Variant report

Variant	nsv569452
Chromosome Location	chr15:54080810-54156980
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	chr15:54122872-54124852	HepG2	liver:	n/a	chr15:54124032-54124048
2	ARID3A	chr15:54125132-54126029	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:54100317-54100664	HepG2	liver:	n/a	chr15:54100560-54100576
4	ARID3A	chr15:54136050-54137124	HepG2	liver:	n/a	n/a
5	BCL3	chr15:54124056-54124467	A549	lung:	n/a	n/a
6	BCL3	chr15:54123951-54124626	A549	lung:	n/a	n/a
7	BHLHE40	chr15:54123267-54123462	HepG2	liver:	n/a	n/a
8	CEBPB	chr15:54136388-54136773	HepG2	liver:	n/a	n/a
9	CEBPB	chr15:54125524-54125854	HepG2	liver:	n/a	n/a
10	CEBPB	chr15:54123281-54123348	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr15:54123075-54123438	HepG2	liver:	n/a	chr15:54123338-54123349
12	CEBPB	chr15:54123077-54123535	A549	lung:	n/a	chr15:54123338-54123349
13	CEBPB	chr15:54123151-54123440	A549	lung:	n/a	chr15:54123338-54123349
14	CEBPB	chr15:54123961-54124628	A549	lung:	n/a	n/a
15	CEBPB	chr15:54125412-54125869	A549	lung:	n/a	n/a
16	CEBPB	chr15:54123212-54123404	HepG2	liver:	n/a	chr15:54123338-54123349
17	CEBPB	chr15:54123168-54123538	HepG2	liver:	n/a	chr15:54123338-54123349
18	CEBPB	chr15:54123158-54123539	HepG2	liver:	n/a	chr15:54123338-54123349
19	CEBPB	chr15:54127592-54127903	A549	lung:	n/a	chr15:54127878-54127891 chr15:54127683-54127696
20	CEBPD	chr15:54123030-54123458	HepG2	liver:	n/a	n/a
21	CEBPD	chr15:54123147-54123399	HepG2	liver:	n/a	n/a
22	CREB1	chr15:54122661-54123645	HepG2	liver:	n/a	n/a
23	CREB1	chr15:54123126-54123420	A549	lung:	n/a	n/a
24	CTCF	chr15:54103840-54103990	HRE	kidney:	n/a	chr15:54103911-54103927 chr15:54103910-54103928 chr15:54103912-54103933
25	CTCF	chr15:54100860-54101010	HFF-Myc	foreskin:	n/a	n/a
26	CTCF	chr15:54103835-54104006	LNCaP	prostate:	n/a	chr15:54103911-54103927 chr15:54103910-54103928 chr15:54103912-54103933
27	CTCF	chr15:54100834-54100901	Fibrobl	skin:	n/a	n/a
28	CTCF	chr15:54103903-54103929	GM13977	blood:	n/a	chr15:54103911-54103927 chr15:54103910-54103928
29	CTCF	chr15:54103880-54104030	Caco-2	colon:	n/a	chr15:54103911-54103927 chr15:54103910-54103928 chr15:54103912-54103933
30	CTCF	chr15:54099840-54099990	HAc	cerebellar:	n/a	n/a
31	CTCF	chr15:54100400-54100550	HMF	breast:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
32	CTCF	chr15:54100320-54100470	GM12870	blood:	n/a	n/a
33	CTCF	chr15:54103860-54104010	GM06990	blood:	n/a	chr15:54103911-54103927 chr15:54103910-54103928 chr15:54103912-54103933
34	CTCF	chr15:54100400-54100550	GM06990	blood:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
35	CTCF	chr15:54129780-54129930	Caco-2	colon:	n/a	n/a
36	CTCF	chr15:54100420-54100570	GM12869	blood:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
37	CTCF	chr15:54100920-54101070	GM12872	blood:	n/a	n/a
38	CTCF	chr15:54100440-54100590	GM12865	blood:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
39	CTCF	chr15:54103860-54104010	HEEpiC	esophagus:	n/a	chr15:54103911-54103927 chr15:54103910-54103928 chr15:54103912-54103933
40	CTCF	chr15:54100400-54100550	GM12873	blood:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
41	CTCF	chr15:54100305-54100667	IMR90	lung:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
42	CTCF	chr15:54100460-54100610	HUVEC	blood vessel:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
43	CTCF	chr15:54100380-54100530	HUVEC	blood vessel:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
44	CTCF	chr15:54100339-54100599	Pancreas_OC	pancreas:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
45	CTCF	chr15:54100400-54100550	HMEC	breast:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
46	CTCF	chr15:54100280-54100430	RPTEC	kidney:	n/a	n/a
47	CTCF	chr15:54143802-54143863	LNCaP	prostate:	n/a	n/a
48	CTCF	chr15:54100440-54100590	HRE	kidney:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498
