Variant report

Variant	rs66713063
Chromosome Location	chr3:105123361-105123362
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs12496827	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13065937	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13070223	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13070790	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13075944	0.88[EUR][1000 genomes]
rs13077096	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13079517	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13079993	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13085657	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13092913	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13095216	0.80[ASN][1000 genomes]
rs13095274	0.80[ASN][1000 genomes]
rs13095691	0.88[EUR][1000 genomes]
rs1438549	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1438551	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16851097	0.98[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs16851175	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2399046	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34198525	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35616213	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4894926	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4894928	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6437582	0.80[ASN][1000 genomes]
rs6437583	0.80[ASN][1000 genomes]
rs6437584	0.80[ASN][1000 genomes]
rs7431148	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7626665	0.80[ASN][1000 genomes]
rs976530	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][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	nsv525071	chr3:105004853-105409321	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv829650	chr3:105070893-105255036	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv877304	chr3:105122214-105198374	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:105114600-105123400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr3:105119000-105133600	Weak transcription	Brain Angular Gyrus	brain
3	chr3:105120000-105130000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr3:105120400-105129400	Weak transcription	Brain Anterior Caudate	brain
5	chr3:105121000-105134800	Weak transcription	NHLF	lung
6	chr3:105121200-105124000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:105121200-105128600	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr3:105121200-105130200	Weak transcription	Brain Hippocampus Middle	brain
9	chr3:105121400-105124600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:105121600-105124000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr3:105121600-105136600	Weak transcription	HSMM	muscle
12	chr3:105121800-105133600	Weak transcription	NH-A	brain
13	chr3:105121800-105133800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr3:105122400-105123600	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr3:105122400-105123800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr3:105122400-105124200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr3:105122400-105124400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr3:105122400-105124800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr3:105122400-105133000	Weak transcription	Gastric	stomach
20	chr3:105122400-105136600	Weak transcription	Osteobl	bone
21	chr3:105122600-105126800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr3:105122600-105133200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr3:105122600-105135800	Weak transcription	NHEK	skin
24	chr3:105123000-105125200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:105123000-105134800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr3:105123200-105124400	Weak transcription	A549	lung

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