Variant report

Variant	nsv902119
Chromosome Location	chr14:81810945-81884857
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:628)
CpG islands
(count:488)
Chromatin interactive
region (count:83)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:628 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:81868069-81868663	K562	blood:	n/a	n/a
2	ARID3A	chr14:81874896-81875252	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:81866603-81866903	K562	blood:	n/a	n/a
4	ARID3A	chr14:81825185-81825197	K562	blood:	n/a	n/a
5	ATF1	chr14:81868376-81868727	K562	blood:	n/a	n/a
6	ATF1	chr14:81866502-81866954	K562	blood:	n/a	n/a
7	ATF1	chr14:81882614-81883897	K562	blood:	n/a	n/a
8	ATF1	chr14:81815860-81816001	K562	blood:	n/a	n/a
9	ATF2	chr14:81867715-81868129	GM12878	blood:	n/a	n/a
10	ATF2	chr14:81867763-81868138	GM12878	blood:	n/a	n/a
11	ATF3	chr14:81866522-81866999	K562	blood:	n/a	chr14:81866678-81866688
12	ATF3	chr14:81868368-81868739	K562	blood:	n/a	n/a
13	BACH1	chr14:81868470-81868670	K562	blood:	n/a	n/a
14	BACH1	chr14:81866712-81867065	K562	blood:	n/a	n/a
15	BATF	chr14:81867798-81868064	GM12878	blood:	n/a	chr14:81868048-81868056
16	BCL11A	chr14:81867776-81868155	GM12878	blood:	n/a	chr14:81868139-81868146
17	BHLHE40	chr14:81868231-81868725	K562	blood:	n/a	n/a
18	BHLHE40	chr14:81882467-81883015	K562	blood:	n/a	n/a
19	BHLHE40	chr14:81866561-81867002	K562	blood:	n/a	n/a
20	BHLHE40	chr14:81867254-81867560	K562	blood:	n/a	n/a
21	BRCA1	chr14:81866499-81868180	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr14:81883354-81883694	K562	blood:	n/a	n/a
23	CBX3	chr14:81868297-81868787	K562	blood:	n/a	n/a
24	CBX3	chr14:81884371-81884937	K562	blood:	n/a	n/a
25	CBX3	chr14:81868336-81868686	K562	blood:	n/a	n/a
26	CCNT2	chr14:81868196-81868749	K562	blood:	n/a	chr14:81868525-81868545
27	CCNT2	chr14:81829196-81829420	K562	blood:	n/a	n/a
28	CCNT2	chr14:81866563-81867034	K562	blood:	n/a	n/a
29	CEBPB	chr14:81878944-81879032	IMR90	lung:	n/a	n/a
30	CEBPB	chr14:81867229-81867613	A549	lung:	n/a	n/a
31	CEBPB	chr14:81882959-81883731	K562	blood:	n/a	chr14:81883531-81883542
32	CEBPB	chr14:81867184-81867615	K562	blood:	n/a	n/a
33	CEBPB	chr14:81867091-81868149	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr14:81851130-81851641	ECC-1	luminal epithelium:	n/a	chr14:81851365-81851376 chr14:81851365-81851378
35	CEBPB	chr14:81867230-81867612	IMR90	lung:	n/a	n/a
36	CEBPB	chr14:81866495-81868320	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr14:81866544-81867026	K562	blood:	n/a	n/a
38	CEBPB	chr14:81878895-81879151	K562	blood:	n/a	n/a
39	CEBPB	chr14:81867061-81868230	HCT-116	colon:	n/a	n/a
40	CEBPB	chr14:81851364-81851417	K562	blood:	n/a	chr14:81851365-81851376 chr14:81851365-81851378
41	CEBPB	chr14:81867890-81868196	IMR90	lung:	n/a	n/a
42	CEBPB	chr14:81883378-81883663	HepG2	liver:	n/a	chr14:81883531-81883542
43	CEBPB	chr14:81866442-81868268	HCT-116	colon:	n/a	n/a
44	CEBPB	chr14:81883338-81883728	K562	blood:	n/a	chr14:81883531-81883542
45	CEBPB	chr14:81867103-81867662	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr14:81867148-81867769	MCF-7	breast:	n/a	n/a
47	CEBPB	chr14:81878850-81879176	A549	lung:	n/a	n/a
48	CEBPB	chr14:81867209-81867616	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr14:81851249-81851609	MCF-7	breast:	n/a	chr14:81851365-81851376 chr14:81851365-81851378
