Variant report

Variant	nsv1019136
Chromosome Location	chr5:104389989-104524312
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	chr5:104475478-104475496	K562	blood:	n/a	n/a
2	BCL11A	chr5:104502865-104503067	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr5:104393511-104393580	GM12878	blood:	n/a	n/a
4	BRCA1	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
5	CBX3	chr5:104393083-104393385	K562	blood:	n/a	n/a
6	CBX3	chr5:104393078-104393434	K562	blood:	n/a	n/a
7	CBX3	chr5:104428357-104428592	K562	blood:	n/a	n/a
8	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
9	CEBPB	chr5:104516185-104516507	IMR90	lung:	n/a	n/a
10	CEBPB	chr5:104391916-104392212	A549	lung:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
11	CEBPB	chr5:104510149-104510395	H1-hESC	embryonic stem cell:	n/a	chr5:104510228-104510239
12	CEBPB	chr5:104423402-104423724	HepG2	liver:	n/a	chr5:104423566-104423577
13	CEBPB	chr5:104484312-104484512	H1-hESC	embryonic stem cell:	n/a	n/a
14	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
15	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
16	CEBPB	chr5:104485759-104485906	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr5:104475581-104475765	H1-hESC	embryonic stem cell:	n/a	n/a
18	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
19	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
20	CEBPB	chr5:104391872-104392206	HepG2	liver:	n/a	chr5:104392017-104392026 chr5:104392042-104392059 chr5:104392015-104392026 chr5:104392045-104392056
21	CEBPB	chr5:104485721-104485921	K562	blood:	n/a	n/a
22	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
23	CEBPB	chr5:104475600-104475772	HepG2	liver:	n/a	n/a
24	CEBPB	chr5:104423410-104423746	IMR90	lung:	n/a	chr5:104423566-104423577
25	CEBPB	chr5:104432081-104432193	HepG2	liver:	n/a	n/a
26	CEBPB	chr5:104423448-104423672	K562	blood:	n/a	chr5:104423566-104423577
27	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
28	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
29	CEBPB	chr5:104510170-104510370	K562	blood:	n/a	chr5:104510228-104510239
30	CEBPB	chr5:104423406-104423707	A549	lung:	n/a	chr5:104423566-104423577
31	CEBPB	chr5:104475627-104475670	K562	blood:	n/a	n/a
32	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
33	CEBPD	chr5:104494206-104494590	K562	blood:	n/a	n/a
34	CHD2	chr5:104502938-104503111	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr5:104497236-104497338	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr5:104484404-104484489	GM20000	blood:	n/a	n/a
37	CTCF	chr5:104471380-104471530	BE2_C	brain:	n/a	n/a
38	CTCF	chr5:104394548-104394560	LNCaP	prostate:	n/a	n/a
39	CTCF	chr5:104448719-104448771	LNCaP	prostate:	n/a	n/a
40	CTCF	chr5:104434155-104434241	GM10248	blood:	n/a	n/a
41	CTCF	chr5:104471340-104471490	HEK293	kidney:	n/a	n/a
42	CTCF	chr5:104506078-104506095	GM10266	blood:	n/a	n/a
43	CTCF	chr5:104471360-104471510	BE2_C	brain:	n/a	n/a
44	CTCF	chr5:104488600-104488750	BE2_C	brain:	n/a	n/a
45	CTCF	chr5:104497253-104497340	GM10248	blood:	n/a	n/a
46	CUX1	chr5:104524102-104524142	K562	blood:	n/a	n/a
47	E2F4	chr5:104454303-104454460	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr5:104399543-104399743	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr5:104480137-104480224	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr5:104445215-104445427	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104435062-104435112	GM12878	blood:	n/a
2	chr5:104434864-104434914	AG09309	skin:	n/a
3	chr5:104435062-104435112	AoSMC	blood vessel:	n/a
4	chr5:104434864-104434914	LNCaP	prostate:	n/a
5	chr5:104434864-104434914	HCPEpiC	choroid plexus:	n/a
6	chr5:104434864-104434914	HUVEC	blood vessel:	n/a
7	chr5:104435608-104435658	ECC-1	luminal epithelium:	n/a
8	chr5:104435062-104435112	AG09319	gingival:	n/a
9	chr5:104434827-104434877	HEEpiC	esophagus:	n/a
10	chr5:104434827-104434877	BE2_C	brain:	n/a
11	chr5:104434827-104434877	NT2-D1	testis:	n/a
12	chr5:104434864-104434914	IMR90	lung:	fetal
13	chr5:104434827-104434877	SK-N-SH_RA	brain:	n/a
14	chr5:104435062-104435112	IMR90	lung:	fetal
15	chr5:104433849-104433899	MCF-7	breast:	n/a
16	chr5:104434864-104434914	HepG2	liver:	n/a
17	chr5:104433849-104433899	HAEpiC	amniotic membrane:	n/a
18	chr5:104434827-104434877	LNCaP	prostate:	n/a
19	chr5:104435608-104435658	IMR90	lung:	fetal
20	chr5:104434827-104434877	HepG2	liver:	n/a
21	chr5:104433849-104433899	PFSK-1	brain:	n/a
22	chr5:104433849-104433899	NH-A	brain:	n/a
23	chr5:104433849-104433899	GM19239	blood:	n/a
24	chr5:104435608-104435658	SAEC	small airway:	n/a
25	chr5:104434864-104434914	GM06990	blood:	n/a
26	chr5:104435608-104435658	HRPEpiC	eye:	n/a
27	chr5:104434864-104434914	SK-N-SH	brain:	n/a
28	chr5:104433849-104433899	NHDF-neo	bronchial:	n/a
29	chr5:104435608-104435658	PrEC	prostate:	n/a
30	chr5:104434864-104434914	PrEC	prostate:	n/a
31	chr5:104435608-104435658	Caco-2	colon:	n/a
32	chr5:104434827-104434877	RPTEC	kidney:	n/a
33	chr5:104434827-104434877	Hepatocyte	liver:	n/a
34	chr5:104435062-104435112	NH-A	brain:	n/a
35	chr5:104434864-104434914	Hela-S3	cervix:	n/a
36	chr5:104433849-104433899	U87	brain:	n/a
37	chr5:104434827-104434877	HIPEpiC	eye:	n/a
38	chr5:104435608-104435658	AG09319	gingival:	n/a
39	chr5:104435608-104435658	HepG2	liver:	n/a
40	chr5:104435608-104435658	SK-N-MC	brain:	n/a
41	chr5:104433849-104433899	PrEC	prostate:	n/a
42	chr5:104435062-104435112	HL-60	blood:	n/a
43	chr5:104435608-104435658	K562	blood:	n/a
44	chr5:104433849-104433899	GM06990	blood:	n/a
45	chr5:104435608-104435658	HL-60	blood:	n/a
46	chr5:104433849-104433899	GM12891	blood:	n/a
47	chr5:104434827-104434877	K562	blood:	n/a
48	chr5:104433849-104433899	GM12878	blood:	n/a
49	chr5:104435062-104435112	ECC-1	luminal epithelium:	n/a
50	chr5:104434864-104434914	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
2	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
3	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
4	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
5	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
6	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
7	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
8	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
9	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
10	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
11	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C5orf30-8	chr5:104435175-104435799	NR_000039
2	lnc-C5orf30-8	chr5:104435174-104435799	NONHSAT103096

