Variant report

Variant	nsv517597
Chromosome Location	chr19:41433613-41508442
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:827)
CpG islands
(count:244)
Chromatin interactive
region (count:25)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:827 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:41506351-41506450	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:41507311-41507499	K562	blood:	n/a	n/a
4	ATF1	chr19:41434897-41435097	K562	blood:	n/a	n/a
5	ATF1	chr19:41468671-41468771	K562	blood:	n/a	n/a
6	ATF3	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
7	ATF3	chr19:41506069-41506786	HCT-116	colon:	n/a	n/a
8	ATF3	chr19:41468329-41468885	A549	lung:	n/a	n/a
9	ATF3	chr19:41506267-41506508	K562	blood:	n/a	n/a
10	BACH1	chr19:41437946-41438301	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr19:41437956-41438260	K562	blood:	n/a	n/a
12	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
14	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
15	BHLHE40	chr19:41507420-41507421	K562	blood:	n/a	n/a
16	BRCA1	chr19:41465957-41466156	GM12878	blood:	n/a	n/a
17	CBX3	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
18	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
19	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
20	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
21	CCNT2	chr19:41434884-41435092	K562	blood:	n/a	n/a
22	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
23	CEBPB	chr19:41434755-41435152	K562	blood:	n/a	n/a
24	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
25	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:41438614-41439244	K562	blood:	n/a	n/a
27	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
28	CEBPB	chr19:41438908-41439279	K562	blood:	n/a	n/a
29	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
30	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
31	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
32	CEBPB	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446
33	CEBPB	chr19:41438982-41439268	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
35	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
36	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
37	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
38	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
39	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
40	CEBPB	chr19:41434742-41435118	K562	blood:	n/a	n/a
41	CEBPB	chr19:41488440-41489019	H1-hESC	embryonic stem cell:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
42	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
43	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
44	CEBPB	chr19:41506208-41506618	A549	lung:	n/a	chr19:41506435-41506446
45	CEBPB	chr19:41434826-41435086	K562	blood:	n/a	n/a
46	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
47	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
48	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	n/a	chr19:41506435-41506446
49	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
50	CEBPB	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41495942-41495992	ProgFib	skin:	n/a
2	chr19:41496043-41496093	MCF-7	breast:	n/a
3	chr19:41496043-41496093	RPTEC	kidney:	n/a
4	chr19:41495942-41495992	H1-hESC	embryonic stem cell:	embryo
5	chr19:41495942-41495992	RPTEC	kidney:	n/a
6	chr19:41497222-41497272	HCM	heart:	n/a
7	chr19:41495942-41495992	GM06990	blood:	n/a
8	chr19:41495942-41495992	NHBE	bronchial:	n/a
9	chr19:41497222-41497272	GM06990	blood:	n/a
10	chr19:41495942-41495992	Caco-2	colon:	n/a
11	chr19:41496749-41496799	PrEC	prostate:	n/a
12	chr19:41496043-41496093	AG04450	lung:	fetal
13	chr19:41497222-41497272	GM12892	blood:	n/a
14	chr19:41495942-41495992	BE2_C	brain:	n/a
15	chr19:41496749-41496799	IMR90	lung:	fetal
