Variant report

Variant	esv3528353
Chromosome Location	chr19:41451614-41517617
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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	chr19:41468671-41468771	K562	blood:	n/a	n/a
5	ATF3	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
6	ATF3	chr19:41506069-41506786	HCT-116	colon:	n/a	n/a
7	ATF3	chr19:41468329-41468885	A549	lung:	n/a	n/a
8	ATF3	chr19:41506267-41506508	K562	blood:	n/a	n/a
9	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
11	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
12	BHLHE40	chr19:41507420-41507421	K562	blood:	n/a	n/a
13	BRCA1	chr19:41465957-41466156	GM12878	blood:	n/a	n/a
14	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
15	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
16	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
17	CBX3	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
18	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
19	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
20	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
21	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
22	CEBPB	chr19:41507152-41507489	K562	blood:	n/a	n/a
23	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
24	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
25	CEBPB	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a
26	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
27	CEBPB	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446
28	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	n/a	chr19:41506435-41506446
30	CEBPB	chr19:41506208-41506618	A549	lung:	n/a	chr19:41506435-41506446
31	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
32	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
33	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
34	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
35	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
36	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
38	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
39	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
40	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
41	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	n/a	chr19:41506435-41506446
42	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
43	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
44	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
45	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
46	CEBPD	chr19:41458422-41458815	K562	blood:	n/a	n/a
47	CHD2	chr19:41465957-41466157	K562	blood:	n/a	n/a
48	CREB1	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr19:41468563-41468752	A549	lung:	n/a	n/a
50	CREB1	chr19:41507218-41507529	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41510243-41510293	Caco-2	colon:	n/a
2	chr19:41496043-41496093	Caco-2	colon:	n/a
3	chr19:41510098-41510148	PANC-1	pancreas:	n/a
4	chr19:41510272-41510322	NH-A	brain:	n/a
5	chr19:41510285-41510335	HepG2	liver:	n/a
6	chr19:41510059-41510109	HMEC	breast:	n/a
7	chr19:41496043-41496093	BE2_C	brain:	n/a
8	chr19:41510243-41510293	AoSMC	blood vessel:	n/a
9	chr19:41496749-41496799	H1-hESC	embryonic stem cell:	embryo
10	chr19:41510243-41510293	AG09319	gingival:	n/a
11	chr19:41510059-41510109	U87	brain:	n/a
12	chr19:41495942-41495992	A549	lung:	n/a
13	chr19:41510098-41510148	BJ	skin:	n/a
14	chr19:41495942-41495992	U87	brain:	n/a
15	chr19:41496043-41496093	NB4	blood:	n/a
16	chr19:41497222-41497272	HNPCEpiC	eye:	n/a
17	chr19:41510059-41510109	SK-N-SH_RA	brain:	n/a
18	chr19:41510026-41510076	NT2-D1	testis:	n/a
19	chr19:41497222-41497272	IMR90	lung:	fetal
20	chr19:41496749-41496799	PANC-1	pancreas:	n/a
21	chr19:41496043-41496093	SK-N-SH	brain:	n/a
22	chr19:41510243-41510293	HEEpiC	esophagus:	n/a
23	chr19:41496043-41496093	MCF10A-Er-Src	breast:	n/a
24	chr19:41510037-41510087	Hepatocyte	liver:	n/a
25	chr19:41496749-41496799	MCF10A-Er-Src	breast:	n/a
26	chr19:41495942-41495992	CMK	blood:	n/a
27	chr19:41496043-41496093	AG04449	skin:	fetal
28	chr19:41510243-41510293	ECC-1	luminal epithelium:	n/a
29	chr19:41510272-41510322	IMR90	lung:	fetal
30	chr19:41510285-41510335	AG10803	skin:	n/a
31	chr19:41497222-41497272	HEK293	kidney:	embryo
32	chr19:41510037-41510087	HAEpiC	amniotic membrane:	n/a
33	chr19:41510243-41510293	AG04450	lung:	fetal
34	chr19:41495942-41495992	BJ	skin:	n/a
35	chr19:41510098-41510148	SKMC	muscle:	n/a
36	chr19:41497222-41497272	AoSMC	blood vessel:	n/a
37	chr19:41510037-41510087	MCF-7	breast:	n/a
38	chr19:41510272-41510322	HL-60	blood:	n/a
39	chr19:41496043-41496093	HAEpiC	amniotic membrane:	n/a
40	chr19:41495942-41495992	PFSK-1	brain:	n/a
41	chr19:41496043-41496093	GM19239	blood:	n/a
42	chr19:41496749-41496799	HRPEpiC	eye:	n/a
43	chr19:41510026-41510076	Hepatocyte	liver:	n/a
44	chr19:41510285-41510335	GM06990	blood:	n/a
45	chr19:41497222-41497272	A549	lung:	n/a
46	chr19:41495942-41495992	ProgFib	skin:	n/a
47	chr19:41510037-41510087	Jurkat	blood:	n/a
48	chr19:41510098-41510148	CMK	blood:	n/a
49	chr19:41510272-41510322	U87	brain:	n/a
50	chr19:41510098-41510148	Hela-S3	cervix:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
2	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
3	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
4	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
5	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
6	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
7	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
8	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
9	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
10	chr10:94639799..94640373-chr19:41475219..41475719,2	K562	blood:
11	chr19:41480412..41481100-chr19:41650028..41650578,2	MCF-7	breast:
12	chr19:41480596..41481177-chr19:41649752..41650983,4	K562	blood:
13	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:

