Variant report

Variant	esv3504662
Chromosome Location	chr14:46340901-46586259
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:802)
CpG islands
(count:122)
Chromatin interactive
region (count:14)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:46375372-46375853	GM12878	blood:	n/a	n/a
2	BACH1	chr14:46351093-46351107	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr14:46559473-46559585	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr14:46368023-46368235	GM12878	blood:	n/a	n/a
5	BATF	chr14:46375483-46375752	GM12878	blood:	n/a	n/a
6	BATF	chr14:46375489-46375749	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:46375429-46375807	GM12878	blood:	n/a	n/a
8	CBX3	chr14:46517423-46517924	HCT-116	colon:	n/a	n/a
9	CEBPB	chr14:46388540-46388874	HepG2	liver:	n/a	chr14:46388709-46388720
10	CEBPB	chr14:46388507-46388949	MCF-7	breast:	n/a	chr14:46388709-46388720
11	CEBPB	chr14:46504563-46504826	IMR90	lung:	n/a	chr14:46504676-46504687
12	CEBPB	chr14:46559949-46560242	HepG2	liver:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
13	CEBPB	chr14:46477968-46478185	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:46357543-46357739	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr14:46547984-46548190	HepG2	liver:	n/a	chr14:46548062-46548073
16	CEBPB	chr14:46504544-46504822	A549	lung:	n/a	chr14:46504676-46504687
17	CEBPB	chr14:46441158-46441496	A549	lung:	n/a	chr14:46441316-46441327
18	CEBPB	chr14:46523694-46524102	IMR90	lung:	n/a	n/a
19	CEBPB	chr14:46441220-46441420	H1-hESC	embryonic stem cell:	n/a	chr14:46441316-46441327
20	CEBPB	chr14:46441175-46441403	HepG2	liver:	n/a	chr14:46441316-46441327
21	CEBPB	chr14:46388459-46388948	MCF-7	breast:	n/a	chr14:46388709-46388720
22	CEBPB	chr14:46559920-46560194	A549	lung:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
23	CEBPB	chr14:46388540-46388897	IMR90	lung:	n/a	chr14:46388709-46388720
24	CEBPB	chr14:46559908-46560222	IMR90	lung:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
25	CEBPB	chr14:46504576-46504826	HepG2	liver:	n/a	chr14:46504676-46504687
26	CEBPB	chr14:46560063-46560127	K562	blood:	n/a	chr14:46560066-46560079 chr14:46560067-46560078 chr14:46560068-46560077 chr14:46560066-46560077 chr14:46560066-46560079
27	CEBPB	chr14:46388556-46388893	A549	lung:	n/a	chr14:46388709-46388720
28	CHD2	chr14:46360235-46360350	HepG2	liver:	n/a	n/a
29	CTCF	chr14:46517440-46517590	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr14:46459580-46459730	GM12864	blood:	n/a	n/a
31	CTCF	chr14:46517460-46517610	GM12873	blood:	n/a	n/a
32	CTCF	chr14:46503625-46503716	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr14:46459640-46459790	HPF	lung:	n/a	n/a
34	CTCF	chr14:46517420-46517570	SAEC	small airway:	n/a	n/a
35	CTCF	chr14:46459580-46459730	HAc	cerebellar:	n/a	n/a
36	CTCF	chr14:46503760-46503910	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr14:46517412-46517610	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr14:46517420-46517570	BE2_C	brain:	n/a	n/a
39	CTCF	chr14:46459620-46459770	SK-N-SH_RA	brain:	n/a	n/a
40	CTCF	chr14:46517360-46517510	HFF	foreskin:	n/a	n/a
41	CTCF	chr14:46517380-46517530	AG04450	lung:	n/a	n/a
42	CTCF	chr14:46517320-46517470	HCM	heart:	n/a	n/a
43	CTCF	chr14:46459480-46459630	RPTEC	kidney:	n/a	n/a
44	CTCF	chr14:46517273-46517849	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr14:46459600-46459750	BJ	skin:	n/a	n/a
46	CTCF	chr14:46517380-46517530	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr14:46409660-46409810	HMEC	breast:	n/a	n/a
48	CTCF	chr14:46500480-46500630	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr14:46500500-46500522	ProgFib	skin:	n/a	n/a
50	CTCF	chr14:46459600-46459750	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:46358139-46358189	Caco-2	colon:	n/a
