Variant report

Variant	nsv901776
Chromosome Location	chr14:43631485-43868912
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	ARID3A	chr14:43642362-43642983	HepG2	liver:	n/a	chr14:43642744-43642760 chr14:43642745-43642761
2	ARID3A	chr14:43770928-43770931	HepG2	liver:	n/a	n/a
3	ATF2	chr14:43638975-43639274	GM12878	blood:	n/a	n/a
4	BATF	chr14:43638998-43639216	GM12878	blood:	n/a	n/a
5	BCL11A	chr14:43635475-43635709	GM12878	blood:	n/a	chr14:43635694-43635703
6	BHLHE40	chr14:43639054-43639242	GM12878	blood:	n/a	n/a
7	BRCA1	chr14:43688380-43688435	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr14:43678094-43678225	HepG2	liver:	n/a	n/a
9	BRCA1	chr14:43744368-43744514	HepG2	liver:	n/a	n/a
10	CEBPB	chr14:43642376-43642711	Hela-S3	cervix:	n/a	chr14:43642536-43642547 chr14:43642575-43642586
11	CEBPB	chr14:43751706-43751924	MCF-7	breast:	n/a	chr14:43751855-43751866
12	CEBPB	chr14:43642322-43642878	HepG2	liver:	n/a	chr14:43642536-43642547 chr14:43642575-43642586
13	CEBPB	chr14:43826288-43826431	HepG2	liver:	n/a	chr14:43826327-43826344
14	CEBPB	chr14:43799516-43799760	HepG2	liver:	n/a	chr14:43799594-43799605 chr14:43799661-43799678 chr14:43799594-43799607
15	CEBPB	chr14:43838957-43839300	A549	lung:	n/a	chr14:43839107-43839118
16	CEBPB	chr14:43826038-43826600	MCF-7	breast:	n/a	chr14:43826327-43826344
17	CEBPB	chr14:43751727-43752031	Hela-S3	cervix:	n/a	chr14:43751855-43751866
18	CEBPB	chr14:43645659-43645980	HepG2	liver:	n/a	chr14:43645837-43645848 chr14:43645837-43645850 chr14:43645837-43645850 chr14:43645839-43645850 chr14:43645708-43645721
19	CEBPB	chr14:43838931-43839289	HepG2	liver:	n/a	chr14:43839107-43839118
20	CEBPB	chr14:43642436-43642637	HepG2	liver:	n/a	chr14:43642536-43642547 chr14:43642575-43642586
21	CEBPB	chr14:43751703-43752032	IMR90	lung:	n/a	chr14:43751855-43751866
22	CEBPB	chr14:43834714-43834907	HepG2	liver:	n/a	chr14:43834795-43834806
23	CEBPB	chr14:43751664-43752043	HepG2	liver:	n/a	chr14:43751855-43751866
24	CEBPB	chr14:43727729-43728009	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:43740863-43741131	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:43797586-43797850	HepG2	liver:	n/a	chr14:43797713-43797724
27	CEBPB	chr14:43634888-43635264	MCF-7	breast:	n/a	n/a
28	CEBPB	chr14:43838901-43839260	MCF-7	breast:	n/a	chr14:43839107-43839118
29	CEBPB	chr14:43743731-43744024	HepG2	liver:	n/a	chr14:43743855-43743866 chr14:43743856-43743867 chr14:43743855-43743868
30	CEBPB	chr14:43642383-43642669	A549	lung:	n/a	chr14:43642536-43642547 chr14:43642575-43642586
31	CEBPB	chr14:43838939-43839283	IMR90	lung:	n/a	chr14:43839107-43839118
32	CEBPB	chr14:43688231-43688372	A549	lung:	n/a	n/a
33	CEBPB	chr14:43751816-43751948	H1-hESC	embryonic stem cell:	n/a	chr14:43751855-43751866
34	CEBPB	chr14:43689962-43690242	HepG2	liver:	n/a	chr14:43690074-43690087 chr14:43690075-43690086
35	CEBPB	chr14:43642364-43642715	A549	lung:	n/a	chr14:43642536-43642547 chr14:43642575-43642586
36	CEBPB	chr14:43758431-43758726	HepG2	liver:	n/a	chr14:43758603-43758614
37	CEBPB	chr14:43826136-43826553	MCF-7	breast:	n/a	chr14:43826327-43826344
38	CEBPB	chr14:43664756-43665100	HepG2	liver:	n/a	chr14:43664905-43664916
39	CEBPB	chr14:43777599-43778357	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr14:43775448-43775758	HepG2	liver:	n/a	chr14:43775607-43775618 chr14:43775606-43775619
41	CEBPB	chr14:43659574-43660192	HepG2	liver:	n/a	chr14:43659655-43659666
42	CEBPB	chr14:43751694-43752036	A549	lung:	n/a	chr14:43751855-43751866
43	CEBPB	chr14:43748607-43748868	HepG2	liver:	n/a	chr14:43748766-43748777 chr14:43748767-43748776 chr14:43748674-43748685 chr14:43748765-43748778 chr14:43748674-43748687 chr14:43748674-43748685
44	CEBPB	chr14:43839045-43839271	K562	blood:	n/a	chr14:43839107-43839118
45	CEBPB	chr14:43655581-43655934	HepG2	liver:	n/a	chr14:43655744-43655755
46	CEBPB	chr14:43642319-43642754	MCF-7	breast:	n/a	chr14:43642536-43642547 chr14:43642575-43642586
47	CEBPZ	chr14:43644554-43644602	HepG2	liver:	n/a	n/a
48	CEBPZ	chr14:43784271-43784461	HepG2	liver:	n/a	n/a
49	CEBPZ	chr14:43654195-43654520	HepG2	liver:	n/a	n/a