49	CTCF	chr15:54103826-54103828	LNCaP	prostate:	n/a	n/a
50	CTCF	chr15:54100380-54100530	HMEC	breast:	n/a	chr15:54100485-54100493 chr15:54100481-54100497 chr15:54100482-54100503 chr15:54100480-54100498

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:54124220-54124270	NH-A	brain:	n/a
2	chr15:54124220-54124270	NH-A	brain:	n/a
3	chr15:54124220-54124270	NHBE	bronchial:	n/a
4	chr15:54124220-54124270	MCF10A-Er-Src	breast:	n/a
5	chr15:54124220-54124270	Jurkat	blood:	n/a
6	chr15:54124220-54124270	AG04449	skin:	fetal
7	chr15:54124220-54124270	GM12878	blood:	n/a
8	chr15:54124220-54124270	U87	brain:	n/a
9	chr15:54124220-54124270	ECC-1	luminal epithelium:	n/a
10	chr15:54124220-54124270	AG04450	lung:	fetal
11	chr15:54124220-54124270	K562	blood:	n/a
12	chr15:54124220-54124270	CMK	blood:	n/a
13	chr15:54124220-54124270	SK-N-SH	brain:	n/a
14	chr15:54124220-54124270	PANC-1	pancreas:	n/a
15	chr15:54124220-54124270	HepG2	liver:	n/a
16	chr15:54124220-54124270	NHDF-neo	bronchial:	n/a
17	chr15:54124220-54124270	HRCEpiC	kidney:	n/a
18	chr15:54124220-54124270	AG09319	gingival:	n/a
19	chr15:54124220-54124270	AoSMC	blood vessel:	n/a
20	chr15:54124220-54124270	LNCaP	prostate:	n/a
21	chr15:54124220-54124270	HCM	heart:	n/a
22	chr15:54124220-54124270	SAEC	small airway:	n/a
23	chr15:54124220-54124270	AG10803	skin:	n/a
24	chr15:54124220-54124270	HUVEC	blood vessel:	n/a
25	chr15:54124220-54124270	PFSK-1	brain:	n/a
26	chr15:54124220-54124270	SK-N-MC	brain:	n/a
27	chr15:54124220-54124270	HCF	heart:	n/a
28	chr15:54124220-54124270	AG09309	skin:	n/a
29	chr15:54124220-54124270	HEK293	kidney:	embryo
30	chr15:54124220-54124270	HL-60	blood:	n/a
31	chr15:54124220-54124270	GM19239	blood:	n/a
32	chr15:54124220-54124270	A549	lung:	n/a
33	chr15:54124220-54124270	HPAEpiC	pulmonary alveolar:	n/a
34	chr15:54124220-54124270	HMEC	breast:	n/a
35	chr15:54124220-54124270	T-47D	breast:	n/a
36	chr15:54124220-54124270	GM12892	blood:	n/a
37	chr15:54124220-54124270	Hepatocyte	liver:	n/a
38	chr15:54124220-54124270	GM06990	blood:	n/a
39	chr15:54124220-54124270	HCT-116	colon:	n/a
40	chr15:54124220-54124270	PrEC	prostate:	n/a
41	chr15:54124220-54124270	NB4	blood:	n/a
42	chr15:54124220-54124270	MCF-7	breast:	n/a
43	chr15:54124220-54124270	Hela-S3	cervix:	n/a
44	chr15:54124220-54124270	NT2-D1	testis:	n/a
45	chr15:54124220-54124270	HEEpiC	esophagus:	n/a
46	chr15:54124220-54124270	BE2_C	brain:	n/a
47	chr15:54124220-54124270	BJ	skin:	n/a
48	chr15:54124220-54124270	HIPEpiC	eye:	n/a
49	chr15:54124220-54124270	RPTEC	kidney:	n/a
50	chr15:54124220-54124270	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:54103478..54104302-chr15:54255062..54255563,2	MCF-7	breast:
2	chr15:54100067..54100735-chr15:54254841..54255517,2	MCF-7	breast:
3	chr15:54082466..54084805-chr15:54086509..54088980,2	K562	blood:
4	chr15:54113534..54116285-chr15:54122883..54124924,2	MCF-7	breast:
5	chr15:54131232..54133067-chr15:54139996..54141988,3	MCF-7	breast:
6	chr15:54131232..54133067-chr15:54139996..54141988,3	MCF-7	breast:
7	chr15:54113534..54116285-chr15:54122883..54124924,2	MCF-7	breast:
8	chr15:54121587..54123725-chr15:55486823..55489231,2	MCF-7	breast:
9	chr1:181074348..181075243-chr15:54127964..54128671,2	MCF-7	breast:
10	chr15:54116856..54119680-chr15:54121215..54123914,2	MCF-7	breast:
11	chr15:54116856..54119680-chr15:54121215..54123914,2	MCF-7	breast:
12	chr15:54082466..54084805-chr15:54086509..54088980,2	K562	blood:
13	chr15:54103533..54104375-chr15:54255060..54255801,2	MCF-7	breast:
14	chr15:54077990..54080956-chr15:54224851..54227112,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR72-3	chr15:54129468-54129757	NONHSAT043971

Variant related genes	Relation type
ENSG00000259301	TF binding region
ENSG00000259301	CpG island
ENSG00000137876	chromatin interactions

Extended variants
