Variant report

Variant	nsv597721
Chromosome Location	chr5:28792713-28877116
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:341)
CpG islands
(count:489)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:341 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:28810841-28811178	K562	blood:	n/a	n/a
2	ARID3A	chr5:28862973-28863184	HepG2	liver:	n/a	n/a
3	BHLHE40	chr5:28816335-28816476	K562	blood:	n/a	n/a
4	BHLHE40	chr5:28808920-28809724	K562	blood:	n/a	n/a
5	BHLHE40	chr5:28810355-28810693	K562	blood:	n/a	chr5:28810481-28810497 chr5:28810394-28810410
6	BHLHE40	chr5:28814502-28814623	K562	blood:	n/a	n/a
7	BRCA1	chr5:28815213-28815234	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr5:28823373-28823651	K562	blood:	n/a	n/a
9	CBX3	chr5:28809015-28809399	K562	blood:	n/a	n/a
10	CBX3	chr5:28823321-28823730	K562	blood:	n/a	n/a
11	CCNT2	chr5:28809192-28810112	K562	blood:	n/a	n/a
12	CCNT2	chr5:28810313-28810825	K562	blood:	n/a	chr5:28810357-28810366
13	CCNT2	chr5:28816425-28816641	K562	blood:	n/a	n/a
14	CEBPB	chr5:28818678-28818966	HepG2	liver:	n/a	chr5:28818791-28818802
15	CEBPB	chr5:28809192-28809322	K562	blood:	n/a	n/a
16	CEBPB	chr5:28862960-28863277	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:28831182-28831450	H1-hESC	embryonic stem cell:	n/a	chr5:28831343-28831354
18	CEBPB	chr5:28834515-28834730	K562	blood:	n/a	chr5:28834587-28834598
19	CEBPB	chr5:28831210-28831505	K562	blood:	n/a	chr5:28831343-28831354
20	CEBPB	chr5:28818648-28818936	K562	blood:	n/a	chr5:28818791-28818802
21	CEBPB	chr5:28850602-28850862	K562	blood:	n/a	n/a
22	CEBPB	chr5:28834436-28834676	HepG2	liver:	n/a	chr5:28834587-28834598
23	CEBPB	chr5:28831177-28831503	A549	lung:	n/a	chr5:28831343-28831354
24	CEBPB	chr5:28831202-28831533	HepG2	liver:	n/a	chr5:28831343-28831354
25	CEBPB	chr5:28828802-28828896	A549	lung:	n/a	n/a
26	CHD2	chr5:28809029-28809592	K562	blood:	n/a	n/a
27	CHD2	chr5:28810617-28810817	K562	blood:	n/a	n/a
28	CHD2	chr5:28810281-28810330	K562	blood:	n/a	n/a
29	CTCF	chr5:28810972-28811116	Gliobla	brain:	n/a	chr5:28811027-28811040
30	CTCF	chr5:28810400-28810550	HVMF	connective:	n/a	n/a
31	CTCF	chr5:28810900-28811050	Hela-S3	cervix:	n/a	chr5:28811027-28811040
32	CTCF	chr5:28810900-28811050	SK-N-SH_RA	brain:	n/a	chr5:28811027-28811040
33	CTCF	chr5:28810930-28811187	K562	blood:	n/a	chr5:28811027-28811040
34	CTCF	chr5:28810960-28811110	RPTEC	kidney:	n/a	chr5:28811027-28811040
35	CTCF	chr5:28810274-28811313	K562	blood:	n/a	chr5:28811027-28811040
36	CTCF	chr5:28810940-28811090	A549	lung:	n/a	chr5:28811027-28811040
37	CTCF	chr5:28810960-28811110	HRPEpiC	eye:	n/a	chr5:28811027-28811040
38	CTCF	chr5:28810880-28811030	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr5:28810920-28811070	HepG2	liver:	n/a	chr5:28811027-28811040
40	CTCF	chr5:28814021-28814081	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr5:28810940-28811090	HEK293	kidney:	n/a	chr5:28811027-28811040
42	CTCF	chr5:28810941-28811090	SK-N-SH_RA	brain:	n/a	chr5:28811027-28811040
43	CTCF	chr5:28821150-28821198	GM20000	blood:	n/a	n/a
44	CTCF	chr5:28810960-28811115	MCF-7	breast:	n/a	chr5:28811027-28811040
45	CTCF	chr5:28810425-28810488	K562	blood:	n/a	n/a
46	CTCF	chr5:28861580-28861730	MCF-7	breast:	n/a	n/a
47	CTCF	chr5:28810640-28810790	HVMF	connective:	n/a	n/a
48	CTCF	chr5:28810960-28811110	HBMEC	blood vessel:	n/a	chr5:28811027-28811040
49	CTCF	chr5:28810980-28811130	HBMEC	blood vessel:	n/a	chr5:28811027-28811040
50	CTCF	chr5:28810925-28811163	K562	blood:	n/a	chr5:28811027-28811040

