Variant report

Variant	nsv880987
Chromosome Location	chr5:29051880-29129027
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	chr5:29070987-29071060	K562	blood:	n/a	n/a
2	ATF1	chr5:29114649-29114850	K562	blood:	n/a	n/a
3	ATF1	chr5:29089739-29090287	K562	blood:	n/a	n/a
4	BATF	chr5:29099772-29100098	GM12878	blood:	n/a	n/a
5	BATF	chr5:29099732-29100010	GM12878	blood:	n/a	n/a
6	BHLHE40	chr5:29089838-29090224	K562	blood:	n/a	n/a
7	BHLHE40	chr5:29114706-29114820	K562	blood:	n/a	n/a
8	BRCA1	chr5:29077488-29077830	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr5:29079757-29080002	K562	blood:	n/a	n/a
10	CCNT2	chr5:29089941-29090240	K562	blood:	n/a	n/a
11	CCNT2	chr5:29051731-29051997	K562	blood:	n/a	chr5:29051832-29051852
12	CEBPB	chr5:29096172-29096477	K562	blood:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
13	CEBPB	chr5:29096184-29096509	IMR90	lung:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
14	CEBPB	chr5:29077957-29078214	A549	lung:	n/a	n/a
15	CEBPB	chr5:29085361-29085554	HepG2	liver:	n/a	n/a
16	CEBPB	chr5:29077432-29078233	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:29096282-29096449	H1-hESC	embryonic stem cell:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
18	CEBPB	chr5:29096216-29096495	Hela-S3	cervix:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
19	CEBPB	chr5:29096209-29096500	HepG2	liver:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
20	CEBPB	chr5:29096194-29096516	A549	lung:	n/a	chr5:29096332-29096343 chr5:29096327-29096344 chr5:29096330-29096343 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096332-29096341 chr5:29096330-29096341
21	CEBPB	chr5:29072750-29072805	HepG2	liver:	n/a	chr5:29072772-29072783
22	CHD1	chr5:29095636-29095675	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD2	chr5:29114366-29114830	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr5:29079997-29080028	Hela-S3	cervix:	n/a	n/a
25	CHD2	chr5:29077610-29077959	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr5:29079960-29080110	A549	lung:	n/a	n/a
27	CTCF	chr5:29079951-29080119	Medullo	brain:	n/a	n/a
28	CTCF	chr5:29115508-29115587	MCF-7	breast:	n/a	n/a
29	CTCF	chr5:29079910-29080169	MCF-7	breast:	n/a	n/a
30	CTCF	chr5:29079990-29080039	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr5:29080000-29080150	K562	blood:	n/a	n/a
32	CTCF	chr5:29079920-29080070	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr5:29079983-29080114	GM12891	blood:	n/a	n/a
34	CTCF	chr5:29079900-29080050	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr5:29079969-29080092	HepG2	liver:	n/a	n/a
36	CTCF	chr5:29080000-29080150	A549	lung:	n/a	n/a
37	CTCF	chr5:29093430-29093630	K562	blood:	n/a	n/a
38	CTCF	chr5:29080000-29080150	Caco-2	colon:	n/a	n/a
39	CTCF	chr5:29120220-29120313	Lung_OC	lung:	n/a	n/a
40	CTCF	chr5:29079950-29080147	MCF-7	breast:	n/a	n/a
41	CTCF	chr5:29079972-29080131	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:29079960-29080110	BE2_C	brain:	n/a	n/a
43	CTCF	chr5:29079881-29080161	K562	blood:	n/a	n/a
44	CTCF	chr5:29079825-29080198	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr5:29080000-29080150	RPTEC	kidney:	n/a	n/a
46	CTCF	chr5:29115340-29115490	BE2_C	brain:	n/a	n/a
47	CTCF	chr5:29079940-29080090	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr5:29080000-29080150	GM12871	blood:	n/a	n/a
49	CTCF	chr5:29126680-29126776	GM20000	blood:	n/a	n/a
50	CTCF	chr5:29079877-29080217	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:29128011-29128061	AG04450	lung:	fetal
2	chr5:29128011-29128061	U87	brain:	n/a
3	chr5:29128011-29128061	ovcar-3	ovarian:	n/a
4	chr5:29128011-29128061	HEEpiC	esophagus:	n/a
5	chr5:29128011-29128061	HEK293	kidney:	embryo
6	chr5:29128011-29128061	PANC-1	pancreas:	n/a
7	chr5:29128011-29128061	MCF10A-Er-Src	breast:	n/a
8	chr5:29128011-29128061	HRPEpiC	eye:	n/a
9	chr5:29128011-29128061	Caco-2	colon:	n/a
10	chr5:29128011-29128061	NHDF-neo	bronchial:	n/a
11	chr5:29128011-29128061	AG09319	gingival:	n/a
12	chr5:29128011-29128061	AG09309	skin:	n/a
13	chr5:29128011-29128061	K562	blood:	n/a
14	chr5:29128011-29128061	GM12878	blood:	n/a
15	chr5:29128011-29128061	PFSK-1	brain:	n/a
16	chr5:29128011-29128061	SKMC	muscle:	n/a
17	chr5:29128011-29128061	NT2-D1	testis:	n/a
18	chr5:29128011-29128061	HepG2	liver:	n/a
19	chr5:29128011-29128061	H1-hESC	embryonic stem cell:	embryo
20	chr5:29128011-29128061	GM06990	blood:	n/a
21	chr5:29128011-29128061	HCPEpiC	choroid plexus:	n/a
22	chr5:29128011-29128061	Jurkat	blood:	n/a
23	chr5:29128011-29128061	ECC-1	luminal epithelium:	n/a
24	chr5:29128011-29128061	ProgFib	skin:	n/a
25	chr5:29128011-29128061	SK-N-SH_RA	brain:	n/a
26	chr5:29128011-29128061	HCT-116	colon:	n/a
27	chr5:29128011-29128061	BJ	skin:	n/a
28	chr5:29128011-29128061	SK-N-SH	brain:	n/a
29	chr5:29128011-29128061	HMEC	breast:	n/a
30	chr5:29128011-29128061	HNPCEpiC	eye:	n/a
31	chr5:29128011-29128061	HIPEpiC	eye:	n/a
32	chr5:29128011-29128061	BE2_C	brain:	n/a
33	chr5:29128011-29128061	IMR90	lung:	fetal
34	chr5:29128011-29128061	HAEpiC	amniotic membrane:	n/a
35	chr5:29128011-29128061	MCF-7	breast:	n/a
36	chr5:29128011-29128061	HL-60	blood:	n/a
37	chr5:29128011-29128061	HCM	heart:	n/a
38	chr5:29128011-29128061	HCF	heart:	n/a
39	chr5:29128011-29128061	RPTEC	kidney:	n/a
40	chr5:29128011-29128061	NHBE	bronchial:	n/a
