Variant report

Variant	rs61783077
Chromosome Location	chr1:77836062-77836063
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs17100499	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61782696	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005183	chr1:77728990-77949309	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv535010	chr1:77728990-77949309	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv932557	chr1:77730247-77958687	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1003714	chr1:77756861-77949309	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	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
6	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
7	esv2764210	chr1:77825478-77838400	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77795000-77836400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:77803400-77839200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr1:77820400-77836400	Weak transcription	Primary T cells from cord blood	blood
4	chr1:77824400-77836400	Weak transcription	Brain Anterior Caudate	brain
5	chr1:77826200-77836400	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr1:77834000-77839800	Enhancers	NHDF-Ad	bronchial
7	chr1:77834200-77836400	Enhancers	Muscle Satellite Cultured Cells	--
8	chr1:77834200-77836600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr1:77834200-77839000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr1:77835200-77837200	Enhancers	Brain Cingulate Gyrus	brain
11	chr1:77835200-77838000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr1:77835600-77836400	Enhancers	NHLF	lung
13	chr1:77835600-77836600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr1:77835600-77837000	Enhancers	HSMMtube	muscle
15	chr1:77835600-77837200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr1:77835600-77837400	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr1:77835600-77837400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr1:77835600-77837400	Enhancers	NH-A	brain
19	chr1:77835600-77838000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr1:77835800-77836600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr1:77835800-77837000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr1:77835800-77837000	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr1:77835800-77837200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr1:77835800-77837200	Enhancers	Fetal Stomach	stomach
25	chr1:77835800-77837400	Enhancers	HMEC	breast
26	chr1:77835800-77846400	Weak transcription	Aorta	Aorta
27	chr1:77836000-77836400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr1:77836000-77836400	Active TSS	Brain Substantia Nigra	brain
29	chr1:77836000-77836600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
30	chr1:77836000-77837000	Weak transcription	Brain Angular Gyrus	brain
31	chr1:77836000-77837000	Enhancers	HSMM	muscle
32	chr1:77836000-77837400	Enhancers	Brain Hippocampus Middle	brain
33	chr1:77836000-77837800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr1:77836000-77837800	Enhancers	Osteobl	bone

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