Variant report

Variant	nsv1054179
Chromosome Location	chr14:42653021-42776098
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	ATF2	chr14:42692066-42692469	GM12878	blood:	n/a	n/a
2	ATF2	chr14:42692045-42692786	GM12878	blood:	n/a	n/a
3	ATF3	chr14:42661867-42662866	A549	lung:	n/a	n/a
4	ATF3	chr14:42662093-42662846	A549	lung:	n/a	n/a
5	BATF	chr14:42692467-42692680	GM12878	blood:	n/a	chr14:42692576-42692587 chr14:42692577-42692587
6	BATF	chr14:42660019-42660349	GM12878	blood:	n/a	n/a
7	BATF	chr14:42662374-42662587	GM12878	blood:	n/a	chr14:42662480-42662491 chr14:42662481-42662491 chr14:42662514-42662525
8	BATF	chr14:42660004-42660257	GM12878	blood:	n/a	n/a
9	BCL11A	chr14:42660008-42660275	GM12878	blood:	n/a	n/a
10	BCL11A	chr14:42692221-42692389	GM12878	blood:	n/a	n/a
11	BCL3	chr14:42662001-42662841	A549	lung:	n/a	chr14:42662483-42662492 chr14:42662517-42662526 chr14:42662484-42662493 chr14:42662518-42662527 chr14:42662042-42662051
12	BCL3	chr14:42661796-42662919	A549	lung:	n/a	chr14:42662483-42662492 chr14:42662517-42662526 chr14:42662484-42662493 chr14:42662518-42662527 chr14:42662042-42662051
13	BHLHE40	chr14:42689589-42689608	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:42691918-42692724	GM12878	blood:	n/a	n/a
15	BRCA1	chr14:42662012-42662838	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr14:42765370-42765423	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr14:42662057-42662909	A549	lung:	n/a	chr14:42662558-42662571
18	CEBPB	chr14:42661986-42662943	MCF-7	breast:	n/a	chr14:42662558-42662571
19	CEBPB	chr14:42689352-42689626	HepG2	liver:	n/a	chr14:42689534-42689547 chr14:42689536-42689547 chr14:42689536-42689545
20	CEBPB	chr14:42661924-42662963	Hela-S3	cervix:	n/a	chr14:42662558-42662571
21	CEBPB	chr14:42686488-42687090	HepG2	liver:	n/a	chr14:42686656-42686669 chr14:42686656-42686667
22	CEBPB	chr14:42681313-42681509	HepG2	liver:	n/a	chr14:42681485-42681496
23	CEBPB	chr14:42686505-42686950	A549	lung:	n/a	chr14:42686656-42686669 chr14:42686656-42686667
24	CEBPB	chr14:42758460-42758763	HepG2	liver:	n/a	chr14:42758619-42758630
25	CEBPB	chr14:42688502-42688706	A549	lung:	n/a	chr14:42688620-42688631
26	CEBPB	chr14:42661759-42662992	A549	lung:	n/a	chr14:42662558-42662571
27	CEBPB	chr14:42662119-42662896	IMR90	lung:	n/a	chr14:42662558-42662571
28	CEBPB	chr14:42686494-42687039	IMR90	lung:	n/a	chr14:42686656-42686669 chr14:42686656-42686667
29	CEBPB	chr14:42662023-42662749	A549	lung:	n/a	chr14:42662558-42662571
30	CEBPB	chr14:42686647-42686957	Hela-S3	cervix:	n/a	chr14:42686656-42686669 chr14:42686656-42686667
31	CEBPB	chr14:42662171-42662962	HCT-116	colon:	n/a	chr14:42662558-42662571
32	CEBPB	chr14:42723181-42723431	HepG2	liver:	n/a	chr14:42723323-42723336
33	CEBPB	chr14:42662264-42662818	HCT-116	colon:	n/a	chr14:42662558-42662571
34	CEBPB	chr14:42662009-42662851	MCF-7	breast:	n/a	chr14:42662558-42662571
35	CEBPB	chr14:42688483-42688798	IMR90	lung:	n/a	chr14:42688620-42688631
36	CEBPB	chr14:42731805-42732164	HepG2	liver:	n/a	chr14:42731982-42731993
37	CEBPB	chr14:42686663-42686863	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr14:42688503-42688783	HepG2	liver:	n/a	chr14:42688620-42688631
39	CHD1	chr14:42667986-42668080	GM12878	blood:	n/a	n/a
40	CHD2	chr14:42661924-42662857	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr14:42693600-42693750	HepG2	liver:	n/a	chr14:42693679-42693695 chr14:42693681-42693694 chr14:42693681-42693690 chr14:42693680-42693701 chr14:42693683-42693693 chr14:42693678-42693696
42	CTCF	chr14:42692500-42692650	HVMF	connective:	n/a	n/a
43	CTCF	chr14:42683600-42683750	AG04450	lung:	n/a	n/a
44	CTCF	chr14:42693620-42693770	HFF	foreskin:	n/a	chr14:42693679-42693695 chr14:42693681-42693694 chr14:42693681-42693690 chr14:42693680-42693701 chr14:42693683-42693693 chr14:42693678-42693696
45	CTCF	chr14:42693575-42693788	GM10248	blood:	n/a	chr14:42693679-42693695 chr14:42693681-42693694 chr14:42693681-42693690 chr14:42693680-42693701 chr14:42693683-42693693 chr14:42693678-42693696
46	CTCF	chr14:42683693-42683773	NHEK	skin:	n/a	n/a
47	CTCF	chr14:42693980-42694130	NHDF-neo	bronchial:	n/a	n/a
48	CTCF	chr14:42693522-42693806	HepG2	liver:	n/a	chr14:42693679-42693695 chr14:42693681-42693694 chr14:42693681-42693690 chr14:42693680-42693701 chr14:42693683-42693693 chr14:42693678-42693696
49	CTCF	chr14:42693620-42693770	AG04449	skin:	n/a	chr14:42693679-42693695 chr14:42693681-42693694 chr14:42693681-42693690 chr14:42693680-42693701 chr14:42693683-42693693 chr14:42693678-42693696
50	CTCF	chr14:42683620-42683770	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:42683574-42683624	HIPEpiC	eye:	n/a
2	chr14:42683574-42683624	NB4	blood:	n/a
3	chr14:42683574-42683624	NHBE	bronchial:	n/a
4	chr14:42662538-42662588	GM06990	blood:	n/a
5	chr14:42662538-42662588	HRE	kidney:	n/a
6	chr14:42683574-42683624	GM12878	blood:	n/a
7	chr14:42683574-42683624	LNCaP	prostate:	n/a
8	chr14:42683574-42683624	SKMC	muscle:	n/a
9	chr14:42683574-42683624	MCF-7	breast:	n/a
10	chr14:42662538-42662588	A549	lung:	n/a
11	chr14:42683574-42683624	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:42683574-42683624	GM19239	blood:	n/a
13	chr14:42683574-42683624	AoSMC	blood vessel:	n/a
14	chr14:42662538-42662588	SKMC	muscle:	n/a
15	chr14:42683574-42683624	HCPEpiC	choroid plexus:	n/a
