Variant report

Variant	nsv1020195
Chromosome Location	chr5:104330773-104510970
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	chr5:104369169-104369636	K562	blood:	n/a	n/a
2	ATF1	chr5:104370024-104370214	K562	blood:	n/a	n/a
3	ATF1	chr5:104475478-104475496	K562	blood:	n/a	n/a
4	ATF1	chr5:104373680-104373755	K562	blood:	n/a	n/a
5	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr5:104369418-104369675	K562	blood:	n/a	n/a
7	BRCA1	chr5:104393511-104393580	GM12878	blood:	n/a	n/a
8	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
9	CBX3	chr5:104393078-104393434	K562	blood:	n/a	n/a
10	CBX3	chr5:104370642-104370939	K562	blood:	n/a	n/a
11	CBX3	chr5:104393083-104393385	K562	blood:	n/a	n/a
12	CBX3	chr5:104428357-104428592	K562	blood:	n/a	n/a
13	CCNT2	chr5:104370115-104370461	K562	blood:	n/a	n/a
14	CCNT2	chr5:104369421-104369754	K562	blood:	n/a	chr5:104369561-104369581
15	CEBPB	chr5:104475581-104475765	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr5:104510170-104510370	K562	blood:	n/a	chr5:104510228-104510239
17	CEBPB	chr5:104437342-104437690	HepG2	liver:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
18	CEBPB	chr5:104510149-104510395	H1-hESC	embryonic stem cell:	n/a	chr5:104510228-104510239
19	CEBPB	chr5:104369982-104370331	K562	blood:	n/a	n/a
20	CEBPB	chr5:104437422-104437706	ECC-1	luminal epithelium:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
21	CEBPB	chr5:104423406-104423707	A549	lung:	n/a	chr5:104423566-104423577
22	CEBPB	chr5:104369173-104369683	K562	blood:	n/a	chr5:104369288-104369301
23	CEBPB	chr5:104485721-104485921	K562	blood:	n/a	n/a
24	CEBPB	chr5:104437340-104437708	ECC-1	luminal epithelium:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
25	CEBPB	chr5:104370063-104370467	A549	lung:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
26	CEBPB	chr5:104370108-104370517	ECC-1	luminal epithelium:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
27	CEBPB	chr5:104370011-104370528	HepG2	liver:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
28	CEBPB	chr5:104391916-104392212	A549	lung:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
29	CEBPB	chr5:104432081-104432193	HepG2	liver:	n/a	n/a
30	CEBPB	chr5:104423448-104423672	K562	blood:	n/a	chr5:104423566-104423577
31	CEBPB	chr5:104369987-104370554	Hela-S3	cervix:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
32	CEBPB	chr5:104484312-104484512	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr5:104423410-104423746	IMR90	lung:	n/a	chr5:104423566-104423577
34	CEBPB	chr5:104475627-104475670	K562	blood:	n/a	n/a
35	CEBPB	chr5:104373830-104373968	HepG2	liver:	n/a	n/a
36	CEBPB	chr5:104437246-104437795	MCF-7	breast:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
37	CEBPB	chr5:104437342-104437688	Hela-S3	cervix:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
38	CEBPB	chr5:104423402-104423724	HepG2	liver:	n/a	chr5:104423566-104423577
39	CEBPB	chr5:104485759-104485906	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr5:104391872-104392206	HepG2	liver:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
41	CEBPB	chr5:104475600-104475772	HepG2	liver:	n/a	n/a
42	CEBPB	chr5:104369993-104370525	K562	blood:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
43	CEBPB	chr5:104334377-104334640	K562	blood:	n/a	chr5:104334524-104334537
44	CEBPB	chr5:104437345-104437662	A549	lung:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
45	CEBPB	chr5:104437313-104437709	MCF-7	breast:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
46	CEBPB	chr5:104370069-104370367	H1-hESC	embryonic stem cell:	n/a	chr5:104370351-104370364 chr5:104370351-104370362 chr5:104370353-104370364
47	CEBPB	chr5:104437346-104437647	K562	blood:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
48	CEBPB	chr5:104437386-104437647	IMR90	lung:	n/a	chr5:104437523-104437534 chr5:104437523-104437532 chr5:104437523-104437532 chr5:104437521-104437534 chr5:104437521-104437532 chr5:104437523-104437532 chr5:104437523-104437532
49	CEBPD	chr5:104369352-104369808	K562	blood:	n/a	n/a
50	CEBPD	chr5:104494206-104494590	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104434864-104434914	AG04449	skin:	fetal
2	chr5:104434864-104434914	AG04449	skin:	fetal
3	chr5:104435608-104435658	HMEC	breast:	n/a
4	chr5:104345171-104345221	PrEC	prostate:	n/a
5	chr5:104435608-104435658	Jurkat	blood:	n/a
6	chr5:104433849-104433899	AG04449	skin:	fetal
7	chr5:104433849-104433899	Jurkat	blood:	n/a
8	chr5:104435062-104435112	Hela-S3	cervix:	n/a
9	chr5:104434827-104434877	AG04449	skin:	fetal
10	chr5:104433849-104433899	AoSMC	blood vessel:	n/a
11	chr5:104435062-104435112	HEEpiC	esophagus:	n/a
12	chr5:104435608-104435658	HEK293	kidney:	embryo
13	chr5:104434827-104434877	HRE	kidney:	n/a
14	chr5:104435608-104435658	NT2-D1	testis:	n/a
15	chr5:104345171-104345221	SAEC	small airway:	n/a
16	chr5:104434864-104434914	AG04450	lung:	fetal
17	chr5:104345171-104345221	AoSMC	blood vessel:	n/a
18	chr5:104434827-104434877	H1-hESC	embryonic stem cell:	embryo
19	chr5:104435062-104435112	AG09319	gingival:	n/a
20	chr5:104345171-104345221	AG10803	skin:	n/a
21	chr5:104434864-104434914	HAEpiC	amniotic membrane:	n/a
22	chr5:104345171-104345221	LNCaP	prostate:	n/a
23	chr5:104345171-104345221	NHBE	bronchial:	n/a
24	chr5:104434864-104434914	GM12878	blood:	n/a
25	chr5:104435608-104435658	RPTEC	kidney:	n/a
26	chr5:104345171-104345221	HIPEpiC	eye:	n/a
