Variant report

Variant	nsv883049
Chromosome Location	chr5:152159184-152399894
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	BATF	chr5:152203895-152204173	GM12878	blood:	n/a	chr5:152204083-152204093 chr5:152204082-152204093
2	BATF	chr5:152203943-152204249	GM12878	blood:	n/a	chr5:152204083-152204093 chr5:152204082-152204093
3	CEBPB	chr5:152162013-152162227	HepG2	liver:	n/a	chr5:152162079-152162090
4	CEBPB	chr5:152250975-152251178	A549	lung:	n/a	chr5:152251072-152251083
5	CEBPB	chr5:152332005-152332335	IMR90	lung:	n/a	chr5:152332151-152332162
6	CEBPB	chr5:152332003-152332331	HepG2	liver:	n/a	chr5:152332151-152332162
7	CEBPB	chr5:152364302-152364664	A549	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
8	CEBPB	chr5:152336837-152337081	IMR90	lung:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
9	CEBPB	chr5:152342360-152342457	HepG2	liver:	n/a	n/a
10	CEBPB	chr5:152374246-152374450	HepG2	liver:	n/a	chr5:152374363-152374374
11	CEBPB	chr5:152336825-152337119	Hela-S3	cervix:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
12	CEBPB	chr5:152336825-152337124	A549	lung:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
13	CEBPB	chr5:152397697-152398071	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr5:152397708-152398049	HepG2	liver:	n/a	n/a
15	CEBPB	chr5:152336869-152337086	K562	blood:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
16	CEBPB	chr5:152336872-152337072	MCF-7	breast:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
17	CEBPB	chr5:152364298-152364669	IMR90	lung:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
18	CEBPB	chr5:152397695-152398058	IMR90	lung:	n/a	n/a
19	CEBPB	chr5:152332064-152332264	H1-hESC	embryonic stem cell:	n/a	chr5:152332151-152332162
20	CEBPB	chr5:152364398-152364644	K562	blood:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
21	CEBPB	chr5:152250941-152251175	HepG2	liver:	n/a	chr5:152251072-152251083
22	CEBPB	chr5:152397710-152398025	A549	lung:	n/a	n/a
23	CEBPB	chr5:152161963-152162188	A549	lung:	n/a	chr5:152162079-152162090
24	CEBPB	chr5:152333400-152333656	HepG2	liver:	n/a	n/a
25	CEBPB	chr5:152336818-152337158	HepG2	liver:	n/a	chr5:152337064-152337072 chr5:152336963-152336974 chr5:152336983-152336994
26	CEBPB	chr5:152332017-152332290	A549	lung:	n/a	chr5:152332151-152332162
27	CEBPB	chr5:152364298-152364651	HepG2	liver:	n/a	chr5:152364474-152364487 chr5:152364474-152364485 chr5:152364476-152364485 chr5:152364476-152364487
28	CEBPB	chr5:152397705-152398057	K562	blood:	n/a	n/a
29	CHD1	chr5:152191653-152191853	GM12878	blood:	n/a	n/a
30	CHD2	chr5:152196898-152196953	GM12878	blood:	n/a	n/a
31	CTCF	chr5:152315496-152315559	Lung_OC	lung:	n/a	n/a
32	CTCF	chr5:152285160-152285310	GM06990	blood:	n/a	n/a
33	CTCF	chr5:152204360-152204510	GM06990	blood:	n/a	n/a
34	CTCF	chr5:152302720-152302870	GM12869	blood:	n/a	n/a
35	CTCF	chr5:152385240-152385390	HMEC	breast:	n/a	n/a
36	CTCF	chr5:152167320-152167470	GM12864	blood:	n/a	n/a
37	CTCF	chr5:152352540-152352690	GM12873	blood:	n/a	n/a
38	CTCF	chr5:152309660-152309810	NHEK	skin:	n/a	n/a
39	CTCF	chr5:152385260-152385410	HMEC	breast:	n/a	n/a
40	CTCF	chr5:152200693-152200727	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr5:152227793-152227902	Lung_OC	lung:	n/a	n/a
42	CTCF	chr5:152205160-152205310	GM06990	blood:	n/a	n/a
43	CTCF	chr5:152385260-152385410	MCF-7	breast:	n/a	n/a
44	CTCF	chr5:152205120-152205270	HEK293	kidney:	n/a	n/a
45	CTCF	chr5:152265726-152265861	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr5:152204760-152204910	GM12864	blood:	n/a	n/a
47	CTCF	chr5:152204940-152205090	GM12864	blood:	n/a	n/a
48	CTCF	chr5:152205120-152205390	NHEK	skin:	n/a	n/a
49	CTCF	chr5:152283080-152283138	GM13976	blood:	n/a	n/a
50	CTCF	chr5:152383240-152383390	GM12869	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:152352697-152352747	AG04450	lung:	fetal
2	chr5:152352697-152352747	AG04450	lung:	fetal
3	chr5:152352468-152352518	GM12878	blood:	n/a
4	chr5:152234077-152234127	IMR90	lung:	fetal
5	chr5:152309662-152309712	HAEpiC	amniotic membrane:	n/a
6	chr5:152352697-152352747	GM19239	blood:	n/a
7	chr5:152279040-152279090	HUVEC	blood vessel:	n/a
8	chr5:152279040-152279090	PFSK-1	brain:	n/a