16	chr14:42683574-42683624	HEK293	kidney:	embryo
17	chr14:42683574-42683624	NH-A	brain:	n/a
18	chr14:42662538-42662588	HEK293	kidney:	embryo
19	chr14:42662538-42662588	SAEC	small airway:	n/a
20	chr14:42662538-42662588	AoSMC	blood vessel:	n/a
21	chr14:42662538-42662588	HRCEpiC	kidney:	n/a
22	chr14:42662538-42662588	AG09319	gingival:	n/a
23	chr14:42662538-42662588	GM12878	blood:	n/a
24	chr14:42683574-42683624	BJ	skin:	n/a
25	chr14:42662538-42662588	SK-N-SH_RA	brain:	n/a
26	chr14:42683574-42683624	AG09309	skin:	n/a
27	chr14:42683574-42683624	NT2-D1	testis:	n/a
28	chr14:42662538-42662588	U87	brain:	n/a
29	chr14:42662538-42662588	Caco-2	colon:	n/a
30	chr14:42662538-42662588	ECC-1	luminal epithelium:	n/a
31	chr14:42683574-42683624	ovcar-3	ovarian:	n/a
32	chr14:42683574-42683624	HepG2	liver:	n/a
33	chr14:42683574-42683624	GM12891	blood:	n/a
34	chr14:42662538-42662588	Hela-S3	cervix:	n/a
35	chr14:42662538-42662588	AG10803	skin:	n/a
36	chr14:42683574-42683624	IMR90	lung:	fetal
37	chr14:42662538-42662588	MCF10A-Er-Src	breast:	n/a
38	chr14:42662538-42662588	AG04450	lung:	fetal
39	chr14:42683574-42683624	AG04450	lung:	fetal
40	chr14:42683574-42683624	SAEC	small airway:	n/a
41	chr14:42662538-42662588	HCPEpiC	choroid plexus:	n/a
42	chr14:42662538-42662588	IMR90	lung:	fetal
43	chr14:42662538-42662588	HRPEpiC	eye:	n/a
44	chr14:42662538-42662588	BJ	skin:	n/a
45	chr14:42662538-42662588	GM12892	blood:	n/a
46	chr14:42662538-42662588	T-47D	breast:	n/a
47	chr14:42662538-42662588	NT2-D1	testis:	n/a
48	chr14:42683574-42683624	AG04449	skin:	fetal
49	chr14:42683574-42683624	PrEC	prostate:	n/a
50	chr14:42683574-42683624	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:42676503..42678368-chr14:42692363..42693936,2	MCF-7	breast:
2	chr14:42676503..42678368-chr14:42692363..42693936,2	MCF-7	breast:
3	chr14:42645764..42648661-chr14:42652288..42655011,2	K562	blood:
4	chr14:42693266..42693778-chr14:43474779..43475522,2	MCF-7	breast:
5	chr14:42706583..42708202-chr2:154103638..154105159,2	MCF-7	breast:
6	chr14:42716738..42718328-chr8:110964082..110966975,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-3	chr14:42737695-42737789	ENSG00000259149
2	lnc-FSCB-3	chr14:42728934-42729156	ENSG00000259149

Variant related genes	Relation type
ENSG00000259149	TF binding region
ENSG00000222084	TF binding region
ENSG00000259149	CpG island
ENSG00000222084	CpG island

Extended variants
information (count: 1398 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:1398 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113781234	chr14:42654014-42654015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs550387301	chr14:42654029-42654030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568630028	chr14:42654098-42654099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs181842221	chr14:42654161-42654162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548279777	chr14:42654169-42654170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs566360351	chr14:42654198-42654199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186455588	chr14:42654223-42654224	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs558609411	chr14:42654271-42654272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76548548	chr14:42654309-42654310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568915292	chr14:42654322-42654323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537692311	chr14:42654332-42654333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555940574	chr14:42654353-42654354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537897541	chr14:42654377-42654378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs201333890	chr14:42654403-42654404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574263241	chr14:42654404-42654405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs578076480	chr14:42654409-42654410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs398118119	chr14:42654413-42654414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541932814	chr14:42654448-42654449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148543531	chr14:42654569-42654570	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117908356	chr14:42654577-42654578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs529350830	chr14:42654595-42654596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564665910	chr14:42654659-42654660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188743448	chr14:42654667-42654668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs142867203	chr14:42654721-42654722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs115212483	chr14:42654768-42654769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529476624	chr14:42654775-42654776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs151208736	chr14:42654793-42654794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566543564	chr14:42654795-42654796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565283755	chr14:42654818-42654819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs180757839	chr14:42654893-42654894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140317919	chr14:42654928-42654929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570065393	chr14:42654964-42654965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs185319572	