Variant report

Variant	rs115625389
Chromosome Location	chr7:64328794-64328795
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:61)
Chromatin interactive
region (count:0)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:64328537-64328820	HepG2	liver:	n/a	chr7:64328659-64328670 chr7:64328659-64328668

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No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:64328759-64328809	HCPEpiC	choroid plexus:	n/a
2	chr7:64328759-64328809	BE2_C	brain:	n/a
3	chr7:64328759-64328809	T-47D	breast:	n/a
4	chr7:64328759-64328809	ovcar-3	ovarian:	n/a
5	chr7:64328759-64328809	IMR90	lung:	fetal
6	chr7:64328759-64328809	AG04450	lung:	fetal
7	chr7:64328759-64328809	SKMC	muscle:	n/a
8	chr7:64328759-64328809	HUVEC	blood vessel:	n/a
9	chr7:64328759-64328809	HNPCEpiC	eye:	n/a
10	chr7:64328759-64328809	Caco-2	colon:	n/a
11	chr7:64328759-64328809	Hela-S3	cervix:	n/a
12	chr7:64328759-64328809	NB4	blood:	n/a
13	chr7:64328759-64328809	SK-N-SH	brain:	n/a
14	chr7:64328759-64328809	GM06990	blood:	n/a
15	chr7:64328759-64328809	HepG2	liver:	n/a
16	chr7:64328759-64328809	HMEC	breast:	n/a
17	chr7:64328759-64328809	SK-N-MC	brain:	n/a
18	chr7:64328759-64328809	PFSK-1	brain:	n/a
19	chr7:64328759-64328809	NT2-D1	testis:	n/a
20	chr7:64328759-64328809	GM12892	blood:	n/a
21	chr7:64328759-64328809	HL-60	blood:	n/a
22	chr7:64328759-64328809	LNCaP	prostate:	n/a
23	chr7:64328759-64328809	HRE	kidney:	n/a
24	chr7:64328759-64328809	NH-A	brain:	n/a
25	chr7:64328759-64328809	HCT-116	colon:	n/a
26	chr7:64328759-64328809	ECC-1	luminal epithelium:	n/a
27	chr7:64328759-64328809	H1-hESC	embryonic stem cell:	embryo
28	chr7:64328759-64328809	AG04449	skin:	fetal
29	chr7:64328759-64328809	AG09309	skin:	n/a
30	chr7:64328759-64328809	HAEpiC	amniotic membrane:	n/a
31	chr7:64328759-64328809	U87	brain:	n/a
32	chr7:64328759-64328809	HRPEpiC	eye:	n/a
33	chr7:64328759-64328809	ProgFib	skin:	n/a
34	chr7:64328759-64328809	Hepatocyte	liver:	n/a
35	chr7:64328759-64328809	Jurkat	blood:	n/a
36	chr7:64328759-64328809	GM12891	blood:	n/a
37	chr7:64328759-64328809	BJ	skin:	n/a
38	chr7:64328759-64328809	A549	lung:	n/a
39	chr7:64328759-64328809	CMK	blood:	n/a
40	chr7:64328759-64328809	HCM	heart:	n/a
41	chr7:64328759-64328809	HCF	heart:	n/a
42	chr7:64328759-64328809	HEK293	kidney:	embryo
43	chr7:64328759-64328809	HEEpiC	esophagus:	n/a
44	chr7:64328759-64328809	PrEC	prostate:	n/a
45	chr7:64328759-64328809	AoSMC	blood vessel:	n/a
46	chr7:64328759-64328809	HRCEpiC	kidney:	n/a
47	chr7:64328759-64328809	GM19239	blood:	n/a
48	chr7:64328759-64328809	GM12878	blood:	n/a
49	chr7:64328759-64328809	NHBE	bronchial:	n/a
50	chr7:64328759-64328809	AG09319	gingival:	n/a

No data

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF117-3	chr7:64327248-64328970	NONHSAT121045
2	lnc-ZNF117-3	chr7:64327248-64328970	NONHSAT121046

No data

Variant related genes	Relation type
ZNF273	TF binding region
ZNF273	CpG island

Extended variants
information (count: 20 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:20 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422405	chr7:63709739-64632341	Enhancers Bivalent Enhancer Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	59 gene(s)	inside rSNPs	diseases
2	nsv427787	chr7:63741770-64419520	Weak transcription Strong transcription Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	esv2755057	chr7:63819849-64345822	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
4	nsv464518	chr7:63881238-64506904	Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
5	nsv607312	chr7:63881238-64506904	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
6	nsv888274	chr7:63990100-64331123	Strong transcription ZNF genes & repeats Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	25 gene(s)	inside rSNPs	diseases
7	nsv888275	chr7:63990100-64468590	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv888276	chr7:63990100-64511564	Strong transcription ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
9	nsv888279	chr7:64094285-64331123	Strong transcription ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
10	nsv1022042	chr7:64226499-64566945	Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
11	nsv1026390	chr7:64240323-64414364	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	nsv1033291	chr7:64273434-64406276	Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
13	nsv508457	chr7:64286522-64391112	Strong transcription Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
14	esv1797468	chr7:64296309-64356050	Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
15	nsv888282	chr7:64299645-64511564	Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
16	nsv1018967	chr7:64318129-64380869	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
17	esv3506582	chr7:64323055-64563984	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
18	esv3506583	chr7:64323055-64563984	Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
19	esv21367	chr7:64328624-64345129	Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
20	esv1818246	chr7:64328632-64344038	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:64322800-64331600	Weak transcription	Right Atrium	heart

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