50	CEBPZ	chr14:43783378-43783823	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:43653106-43653156	PANC-1	pancreas:	n/a
2	chr14:43723010-43723060	HCPEpiC	choroid plexus:	n/a
3	chr14:43653106-43653156	T-47D	breast:	n/a
4	chr14:43653106-43653156	ECC-1	luminal epithelium:	n/a
5	chr14:43723010-43723060	ProgFib	skin:	n/a
6	chr14:43653106-43653156	HAEpiC	amniotic membrane:	n/a
7	chr14:43653106-43653156	NHBE	bronchial:	n/a
8	chr14:43653106-43653156	IMR90	lung:	fetal
9	chr14:43723010-43723060	AG09319	gingival:	n/a
10	chr14:43653106-43653156	LNCaP	prostate:	n/a
11	chr14:43723010-43723060	RPTEC	kidney:	n/a
12	chr14:43723010-43723060	HAEpiC	amniotic membrane:	n/a
13	chr14:43723010-43723060	HRPEpiC	eye:	n/a
14	chr14:43723010-43723060	HCM	heart:	n/a
15	chr14:43723010-43723060	AoSMC	blood vessel:	n/a
16	chr14:43723010-43723060	AG10803	skin:	n/a
17	chr14:43723010-43723060	GM12891	blood:	n/a
18	chr14:43723010-43723060	HEEpiC	esophagus:	n/a
19	chr14:43723010-43723060	U87	brain:	n/a
20	chr14:43653106-43653156	HMEC	breast:	n/a
21	chr14:43723010-43723060	SKMC	muscle:	n/a
22	chr14:43653106-43653156	MCF-7	breast:	n/a
23	chr14:43723010-43723060	HCT-116	colon:	n/a
24	chr14:43723010-43723060	A549	lung:	n/a
25	chr14:43653106-43653156	HCM	heart:	n/a
26	chr14:43723010-43723060	K562	blood:	n/a
27	chr14:43723010-43723060	T-47D	breast:	n/a
28	chr14:43653106-43653156	AG10803	skin:	n/a
29	chr14:43723010-43723060	GM12878	blood:	n/a
30	chr14:43723010-43723060	Jurkat	blood:	n/a
31	chr14:43653106-43653156	H1-hESC	embryonic stem cell:	embryo
32	chr14:43653106-43653156	Jurkat	blood:	n/a
33	chr14:43653106-43653156	SK-N-SH_RA	brain:	n/a
34	chr14:43653106-43653156	HCT-116	colon:	n/a
35	chr14:43653106-43653156	AoSMC	blood vessel:	n/a
36	chr14:43653106-43653156	HUVEC	blood vessel:	n/a
37	chr14:43723010-43723060	NB4	blood:	n/a
38	chr14:43653106-43653156	CMK	blood:	n/a
39	chr14:43653106-43653156	HRCEpiC	kidney:	n/a
40	chr14:43723010-43723060	HCF	heart:	n/a
41	chr14:43723010-43723060	NHDF-neo	bronchial:	n/a
42	chr14:43653106-43653156	RPTEC	kidney:	n/a
43	chr14:43723010-43723060	AG09309	skin:	n/a
44	chr14:43653106-43653156	SAEC	small airway:	n/a
45	chr14:43653106-43653156	GM12891	blood:	n/a
46	chr14:43653106-43653156	A549	lung:	n/a
47	chr14:43723010-43723060	Hepatocyte	liver:	n/a
48	chr14:43723010-43723060	HIPEpiC	eye:	n/a
49	chr14:43653106-43653156	SK-N-MC	brain:	n/a
50	chr14:43653106-43653156	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:43786117..43788131-chr14:43802827..43805151,2	MCF-7	breast:
2	chr14:43786117..43788131-chr14:43802827..43805151,2	MCF-7	breast:
3	chr14:43852687..43854424-chr14:43860035..43862313,2	K562	blood:
4	chr14:43632646..43635519-chr14:43636829..43638546,2	K562	blood:
5	chr14:43698955..43701264-chr14:43718392..43721075,2	MCF-7	breast:
6	chr14:43852687..43854424-chr14:43860035..43862313,2	K562	blood:
7	chr14:43753082..43755814-chr14:43755842..43757699,2	MCF-7	breast:
8	chr14:43698955..43701264-chr14:43718392..43721075,2	MCF-7	breast:
9	chr14:43670589..43672265-chr14:43673171..43675678,2	MCF-7	breast:
10	chr14:43819328..43821772-chr14:43825772..43828507,2	MCF-7	breast:
11	chr14:43574936..43576620-chr14:43639722..43642380,2	MCF-7	breast:
12	chr14:43632646..43635519-chr14:43636829..43638546,2	K562	blood:
13	chr14:43670589..43672265-chr14:43673171..43675678,2	MCF-7	breast:
14	chr14:43821381..43823520-chr14:43862265..43864179,2	MCF-7	breast:
15	chr14:43753082..43755814-chr14:43755842..43757699,2	MCF-7	breast:
16	chr14:43865357..43867874-chr14:43869727..43871855,2	MCF-7	breast:
17	chr14:43819328..43821772-chr14:43825772..43828507,2	MCF-7	breast:
18	chr14:43821381..43823520-chr14:43862265..43864179,2	MCF-7	breast:
19	chr14:43627304..43628817-chr14:43633953..43636435,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-214N1.1.1-7	chr14:43769466-43769798	NONHSAT036596

Variant related genes	Relation type
HNRNPUP1	TF binding region
ENSG00000258406	TF binding region
HNRNPUP1	CpG island
ENSG00000258406	CpG island

Extended variants
