Variant report

Variant	rs6772383
Chromosome Location	chr3:69797020-69797021
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:69794951..69797819-chr3:69799662..69801959,2	K562	blood:
2	chr3:69787097..69790813-chr3:69794141..69797560,3	K562	blood:
3	chr3:69792105..69794601-chr3:69795513..69798225,3	K562	blood:
4	chr3:69796755..69798607-chr3:69808802..69811346,2	K562	blood:

Variant related genes	Relation type
ENSG00000187098	Chromatin interaction

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs13314892	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13318796	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17006419	0.82[AMR][1000 genomes]
rs17043851	0.80[EUR][1000 genomes]
rs2114660	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2315497	0.81[AMR][1000 genomes]
rs4855323	0.84[AMR][1000 genomes]
rs4855447	0.82[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs56386221	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs57078287	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58244283	0.84[AMR][1000 genomes]
rs58529025	0.84[AMR][1000 genomes]
rs60551165	0.84[AMR][1000 genomes]
rs60843510	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs62250977	0.84[AMR][1000 genomes]
rs9817946	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9869047	0.93[AMR][1000 genomes];0.90[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	nsv834723	chr3:69643641-69811601	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:54 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:69790200-69797400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr3:69790600-69802200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:69790800-69797400	Weak transcription	Brain Anterior Caudate	brain
4	chr3:69791000-69798200	Enhancers	Fetal Thymus	thymus
5	chr3:69792000-69797400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:69792200-69798000	Enhancers	Adipose Nuclei	Adipose
7	chr3:69792800-69798400	Enhancers	Thymus	Thymus
8	chr3:69793200-69798600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr3:69794200-69801200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr3:69794400-69799000	Enhancers	NHDF-Ad	bronchial
11	chr3:69794400-69799600	Enhancers	NHLF	lung
12	chr3:69794400-69800400	Enhancers	Fetal Heart	heart
13	chr3:69794600-69798200	Enhancers	Brain Hippocampus Middle	brain
14	chr3:69794800-69798000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:69795000-69797400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr3:69795000-69801600	Enhancers	Colon Smooth Muscle	Colon
17	chr3:69795000-69802000	Weak transcription	Lung	lung
18	chr3:69795000-69802200	Weak transcription	Esophagus	oesophagus
19	chr3:69795000-69810600	Weak transcription	Pancreas	Pancrea
20	chr3:69795200-69798000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr3:69795200-69798600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr3:69795400-69798400	Weak transcription	Fetal Lung	lung
23	chr3:69795600-69799400	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr3:69795600-69801200	Enhancers	Psoas Muscle	Psoas
25	chr3:69795800-69801000	Enhancers	Duodenum Smooth Muscle	Duodenum
26	chr3:69796000-69797200	Enhancers	Right Ventricle	heart
27	chr3:69796000-69798000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr3:69796000-69798000	Enhancers	Left Ventricle	heart
29	chr3:69796200-69801200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr3:69796200-69802200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr3:69796400-69797600	Weak transcription	K562	blood
32	chr3:69796400-69798000	Enhancers	Muscle Satellite Cultured Cells	--
33	chr3:69796400-69798000	Enhancers	Osteobl	bone
34	chr3:69796400-69798400	Weak transcription	Fetal Muscle Leg	muscle
35	chr3:69796400-69798600	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr3:69796400-69798600	Enhancers	Ovary	ovary
37	chr3:69796400-69799800	Weak transcription	Duodenum Mucosa	Duodenum
38	chr3:69796600-69797600	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr3:69796600-69797600	Weak transcription	Small Intestine	intestine
40	chr3:69796600-69797800	Weak transcription	Aorta	Aorta
41	chr3:69796600-69798000	Enhancers	HSMMtube	muscle
42	chr3:69796600-69798200	Enhancers	Primary T cells from cord blood	blood
43	chr3:69796600-69798400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:69796600-69798800	Weak transcription	Colonic Mucosa	Colon
45	chr3:69796800-69797200	Weak transcription	Right Atrium	heart
46	chr3:69796800-69797200	Flanking Active TSS	Stomach Smooth Muscle	stomach
47	chr3:69796800-69797800	Weak transcription	Brain Cingulate Gyrus	brain
48	chr3:69796800-69798000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr3:69796800-69800400	Weak transcription	Brain Substantia Nigra	brain
50	chr3:69797000-69797200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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