Variant report

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr6:132448020-132448170	HRPEpiC	eye:	n/a	n/a

No data

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	6:132176847-132180372..6:132441471-132451441	K562	blood:
2	6:132182612-132191683..6:132441471-132451441	Hela-S3	cervix:
3	6:132441471-132451441..6:132646256-132647474	K562	blood:
4	6:132269655-132282174..6:132441471-132451441	GM12878	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ENPP1-6	chr6:132447917-132448119	NONHSAT114941

No data

rSNPs within LD-proxies of this variant (count:3)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762616	chr6:132404708-132584324	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:132444400-132451000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr6:132445000-132450600	Weak transcription	Fetal Muscle Leg	muscle
3	chr6:132445400-132451600	Weak transcription	Brain Angular Gyrus	brain
4	chr6:132446000-132450400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:132446600-132451600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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