Variant report

Variant	esv3348162
Chromosome Location	chr19:41443405-41524477
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	chr19:41507311-41507499	K562	blood:	n/a	n/a
2	ARID3A	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:41506351-41506450	HepG2	liver:	n/a	n/a
4	ATF1	chr19:41468671-41468771	K562	blood:	n/a	n/a
5	ATF3	chr19:41468329-41468885	A549	lung:	n/a	n/a
6	ATF3	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
7	ATF3	chr19:41506267-41506508	K562	blood:	n/a	n/a
8	ATF3	chr19:41506069-41506786	HCT-116	colon:	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	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
16	CBX3	chr19:41482345-41482685	K562	blood:	n/a	n/a
17	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
18	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
19	CEBPB	chr19:41446714-41446729	A549	lung:	n/a	n/a
20	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
21	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	n/a	chr19:41506435-41506446
22	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
23	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
24	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
25	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	n/a	chr19:41506435-41506446
27	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
28	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
29	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
30	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
31	CEBPB	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446
32	CEBPB	chr19:41506208-41506618	A549	lung:	n/a	chr19:41506435-41506446
33	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
34	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
35	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
36	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
37	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
38	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
39	CEBPB	chr19:41507152-41507489	K562	blood:	n/a	n/a
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	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
42	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
43	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
44	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
45	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
46	CEBPB	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPD	chr19:41458422-41458815	K562	blood:	n/a	n/a
48	CHD2	chr19:41465957-41466157	K562	blood:	n/a	n/a
49	CREB1	chr19:41507218-41507529	K562	blood:	n/a	n/a
50	CREB1	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41524298-41524348	A549	lung:	n/a
2	chr19:41524298-41524348	A549	lung:	n/a
3	chr19:41497222-41497272	IMR90	lung:	fetal
4	chr19:41496043-41496093	HL-60	blood:	n/a
5	chr19:41497222-41497272	AG09309	skin:	n/a
6	chr19:41510026-41510076	CMK	blood:	n/a
7	chr19:41496749-41496799	SAEC	small airway:	n/a
8	chr19:41510037-41510087	SK-N-SH	brain:	n/a
9	chr19:41510272-41510322	HUVEC	blood vessel:	n/a
