Variant report

Variant	nsv901743
Chromosome Location	chr14:42672410-43030843
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	chr14:42890942-42891236	GM12878	blood:	n/a	n/a
2	ATF2	chr14:42692045-42692786	GM12878	blood:	n/a	n/a
3	ATF2	chr14:42898121-42898501	GM12878	blood:	n/a	n/a
4	ATF2	chr14:42898123-42898538	GM12878	blood:	n/a	n/a
5	ATF2	chr14:42692066-42692469	GM12878	blood:	n/a	n/a
6	BATF	chr14:42992903-42993204	GM12878	blood:	n/a	n/a
7	BATF	chr14:42898158-42898555	GM12878	blood:	n/a	n/a
8	BATF	chr14:42807386-42807601	GM12878	blood:	n/a	chr14:42807519-42807530
9	BATF	chr14:42890928-42891203	GM12878	blood:	n/a	chr14:42891116-42891127 chr14:42891154-42891165
10	BATF	chr14:42692467-42692680	GM12878	blood:	n/a	chr14:42692576-42692587 chr14:42692577-42692587
11	BATF	chr14:42890963-42891282	GM12878	blood:	n/a	chr14:42891116-42891127 chr14:42891154-42891165
12	BCL11A	chr14:42805119-42805441	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr14:42992865-42993250	GM12878	blood:	n/a	n/a
14	BCL11A	chr14:42792249-42792451	GM12878	blood:	n/a	n/a
15	BCL11A	chr14:42692221-42692389	GM12878	blood:	n/a	n/a
16	BCL11A	chr14:42898127-42898592	GM12878	blood:	n/a	n/a
17	BCL11A	chr14:42944608-42944827	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr14:42805184-42805444	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr14:42898070-42898555	GM12878	blood:	n/a	n/a
20	BCL11A	chr14:42890931-42891249	GM12878	blood:	n/a	n/a
21	BHLHE40	chr14:42691918-42692724	GM12878	blood:	n/a	n/a
22	BHLHE40	chr14:42898065-42898516	GM12878	blood:	n/a	n/a
23	BHLHE40	chr14:42689589-42689608	GM12878	blood:	n/a	n/a
24	BRCA1	chr14:43010506-43011087	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr14:42765370-42765423	Hela-S3	cervix:	n/a	n/a
26	CCNT2	chr14:42932649-42932849	K562	blood:	n/a	n/a
27	CEBPB	chr14:42681313-42681509	HepG2	liver:	n/a	chr14:42681485-42681496
28	CEBPB	chr14:42689352-42689626	HepG2	liver:	n/a	chr14:42689534-42689547 chr14:42689536-42689547 chr14:42689536-42689545
29	CEBPB	chr14:42686494-42687039	IMR90	lung:	n/a	chr14:42686656-42686669 chr14:42686656-42686667
30	CEBPB	chr14:42854827-42854835	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:42758460-42758763	HepG2	liver:	n/a	chr14:42758619-42758630
32	CEBPB	chr14:42686505-42686950	A549	lung:	n/a	chr14:42686656-42686669 chr14:42686656-42686667
33	CEBPB	chr14:42688503-42688783	HepG2	liver:	n/a	chr14:42688620-42688631
34	CEBPB	chr14:42686488-42687090	HepG2	liver:	n/a	chr14:42686656-42686669 chr14:42686656-42686667
35	CEBPB	chr14:42973675-42974008	IMR90	lung:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
36	CEBPB	chr14:42973667-42974028	HepG2	liver:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
37	CEBPB	chr14:42686663-42686863	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr14:42973656-42974004	Hela-S3	cervix:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
39	CEBPB	chr14:42973693-42973995	A549	lung:	n/a	chr14:42973833-42973846 chr14:42973851-42973862 chr14:42973834-42973845 chr14:42973849-42973860 chr14:42973851-42973860
40	CEBPB	chr14:42688502-42688706	A549	lung:	n/a	chr14:42688620-42688631
41	CEBPB	chr14:42826701-42826845	A549	lung:	n/a	chr14:42826760-42826771
42	CEBPB	chr14:42968773-42969081	HepG2	liver:	n/a	chr14:42968894-42968905 chr14:42968918-42968929
43	CEBPB	chr14:42995827-42996065	HepG2	liver:	n/a	chr14:42995926-42995937 chr14:42995924-42995935
44	CEBPB	chr14:42898784-42898952	HepG2	liver:	n/a	chr14:42898837-42898848
45	CEBPB	chr14:42968792-42969062	IMR90	lung:	n/a	chr14:42968894-42968905 chr14:42968918-42968929
46	CEBPB	chr14:42941893-42942056	HepG2	liver:	n/a	chr14:42941935-42941946
47	CEBPB	chr14:42686647-42686957	Hela-S3	cervix:	n/a	chr14:42686656-42686669 chr14:42686656-42686667
48	CEBPB	chr14:42917905-42918115	HepG2	liver:	n/a	chr14:42918004-42918015
49	CEBPB	chr14:42970807-42970999	HepG2	liver:	n/a	chr14:42970856-42970867
50	CEBPB	chr14:43009532-43009798	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:42683574-42683624	NHDF-neo	bronchial:	n/a
2	chr14:42683574-42683624	AoSMC	blood vessel:	n/a
3	chr14:42683574-42683624	K562	blood:	n/a
4	chr14:42683574-42683624	ProgFib	skin:	n/a