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:28810402-28810452	MCF10A-Er-Src	breast:	n/a
2	chr5:28810402-28810452	MCF10A-Er-Src	breast:	n/a
3	chr5:28810402-28810452	HCM	heart:	n/a
4	chr5:28809121-28809171	CMK	blood:	n/a
5	chr5:28810148-28810198	PFSK-1	brain:	n/a
6	chr5:28810402-28810452	HCT-116	colon:	n/a
7	chr5:28799238-28799288	HepG2	liver:	n/a
8	chr5:28799238-28799288	MCF10A-Er-Src	breast:	n/a
9	chr5:28810645-28810695	LNCaP	prostate:	n/a
10	chr5:28810645-28810695	K562	blood:	n/a
11	chr5:28809997-28810047	HPAEpiC	pulmonary alveolar:	n/a
12	chr5:28809997-28810047	HCPEpiC	choroid plexus:	n/a
13	chr5:28799238-28799288	A549	lung:	n/a
14	chr5:28810645-28810695	AoSMC	blood vessel:	n/a
15	chr5:28809997-28810047	ovcar-3	ovarian:	n/a
16	chr5:28809037-28809087	GM19239	blood:	n/a
17	chr5:28809622-28809672	GM12891	blood:	n/a
18	chr5:28799238-28799288	Hepatocyte	liver:	n/a
19	chr5:28810148-28810198	SK-N-SH_RA	brain:	n/a
20	chr5:28809997-28810047	BE2_C	brain:	n/a
21	chr5:28810402-28810452	GM06990	blood:	n/a
22	chr5:28810645-28810695	SK-N-SH_RA	brain:	n/a
23	chr5:28810402-28810452	SK-N-SH	brain:	n/a
24	chr5:28809622-28809672	PrEC	prostate:	n/a
25	chr5:28809037-28809087	ECC-1	luminal epithelium:	n/a
26	chr5:28809037-28809087	HRPEpiC	eye:	n/a
27	chr5:28810645-28810695	SKMC	muscle:	n/a
28	chr5:28810148-28810198	GM12878	blood:	n/a
29	chr5:28799238-28799288	NHDF-neo	bronchial:	n/a
30	chr5:28810148-28810198	AG04450	lung:	fetal
31	chr5:28809997-28810047	AoSMC	blood vessel:	n/a
32	chr5:28809121-28809171	BJ	skin:	n/a
33	chr5:28810148-28810198	SK-N-SH	brain:	n/a
34	chr5:28799238-28799288	AG04449	skin:	fetal
35	chr5:28810148-28810198	GM19239	blood:	n/a
36	chr5:28799238-28799288	MCF-7	breast:	n/a
37	chr5:28809997-28810047	HRCEpiC	kidney:	n/a
38	chr5:28809037-28809087	NHDF-neo	bronchial:	n/a
39	chr5:28809121-28809171	HRCEpiC	kidney:	n/a
40	chr5:28809997-28810047	ProgFib	skin:	n/a
41	chr5:28810645-28810695	HRCEpiC	kidney:	n/a
42	chr5:28810645-28810695	Jurkat	blood:	n/a
43	chr5:28809037-28809087	AG09309	skin:	n/a
44	chr5:28809121-28809171	HRE	kidney:	n/a
45	chr5:28809997-28810047	U87	brain:	n/a
46	chr5:28810402-28810452	HUVEC	blood vessel:	n/a
47	chr5:28799238-28799288	HPAEpiC	pulmonary alveolar:	n/a
48	chr5:28810645-28810695	BE2_C	brain:	n/a
49	chr5:28809997-28810047	HIPEpiC	eye:	n/a
50	chr5:28810402-28810452	SAEC	small airway:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:28808032..28811102-chr5:28813971..28817710,5	K562	blood:
2	chr5:28786798..28789363-chr5:28791647..28793398,2	K562	blood:
3	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
4	chr5:28811938..28814493-chr5:28819966..28823203,3	K562	blood:
5	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:
6	chr5:28765020..28766870-chr5:28809812..28812642,2	K562	blood:
7	chr5:28809387..28811298-chr5:29193650..29195834,2	K562	blood:
8	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
9	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
10	chr5:28836092..28838497-chr5:28839805..28842751,2	MCF-7	breast:
11	chr5:28827388..28830378-chr5:28832041..28834686,2	K562	blood:
12	chr5:28806282..28808048-chr5:28853726..28856182,2	K562	blood:
13	chr5:28848991..28851784-chr5:28856691..28858212,2	K562	blood:
14	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
15	chr5:28805163..28807259-chr5:28812094..28813798,2	K562	blood:
16	chr5:28806282..28808048-chr5:28853726..28856182,2	K562	blood:
17	chr5:28805922..28808420-chr5:28809202..28811186,4	K562	blood:
18	chr5:28826049..28828145-chr5:28828270..28829851,2	K562	blood:
19	chr5:28816134..28818756-chr5:28819776..28822041,3	K562	blood:
20	chr5:28811938..28814493-chr5:28819966..28823203,3	K562	blood:
21	chr5:28743630..28746249-chr5:28809920..28812616,2	K562	blood:
22	chr5:28823907..28826639-chr5:28834141..28835828,2	K562	blood:
23	chr5:28851055..28851753-chr7:86185395..86186230,2	MCF-7	breast:
24	chr5:28848991..28851784-chr5:28856691..28858212,2	K562	blood:
25	chr5:28836092..28838497-chr5:28839805..28842751,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CDH6-16	chr5:28808645-28809362	NONHSAT100821
2	lnc-CDH9-6	chr5:28809063-28809356	ENSG00000250453

