Variant report

Variant	rs2892795
Chromosome Location	chr6:121803816-121803817
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10872223	1.00[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs12195627	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12196049	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12196172	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12198502	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12201990	0.91[ASN][1000 genomes]
rs12204055	0.84[ASN][1000 genomes]
rs12215552	0.83[ASN][1000 genomes]
rs58614102	0.94[ASN][1000 genomes]
rs716013	1.00[AFR][1000 genomes];0.98[ASN][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	nsv966657	chr6:121786080-121806494	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv5458	chr6:121787521-121823054	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121801000-121806200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr6:121801600-121806200	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr6:121802600-121804000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:121802600-121804000	Enhancers	HUVEC	blood vessel
5	chr6:121802600-121808600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:121803000-121804000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:121803000-121806000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr6:121803000-121806200	Weak transcription	HMEC	breast
9	chr6:121803200-121805600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr6:121803200-121806200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr6:121803200-121806200	Weak transcription	NHEK	skin
12	chr6:121803200-121806400	Weak transcription	Hela-S3	cervix
13	chr6:121803400-121805400	Weak transcription	A549	lung
14	chr6:121803400-121806400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:121803600-121805600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr6:121803800-121804600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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