information (count: 1729 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1729 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1381195	chr15:54080810-54080811	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532986902	chr15:54080815-54080816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142872950	chr15:54080816-54080817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs560476407	chr15:54080896-54080897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs13379509	chr15:54080898-54080899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs548906234	chr15:54080904-54080905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569304407	chr15:54080916-54080917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs689705	chr15:54080919-54080920	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs117999091	chr15:54080936-54080937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571284285	chr15:54080937-54080938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539945631	chr15:54080939-54080940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554034596	chr15:54080954-54080955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567872867	chr15:54081004-54081005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559898065	chr15:54081006-54081007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184189914	chr15:54081007-54081008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576611734	chr15:54081058-54081059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573058350	chr15:54081090-54081091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557932999	chr15:54081108-54081109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs567531566	chr15:54081109-54081110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs577705325	chr15:54081137-54081138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188127561	chr15:54081163-54081164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs180851108	chr15:54081193-54081194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560351000	chr15:54081209-54081210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs689727	chr15:54081226-54081227	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs78690600	chr15:54081262-54081263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs689741	chr15:54081332-54081333	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs79507555	chr15:54081344-54081345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183966121	chr15:54081349-54081350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149764819	chr15:54081360-54081361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs527639192	chr15:54081361-54081362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547409655	chr15:54081378-54081379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567915904	chr15:54081421-54081422	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs55658802	chr15:54081459-54081460	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs551997164	chr15:54081558-54081559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550479011	chr15:54081562-54081563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs35986065	chr15:54081579-54081580	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs539282243	chr15:54081593-54081594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147872158	chr15:54081609-54081610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs520793	chr15:54081622-54081623	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs533738390	chr15:54081639-54081640	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141480696	chr15:54081659-54081660	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113885621	chr15:54081706-54081707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs547195908	chr15:54081746-54081747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542533765	chr15:54081757-54081758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375523673	chr15:54081768-54081769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76720982	chr15:54081777-54081778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370159958	chr15:54081811-54081812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190557718	chr15:54081847-54081848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs538819410	chr15:54081875-54081876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369764000	chr15:54081887-54081888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:54078600-54081400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr15:54079800-54082400	Weak transcription	Fetal Intestine Small	intestine
