Variant report

Variant	esv1831511
Chromosome Location	chr5:97666860-97678414
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	CEBPB	chr5:97676744-97677715	IMR90	lung:	n/a	chr5:97677511-97677524
2	CTCF	chr5:97667760-97667910	AG09309	skin:	n/a	n/a
3	CTCF	chr5:97667063-97667119	GM13976	blood:	n/a	n/a
4	E2F4	chr5:97676873-97677016	MCF10A-Er-Src	breast:	n/a	n/a
5	E2F4	chr5:97669784-97670391	MCF10A-Er-Src	breast:	n/a	n/a
6	EP300	chr5:97673811-97673892	K562	blood:	n/a	n/a
7	EP300	chr5:97676534-97677417	SK-N-SH	brain:	n/a	chr5:97676651-97676665 chr5:97676664-97676678
8	EP300	chr5:97676369-97677415	SK-N-SH	brain:	n/a	chr5:97676651-97676665 chr5:97676664-97676678
9	FOS	chr5:97676969-97677024	MCF10A-Er-Src	breast:	n/a	n/a
10	FOS	chr5:97676868-97677068	MCF10A-Er-Src	breast:	n/a	chr5:97677059-97677068
11	FOS	chr5:97669671-97669949	MCF10A-Er-Src	breast:	n/a	chr5:97669815-97669825 chr5:97669876-97669884 chr5:97669816-97669823 chr5:97669815-97669825 chr5:97669815-97669825 chr5:97669816-97669824 chr5:97669815-97669825 chr5:97669816-97669824
12	FOS	chr5:97669670-97669966	MCF10A-Er-Src	breast:	n/a	chr5:97669815-97669825 chr5:97669876-97669884 chr5:97669816-97669823 chr5:97669815-97669825 chr5:97669815-97669825 chr5:97669816-97669824 chr5:97669815-97669825 chr5:97669816-97669824
13	FOS	chr5:97669749-97669966	MCF10A-Er-Src	breast:	n/a	chr5:97669815-97669825 chr5:97669876-97669884 chr5:97669816-97669823 chr5:97669815-97669825 chr5:97669815-97669825 chr5:97669816-97669824 chr5:97669815-97669825 chr5:97669816-97669824
14	FOS	chr5:97669686-97669959	MCF10A-Er-Src	breast:	n/a	chr5:97669815-97669825 chr5:97669876-97669884 chr5:97669816-97669823 chr5:97669815-97669825 chr5:97669815-97669825 chr5:97669816-97669824 chr5:97669815-97669825 chr5:97669816-97669824
15	FOS	chr5:97666509-97667015	HUVEC	blood vessel:	n/a	n/a
16	FOS	chr5:97676986-97677031	MCF10A-Er-Src	breast:	n/a	n/a
17	FOSL2	chr5:97676557-97677325	SK-N-SH	brain:	n/a	chr5:97677059-97677068 chr5:97676666-97676675 chr5:97676727-97676741
18	FOSL2	chr5:97676726-97677241	SK-N-SH	brain:	n/a	chr5:97677059-97677068 chr5:97676727-97676741
19	GABPA	chr5:97667810-97667898	Hela-S3	cervix:	n/a	n/a
20	GATA2	chr5:97666647-97666964	HUVEC	blood vessel:	n/a	n/a
21	GATA3	chr5:97676390-97677679	SK-N-SH	brain:	n/a	chr5:97676790-97676799 chr5:97676809-97676820 chr5:97676818-97676828
22	GATA3	chr5:97676382-97677623	SK-N-SH	brain:	n/a	chr5:97676790-97676799 chr5:97676809-97676820 chr5:97676818-97676828
23	HEY1	chr5:97675483-97675675	K562	blood:	n/a	n/a
24	HEY1	chr5:97675990-97676158	K562	blood:	n/a	n/a
25	JUND	chr5:97676522-97677426	SK-N-SH	brain:	n/a	chr5:97677059-97677068 chr5:97676666-97676675 chr5:97676727-97676741
26	JUND	chr5:97676489-97677351	SK-N-SH	brain:	n/a	chr5:97677059-97677068 chr5:97676666-97676675 chr5:97676727-97676741
27	MAFF	chr5:97677513-97677734	K562	blood:	n/a	chr5:97677637-97677651 chr5:97677638-97677656
28	MAFF	chr5:97677473-97677791	HepG2	liver:	n/a	chr5:97677637-97677651 chr5:97677638-97677656
29	MAFK	chr5:97677514-97677768	K562	blood:	n/a	chr5:97677641-97677650 chr5:97677639-97677654 chr5:97677640-97677650 chr5:97677637-97677651 chr5:97677634-97677654 chr5:97677636-97677652 chr5:97677639-97677655 chr5:97677644-97677655
30	MAFK	chr5:97677486-97677818	HepG2	liver:	n/a	chr5:97677641-97677650 chr5:97677639-97677654 chr5:97677640-97677650 chr5:97677637-97677651 chr5:97677634-97677654 chr5:97677636-97677652 chr5:97677639-97677655 chr5:97677644-97677655
31	MAFK	chr5:97677468-97677823	HepG2	liver:	n/a	chr5:97677641-97677650 chr5:97677639-97677654 chr5:97677640-97677650 chr5:97677637-97677651 chr5:97677634-97677654 chr5:97677636-97677652 chr5:97677639-97677655 chr5:97677644-97677655
32	MAFK	chr5:97676797-97677841	IMR90	lung:	n/a	chr5:97677641-97677650 chr5:97677639-97677654 chr5:97677640-97677650 chr5:97677637-97677651 chr5:97677634-97677654 chr5:97677636-97677652 chr5:97677639-97677655 chr5:97677644-97677655
