Variant report

Variant	nsv599435
Chromosome Location	chr5:113957246-114166068
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	BHLHE40	chr5:114125586-114125762	GM12878	blood:	n/a	n/a
2	BHLHE40	chr5:113993492-113993685	K562	blood:	n/a	n/a
3	CEBPB	chr5:114118689-114118754	HepG2	liver:	n/a	n/a
4	CEBPB	chr5:113970220-113970599	A549	lung:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
5	CEBPB	chr5:113970237-113970569	MCF-7	breast:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
6	CEBPB	chr5:114133961-114134206	HepG2	liver:	n/a	chr5:114134096-114134107
7	CEBPB	chr5:114108964-114109264	HepG2	liver:	n/a	chr5:114109077-114109088
8	CEBPB	chr5:114139498-114139808	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr5:114102319-114102498	HepG2	liver:	n/a	chr5:114102441-114102452
10	CEBPB	chr5:113993485-113993747	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr5:113970217-113970599	H1-hESC	embryonic stem cell:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
12	CEBPB	chr5:114073815-114073987	HepG2	liver:	n/a	chr5:114073883-114073894 chr5:114073880-114073897
13	CEBPB	chr5:113993507-113993646	K562	blood:	n/a	n/a
14	CEBPB	chr5:114014575-114014744	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr5:113970317-113970507	A549	lung:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
16	CEBPB	chr5:113987524-113987814	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr5:114108963-114109257	A549	lung:	n/a	chr5:114109077-114109088
18	CEBPB	chr5:113970241-113970588	Hela-S3	cervix:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
19	CEBPB	chr5:114085188-114085505	HepG2	liver:	n/a	chr5:114085314-114085325
20	CEBPB	chr5:114136917-114136942	A549	lung:	n/a	n/a
21	CEBPB	chr5:114118687-114118856	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr5:113970223-113970601	IMR90	lung:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
23	CEBPB	chr5:114139403-114139746	HCT-116	colon:	n/a	n/a
24	CEBPB	chr5:114109020-114109117	H1-hESC	embryonic stem cell:	n/a	chr5:114109077-114109088
25	CEBPB	chr5:114014252-114014275	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr5:113970213-113970582	A549	lung:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
27	CEBPB	chr5:114108944-114109200	IMR90	lung:	n/a	chr5:114109077-114109088
28	CEBPB	chr5:113966175-113966410	HepG2	liver:	n/a	chr5:113966248-113966260 chr5:113966289-113966300
29	CEBPB	chr5:114085307-114085500	A549	lung:	n/a	chr5:114085314-114085325
30	CEBPB	chr5:113970220-113970587	K562	blood:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
31	CEBPB	chr5:114085288-114085512	IMR90	lung:	n/a	chr5:114085314-114085325
32	CEBPB	chr5:114016852-114017040	A549	lung:	n/a	chr5:114016923-114016934
33	CEBPB	chr5:114016801-114017079	HepG2	liver:	n/a	chr5:114016923-114016934
34	CEBPB	chr5:113970218-113970603	HepG2	liver:	n/a	chr5:113970406-113970415 chr5:113970404-113970417 chr5:113970406-113970415 chr5:113970404-113970415 chr5:113970406-113970415
35	CTCF	chr5:114139100-114139250	GM12873	blood:	n/a	chr5:114139207-114139225 chr5:114139202-114139223 chr5:114139208-114139224
36	CTCF	chr5:114139860-114140010	NHEK	skin:	n/a	n/a
37	CTCF	chr5:114125580-114125730	GM12874	blood:	n/a	chr5:114125655-114125673 chr5:114125650-114125671 chr5:114125656-114125672
38	CTCF	chr5:114139180-114139330	GM12871	blood:	n/a	chr5:114139207-114139225 chr5:114139202-114139223 chr5:114139208-114139224
39	CTCF	chr5:114139300-114139450	GM12872	blood:	n/a	n/a
40	CTCF	chr5:114125560-114125710	SK-N-SH_RA	brain:	n/a	chr5:114125655-114125673 chr5:114125650-114125671 chr5:114125656-114125672
41	CTCF	chr5:114139220-114139370	GM12864	blood:	n/a	n/a
42	CTCF	chr5:114125512-114125788	K562	blood:	n/a	chr5:114125655-114125673 chr5:114125650-114125671 chr5:114125656-114125672
43	CTCF	chr5:114125560-114125710	HepG2	liver:	n/a	chr5:114125655-114125673 chr5:114125650-114125671 chr5:114125656-114125672
44	CTCF	chr5:114081505-114081576	GM12878	blood:	n/a	n/a
45	CTCF	chr5:114133718-114133949	MCF-7	breast:	n/a	chr5:114133848-114133861
46	CTCF	chr5:114125600-114125750	GM12872	blood:	n/a	chr5:114125655-114125673 chr5:114125650-114125671 chr5:114125656-114125672
47	CTCF	chr5:114125540-114125690	HRPEpiC	eye:	n/a	chr5:114125655-114125673 chr5:114125650-114125671 chr5:114125656-114125672
48	CTCF	chr5:114139520-114139670	HEK293	kidney:	n/a	n/a
49	CTCF	chr5:114125620-114125770	RPTEC	kidney:	n/a	chr5:114125655-114125673 chr5:114125650-114125671 chr5:114125656-114125672
50	CTCF	chr5:114125580-114125730	BE2_C	brain:	n/a	chr5:114125655-114125673 chr5:114125650-114125671 chr5:114125656-114125672

