Variant report

Variant	rs567460882
Chromosome Location	chr19:45074280-45074281
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:195)
CpG islands
(count:0)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:195 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr19:45074220-45074370	AoAF	blood vessel:	n/a	n/a
2	RAD21	chr19:45074162-45074564	HepG2	liver:	n/a	n/a
3	CTCF	chr19:45074209-45074355	GM19239	blood:	n/a	n/a
4	CTCF	chr19:45074200-45074350	GM12878	blood:	n/a	n/a
5	CTCF	chr19:45074204-45074395	LNCaP	prostate:	n/a	n/a
6	ELF1	chr19:45073932-45074425	A549	lung:	n/a	n/a
7	RAD21	chr19:45074027-45074591	HCT-116	colon:	n/a	n/a
8	TEAD4	chr19:45074017-45074493	K562	blood:	n/a	n/a
9	RAD21	chr19:45074125-45074794	HepG2	liver:	n/a	n/a
10	CTCF	chr19:45074240-45074390	HPAF	blood vessel:	n/a	n/a
11	CTCF	chr19:45074241-45074333	MCF-7	breast:	n/a	n/a
12	RAD21	chr19:45073998-45074635	A549	lung:	n/a	n/a
13	CTCF	chr19:45074200-45074350	NHDF-neo	bronchial:	n/a	n/a
14	CTCF	chr19:45074157-45074489	K562	blood:	n/a	n/a
15	RAD21	chr19:45074035-45074576	MCF-7	breast:	n/a	n/a
16	CTCF	chr19:45074280-45074430	GM12875	blood:	n/a	n/a
17	ZNF143	chr19:45074237-45074420	GM12878	blood:	n/a	n/a
18	CTCF	chr19:45074060-45074582	HCT-116	colon:	n/a	n/a
19	RAD21	chr19:45074054-45074543	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr19:45074111-45074505	K562	blood:	n/a	n/a
21	RAD21	chr19:45074139-45074509	A549	lung:	n/a	n/a
22	CTCF	chr19:45074140-45074290	HFF-Myc	foreskin:	n/a	n/a
23	SMC3	chr19:45074165-45074478	GM12878	blood:	n/a	n/a
24	CTCF	chr19:45074220-45074370	NHLF	lung:	n/a	n/a
25	CTCF	chr19:45074240-45074390	HRPEpiC	eye:	n/a	n/a
26	CTCF	chr19:45074260-45074410	SAEC	small airway:	n/a	n/a
27	SMC3	chr19:45074153-45074465	HepG2	liver:	n/a	n/a
28	CTCF	chr19:45073959-45074610	SK-N-SH	brain:	n/a	n/a
29	CTCF	chr19:45074240-45074390	GM12866	blood:	n/a	n/a
30	CTCF	chr19:45074164-45074378	Fibrobl	skin:	n/a	n/a
31	E2F4	chr19:45074256-45074360	MCF10A-Er-Src	breast:	n/a	n/a
32	CTCF	chr19:45074240-45074390	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr19:45074106-45074493	GM12878	blood:	n/a	n/a
34	CTCF	chr19:45074240-45074390	GM12873	blood:	n/a	n/a
35	CTCF	chr19:45074149-45074386	SK-N-SH_RA	brain:	n/a	n/a
36	RAD21	chr19:45074041-45074598	MCF-7	breast:	n/a	n/a
37	CTCF	chr19:45074240-45074390	RPTEC	kidney:	n/a	n/a
38	CTCF	chr19:45074232-45074384	GM13976	blood:	n/a	n/a
39	CTCF	chr19:45074127-45074488	K562	blood:	n/a	n/a
40	CTCF	chr19:45074260-45074410	WI-38	lung:	n/a	n/a
41	CTCF	chr19:45074143-45074407	ProgFib	skin:	n/a	n/a
42	CTCF	chr19:45074240-45074390	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr19:45074188-45074384	GM19238	blood:	n/a	n/a
44	CTCF	chr19:45074240-45074390	GM12871	blood:	n/a	n/a
45	CTCF	chr19:45074240-45074390	HA-sp	spinal cord:	n/a	n/a
46	CTCF	chr19:45074160-45074310	HVMF	connective:	n/a	n/a
47	RAD21	chr19:45074008-45074629	ECC-1	luminal epithelium:	n/a	n/a
48	CTCF	chr19:45074157-45074443	Gliobla	brain:	n/a	n/a
49	CTCF	chr19:45074260-45074410	SK-N-SH_RA	brain:	n/a	n/a
50	RAD21	chr19:45073977-45074629	HCT-116	colon:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr19:45016284..45016826-chr19:45073849..45074372,2	MCF-7	breast:
2	chr19:45073833..45074821-chr19:45348052..45348614,3	K562	blood:
3	chr19:45074225..45075084-chr19:45160196..45161185,6	K562	blood:
4	chr19:45074025..45075864-chr19:45246101..45248322,2	MCF-7	breast:
5	chr19:45074128..45076823-chr19:45084175..45086201,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000224366	TF binding region

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv1062812	chr19:45042262-45214796	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv960931	chr19:45073821-45102725	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 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	chr19:45070000-45074400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr19:45070400-45080400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr19:45070600-45075200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr19:45073800-45076400	Enhancers	K562	blood
5	chr19:45074200-45074400	Active TSS	Liver	Liver
6	chr19:45074200-45075600	Enhancers	A549	lung
7	chr19:45074200-45076000	Flanking Active TSS	HepG2	liver

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