Variant report

Variant	esv2757129
Chromosome Location	chr5:104424297-104528125
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	chr5:104488401-104488414	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr5:104428357-104428592	K562	blood:	n/a	n/a
5	CEBPB	chr5:104510170-104510370	K562	blood:	n/a	chr5:104510228-104510239
6	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
7	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
8	CEBPB	chr5:104475600-104475772	HepG2	liver:	n/a	n/a
9	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
10	CEBPB	chr5:104526203-104526286	K562	blood:	n/a	n/a
11	CEBPB	chr5:104510149-104510395	H1-hESC	embryonic stem cell:	n/a	chr5:104510228-104510239
12	CEBPB	chr5:104485721-104485921	K562	blood:	n/a	n/a
13	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
14	CEBPB	chr5:104485759-104485906	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr5:104475627-104475670	K562	blood:	n/a	n/a
16	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
17	CEBPB	chr5:104475581-104475765	H1-hESC	embryonic stem cell:	n/a	n/a
18	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
19	CEBPB	chr5:104432081-104432193	HepG2	liver:	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	chr5:104437342-104437688	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
22	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
23	CEBPB	chr5:104484312-104484512	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr5:104516185-104516507	IMR90	lung:	n/a	n/a
25	CEBPD	chr5:104494206-104494590	K562	blood:	n/a	n/a
26	CHD2	chr5:104502938-104503111	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr5:104434155-104434241	GM10248	blood:	n/a	n/a
28	CTCF	chr5:104506078-104506095	GM10266	blood:	n/a	n/a
29	CTCF	chr5:104497253-104497340	GM10248	blood:	n/a	n/a
30	CTCF	chr5:104471360-104471510	BE2_C	brain:	n/a	n/a
31	CTCF	chr5:104497236-104497338	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr5:104471380-104471530	BE2_C	brain:	n/a	n/a
33	CTCF	chr5:104471340-104471490	HEK293	kidney:	n/a	n/a
34	CTCF	chr5:104484404-104484489	GM20000	blood:	n/a	n/a
35	CTCF	chr5:104488600-104488750	BE2_C	brain:	n/a	n/a
36	CTCF	chr5:104448719-104448771	LNCaP	prostate:	n/a	n/a
37	CUX1	chr5:104524102-104524142	K562	blood:	n/a	n/a
38	E2F4	chr5:104527912-104528169	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr5:104474409-104474580	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr5:104480137-104480224	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr5:104445215-104445427	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr5:104454303-104454460	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr5:104457846-104457897	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F6	chr5:104503661-104504240	H1-hESC	embryonic stem cell:	n/a	n/a
45	EP300	chr5:104459435-104459684	SK-N-SH_RA	brain:	n/a	n/a
46	EP300	chr5:104440417-104441093	MCF-7	breast:	n/a	chr5:104440714-104440724
47	EP300	chr5:104459190-104459771	SK-N-SH	brain:	n/a	n/a
48	FAM48A	chr5:104424879-104425034	GM12878	blood:	n/a	n/a
49	FOS	chr5:104504538-104504934	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr5:104482572-104482914	MCF10A-Er-Src	breast:	n/a	chr5:104482738-104482745 chr5:104482737-104482746 chr5:104482737-104482745 chr5:104482733-104482744 chr5:104482735-104482747

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:104435608-104435658	SK-N-SH_RA	brain:	n/a
2	chr5:104435608-104435658	NHBE	bronchial:	n/a
3	chr5:104435608-104435658	GM12878	blood:	n/a
4	chr5:104434827-104434877	HRE	kidney:	n/a
5	chr5:104435608-104435658	ECC-1	luminal epithelium:	n/a
6	chr5:104435062-104435112	SAEC	small airway:	n/a
7	chr5:104435608-104435658	Jurkat	blood:	n/a
8	chr5:104433849-104433899	AoSMC	blood vessel:	n/a
9	chr5:104435062-104435112	HMEC	breast:	n/a
10	chr5:104434864-104434914	HMEC	breast:	n/a
11	chr5:104435608-104435658	AG04449	skin:	fetal
12	chr5:104434827-104434877	ovcar-3	ovarian:	n/a
13	chr5:104434827-104434877	SK-N-MC	brain:	n/a
14	chr5:104435062-104435112	ECC-1	luminal epithelium:	n/a
15	chr5:104435608-104435658	ProgFib	skin:	n/a
16	chr5:104435608-104435658	HUVEC	blood vessel:	n/a
17	chr5:104434827-104434877	HL-60	blood:	n/a
18	chr5:104434864-104434914	HUVEC	blood vessel:	n/a
19	chr5:104433849-104433899	Hepatocyte	liver:	n/a
20	chr5:104435062-104435112	SK-N-SH_RA	brain:	n/a
21	chr5:104434864-104434914	GM12892	blood:	n/a
22	chr5:104435062-104435112	HEEpiC	esophagus:	n/a
23	chr5:104433849-104433899	HRE	kidney:	n/a
24	chr5:104435062-104435112	MCF-7	breast:	n/a
25	chr5:104435062-104435112	ovcar-3	ovarian:	n/a
26	chr5:104435062-104435112	HRPEpiC	eye:	n/a
27	chr5:104435608-104435658	AG10803	skin:	n/a
28	chr5:104433849-104433899	A549	lung:	n/a
29	chr5:104433849-104433899	HPAEpiC	pulmonary alveolar:	n/a
30	chr5:104434827-104434877	HepG2	liver:	n/a
31	chr5:104433849-104433899	SK-N-SH	brain:	n/a
32	chr5:104433849-104433899	BE2_C	brain:	n/a
33	chr5:104433849-104433899	NB4	blood:	n/a
34	chr5:104435062-104435112	K562	blood:	n/a
35	chr5:104433849-104433899	T-47D	breast:	n/a
36	chr5:104435062-104435112	LNCaP	prostate:	n/a
37	chr5:104435608-104435658	GM12891	blood:	n/a
38	chr5:104435608-104435658	GM06990	blood:	n/a
39	chr5:104435062-104435112	HNPCEpiC	eye:	n/a
40	chr5:104434864-104434914	PFSK-1	brain:	n/a
41	chr5:104433849-104433899	HIPEpiC	eye:	n/a
42	chr5:104434864-104434914	AG04450	lung:	fetal
43	chr5:104435062-104435112	NHDF-neo	bronchial:	n/a
44	chr5:104435062-104435112	PFSK-1	brain:	n/a
45	chr5:104435062-104435112	PANC-1	pancreas:	n/a
46	chr5:104434827-104434877	Hela-S3	cervix:	n/a
47	chr5:104433849-104433899	HEK293	kidney:	embryo
48	chr5:104434864-104434914	MCF-7	breast:	n/a
49	chr5:104433849-104433899	SAEC	small airway:	n/a
50	chr5:104435608-104435658	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
2	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
3	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
4	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
5	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
6	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
7	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
8	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
9	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
10	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
11	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
12	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:

