Variant report

Variant	nsv882566
Chromosome Location	chr5:104394274-104540026
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	chr5:104437340-104437708	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
6	CEBPB	chr5:104423410-104423746	IMR90	lung:	n/a	chr5:104423566-104423577
7	CEBPB	chr5:104475627-104475670	K562	blood:	n/a	n/a
8	CEBPB	chr5:104484312-104484512	H1-hESC	embryonic stem cell:	n/a	n/a
9	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
10	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
11	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
12	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
13	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
14	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
15	CEBPB	chr5:104485721-104485921	K562	blood:	n/a	n/a
16	CEBPB	chr5:104475600-104475772	HepG2	liver:	n/a	n/a
17	CEBPB	chr5:104526203-104526286	K562	blood:	n/a	n/a
18	CEBPB	chr5:104423406-104423707	A549	lung:	n/a	chr5:104423566-104423577
19	CEBPB	chr5:104423448-104423672	K562	blood:	n/a	chr5:104423566-104423577
20	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
21	CEBPB	chr5:104423402-104423724	HepG2	liver:	n/a	chr5:104423566-104423577
22	CEBPB	chr5:104485759-104485906	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr5:104534357-104534498	HepG2	liver:	n/a	chr5:104534396-104534407
24	CEBPB	chr5:104510170-104510370	K562	blood:	n/a	chr5:104510228-104510239
25	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
26	CEBPB	chr5:104516185-104516507	IMR90	lung:	n/a	n/a
27	CEBPB	chr5:104510149-104510395	H1-hESC	embryonic stem cell:	n/a	chr5:104510228-104510239
28	CEBPB	chr5:104475581-104475765	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr5:104432081-104432193	HepG2	liver:	n/a	n/a
30	CEBPD	chr5:104494206-104494590	K562	blood:	n/a	n/a
31	CHD2	chr5:104502938-104503111	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:104471340-104471490	HEK293	kidney:	n/a	n/a
33	CTCF	chr5:104535035-104535150	Spleen_OC	spleen:	n/a	n/a
34	CTCF	chr5:104471360-104471510	BE2_C	brain:	n/a	n/a
35	CTCF	chr5:104434155-104434241	GM10248	blood:	n/a	n/a
36	CTCF	chr5:104471380-104471530	BE2_C	brain:	n/a	n/a
37	CTCF	chr5:104448719-104448771	LNCaP	prostate:	n/a	n/a
38	CTCF	chr5:104497236-104497338	Kidney_OC	kidney:	n/a	n/a
39	CTCF	chr5:104506078-104506095	GM10266	blood:	n/a	n/a
40	CTCF	chr5:104394548-104394560	LNCaP	prostate:	n/a	n/a
41	CTCF	chr5:104539330-104539410	Medullo	brain:	n/a	n/a
42	CTCF	chr5:104484404-104484489	GM20000	blood:	n/a	n/a
43	CTCF	chr5:104488600-104488750	BE2_C	brain:	n/a	n/a
44	CTCF	chr5:104497253-104497340	GM10248	blood:	n/a	n/a
45	CUX1	chr5:104524102-104524142	K562	blood:	n/a	n/a
46	E2F4	chr5:104454303-104454460	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr5:104527912-104528169	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr5:104474409-104474580	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr5:104399543-104399743	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	chr5:104434864-104434914	ovcar-3	ovarian:	n/a
2	chr5:104434864-104434914	RPTEC	kidney:	n/a
3	chr5:104434864-104434914	NHDF-neo	bronchial:	n/a
4	chr5:104434864-104434914	Hela-S3	cervix:	n/a
5	chr5:104435608-104435658	Hela-S3	cervix:	n/a
6	chr5:104433849-104433899	AoSMC	blood vessel:	n/a
7	chr5:104435062-104435112	GM06990	blood:	n/a
8	chr5:104434864-104434914	HRE	kidney:	n/a
9	chr5:104435062-104435112	AG09319	gingival:	n/a
10	chr5:104433849-104433899	MCF-7	breast:	n/a
11	chr5:104434827-104434877	HCM	heart:	n/a
12	chr5:104435062-104435112	HIPEpiC	eye:	n/a
13	chr5:104435062-104435112	HRPEpiC	eye:	n/a
14	chr5:104433849-104433899	HCT-116	colon:	n/a
15	chr5:104434864-104434914	GM12878	blood:	n/a
16	chr5:104435062-104435112	PANC-1	pancreas:	n/a
17	chr5:104434864-104434914	AG09319	gingival:	n/a
18	chr5:104435062-104435112	HPAEpiC	pulmonary alveolar:	n/a
19	chr5:104434827-104434877	H1-hESC	embryonic stem cell:	embryo
20	chr5:104435608-104435658	AG04449	skin:	fetal
21	chr5:104435062-104435112	GM12891	blood:	n/a
22	chr5:104433849-104433899	GM06990	blood:	n/a
23	chr5:104433849-104433899	BE2_C	brain:	n/a
24	chr5:104435062-104435112	ECC-1	luminal epithelium:	n/a
25	chr5:104435062-104435112	SK-N-SH	brain:	n/a
26	chr5:104434827-104434877	U87	brain:	n/a
27	chr5:104433849-104433899	AG04449	skin:	fetal
28	chr5:104434864-104434914	HIPEpiC	eye:	n/a
29	chr5:104435608-104435658	HCM	heart:	n/a
30	chr5:104435608-104435658	RPTEC	kidney:	n/a
31	chr5:104434827-104434877	AG10803	skin:	n/a
32	chr5:104435608-104435658	Jurkat	blood:	n/a
33	chr5:104434827-104434877	HEK293	kidney:	embryo
34	chr5:104435608-104435658	NB4	blood:	n/a
35	chr5:104435062-104435112	NB4	blood:	n/a
36	chr5:104433849-104433899	SK-N-SH	brain:	n/a
37	chr5:104435608-104435658	HCF	heart:	n/a
38	chr5:104435608-104435658	Caco-2	colon:	n/a
39	chr5:104434864-104434914	GM06990	blood:	n/a
40	chr5:104434864-104434914	HUVEC	blood vessel:	n/a
41	chr5:104435608-104435658	BE2_C	brain:	n/a
42	chr5:104433849-104433899	HPAEpiC	pulmonary alveolar:	n/a
43	chr5:104433849-104433899	RPTEC	kidney:	n/a
44	chr5:104435062-104435112	GM12878	blood:	n/a
45	chr5:104434827-104434877	HepG2	liver:	n/a
46	chr5:104434864-104434914	SK-N-MC	brain:	n/a
47	chr5:104434864-104434914	SK-N-SH	brain:	n/a
48	chr5:104434827-104434877	RPTEC	kidney:	n/a
49	chr5:104435062-104435112	HCM	heart:	n/a
50	chr5:104434827-104434877	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr5:104524711..104526370-chr5:104889242..104892104,2	K562	blood:
2	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
3	chr5:104454743..104457659-chr5:104458109..104460411,2	MCF-7	breast:
4	chr12:23105697..23106553-chr5:104539343..104540254,2	MCF-7	breast:
5	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
6	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
7	chr5:104528561..104530726-chr5:104532311..104534213,2	K562	blood:
8	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
9	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
10	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
11	chr5:104438251..104441149-chr5:104441695..104444269,2	K562	blood:
12	chr5:104443161..104444832-chr5:104444978..104447101,2	MCF-7	breast:
13	chr5:104482838..104485793-chr5:104489379..104492370,3	MCF-7	breast:
14	chr5:104423554..104425423-chr5:104426738..104428780,3	K562	blood:
15	chr5:104528561..104530726-chr5:104532311..104534213,2	K562	blood:

