Variant report

No.	Distal block	Cell Line	Cell type
1	chr9:93740191..93743980-chr9:93753139..93756785,4	MCF-7	breast:
2	chr9:93728320..93731079-chr9:93741313..93742989,2	MCF-7	breast:
3	chr9:93676159..93678392-chr9:93740956..93744804,3	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10115615	0.94[EUR][1000 genomes]
rs10121625	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs10465159	0.82[EUR][1000 genomes]
rs10820823	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10991703	0.82[EUR][1000 genomes]
rs10991704	0.82[EUR][1000 genomes]
rs10991705	0.82[EUR][1000 genomes]
rs10991729	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs10991734	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10991738	0.89[ASN][1000 genomes]
rs12236287	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12352804	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13294492	0.82[EUR][1000 genomes]
rs16907055	0.83[AFR][1000 genomes]
rs28425571	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs296725	0.86[AFR][1000 genomes]
rs36034099	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4452924	0.91[EUR][1000 genomes]
rs7030712	0.94[EUR][1000 genomes]
rs71509677	0.85[ASN][1000 genomes]
rs715728	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes]
rs73653514	0.94[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046989	chr9:93353987-93800416	Transcr. at gene 5' and 3' Weak transcription Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv893568	chr9:93539879-93774385	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:93730400-93741600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr9:93740400-93746200	Weak transcription	Dnd41	blood
3	chr9:93740800-93743200	Enhancers	HMEC	breast
4	chr9:93741000-93741800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:93741000-93742000	Enhancers	NHEK	skin
6	chr9:93741000-93742200	Enhancers	Pancreas	Pancrea
7	chr9:93741000-93742400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr9:93741000-93742600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:93741200-93741600	Active TSS	Rectal Mucosa Donor 29	rectum
10	chr9:93741200-93742000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr9:93741200-93742000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr9:93741400-93741600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:93741400-93741800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr9:93741400-93741800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr9:93741400-93741800	Enhancers	Esophagus	oesophagus
16	chr9:93741400-93742000	Enhancers	Placenta Amnion	Placenta Amnion
17	chr9:93741400-93742000	Enhancers	Hela-S3	cervix

Quick Search: