Variant report

Variant	nsv901825
Chromosome Location	chr14:44595346-44947663
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1097)
CpG islands
(count:62)
Chromatin interactive
region (count:34)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1097 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:44786027-44786367	K562	blood:	n/a	n/a
2	ARID3A	chr14:44786011-44786505	HepG2	liver:	n/a	n/a
3	ATF1	chr14:44918300-44918537	K562	blood:	n/a	n/a
4	ATF1	chr14:44786110-44786462	K562	blood:	n/a	n/a
5	ATF3	chr14:44786000-44786531	HCT-116	colon:	n/a	n/a
6	ATF3	chr14:44786197-44786335	K562	blood:	n/a	n/a
7	ATF3	chr14:44786082-44786534	A549	lung:	n/a	n/a
8	ATF3	chr14:44786091-44786377	K562	blood:	n/a	n/a
9	ATF3	chr14:44786185-44786384	HepG2	liver:	n/a	n/a
10	ATF3	chr14:44786106-44786596	HCT-116	colon:	n/a	n/a
11	BACH1	chr14:44862483-44862496	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr14:44632100-44632238	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr14:44786155-44786410	GM12878	blood:	n/a	n/a
14	BATF	chr14:44786178-44786410	GM12878	blood:	n/a	n/a
15	BCL11A	chr14:44673306-44673565	H1-hESC	embryonic stem cell:	n/a	n/a
16	BCL3	chr14:44786061-44786449	GM12878	blood:	n/a	n/a
17	BHLHE40	chr14:44918875-44919187	HepG2	liver:	n/a	n/a
18	BHLHE40	chr14:44786136-44786463	HepG2	liver:	n/a	n/a
19	BHLHE40	chr14:44918215-44918640	K562	blood:	n/a	n/a
20	BHLHE40	chr14:44918841-44919166	HepG2	liver:	n/a	n/a
21	BHLHE40	chr14:44786155-44786484	K562	blood:	n/a	n/a
22	BRCA1	chr14:44618833-44619126	H1-hESC	embryonic stem cell:	n/a	n/a
23	BRCA1	chr14:44887139-44887316	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr14:44785944-44786626	HCT-116	colon:	n/a	n/a
25	CCNT2	chr14:44918261-44918573	K562	blood:	n/a	n/a
26	CCNT2	chr14:44870973-44871349	K562	blood:	n/a	n/a
27	CEBPB	chr14:44599593-44600126	A549	lung:	n/a	chr14:44599949-44599960
28	CEBPB	chr14:44822861-44823165	K562	blood:	n/a	chr14:44823024-44823035
29	CEBPB	chr14:44804504-44804827	A549	lung:	n/a	chr14:44804642-44804653
30	CEBPB	chr14:44825168-44825407	HepG2	liver:	n/a	n/a
31	CEBPB	chr14:44657629-44657829	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr14:44618834-44619117	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr14:44605796-44606154	Hela-S3	cervix:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
34	CEBPB	chr14:44595859-44595978	A549	lung:	n/a	n/a
35	CEBPB	chr14:44822869-44823209	HepG2	liver:	n/a	chr14:44823024-44823035
36	CEBPB	chr14:44865484-44865848	HepG2	liver:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
37	CEBPB	chr14:44822866-44823194	H1-hESC	embryonic stem cell:	n/a	chr14:44823024-44823035
38	CEBPB	chr14:44804468-44804813	HepG2	liver:	n/a	chr14:44804642-44804653
39	CEBPB	chr14:44860656-44860866	HepG2	liver:	n/a	chr14:44860752-44860763
40	CEBPB	chr14:44633192-44633496	Hela-S3	cervix:	n/a	chr14:44633351-44633362
41	CEBPB	chr14:44865546-44865783	Hela-S3	cervix:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
42	CEBPB	chr14:44865547-44865773	H1-hESC	embryonic stem cell:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
43	CEBPB	chr14:44605865-44606139	A549	lung:	n/a	chr14:44605990-44606001 chr14:44605988-44606001 chr14:44605988-44605999 chr14:44605990-44606001
44	CEBPB	chr14:44595881-44596093	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:44892241-44892441	IMR90	lung:	n/a	chr14:44892371-44892382
46	CEBPB	chr14:44865514-44865808	IMR90	lung:	n/a	chr14:44865665-44865674 chr14:44865621-44865632
47	CEBPB	chr14:44606767-44606976	H1-hESC	embryonic stem cell:	n/a	chr14:44606862-44606873
48	CEBPB	chr14:44801528-44801807	A549	lung:	n/a	chr14:44801651-44801662 chr14:44801651-44801664
49	CEBPB	chr14:44822632-44823413	MCF-7	breast:	n/a	chr14:44823024-44823035
50	CEBPB	chr14:44599875-44600120	HepG2	liver:	n/a	chr14:44599949-44599960

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:44853952-44854002	T-47D	breast:	n/a
2	chr14:44853952-44854002	T-47D	breast:	n/a
3	chr14:44853952-44854002	HNPCEpiC	eye:	n/a
4	chr14:44853952-44854002	HCPEpiC	choroid plexus:	n/a
5	chr14:44853952-44854002	Caco-2	colon:	n/a
6	chr14:44853952-44854002	K562	blood:	n/a
7	chr14:44853952-44854002	HCM	heart:	n/a
8	chr14:44853952-44854002	HepG2	liver:	n/a
9	chr14:44853952-44854002	NH-A	brain:	n/a
10	chr14:44853952-44854002	AG10803	skin:	n/a
11	chr14:44853952-44854002	GM12878	blood:	n/a
12	chr14:44853952-44854002	SK-N-SH_RA	brain:	n/a
13	chr14:44853952-44854002	NT2-D1	testis:	n/a
14	chr14:44853952-44854002	NHDF-neo	bronchial:	n/a
15	chr14:44853952-44854002	HAEpiC	amniotic membrane:	n/a
16	chr14:44853952-44854002	A549	lung:	n/a