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:114110567-114110617	HNPCEpiC	eye:	n/a
2	chr5:114110567-114110617	AoSMC	blood vessel:	n/a
3	chr5:114110567-114110617	HCM	heart:	n/a
4	chr5:114109705-114109755	HPAEpiC	pulmonary alveolar:	n/a
5	chr5:114026851-114026901	HRCEpiC	kidney:	n/a
6	chr5:114110567-114110617	T-47D	breast:	n/a
7	chr5:114109705-114109755	HCT-116	colon:	n/a
8	chr5:114026851-114026901	Hela-S3	cervix:	n/a
9	chr5:114110567-114110617	GM12878	blood:	n/a
10	chr5:114026851-114026901	U87	brain:	n/a
11	chr5:114110567-114110617	GM12891	blood:	n/a
12	chr5:114110567-114110617	HCT-116	colon:	n/a
13	chr5:114109705-114109755	GM06990	blood:	n/a
14	chr5:114026851-114026901	HNPCEpiC	eye:	n/a
15	chr5:114109705-114109755	AG04450	lung:	fetal
16	chr5:114109705-114109755	AG09319	gingival:	n/a
17	chr5:114026851-114026901	HAEpiC	amniotic membrane:	n/a
18	chr5:114110567-114110617	HEK293	kidney:	embryo
19	chr5:114109705-114109755	NHDF-neo	bronchial:	n/a
20	chr5:114109705-114109755	T-47D	breast:	n/a
21	chr5:114109705-114109755	HCM	heart:	n/a
22	chr5:114109705-114109755	ovcar-3	ovarian:	n/a
23	chr5:114110567-114110617	BE2_C	brain:	n/a
24	chr5:114110567-114110617	U87	brain:	n/a
25	chr5:114026851-114026901	AG09309	skin:	n/a
26	chr5:114109705-114109755	HUVEC	blood vessel:	n/a
27	chr5:114110567-114110617	Hepatocyte	liver:	n/a
28	chr5:114026851-114026901	AG04450	lung:	fetal
29	chr5:114109705-114109755	Hepatocyte	liver:	n/a
30	chr5:114110567-114110617	SK-N-SH_RA	brain:	n/a
31	chr5:114026851-114026901	NB4	blood:	n/a
32	chr5:114026851-114026901	HepG2	liver:	n/a
33	chr5:114026851-114026901	NH-A	brain:	n/a
34	chr5:114109705-114109755	RPTEC	kidney:	n/a
35	chr5:114109705-114109755	PFSK-1	brain:	n/a
36	chr5:114109705-114109755	GM12892	blood:	n/a
37	chr5:114026851-114026901	GM12878	blood:	n/a
38	chr5:114026851-114026901	HCPEpiC	choroid plexus:	n/a
39	chr5:114109705-114109755	IMR90	lung:	fetal
40	chr5:114109705-114109755	NB4	blood:	n/a
41	chr5:114110567-114110617	GM19239	blood:	n/a
42	chr5:114110567-114110617	ECC-1	luminal epithelium:	n/a
43	chr5:114110567-114110617	AG09309	skin:	n/a
44	chr5:114109705-114109755	GM19239	blood:	n/a
45	chr5:114026851-114026901	HEEpiC	esophagus:	n/a
46	chr5:114026851-114026901	T-47D	breast:	n/a
47	chr5:114026851-114026901	Jurkat	blood:	n/a
48	chr5:114110567-114110617	AG10803	skin:	n/a
49	chr5:114109705-114109755	NH-A	brain:	n/a
50	chr5:114110567-114110617	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:114028110..114029775-chr5:114042253..114044572,2	K562	blood:
2	chr5:114133331..114134215-chr5:114369304..114370183,3	MCF-7	breast:
3	chr5:114138711..114139387-chr5:114369334..114369873,2	MCF-7	breast:
4	chr5:114125530..114126082-chr5:114137895..114138833,2	MCF-7	breast:
5	chr5:114125530..114126082-chr5:114137895..114138833,2	MCF-7	breast:
6	chr5:114041267..114043614-chr5:114045209..114048129,2	K562	blood:
7	chr5:114139161..114139984-chr5:114369361..114370136,2	MCF-7	breast:
8	chr5:114028110..114029775-chr5:114042253..114044572,2	K562	blood:
9	chr17:56708890..56709453-chr5:113999791..114000291,2	Hela-S3	cervix:
10	chr5:113985866..113987952-chr5:113988127..113990699,2	K562	blood:
11	chr5:114041267..114043614-chr5:114045209..114048129,2	K562	blood:
12	chr5:114139185..114139978-chr5:114404825..114405439,2	MCF-7	breast:
13	chr5:113985866..113987952-chr5:113988127..113990699,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM36-4	chr5:114003306-114003444	ENSG00000246316.3
2	lnc-TRIM36-4	chr5:113998658-113998922	ENSG00000246316.3
3	lnc-TRIM36-4	chr5:114003805-114003928	ENSG00000246316.3
4	lnc-TRIM36-4	chr5:114004040-114004103	ENSG00000246316.3

