Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:107736265..107740487-chr7:107741777..107745446,6	K562	blood:
2	chr7:107738530..107740733-chr7:107749909..107751465,2	K562	blood:
3	chr7:107729546..107731523-chr7:107740327..107742242,2	K562	blood:
4	chr7:107733842..107736085-chr7:107740021..107742825,3	K562	blood:

rSNPs within LD-proxies of this variant (count:7)

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	nsv1033979	chr7:107003734-107877761	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv949344	chr7:107396502-107987085	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv831089	chr7:107687618-107877240	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107736200-107744600	Weak transcription	Fetal Muscle Leg	muscle
2	chr7:107736200-107753400	Weak transcription	Right Atrium	heart
3	chr7:107736400-107744200	Weak transcription	Osteobl	bone
4	chr7:107736400-107756400	Weak transcription	Pancreas	Pancrea
5	chr7:107736600-107742800	Weak transcription	K562	blood
6	chr7:107736600-107747400	Weak transcription	Duodenum Mucosa	Duodenum
7	chr7:107737000-107744600	Weak transcription	Fetal Lung	lung
8	chr7:107737800-107740400	Weak transcription	Fetal Kidney	kidney
9	chr7:107737800-107742400	Weak transcription	HepG2	liver
10	chr7:107738800-107741200	Enhancers	NHLF	lung
11	chr7:107739200-107741800	Enhancers	NHDF-Ad	bronchial
12	chr7:107739200-107744200	Weak transcription	A549	lung
13	chr7:107739400-107740600	Enhancers	Fetal Stomach	stomach
14	chr7:107739400-107740800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:107739600-107741200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr7:107739800-107741000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr7:107740000-107740600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr7:107740000-107743200	Weak transcription	Placenta	Placenta
19	chr7:107740000-107743400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr7:107740200-107743200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:107740200-107743200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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