Variant report

Variant	nsv564198
Chromosome Location	chr14:35118196-35152084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:702)
CpG islands
(count:122)
Chromatin interactive
region (count:34)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:702 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35122450-35122628	K562	blood:	n/a	n/a
2	ARID3A	chr14:35120180-35120293	K562	blood:	n/a	n/a
3	ARID3A	chr14:35135438-35135510	K562	blood:	n/a	n/a
4	ATF1	chr14:35122319-35122681	K562	blood:	n/a	n/a
5	ATF2	chr14:35151763-35152397	GM12878	blood:	n/a	n/a
6	ATF3	chr14:35120100-35120458	K562	blood:	n/a	n/a
7	ATF3	chr14:35120025-35120546	A549	lung:	n/a	n/a
8	BCL3	chr14:35119887-35120614	A549	lung:	n/a	n/a
9	BHLHE40	chr14:35150485-35150595	K562	blood:	n/a	n/a
10	BHLHE40	chr14:35122438-35122531	K562	blood:	n/a	n/a
11	CBX3	chr14:35119980-35120560	HCT-116	colon:	n/a	n/a
12	CBX3	chr14:35119917-35120633	HCT-116	colon:	n/a	n/a
13	CBX3	chr14:35120163-35120474	K562	blood:	n/a	n/a
14	CCNT2	chr14:35147270-35147358	K562	blood:	n/a	n/a
15	CCNT2	chr14:35125305-35125505	K562	blood:	n/a	n/a
16	CEBPB	chr14:35132965-35132992	A549	lung:	n/a	n/a
17	CEBPB	chr14:35117900-35118387	MCF-7	breast:	n/a	n/a
18	CEBPB	chr14:35122373-35122856	K562	blood:	n/a	n/a
19	CEBPB	chr14:35117871-35118372	MCF-7	breast:	n/a	n/a
20	CEBPB	chr14:35122283-35122841	K562	blood:	n/a	n/a
21	CEBPB	chr14:35132959-35133093	K562	blood:	n/a	n/a
22	CEBPB	chr14:35141597-35141623	A549	lung:	n/a	n/a
23	CEBPB	chr14:35147136-35147443	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr14:35119913-35120724	HCT-116	colon:	n/a	n/a
25	CEBPB	chr14:35119923-35120648	HCT-116	colon:	n/a	n/a
26	CEBPB	chr14:35119933-35120650	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr14:35132919-35133126	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr14:35120153-35120445	K562	blood:	n/a	n/a
29	CEBPB	chr14:35119880-35120558	A549	lung:	n/a	n/a
30	CEBPB	chr14:35137416-35137498	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:35147054-35147685	HCT-116	colon:	n/a	n/a
32	CEBPB	chr14:35119953-35120653	A549	lung:	n/a	n/a
33	CEBPB	chr14:35147128-35147480	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:35135194-35135704	A549	lung:	n/a	n/a
35	CEBPB	chr14:35120045-35120582	MCF-7	breast:	n/a	n/a
36	CEBPB	chr14:35119938-35120515	IMR90	lung:	n/a	n/a
37	CEBPB	chr14:35147090-35147488	ECC-1	luminal epithelium:	n/a	n/a
38	CEBPB	chr14:35119868-35120784	A549	lung:	n/a	n/a
39	CEBPD	chr14:35122197-35122711	K562	blood:	n/a	n/a
40	CEBPD	chr14:35122219-35122589	K562	blood:	n/a	n/a
41	CHD1	chr14:35141641-35142218	IMR90	lung:	n/a	n/a
42	CHD1	chr14:35146988-35147639	IMR90	lung:	n/a	n/a
43	CHD1	chr14:35151152-35151161	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr14:35139280-35139430	BE2_C	brain:	n/a	n/a
45	CTCF	chr14:35141900-35142050	NHLF	lung:	n/a	chr14:35141957-35141975 chr14:35141959-35141980 chr14:35141960-35141973 chr14:35141958-35141974
46	CTCF	chr14:35141480-35141630	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr14:35141860-35142010	GM12872	blood:	n/a	chr14:35141957-35141975 chr14:35141959-35141980 chr14:35141960-35141973 chr14:35141958-35141974
48	CTCF	chr14:35141860-35142010	AG04449	skin:	n/a	chr14:35141957-35141975 chr14:35141959-35141980 chr14:35141960-35141973 chr14:35141958-35141974
49	CTCF	chr14:35141500-35141650	HRE	kidney:	n/a	n/a
50	CTCF	chr14:35141860-35142010	HUVEC	blood vessel:	n/a	chr14:35141957-35141975 chr14:35141959-35141980 chr14:35141960-35141973 chr14:35141958-35141974