17	chr14:44853952-44854002	AG04449	skin:	fetal
18	chr14:44853952-44854002	NHBE	bronchial:	n/a
19	chr14:44853952-44854002	LNCaP	prostate:	n/a
20	chr14:44853952-44854002	SK-N-SH	brain:	n/a
21	chr14:44853952-44854002	GM12892	blood:	n/a
22	chr14:44853952-44854002	AoSMC	blood vessel:	n/a
23	chr14:44853952-44854002	PrEC	prostate:	n/a
24	chr14:44853952-44854002	HRE	kidney:	n/a
25	chr14:44853952-44854002	H1-hESC	embryonic stem cell:	embryo
26	chr14:44853952-44854002	Hela-S3	cervix:	n/a
27	chr14:44853952-44854002	HRPEpiC	eye:	n/a
28	chr14:44853952-44854002	NB4	blood:	n/a
29	chr14:44853952-44854002	IMR90	lung:	fetal
30	chr14:44853952-44854002	SAEC	small airway:	n/a
31	chr14:44853952-44854002	ovcar-3	ovarian:	n/a
32	chr14:44853952-44854002	HUVEC	blood vessel:	n/a
33	chr14:44853952-44854002	HEK293	kidney:	embryo
34	chr14:44853952-44854002	SK-N-MC	brain:	n/a
35	chr14:44853952-44854002	HEEpiC	esophagus:	n/a
36	chr14:44853952-44854002	HIPEpiC	eye:	n/a
37	chr14:44853952-44854002	PFSK-1	brain:	n/a
38	chr14:44853952-44854002	HRCEpiC	kidney:	n/a
39	chr14:44853952-44854002	HL-60	blood:	n/a
40	chr14:44853952-44854002	HCF	heart:	n/a
41	chr14:44853952-44854002	U87	brain:	n/a
42	chr14:44853952-44854002	RPTEC	kidney:	n/a
43	chr14:44853952-44854002	AG04450	lung:	fetal
44	chr14:44853952-44854002	SKMC	muscle:	n/a
45	chr14:44853952-44854002	PANC-1	pancreas:	n/a
46	chr14:44853952-44854002	BJ	skin:	n/a
47	chr14:44853952-44854002	BE2_C	brain:	n/a
48	chr14:44853952-44854002	HPAEpiC	pulmonary alveolar:	n/a
49	chr14:44853952-44854002	ECC-1	luminal epithelium:	n/a
50	chr14:44853952-44854002	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
2	chr1:17231477..17232007-chr14:44939008..44939528,2	Hela-S3	cervix:
3	chr14:44370246..44372256-chr14:44617257..44619025,2	MCF-7	breast:
4	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
5	chr14:44799704..44802515-chr14:44803665..44805548,2	K562	blood:
6	chr14:44754776..44756782-chr14:44760420..44763272,3	MCF-7	breast:
7	chr14:44803036..44805789-chr14:44807681..44809917,2	MCF-7	breast:
8	chr14:44838612..44839205-chr14:44974588..44975472,2	MCF-7	breast:
9	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
10	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
11	chr14:44659162..44661192-chr14:44662497..44664945,3	MCF-7	breast:
12	chr14:44606810..44610792-chr14:44612494..44615788,3	K562	blood:
13	chr14:44755644..44758887-chr14:44761125..44763162,3	K562	blood:
14	chr14:44836359..44838272-chr14:44839234..44841841,3	K562	blood:
15	chr14:44659162..44661192-chr14:44662497..44664945,3	MCF-7	breast:
16	chr14:44785511..44787603-chr14:44801475..44804165,2	MCF-7	breast:
17	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
18	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
19	chr14:44856514..44860245-chr14:44862169..44864602,3	K562	blood:
20	chr14:44838296..44838875-chr14:45126583..45127520,3	MCF-7	breast:
21	chr14:44834762..44837688-chr14:44839758..44841386,2	MCF-7	breast:
22	chr14:44795723..44798432-chr14:44798850..44801579,2	MCF-7	breast:
23	chr14:44838166..44839882-chr14:44873785..44875324,2	MCF-7	breast:
24	chr14:44795723..44798432-chr14:44798850..44801579,2	MCF-7	breast:
25	chr14:44922572..44923387-chr14:45126451..45127121,2	MCF-7	breast:
26	chr14:44755644..44758887-chr14:44761125..44763162,3	K562	blood:
27	chr14:44857399..44860693-chr14:44862169..44864634,3	K562	blood:
28	chr14:44600217..44602036-chr14:44604194..44606588,2	K562	blood:
29	chr14:44836359..44838272-chr14:44839234..44841841,2	K562	blood:
30	chr14:44562970..44563903-chr14:44618440..44619350,3	MCF-7	breast:
31	chr14:44799704..44802515-chr14:44803665..44805548,2	K562	blood:
32	chr14:44803036..44805789-chr14:44807681..44809917,2	MCF-7	breast:
33	chr14:44370633..44373508-chr14:44616084..44618482,2	MCF-7	breast:
34	chr14:44785511..44787603-chr14:44801475..44804165,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FSCB-1	chr14:44936162-44936372	XLOC_011007
2	lnc-FSCB-2	chr14:44853680-44853748	ENSG00000258969
3	lnc-FSCB-1	chr14:44862812-44862997	XLOC_011006
4	lnc-FSCB-6	chr14:44622029-44622354	l_977_chr14:44621312-44622966_testes
5	lnc-FSCB-5	chr14:44760200-44760921	NONHSAT036604
6	lnc-FSCB-1	chr14:44936293-44936372	XLOC_011007
7	lnc-FSCB-6	chr14:44621821-44621918	l_977_chr14:44621312-44622966_testes
8	lnc-FSCB-1	chr14:44913950-44914025	ENSG00000258487
9	lnc-FSCB-1	chr14:44913910-44914002	XLOC_011006
10	lnc-FSCB-1	chr14:44862209-44862941	XLOC_011006
11	lnc-FSCB-1	chr14:44936161-44936372	ENSG00000258487
12	lnc-FSCB-1	chr14:44862821-44862919	ENSG00000259126
13	lnc-FSCB-1	chr14:44861745-44861893	ENSG00000259126
14	lnc-FSCB-6	chr14:44621313-44621629	l_977_chr14:44621312-44622966_testes
15	lnc-FSCB-1	chr14:44915851-44915996	ENSG00000258487
16	lnc-FSCB-1	chr14:44861702-44861893	XLOC_011006
17	lnc-FSCB-6	chr14:44622425-44622966	l_977_chr14:44621312-44622966_testes
18	lnc-FSCB-1	chr14:44913926-44914025	NONHSAT036608
19	lnc-FSCB-1	chr14:44861734-44861893	ENSG00000259126
20	lnc-FSCB-1	chr14:44862812-44862914	ENSG00000259126

No data

Variant related genes	Relation type
ENSG00000259148	TF binding region
ENSG00000258969	TF binding region
ENSG00000259126	TF binding region
ENSG00000259148	CpG island
ENSG00000258969	CpG island
ENSG00000259126	CpG island
ENSG00000259126	chromatin interactions
ENSG00000259148	chromatin interactions
B4GALT1	miRNA target sites
FAM134B	miRNA target sites

Extended variants
information (count: 4714 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4714 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149356244	chr14:44605213-44605214	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs34460235	chr14:44605229-44605230	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs557637878	chr14:44605242-44605243	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs117447894	chr14:44605286-44605287	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs144105856	chr14:44605302-44605303	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs554216997	chr14:44605332-44605333	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs148686229	chr14:44605347-44605348	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs184039184	chr14:44605358-44605359	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs1950546	chr14:44605399-44605400	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs79769978	chr14:44605403-44605404	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs577061535	chr14:44605421-44605422	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs74742942	chr14:44605426-44605427	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs562809863	chr14:44605430-44605431	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs189059091	chr14:44605440-44605441	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs575675550	chr14:44605454-44605455	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs181006643	chr14:44605455-44605456	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs561346062	chr14:44605464-44605465	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs528638261	chr14:44605489-44605490	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs185484108	chr14:44605492-44605493	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs538512977	chr14:44606466-44606467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs10150365	chr14:44606505-44606506	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs565397263	chr14:44606522-44606523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185917563	chr14:44606540-44606541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551186562	chr14:44606541-44606542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562829131	chr14:44606578-44606579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs537416423	chr14:44606597-44606598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs557751805	chr14:44606613-44606614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs10139773	chr14:44606721-44606722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10139865	chr14:44606779-44606780	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs545357613	chr14:44608403-44608404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549869573	chr14:44608433-44608434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs10133756	chr14:44608436-44608437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563025862	chr14:44608440-44608441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534073589	chr14:44608475-44608476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529079366	chr14:44608478-44608479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547648426	chr14:44608489-44608490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554146097	chr14:44608497-44608498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149001805	chr14:44608512-44608513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377110496	chr14:44608525-44608526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531952303	chr14:44608529-44608530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552095132	chr14:44608581-44608582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10146082	chr14:44608583-44608584	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs138405715	chr14:44608640-44608641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139365272	chr14:44608660-44608661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs35337895	chr14:44608664-44608665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs574619414	chr14:44608754-44608755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576417094	chr14:44608765-44608766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs75015372	chr14:44608777-44608778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs375312268	chr14:44608818-44608819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs201794980	chr14:44608834-44608835	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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
Renal cell carcinoma	18194544	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ovarian cancer	21781307	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Williams Syndrome	20824207	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:44605200-44605600	Active TSS	A549	lung
2	chr14:44606400-44606800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr14:44608400-44609000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr14:44618800-44619000	Enhancers	Pancreas	Pancrea
5	chr14:44620200-44623600	Weak transcription	Pancreas	Pancrea
6	chr14:44623600-44624200	ZNF genes & repeats	Pancreas	Pancrea
7	chr14:44623800-44624200	Enhancers	NHDF-Ad	bronchial
8	chr14:44626800-44627200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr14:44629600-44630000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr14:44631400-44631800	Enhancers	HepG2	liver
11	chr14:44631800-44632000	ZNF genes & repeats	Fetal Intestine Small	intestine
12	chr14:44631800-44632000	Flanking Active TSS	HepG2	liver
13	chr14:44632000-44635200	Weak transcription	Fetal Intestine Small	intestine
14	chr14:44633200-44633600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr14:44633600-44636800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr14:44634600-44634800	Enhancers	Fetal Lung	lung
17	chr14:44635200-44635600	Enhancers	Fetal Intestine Small	intestine
18	chr14:44635600-44639000	Weak transcription	Fetal Intestine Small	intestine
19	chr14:44636800-44638200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr14:44639000-44640600	Enhancers	Fetal Intestine Small	intestine
21	chr14:44639400-44640800	Enhancers	Liver	Liver
22	chr14:44639800-44640800	Enhancers	Fetal Intestine Large	intestine
23	chr14:44649800-44650600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr14:44650200-44650600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr14:44650200-44650800	Enhancers	Fetal Lung	lung
26	chr14:44660600-44661800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr14:44661200-44661600	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr14:44661600-44661800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr14:44665200-44665800	Enhancers	Fetal Brain Male	brain
30	chr14:44672600-44673200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr14:44672800-44673600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr14:44673000-44673800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr14:44673000-44674000	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr14:44673200-44673800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr14:44673200-44674400	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr14:44673200-44674400	Enhancers	Fetal Heart	heart
37	chr14:44673200-44675800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr14:44673400-44675400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr14:44673600-44673800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr14:44673600-44674000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr14:44673600-44674000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr14:44673600-44674600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr14:44673800-44674200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr14:44673800-44674400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr14:44674000-44674600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr14:44674000-44675000	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr14:44674200-44674400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr14:44674400-44674800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr14:44674400-44675000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr14:44674600-44675600	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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