Variant report

Variant	rs624092
Chromosome Location	chr1:79658675-79658676
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11162650	0.80[AMR][1000 genomes]
rs182761	0.80[AMR][1000 genomes]
rs228549	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs228550	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs228551	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs401462	0.80[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv491784	chr1:79146141-79853482	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv830326	chr1:79573379-79735667	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv871182	chr1:79614989-79822735	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv999471	chr1:79650363-79774433	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79654200-79659000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr1:79654400-79658800	Weak transcription	GM12878-XiMat	blood
3	chr1:79654400-79658800	Weak transcription	HMEC	breast
4	chr1:79654400-79659000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:79654600-79658800	Weak transcription	NH-A	brain
6	chr1:79654600-79658800	Weak transcription	Osteobl	bone
7	chr1:79654800-79658800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr1:79655600-79658800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr1:79657800-79658800	Enhancers	HUVEC	blood vessel
10	chr1:79658000-79658800	Enhancers	Hela-S3	cervix
11	chr1:79658000-79659800	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr1:79658200-79659200	Enhancers	Thymus	Thymus
13	chr1:79658400-79658800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr1:79658400-79659000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr1:79658600-79658800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:79658600-79659400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr1:79658600-79659400	Enhancers	Fetal Thymus	thymus

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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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