information (count: 2132 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:2132 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11849781	chr14:43631485-43631486	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs111800240	chr14:43631525-43631526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561293464	chr14:43631530-43631531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79762948	chr14:43631565-43631566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs547708039	chr14:43631618-43631619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs184453383	chr14:43631649-43631650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74981124	chr14:43631673-43631674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551157389	chr14:43631740-43631741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553373628	chr14:43631832-43631833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572035623	chr14:43631864-43631865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs74047577	chr14:43631916-43631917	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs139282135	chr14:43631924-43631925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72668993	chr14:43631927-43631928	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs554282217	chr14:43631931-43631932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574200924	chr14:43631934-43631935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531525690	chr14:43632009-43632010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535003167	chr14:43632032-43632033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553631393	chr14:43632055-43632056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377109441	chr14:43632075-43632076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539236198	chr14:43632099-43632100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557145238	chr14:43632128-43632129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79237605	chr14:43632168-43632169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149722070	chr14:43632195-43632196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs144529898	chr14:43632278-43632279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs181092573	chr14:43632284-43632285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185512784	chr14:43632293-43632294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548118312	chr14:43632294-43632295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532956722	chr14:43632299-43632300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs545166687	chr14:43632307-43632308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs563178723	chr14:43632308-43632309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530512841	chr14:43632327-43632328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs367942174	chr14:43632335-43632336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548716253	chr14:43632348-43632349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190598946	chr14:43632377-43632378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181081060	chr14:43632440-43632441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76641829	chr14:43632469-43632470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs10137594	chr14:43632481-43632482	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs538989936	chr14:43632485-43632486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs187156275	chr14:43632529-43632530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192452389	chr14:43632542-43632543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536738936	chr14:43632548-43632549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182962421	chr14:43632584-43632585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148487677	chr14:43632613-43632614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs540646360	chr14:43632674-43632675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542480304	chr14:43632683-43632684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10148798	chr14:43632695-43632696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs545015716	chr14:43632767-43632768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144138017	chr14:43632797-43632798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs79614780	chr14:43632806-43632807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532176166	chr14:43632851-43632852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