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

Variant related genes	Relation type
CYP2B6	TF binding region
ENSG00000269353	TF binding region
CYP2B6	CpG island
ENSG00000269353	CpG island

Extended variants
information (count: 2738 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2738 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141315369	chr19:41451666-41451667	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs532858149	chr19:41451728-41451729	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375606155	chr19:41451732-41451733	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559309179	chr19:41451733-41451734	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs143712583	chr19:41451750-41451751	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs530077475	chr19:41451751-41451752	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs188877782	chr19:41451759-41451760	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs570100443	chr19:41451770-41451771	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs530720328	chr19:41451776-41451777	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs551961508	chr19:41451779-41451780	ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs4560022	chr19:41451810-41451811	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs36003149	chr19:41451811-41451812	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs534623357	chr19:41451831-41451832	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs4560023	chr19:41451893-41451894	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs568031783	chr19:41451903-41451904	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs535131811	chr19:41451908-41451909	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs181589518	chr19:41451923-41451924	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs111955502	chr19:41451953-41451954	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs543987718	chr19:41451987-41451988	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs12461995	chr19:41451996-41451997	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs111724462	chr19:41451997-41451998	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs541733356	chr19:41452016-41452017	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs189779372	chr19:41452020-41452021	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs180981496	chr19:41452025-41452026	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs530105116	chr19:41452053-41452054	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs541901512	chr19:41452054-41452055	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs563760969	chr19:41452057-41452058	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530909131	chr19:41452070-41452071	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs551922846	chr19:41452095-41452096	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570327591	chr19:41452113-41452114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs185976825	chr19:41452119-41452120	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs150365167	chr19:41452185-41452186	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs10411962	chr19:41452212-41452213	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs112908268	chr19:41452248-41452249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs71173697	chr19:41452252-41452253	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
36	rs202061923	chr19:41452268-41452269	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs138108153	chr19:41452282-41452283	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs116015689	chr19:41452283-41452284	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs7251436	chr19:41452293-41452294	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs190961667	chr19:41452417-41452418	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs557923903	chr19:41452423-41452424	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs577494024	chr19:41452440-41452441	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs535283734	chr19:41452441-41452442	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
44	rs553623280	chr19:41452457-41452458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181753516	chr19:41452492-41452493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575038923	chr19:41452493-41452494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185881160	chr19:41452494-41452495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146008021	chr19:41452503-41452504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190694655	chr19:41452504-41452505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112486847	chr19:41452573-41452574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	22522925	CNVD

Chromatin state (count:268 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
2	chr19:41449600-41451800	Strong transcription	Liver	Liver
3	chr19:41450800-41451800	ZNF genes & repeats	Fetal Intestine Small	intestine
4	chr19:41451400-41451800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:41451400-41452200	Flanking Active TSS	K562	blood
6	chr19:41451800-41452200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr19:41451800-41455200	Weak transcription	Liver	Liver
8	chr19:41451800-41456200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr19:41451800-41456200	Weak transcription	Fetal Intestine Small	intestine
10	chr19:41452200-41452400	Enhancers	K562	blood
11	chr19:41453800-41458200	Weak transcription	Right Atrium	heart
12	chr19:41456200-41456400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:41459600-41460800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
14	chr19:41460000-41460800	ZNF genes & repeats	Brain Hippocampus Middle	brain
15	chr19:41460000-41461600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr19:41460200-41460400	ZNF genes & repeats	A549	lung
17	chr19:41460200-41461400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
18	chr19:41464600-41464800	Enhancers	Fetal Intestine Small	intestine
19	chr19:41464800-41466400	Weak transcription	Fetal Intestine Small	intestine
20	chr19:41465200-41466600	Enhancers	Esophagus	oesophagus
21	chr19:41465400-41465800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:41465400-41465800	Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr19:41465400-41466000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr19:41465800-41466000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr19:41465800-41466000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
26	chr19:41465800-41466200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
28	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
29	chr19:41466000-41466200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr19:41466000-41466200	Bivalent Enhancer	Adipose Nuclei	Adipose
31	chr19:41466000-41466200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
32	chr19:41466200-41466600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
33	chr19:41466200-41466600	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr19:41466200-41466800	Enhancers	Adipose Nuclei	Adipose
35	chr19:41466200-41469800	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr19:41466200-41469800	Enhancers	Ovary	ovary
37	chr19:41466400-41466600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr19:41466400-41466800	Enhancers	Fetal Intestine Large	intestine
39	chr19:41466400-41466800	Enhancers	Fetal Intestine Small	intestine
40	chr19:41466600-41468000	Weak transcription	Esophagus	oesophagus
41	chr19:41466800-41467000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
42	chr19:41466800-41467000	Bivalent Enhancer	A549	lung
43	chr19:41466800-41467200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr19:41466800-41468000	Weak transcription	Adipose Nuclei	Adipose
45	chr19:41467800-41468000	Bivalent Enhancer	A549	lung
46	chr19:41467800-41469600	Enhancers	HepG2	liver
47	chr19:41467800-41469800	Enhancers	Hela-S3	cervix
48	chr19:41468000-41468200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
49	chr19:41468000-41468200	Enhancers	Esophagus	oesophagus
50	chr19:41468000-41468200	Enhancers	Placenta	Placenta

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