3	chr15:54081400-54081800	Enhancers	Duodenum Mucosa	Duodenum
4	chr15:54081800-54083000	Weak transcription	Duodenum Mucosa	Duodenum
5	chr15:54082000-54084000	Enhancers	Stomach Mucosa	stomach
6	chr15:54082400-54083800	Enhancers	Fetal Intestine Small	intestine
7	chr15:54083000-54083200	Enhancers	Small Intestine	intestine
8	chr15:54083000-54083400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr15:54083000-54084600	Enhancers	Duodenum Mucosa	Duodenum
10	chr15:54083200-54083400	Flanking Bivalent TSS/Enh	Left Ventricle	heart
11	chr15:54083800-54084400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr15:54084000-54084600	Weak transcription	Stomach Mucosa	stomach
13	chr15:54084600-54084800	Enhancers	Stomach Mucosa	stomach
14	chr15:54099600-54099800	Enhancers	Duodenum Mucosa	Duodenum
15	chr15:54099600-54100000	Enhancers	Stomach Smooth Muscle	stomach
16	chr15:54099600-54100200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr15:54099600-54100400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr15:54099600-54100400	Enhancers	Brain Hippocampus Middle	brain
19	chr15:54099600-54101000	Enhancers	Fetal Lung	lung
20	chr15:54099600-54101200	Enhancers	Fetal Stomach	stomach
21	chr15:54099800-54100000	Enhancers	Brain Angular Gyrus	brain
22	chr15:54099800-54100000	Enhancers	Fetal Intestine Large	intestine
23	chr15:54099800-54100200	Enhancers	Brain Germinal Matrix	brain
24	chr15:54099800-54100200	Enhancers	Stomach Mucosa	stomach
25	chr15:54099800-54100400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr15:54099800-54100400	Enhancers	Fetal Kidney	kidney
27	chr15:54099800-54104200	Enhancers	HepG2	liver
28	chr15:54100000-54100200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr15:54100000-54101000	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr15:54100000-54104000	Weak transcription	Fetal Intestine Large	intestine
31	chr15:54100200-54101000	Enhancers	Fetal Intestine Small	intestine
32	chr15:54100200-54101000	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr15:54100200-54104400	Weak transcription	Stomach Mucosa	stomach
34	chr15:54100400-54101000	Enhancers	Duodenum Mucosa	Duodenum
35	chr15:54100400-54101600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr15:54100400-54101600	Weak transcription	Fetal Kidney	kidney
37	chr15:54101000-54101800	Weak transcription	Fetal Intestine Small	intestine
38	chr15:54101000-54103000	Weak transcription	Fetal Lung	lung
39	chr15:54101200-54105600	Weak transcription	Fetal Stomach	stomach
40	chr15:54101600-54101800	Enhancers	Fetal Kidney	kidney
41	chr15:54101600-54102600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr15:54101800-54102200	Enhancers	Fetal Intestine Small	intestine
43	chr15:54102200-54104600	Weak transcription	Fetal Intestine Small	intestine
44	chr15:54102600-54103000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr15:54103000-54103200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr15:54103000-54103400	Enhancers	Fetal Lung	lung
47	chr15:54103200-54103600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr15:54103600-54103800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr15:54103800-54104400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr15:54104000-54105400	Enhancers	Fetal Intestine Large	intestine

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