Variant report

Variant	nsv882762
Chromosome Location	chr5:117499480-117706786
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	ATF1	chr5:117540315-117540489	K562	blood:	n/a	n/a
2	ATF2	chr5:117572082-117572630	GM12878	blood:	n/a	n/a
3	BACH1	chr5:117647727-117647789	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr5:117661095-117661110	K562	blood:	n/a	n/a
5	BATF	chr5:117620020-117620314	GM12878	blood:	n/a	n/a
6	BATF	chr5:117619990-117620322	GM12878	blood:	n/a	n/a
7	BHLHE40	chr5:117572143-117572515	GM12878	blood:	n/a	n/a
8	CBX3	chr5:117587070-117587579	HCT-116	colon:	n/a	n/a
9	CEBPB	chr5:117654150-117654245	A549	lung:	n/a	chr5:117654199-117654212
10	CEBPB	chr5:117670911-117671221	IMR90	lung:	n/a	chr5:117671060-117671071
11	CEBPB	chr5:117499546-117499809	A549	lung:	n/a	chr5:117499709-117499722 chr5:117499668-117499681 chr5:117499710-117499721 chr5:117499709-117499720
12	CEBPB	chr5:117581014-117581285	A549	lung:	n/a	chr5:117581160-117581171
13	CEBPB	chr5:117581079-117581323	HepG2	liver:	n/a	chr5:117581160-117581171
14	CEBPB	chr5:117689722-117689920	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr5:117578822-117579114	MCF-7	breast:	n/a	n/a
16	CEBPB	chr5:117510385-117510730	HepG2	liver:	n/a	chr5:117510553-117510562 chr5:117510551-117510564 chr5:117510553-117510562 chr5:117510551-117510562 chr5:117510553-117510562 chr5:117510552-117510563 chr5:117510553-117510562 chr5:117510551-117510564
17	CEBPB	chr5:117670914-117671189	A549	lung:	n/a	chr5:117671060-117671071
18	CEBPB	chr5:117510394-117510741	IMR90	lung:	n/a	chr5:117510553-117510562 chr5:117510551-117510564 chr5:117510553-117510562 chr5:117510551-117510562 chr5:117510553-117510562 chr5:117510552-117510563 chr5:117510553-117510562 chr5:117510551-117510564
19	CEBPB	chr5:117510395-117510722	A549	lung:	n/a	chr5:117510553-117510562 chr5:117510551-117510564 chr5:117510553-117510562 chr5:117510551-117510562 chr5:117510553-117510562 chr5:117510552-117510563 chr5:117510553-117510562 chr5:117510551-117510564
20	CEBPB	chr5:117670935-117671234	HepG2	liver:	n/a	chr5:117671060-117671071
21	CEBPB	chr5:117657498-117657812	IMR90	lung:	n/a	n/a
22	CEBPB	chr5:117581577-117581786	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:117627601-117627904	IMR90	lung:	n/a	chr5:117627762-117627773
24	CEBPB	chr5:117578882-117579162	H1-hESC	embryonic stem cell:	n/a	chr5:117579136-117579147 chr5:117579136-117579149 chr5:117579136-117579147 chr5:117579136-117579149 chr5:117579136-117579149
25	CEBPB	chr5:117499596-117499835	HepG2	liver:	n/a	chr5:117499709-117499722 chr5:117499668-117499681 chr5:117499710-117499721 chr5:117499709-117499720
26	CEBPB	chr5:117627685-117627933	HepG2	liver:	n/a	chr5:117627762-117627773
27	CEBPB	chr5:117581099-117581191	K562	blood:	n/a	chr5:117581160-117581171
28	CEBPB	chr5:117510392-117510721	H1-hESC	embryonic stem cell:	n/a	chr5:117510553-117510562 chr5:117510551-117510564 chr5:117510553-117510562 chr5:117510551-117510562 chr5:117510553-117510562 chr5:117510552-117510563 chr5:117510553-117510562 chr5:117510551-117510564
29	CHD2	chr5:117572190-117572292	GM12878	blood:	n/a	n/a
30	CTCF	chr5:117591187-117591238	MCF-7	breast:	n/a	n/a
31	CTCF	chr5:117656780-117656930	A549	lung:	n/a	n/a
32	CTCF	chr5:117523300-117523450	Caco-2	colon:	n/a	chr5:117523337-117523355 chr5:117523332-117523353
33	CTCF	chr5:117656819-117656867	HepG2	liver:	n/a	n/a
34	CTCF	chr5:117582920-117583070	HEK293	kidney:	n/a	n/a
35	CTCF	chr5:117589580-117589730	AG09319	gingival:	n/a	n/a
36	CTCF	chr5:117620029-117620053	Lung_OC	lung:	n/a	n/a
37	CTCF	chr5:117632260-117632410	GM12878	blood:	n/a	n/a
38	CTCF	chr5:117523321-117523359	GM12878	blood:	n/a	chr5:117523337-117523355 chr5:117523332-117523353
39	CTCF	chr5:117591150-117591253	MCF-7	breast:	n/a	n/a
40	CTCF	chr5:117501960-117502110	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr5:117591175-117591229	MCF-7	breast:	n/a	n/a
42	CTCF	chr5:117580760-117580910	HMF	breast:	n/a	n/a
43	CTCF	chr5:117589600-117589750	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr5:117656680-117656830	RPTEC	kidney:	n/a	n/a
45	CUX1	chr5:117702320-117702322	K562	blood:	n/a	n/a
46	E2F4	chr5:117522783-117523016	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr5:117526329-117526792	MCF10A-Er-Src	breast:	n/a	chr5:117526524-117526535