33	MAX	chr5:97676692-97677264	SK-N-SH	brain:	n/a	n/a
34	MAX	chr5:97676593-97677261	SK-N-SH	brain:	n/a	n/a
35	MAZ	chr5:97673527-97673549	HepG2	liver:	n/a	n/a
36	MXI1	chr5:97669908-97669991	GM12878	blood:	n/a	n/a
37	MYC	chr5:97673438-97673535	MCF10A-Er-Src	breast:	n/a	n/a
38	MYC	chr5:97674946-97674954	H1-hESC	embryonic stem cell:	n/a	n/a
39	MYC	chr5:97674400-97674452	MCF-7	breast:	n/a	n/a
40	MYC	chr5:97674993-97675009	MCF-7	breast:	n/a	n/a
41	MYC	chr5:97676928-97677129	MCF10A-Er-Src	breast:	n/a	n/a
42	MYC	chr5:97674974-97674987	H1-hESC	embryonic stem cell:	n/a	n/a
43	MYC	chr5:97674840-97674983	MCF-7	breast:	n/a	n/a
44	MYC	chr5:97675011-97675039	H1-hESC	embryonic stem cell:	n/a	n/a
45	NFIC	chr5:97676480-97677413	SK-N-SH	brain:	n/a	n/a
46	PBX3	chr5:97676473-97677383	SK-N-SH	brain:	n/a	n/a
47	PBX3	chr5:97676561-97677268	SK-N-SH	brain:	n/a	n/a
48	POLR2A	chr5:97675421-97675654	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr5:97675327-97675705	GM12892	blood:	n/a	n/a
50	POLR2A	chr5:97674781-97674985	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:97676915-97676965	AoSMC	blood vessel:	n/a
2	chr5:97676915-97676965	NB4	blood:	n/a
3	chr5:97676915-97676965	GM19239	blood:	n/a
4	chr5:97676915-97676965	AG04450	lung:	fetal
5	chr5:97676915-97676965	LNCaP	prostate:	n/a
6	chr5:97676915-97676965	AG09319	gingival:	n/a
7	chr5:97676915-97676965	HCF	heart:	n/a
8	chr5:97676915-97676965	AG10803	skin:	n/a
9	chr5:97676915-97676965	BE2_C	brain:	n/a
10	chr5:97676915-97676965	CMK	blood:	n/a
11	chr5:97676915-97676965	HIPEpiC	eye:	n/a
12	chr5:97676915-97676965	AG09309	skin:	n/a
13	chr5:97676915-97676965	Hela-S3	cervix:	n/a
14	chr5:97676915-97676965	ProgFib	skin:	n/a
15	chr5:97676915-97676965	HRE	kidney:	n/a
16	chr5:97676915-97676965	HCT-116	colon:	n/a
17	chr5:97676915-97676965	SK-N-SH_RA	brain:	n/a
18	chr5:97676915-97676965	Hepatocyte	liver:	n/a
19	chr5:97676915-97676965	HRCEpiC	kidney:	n/a
20	chr5:97676915-97676965	MCF10A-Er-Src	breast:	n/a
21	chr5:97676915-97676965	HL-60	blood:	n/a
22	chr5:97676915-97676965	HEEpiC	esophagus:	n/a
23	chr5:97676915-97676965	NH-A	brain:	n/a
24	chr5:97676915-97676965	K562	blood:	n/a
25	chr5:97676915-97676965	GM12878	blood:	n/a
26	chr5:97676915-97676965	U87	brain:	n/a
27	chr5:97676915-97676965	HNPCEpiC	eye:	n/a
28	chr5:97676915-97676965	NHBE	bronchial:	n/a
29	chr5:97676915-97676965	GM12892	blood:	n/a
30	chr5:97676915-97676965	Caco-2	colon:	n/a
31	chr5:97676915-97676965	HMEC	breast:	n/a
32	chr5:97676915-97676965	GM06990	blood:	n/a
33	chr5:97676915-97676965	NT2-D1	testis:	n/a
34	chr5:97676915-97676965	HCM	heart:	n/a
35	chr5:97676915-97676965	SAEC	small airway:	n/a
36	chr5:97676915-97676965	A549	lung:	n/a
37	chr5:97676915-97676965	GM12891	blood:	n/a
38	chr5:97676915-97676965	PFSK-1	brain:	n/a
39	chr5:97676915-97676965	SK-N-SH	brain:	n/a
40	chr5:97676915-97676965	PANC-1	pancreas:	n/a
41	chr5:97676915-97676965	HCPEpiC	choroid plexus:	n/a
42	chr5:97676915-97676965	PrEC	prostate:	n/a
43	chr5:97676915-97676965	BJ	skin:	n/a
44	chr5:97676915-97676965	HAEpiC	amniotic membrane:	n/a
45	chr5:97676915-97676965	SKMC	muscle:	n/a
46	chr5:97676915-97676965	SK-N-MC	brain:	n/a
47	chr5:97676915-97676965	RPTEC	kidney:	n/a
48	chr5:97676915-97676965	HEK293	kidney:	embryo
49	chr5:97676915-97676965	ovcar-3	ovarian:	n/a
50	chr5:97676915-97676965	AG04449	skin:	fetal

Variant related genes	Relation type
ENSG00000176183	TF binding region
ENSG00000176183	CpG island

Extended variants