5	chr14:42683574-42683624	Hela-S3	cervix:	n/a
6	chr14:42683574-42683624	HAEpiC	amniotic membrane:	n/a
7	chr14:42683574-42683624	MCF-7	breast:	n/a
8	chr14:42683574-42683624	PANC-1	pancreas:	n/a
9	chr14:42683574-42683624	BE2_C	brain:	n/a
10	chr14:42683574-42683624	SK-N-SH_RA	brain:	n/a
11	chr14:42683574-42683624	HRCEpiC	kidney:	n/a
12	chr14:42683574-42683624	NH-A	brain:	n/a
13	chr14:42683574-42683624	HRE	kidney:	n/a
14	chr14:42683574-42683624	AG09319	gingival:	n/a
15	chr14:42683574-42683624	CMK	blood:	n/a
16	chr14:42683574-42683624	HCF	heart:	n/a
17	chr14:42683574-42683624	H1-hESC	embryonic stem cell:	embryo
18	chr14:42683574-42683624	GM06990	blood:	n/a
19	chr14:42683574-42683624	ovcar-3	ovarian:	n/a
20	chr14:42683574-42683624	GM12878	blood:	n/a
21	chr14:42683574-42683624	HCPEpiC	choroid plexus:	n/a
22	chr14:42683574-42683624	HCM	heart:	n/a
23	chr14:42683574-42683624	Caco-2	colon:	n/a
24	chr14:42683574-42683624	Hepatocyte	liver:	n/a
25	chr14:42683574-42683624	IMR90	lung:	fetal
26	chr14:42683574-42683624	HUVEC	blood vessel:	n/a
27	chr14:42683574-42683624	A549	lung:	n/a
28	chr14:42683574-42683624	AG04449	skin:	fetal
29	chr14:42683574-42683624	NB4	blood:	n/a
30	chr14:42683574-42683624	GM19239	blood:	n/a
31	chr14:42683574-42683624	SK-N-SH	brain:	n/a
32	chr14:42683574-42683624	PFSK-1	brain:	n/a
33	chr14:42683574-42683624	T-47D	breast:	n/a
34	chr14:42683574-42683624	AG10803	skin:	n/a
35	chr14:42683574-42683624	HEEpiC	esophagus:	n/a
36	chr14:42683574-42683624	HNPCEpiC	eye:	n/a
37	chr14:42683574-42683624	ECC-1	luminal epithelium:	n/a
38	chr14:42683574-42683624	BJ	skin:	n/a
39	chr14:42683574-42683624	SKMC	muscle:	n/a
40	chr14:42683574-42683624	LNCaP	prostate:	n/a
41	chr14:42683574-42683624	U87	brain:	n/a
42	chr14:42683574-42683624	AG04450	lung:	fetal
43	chr14:42683574-42683624	MCF10A-Er-Src	breast:	n/a
44	chr14:42683574-42683624	SK-N-MC	brain:	n/a
45	chr14:42683574-42683624	NHBE	bronchial:	n/a
46	chr14:42683574-42683624	HIPEpiC	eye:	n/a
47	chr14:42683574-42683624	Jurkat	blood:	n/a
48	chr14:42683574-42683624	SAEC	small airway:	n/a
49	chr14:42683574-42683624	HCT-116	colon:	n/a
50	chr14:42683574-42683624	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:42716738..42718328-chr8:110964082..110966975,2	MCF-7	breast:
2	chr14:42871630..42873900-chr14:42876970..42879114,2	MCF-7	breast:
3	chr14:42871630..42873900-chr14:42876970..42879114,2	MCF-7	breast:
4	chr14:42933700..42935505-chr14:42937514..42939043,2	MCF-7	breast:
5	chr14:43030553..43031053-chr17:8338863..8339416,2	Hela-S3	cervix:
6	chr14:42995581..42997108-chr14:42999086..43001857,2	K562	blood:
7	chr14:42854900..42857464-chr14:42857634..42860608,2	MCF-7	breast:
8	chr14:42955061..42956041-chr18:32446617..32447280,2	MCF-7	breast:
9	chr14:42933700..42935505-chr14:42937514..42939043,2	MCF-7	breast:
10	chr14:42933286..42933984-chr3:29810719..29811455,2	MCF-7	breast:
11	chr14:42676503..42678368-chr14:42692363..42693936,2	MCF-7	breast:
12	chr14:42854900..42857464-chr14:42857634..42860608,2	MCF-7	breast:
13	chr14:42790692..42792450-chr14:42801986..42803943,2	MCF-7	breast:
14	chr14:42995581..42997108-chr14:42999086..43001857,2	K562	blood:
15	chr14:42676503..42678368-chr14:42692363..42693936,2	MCF-7	breast:
16	chr14:42706583..42708202-chr2:154103638..154105159,2	MCF-7	breast:
17	chr14:42790692..42792450-chr14:42801986..42803943,2	MCF-7	breast:
18	chr14:42693266..42693778-chr14:43474779..43475522,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-214N1.1.1-2	chr14:42998014-42998060	NONHSAT036588
2	lnc-FSCB-3	chr14:42737695-42737789	ENSG00000259149
3	lnc-RP11-214N1.1.1-1	chr14:42832186-42832203	ENSG00000258394.1
4	lnc-FSCB-3	chr14:42728934-42729156	ENSG00000259149
5	lnc-RP11-214N1.1.1-2	chr14:42972301-42972709	NONHSAT036588
6	lnc-RP11-214N1.1.1-2	chr14:42881776-42882409	ENSG00000258850.1
7	lnc-RP11-214N1.1.1-2	chr14:42997872-42998091	ENSG00000258850.1
8	lnc-RP11-214N1.1.1-2	chr14:42997872-42998001	NONHSAT036588
9	lnc-RP11-214N1.1.1-2	chr14:42881776-42883030	NONHSAT036588
10	lnc-RP11-214N1.1.1-1	chr14:42864148-42864295	ENSG00000258394.1

Variant related genes	Relation type
ENSG00000259149	TF binding region
ENSG00000222084	TF binding region
ENSG00000258850	TF binding region
ENSG00000258394	TF binding region
ENSG00000259149	CpG island
ENSG00000222084	CpG island
ENSG00000258850	CpG island
ENSG00000258394	CpG island
ENSG00000166579	chromatin interactions

Extended variants
information (count: 5070 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:5070 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556970637	chr14:42683009-42683010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559880406	chr14:42683013-42683014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575224949	chr14:42683051-42683052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs543353123	chr14:42683093-42683094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs554967981	chr14:42683095-42683096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567708583	chr14:42683148-42683149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs1273438	chr14:42683158-42683159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs540488161	chr14:42683225-42683226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565453656	chr14:42683243-42683244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs533090226	chr14:42683285-42683286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs56068672	chr14:42683385-42683386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563310891	chr14:42683391-42683392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529171520	chr14:42683524-42683525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs548817133	chr14:42683538-42683539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369415037	chr14:42683547-42683548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs567456490	chr14:42683606-42683607	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs113395758	chr14:42683685-42683686	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs118027845	chr14:42683746-42683747	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs571095080	chr14:42683816-42683817	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs112179727	chr14:42683828-42683829	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs114027278	chr14:42683836-42683837	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs376010362	chr14:42683861-42683862	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs551746208	chr14:42683870-42683871	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs571674779	chr14:42683893-42683894	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs534267239	chr14:42683908-42683909	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs369056958	chr14:42683956-42683957	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs554917198	chr14:42684064-42684065	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs184944487	chr14:42684077-42684078	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs540902519	chr14:42684118-42684119	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs559226959	chr14:42684130-42684131	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs189437958	chr14:42684187-42684188	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs545169444	chr14:42684327-42684328	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs78160559	chr14:42684328-42684329	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563372568	chr14:42684398-42684399	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10498364	chr14:42684415-42684416	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs542272198	chr14:42684421-42684422	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560910463	chr14:42684423-42684424	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs528403132	chr14:42684450-42684451	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373146995	chr14:42684462-42684463	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35641090	chr14:42684471-42684472	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567814987	chr14:42684523-42684524	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192424490	chr14:42684560-42684561	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573947777	chr14:42684568-42684569	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs571155518	chr14:42684616-42684617	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs72674307	chr14:42684626-42684627	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs550321444	chr14:42684633-42684634	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569027240	chr14:42684690-42684691	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184636869	chr14:42684707-42684708	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs386776855	chr14:42684817-42684818	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72674309	chr14:42684819-42684820	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:66)

