Variant report

Variant	nsv1061228
Chromosome Location	chr19:41436546-41513333
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	chr19:41507311-41507499	K562	blood:	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	chr19:41506267-41506508	K562	blood:	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	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
9	BACH1	chr19:41437946-41438301	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr19:41437956-41438260	K562	blood:	n/a	n/a
11	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr19:41468223-41469050	A549	lung:	n/a	n/a
13	BCL3	chr19:41468291-41469001	A549	lung:	n/a	n/a
14	BHLHE40	chr19:41507420-41507421	K562	blood:	n/a	n/a
15	BRCA1	chr19:41465957-41466156	GM12878	blood:	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	CBX3	chr19:41460404-41460899	K562	blood:	n/a	n/a
19	CBX3	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
20	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
21	CEBPB	chr19:41446714-41446729	A549	lung:	n/a	n/a
22	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
23	CEBPB	chr19:41468165-41469078	A549	lung:	n/a	chr19:41468797-41468810
24	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
25	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
26	CEBPB	chr19:41468301-41468559	HepG2	liver:	n/a	n/a
27	CEBPB	chr19:41438982-41439268	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
29	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
30	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	n/a	chr19:41506435-41506446
31	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	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	chr19:41468308-41469019	Hela-S3	cervix:	n/a	chr19:41468797-41468810
34	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
35	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
36	CEBPB	chr19:41438733-41439296	A549	lung:	n/a	n/a
37	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
38	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
39	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
40	CEBPB	chr19:41488308-41488880	A549	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	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr19:41438908-41439279	K562	blood:	n/a	n/a
44	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
45	CEBPB	chr19:41438614-41439244	K562	blood:	n/a	n/a
46	CEBPB	chr19:41507152-41507489	K562	blood:	n/a	n/a
47	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
48	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
49	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
50	CEBPB	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41510243-41510293	K562	blood:	n/a
2	chr19:41510243-41510293	K562	blood:	n/a
3	chr19:41510098-41510148	K562	blood:	n/a
4	chr19:41510272-41510322	HepG2	liver:	n/a
5	chr19:41510285-41510335	HRCEpiC	kidney:	n/a
6	chr19:41510059-41510109	ProgFib	skin:	n/a
7	chr19:41510243-41510293	Hela-S3	cervix:	n/a
8	chr19:41510285-41510335	GM12878	blood:	n/a
9	chr19:41510026-41510076	SKMC	muscle:	n/a
10	chr19:41496043-41496093	RPTEC	kidney:	n/a
11	chr19:41510059-41510109	HCM	heart:	n/a
12	chr19:41510285-41510335	ovcar-3	ovarian:	n/a
13	chr19:41496043-41496093	AG04449	skin:	fetal
14	chr19:41495942-41495992	SK-N-SH_RA	brain:	n/a
15	chr19:41510037-41510087	BJ	skin:	n/a
16	chr19:41496043-41496093	A549	lung:	n/a
17	chr19:41510059-41510109	AG09319	gingival:	n/a
18	chr19:41510037-41510087	HepG2	liver:	n/a
19	chr19:41497222-41497272	HPAEpiC	pulmonary alveolar:	n/a
20	chr19:41496749-41496799	AG04450	lung:	fetal
21	chr19:41496749-41496799	Hepatocyte	liver:	n/a
22	chr19:41495942-41495992	HEEpiC	esophagus:	n/a
23	chr19:41510272-41510322	BE2_C	brain:	n/a
24	chr19:41510285-41510335	CMK	blood:	n/a
25	chr19:41496749-41496799	SAEC	small airway:	n/a
26	chr19:41510272-41510322	PrEC	prostate:	n/a
27	chr19:41510026-41510076	PANC-1	pancreas:	n/a
28	chr19:41496749-41496799	AG10803	skin:	n/a
29	chr19:41495942-41495992	U87	brain:	n/a
30	chr19:41510037-41510087	H1-hESC	embryonic stem cell:	embryo
31	chr19:41496749-41496799	HPAEpiC	pulmonary alveolar:	n/a
32	chr19:41510272-41510322	SK-N-SH	brain:	n/a
33	chr19:41496043-41496093	MCF-7	breast:	n/a
34	chr19:41510037-41510087	GM12892	blood:	n/a
35	chr19:41495942-41495992	IMR90	lung:	fetal
36	chr19:41510037-41510087	T-47D	breast:	n/a
37	chr19:41496749-41496799	LNCaP	prostate:	n/a
38	chr19:41510059-41510109	ECC-1	luminal epithelium:	n/a
39	chr19:41510272-41510322	MCF-7	breast:	n/a
40	chr19:41510272-41510322	SKMC	muscle:	n/a
41	chr19:41510285-41510335	AG09309	skin:	n/a
42	chr19:41510037-41510087	GM12878	blood:	n/a
43	chr19:41510059-41510109	HPAEpiC	pulmonary alveolar:	n/a
44	chr19:41510098-41510148	A549	lung:	n/a
45	chr19:41510037-41510087	Hepatocyte	liver:	n/a
46	chr19:41510285-41510335	HEEpiC	esophagus:	n/a
47	chr19:41495942-41495992	GM06990	blood:	n/a
48	chr19:41496043-41496093	PrEC	prostate:	n/a
49	chr19:41496043-41496093	GM12892	blood:	n/a
50	chr19:41495942-41495992	ECC-1	luminal epithelium:	n/a