41	chr5:29128011-29128061	T-47D	breast:	n/a
42	chr5:29128011-29128061	GM19239	blood:	n/a
43	chr5:29128011-29128061	PrEC	prostate:	n/a
44	chr5:29128011-29128061	GM12891	blood:	n/a
45	chr5:29128011-29128061	AoSMC	blood vessel:	n/a
46	chr5:29128011-29128061	A549	lung:	n/a
47	chr5:29128011-29128061	NB4	blood:	n/a
48	chr5:29128011-29128061	SK-N-MC	brain:	n/a
49	chr5:29128011-29128061	Hepatocyte	liver:	n/a
50	chr5:29128011-29128061	AG10803	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:29050111..29052926-chr5:29053158..29054737,2	MCF-7	breast:
2	chr5:29059482..29062466-chr5:29065874..29068673,2	MCF-7	breast:
3	chr5:29050111..29052926-chr5:29053158..29054737,2	MCF-7	breast:
4	chr5:29059482..29062466-chr5:29065874..29068673,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH6-12	chr5:29104987-29105152	NONHSAT100833
2	lnc-CDH6-3	chr5:29066381-29070363	NR_109948
3	lnc-CDH6-3	chr5:29065946-29066069	ENSG00000249322
4	lnc-CDH6-3	chr5:29073007-29073330	NR_109948
5	lnc-CDH9-14	chr5:29105675-29106968	NONHSAT100834
6	lnc-CDH6-3	chr5:29066381-29070363	ENSG00000249322
7	lnc-CDH6-11	chr5:29106999-29107219	NONHSAT100835
8	lnc-CDH6-3	chr5:29065351-29065724	NR_109948
9	lnc-CDH6-3	chr5:29065946-29066069	NR_109948
10	lnc-CDH6-3	chr5:29065351-29065724	ENSG00000249322
11	lnc-CDH6-3	chr5:29073007-29073329	ENSG00000249322
12	lnc-CDH6-11	chr5:29126624-29126682	NONHSAT100835
13	lnc-CDH6-12	chr5:29105449-29105545	NONHSAT100833

Variant related genes	Relation type
ENSG00000252601	TF binding region
ENSG00000248687	TF binding region
ENSG00000270430	TF binding region
ENSG00000252601	CpG island
ENSG00000248687	CpG island
ENSG00000270430	CpG island
FOXD1	miRNA target sites
CBFB	miRNA target sites

Extended variants
information (count: 1097 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12153251	chr5:29051880-29051881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115744317	chr5:29051892-29051893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537523289	chr5:29051927-29051928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190367279	chr5:29051937-29051938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs537282171	chr5:29051949-29051950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs199910714	chr5:29051950-29051951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138616513	chr5:29051954-29051955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs573174306	chr5:29051985-29051986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs540660203	chr5:29051994-29051995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555811649	chr5:29052021-29052022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs555457845	chr5:29052068-29052069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576068508	chr5:29052071-29052072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182212557	chr5:29052095-29052096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs562683416	chr5:29052116-29052117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577867736	chr5:29052121-29052122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs372604423	chr5:29052168-29052169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116188659	chr5:29052172-29052173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142900558	chr5:29052187-29052188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527575594	chr5:29052222-29052223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187217909	chr5:29052232-29052233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535065113	chr5:29052273-29052274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs79663099	chr5:29052279-29052280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531342570	chr5:29052281-29052282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545734116	chr5:29052296-29052297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549423867	chr5:29052319-29052320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs516107	chr5:29052337-29052338	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs114260977	chr5:29052367-29052368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539449687	chr5:29052384-29052385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572680238	chr5:29052410-29052411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs115176523	chr5:29052423-29052424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567184430	chr5:29052490-29052491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs191698204	chr5:29052517-29052518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183528706	chr5:29052518-29052519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574042730	chr5:29052546-29052547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs517935	chr5:29052547-29052548	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs554204499	chr5:29052565-29052566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185630164	chr5:29052595-29052596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370595217	chr5:29052597-29052598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs602489	chr5:29052682-29052683	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs202188463	chr5:29052692-29052693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs519037	chr5:29052704-29052705	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs572349518	