48	E2F4	chr5:117577312-117577421	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr5:117507304-117507542	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr5:117525029-117525234	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:117645500-117645550	Hela-S3	cervix:	n/a
2	chr5:117543401-117543451	RPTEC	kidney:	n/a
3	chr5:117645500-117645550	Hela-S3	cervix:	n/a
4	chr5:117543401-117543451	RPTEC	kidney:	n/a
5	chr5:117543966-117544016	NHBE	bronchial:	n/a
6	chr5:117645500-117645550	BJ	skin:	n/a
7	chr5:117645500-117645550	HRCEpiC	kidney:	n/a
8	chr5:117645500-117645550	GM12892	blood:	n/a
9	chr5:117645500-117645550	A549	lung:	n/a
10	chr5:117645500-117645550	SAEC	small airway:	n/a
11	chr5:117532041-117532091	ProgFib	skin:	n/a
12	chr5:117617841-117617891	K562	blood:	n/a
13	chr5:117543681-117543731	PFSK-1	brain:	n/a
14	chr5:117532041-117532091	HL-60	blood:	n/a
15	chr5:117645500-117645550	K562	blood:	n/a
16	chr5:117645500-117645550	ECC-1	luminal epithelium:	n/a
17	chr5:117543966-117544016	HNPCEpiC	eye:	n/a
18	chr5:117630841-117630891	Hela-S3	cervix:	n/a
19	chr5:117645500-117645550	RPTEC	kidney:	n/a
20	chr5:117618514-117618564	GM19239	blood:	n/a
21	chr5:117617841-117617891	MCF10A-Er-Src	breast:	n/a
22	chr5:117645500-117645550	NHDF-neo	bronchial:	n/a
23	chr5:117645500-117645550	HAEpiC	amniotic membrane:	n/a
24	chr5:117630841-117630891	NT2-D1	testis:	n/a
25	chr5:117543401-117543451	NHDF-neo	bronchial:	n/a
26	chr5:117618514-117618564	AG10803	skin:	n/a
27	chr5:117630841-117630891	SK-N-SH	brain:	n/a
28	chr5:117630841-117630891	ECC-1	luminal epithelium:	n/a
29	chr5:117543966-117544016	IMR90	lung:	fetal
30	chr5:117543401-117543451	SK-N-MC	brain:	n/a
31	chr5:117543401-117543451	Caco-2	colon:	n/a
32	chr5:117645500-117645550	HPAEpiC	pulmonary alveolar:	n/a
33	chr5:117543401-117543451	HL-60	blood:	n/a
34	chr5:117645500-117645550	HCPEpiC	choroid plexus:	n/a
35	chr5:117618514-117618564	PFSK-1	brain:	n/a
36	chr5:117630841-117630891	MCF10A-Er-Src	breast:	n/a
37	chr5:117532041-117532091	CMK	blood:	n/a
38	chr5:117532041-117532091	HUVEC	blood vessel:	n/a
39	chr5:117617841-117617891	NB4	blood:	n/a
40	chr5:117617841-117617891	HCPEpiC	choroid plexus:	n/a
41	chr5:117630841-117630891	GM06990	blood:	n/a
42	chr5:117543401-117543451	HAEpiC	amniotic membrane:	n/a
43	chr5:117543966-117544016	BE2_C	brain:	n/a
44	chr5:117618514-117618564	SK-N-SH	brain:	n/a
45	chr5:117630841-117630891	IMR90	lung:	fetal
46	chr5:117543681-117543731	NHBE	bronchial:	n/a
47	chr5:117645500-117645550	ProgFib	skin:	n/a
48	chr5:117543966-117544016	Jurkat	blood:	n/a
49	chr5:117618514-117618564	A549	lung:	n/a
50	chr5:117532041-117532091	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:117564627..117566245-chr5:117569681..117572148,3	MCF-7	breast:
2	chr5:117499273..117500993-chr5:117501863..117504364,2	MCF-7	breast:
3	chr5:117584101..117585840-chr5:117595534..117597054,2	MCF-7	breast:
4	chr5:116790798..116792666-chr5:117532580..117535246,2	MCF-7	breast:
5	chr5:117662110..117664653-chr5:117666113..117667800,2	MCF-7	breast:
6	chr5:117501309..117503811-chr5:117506709..117509666,2	MCF-7	breast:
7	chr5:117607162..117609228-chr5:117612634..117615234,2	MCF-7	breast:
8	chr5:117501309..117503811-chr5:117506709..117509666,2	MCF-7	breast:
9	chr5:117564627..117566245-chr5:117569681..117572148,3	MCF-7	breast:
10	chr5:117662110..117664653-chr5:117666113..117667800,2	MCF-7	breast:
11	chr5:117499273..117500993-chr5:117501863..117504364,2	MCF-7	breast:
12	chr5:117584101..117585840-chr5:117595534..117597054,2	MCF-7	breast:
13	chr5:117701000..117704455-chr5:117706374..117709409,3	MCF-7	breast:
14	chr5:117573331..117574961-chr5:117577405..117579413,2	K562	blood:
15	chr5:117502319..117505069-chr5:118158604..118161182,2	K562	blood:
16	chr14:81686696..81687602-chr5:117664674..117665194,3	HCT-116	colon:
17	chr5:117607162..117609228-chr5:117612634..117615234,2	MCF-7	breast:
18	chr5:117701000..117704455-chr5:117706374..117709409,3	MCF-7	breast:
19	chr5:117573331..117574961-chr5:117577405..117579413,2	K562	blood:
20	chr5:117679557..117681634-chr5:117711905..117714203,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DMXL1-4	chr5:117523162-117523286	XLOC_004524
2	lnc-DMXL1-9	chr5:117646168-117646321	ucscGeneNc_uc003krz_2
3	lnc-DTWD2-3	chr5:117686661-117687202	NONHSAT103396
4	lnc-DMXL1-4	chr5:117523161-117523286	XLOC_004524
5	lnc-DTWD2-3	chr5:117686667-117687202	NR_104610
6	lnc-DMXL1-4	chr5:117542415-117542666	XLOC_004524
7	lnc-DMXL1-4	chr5:117601049-117601757	NR_104997
