Variant report

Variant	nsv433319
Chromosome Location	chr19:41448734-41510030
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	chr19:41486058-41486085	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:41506351-41506450	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	chr19:41506267-41506508	K562	blood:	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	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
9	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
11	BCL3	chr19:41468223-41469050	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	chr19:41482345-41482685	K562	blood:	n/a	n/a
16	CBX3	chr19:41460434-41460907	K562	blood:	n/a	n/a
17	CBX3	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
18	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	n/a	chr19:41506435-41506446
19	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
20	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
21	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
22	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
23	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
24	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
25	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
26	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
28	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
29	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
30	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
31	CEBPB	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446
32	CEBPB	chr19:41507152-41507489	K562	blood:	n/a	n/a
33	CEBPB	chr19:41506208-41506618	A549	lung:	n/a	chr19:41506435-41506446
34	CEBPB	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
36	CEBPB	chr19:41468360-41468789	A549	lung:	n/a	n/a
37	CEBPB	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
38	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
39	CEBPB	chr19:41488434-41488797	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
40	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	n/a	chr19:41506435-41506446
41	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
42	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
43	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
44	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
45	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
46	CEBPD	chr19:41458422-41458815	K562	blood:	n/a	n/a
47	CHD2	chr19:41465957-41466157	K562	blood:	n/a	n/a
48	CREB1	chr19:41468563-41468752	A549	lung:	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	chr19:41496043-41496093	IMR90	lung:	fetal
2	chr19:41495942-41495992	HCT-116	colon:	n/a
3	chr19:41496043-41496093	Hela-S3	cervix:	n/a
4	chr19:41496043-41496093	HRE	kidney:	n/a
5	chr19:41496749-41496799	NT2-D1	testis:	n/a
6	chr19:41495942-41495992	LNCaP	prostate:	n/a
7	chr19:41496749-41496799	GM19239	blood:	n/a
8	chr19:41496749-41496799	Hepatocyte	liver:	n/a
9	chr19:41496749-41496799	AG10803	skin:	n/a
10	chr19:41495942-41495992	NH-A	brain:	n/a
11	chr19:41510026-41510076	SK-N-SH	brain:	n/a
12	chr19:41496749-41496799	NB4	blood:	n/a
13	chr19:41497222-41497272	GM12892	blood:	n/a
14	chr19:41496749-41496799	SK-N-MC	brain:	n/a
15	chr19:41497222-41497272	HCPEpiC	choroid plexus:	n/a
16	chr19:41496043-41496093	SK-N-MC	brain:	n/a
17	chr19:41496749-41496799	HCF	heart:	n/a
18	chr19:41495942-41495992	SK-N-SH	brain:	n/a
19	chr19:41510026-41510076	HIPEpiC	eye:	n/a
20	chr19:41497222-41497272	PrEC	prostate:	n/a
21	chr19:41496043-41496093	LNCaP	prostate:	n/a
22	chr19:41496043-41496093	AoSMC	blood vessel:	n/a
23	chr19:41510026-41510076	NHDF-neo	bronchial:	n/a
24	chr19:41495942-41495992	AG04450	lung:	fetal
25	chr19:41497222-41497272	NT2-D1	testis:	n/a
26	chr19:41496043-41496093	PFSK-1	brain:	n/a
27	chr19:41495942-41495992	HUVEC	blood vessel:	n/a
28	chr19:41496043-41496093	AG09309	skin:	n/a
29	chr19:41496749-41496799	H1-hESC	embryonic stem cell:	embryo
30	chr19:41496749-41496799	ProgFib	skin:	n/a
31	chr19:41495942-41495992	AG10803	skin:	n/a
32	chr19:41496043-41496093	GM06990	blood:	n/a
33	chr19:41496043-41496093	HMEC	breast:	n/a
34	chr19:41497222-41497272	HEEpiC	esophagus:	n/a
35	chr19:41497222-41497272	SK-N-SH_RA	brain:	n/a
36	chr19:41495942-41495992	HL-60	blood:	n/a
37	chr19:41496749-41496799	LNCaP	prostate:	n/a
38	chr19:41495942-41495992	HCPEpiC	choroid plexus:	n/a
39	chr19:41510026-41510076	SK-N-SH_RA	brain:	n/a
40	chr19:41497222-41497272	Hepatocyte	liver:	n/a
41	chr19:41496043-41496093	ovcar-3	ovarian:	n/a
42	chr19:41496749-41496799	SK-N-SH_RA	brain:	n/a
43	chr19:41510026-41510076	GM12892	blood:	n/a
44	chr19:41510026-41510076	BE2_C	brain:	n/a
45	chr19:41496043-41496093	BJ	skin:	n/a
46	chr19:41495942-41495992	K562	blood:	n/a
47	chr19:41495942-41495992	HRE	kidney:	n/a
48	chr19:41510026-41510076	HNPCEpiC	eye:	n/a
49	chr19:41495942-41495992	BJ	skin:	n/a
50	chr19:41497222-41497272	IMR90	lung:	fetal

