Variant report

Variant	rs72975025
Chromosome Location	chr2:141773685-141773686
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:2)

rs_ID	r²[population]
rs72975015	0.87[AFR][1000 genomes]
rs72975050	1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583198	chr2:141510791-142150620	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv875208	chr2:141657878-141795620	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1014208	chr2:141707558-141790148	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv817518	chr2:141714174-142287302	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv875210	chr2:141764693-141818657	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv875211	chr2:141764693-141846346	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:141771800-141774600	Enhancers	Cortex derived primary cultured neurospheres	brain
2	chr2:141772200-141774400	Enhancers	Fetal Heart	heart
3	chr2:141772200-141774600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:141772200-141774600	Enhancers	Brain Hippocampus Middle	brain
5	chr2:141772400-141773800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr2:141772400-141774200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr2:141772600-141773800	Enhancers	Brain Substantia Nigra	brain
8	chr2:141772800-141773800	Enhancers	Fetal Lung	lung
9	chr2:141773000-141773800	Enhancers	Brain Anterior Caudate	brain
10	chr2:141773000-141774000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr2:141773000-141774400	Enhancers	Brain Cingulate Gyrus	brain
12	chr2:141773600-141773800	Enhancers	HSMMtube	muscle
13	chr2:141773600-141774200	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr2:141773600-141777400	Weak transcription	HSMM	muscle
15	chr2:141773600-141806800	Weak transcription	Brain Angular Gyrus	brain

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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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