chr14:42654973-42654974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs61993274	chr14:42655041-42655042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs567945884	chr14:42655080-42655081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs535249100	chr14:42655087-42655088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547506981	chr14:42655130-42655131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190871423	chr14:42655189-42655190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554356499	chr14:42655222-42655223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572491582	chr14:42655225-42655226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184014867	chr14:42655245-42655246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558137038	chr14:42655258-42655259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2154294	chr14:42655275-42655276	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
44	rs187397729	chr14:42655277-42655278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144155024	chr14:42655294-42655295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75758584	chr14:42655302-42655303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541613339	chr14:42655308-42655309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560032807	chr14:42655335-42655336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs117195041	chr14:42655350-42655351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551956414	chr14:42655364-42655365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21858162	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Thyroid cancer	19470727	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Immune disease	21076436	CNVD
Immune disease	21042300	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Bipolar disorder	19114987	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:223 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42654000-42654600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr14:42654400-42654800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr14:42654800-42662000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr14:42656800-42658000	Enhancers	Muscle Satellite Cultured Cells	--
5	chr14:42657000-42657600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr14:42657000-42657800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr14:42657400-42657800	Enhancers	Osteobl	bone
8	chr14:42657600-42661200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr14:42657800-42658000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr14:42657800-42661600	Weak transcription	Osteobl	bone
11	chr14:42657800-42661800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr14:42658000-42661400	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr14:42658200-42661600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr14:42661200-42661800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr14:42661200-42661800	Enhancers	A549	lung
16	chr14:42661200-42661800	Enhancers	HUVEC	blood vessel
17	chr14:42661200-42661800	Enhancers	NHDF-Ad	bronchial
18	chr14:42661400-42661800	Enhancers	Muscle Satellite Cultured Cells	--
19	chr14:42661400-42664200	Enhancers	Hela-S3	cervix
20	chr14:42661600-42661800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr14:42661600-42661800	Enhancers	NH-A	brain
22	chr14:42661600-42661800	Enhancers	NHLF	lung
23	chr14:42661600-42661800	Enhancers	Osteobl	bone
24	chr14:42661600-42662000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr14:42661600-42662000	Enhancers	NHEK	skin
26	chr14:42661600-42663600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr14:42661600-42663600	Enhancers	HMEC	breast
28	chr14:42661800-42662000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr14:42661800-42662200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr14:42661800-42662200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr14:42661800-42662200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr14:42661800-42662200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr14:42661800-42662200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr14:42661800-42662200	Enhancers	Small Intestine	intestine
35	chr14:42661800-42662200	Flanking Active TSS	A549	lung
36	chr14:42661800-42662400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr14:42661800-42662400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
38	chr14:42661800-42662400	Flanking Active TSS	HUVEC	blood vessel
39	chr14:42661800-42662400	Flanking Active TSS	NH-A	brain
40	chr14:42661800-42662400	Flanking Active TSS	NHDF-Ad	bronchial
41	chr14:42661800-42662400	Flanking Active TSS	NHLF	lung
42	chr14:42661800-42662400	Flanking Active TSS	Osteobl	bone
43	chr14:42661800-42662800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr14:42661800-42663000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:42661800-42663200	Enhancers	HSMM	muscle
46	chr14:42661800-42663400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr14:42661800-42663400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr14:42661800-42663400	Enhancers	Colon Smooth Muscle	Colon
49	chr14:42662000-42662400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr14:42662000-42662400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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