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
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	21364760	CNVD
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Type 2 diabetes	21526130	CNVD
Breast cancer	22522925	CNVD
Melanoma	17363583	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:43631000-43634600	Weak transcription	A549	lung
2	chr14:43634600-43635000	Active TSS	A549	lung
3	chr14:43634600-43636600	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr14:43635000-43635200	Flanking Active TSS	A549	lung
5	chr14:43635200-43635400	Enhancers	A549	lung
6	chr14:43635400-43635600	Flanking Active TSS	A549	lung
7	chr14:43635600-43636200	Enhancers	A549	lung
8	chr14:43636200-43637600	Weak transcription	A549	lung
9	chr14:43636600-43637000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr14:43636800-43637000	Enhancers	Fetal Intestine Small	intestine
11	chr14:43636800-43638800	Enhancers	Fetal Intestine Large	intestine
12	chr14:43637000-43637600	Weak transcription	Fetal Intestine Small	intestine
13	chr14:43637000-43637800	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr14:43637600-43637800	Enhancers	A549	lung
15	chr14:43637600-43638800	Enhancers	Fetal Intestine Small	intestine
16	chr14:43637800-43638200	Enhancers	Fetal Lung	lung
17	chr14:43637800-43638200	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr14:43638200-43638600	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr14:43638200-43641800	Weak transcription	Fetal Lung	lung
20	chr14:43638800-43641800	Weak transcription	Fetal Intestine Large	intestine
21	chr14:43641200-43643200	Enhancers	Liver	Liver
22	chr14:43641800-43642200	Enhancers	Fetal Lung	lung
23	chr14:43641800-43643200	Enhancers	Fetal Intestine Large	intestine
24	chr14:43642200-43645000	Weak transcription	Fetal Lung	lung
25	chr14:43645000-43645400	Enhancers	Fetal Lung	lung
26	chr14:43652000-43653600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr14:43652000-43654400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr14:43652000-43654600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr14:43652200-43653800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr14:43652200-43654400	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr14:43652200-43654400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr14:43653200-43654000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr14:43653800-43654200	Enhancers	Ovary	ovary
34	chr14:43653800-43654400	Enhancers	H1 Cell Line	embryonic stem cell
35	chr14:43657400-43657800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr14:43657800-43658200	Enhancers	Fetal Intestine Large	intestine
37	chr14:43714400-43715000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr14:43727800-43728200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr14:43743400-43745600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr14:43746600-43747200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
41	chr14:43746800-43747200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr14:43777600-43778400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr14:43782800-43783200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr14:43783200-43783600	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr14:43795600-43796200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
46	chr14:43795800-43796200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:43816600-43829600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr14:43825800-43827200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
49	chr14:43826000-43826800	Enhancers	Pancreas	Pancrea
50	chr14:43826000-43827200	Enhancers	Pancreatic Islets	Pancreatic Islet

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