Variant related genes	Relation type
ENSG00000246316	TF binding region
ENSG00000246316	CpG island
ENSG00000212195	chromatin interactions

Extended variants
information (count: 1960 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1960 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532051388	chr5:113971018-113971019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs146857710	chr5:113971039-113971040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs376996113	chr5:113971041-113971042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs570879816	chr5:113971055-113971056	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs140269948	chr5:113971056-113971057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs542135772	chr5:113971106-113971107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370734731	chr5:113971121-113971122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150324676	chr5:113971134-113971135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs375362912	chr5:113971171-113971172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs137864909	chr5:113971194-113971195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs186817797	chr5:113971209-113971210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564123307	chr5:113971227-113971228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs386691328	chr5:113971241-113971242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs78818346	chr5:113971242-113971243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547627754	chr5:113971270-113971271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375569442	chr5:113971286-113971287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs149455241	chr5:113971312-113971313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs548895634	chr5:113971327-113971328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs570149741	chr5:113971329-113971330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143052116	chr5:113971331-113971332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558737978	chr5:113971337-113971338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368277348	chr5:113971351-113971352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs534813833	chr5:113971367-113971368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552927230	chr5:113971378-113971379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574809799	chr5:113971384-113971385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541748484	chr5:113971402-113971403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs563647097	chr5:113971428-113971429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192125208	chr5:113971466-113971467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs545941165	chr5:113971477-113971478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs77403588	chr5:113971503-113971504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371854309	chr5:113971533-113971534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540355296	chr5:113971549-113971550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561648879	chr5:113971551-113971552	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs528932484	chr5:113971559-113971560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567746512	chr5:113971574-113971575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs550311999	chr5:113971580-113971581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs533607102	chr5:113971635-113971636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs570291405	chr5:113971644-113971645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531127725	chr5:113971713-113971714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs538314159	chr5:113971750-113971751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs556710064	chr5:113971752-113971753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183905391	chr5:113971758-113971759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570740474	chr5:113971762-113971763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs374374559	chr5:113971811-113971812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1820382	chr5:113971833-113971834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs138908935	chr5:113971848-113971849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142931293	chr5:113971878-113971879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535793773	chr5:113971900-113971901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs557086128	chr5:113971907-113971908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147396292	chr5:113971930-113971931	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	16272173	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
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Sezary syndrome	18413736	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:113971000-113972200	Enhancers	Colon Smooth Muscle	Colon
2	chr5:113980000-113980600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:113980400-113981000	Enhancers	Brain Substantia Nigra	brain
4	chr5:113985200-113986200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr5:113985800-113986200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr5:113992800-113994800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr5:113993400-113994200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:113993400-113994800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr5:113993600-113994000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr5:113994800-113996800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr5:113997000-113997200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr5:114001000-114001600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr5:114001000-114001800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr5:114021600-114022000	Enhancers	Fetal Brain Male	brain
15	chr5:114031000-114031400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
16	chr5:114041200-114041600	Bivalent/Poised TSS	Aorta	Aorta
17	chr5:114051800-114052600	Active TSS	Right Atrium	heart
18	chr5:114052600-114054400	Weak transcription	Right Atrium	heart
19	chr5:114058400-114059000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chr5:114061600-114063000	Enhancers	HSMMtube	muscle
21	chr5:114062800-114063200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:114062800-114063400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr5:114084800-114085000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr5:114085000-114085600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:114085000-114085800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr5:114085600-114091200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr5:114085800-114086000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr5:114086000-114086800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr5:114086800-114087200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr5:114091200-114091800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:114091800-114095000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:114095000-114095200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:114095200-114095800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:114095800-114096000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:114108200-114110200	Enhancers	Adipose Nuclei	Adipose
36	chr5:114109400-114110200	Enhancers	Fetal Brain Female	brain
37	chr5:114110200-114118400	Weak transcription	Adipose Nuclei	Adipose
38	chr5:114111800-114112800	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr5:114112800-114118000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr5:114117800-114118800	Enhancers	Fetal Muscle Leg	muscle
41	chr5:114118000-114118400	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr5:114118400-114118600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr5:114118400-114119000	Enhancers	Adipose Nuclei	Adipose
44	chr5:114118600-114119000	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr5:114118600-114119000	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr5:114119000-114119600	Weak transcription	Adipose Nuclei	Adipose
47	chr5:114119600-114120800	Enhancers	Adipose Nuclei	Adipose
48	chr5:114125400-114126000	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr5:114129200-114129800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr5:114141600-114142200	Enhancers	Breast Myoepithelial Primary Cells	Breast

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