16	chr19:41497222-41497272	HMEC	breast:	n/a
17	chr19:41497222-41497272	PrEC	prostate:	n/a
18	chr19:41496043-41496093	T-47D	breast:	n/a
19	chr19:41496749-41496799	Hepatocyte	liver:	n/a
20	chr19:41495942-41495992	CMK	blood:	n/a
21	chr19:41496043-41496093	SK-N-SH	brain:	n/a
22	chr19:41496043-41496093	BE2_C	brain:	n/a
23	chr19:41495942-41495992	AG04449	skin:	fetal
24	chr19:41496749-41496799	LNCaP	prostate:	n/a
25	chr19:41496749-41496799	HepG2	liver:	n/a
26	chr19:41495942-41495992	HCF	heart:	n/a
27	chr19:41497222-41497272	GM12878	blood:	n/a
28	chr19:41495942-41495992	PANC-1	pancreas:	n/a
29	chr19:41496749-41496799	PANC-1	pancreas:	n/a
30	chr19:41497222-41497272	HRE	kidney:	n/a
31	chr19:41496749-41496799	HCF	heart:	n/a
32	chr19:41496043-41496093	HCT-116	colon:	n/a
33	chr19:41496043-41496093	NB4	blood:	n/a
34	chr19:41496043-41496093	HEEpiC	esophagus:	n/a
35	chr19:41496749-41496799	GM12892	blood:	n/a
36	chr19:41496043-41496093	AG04449	skin:	fetal
37	chr19:41497222-41497272	HIPEpiC	eye:	n/a
38	chr19:41497222-41497272	IMR90	lung:	fetal
39	chr19:41497222-41497272	HL-60	blood:	n/a
40	chr19:41496043-41496093	H1-hESC	embryonic stem cell:	embryo
41	chr19:41496043-41496093	GM12892	blood:	n/a
42	chr19:41496043-41496093	SKMC	muscle:	n/a
43	chr19:41497222-41497272	NB4	blood:	n/a
44	chr19:41496749-41496799	AG10803	skin:	n/a
45	chr19:41496749-41496799	HRPEpiC	eye:	n/a
46	chr19:41495942-41495992	NHDF-neo	bronchial:	n/a
47	chr19:41495942-41495992	SAEC	small airway:	n/a
48	chr19:41496043-41496093	ECC-1	luminal epithelium:	n/a
49	chr19:41496749-41496799	NHDF-neo	bronchial:	n/a
50	chr19:41496043-41496093	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr19:41429883..41432599-chr19:41435321..41438137,2	MCF-7	breast:
2	chr19:41438993..41440711-chr19:41442295..41445002,2	MCF-7	breast:
3	chr19:41435849..41437489-chr19:41440022..41442246,2	MCF-7	breast:
4	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
5	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
6	chr19:41438993..41440711-chr19:41442295..41445002,2	MCF-7	breast:
7	chr19:41400931..41403268-chr19:41432541..41435329,2	K562	blood:
8	chr10:94639799..94640373-chr19:41475219..41475719,2	K562	blood:
9	chr19:41433604..41436108-chr19:41440713..41443622,2	MCF-7	breast:
10	chr19:41480596..41481177-chr19:41649752..41650983,4	K562	blood:
11	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
12	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
13	chr19:41435849..41437489-chr19:41440022..41442246,2	MCF-7	breast:
14	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
15	chr19:41433604..41436108-chr19:41440713..41443622,2	MCF-7	breast:
16	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
17	chr19:41303781..41306051-chr19:41433024..41435492,2	MCF-7	breast:
18	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
19	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
20	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
21	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
22	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
23	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
24	chr19:41480412..41481100-chr19:41650028..41650578,2	MCF-7	breast:
25	chr19:41444451..41445965-chr19:41446160..41448128,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2B6-1	chr19:41492504-41492600	l_1687_chr19:41492503-41503928_testes
2	lnc-CYP2B6-2	chr19:41452252-41452450	ENSG00000269353.1
3	lnc-CYP2B6-1	chr19:41503762-41503928	l_1687_chr19:41492503-41503928_testes
4	lnc-CYP2B6-1	chr19:41493956-41494534	l_1687_chr19:41492503-41503928_testes
5	lnc-CYP2B6-2	chr19:41453006-41453355	ENSG00000269353.1
6	lnc-CYP2B6-1	chr19:41493177-41493736	l_1687_chr19:41492503-41503928_testes
7	lnc-CYP2B6-1	chr19:41495264-41495408	l_1687_chr19:41492503-41503928_testes