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
Osteosarcoma	21215367	CNVD
Glioblastoma multiforme	21569311	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:42683000-42683600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr14:42683000-42685000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr14:42683200-42684600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr14:42683400-42685000	Enhancers	HMEC	breast
5	chr14:42683400-42685400	Enhancers	NHEK	skin
6	chr14:42683600-42683800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr14:42683600-42684000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
8	chr14:42683600-42684200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr14:42683600-42684200	Enhancers	Adipose Nuclei	Adipose
10	chr14:42683600-42684200	Active TSS	Skeletal Muscle Female	skeletal muscle
11	chr14:42683600-42684400	Enhancers	Left Ventricle	heart
12	chr14:42683600-42684400	Enhancers	Psoas Muscle	Psoas
13	chr14:42683600-42684600	Enhancers	HSMM	muscle
14	chr14:42683600-42684800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr14:42683600-42684800	Enhancers	Colon Smooth Muscle	Colon
16	chr14:42683600-42684800	Enhancers	Hela-S3	cervix
17	chr14:42683600-42684800	Enhancers	HSMMtube	muscle
18	chr14:42683600-42684800	Enhancers	HUVEC	blood vessel
19	chr14:42683600-42685000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr14:42683600-42685000	Enhancers	NH-A	brain
21	chr14:42683600-42685600	Enhancers	Osteobl	bone
22	chr14:42683600-42685800	Enhancers	NHDF-Ad	bronchial
23	chr14:42683800-42684800	Enhancers	Stomach Smooth Muscle	stomach
24	chr14:42683800-42691400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr14:42684000-42684400	Enhancers	Muscle Satellite Cultured Cells	--
26	chr14:42684000-42685000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr14:42684000-42685000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr14:42684200-42684400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
29	chr14:42684200-42684600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr14:42684200-42684600	Flanking Active TSS	Adipose Nuclei	Adipose
31	chr14:42684200-42684600	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr14:42684200-42684600	Enhancers	NHLF	lung
33	chr14:42684200-42684800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr14:42684200-42684800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr14:42684200-42684800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr14:42684200-42684800	Enhancers	Rectal Smooth Muscle	rectum
37	chr14:42684200-42684800	Enhancers	A549	lung
38	chr14:42684400-42684800	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr14:42684400-42685000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr14:42684600-42684800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr14:42684600-42684800	Enhancers	Adipose Nuclei	Adipose
42	chr14:42684600-42685000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr14:42684800-42686000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr14:42684800-42686000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr14:42684800-42686600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr14:42685000-42685600	Enhancers	Muscle Satellite Cultured Cells	--
47	chr14:42685000-42686000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr14:42685000-42686600	Weak transcription	HMEC	breast
49	chr14:42685400-42685800	Weak transcription	NHEK	skin
50	chr14:42685600-42691000	Weak transcription	Osteobl	bone

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