Variant report

Variant	rs73708225
Chromosome Location	chr8:129869622-129869623
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:7)

rs_ID	r²[population]
rs55816406	1.00[AMR][1000 genomes]
rs59286366	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61574305	1.00[AMR][1000 genomes]
rs73708250	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73708255	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73708278	1.00[AMR][1000 genomes]
rs73708281	1.00[AMR][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	nsv517445	chr8:129859924-129881299	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 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	chr8:129864200-129873200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr8:129864200-129873200	Weak transcription	NH-A	brain
3	chr8:129864400-129873400	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr8:129866600-129873200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:129867200-129873200	Weak transcription	Osteobl	bone
6	chr8:129867800-129870600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr8:129868000-129873000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr8:129869200-129870200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:129869200-129871800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr8:129869200-129871800	Weak transcription	NHDF-Ad	bronchial
11	chr8:129869200-129873000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr8:129869400-129870400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr8:129869600-129869800	Enhancers	Dnd41	blood

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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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