2	chr14:46358279-46358329	HUVEC	blood vessel:	n/a
3	chr14:46358279-46358329	HEEpiC	esophagus:	n/a
4	chr14:46358139-46358189	HCM	heart:	n/a
5	chr14:46358139-46358189	RPTEC	kidney:	n/a
6	chr14:46358139-46358189	SAEC	small airway:	n/a
7	chr14:46358139-46358189	GM12878	blood:	n/a
8	chr14:46358279-46358329	AG10803	skin:	n/a
9	chr14:46358139-46358189	SK-N-SH	brain:	n/a
10	chr14:46358139-46358189	SK-N-MC	brain:	n/a
11	chr14:46358139-46358189	HepG2	liver:	n/a
12	chr14:46358279-46358329	U87	brain:	n/a
13	chr14:46358139-46358189	GM12892	blood:	n/a
14	chr14:46358139-46358189	HCPEpiC	choroid plexus:	n/a
15	chr14:46358279-46358329	HCT-116	colon:	n/a
16	chr14:46358279-46358329	HL-60	blood:	n/a
17	chr14:46358139-46358189	Hepatocyte	liver:	n/a
18	chr14:46358279-46358329	HCF	heart:	n/a
19	chr14:46358279-46358329	K562	blood:	n/a
20	chr14:46358279-46358329	H1-hESC	embryonic stem cell:	embryo
21	chr14:46358279-46358329	HCM	heart:	n/a
22	chr14:46358279-46358329	HEK293	kidney:	embryo
23	chr14:46358279-46358329	GM06990	blood:	n/a
24	chr14:46358279-46358329	SK-N-SH	brain:	n/a
25	chr14:46358139-46358189	HL-60	blood:	n/a
26	chr14:46358279-46358329	GM12891	blood:	n/a
27	chr14:46358279-46358329	BJ	skin:	n/a
28	chr14:46358139-46358189	BJ	skin:	n/a
29	chr14:46358139-46358189	ovcar-3	ovarian:	n/a
30	chr14:46358139-46358189	GM12891	blood:	n/a
31	chr14:46358279-46358329	SAEC	small airway:	n/a
32	chr14:46358139-46358189	NH-A	brain:	n/a
33	chr14:46358139-46358189	AoSMC	blood vessel:	n/a
34	chr14:46358279-46358329	HRCEpiC	kidney:	n/a
35	chr14:46358279-46358329	A549	lung:	n/a
36	chr14:46358279-46358329	CMK	blood:	n/a
37	chr14:46358279-46358329	LNCaP	prostate:	n/a
38	chr14:46358139-46358189	NB4	blood:	n/a
39	chr14:46358279-46358329	AG04450	lung:	fetal
40	chr14:46358279-46358329	PFSK-1	brain:	n/a
41	chr14:46358279-46358329	NB4	blood:	n/a
42	chr14:46358139-46358189	NHBE	bronchial:	n/a
43	chr14:46358139-46358189	T-47D	breast:	n/a
44	chr14:46358139-46358189	NHDF-neo	bronchial:	n/a
45	chr14:46358279-46358329	HRPEpiC	eye:	n/a
46	chr14:46358279-46358329	SKMC	muscle:	n/a
47	chr14:46358279-46358329	GM19239	blood:	n/a
48	chr14:46358139-46358189	MCF-7	breast:	n/a
49	chr14:46358139-46358189	HCT-116	colon:	n/a
50	chr14:46358139-46358189	HRCEpiC	kidney:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:46308036..46308555-chr14:46409283..46409960,2	MCF-7	breast:
2	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
3	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
4	chr14:46346207..46348483-chr14:46349392..46352093,2	K562	blood:
5	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
6	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
7	chr12:122908054..122908892-chr14:46408991..46409734,2	MCF-7	breast:
8	chr14:46368837..46370409-chr14:46372784..46375382,2	K562	blood:
9	chr14:46557288..46558270-chr17:53789584..53790485,2	MCF-7	breast:
10	chr14:46375125..46377270-chr14:46379726..46383333,3	K562	blood:
11	chr14:46385119..46386937-chr14:46388253..46390395,2	MCF-7	breast:
12	chr14:46538407..46539085-chr4:43195045..43195862,2	MCF-7	breast:
13	chr14:46517458..46517985-chr14:47049934..47050581,2	MCF-7	breast:
14	chr14:46517075..46517958-chr14:46813262..46814074,4	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FANCM-9	chr14:46359392-46359577	NONHSAT036675
2	lnc-FANCM-6	chr14:46533362-46533419	NONHSAT036679
3	lnc-FANCM-10	chr14:46484296-46484458	NONHSAT036677
4	lnc-FANCM-10	chr14:46483700-46483934	NONHSAT036677
5	lnc-FANCM-6	chr14:46533362-46533419	NONHSAT036678
6	lnc-FANCM-6	chr14:46410146-46410221	ENSG00000258700
7	lnc-FANCM-9	chr14:46376825-46376872	NONHSAT036675
8	lnc-FANCM-6	chr14:46533362-46533419	ENSG00000258700

