Variant report

Variant	nsv1040350
Chromosome Location	chr14:35196524-35245409
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:122)
Chromatin interactive
region (count:31)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:323 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr14:35209799-35210064	GM12878	blood:	n/a	n/a
2	BCL3	chr14:35203787-35204534	GM12878	blood:	n/a	n/a
3	BCL3	chr14:35203782-35204497	GM12878	blood:	n/a	n/a
4	CBX3	chr14:35202370-35202940	HCT-116	colon:	n/a	n/a
5	CEBPB	chr14:35227987-35228149	HepG2	liver:	n/a	n/a
6	CEBPB	chr14:35213102-35213384	K562	blood:	n/a	chr14:35213219-35213230
7	CEBPB	chr14:35220011-35220215	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr14:35213091-35213314	IMR90	lung:	n/a	chr14:35213219-35213230
9	CEBPB	chr14:35217157-35217214	K562	blood:	n/a	chr14:35217198-35217209
10	CEBPB	chr14:35213203-35213245	H1-hESC	embryonic stem cell:	n/a	chr14:35213219-35213230
11	CEBPB	chr14:35234216-35234404	A549	lung:	n/a	n/a
12	CEBPB	chr14:35217104-35217278	HepG2	liver:	n/a	chr14:35217198-35217209
13	CEBPB	chr14:35211862-35212140	HepG2	liver:	n/a	n/a
14	CEBPB	chr14:35202411-35202871	MCF-7	breast:	n/a	chr14:35202785-35202798
15	CEBPB	chr14:35234268-35234374	HepG2	liver:	n/a	n/a
16	CEBPB	chr14:35213076-35213377	HepG2	liver:	n/a	chr14:35213219-35213230
17	CEBPB	chr14:35213096-35213296	A549	lung:	n/a	chr14:35213219-35213230
18	CEBPB	chr14:35219904-35220225	IMR90	lung:	n/a	n/a
19	CEBPB	chr14:35211921-35212074	A549	lung:	n/a	n/a
20	CREB1	chr14:35201995-35202452	HepG2	liver:	n/a	n/a
21	CTCF	chr14:35235440-35235590	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr14:35235380-35235530	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr14:35235460-35235610	GM06990	blood:	n/a	n/a
24	CTCF	chr14:35235440-35235590	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr14:35204073-35204415	MCF-7	breast:	n/a	n/a
26	CTCF	chr14:35235420-35235570	Caco-2	colon:	n/a	n/a
27	CTCF	chr14:35235340-35235490	GM12878	blood:	n/a	n/a
28	CTCF	chr14:35235500-35235650	HFF	foreskin:	n/a	n/a
29	CTCF	chr14:35235400-35235550	HCM	heart:	n/a	n/a
30	CTCF	chr14:35235220-35235370	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr14:35235340-35235490	GM12874	blood:	n/a	n/a
32	CTCF	chr14:35235400-35235550	BE2_C	brain:	n/a	n/a
33	CTCF	chr14:35235340-35235490	HVMF	connective:	n/a	n/a
34	CTCF	chr14:35235360-35235510	A549	lung:	n/a	n/a
35	CTCF	chr14:35235380-35235530	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr14:35235360-35235510	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr14:35217047-35217108	GM13976	blood:	n/a	n/a
38	CTCF	chr14:35235340-35235490	GM12864	blood:	n/a	n/a
39	CTCF	chr14:35235420-35235570	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr14:35213960-35214110	HepG2	liver:	n/a	n/a
41	CTCF	chr14:35235440-35235590	HMF	breast:	n/a	n/a
42	CTCF	chr14:35235380-35235530	HL-60	blood:	n/a	n/a
43	CTCF	chr14:35235205-35235849	HepG2	liver:	n/a	n/a
44	CTCF	chr14:35235420-35235570	HRE	kidney:	n/a	n/a
45	CTCF	chr14:35235160-35235310	HVMF	connective:	n/a	n/a
46	CTCF	chr14:35235380-35235530	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr14:35235360-35235510	GM12871	blood:	n/a	n/a
48	CTCF	chr14:35235420-35235570	HMF	breast:	n/a	n/a
49	CTCF	chr14:35235356-35235616	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr14:35235400-35235550	GM12873	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35203968-35204018	T-47D	breast:	n/a
2	chr14:35236912-35236962	PANC-1	pancreas:	n/a
3	chr14:35203968-35204018	MCF10A-Er-Src	breast:	n/a
4	chr14:35203968-35204018	SK-N-SH_RA	brain:	n/a
5	chr14:35203968-35204018	AG10803	skin:	n/a
6	chr14:35203968-35204018	SAEC	small airway:	n/a
7	chr14:35236912-35236962	NHDF-neo	bronchial:	n/a
8	chr14:35236912-35236962	MCF-7	breast:	n/a
9	chr14:35236912-35236962	HPAEpiC	pulmonary alveolar:	n/a
10	chr14:35203968-35204018	ovcar-3	ovarian:	n/a
11	chr14:35203968-35204018	BE2_C	brain:	n/a
12	chr14:35203968-35204018	HIPEpiC	eye:	n/a
13	chr14:35203968-35204018	Hepatocyte	liver:	n/a
14	chr14:35236912-35236962	RPTEC	kidney:	n/a
