400	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr11:119756400-119757400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:119756400-119757400	Enhancers	Rectal Mucosa Donor 31	rectum
10	chr11:119756400-119757800	Enhancers	Sigmoid Colon	Sigmoid Colon

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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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