No data

Variant related genes	Relation type
LINC00871	TF binding region
LINC00871	CpG island

Extended variants
information (count: 2744 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2744 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113517575	chr14:46357608-46357609	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs562550766	chr14:46357627-46357628	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10142032	chr14:46357634-46357635	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs180884203	chr14:46357670-46357671	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs543212284	chr14:46357681-46357682	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs561592209	chr14:46357686-46357687	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2768516	chr14:46357687-46357688	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs546979467	chr14:46357688-46357689	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547470059	chr14:46357693-46357694	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561663786	chr14:46357706-46357707	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs393645	chr14:46357712-46357713	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs77536935	chr14:46357719-46357720	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568992514	chr14:46357740-46357741	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs393678	chr14:46357747-46357748	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192513622	chr14:46357751-46357752	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201145308	chr14:46357753-46357754	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376217815	chr14:46357754-46357755	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs547952959	chr14:46357774-46357775	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183795495	chr14:46357787-46357788	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs201652586	chr14:46357808-46357809	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs566439462	chr14:46357851-46357852	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs146932058	chr14:46357854-46357855	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs558813462	chr14:46357869-46357870	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576792858	chr14:46357930-46357931	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs537835406	chr14:46357937-46357938	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs556312129	chr14:46357958-46357959	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs574560482	chr14:46357960-46357961	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs71517479	chr14:46357977-46357978	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs561425275	chr14:46357978-46357979	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs573373123	chr14:46357997-46357998	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs551463943	chr14:46358013-46358014	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540616252	chr14:46358014-46358015	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs4333557	chr14:46358015-46358016	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs4507734	chr14:46358023-46358024	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs112086196	chr14:46358042-46358043	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs79246215	chr14:46358049-46358050	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76469102	chr14:46358050-46358051	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs75342822	chr14:46358054-46358055	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs80246264	chr14:46358058-46358059	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76831952	chr14:46358059-46358060	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs533832003	chr14:46358061-46358062	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs71626862	chr14:46358062-46358063	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs74741492	chr14:46358064-46358065	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74508066	chr14:46358068-46358069	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79379947	chr14:46358078-46358079	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs76453467	chr14:46358080-46358081	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs550526370	chr14:46358082-46358083	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs78281017	chr14:46358083-46358084	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74533924	chr14:46358084-46358085	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs79614853	chr14:46358085-46358086	Active TSS Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	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
Oral squamous cell carcinoma	17134496	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	19907438	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:224 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:46357600-46357800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr14:46357600-46358200	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr14:46357600-46358200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:46357600-46358400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:46357600-46358600	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr14:46357600-46358600	Active TSS	HUES64 Cell Line	embryonic stem cell
7	chr14:46357800-46358600	Active TSS	H9 Cell Line	embryonic stem cell
8	chr14:46357800-46358600	Active TSS	iPS-15b Cell Line	embryonic stem cell
9	chr14:46358000-46358200	Active TSS	H1 Cell Line	embryonic stem cell
10	chr14:46358000-46358200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:46358000-46358600	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr14:46358000-46360800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:46358200-46358400	Flanking Active TSS	H1 Cell Line	embryonic stem cell
14	chr14:46358200-46358400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr14:46358200-46358400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr14:46358400-46358600	Active TSS	HUES48 Cell Line	embryonic stem cell
17	chr14:46358400-46358600	Weak transcription	Pancreas	Pancrea
18	chr14:46358400-46360800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr14:46358400-46360800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr14:46358400-46361000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr14:46358600-46359000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr14:46358600-46359000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr14:46358600-46360200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr14:46358600-46360400	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr14:46358600-46360400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr14:46358600-46360800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr14:46359000-46360200	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr14:46359000-46360600	Weak transcription	HUES6 Cell Line	embryonic stem cell
29	chr14:46359200-46359600	Enhancers	Fetal Kidney	kidney
30	chr14:46359600-46360000	Weak transcription	Fetal Kidney	kidney
31	chr14:46360000-46360600	Enhancers	Fetal Kidney	kidney
32	chr14:46360200-46360600	Active TSS	ES-I3 Cell Line	embryonic stem cell
33	chr14:46360200-46360800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr14:46360200-46360800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr14:46360200-46360800	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr14:46360200-46360800	Enhancers	HMEC	breast
37	chr14:46360200-46361400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr14:46360200-46362200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr14:46360400-46360600	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr14:46360400-46360600	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr14:46360400-46360600	Enhancers	NHEK	skin
42	chr14:46360400-46360800	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr14:46360400-46360800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr14:46360400-46361000	Enhancers	Colon Smooth Muscle	Colon
45	chr14:46360400-46361600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr14:46360600-46360800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr14:46360600-46360800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr14:46360600-46360800	Enhancers	Esophagus	oesophagus
49	chr14:46360600-46360800	Enhancers	Ovary	ovary
50	chr14:46360600-46360800	Enhancers	Pancreas	Pancrea

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