Variant report

Variant	rs7276931
Chromosome Location	chr21:16644635-16644636
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs16980826	1.00[EUR][1000 genomes]
rs16980835	1.00[EUR][1000 genomes]
rs16980843	1.00[EUR][1000 genomes]
rs16980928	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17275037	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220271	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220272	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220273	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220274	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220275	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220276	1.00[EUR][1000 genomes]
rs62220277	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62220278	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7277875	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7278014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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	nsv1063385	chr21:16521617-16926212	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	7 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	chr21:16636200-16653200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr21:16643200-16647000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr21:16643600-16644800	Enhancers	Placenta	Placenta
4	chr21:16644000-16646000	Enhancers	Primary hematopoietic stem cells	blood
5	chr21:16644400-16644800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr21:16644400-16647000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr21:16644600-16645000	Enhancers	Muscle Satellite Cultured Cells	--
8	chr21:16644600-16645000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr21:16644600-16645000	Enhancers	Adipose Nuclei	Adipose
10	chr21:16644600-16645000	Enhancers	NH-A	brain
11	chr21:16644600-16645400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr21:16644600-16645400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr21:16644600-16645600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr21:16644600-16645600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr21:16644600-16645600	Enhancers	HSMM	muscle
16	chr21:16644600-16645600	Enhancers	HSMMtube	muscle

Quick Search:

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

what's new

Quick links