15	chr14:35236912-35236962	AG10803	skin:	n/a
16	chr14:35203968-35204018	Caco-2	colon:	n/a
17	chr14:35203968-35204018	GM12892	blood:	n/a
18	chr14:35236912-35236962	AoSMC	blood vessel:	n/a
19	chr14:35236912-35236962	ProgFib	skin:	n/a
20	chr14:35236912-35236962	GM12891	blood:	n/a
21	chr14:35203968-35204018	AG09309	skin:	n/a
22	chr14:35203968-35204018	HPAEpiC	pulmonary alveolar:	n/a
23	chr14:35236912-35236962	PrEC	prostate:	n/a
24	chr14:35203968-35204018	NHDF-neo	bronchial:	n/a
25	chr14:35236912-35236962	GM19239	blood:	n/a
26	chr14:35203968-35204018	HRE	kidney:	n/a
27	chr14:35203968-35204018	PANC-1	pancreas:	n/a
28	chr14:35203968-35204018	NB4	blood:	n/a
29	chr14:35236912-35236962	Jurkat	blood:	n/a
30	chr14:35236912-35236962	T-47D	breast:	n/a
31	chr14:35236912-35236962	BJ	skin:	n/a
32	chr14:35203968-35204018	RPTEC	kidney:	n/a
33	chr14:35203968-35204018	HL-60	blood:	n/a
34	chr14:35203968-35204018	HCT-116	colon:	n/a
35	chr14:35203968-35204018	HEK293	kidney:	embryo
36	chr14:35236912-35236962	NB4	blood:	n/a
37	chr14:35203968-35204018	IMR90	lung:	fetal
38	chr14:35203968-35204018	K562	blood:	n/a
39	chr14:35236912-35236962	AG09319	gingival:	n/a
40	chr14:35236912-35236962	SK-N-SH	brain:	n/a
41	chr14:35236912-35236962	HCF	heart:	n/a
42	chr14:35203968-35204018	HCF	heart:	n/a
43	chr14:35236912-35236962	SK-N-SH_RA	brain:	n/a
44	chr14:35203968-35204018	NHBE	bronchial:	n/a
45	chr14:35203968-35204018	BJ	skin:	n/a
46	chr14:35203968-35204018	HMEC	breast:	n/a
47	chr14:35236912-35236962	HCM	heart:	n/a
48	chr14:35236912-35236962	PFSK-1	brain:	n/a
49	chr14:35203968-35204018	GM12891	blood:	n/a
50	chr14:35203968-35204018	Hela-S3	cervix:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35216580..35218836-chr14:35224214..35226003,2	MCF-7	breast:
2	chr14:35244032..35246087-chr14:35246234..35248911,2	K562	blood:
3	chr14:35022505..35025054-chr14:35199460..35201377,2	MCF-7	breast:
4	chr14:35182351..35184361-chr14:35202721..35204488,2	MCF-7	breast:
5	chr14:35216580..35218836-chr14:35224214..35226003,2	MCF-7	breast:
6	chr14:35237218..35239739-chr14:35251859..35254380,2	K562	blood:
7	chr14:35239089..35240652-chr14:35244321..35246894,2	MCF-7	breast:
8	chr14:35019137..35020709-chr14:35232783..35235542,2	MCF-7	breast:
9	chr14:35219442..35221288-chr14:35451553..35453425,2	MCF-7	breast:
10	chr14:35023215..35025386-chr14:35216421..35218330,2	MCF-7	breast:
11	chr14:35149549..35152323-chr14:35213699..35215325,2	MCF-7	breast:
12	chr14:35141750..35142455-chr14:35235000..35235957,3	MCF-7	breast:
13	chr14:35234999..35235707-chr14:35882228..35882732,2	MCF-7	breast:
14	chr14:35201332..35203966-chr14:35218977..35221479,2	MCF-7	breast:
15	chr14:35239089..35240652-chr14:35244321..35246894,2	MCF-7	breast:
16	chr14:35220615..35223020-chr14:35450573..35452983,2	K562	blood:
17	chr14:35169173..35171973-chr14:35214224..35216870,2	MCF-7	breast:
18	chr14:35182088..35184140-chr14:35204016..35205651,2	MCF-7	breast:
19	chr14:35227474..35229033-chr14:35341739..35343496,2	MCF-7	breast:
20	chr14:35191597..35194615-chr14:35196317..35199532,3	MCF-7	breast:
21	chr14:35232989..35235688-chr14:35236337..35238801,2	K562	blood:
22	chr14:35021191..35023610-chr14:35210750..35213558,2	MCF-7	breast:
23	chr14:35193866..35196753-chr7:148818833..148820454,2	MCF-7	breast:
24	chr14:35237464..35239910-chr14:35248990..35251298,2	K562	blood:
25	chr14:35235389..35237760-chr14:35341826..35344219,2	MCF-7	breast:
26	chr14:35201332..35203966-chr14:35218977..35221479,2	MCF-7	breast:
27	chr14:35139329..35142128-chr14:35231474..35234080,2	MCF-7	breast:
28	chr14:35232989..35235688-chr14:35236337..35238801,2	K562	blood:
29	chr14:35173049..35174992-chr14:35202703..35204231,2	MCF-7	breast:
30	chr14:35239285..35241333-chr14:35342948..35344948,2	MCF-7	breast:
31	chr14:35022083..35024389-chr14:35233897..35236737,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CFL2-2	chr14:35228119-35228334	expReg_chr14_2115_-
2	lnc-CFL2-3	chr14:35228545-35228769	expReg_chr14_2118_-
3	lnc-CFL2-4	chr14:35227420-35227870	expReg_chr14_2111_-

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BAZ1A	hsa-miR-373-3p	chr14:35222566-35222587

Variant related genes	Relation type
ENSG00000243824	TF binding region
BAZ1A	TF binding region
ENSG00000243824	CpG island
BAZ1A	CpG island
ENSG00000165410	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000198604	chromatin interactions

Extended variants
information (count: 2070 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:2070 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182424983	chr14:35196550-35196551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558257166	chr14:35196624-35196625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572103023	chr14:35196647-35196648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372109382	chr14:35196667-35196668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144553532	chr14:35196668-35196669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs2383669	chr14:35196693-35196694	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs186706049	chr14:35196749-35196750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs543653929	chr14:35196768-35196769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs563756890	chr14:35196777-35196778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532497162	chr14:35196793-35196794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192692379	chr14:35196806-35196807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2383670	chr14:35196807-35196808	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs528488287	chr14:35196816-35196817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76741172	chr14:35196905-35196906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76127410	chr14:35196907-35196908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539689928	chr14:35196916-35196917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537200640	chr14:35196942-35196943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557267757	chr14:35196945-35196946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557780776	chr14:35196951-35196952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184752832	chr14:35196962-35196963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538337456	chr14:35196974-35196975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs558649558	chr14:35197002-35197003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572044940	chr14:35197024-35197025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189999327	chr14:35197034-35197035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2383671	chr14:35197041-35197042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs527534513	chr14:35197062-35197063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7144989	chr14:35197235-35197236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs13313361	chr14:35197256-35197257	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs115154327	chr14:35197272-35197273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs7144858	chr14:35197285-35197286	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs545952436	chr14:35197305-35197306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544333311	chr14:35197312-35197313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563845523	chr14:35197323-35197324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559811362	chr14:35197380-35197381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528428583	chr14:35197402-35197403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548180406	chr14:35197403-35197404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs568160737	chr14:35197423-35197424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs58803997	chr14:35197453-35197454	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs551288833	chr14:35197459-35197460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112516265	chr14:35197480-35197481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13313362	chr14:35197484-35197485	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs193051125	chr14:35197546-35197547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565791654	