information (count: 474 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:474 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6882939	chr5:97666860-97666861	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs189917812	chr5:97666885-97666886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs72769658	chr5:97666895-97666896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370368486	chr5:97666904-97666905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558992535	chr5:97666930-97666931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182955914	chr5:97666951-97666952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs563368971	chr5:97666960-97666961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530796915	chr5:97666980-97666981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs549222701	chr5:97667007-97667008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111918370	chr5:97667032-97667033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs6887168	chr5:97667081-97667082	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs111359807	chr5:97667114-97667115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565872901	chr5:97667158-97667159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539794595	chr5:97667224-97667225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375223940	chr5:97667278-97667279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs367598877	chr5:97667347-97667348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs13355852	chr5:97667357-97667358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs111592538	chr5:97667366-97667367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537016859	chr5:97667379-97667380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376265406	chr5:97667396-97667397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555194651	chr5:97667428-97667429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs567309440	chr5:97667440-97667441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558412111	chr5:97667459-97667460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554759496	chr5:97667492-97667493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs148645179	chr5:97667493-97667494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140579575	chr5:97667525-97667526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577794591	chr5:97667527-97667528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs545328729	chr5:97667534-97667535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150462253	chr5:97667537-97667538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146189165	chr5:97667578-97667579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61375328	chr5:97667581-97667582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539277983	chr5:97667594-97667595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs542959126	chr5:97667604-97667605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561232884	chr5:97667613-97667614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528628836	chr5:97667651-97667652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs540370477	chr5:97667657-97667658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186829922	chr5:97667661-97667662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191510062	chr5:97667663-97667664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs184154727	chr5:97667673-97667674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs55862280	chr5:97667707-97667708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372483432	chr5:97667747-97667748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs61294285	chr5:97667768-97667769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs569939643	chr5:97667797-97667798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554165709	chr5:97667810-97667811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530428596	chr5:97667816-97667817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549002153	chr5:97667834-97667835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs557787815	chr5:97667839-97667840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534743629	chr5:97667840-97667841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs571520216	chr5:97667842-97667843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13355960	chr5:97667843-97667844	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
