Variant report

Variant	rs61777066
Chromosome Location	chr1:77974662-77974663
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:77966991..77969632-chr1:77973867..77975954,2	MCF-7	breast:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1874816	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61777063	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61777064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61777065	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61777068	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61777069	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61777070	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61777071	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61778697	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61778699	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61778700	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61778702	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61778703	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61778704	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61778705	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61778707	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61778708	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs61784764	0.88[AMR][1000 genomes]
rs61784767	0.94[AMR][1000 genomes]
rs61784770	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61784771	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61784772	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6678173	0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470719	chr1:77774413-78269207	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv546591	chr1:77774413-78269207	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv871143	chr1:77955577-78031994	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77956200-77975600	Weak transcription	HSMMtube	muscle
2	chr1:77958200-77974800	Weak transcription	Brain Angular Gyrus	brain
3	chr1:77969600-77981600	Enhancers	HUVEC	blood vessel
4	chr1:77971000-77974800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr1:77971000-77980400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr1:77971200-77978800	Weak transcription	Primary T cells from cord blood	blood
7	chr1:77971200-77980600	Weak transcription	Primary hematopoietic stem cells	blood
8	chr1:77972800-77979200	Weak transcription	Fetal Muscle Trunk	muscle
9	chr1:77973000-77977200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr1:77973200-77975800	Weak transcription	A549	lung
11	chr1:77973600-77983400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr1:77974000-77976000	Enhancers	Brain Substantia Nigra	brain
13	chr1:77974000-77976000	Enhancers	Fetal Muscle Leg	muscle
14	chr1:77974200-77976000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr1:77974200-77977400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr1:77974400-77978200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr1:77974600-77974800	Enhancers	Hela-S3	cervix
18	chr1:77974600-77975200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr1:77974600-77975200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr1:77974600-77975200	Enhancers	NHLF	lung
21	chr1:77974600-77975800	Enhancers	Brain Cingulate Gyrus	brain
22	chr1:77974600-77976000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:77974600-77976000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr1:77974600-77976200	Enhancers	Brain Hippocampus Middle	brain
25	chr1:77974600-77976400	Enhancers	Brain Anterior Caudate	brain
26	chr1:77974600-77977400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr1:77974600-77977400	Enhancers	HSMM	muscle
28	chr1:77974600-77977400	Enhancers	Osteobl	bone
29	chr1:77974600-77978200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:77974600-77982200	Enhancers	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links