Variant report

No.	Distal block	Cell Line	Cell type
1	chr14:70046589..70048780-chr14:70243227..70244805,2	MCF-7	breast:
2	chr14:70045745..70047839-chr14:70232582..70236616,4	K562	blood:
3	chr14:70046515..70047542-chr14:70193403..70194180,5	MCF-7	breast:
4	chr14:70044893..70047261-chr14:70192485..70195445,3	K562	blood:
5	chr14:70044627..70046904-chr14:70192270..70194531,2	K562	blood:
6	chr14:70046299..70047841-chr14:70240558..70242484,2	K562	blood:
7	chr14:70046536..70047298-chr14:70193410..70194236,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000100650	Chromatin interaction

rSNPs within LD-proxies of this variant (count:33)

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	nsv1335	chr14:70036126-70062584	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1049280	chr14:70036804-70172630	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv542124	chr14:70036804-70172630	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr14:70041600-70046800	Weak transcription	Pancreas	Pancrea
2	chr14:70041600-70060400	Weak transcription	Esophagus	oesophagus
3	chr14:70043800-70067200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:70045800-70047400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr14:70045800-70052600	Weak transcription	Right Atrium	heart
6	chr14:70046000-70047400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr14:70046200-70047000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr14:70046200-70047400	Enhancers	Fetal Intestine Large	intestine
9	chr14:70046200-70047400	Enhancers	HepG2	liver
10	chr14:70046200-70047400	Enhancers	Osteobl	bone
11	chr14:70046400-70046600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:70046400-70046800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr14:70046400-70046800	Flanking Active TSS	Hela-S3	cervix
14	chr14:70046400-70046800	Enhancers	NH-A	brain
15	chr14:70046400-70047200	Enhancers	Duodenum Mucosa	Duodenum
16	chr14:70046400-70047400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr14:70046400-70047400	Enhancers	Liver	Liver
18	chr14:70046400-70047400	Enhancers	Fetal Intestine Small	intestine
19	chr14:70046400-70047400	Enhancers	Stomach Mucosa	stomach
20	chr14:70046400-70047400	Enhancers	K562	blood

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