No data

Variant related genes	Relation type
CYP2B6	TF binding region
ENSG00000269353	TF binding region
CYP2B7P	TF binding region
CYP2B6	CpG island
ENSG00000269353	CpG island
CYP2B7P	CpG island
ENSG00000256612	chromatin interactions
ENSG00000269858	chromatin interactions

Extended variants
information (count: 2928 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2928 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4609955	chr19:41433613-41433614	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531763458	chr19:41433621-41433622	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs183543034	chr19:41433640-41433641	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs532824885	chr19:41433658-41433659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs527815131	chr19:41433728-41433729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372401244	chr19:41433773-41433774	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs567472416	chr19:41433783-41433784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs537700235	chr19:41433789-41433790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs4099161	chr19:41433818-41433819	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs571607923	chr19:41433844-41433845	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs374353764	chr19:41433847-41433848	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs190473122	chr19:41433850-41433851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182246446	chr19:41433868-41433869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs186790089	chr19:41433917-41433918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs191634701	chr19:41433922-41433923	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs3843043	chr19:41433931-41433932	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs544537593	chr19:41433942-41433943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181594133	chr19:41433978-41433979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs577965942	chr19:41433979-41433980	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs185862472	chr19:41433981-41433982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs139828937	chr19:41433982-41433983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs3844444	chr19:41434047-41434048	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs56302534	chr19:41434054-41434055	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs3844445	chr19:41434106-41434107	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs145387799	chr19:41434148-41434149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs539240839	chr19:41434212-41434213	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs571542623	chr19:41434280-41434281	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs532482263	chr19:41434281-41434282	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs80178153	chr19:41434294-41434295	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs561462966	chr19:41434352-41434353	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs535921784	chr19:41434395-41434396	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs190184890	chr19:41434410-41434411	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs569692065	chr19:41434461-41434462	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12150973	chr19:41434524-41434525	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs182398563	chr19:41434577-41434578	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185982692	chr19:41434579-41434580	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs560866209	chr19:41434617-41434618	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs549204655	chr19:41434618-41434619	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs545313106	chr19:41434637-41434638	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs553724663	chr19:41434644-41434645	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs192023060	chr19:41434707-41434708	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs376686085	chr19:41434732-41434733	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561428585	chr19:41434741-41434742	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs183902227	chr19:41434751-41434752	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs562355325	chr19:41434783-41434784	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543625296	chr19:41434797-41434798	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565091202	chr19:41434807-41434808	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs532420040	chr19:41434884-41434885	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs547717217	chr19:41434944-41434945	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs151009564	chr19:41434945-41434946	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41429000-41434200	Weak transcription	K562	blood
2	chr19:41429200-41434600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr19:41432200-41447600	Weak transcription	Liver	Liver
4	chr19:41432600-41434600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr19:41433000-41435200	Enhancers	Fetal Intestine Small	intestine
6	chr19:41433000-41437800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr19:41433200-41434400	Enhancers	Fetal Intestine Large	intestine
8	chr19:41434200-41434400	Bivalent Enhancer	A549	lung
9	chr19:41434200-41436000	Enhancers	K562	blood
10	chr19:41434400-41434800	Flanking Active TSS	Fetal Intestine Large	intestine
11	chr19:41434600-41435000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr19:41434600-41435000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr19:41434800-41436200	Enhancers	Fetal Intestine Large	intestine
14	chr19:41435000-41435600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr19:41435200-41435400	Flanking Active TSS	Fetal Intestine Small	intestine
16	chr19:41435400-41436200	Enhancers	Fetal Intestine Small	intestine
17	chr19:41436000-41437600	Weak transcription	K562	blood
18	chr19:41436200-41436600	Weak transcription	Fetal Intestine Small	intestine
19	chr19:41436200-41437800	Weak transcription	Fetal Intestine Large	intestine
20	chr19:41436600-41437000	Strong transcription	Fetal Intestine Small	intestine
21	chr19:41437000-41437800	Weak transcription	Fetal Intestine Small	intestine
22	chr19:41437600-41438000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr19:41437600-41439800	Enhancers	K562	blood
24	chr19:41437800-41438000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr19:41437800-41438000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr19:41437800-41438200	Genic enhancers	Fetal Intestine Small	intestine
27	chr19:41437800-41438600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr19:41437800-41438800	Enhancers	Fetal Intestine Large	intestine
29	chr19:41438000-41439400	Bivalent Enhancer	A549	lung
30	chr19:41438200-41438400	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr19:41438200-41438600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr19:41438200-41442000	Weak transcription	Fetal Intestine Small	intestine
33	chr19:41438400-41438800	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr19:41438400-41439000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr19:41438400-41439000	Enhancers	Placenta	Placenta
36	chr19:41438600-41439000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr19:41438600-41439600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr19:41438800-41444000	Weak transcription	Fetal Intestine Large	intestine
39	chr19:41439000-41439200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr19:41439000-41439200	Enhancers	Stomach Mucosa	stomach
41	chr19:41439000-41439800	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr19:41439200-41447800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr19:41439200-41448000	Weak transcription	Stomach Mucosa	stomach
44	chr19:41439600-41439800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr19:41439800-41441600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
46	chr19:41440600-41442400	Weak transcription	Lung	lung
47	chr19:41441600-41441800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr19:41442000-41442400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr19:41442000-41445400	Strong transcription	Fetal Intestine Small	intestine
50	chr19:41442400-41442600	Strong transcription	Lung	lung

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