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35135441-35135491	HIPEpiC	eye:	n/a
2	chr14:35135441-35135491	LNCaP	prostate:	n/a
3	chr14:35135441-35135491	SK-N-MC	brain:	n/a
4	chr14:35119021-35119071	U87	brain:	n/a
5	chr14:35119021-35119071	Hela-S3	cervix:	n/a
6	chr14:35135441-35135491	K562	blood:	n/a
7	chr14:35119021-35119071	RPTEC	kidney:	n/a
8	chr14:35135441-35135491	SAEC	small airway:	n/a
9	chr14:35135441-35135491	NHBE	bronchial:	n/a
10	chr14:35119021-35119071	AG10803	skin:	n/a
11	chr14:35119021-35119071	HCT-116	colon:	n/a
12	chr14:35135441-35135491	NB4	blood:	n/a
13	chr14:35135441-35135491	ovcar-3	ovarian:	n/a
14	chr14:35119021-35119071	SAEC	small airway:	n/a
15	chr14:35135441-35135491	NHDF-neo	bronchial:	n/a
16	chr14:35135441-35135491	ECC-1	luminal epithelium:	n/a
17	chr14:35119021-35119071	HCF	heart:	n/a
18	chr14:35119021-35119071	Hepatocyte	liver:	n/a
19	chr14:35119021-35119071	HMEC	breast:	n/a
20	chr14:35135441-35135491	AG04450	lung:	fetal
21	chr14:35119021-35119071	AoSMC	blood vessel:	n/a
22	chr14:35119021-35119071	Caco-2	colon:	n/a
23	chr14:35135441-35135491	HEK293	kidney:	embryo
24	chr14:35135441-35135491	NT2-D1	testis:	n/a
25	chr14:35135441-35135491	T-47D	breast:	n/a
26	chr14:35119021-35119071	HL-60	blood:	n/a
27	chr14:35135441-35135491	Hela-S3	cervix:	n/a
28	chr14:35119021-35119071	GM12891	blood:	n/a
29	chr14:35135441-35135491	Caco-2	colon:	n/a
30	chr14:35119021-35119071	HCM	heart:	n/a
31	chr14:35135441-35135491	HPAEpiC	pulmonary alveolar:	n/a
32	chr14:35135441-35135491	HepG2	liver:	n/a
33	chr14:35119021-35119071	ECC-1	luminal epithelium:	n/a
34	chr14:35119021-35119071	K562	blood:	n/a
35	chr14:35135441-35135491	HEEpiC	esophagus:	n/a
36	chr14:35135441-35135491	HCM	heart:	n/a
37	chr14:35135441-35135491	AoSMC	blood vessel:	n/a
38	chr14:35135441-35135491	GM06990	blood:	n/a
39	chr14:35135441-35135491	BJ	skin:	n/a
40	chr14:35135441-35135491	AG09319	gingival:	n/a
41	chr14:35119021-35119071	SK-N-MC	brain:	n/a
42	chr14:35119021-35119071	LNCaP	prostate:	n/a
43	chr14:35119021-35119071	BE2_C	brain:	n/a
44	chr14:35135441-35135491	H1-hESC	embryonic stem cell:	embryo
45	chr14:35119021-35119071	MCF10A-Er-Src	breast:	n/a
46	chr14:35119021-35119071	NT2-D1	testis:	n/a
47	chr14:35135441-35135491	PANC-1	pancreas:	n/a
48	chr14:35135441-35135491	HRE	kidney:	n/a
49	chr14:35119021-35119071	PrEC	prostate:	n/a
50	chr14:35119021-35119071	HEK293	kidney:	embryo

