Variant report

Variant	nsv470142
Chromosome Location	chr19:41482742-41524153
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	ATF3	chr19:41506069-41506786	HCT-116	colon:	n/a	n/a
5	ATF3	chr19:41506267-41506508	K562	blood:	n/a	n/a
6	ATF3	chr19:41506140-41506734	HCT-116	colon:	n/a	n/a
7	BACH1	chr19:41488176-41489166	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr19:41507420-41507421	K562	blood:	n/a	n/a
9	CBX3	chr19:41505993-41506787	HCT-116	colon:	n/a	n/a
10	CEBPB	chr19:41505976-41507518	HCT-116	colon:	n/a	chr19:41506435-41506446
11	CEBPB	chr19:41507207-41507407	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr19:41507152-41507489	K562	blood:	n/a	n/a
13	CEBPB	chr19:41488308-41488880	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
14	CEBPB	chr19:41488481-41488681	Hela-S3	cervix:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
15	CEBPB	chr19:41506263-41507465	K562	blood:	n/a	chr19:41506435-41506446
16	CEBPB	chr19:41488522-41488635	HepG2	liver:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
17	CEBPB	chr19:41488408-41488845	MCF-7	breast:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
18	CEBPB	chr19:41488434-41488797	HepG2	liver:	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	chr19:41506068-41507138	HCT-116	colon:	n/a	chr19:41506435-41506446
21	CEBPB	chr19:41506256-41506628	Hela-S3	cervix:	n/a	chr19:41506435-41506446
22	CEBPB	chr19:41486262-41486477	HepG2	liver:	n/a	n/a
23	CEBPB	chr19:41506244-41506603	ECC-1	luminal epithelium:	n/a	chr19:41506435-41506446
24	CEBPB	chr19:41506205-41506669	MCF-7	breast:	n/a	chr19:41506435-41506446
25	CEBPB	chr19:41488422-41488791	A549	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
26	CEBPB	chr19:41488441-41488804	IMR90	lung:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
27	CEBPB	chr19:41506189-41507135	A549	lung:	n/a	chr19:41506435-41506446
28	CEBPB	chr19:41506268-41506934	HepG2	liver:	n/a	chr19:41506435-41506446
29	CEBPB	chr19:41506284-41507442	A549	lung:	n/a	chr19:41506435-41506446
30	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
31	CEBPB	chr19:41506884-41506987	IMR90	lung:	n/a	n/a
32	CEBPB	chr19:41488438-41488777	K562	blood:	n/a	chr19:41488609-41488620 chr19:41488607-41488620 chr19:41488609-41488618 chr19:41488607-41488618 chr19:41488607-41488620
33	CEBPB	chr19:41486382-41486422	K562	blood:	n/a	n/a
34	CREB1	chr19:41486321-41486531	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr19:41507218-41507529	K562	blood:	n/a	n/a
36	CTCF	chr19:41507260-41507410	MCF-7	breast:	n/a	n/a
37	CTCF	chr19:41510420-41510570	K562	blood:	n/a	n/a
38	CTCF	chr19:41483596-41483708	K562	blood:	n/a	n/a
39	CTCF	chr19:41483545-41483745	MCF-7	breast:	n/a	n/a
40	CTCF	chr19:41507246-41507415	Gliobla	brain:	n/a	n/a
41	CTCF	chr19:41507220-41507370	HEK293	kidney:	n/a	n/a
42	CTCF	chr19:41507215-41507476	K562	blood:	n/a	n/a
43	CTCF	chr19:41507320-41507470	HepG2	liver:	n/a	n/a
44	CTCF	chr19:41507237-41507437	MCF-7	breast:	n/a	n/a
45	CTCF	chr19:41507300-41507450	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr19:41507200-41507350	RPTEC	kidney:	n/a	n/a
47	CTCF	chr19:41507180-41507330	HCT-116	colon:	n/a	n/a
48	CTCF	chr19:41483589-41483594	K562	blood:	n/a	n/a
49	CTCF	chr19:41507280-41507430	GM12873	blood:	n/a	n/a
50	CTCF	chr19:41507257-41507415	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:41510098-41510148	MCF10A-Er-Src	breast:	n/a
2	chr19:41496043-41496093	A549	lung:	n/a
3	chr19:41510098-41510148	MCF10A-Er-Src	breast:	n/a
4	chr19:41496043-41496093	A549	lung:	n/a
5	chr19:41510272-41510322	AG09319	gingival:	n/a
6	chr19:41496749-41496799	NH-A	brain:	n/a
7	chr19:41510272-41510322	HNPCEpiC	eye:	n/a
8	chr19:41510059-41510109	AG09319	gingival:	n/a
9	chr19:41510098-41510148	ovcar-3	ovarian:	n/a
10	chr19:41510026-41510076	AG04450	lung:	fetal
11	chr19:41510272-41510322	GM12878	blood:	n/a
12	chr19:41510285-41510335	AoSMC	blood vessel:	n/a
13	chr19:41496749-41496799	NB4	blood:	n/a
14	chr19:41510098-41510148	HAEpiC	amniotic membrane:	n/a
15	chr19:41510098-41510148	SK-N-SH	brain:	n/a
16	chr19:41496043-41496093	Hela-S3	cervix:	n/a
17	chr19:41510037-41510087	HMEC	breast:	n/a
18	chr19:41510285-41510335	HCF	heart:	n/a
19	chr19:41510098-41510148	IMR90	lung:	fetal
20	chr19:41510059-41510109	HUVEC	blood vessel:	n/a
21	chr19:41510285-41510335	NH-A	brain:	n/a
22	chr19:41510285-41510335	HRE	kidney:	n/a
23	chr19:41495942-41495992	SAEC	small airway:	n/a
24	chr19:41496043-41496093	IMR90	lung:	fetal
25	chr19:41510026-41510076	HCF	heart:	n/a
26	chr19:41510272-41510322	AG04450	lung:	fetal
27	chr19:41495942-41495992	MCF-7	breast:	n/a
28	chr19:41510026-41510076	ovcar-3	ovarian:	n/a
29	chr19:41510059-41510109	ovcar-3	ovarian:	n/a
30	chr19:41510098-41510148	HCT-116	colon:	n/a
31	chr19:41496749-41496799	GM12878	blood:	n/a