Variant related genes	Relation type
RAB9BP1	TF binding region
RAB9BP1	CpG island

Extended variants
information (count: 1269 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1269 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562797695	chr5:104390003-104390004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs202061297	chr5:104390029-104390030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs531208500	chr5:104390031-104390032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548125729	chr5:104390034-104390035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551551448	chr5:104390035-104390036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527355664	chr5:104390117-104390118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs369991619	chr5:104390249-104390250	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs189259417	chr5:104390262-104390263	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191502889	chr5:104390285-104390286	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539645026	chr5:104390306-104390307	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550212744	chr5:104390324-104390325	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs148561048	chr5:104390389-104390390	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372367310	chr5:104390427-104390428	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142856814	chr5:104390430-104390431	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs569246438	chr5:104390463-104390464	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555706181	chr5:104390484-104390485	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184028286	chr5:104390509-104390510	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs535156386	chr5:104390528-104390529	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574675283	chr5:104390564-104390565	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs538553205	chr5:104390574-104390575	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200880208	chr5:104390598-104390599	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545933111	chr5:104390625-104390626	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs188713585	chr5:104390642-104390643	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576250844	chr5:104390698-104390699	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs567613106	chr5:104390730-104390731	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs377597043	chr5:104390760-104390761	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs541481046	chr5:104390761-104390762	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs112712024	chr5:104390763-104390764	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs527284259	chr5:104390817-104390818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7700782	chr5:104390848-104390849	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs181543827	chr5:104390955-104390956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs538111597	chr5:104390956-104390957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533371845	chr5:104390960-104390961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs186873502	chr5:104391024-104391025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540866065	chr5:104391052-104391053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536175566	chr5:104391053-104391054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554065099	chr5:104391088-104391089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs549980484	chr5:104391137-104391138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151067376	chr5:104391171-104391172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs566118160	chr5:104391270-104391271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535012919	chr5:104391313-104391314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558286692	chr5:104391379-104391380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141010521	chr5:104391395-104391396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539269998	chr5:104391439-104391440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556292685	chr5:104391440-104391441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs76925010	chr5:104391458-104391459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190563292	chr5:104391470-104391471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs182172383	chr5:104391486-104391487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571714229	chr5:104391505-104391506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540587205	chr5:104391520-104391521	Weak transcription	n/a	n/a	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
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
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104388000-104392400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:104389600-104390600	Enhancers	Fetal Lung	lung
3	chr5:104390200-104390800	Active TSS	Fetal Brain Male	brain
4	chr5:104392400-104393200	ZNF genes & repeats	Esophagus	oesophagus
5	chr5:104392400-104394000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:104392400-104394000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:104392400-104394000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:104398800-104402000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr5:104421400-104421600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr5:104421600-104422200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:104422400-104422600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr5:104422600-104423600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:104423600-104425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:104424000-104424400	Enhancers	Primary hematopoietic stem cells	blood
15	chr5:104425000-104428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr5:104428000-104428200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr5:104437400-104438000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr5:104446800-104447200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr5:104451200-104451400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:104453600-104455000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr5:104459600-104460200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr5:104468200-104468800	Enhancers	Brain Germinal Matrix	brain
23	chr5:104469400-104470600	Enhancers	Liver	Liver
24	chr5:104472600-104473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr5:104473200-104474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr5:104474200-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr5:104485600-104486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr5:104486000-104486600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr5:104488800-104489000	Enhancers	Fetal Lung	lung
30	chr5:104489000-104490800	Weak transcription	Fetal Lung	lung
31	chr5:104490800-104491200	ZNF genes & repeats	Fetal Lung	lung
32	chr5:104492600-104492800	ZNF genes & repeats	Aorta	Aorta
33	chr5:104492800-104494200	Weak transcription	Aorta	Aorta
34	chr5:104494000-104495600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr5:104503600-104504400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:104503800-104504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr5:104503800-104504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr5:104503800-104504600	Enhancers	Hela-S3	cervix
39	chr5:104504400-104505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr5:104505800-104506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chr5:104512000-104512400	Active TSS	Breast Myoepithelial Primary Cells	Breast

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