8	lnc-DMXL1-4	chr5:117542415-117542551	XLOC_004524
9	lnc-DMXL1-4	chr5:117542415-117542631	XLOC_004524
10	lnc-DMXL1-4	chr5:117523160-117523290	XLOC_004524
11	lnc-DMXL1-4	chr5:117601049-117601730	XLOC_004524
12	lnc-DMXL1-9	chr5:117647307-117648354	ucscGeneNc_uc003krz_2

Variant related genes	Relation type
ENSG00000250427	TF binding region
ENSG00000249797	TF binding region
ENSG00000250427	CpG island
ENSG00000249797	CpG island
ENSG00000248663	chromatin interactions
ENSG00000165417	chromatin interactions

Extended variants
information (count: 4081 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4081 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146850451	chr5:117507821-117507822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183622927	chr5:117507862-117507863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs555542076	chr5:117507897-117507898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs568471917	chr5:117507901-117507902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374757071	chr5:117507920-117507921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189209120	chr5:117507993-117507994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555920882	chr5:117508010-117508011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539902053	chr5:117508025-117508026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs553315757	chr5:117508032-117508033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs13187513	chr5:117508036-117508037	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs17430818	chr5:117508047-117508048	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs373093542	chr5:117508094-117508095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs199733009	chr5:117508096-117508097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140639499	chr5:117508104-117508105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113067794	chr5:117508105-117508106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562709513	chr5:117508119-117508120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564093241	chr5:117508130-117508131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577691591	chr5:117508145-117508146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540295533	chr5:117508179-117508180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148886256	chr5:117518064-117518065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs532429500	chr5:117518138-117518139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368042013	chr5:117518139-117518140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143540100	chr5:117518153-117518154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371806380	chr5:117518162-117518163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146831615	chr5:117518179-117518180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552558694	chr5:117518182-117518183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs572751714	chr5:117518284-117518285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541458672	chr5:117518339-117518340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375148252	chr5:117518389-117518390	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs147641023	chr5:117518423-117518424	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs10066475	chr5:117518432-117518433	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs548279091	chr5:117518879-117518880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs376818276	chr5:117518927-117518928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs73246751	chr5:117518968-117518969	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs550783882	chr5:117519018-117519019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570676606	chr5:117519088-117519089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs11739202	chr5:117519113-117519114	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs145671772	chr5:117519137-117519138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138220017	chr5:117519138-117519139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186386610	chr5:117519185-117519186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs141824475	chr5:117519196-117519197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369102589	chr5:117519280-117519281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs55955007	chr5:117519341-117519342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs56210549	