Variant report

(count:25 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	E2F6	chr10:91318123-91318610	H1-hESC	embryonic stem cell:	n/a	n/a
2	CTCF	chr10:91318200-91318350	RPTEC	kidney:	n/a	n/a
3	POLR2A	chr10:91318108-91318456	K562	blood:	n/a	n/a
4	CTCF	chr10:91318260-91318410	HBMEC	blood vessel:	n/a	n/a
5	CTCF	chr10:91318200-91318350	HEK293	kidney:	n/a	n/a
6	CTCF	chr10:91318200-91318350	WERI-Rb-1	eye:	n/a	n/a
7	POLR2A	chr10:91318194-91318755	H1-hESC	embryonic stem cell:	n/a	n/a
8	ZNF384	chr10:91318045-91318404	K562	blood:	n/a	n/a
9	E2F6	chr10:91318180-91318350	K562	blood:	n/a	n/a
10	E2F6	chr10:91318167-91318394	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr10:91318200-91318350	BE2_C	brain:	n/a	n/a
12	POLR2A	chr10:91318272-91318800	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr10:91318200-91318350	HVMF	connective:	n/a	n/a
14	CTCF	chr10:91318200-91318350	K562	blood:	n/a	n/a
15	CTCF	chr10:91318220-91318370	HepG2	liver:	n/a	n/a
16	CTCF	chr10:91318112-91318311	K562	blood:	n/a	n/a
17	RCOR1	chr10:91318213-91318416	K562	blood:	n/a	n/a
18	CTCF	chr10:91318178-91318325	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr10:91318260-91318410	GM12872	blood:	n/a	n/a
20	RAD21	chr10:91318146-91318386	H1-hESC	embryonic stem cell:	n/a	n/a
21	MYC	chr10:91318261-91318932	K562	blood:	n/a	n/a
22	ZNF143	chr10:91318228-91319017	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr10:91318136-91318566	K562	blood:	n/a	n/a
24	CTCF	chr10:91318180-91318330	HCT-116	colon:	n/a	n/a
25	HEY1	chr10:91318154-91318610	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr10:91317394..91320860-chr10:91322382..91324192,3	K562	blood:
2	chr10:91291214..91293702-chr10:91316948..91318606,2	K562	blood:
3	chr10:91316904..91318893-chr10:91326946..91328940,2	MCF-7	breast:
4	chr10:91313371..91315755-chr10:91316862..91319102,2	K562	blood:

No data

Variant related genes	Relation type
SLC16A12	TF binding region

rSNPs within LD-proxies of this variant (count:14)

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	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:91313600-91324600	Weak transcription	Aorta	Aorta
2	chr10:91314400-91319800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:91314600-91324600	Weak transcription	Pancreas	Pancrea
4	chr10:91315800-91318400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr10:91317200-91321400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr10:91318200-91318400	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr10:91318200-91319400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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