Variant report

Variant	esv3584954
Chromosome Location	chr19:41445949-41517079
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	chr19:41468329-41468885	A549	lung:	n/a	n/a
7	ATF3	chr19:41506069-41506786	HCT-116	colon:	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	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
19	CEBPB	chr19:41506208-41506618	A549	lung:	n/a	chr19:41506435-41506446
20	CEBPB	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
22	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
23	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
24	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
25	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
26	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
27	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
28	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
29	CEBPB	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446
30	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
31	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	n/a	chr19:41506435-41506446
32	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
33	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
34	CEBPB	chr19:41446714-41446729	A549	lung:	n/a	n/a
35	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
36	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
37	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
38	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
39	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
40	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
41	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
43	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
44	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
45	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	n/a	chr19:41506435-41506446
46	CEBPB	chr19:41507152-41507489	K562	blood:	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	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	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	chr19:41495942-41495992	AG04449	skin:	fetal
2	chr19:41497222-41497272	HL-60	blood:	n/a
3	chr19:41495942-41495992	AG04449	skin:	fetal
4	chr19:41497222-41497272	HL-60	blood:	n/a
5	chr19:41496749-41496799	GM06990	blood:	n/a
6	chr19:41496043-41496093	HepG2	liver:	n/a
7	chr19:41496749-41496799	SK-N-SH_RA	brain:	n/a
8	chr19:41496043-41496093	HEEpiC	esophagus:	n/a
9	chr19:41510243-41510293	H1-hESC	embryonic stem cell:	embryo
10	chr19:41510243-41510293	SAEC	small airway:	n/a
11	chr19:41495942-41495992	NHBE	bronchial:	n/a
12	chr19:41510285-41510335	HEEpiC	esophagus:	n/a
13	chr19:41495942-41495992	NH-A	brain:	n/a
14	chr19:41510098-41510148	SK-N-SH	brain:	n/a
15	chr19:41510098-41510148	CMK	blood:	n/a
16	chr19:41510243-41510293	HEEpiC	esophagus:	n/a
17	chr19:41510272-41510322	GM19239	blood:	n/a
18	chr19:41496749-41496799	AG09319	gingival:	n/a
19	chr19:41510059-41510109	HRE	kidney:	n/a
20	chr19:41510285-41510335	Jurkat	blood:	n/a
21	chr19:41510272-41510322	NHDF-neo	bronchial:	n/a
22	chr19:41510037-41510087	RPTEC	kidney:	n/a
23	chr19:41510026-41510076	HEEpiC	esophagus:	n/a
24	chr19:41497222-41497272	ProgFib	skin:	n/a
25	chr19:41510037-41510087	GM12878	blood:	n/a
26	chr19:41510285-41510335	HIPEpiC	eye:	n/a
27	chr19:41510059-41510109	HRCEpiC	kidney:	n/a
28	chr19:41496749-41496799	BE2_C	brain:	n/a
29	chr19:41497222-41497272	NB4	blood:	n/a
30	chr19:41510243-41510293	HEK293	kidney:	embryo
31	chr19:41496043-41496093	MCF10A-Er-Src	breast:	n/a
32	chr19:41496043-41496093	PANC-1	pancreas:	n/a
33	chr19:41496749-41496799	NHDF-neo	bronchial:	n/a
34	chr19:41510243-41510293	SKMC	muscle:	n/a
35	chr19:41496749-41496799	HRCEpiC	kidney:	n/a
36	chr19:41510285-41510335	AG04450	lung:	fetal
37	chr19:41510285-41510335	HMEC	breast:	n/a
38	chr19:41510098-41510148	HPAEpiC	pulmonary alveolar:	n/a
39	chr19:41510285-41510335	BJ	skin:	n/a
40	chr19:41510037-41510087	SAEC	small airway:	n/a
41	chr19:41497222-41497272	AG09319	gingival:	n/a
42	chr19:41510098-41510148	IMR90	lung:	fetal
43	chr19:41510026-41510076	NB4	blood:	n/a
44	chr19:41495942-41495992	U87	brain:	n/a
45	chr19:41510098-41510148	AoSMC	blood vessel:	n/a
46	chr19:41510272-41510322	K562	blood:	n/a
47	chr19:41497222-41497272	HPAEpiC	pulmonary alveolar:	n/a
48	chr19:41510059-41510109	LNCaP	prostate:	n/a
49	chr19:41510098-41510148	MCF-7	breast:	n/a
50	chr19:41510272-41510322	HL-60	blood:	n/a

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CYP2B6-1	chr19:41492504-41492600	l_1687_chr19:41492503-41503928_testes
2	lnc-CYP2B6-2	chr19:41453006-41453355	ENSG00000269353.1
3	lnc-CYP2B6-2	chr19:41452252-41452450	ENSG00000269353.1
4	lnc-CYP2B6-1	chr19:41493956-41494534	l_1687_chr19:41492503-41503928_testes
5	lnc-CYP2B6-1	chr19:41503762-41503928	l_1687_chr19:41492503-41503928_testes
6	lnc-CYP2B6-1	chr19:41495264-41495408	l_1687_chr19:41492503-41503928_testes
7	lnc-CYP2B6-1	chr19:41493177-41493736	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: 3014 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3014 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs202025444	chr19:41446012-41446013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs538159639	chr19:41446025-41446026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs34012880	chr19:41446031-41446032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs77057193	chr19:41446043-41446044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543109051	chr19:41446044-41446045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10405736	chr19:41446045-41446046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28491266	chr19:41446046-41446047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553951942	chr19:41446047-41446048	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572617273	chr19:41446055-41446056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs386809307	chr19:41446076-41446077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10405755	chr19:41446078-41446079	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs140318071	chr19:41446084-41446085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192919054	chr19:41446093-41446094	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs367953541	chr19:41446097-41446098	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565218699	chr19:41446103-41446104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs10405934	chr19:41446104-41446105	