chr5:117519344-117519345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575322990	chr5:117519348-117519349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544292652	chr5:117519355-117519356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190493668	chr5:117519361-117519362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77837906	chr5:117519397-117519398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540424109	chr5:117519406-117519407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs113969018	chr5:117519428-117519429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Breast cancer	21509527	CNVD
Autism	22543975	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:117507800-117508200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:117518000-117518200	Enhancers	Fetal Lung	lung
3	chr5:117518000-117518400	Enhancers	Brain Germinal Matrix	brain
4	chr5:117518800-117520200	Weak transcription	Fetal Lung	lung
5	chr5:117520200-117520600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr5:117520200-117521400	Enhancers	Fetal Lung	lung
7	chr5:117520400-117521000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr5:117520600-117521000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr5:117520600-117521200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr5:117520800-117521200	Enhancers	Ovary	ovary
11	chr5:117523000-117523400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:117525200-117525800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr5:117529000-117529800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr5:117529400-117529800	Enhancers	Colon Smooth Muscle	Colon
15	chr5:117529800-117530800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr5:117529800-117531000	Weak transcription	Colon Smooth Muscle	Colon
17	chr5:117530600-117531400	Enhancers	Liver	Liver
18	chr5:117530600-117532200	Enhancers	Rectal Smooth Muscle	rectum
19	chr5:117530800-117531000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr5:117530800-117531000	Active TSS	Duodenum Smooth Muscle	Duodenum
21	chr5:117530800-117531200	Active TSS	Right Atrium	heart
22	chr5:117530800-117531400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr5:117531000-117531200	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr5:117531000-117531200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr5:117531000-117531200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
26	chr5:117531000-117531600	Enhancers	Colon Smooth Muscle	Colon
27	chr5:117531200-117531400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr5:117531200-117531400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr5:117531200-117531800	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr5:117531200-117534200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr5:117531400-117534800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr5:117531800-117533000	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr5:117531800-117533200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr5:117532000-117532800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr5:117532200-117533600	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr5:117532800-117533000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:117532800-117535000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr5:117533000-117535200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
39	chr5:117533000-117535600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr5:117533200-117535200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr5:117533600-117534800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr5:117534200-117534600	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr5:117534600-117536200	Enhancers	HUES48 Cell Line	embryonic stem cell
44	chr5:117534800-117535600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr5:117534800-117536000	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr5:117535000-117536600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr5:117535200-117535600	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr5:117535200-117536600	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr5:117535600-117536000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr5:117535600-117541400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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