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
Merkel cell carcinoma	19020549	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
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17053054	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	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
Breast cancer	21611746	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:97660000-97669800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:97663800-97669600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:97665800-97667200	Enhancers	HUVEC	blood vessel
4	chr5:97666000-97667000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr5:97666400-97667000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:97669400-97670200	Enhancers	NHDF-Ad	bronchial
7	chr5:97669600-97670400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr5:97669800-97670000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr5:97669800-97670000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:97670400-97671400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:97671400-97673600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr5:97672000-97672400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr5:97672400-97674400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:97672800-97676400	Weak transcription	Osteobl	bone
15	chr5:97673600-97676800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr5:97674000-97674800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr5:97674400-97674600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr5:97674400-97674800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr5:97674400-97675400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr5:97674400-97675600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr5:97674800-97675200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr5:97674800-97675400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr5:97675000-97675200	ZNF genes & repeats	NHLF	lung
24	chr5:97675200-97676400	Weak transcription	NHLF	lung
25	chr5:97675200-97676600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr5:97675400-97678200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr5:97675400-97678800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr5:97675600-97676600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr5:97676200-97677200	Enhancers	NHDF-Ad	bronchial
30	chr5:97676400-97676600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr5:97676400-97677600	Enhancers	NH-A	brain
32	chr5:97676400-97678200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:97676400-97678200	Enhancers	Muscle Satellite Cultured Cells	--
34	chr5:97676400-97678200	Enhancers	HSMMtube	muscle
35	chr5:97676400-97678400	Enhancers	HSMM	muscle
36	chr5:97676400-97678400	Enhancers	NHLF	lung
37	chr5:97676400-97678600	Enhancers	Osteobl	bone
38	chr5:97676400-97678800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr5:97676600-97677400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr5:97676600-97677400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr5:97676600-97677400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr5:97676600-97677600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr5:97676600-97677600	Enhancers	Fetal Intestine Large	intestine
44	chr5:97676600-97677600	Enhancers	Fetal Intestine Small	intestine
45	chr5:97676800-97677000	Enhancers	Gastric	stomach
46	chr5:97676800-97677400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr5:97676800-97677400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
48	chr5:97676800-97677600	Enhancers	Fetal Stomach	stomach
49	chr5:97676800-97677600	Enhancers	NHEK	skin
50	chr5:97676800-97678000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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