chr5:29052729-29052730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542546377	chr5:29052736-29052737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2644949	chr5:29052744-29052745	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs559298628	chr5:29052773-29052774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531160430	chr5:29052799-29052800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549481559	chr5:29052805-29052806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564674540	chr5:29052820-29052821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs520670	chr5:29052833-29052834	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs552000203	chr5:29052864-29052865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Kartagener syndrome	16639409	CNVD
Medulloblastoma	21979893	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Non-small cell lung cancer	20864512	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Multiple myeloma	17550852	CNVD
prenatal diagnosis	22389664	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Breast cancer	21858162	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Intellectual disability	22102821	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-small cell lung cancer	19010865	CNVD
Glioblastoma multiforme	22286061	CNVD
Compulsive disorder	18923513	CNVD
Epilepsy	18923513	CNVD
Prader-willi syndrome	18923513	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20409316	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	19553991	CNVD
Lung cancer	19553991	CNVD
Melanoma	19553991	CNVD
Ovarian cancer	19553991	CNVD
Prostate cancer	19553991	CNVD
Non-small cell lung cancer	17156491	CNVD
Breast cancer	17133270	CNVD
Bipolar disorder	19114987	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:29051200-29052400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr5:29052400-29054600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:29054200-29054400	Enhancers	Fetal Heart	heart
4	chr5:29054400-29054800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr5:29054400-29054800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:29054400-29054800	Flanking Active TSS	Fetal Heart	heart
7	chr5:29054400-29055000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr5:29054400-29055000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr5:29054600-29054800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:29054800-29055000	Enhancers	Fetal Heart	heart
11	chr5:29061400-29061800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:29067600-29067800	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr5:29067800-29068200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
14	chr5:29067800-29068200	Enhancers	Stomach Mucosa	stomach
15	chr5:29068000-29068400	Enhancers	Rectal Mucosa Donor 29	rectum
16	chr5:29068200-29068400	Active TSS	Rectal Mucosa Donor 31	rectum
17	chr5:29068400-29068600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
18	chr5:29068400-29068600	Weak transcription	Stomach Mucosa	stomach
19	chr5:29068400-29068800	Active TSS	Pancreatic Islets	Pancreatic Islet
20	chr5:29068400-29069200	Enhancers	Pancreas	Pancrea
21	chr5:29068400-29069200	Enhancers	HepG2	liver
22	chr5:29068400-29070200	Active TSS	Rectal Mucosa Donor 29	rectum
23	chr5:29068600-29069000	Active TSS	Rectal Mucosa Donor 31	rectum
24	chr5:29068600-29069000	Active TSS	Stomach Mucosa	stomach
25	chr5:29069000-29069200	Flanking Active TSS	Stomach Mucosa	stomach
26	chr5:29069000-29069400	Active TSS	Rectal Smooth Muscle	rectum
27	chr5:29069000-29069600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
28	chr5:29069200-29069600	Enhancers	Stomach Mucosa	stomach
29	chr5:29069600-29070800	Enhancers	Rectal Mucosa Donor 31	rectum
30	chr5:29077400-29078000	Enhancers	A549	lung
31	chr5:29077400-29078400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr5:29077400-29078400	Enhancers	Hela-S3	cervix
33	chr5:29077600-29078000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:29079200-29080000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr5:29085000-29085800	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr5:29090200-29090600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr5:29095400-29095800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:29095600-29096000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr5:29095600-29096000	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr5:29095800-29096200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr5:29097000-29097400	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr5:29102600-29103600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr5:29105600-29106600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr5:29105800-29106600	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:29106000-29106600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr5:29106200-29106600	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr5:29107000-29107400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr5:29109200-29111200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:29111200-29112200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:29112200-29112600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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