Variant report

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:125826373..125828748-chr8:126103559..126105908,3	K562	blood:
2	chr8:125710029..125712501-chr8:125825729..125827888,2	K562	blood:
3	chr8:125825097..125827152-chr8:125954026..125955996,2	K562	blood:
4	chr8:125825562..125827857-chr8:125852824..125856863,3	MCF-7	breast:
5	chr8:125548570..125552806-chr8:125825742..125828762,4	K562	blood:
6	chr8:125549492..125551989-chr8:125824960..125829256,5	K562	blood:
7	chr8:125825851..125829198-chr8:125950064..125952936,3	K562	blood:
8	chr8:125824915..125827447-chr8:125870554..125873163,2	K562	blood:
9	chr8:125755220..125757743-chr8:125826134..125827699,2	MCF-7	breast:
10	chr8:125730674..125732693-chr8:125825139..125827888,2	K562	blood:
11	chr8:125822757..125824811-chr8:125825500..125827545,2	MCF-7	breast:
12	chr8:125825929..125828748-chr8:126103559..126105908,4	K562	blood:
13	chr8:125826305..125827862-chr8:126015361..126017924,2	K562	blood:
14	chr8:125653582..125656116-chr8:125824961..125827801,3	K562	blood:
15	chr8:125633171..125635240-chr8:125826139..125827745,2	K562	blood:
16	chr8:125826381..125829374-chr8:125860039..125861622,2	K562	blood:
17	chr8:125825958..125827774-chr8:125846394..125847974,2	K562	blood:
18	chr8:125825718..125829730-chr8:126008807..126013107,8	K562	blood:

No data

rSNPs within LD-proxies of this variant (count:5)

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	nsv891434	chr8:125630655-126324432	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv1016502	chr8:125657664-125845074	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125821600-125827000	Weak transcription	Fetal Lung	lung
2	chr8:125821800-125827200	Weak transcription	Adipose Nuclei	Adipose
3	chr8:125821800-125827400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr8:125822200-125827000	Weak transcription	Osteobl	bone
5	chr8:125823800-125827000	Weak transcription	Fetal Brain Male	brain
6	chr8:125825200-125827400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:125826200-125827800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr8:125826200-125828400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr8:125826400-125827200	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr8:125826400-125827400	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr8:125826400-125827400	Enhancers	HSMM	muscle
12	chr8:125826400-125827400	Enhancers	NHDF-Ad	bronchial
13	chr8:125826400-125827600	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr8:125826400-125828800	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr8:125826600-125826800	Enhancers	Psoas Muscle	Psoas
16	chr8:125826600-125826800	Enhancers	Right Atrium	heart
17	chr8:125826600-125827200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr8:125826600-125827200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr8:125826600-125827400	Enhancers	Fetal Heart	heart
20	chr8:125826600-125827400	Enhancers	HSMMtube	muscle

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