No data

Variant related genes	Relation type
ENSG00000250453	TF binding region
ENSG00000270495	TF binding region
ENSG00000250453	CpG island
ENSG00000270495	CpG island
ENSG00000270495	chromatin interactions
ENSG00000250453	chromatin interactions

Extended variants
information (count: 751 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:751 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150489393	chr5:28805826-28805827	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs372063615	chr5:28805841-28805842	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs193037802	chr5:28805869-28805870	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs113129104	chr5:28805878-28805879	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs558096279	chr5:28805972-28805973	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs577719419	chr5:28805989-28805990	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs75724662	chr5:28805992-28805993	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs185834107	chr5:28806031-28806032	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555483576	chr5:28806053-28806054	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573500364	chr5:28806102-28806103	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544425655	chr5:28806107-28806108	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs554626887	chr5:28806114-28806115	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146480417	chr5:28806115-28806116	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12652228	chr5:28806119-28806120	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs533220339	chr5:28806159-28806160	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs544997477	chr5:28806164-28806165	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs560145291	chr5:28806169-28806170	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs527291703	chr5:28806187-28806188	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs549089010	chr5:28806217-28806218	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs560196932	chr5:28806218-28806219	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs529276039	chr5:28806230-28806231	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542608763	chr5:28806231-28806232	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs369825077	chr5:28806239-28806240	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs2548005	chr5:28806256-28806257	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs551186705	chr5:28806284-28806285	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs563109734	chr5:28806312-28806313	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs193192287	chr5:28806321-28806322	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs376383516	chr5:28806328-28806329	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184560921	chr5:28806332-28806333	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566521445	chr5:28806343-28806344	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs533980934	chr5:28806367-28806368	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555421789	chr5:28806414-28806415	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs188484449	chr5:28806443-28806444	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs72758537	chr5:28806489-28806490	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146665005	chr5:28806618-28806619	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs138773380	chr5:28806622-28806623	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs545246215	chr5:28806649-28806650	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs181341454	chr5:28806674-28806675	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs572067334	chr5:28806709-28806710	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs200288764	chr5:28806719-28806720	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566164333	chr5:28806733-28806734	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs542671915	chr5:28806762-28806763	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs16898167	chr5:28806780-28806781	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142746889	chr5:28806782-28806783	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549630885	chr5:28806828-28806829	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2554914	chr5:28806835-28806836	Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs569683999	chr5:28806861-28806862	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs377143232	chr5:28806867-28806868	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551657542	chr5:28806977-28806978	Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs368384422	chr5:28807006-28807007	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
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
Lung cancer	16740712	CNVD
Renal cell carcinoma	18194544	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:28806200-28813200	Active TSS	K562	blood
2	chr5:28807200-28807800	Enhancers	Hela-S3	cervix
3	chr5:28808400-28808600	Enhancers	Placenta	Placenta
4	chr5:28808400-28809200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:28808600-28810800	ZNF genes & repeats	Placenta	Placenta
6	chr5:28809000-28810600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:28809200-28809400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:28809400-28809800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr5:28809800-28810400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:28810800-28811400	Active TSS	Placenta	Placenta
11	chr5:28813200-28816600	Weak transcription	K562	blood
12	chr5:28822200-28822800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:28823200-28823800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
14	chr5:28825600-28827000	Enhancers	Fetal Heart	heart
15	chr5:28857600-28859800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:28859800-28860000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr5:28860000-28861600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:28861400-28862600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr5:28861600-28862000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:28862000-28862400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:28862200-28863000	Enhancers	HepG2	liver
22	chr5:28862400-28863600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:28863600-28864200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:28876800-28877400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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