9	chr5:152374989-152375039	GM12891	blood:	n/a
10	chr5:152352468-152352518	HCT-116	colon:	n/a
11	chr5:152234077-152234127	MCF-7	breast:	n/a
12	chr5:152352697-152352747	SK-N-SH	brain:	n/a
13	chr5:152352468-152352518	AG04449	skin:	fetal
14	chr5:152374989-152375039	HIPEpiC	eye:	n/a
15	chr5:152234077-152234127	BE2_C	brain:	n/a
16	chr5:152374989-152375039	HRE	kidney:	n/a
17	chr5:152309662-152309712	LNCaP	prostate:	n/a
18	chr5:152352697-152352747	NB4	blood:	n/a
19	chr5:152352468-152352518	HL-60	blood:	n/a
20	chr5:152352697-152352747	NT2-D1	testis:	n/a
21	chr5:152234077-152234127	SKMC	muscle:	n/a
22	chr5:152376702-152376752	NT2-D1	testis:	n/a
23	chr5:152309662-152309712	HUVEC	blood vessel:	n/a
24	chr5:152376702-152376752	NH-A	brain:	n/a
25	chr5:152352468-152352518	HRPEpiC	eye:	n/a
26	chr5:152309662-152309712	AG09319	gingival:	n/a
27	chr5:152352697-152352747	BE2_C	brain:	n/a
28	chr5:152352468-152352518	A549	lung:	n/a
29	chr5:152352697-152352747	Hepatocyte	liver:	n/a
30	chr5:152309662-152309712	HPAEpiC	pulmonary alveolar:	n/a
31	chr5:152352697-152352747	PrEC	prostate:	n/a
32	chr5:152374989-152375039	Hela-S3	cervix:	n/a
33	chr5:152376702-152376752	U87	brain:	n/a
34	chr5:152309662-152309712	MCF10A-Er-Src	breast:	n/a
35	chr5:152376702-152376752	MCF10A-Er-Src	breast:	n/a
36	chr5:152352468-152352518	MCF10A-Er-Src	breast:	n/a
37	chr5:152376702-152376752	AG09319	gingival:	n/a
38	chr5:152374989-152375039	PrEC	prostate:	n/a
39	chr5:152234077-152234127	SAEC	small airway:	n/a
40	chr5:152279040-152279090	HCM	heart:	n/a
41	chr5:152374989-152375039	AG04450	lung:	fetal
42	chr5:152309662-152309712	NHBE	bronchial:	n/a
43	chr5:152309662-152309712	ovcar-3	ovarian:	n/a
44	chr5:152234077-152234127	HNPCEpiC	eye:	n/a
45	chr5:152352468-152352518	RPTEC	kidney:	n/a
46	chr5:152376702-152376752	K562	blood:	n/a
47	chr5:152234077-152234127	HepG2	liver:	n/a
48	chr5:152234077-152234127	PrEC	prostate:	n/a
49	chr5:152309662-152309712	ECC-1	luminal epithelium:	n/a
50	chr5:152376702-152376752	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr5:152247556..152250256-chr5:152250400..152252605,2	K562	blood:
2	chr5:152180042..152181863-chr5:152182036..152183664,2	MCF-7	breast:
3	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:
4	chr5:152177163..152179872-chr5:152182805..152185020,2	K562	blood:
5	chr5:152354651..152356569-chr5:152358890..152361095,2	K562	blood:
6	chr5:152177163..152179872-chr5:152182805..152185020,2	K562	blood:
7	chr5:152247556..152250256-chr5:152250400..152252605,2	K562	blood:
8	chr5:152180042..152181863-chr5:152182036..152183664,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMUR2-1	chr5:152264987-152265188	XLOC_005056
2	lnc-NMUR2-1	chr5:152351574-152351793	XLOC_005056
3	lnc-NMUR2-1	chr5:152318398-152318551	XLOC_005056
4	lnc-NMUR2-1	chr5:152345801-152345894	ENSG00000249484
5	lnc-NMUR2-1	chr5:152199805-152199860	ENSG00000249484
6	lnc-NMUR2-1	chr5:152351274-152351346	XLOC_005056
7	lnc-NMUR2-1	chr5:152345801-152345909	XLOC_005056
8	lnc-NMUR2-1	chr5:152318398-152318551	ENSG00000249484.4
9	lnc-NMUR2-1	chr5:152352638-152352763	XLOC_005056
10	lnc-NMUR2-1	chr5:152351274-152351346	ENSG00000249484.4
11	lnc-NMUR2-1	chr5:152199805-152199860	XLOC_005056
12	lnc-NMUR2-1	chr5:152352638-152352763	ENSG00000249484.4
13	lnc-NMUR2-1	chr5:152345801-152345894	ENSG00000249484.4
14	lnc-NMUR2-1	chr5:152351574-152351793	ENSG00000249484.4
15	lnc-NMUR2-1	chr5:152351274-152351343	XLOC_005056
16	lnc-NMUR2-1	chr5:152346653-152346666	ENSG00000249484.4
17	lnc-NMUR2-1	chr5:152345801-152345894	XLOC_005056
18	lnc-NMUR2-1	chr5:152351826-152351909	ENSG00000249484
19	lnc-NMUR2-1	chr5:152345801-152345894	XLOC_005056
20	lnc-NMUR2-1	chr5:152351826-152351909	XLOC_005056

Variant related genes	Relation type
ENSG00000249484	TF binding region
ENSG00000249484	CpG island
DPYSL2	miRNA target sites
DICER1	miRNA target sites
FAM122A	miRNA target sites

Extended variants