32	chr19:41510243-41510293	A549	lung:	n/a
33	chr19:41497222-41497272	HPAEpiC	pulmonary alveolar:	n/a
34	chr19:41510037-41510087	HCT-116	colon:	n/a
35	chr19:41510098-41510148	PrEC	prostate:	n/a
36	chr19:41496749-41496799	NHDF-neo	bronchial:	n/a
37	chr19:41510026-41510076	Hepatocyte	liver:	n/a
38	chr19:41510059-41510109	GM19239	blood:	n/a
39	chr19:41497222-41497272	PANC-1	pancreas:	n/a
40	chr19:41510243-41510293	PFSK-1	brain:	n/a
41	chr19:41495942-41495992	GM12878	blood:	n/a
42	chr19:41510243-41510293	HPAEpiC	pulmonary alveolar:	n/a
43	chr19:41510243-41510293	HRCEpiC	kidney:	n/a
44	chr19:41496043-41496093	Caco-2	colon:	n/a
45	chr19:41510098-41510148	NH-A	brain:	n/a
46	chr19:41510059-41510109	GM12878	blood:	n/a
47	chr19:41495942-41495992	U87	brain:	n/a
48	chr19:41496749-41496799	IMR90	lung:	fetal
49	chr19:41510272-41510322	HRE	kidney:	n/a
50	chr19:41496749-41496799	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:41489930..41492049-chr19:41494201..41495851,2	K562	blood:
2	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-CYP2B6-1	chr19:41495264-41495408	l_1687_chr19:41492503-41503928_testes
4	lnc-CYP2B6-1	chr19:41503762-41503928	l_1687_chr19:41492503-41503928_testes
5	lnc-CYP2B6-1	chr19:41492504-41492600	l_1687_chr19:41492503-41503928_testes

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

Extended variants
information (count: 2361 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2361 , 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	rs12971445	chr19:41484602-41484603	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574489240	chr19:41484606-41484607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541907407	chr19:41484644-41484645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs563388616	chr19:41484645-41484646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs576552517	chr19:41484710-41484711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs145273754	chr19:41484735-41484736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs183061689	chr19:41484797-41484798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs147651450	chr19:41484798-41484799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548115187	chr19:41484824-41484825	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367686951	chr19:41484857-41484858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs554751904	chr19:41484886-41484887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79152072	chr19:41484890-41484891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs548239167	chr19:41484909-41484910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188471028	chr19:41484922-41484923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537589622	chr19:41484927-41484928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs552081081	chr19:41484930-41484931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs77159062	chr19:41484943-41484944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs75889152	chr19:41485007-41485008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543649116	chr19:41485050-41485051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs553314378	chr19:41485144-41485145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1808002	chr19:41485194-41485195	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs535464775	chr19:41485211-41485212	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397970243	chr19:41485243-41485244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372605508	chr19:41485244-41485245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557024332	chr19:41485282-41485283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559166276	chr19:41485302-41485303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192894682	chr19:41485310-41485311	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs151166009	chr19:41485328-41485329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545908382	chr19:41485346-41485347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56881024	chr19:41485380-41485381	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs371708821	chr19:41485381-41485382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11443247	chr19:41485405-41485406	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs71358953	chr19:41485408-41485409	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs374975103	chr19:41485439-41485440	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs367902385	chr19:41485450-41485451	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs554458842	chr19:41485451-41485452	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs559632408	chr19:41485462-41485463	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs530006139	chr19:41485476-41485477	