27	chr5:104433849-104433899	MCF10A-Er-Src	breast:	n/a
28	chr5:104435062-104435112	AG04449	skin:	fetal
29	chr5:104435062-104435112	Hepatocyte	liver:	n/a
30	chr5:104434864-104434914	AG09309	skin:	n/a
31	chr5:104434827-104434877	ECC-1	luminal epithelium:	n/a
32	chr5:104435608-104435658	HAEpiC	amniotic membrane:	n/a
33	chr5:104435062-104435112	A549	lung:	n/a
34	chr5:104434864-104434914	HPAEpiC	pulmonary alveolar:	n/a
35	chr5:104345171-104345221	HEEpiC	esophagus:	n/a
36	chr5:104434864-104434914	A549	lung:	n/a
37	chr5:104433849-104433899	NB4	blood:	n/a
38	chr5:104435062-104435112	BJ	skin:	n/a
39	chr5:104433849-104433899	Caco-2	colon:	n/a
40	chr5:104435608-104435658	PFSK-1	brain:	n/a
41	chr5:104434827-104434877	HepG2	liver:	n/a
42	chr5:104434864-104434914	NB4	blood:	n/a
43	chr5:104433849-104433899	Hela-S3	cervix:	n/a
44	chr5:104435608-104435658	HL-60	blood:	n/a
45	chr5:104435062-104435112	BE2_C	brain:	n/a
46	chr5:104434827-104434877	IMR90	lung:	fetal
47	chr5:104434827-104434877	CMK	blood:	n/a
48	chr5:104435608-104435658	NHDF-neo	bronchial:	n/a
49	chr5:104345171-104345221	SK-N-SH_RA	brain:	n/a
50	chr5:104434864-104434914	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
2	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
3	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
4	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
5	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
6	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
7	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
8	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
9	chr5:104369671..104371200-chr5:104727235..104729208,2	K562	blood:
10	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
11	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
12	chr5:104369743..104372595-chr5:104912590..104914639,2	K562	blood:
13	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
14	chr5:104370391..104373072-chr5:104374539..104377725,3	K562	blood:
15	chr5:104370391..104371902-chr5:104374539..104376562,2	K562	blood:
16	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104344562-104344618	ENSG00000253584
2	lnc-C5orf30-8	chr5:104435175-104435799	NR_000039
3	lnc-C5orf30-8	chr5:104435174-104435799	NONHSAT103096
4	lnc-NUDT12-7	chr5:104344562-104344612	ENSG00000253584

Variant related genes	Relation type
ENSG00000253584	TF binding region
RAB9BP1	TF binding region
ENSG00000253584	CpG island
RAB9BP1	CpG island
ENSG00000251574	chromatin interactions

Extended variants
information (count: 1499 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1499 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529027939	chr5:104344563-104344564	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs144660050	chr5:104344616-104344617	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs528159885	chr5:104345171-104345172	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
4	rs144882081	chr5:104345172-104345173	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
5	rs562782909	chr5:104345204-104345205	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
6	rs371559449	chr5:104346738-104346739	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs552723532	chr5:104346786-104346787	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs562877915	chr5:104346858-104346859	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs573585961	chr5:104346860-104346861	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs4360012	chr5:104347140-104347141	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs4277888	chr5:104347167-104347168	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs146035872	chr5:104347185-104347186	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs200713162	chr5:104347186-104347187	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs577599129	chr5:104347205-104347206	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs546249765	chr5:104347211-104347212	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs562899655	chr5:104347216-104347217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs4461607	chr5:104347357-104347358	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs538968373	chr5:104347369-104347370	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs111798210	chr5:104347378-104347379	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs4501314	chr5:104347392-104347393	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs4260638	chr5:104347428-104347429	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs4512105	chr5:104347459-104347460	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs546504869	chr5:104347470-104347471	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs571456642	chr5:104347497-104347498	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs532251387	chr5:104347511-104347512	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs551173771	chr5:104369411-104369412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs567724461	chr5:104369424-104369425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs80213085	chr5:104369447-104369448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs13168070	chr5:104369455-104369456	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs567169618	chr5:104369459-104369460	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539076977	