Variant report

Variant	rs4149465
Chromosome Location	chr7:65798988-65798989
allele	A/G
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:12)

rs_ID	r²[population]
rs11560207	0.83[AMR][1000 genomes]
rs11561738	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13311614	0.81[EUR][1000 genomes]
rs2859839	0.92[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs3823606	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4149458	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4149459	1.00[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4149460	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4149462	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4149464	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4149466	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9647880	1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532124	chr7:65371521-66234730	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
2	nsv1026559	chr7:65617368-66370805	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases
3	nsv508458	chr7:65724222-65842639	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
4	nsv1034195	chr7:65743409-65828266	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65791800-65799600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:65791800-65800400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:65792600-65799800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:65793000-65800200	Weak transcription	HSMM	muscle
5	chr7:65795800-65799200	Enhancers	Fetal Lung	lung
6	chr7:65796200-65799800	Weak transcription	Pancreas	Pancrea
7	chr7:65796200-65801600	Weak transcription	Left Ventricle	heart
8	chr7:65796200-65809000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr7:65796400-65800000	Weak transcription	Fetal Stomach	stomach
10	chr7:65796400-65800400	Weak transcription	Fetal Muscle Leg	muscle
11	chr7:65796600-65799000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:65796800-65800200	Weak transcription	NHLF	lung
13	chr7:65796800-65809200	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr7:65797200-65811600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:65797600-65799400	Enhancers	Liver	Liver
16	chr7:65797800-65799200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:65797800-65799200	Enhancers	Fetal Intestine Large	intestine
18	chr7:65797800-65799200	Enhancers	Fetal Intestine Small	intestine
19	chr7:65797800-65799200	Enhancers	Fetal Kidney	kidney
20	chr7:65797800-65800000	Enhancers	HepG2	liver
21	chr7:65798200-65809000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr7:65798400-65799200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:65798600-65799200	Enhancers	A549	lung
24	chr7:65798800-65800200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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