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs531992207	chr19:41446109-41446110	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541068427	chr19:41446159-41446160	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs372322352	chr19:41446198-41446199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559012724	chr19:41446273-41446274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529748036	chr19:41446328-41446329	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184148263	chr19:41446330-41446331	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143781396	chr19:41446333-41446334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs188506290	chr19:41446336-41446337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs531995403	chr19:41446338-41446339	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550188189	chr19:41446345-41446346	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs180971674	chr19:41446352-41446353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538650745	chr19:41446355-41446356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7248682	chr19:41446402-41446403	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs566134272	chr19:41446442-41446443	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs183563190	chr19:41446444-41446445	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs536769014	chr19:41446448-41446449	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs554772442	chr19:41446473-41446474	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs147747163	chr19:41446506-41446507	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs377253572	chr19:41446507-41446508	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7249720	chr19:41446535-41446536	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs372635520	chr19:41446567-41446568	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs190724724	chr19:41446662-41446663	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs566522560	chr19:41446677-41446678	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs562909698	chr19:41446682-41446683	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs78459083	chr19:41446683-41446684	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs73931401	chr19:41446691-41446692	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs369566587	chr19:41446771-41446772	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs187017485	chr19:41446790-41446791	Weak transcription Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs150258088	chr19:41446811-41446812	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs541539960	chr19:41446813-41446814	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs376327530	chr19:41446823-41446824	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs368214171	chr19:41446897-41446898	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs563075437	chr19:41446907-41446908	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs367668090	chr19:41447000-41447001	Weak transcription Enhancers	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:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41432200-41447600	Weak transcription	Liver	Liver
2	chr19:41439200-41447800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr19:41439200-41448000	Weak transcription	Stomach Mucosa	stomach
4	chr19:41442400-41451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr19:41442600-41450200	Weak transcription	Lung	lung
6	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
7	chr19:41445400-41450200	Weak transcription	Fetal Intestine Small	intestine
8	chr19:41445800-41449200	Enhancers	HUVEC	blood vessel
9	chr19:41446400-41446600	Enhancers	A549	lung
10	chr19:41446600-41446800	Flanking Active TSS	A549	lung
11	chr19:41446800-41447200	Enhancers	A549	lung
12	chr19:41447200-41447600	Bivalent Enhancer	A549	lung
13	chr19:41447400-41448000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr19:41447600-41447800	Flanking Bivalent TSS/Enh	A549	lung
15	chr19:41447600-41448200	Strong transcription	Liver	Liver
16	chr19:41447800-41448200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr19:41447800-41448200	Bivalent Enhancer	A549	lung
18	chr19:41447800-41448200	Bivalent Enhancer	K562	blood
19	chr19:41448200-41449600	Weak transcription	Liver	Liver
20	chr19:41449600-41451800	Strong transcription	Liver	Liver
21	chr19:41450200-41450400	Bivalent Enhancer	Esophagus	oesophagus
22	chr19:41450200-41450600	ZNF genes & repeats	Lung	lung
23	chr19:41450200-41450800	Strong transcription	Fetal Intestine Small	intestine
24	chr19:41450800-41451800	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chr19:41451400-41451800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr19:41451400-41452200	Flanking Active TSS	K562	blood
27	chr19:41451800-41452200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr19:41451800-41455200	Weak transcription	Liver	Liver
29	chr19:41451800-41456200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr19:41451800-41456200	Weak transcription	Fetal Intestine Small	intestine
31	chr19:41452200-41452400	Enhancers	K562	blood
32	chr19:41453800-41458200	Weak transcription	Right Atrium	heart
33	chr19:41456200-41456400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr19:41459600-41460800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
35	chr19:41460000-41460800	ZNF genes & repeats	Brain Hippocampus Middle	brain
36	chr19:41460000-41461600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr19:41460200-41460400	ZNF genes & repeats	A549	lung
38	chr19:41460200-41461400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
39	chr19:41464600-41464800	Enhancers	Fetal Intestine Small	intestine
40	chr19:41464800-41466400	Weak transcription	Fetal Intestine Small	intestine
41	chr19:41465200-41466600	Enhancers	Esophagus	oesophagus
42	chr19:41465400-41465800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
43	chr19:41465400-41465800	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr19:41465400-41466000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr19:41465800-41466000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr19:41465800-41466000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
47	chr19:41465800-41466200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
49	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
50	chr19:41466000-41466200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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