chr5:104369475-104369476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529169327	chr5:104369491-104369492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs558639915	chr5:104369503-104369504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs549198741	chr5:104369506-104369507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs575697070	chr5:104369514-104369515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568940603	chr5:104369547-104369548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544354833	chr5:104369582-104369583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs557137686	chr5:104369592-104369593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369630905	chr5:104369605-104369606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370273956	chr5:104369717-104369718	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573791045	chr5:104369739-104369740	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs34567596	chr5:104369804-104369805	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs542393671	chr5:104369836-104369837	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7709488	chr5:104369901-104369902	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs528326636	chr5:104369906-104369907	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544604571	chr5:104369921-104369922	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs564695647	chr5:104369937-104369938	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs62366393	chr5:104369953-104369954	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs550436959	chr5:104369954-104369955	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs118109132	chr5:104369955-104369956	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	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
Retinoblastoma	22278416	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
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Obesity	20622171	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104369400-104369800	Enhancers	K562	blood
2	chr5:104369400-104370000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr5:104369400-104370200	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr5:104369800-104370200	Flanking Active TSS	K562	blood
5	chr5:104370200-104370400	Enhancers	K562	blood
6	chr5:104370200-104370600	Enhancers	Hela-S3	cervix
7	chr5:104370400-104371600	Weak transcription	K562	blood
8	chr5:104376200-104376600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:104380200-104380600	Enhancers	Fetal Brain Male	brain
10	chr5:104388000-104392400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr5:104389600-104390600	Enhancers	Fetal Lung	lung
12	chr5:104390200-104390800	Active TSS	Fetal Brain Male	brain
13	chr5:104392400-104393200	ZNF genes & repeats	Esophagus	oesophagus
14	chr5:104392400-104394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr5:104392400-104394000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr5:104392400-104394000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:104398800-104402000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr5:104421400-104421600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:104421600-104422200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:104422400-104422600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr5:104422600-104423600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr5:104423600-104425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:104424000-104424400	Enhancers	Primary hematopoietic stem cells	blood
24	chr5:104425000-104428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:104428000-104428200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:104437400-104438000	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr5:104446800-104447200	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr5:104451200-104451400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr5:104453600-104455000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr5:104459600-104460200	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr5:104468200-104468800	Enhancers	Brain Germinal Matrix	brain
32	chr5:104469400-104470600	Enhancers	Liver	Liver
33	chr5:104472600-104473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr5:104473200-104474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr5:104474200-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr5:104485600-104486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr5:104486000-104486600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:104488800-104489000	Enhancers	Fetal Lung	lung
39	chr5:104489000-104490800	Weak transcription	Fetal Lung	lung
40	chr5:104490800-104491200	ZNF genes & repeats	Fetal Lung	lung
41	chr5:104492600-104492800	ZNF genes & repeats	Aorta	Aorta
42	chr5:104492800-104494200	Weak transcription	Aorta	Aorta
43	chr5:104494000-104495600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr5:104503600-104504400	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr5:104503800-104504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr5:104503800-104504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr5:104503800-104504600	Enhancers	Hela-S3	cervix
48	chr5:104504400-104505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr5:104505800-104506000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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