information (count: 3019 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3019 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6579967	chr5:152165010-152165011	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543814568	chr5:152165064-152165065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs4132712	chr5:152165088-152165089	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs4132713	chr5:152165129-152165130	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs200411282	chr5:152165137-152165138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528356799	chr5:152165139-152165140	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4484413	chr5:152165140-152165141	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs34966881	chr5:152165146-152165147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs187076006	chr5:152165151-152165152	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370776339	chr5:152165194-152165195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35815566	chr5:152165254-152165255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs149506732	chr5:152165316-152165317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557436981	chr5:152165317-152165318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs577021026	chr5:152165337-152165338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544445010	chr5:152165390-152165391	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs574614635	chr5:152165400-152165401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542143742	chr5:152165454-152165455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs563024489	chr5:152165482-152165483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75777158	chr5:152165515-152165516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs191940880	chr5:152165536-152165537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs547075597	chr5:152165541-152165542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560364324	chr5:152165554-152165555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527688598	chr5:152165556-152165557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs565580475	chr5:152165558-152165559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115467457	chr5:152165585-152165586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs144069124	chr5:152165589-152165590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527528569	chr5:152165627-152165628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73799121	chr5:152165643-152165644	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs146276046	chr5:152165678-152165679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs552691157	chr5:152165705-152165706	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547386984	chr5:152165731-152165732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs112721476	chr5:152165778-152165779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74366734	chr5:152165791-152165792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs35027049	chr5:152181604-152181605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556619812	chr5:152181704-152181705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11959469	chr5:152181709-152181710	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs34719342	chr5:152181730-152181731	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs116194011	chr5:152181735-152181736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546516983	chr5:152181766-152181767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs527419713	chr5:152181768-152181769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564733747	chr5:152181814-152181815	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572242836	chr5:152181869-152181870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372755226	chr5:152181895-152181896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187742448	chr5:152181899-152181900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531521966	chr5:152181914-152181915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs147799239	chr5:152181915-152181916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs116368477	chr5:152181951-152181952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528935430	chr5:152181958-152181959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs547516253	chr5:152181979-152181980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114543069	chr5:152181983-152181984	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	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