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

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

Extended variants
information (count: 2368 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2368 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8112043	chr19:41448734-41448735	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549076768	chr19:41448757-41448758	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs578039842	chr19:41448780-41448781	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs187115902	chr19:41448792-41448793	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs536036176	chr19:41448799-41448800	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs142397253	chr19:41448843-41448844	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs575845484	chr19:41448856-41448857	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs191569579	chr19:41448868-41448869	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs537060203	chr19:41448871-41448872	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs546028060	chr19:41448888-41448889	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs183669511	chr19:41448909-41448910	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs8100958	chr19:41448912-41448913	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs74620033	chr19:41448946-41448947	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs57518414	chr19:41448947-41448948	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs77520437	chr19:41449013-41449014	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs564225059	chr19:41449049-41449050	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs574059973	chr19:41449057-41449058	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs544349499	chr19:41449091-41449092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373398907	chr19:41449117-41449118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151291922	chr19:41449136-41449137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533218290	chr19:41449154-41449155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140563081	chr19:41449192-41449193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189014761	chr19:41449209-41449210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560472024	chr19:41449257-41449258	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs527272230	chr19:41449267-41449268	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs549039816	chr19:41449276-41449277	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs377089269	chr19:41449289-41449290	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs193259061	chr19:41449317-41449318	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs57637045	chr19:41449321-41449322	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs551124330	chr19:41449339-41449340	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs531659292	chr19:41449343-41449344	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs569338640	chr19:41449385-41449386	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs540053838	chr19:41449387-41449388	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs558027655	chr19:41449415-41449416	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs185753570	chr19:41449424-41449425	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs550063601	chr19:41449426-41449427	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs375631421	chr19:41449444-41449445	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs368733670	chr19:41449452-41449453	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs11083593	chr19:41449455-41449456	Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs555347903	chr19:41449467-41449468	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs574054135	chr19:41449479-41449480	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs545859275	chr19:41449495-41449496	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs146580417	chr19:41449513-41449514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556650289	chr19:41449544-41449545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs528909033	chr19:41449593-41449594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4124633	chr19:41449603-41449604	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs141208568	chr19:41449627-41449628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565647874	chr19:41449631-41449632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369907109	chr19:41449657-41449658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527593504	chr19:41449727-41449728	Weak transcription Strong transcription	n/a	n/a	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:264 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41442400-41451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:41442600-41450200	Weak transcription	Lung	lung
3	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
4	chr19:41445400-41450200	Weak transcription	Fetal Intestine Small	intestine
5	chr19:41445800-41449200	Enhancers	HUVEC	blood vessel
6	chr19:41448200-41449600	Weak transcription	Liver	Liver
7	chr19:41449600-41451800	Strong transcription	Liver	Liver
8	chr19:41450200-41450400	Bivalent Enhancer	Esophagus	oesophagus
9	chr19:41450200-41450600	ZNF genes & repeats	Lung	lung
10	chr19:41450200-41450800	Strong transcription	Fetal Intestine Small	intestine
11	chr19:41450800-41451800	ZNF genes & repeats	Fetal Intestine Small	intestine
12	chr19:41451400-41451800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr19:41451400-41452200	Flanking Active TSS	K562	blood
14	chr19:41451800-41452200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr19:41451800-41455200	Weak transcription	Liver	Liver
16	chr19:41451800-41456200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:41451800-41456200	Weak transcription	Fetal Intestine Small	intestine
18	chr19:41452200-41452400	Enhancers	K562	blood
19	chr19:41453800-41458200	Weak transcription	Right Atrium	heart
20	chr19:41456200-41456400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr19:41459600-41460800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
22	chr19:41460000-41460800	ZNF genes & repeats	Brain Hippocampus Middle	brain
23	chr19:41460000-41461600	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr19:41460200-41460400	ZNF genes & repeats	A549	lung
25	chr19:41460200-41461400	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
26	chr19:41464600-41464800	Enhancers	Fetal Intestine Small	intestine
27	chr19:41464800-41466400	Weak transcription	Fetal Intestine Small	intestine
28	chr19:41465200-41466600	Enhancers	Esophagus	oesophagus
29	chr19:41465400-41465800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
30	chr19:41465400-41465800	Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr19:41465400-41466000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr19:41465800-41466000	Bivalent Enhancer	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr19:41465800-41466000	Flanking Bivalent TSS/Enh	Brain Dorsolateral Prefrontal Cortex	brain
34	chr19:41465800-41466200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
36	chr19:41465800-41466200	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
37	chr19:41466000-41466200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr19:41466000-41466200	Bivalent Enhancer	Adipose Nuclei	Adipose
39	chr19:41466000-41466200	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
40	chr19:41466200-41466600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr19:41466200-41466600	Enhancers	Sigmoid Colon	Sigmoid Colon
42	chr19:41466200-41466800	Enhancers	Adipose Nuclei	Adipose
43	chr19:41466200-41469800	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr19:41466200-41469800	Enhancers	Ovary	ovary
45	chr19:41466400-41466600	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr19:41466400-41466800	Enhancers	Fetal Intestine Large	intestine
47	chr19:41466400-41466800	Enhancers	Fetal Intestine Small	intestine
48	chr19:41466600-41468000	Weak transcription	Esophagus	oesophagus
49	chr19:41466800-41467000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
50	chr19:41466800-41467000	Bivalent Enhancer	A549	lung

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