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35023387..35025537-chr14:35125652..35127152,2	MCF-7	breast:
2	chr14:35135275..35136944-chr14:35151040..35152580,2	MCF-7	breast:
3	chr14:35150230..35152765-chr14:35168085..35171120,3	MCF-7	breast:
4	chr14:35141750..35142455-chr14:35235000..35235957,3	MCF-7	breast:
5	chr14:35120647..35123453-chr14:35134189..35136107,2	MCF-7	breast:
6	chr14:35139329..35142128-chr14:35231474..35234080,2	MCF-7	breast:
7	chr14:35141519..35142408-chr14:35192106..35192849,2	K562	blood:
8	chr14:35146210..35148621-chr14:35155232..35157199,2	MCF-7	breast:
9	chr14:35103973..35106509-chr14:35117782..35119447,2	K562	blood:
10	chr14:35016452..35018611-chr14:35133910..35135545,2	K562	blood:
11	chr14:35129877..35132741-chr14:35133755..35136058,2	MCF-7	breast:
12	chr14:35145594..35147705-chr14:35179557..35182556,3	MCF-7	breast:
13	chr14:35099347..35101109-chr14:35116790..35118482,2	K562	blood:
14	chr14:35129877..35132741-chr14:35133755..35136058,2	MCF-7	breast:
15	chr14:35141536..35142451-chr14:35451492..35451997,2	MCF-7	breast:
16	chr14:35118550..35121820-chr14:35125434..35129120,4	MCF-7	breast:
17	chr14:35017489..35019232-chr14:35116363..35118749,2	MCF-7	breast:
18	chr14:35130824..35132535-chr14:35133653..35135571,2	K562	blood:
19	chr14:35141525..35142623-chr14:35191837..35192837,6	MCF-7	breast:
20	chr14:35117978..35120935-chr14:35181287..35183685,2	MCF-7	breast:
21	chr14:35103930..35106002-chr14:35116842..35119484,2	MCF-7	breast:
22	chr14:35114358..35116141-chr14:35116901..35120753,3	MCF-7	breast:
23	chr14:35130824..35132535-chr14:35133653..35135571,2	K562	blood:
24	chr14:35120647..35123453-chr14:35134189..35136107,2	MCF-7	breast:
25	chr14:35150818..35153695-chr14:36294438..36295963,2	MCF-7	breast:
26	chr14:35118550..35121820-chr14:35125434..35129120,4	MCF-7	breast:
27	chr14:35139485..35141346-chr14:35514418..35517178,2	MCF-7	breast:
28	chr14:35022004..35024254-chr14:35128832..35131570,2	MCF-7	breast:
29	chr14:35107496..35110407-chr14:35118041..35119624,2	MCF-7	breast:
30	chr14:35135275..35136944-chr14:35151040..35152580,2	MCF-7	breast:
31	chr14:35149872..35152773-chr14:35155685..35158486,2	MCF-7	breast:
32	chr14:35150005..35152867-chr14:35168615..35170921,2	MCF-7	breast:
33	chr14:35149549..35152323-chr14:35213699..35215325,2	MCF-7	breast:
34	chr14:35103956..35105473-chr14:35117782..35120594,2	K562	blood:

No data

Variant related genes	Relation type
RNU6-1261P	TF binding region
RNU6-1261P	CpG island
ENSG00000258704	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000100916	chromatin interactions
ENSG00000165410	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000129515	chromatin interactions

