Variant report

Variant	rs1837098
Chromosome Location	chr11:16384447-16384448
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs73429680	1.00[EUR][1000 genomes]
rs73429682	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529731	chr11:16122782-16468170	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv553566	chr11:16329009-16799044	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16379000-16387200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr11:16379200-16387400	Weak transcription	Fetal Muscle Leg	muscle
3	chr11:16379800-16386600	Weak transcription	Fetal Brain Female	brain
4	chr11:16380400-16385400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr11:16380400-16387200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:16381000-16385000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr11:16381600-16385000	Weak transcription	Fetal Heart	heart
8	chr11:16381600-16386000	Enhancers	K562	blood
9	chr11:16381800-16385000	Weak transcription	Fetal Intestine Large	intestine
10	chr11:16382000-16385400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr11:16382800-16385400	Weak transcription	Fetal Intestine Small	intestine
12	chr11:16383800-16386000	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr11:16384200-16384600	Enhancers	Pancreatic Islets	Pancreatic Islet

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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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