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs185044055	chr19:41485496-41485497	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs563385724	chr19:41485521-41485522	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs189508457	chr19:41485529-41485530	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs552646282	chr19:41485621-41485622	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs570514388	chr19:41485652-41485653	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs76421816	chr19:41485688-41485689	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs183528325	chr19:41485696-41485697	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs568340012	chr19:41485697-41485698	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs535781998	chr19:41485698-41485699	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs556987149	chr19:41485740-41485741	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs8106966	chr19:41485821-41485822	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs189390480	chr19:41485826-41485827	Enhancers 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	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:194 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:41484600-41485000	Enhancers	Stomach Mucosa	stomach
2	chr19:41484600-41489200	Enhancers	Fetal Intestine Large	intestine
3	chr19:41484600-41489200	Enhancers	Fetal Intestine Small	intestine
4	chr19:41484600-41489800	Enhancers	Liver	Liver
5	chr19:41484800-41485800	Enhancers	Colonic Mucosa	Colon
6	chr19:41484800-41487200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr19:41485000-41485200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr19:41485000-41485400	Weak transcription	Stomach Mucosa	stomach
9	chr19:41485200-41485400	Enhancers	Duodenum Mucosa	Duodenum
10	chr19:41485400-41485800	Flanking Active TSS	Duodenum Mucosa	Duodenum
11	chr19:41485400-41486200	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr19:41485400-41487000	Enhancers	Stomach Mucosa	stomach
13	chr19:41485600-41487000	Enhancers	HepG2	liver
14	chr19:41485800-41486000	Enhancers	Duodenum Mucosa	Duodenum
15	chr19:41485800-41486800	Weak transcription	Colonic Mucosa	Colon
16	chr19:41486000-41486600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr19:41486000-41488000	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr19:41486000-41488400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr19:41486200-41486400	Active TSS	Rectal Mucosa Donor 29	rectum
20	chr19:41486200-41486600	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr19:41486200-41486800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr19:41486200-41487000	Enhancers	H9 Cell Line	embryonic stem cell
23	chr19:41486200-41488000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr19:41486200-41488200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr19:41486200-41489800	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr19:41486200-41490000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr19:41486400-41486800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
28	chr19:41486400-41487000	Enhancers	Pancreas	Pancrea
29	chr19:41486400-41487400	Enhancers	Sigmoid Colon	Sigmoid Colon
30	chr19:41486400-41487800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr19:41486400-41488200	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr19:41486600-41486800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr19:41486600-41486800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr19:41486600-41487600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr19:41486600-41488800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
36	chr19:41486600-41489200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr19:41486800-41487000	Enhancers	Colonic Mucosa	Colon
38	chr19:41486800-41487200	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr19:41486800-41487200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
40	chr19:41486800-41487200	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr19:41486800-41489600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr19:41487000-41487400	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr19:41487000-41488400	Weak transcription	Pancreas	Pancrea
44	chr19:41487000-41490200	Weak transcription	Colonic Mucosa	Colon
45	chr19:41487200-41487800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr19:41487200-41490000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr19:41487200-41490200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr19:41487400-41490400	Enhancers	H9 Cell Line	embryonic stem cell
49	chr19:41487600-41488000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr19:41487800-41488000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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