chr14:35197557-35197558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184834550	chr14:35197570-35197571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs189973687	chr14:35197586-35197587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs11845001	chr14:35197589-35197590	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs376674832	chr14:35197599-35197600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149831497	chr14:35197640-35197641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58921719	chr14:35197653-35197654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536931400	chr14:35197664-35197665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:886 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35184400-35204000	Weak transcription	Pancreas	Pancrea
2	chr14:35192600-35202000	Weak transcription	HSMMtube	muscle
3	chr14:35198800-35199000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr14:35199000-35199600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr14:35199600-35203000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr14:35201200-35201400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr14:35201400-35203200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr14:35202000-35202400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:35202000-35202400	Enhancers	A549	lung
10	chr14:35202000-35202400	Enhancers	NHLF	lung
11	chr14:35202000-35202600	Enhancers	NHEK	skin
12	chr14:35202000-35202800	Enhancers	HSMMtube	muscle
13	chr14:35202000-35203000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr14:35202000-35203000	Enhancers	HepG2	liver
15	chr14:35202000-35203000	Enhancers	HSMM	muscle
16	chr14:35202000-35203200	Enhancers	HMEC	breast
17	chr14:35202000-35203400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:35202000-35203600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr14:35202200-35202600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr14:35202200-35203000	Enhancers	Muscle Satellite Cultured Cells	--
21	chr14:35202200-35203000	Enhancers	Placenta Amnion	Placenta Amnion
22	chr14:35202200-35203000	Enhancers	NH-A	brain
23	chr14:35202200-35203200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr14:35202200-35203200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr14:35202200-35203200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr14:35202400-35202800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr14:35202400-35203000	Flanking Active TSS	A549	lung
28	chr14:35202400-35203200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr14:35202400-35203200	Enhancers	Osteobl	bone
30	chr14:35202600-35203000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr14:35202600-35203000	Flanking Active TSS	NHEK	skin
32	chr14:35203000-35203200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr14:35203000-35203200	Enhancers	NHEK	skin
34	chr14:35203200-35203400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:35203200-35204600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr14:35203400-35204000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr14:35203800-35204000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr14:35204000-35204200	Weak transcription	Gastric	stomach
39	chr14:35204000-35204200	Enhancers	Pancreas	Pancrea
40	chr14:35204000-35204400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr14:35204000-35204400	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr14:35204000-35204400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr14:35204200-35204400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr14:35204200-35204400	Enhancers	Gastric	stomach
45	chr14:35204200-35205200	Weak transcription	Pancreas	Pancrea
46	chr14:35204400-35204600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr14:35204400-35210400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr14:35209400-35209600	Bivalent Enhancer	HepG2	liver
49	chr14:35209800-35222600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:35210400-35210600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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