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Renal cell carcinoma	18592004	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	17603634	CNVD
Crohn''s disease	20106866	CNVD
Breast cancer	20409316	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Deafness	19353646	CNVD
Developmental delay	19353646	CNVD
dysmorphism	19353646	CNVD
feeding difficulties	19353646	CNVD
strabismus	19353646	CNVD
Gastric adenocarcinoma	19115996	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:152165000-152165800	Enhancers	Esophagus	oesophagus
2	chr5:152181600-152182200	Enhancers	Fetal Lung	lung
3	chr5:152183800-152184200	Enhancers	Fetal Kidney	kidney
4	chr5:152189200-152191800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr5:152191200-152192600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr5:152191600-152191800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr5:152191600-152192800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:152191800-152192000	Enhancers	Fetal Brain Male	brain
9	chr5:152191800-152192600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:152191800-152192800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:152192000-152193000	Weak transcription	Fetal Brain Male	brain
12	chr5:152192400-152194000	Enhancers	Brain Germinal Matrix	brain
13	chr5:152192800-152196000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:152193000-152193400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr5:152193000-152193400	Enhancers	Fetal Brain Male	brain
16	chr5:152193000-152193400	Enhancers	Stomach Smooth Muscle	stomach
17	chr5:152193200-152193600	Enhancers	Brain Substantia Nigra	brain
18	chr5:152193400-152195800	Weak transcription	Fetal Brain Male	brain
19	chr5:152194000-152197800	Weak transcription	Brain Germinal Matrix	brain
20	chr5:152195800-152198000	Enhancers	Fetal Brain Male	brain
21	chr5:152196000-152196200	Enhancers	Fetal Brain Female	brain
22	chr5:152196000-152196800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:152196200-152196400	Flanking Active TSS	Fetal Brain Female	brain
24	chr5:152196400-152196800	Active TSS	Fetal Brain Female	brain
25	chr5:152196800-152197000	Flanking Active TSS	Fetal Brain Female	brain
26	chr5:152196800-152198600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:152197000-152198000	Enhancers	Fetal Brain Female	brain
28	chr5:152197400-152198000	Enhancers	Fetal Kidney	kidney
29	chr5:152197800-152198200	Enhancers	Brain Germinal Matrix	brain
30	chr5:152198600-152199200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:152198800-152199800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr5:152199200-152199600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:152213000-152213200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:152213200-152218000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr5:152217800-152218600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr5:152218000-152218200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr5:152218000-152218400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:152218000-152218600	Active TSS	Liver	Liver
39	chr5:152218000-152218800	Enhancers	Colon Smooth Muscle	Colon
40	chr5:152231400-152232000	Enhancers	Stomach Mucosa	stomach
41	chr5:152232000-152235200	Weak transcription	Stomach Mucosa	stomach
42	chr5:152232800-152235200	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr5:152233000-152233400	Enhancers	H9 Cell Line	embryonic stem cell
44	chr5:152233000-152233800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr5:152233000-152234600	Enhancers	H1 Cell Line	embryonic stem cell
46	chr5:152233000-152235400	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr5:152233000-152236200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr5:152233200-152235600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr5:152233200-152235800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr5:152233400-152233800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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