Extended variants
information (count: 1307 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1307 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56054430	chr14:35118196-35118197	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs142424394	chr14:35118202-35118203	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs183957751	chr14:35118266-35118267	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs111532401	chr14:35118333-35118334	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs146657822	chr14:35118347-35118348	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs79799683	chr14:35118382-35118383	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs189212588	chr14:35118395-35118396	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs180695043	chr14:35118416-35118417	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs542800557	chr14:35118458-35118459	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs562784681	chr14:35118469-35118470	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs75062331	chr14:35118502-35118503	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs145682824	chr14:35118505-35118506	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187309026	chr14:35118536-35118537	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs112361281	chr14:35118553-35118554	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547491154	chr14:35118669-35118670	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs376215646	chr14:35118690-35118691	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs190509151	chr14:35118745-35118746	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs199714118	chr14:35118754-35118755	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs570548687	chr14:35118779-35118780	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536465044	chr14:35118792-35118793	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs181887317	chr14:35118832-35118833	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs56366512	chr14:35118865-35118866	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs570356823	chr14:35118904-35118905	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs534648559	chr14:35118916-35118917	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538947061	chr14:35118934-35118935	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557774309	chr14:35118957-35118958	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs577562358	chr14:35119001-35119002	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs537334837	chr14:35119002-35119003	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs533735719	chr14:35119021-35119022	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs553003730	chr14:35119043-35119044	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs57855649	chr14:35119060-35119061	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs576744048	chr14:35119114-35119115	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534324480	chr14:35119148-35119149	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs148931906	chr14:35119170-35119171	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs574185128	chr14:35119209-35119210	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs576328693	chr14:35119280-35119281	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs541571987	chr14:35119284-35119285	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs58615877	chr14:35119285-35119286	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs115166865	chr14:35119290-35119291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs565143796	chr14:35119293-35119294	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs367652886	chr14:35119294-35119295	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs576595058	chr14:35119303-35119304	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs371889083	chr14:35119325-35119326	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs527697919	chr14:35119341-35119342	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547352663	chr14:35119343-35119344	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs113083594	chr14:35119392-35119393	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561070041	chr14:35119452-35119453	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs55727965	chr14:35119472-35119473	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530113087	chr14:35119537-35119538	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs113535936	chr14:35119590-35119591	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35115600-35119200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr14:35117000-35121600	Enhancers	Placenta	Placenta
3	chr14:35117600-35118200	Enhancers	A549	lung
4	chr14:35117600-35118200	Enhancers	K562	blood
5	chr14:35117600-35120000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr14:35118000-35118200	Enhancers	Muscle Satellite Cultured Cells	--
7	chr14:35118000-35118200	Flanking Active TSS	Hela-S3	cervix
8	chr14:35118000-35118200	Enhancers	Osteobl	bone
9	chr14:35118000-35118400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr14:35118000-35118400	Flanking Bivalent TSS/Enh	HepG2	liver
11	chr14:35118000-35118400	Enhancers	NH-A	brain
12	chr14:35118000-35120600	Enhancers	NHDF-Ad	bronchial
13	chr14:35118000-35120800	Enhancers	NHLF	lung
14	chr14:35118200-35118400	Flanking Active TSS	A549	lung
15	chr14:35118200-35118400	Enhancers	Hela-S3	cervix
16	chr14:35118200-35118400	Flanking Active TSS	K562	blood
17	chr14:35118200-35118600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
18	chr14:35118200-35118600	Flanking Active TSS	Osteobl	bone
19	chr14:35118200-35118800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr14:35118200-35119800	Enhancers	HSMM	muscle
21	chr14:35118200-35120200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr14:35118200-35120400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr14:35118200-35120800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:35118200-35120800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr14:35118200-35120800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:35118200-35120800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr14:35118200-35120800	Enhancers	HUVEC	blood vessel
28	chr14:35118200-35120800	Enhancers	NHEK	skin
29	chr14:35118200-35122400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr14:35118400-35118600	Enhancers	A549	lung
31	chr14:35118400-35118600	Flanking Active TSS	Hela-S3	cervix
32	chr14:35118400-35118600	Flanking Active TSS	NH-A	brain
33	chr14:35118400-35118800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr14:35118400-35118800	Bivalent Enhancer	HepG2	liver
35	chr14:35118400-35119400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr14:35118400-35120600	Enhancers	HSMMtube	muscle
37	chr14:35118400-35120800	Enhancers	HMEC	breast
38	chr14:35118400-35122000	Enhancers	K562	blood
39	chr14:35118600-35118800	Flanking Active TSS	A549	lung
40	chr14:35118600-35118800	Enhancers	NH-A	brain
41	chr14:35118600-35119800	Enhancers	Hela-S3	cervix
42	chr14:35118600-35120000	Enhancers	Osteobl	bone
43	chr14:35118600-35120200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr14:35118600-35120800	Enhancers	Muscle Satellite Cultured Cells	--
45	chr14:35118600-35120800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr14:35118800-35119000	Flanking Active TSS	NH-A	brain
47	chr14:35118800-35119400	Enhancers	A549	lung
48	chr14:35118800-35119800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr14:35118800-35120600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:35119000-35121000	Enhancers	NH-A	brain

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