10	chr19:41510272-41510322	HPAEpiC	pulmonary alveolar:	n/a
11	chr19:41510272-41510322	Jurkat	blood:	n/a
12	chr19:41524298-41524348	Jurkat	blood:	n/a
13	chr19:41510026-41510076	SAEC	small airway:	n/a
14	chr19:41510098-41510148	HRPEpiC	eye:	n/a
15	chr19:41510059-41510109	SK-N-SH_RA	brain:	n/a
16	chr19:41510026-41510076	GM19239	blood:	n/a
17	chr19:41510272-41510322	A549	lung:	n/a
18	chr19:41510243-41510293	PANC-1	pancreas:	n/a
19	chr19:41510037-41510087	ECC-1	luminal epithelium:	n/a
20	chr19:41495942-41495992	HCF	heart:	n/a
21	chr19:41524298-41524348	HCT-116	colon:	n/a
22	chr19:41510098-41510148	H1-hESC	embryonic stem cell:	embryo
23	chr19:41510059-41510109	H1-hESC	embryonic stem cell:	embryo
24	chr19:41510243-41510293	HL-60	blood:	n/a
25	chr19:41510059-41510109	HAEpiC	amniotic membrane:	n/a
26	chr19:41510037-41510087	NHDF-neo	bronchial:	n/a
27	chr19:41496043-41496093	LNCaP	prostate:	n/a
28	chr19:41510285-41510335	ProgFib	skin:	n/a
29	chr19:41510026-41510076	HPAEpiC	pulmonary alveolar:	n/a
30	chr19:41497222-41497272	HRE	kidney:	n/a
31	chr19:41510243-41510293	AG04450	lung:	fetal
32	chr19:41510059-41510109	ECC-1	luminal epithelium:	n/a
33	chr19:41510285-41510335	PANC-1	pancreas:	n/a
34	chr19:41524298-41524348	HEEpiC	esophagus:	n/a
35	chr19:41496043-41496093	GM12892	blood:	n/a
36	chr19:41510026-41510076	NB4	blood:	n/a
37	chr19:41510026-41510076	BJ	skin:	n/a
38	chr19:41496043-41496093	HIPEpiC	eye:	n/a
39	chr19:41510098-41510148	Jurkat	blood:	n/a
40	chr19:41495942-41495992	Jurkat	blood:	n/a
41	chr19:41510026-41510076	GM12891	blood:	n/a
42	chr19:41510037-41510087	U87	brain:	n/a
43	chr19:41496043-41496093	HNPCEpiC	eye:	n/a
44	chr19:41496749-41496799	HPAEpiC	pulmonary alveolar:	n/a
45	chr19:41497222-41497272	GM12891	blood:	n/a
46	chr19:41524298-41524348	SK-N-MC	brain:	n/a
47	chr19:41524298-41524348	AG04449	skin:	fetal
48	chr19:41496749-41496799	HL-60	blood:	n/a
49	chr19:41510098-41510148	Caco-2	colon:	n/a
50	chr19:41510098-41510148	AG09319	gingival:	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
2	chr19:41480412..41481100-chr19:41650028..41650578,2	MCF-7	breast:
3	chr19:41444451..41445965-chr19:41446160..41448128,2	MCF-7	breast:
4	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
5	chr19:41463243..41465087-chr19:41467190..41469905,2	K562	blood:
6	chr19:41436490..41439337-chr19:41447432..41449781,2	MCF-7	breast:
7	chr10:94639799..94640373-chr19:41475219..41475719,2	K562	blood:
8	chr19:41480596..41481177-chr19:41649752..41650983,4	K562	blood:
9	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
10	chr19:41463496..41465246-chr19:41466230..41468956,2	K562	blood:
11	chr19:41438993..41440711-chr19:41442295..41445002,2	MCF-7	breast:
12	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
13	chr19:41433604..41436108-chr19:41440713..41443622,2	MCF-7	breast:
14	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
15	chr19:41458951..41460963-chr19:41463374..41465958,2	K562	blood:
16	chr19:41455358..41456878-chr19:41467418..41469286,2	K562	blood:
17	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:

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

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

Extended variants
information (count: 3731 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3731 , 50 per page) page: 1 2 3 4 5 6 7 ... 75

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572805092	chr19:41443455-41443456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140051743	chr19:41443468-41443469	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559952772	chr19:41443532-41443533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542032635	chr19:41443537-41443538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575070567	chr19:41443543-41443544	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542470724	chr19:41443546-41443547	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs563967942	chr19:41443549-41443550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs531275052	chr19:41443550-41443551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552246671	chr19:41443556-41443557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs116520699	chr19:41443625-41443626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs528548027	chr19:41443638-41443639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs547058155	chr19:41443644-41443645	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560885923	chr19:41443689-41443690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs8182581	chr19:41443788-41443789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs535268543	chr19:41443801-41443802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147951149	chr19:41443819-41443820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568772057	chr19:41443828-41443829	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539724736	chr19:41443838-41443839	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs527968008	chr19:41443853-41443854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs56060439	chr19:41443862-41443863	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs138198655	chr19:41443868-41443869	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371327360	chr19:41443877-41443878	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs190835825	chr19:41443882-41443883	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560596473	chr19:41443894-41443895	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs141895590	chr19:41443904-41443905	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555479951	chr19:41443905-41443906	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs56352639	chr19:41443929-41443930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573826641	chr19:41443933-41443934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs56039458	chr19:41443935-41443936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147118572	chr19:41443939-41443940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564092136	chr19:41443951-41443952	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147712752	chr19:41443964-41443965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575799696	chr19:41443992-41443993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546495859	chr19:41444039-41444040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs55722903	chr19:41444042-41444043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs55669130	chr19:41444064-41444065	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56249515	chr19:41444072-41444073	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs56190530	chr19:41444078-41444079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569816857	chr19:41444089-41444090	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531712564	chr19:41444105-41444106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149191868	chr19:41444114-41444115	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs528468328	chr19:41444125-41444126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371144694	chr19:41444150-41444151	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369904096	chr19:41444188-41444189	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144682800	chr19:41444189-41444190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs386809305	chr19:41444193-41444194	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs550315253	chr19:41444211-41444212	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs568735190	chr19:41444249-41444250	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs115210543	chr19:41444370-41444371	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs551638301	chr19:41444371-41444372	Weak transcription Strong transcription	TF binding region	1 gene(s)	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:304 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41432200-41447600	Weak transcription	Liver	Liver
2	chr19:41438800-41444000	Weak transcription	Fetal Intestine Large	intestine
3	chr19:41439200-41447800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr19:41439200-41448000	Weak transcription	Stomach Mucosa	stomach
5	chr19:41442000-41445400	Strong transcription	Fetal Intestine Small	intestine
6	chr19:41442400-41451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr19:41442600-41450200	Weak transcription	Lung	lung
8	chr19:41444000-41444800	Strong transcription	Fetal Intestine Large	intestine
9	chr19:41444400-41445400	Bivalent Enhancer	A549	lung
10	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
11	chr19:41445400-41450200	Weak transcription	Fetal Intestine Small	intestine
12	chr19:41445800-41449200	Enhancers	HUVEC	blood vessel
13	chr19:41446400-41446600	Enhancers	A549	lung
14	chr19:41446600-41446800	Flanking Active TSS	A549	lung
15	chr19:41446800-41447200	Enhancers	A549	lung
16	chr19:41447200-41447600	Bivalent Enhancer	A549	lung
17	chr19:41447400-41448000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr19:41447600-41447800	Flanking Bivalent TSS/Enh	A549	lung
19	chr19:41447600-41448200	Strong transcription	Liver	Liver
20	chr19:41447800-41448200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr19:41447800-41448200	Bivalent Enhancer	A549	lung
22	chr19:41447800-41448200	Bivalent Enhancer	K562	blood
23	chr19:41448200-41449600	Weak transcription	Liver	Liver
24	chr19:41449600-41451800	Strong transcription	Liver	Liver
25	chr19:41450200-41450400	Bivalent Enhancer	Esophagus	oesophagus
26	chr19:41450200-41450600	ZNF genes & repeats	Lung	lung
27	chr19:41450200-41450800	Strong transcription	Fetal Intestine Small	intestine
28	chr19:41450800-41451800	ZNF genes & repeats	Fetal Intestine Small	intestine
29	chr19:41451400-41451800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr19:41451400-41452200	Flanking Active TSS	K562	blood
31	chr19:41451800-41452200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr19:41451800-41455200	Weak transcription	Liver	Liver
33	chr19:41451800-41456200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr19:41451800-41456200	Weak transcription	Fetal Intestine Small	intestine
35	chr19:41452200-41452400	Enhancers	K562	blood
36	chr19:41453800-41458200	Weak transcription	Right Atrium	heart
37	chr19:41456200-41456400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr19:41459600-41460800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
39	chr19:41460000-41460800	ZNF genes & repeats	Brain Hippocampus Middle	brain
40	chr19:41460000-41461600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr19:41460200-41460400	ZNF genes & repeats	A549	lung
42	chr19:41460200-41461400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
43	chr19:41464600-41464800	Enhancers	Fetal Intestine Small	intestine
44	chr19:41464800-41466400	Weak transcription	Fetal Intestine Small	intestine
45	chr19:41465200-41466600	Enhancers	Esophagus	oesophagus
46	chr19:41465400-41465800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
47	chr19:41465400-41465800	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr19:41465400-41466000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr19:41465800-41466000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr19:41465800-41466000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain

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