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

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

Extended variants
information (count: 1108 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1108 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560103429	chr5:104398847-104398848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs553525926	chr5:104398878-104398879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573430643	chr5:104398887-104398888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545661088	chr5:104398888-104398889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565175963	chr5:104398893-104398894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188497376	chr5:104398899-104398900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142707449	chr5:104398900-104398901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs561009293	chr5:104398920-104398921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114624752	chr5:104398925-104398926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs73211631	chr5:104399029-104399030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs76471278	chr5:104399048-104399049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192882770	chr5:104399050-104399051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs528406797	chr5:104399063-104399064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551640468	chr5:104399065-104399066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs74836865	chr5:104399108-104399109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs144460525	chr5:104399145-104399146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557101628	chr5:104399156-104399157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs567334463	chr5:104399162-104399163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148161896	chr5:104399194-104399195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553318001	chr5:104399237-104399238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573377023	chr5:104399268-104399269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536036967	chr5:104399335-104399336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7705466	chr5:104399356-104399357	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs374447012	chr5:104399394-104399395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575559792	chr5:104399395-104399396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs74901155	chr5:104399399-104399400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114026862	chr5:104399404-104399405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530164920	chr5:104399440-104399441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs112362399	chr5:104399494-104399495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs533595092	chr5:104399496-104399497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs559323507	chr5:104399497-104399498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs78564137	chr5:104399502-104399503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551388238	chr5:104399508-104399509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571476342	chr5:104399592-104399593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530535468	chr5:104399600-104399601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368614449	chr5:104399749-104399750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77799122	chr5:104399750-104399751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79749337	chr5:104399751-104399752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142034540	chr5:104399752-104399753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs199700375	chr5:104399753-104399754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375100943	chr5:104399888-104399889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs537114416	chr5:104399935-104399936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201859661	chr5:104399942-104399943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539184178	chr5:104399946-104399947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185468349	chr5:104399963-104399964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575506842	chr5:104399969-104399970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558702667	chr5:104399986-104399987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554580499	chr5:104399991-104399992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs189410391	chr5:104400023-104400024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574480447	chr5:104400079-104400080	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:34 , 50 per page) page: 1

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

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