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

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

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: 3208 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:3208 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1820025	chr19:41436546-41436547	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34207755	chr19:41436569-41436570	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs536692549	chr19:41436577-41436578	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369797583	chr19:41436599-41436600	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551798925	chr19:41436619-41436620	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs150274956	chr19:41436672-41436673	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs528203528	chr19:41436712-41436713	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs547935338	chr19:41436727-41436728	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs566162072	chr19:41436734-41436735	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536902602	chr19:41436739-41436740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs12459233	chr19:41436785-41436786	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs77573739	chr19:41436814-41436815	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs566863631	chr19:41436817-41436818	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs143215384	chr19:41436820-41436821	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147481109	chr19:41436845-41436846	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534824882	chr19:41436881-41436882	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs553106449	chr19:41436960-41436961	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs189291945	chr19:41436985-41436986	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs193099296	chr19:41436997-41436998	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs185880518	chr19:41437010-41437011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs190353143	chr19:41437029-41437030	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181710516	chr19:41437035-41437036	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542070229	chr19:41437065-41437066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs556831506	chr19:41437102-41437103	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575187262	chr19:41437137-41437138	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545376061	chr19:41437176-41437177	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs534253240	chr19:41437253-41437254	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs186010610	chr19:41437369-41437370	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs7248187	chr19:41437426-41437427	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs539953939	chr19:41437428-41437429	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs7247910	chr19:41437440-41437441	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs77043975	chr19:41437454-41437455	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs538429036	chr19:41437455-41437456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs556862272	chr19:41437472-41437473	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs114675593	chr19:41437495-41437496	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs141404142	chr19:41437525-41437526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570342525	chr19:41437564-41437565	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs7249124	chr19:41437619-41437620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs542254888	chr19:41437658-41437659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs560900183	chr19:41437667-41437668	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs552571480	chr19:41437676-41437677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs552685733	chr19:41437682-41437683	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs188775062	chr19:41437709-41437710	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs6508960	chr19:41437717-41437718	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs9916983	chr19:41437730-41437731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535269018	chr19:41437794-41437795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564815244	chr19:41437800-41437801	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs543586531	chr19:41437802-41437803	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556770048	chr19:41437847-41437848	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs575159522	chr19:41437882-41437883	Enhancers Weak transcription Genic enhancers	Chromatin interactive 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:321 , 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	chr19:41433000-41437800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr19:41436000-41437600	Weak transcription	K562	blood
4	chr19:41436200-41436600	Weak transcription	Fetal Intestine Small	intestine
5	chr19:41436200-41437800	Weak transcription	Fetal Intestine Large	intestine
6	chr19:41436600-41437000	Strong transcription	Fetal Intestine Small	intestine
7	chr19:41437000-41437800	Weak transcription	Fetal Intestine Small	intestine
8	chr19:41437600-41438000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr19:41437600-41439800	Enhancers	K562	blood
10	chr19:41437800-41438000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr19:41437800-41438000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr19:41437800-41438200	Genic enhancers	Fetal Intestine Small	intestine
13	chr19:41437800-41438600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr19:41437800-41438800	Enhancers	Fetal Intestine Large	intestine
15	chr19:41438000-41439400	Bivalent Enhancer	A549	lung
16	chr19:41438200-41438400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr19:41438200-41438600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
18	chr19:41438200-41442000	Weak transcription	Fetal Intestine Small	intestine
19	chr19:41438400-41438800	Enhancers	Primary neutrophils fromperipheralblood	blood
20	chr19:41438400-41439000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr19:41438400-41439000	Enhancers	Placenta	Placenta
22	chr19:41438600-41439000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr19:41438600-41439600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr19:41438800-41444000	Weak transcription	Fetal Intestine Large	intestine
25	chr19:41439000-41439200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr19:41439000-41439200	Enhancers	Stomach Mucosa	stomach
27	chr19:41439000-41439800	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr19:41439200-41447800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr19:41439200-41448000	Weak transcription	Stomach Mucosa	stomach
30	chr19:41439600-41439800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr19:41439800-41441600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
32	chr19:41440600-41442400	Weak transcription	Lung	lung
33	chr19:41441600-41441800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr19:41442000-41442400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr19:41442000-41445400	Strong transcription	Fetal Intestine Small	intestine
36	chr19:41442400-41442600	Strong transcription	Lung	lung
37	chr19:41442400-41451400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr19:41442600-41442800	Bivalent Enhancer	Stomach Smooth Muscle	stomach
39	chr19:41442600-41450200	Weak transcription	Lung	lung
40	chr19:41444000-41444800	Strong transcription	Fetal Intestine Large	intestine
41	chr19:41444400-41445400	Bivalent Enhancer	A549	lung
42	chr19:41444800-41455800	Weak transcription	Fetal Intestine Large	intestine
43	chr19:41445400-41450200	Weak transcription	Fetal Intestine Small	intestine
44	chr19:41445800-41449200	Enhancers	HUVEC	blood vessel
45	chr19:41446400-41446600	Enhancers	A549	lung
46	chr19:41446600-41446800	Flanking Active TSS	A549	lung
47	chr19:41446800-41447200	Enhancers	A549	lung
48	chr19:41447200-41447600	Bivalent Enhancer	A549	lung
49	chr19:41447400-41448000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr19:41447600-41447800	Flanking Bivalent TSS/Enh	A549	lung

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