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: 871 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6596598	chr5:104424297-104424298	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs73194503	chr5:104424335-104424336	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs181347630	chr5:104424409-104424410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186776367	chr5:104424420-104424421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs10038585	chr5:104424483-104424484	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs17367942	chr5:104424487-104424488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540878194	chr5:104424521-104424522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116049579	chr5:104424535-104424536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191545334	chr5:104424578-104424579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs532506653	chr5:104424621-104424622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10035756	chr5:104424634-104424635	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs569408541	chr5:104424635-104424636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs531832686	chr5:104424686-104424687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs550841429	chr5:104424693-104424694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369075604	chr5:104424715-104424716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs115369132	chr5:104424718-104424719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs151330619	chr5:104424722-104424723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10035777	chr5:104424730-104424731	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs565518717	chr5:104424738-104424739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183848789	chr5:104424742-104424743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188693700	chr5:104424817-104424818	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs566368247	chr5:104424844-104424845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192446429	chr5:104424859-104424860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs558117612	chr5:104424868-104424869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575039813	chr5:104424880-104424881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs182100666	chr5:104424941-104424942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs10038726	chr5:104424956-104424957	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs540590030	chr5:104424957-104424958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10035820	chr5:104424968-104424969	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs554633913	chr5:104424993-104424994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561848264	chr5:104424999-104425000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs186735498	chr5:104425036-104425037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs10050446	chr5:104425043-104425044	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs531845825	chr5:104425085-104425086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548662662	chr5:104425186-104425187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561082686	chr5:104425233-104425234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140231585	chr5:104425270-104425271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs546458608	chr5:104425275-104425276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111968642	chr5:104425277-104425278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538550389	chr5:104425278-104425279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537457564	chr5:104425284-104425285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551804975	chr5:104425317-104425318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191502845	chr5:104425326-104425327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537560888	chr5:104425376-104425377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184028994	chr5:104425509-104425510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554212922	chr5:104425512-104425513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574425378	chr5:104425520-104425521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534437903	chr5:104425548-104425549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145530138	chr5:104425576-104425577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs577512722	chr5:104425579-104425580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104423600-104425000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr5:104424000-104424400	Enhancers	Primary hematopoietic stem cells	blood
3	chr5:104425000-104428000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:104428000-104428200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:104437400-104438000	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr5:104446800-104447200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr5:104451200-104451400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr5:104453600-104455000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr5:104459600-104460200	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr5:104468200-104468800	Enhancers	Brain Germinal Matrix	brain
11	chr5:104469400-104470600	Enhancers	Liver	Liver
12	chr5:104472600-104473200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr5:104473200-104474200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:104474200-104474400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:104485600-104486600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr5:104486000-104486600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:104488800-104489000	Enhancers	Fetal Lung	lung
18	chr5:104489000-104490800	Weak transcription	Fetal Lung	lung
19	chr5:104490800-104491200	ZNF genes & repeats	Fetal Lung	lung
20	chr5:104492600-104492800	ZNF genes & repeats	Aorta	Aorta
21	chr5:104492800-104494200	Weak transcription	Aorta	Aorta
22	chr5:104494000-104495600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr5:104503600-104504400	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr5:104503800-104504400	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr5:104503800-104504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr5:104503800-104504600	Enhancers	Hela-S3	cervix
27	chr5:104504400-104505400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr5:104505800-104506000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr5:104512000-104512400	Active TSS	Breast Myoepithelial Primary Cells	Breast

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