50	CEBPB	chr14:81851175-81851580	Hela-S3	cervix:	n/a	chr14:81851365-81851376 chr14:81851365-81851378

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:81864899-81864949	HMEC	breast:	n/a
2	chr14:81865007-81865057	Hepatocyte	liver:	n/a
3	chr14:81864899-81864949	U87	brain:	n/a
4	chr14:81864899-81864949	RPTEC	kidney:	n/a
5	chr14:81879375-81879425	Hela-S3	cervix:	n/a
6	chr14:81865007-81865057	HEEpiC	esophagus:	n/a
7	chr14:81864643-81864693	HAEpiC	amniotic membrane:	n/a
8	chr14:81865007-81865057	SK-N-SH	brain:	n/a
9	chr14:81864623-81864673	HepG2	liver:	n/a
10	chr14:81879247-81879297	HEEpiC	esophagus:	n/a
11	chr14:81832422-81832472	K562	blood:	n/a
12	chr14:81864623-81864673	BJ	skin:	n/a
13	chr14:81864623-81864673	GM12878	blood:	n/a
14	chr14:81865007-81865057	U87	brain:	n/a
15	chr14:81864643-81864693	K562	blood:	n/a
16	chr14:81864899-81864949	GM12878	blood:	n/a
17	chr14:81832422-81832472	SKMC	muscle:	n/a
18	chr14:81879375-81879425	K562	blood:	n/a
19	chr14:81879247-81879297	HRCEpiC	kidney:	n/a
20	chr14:81879375-81879425	Jurkat	blood:	n/a
21	chr14:81864623-81864673	CMK	blood:	n/a
22	chr14:81864899-81864949	LNCaP	prostate:	n/a
23	chr14:81832422-81832472	HNPCEpiC	eye:	n/a
24	chr14:81864643-81864693	SK-N-MC	brain:	n/a
25	chr14:81879375-81879425	NT2-D1	testis:	n/a
26	chr14:81865007-81865057	AG09309	skin:	n/a
27	chr14:81864899-81864949	HRPEpiC	eye:	n/a
28	chr14:81879247-81879297	MCF10A-Er-Src	breast:	n/a
29	chr14:81832422-81832472	H1-hESC	embryonic stem cell:	embryo
30	chr14:81865007-81865057	HRPEpiC	eye:	n/a
31	chr14:81864899-81864949	SKMC	muscle:	n/a
32	chr14:81879375-81879425	Hepatocyte	liver:	n/a
33	chr14:81832422-81832472	SK-N-SH	brain:	n/a
34	chr14:81864623-81864673	HCT-116	colon:	n/a
35	chr14:81864643-81864693	HCF	heart:	n/a
36	chr14:81879247-81879297	AG09309	skin:	n/a
37	chr14:81865007-81865057	HAEpiC	amniotic membrane:	n/a
38	chr14:81865007-81865057	ECC-1	luminal epithelium:	n/a
39	chr14:81865007-81865057	AG04450	lung:	fetal
40	chr14:81852444-81852494	Hela-S3	cervix:	n/a
41	chr14:81865007-81865057	HMEC	breast:	n/a
42	chr14:81832422-81832472	HIPEpiC	eye:	n/a
43	chr14:81879375-81879425	AoSMC	blood vessel:	n/a
44	chr14:81864643-81864693	NHBE	bronchial:	n/a
45	chr14:81864643-81864693	HPAEpiC	pulmonary alveolar:	n/a
46	chr14:81832422-81832472	NH-A	brain:	n/a
47	chr14:81879375-81879425	SK-N-SH	brain:	n/a
48	chr14:81879375-81879425	HCM	heart:	n/a
49	chr14:81864899-81864949	AoSMC	blood vessel:	n/a
50	chr14:81879375-81879425	BJ	skin:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:81816828..81818366-chr14:81868014..81870055,2	K562	blood:
2	chr14:81865287..81867829-chr14:81917916..81919892,2	K562	blood:
3	chr14:81837694..81839198-chr14:81840938..81842642,2	MCF-7	breast:
4	chr14:81684553..81687332-chr14:81856686..81858470,2	MCF-7	breast:
5	chr14:81835420..81837863-chr14:81857937..81859970,2	MCF-7	breast:
6	chr14:81867029..81868586-chr14:81887440..81889989,2	K562	blood:
7	chr14:81685691..81688551-chr14:81879364..81882605,3	K562	blood:
8	chr14:81810357..81812474-chr14:81820150..81822566,2	K562	blood:
9	chr14:81685583..81687332-chr14:81866862..81869553,2	K562	blood:
10	chr14:81876407..81878625-chr14:81895373..81897999,2	K562	blood:
11	chr14:81852266..81853780-chr14:81865825..81868508,2	K562	blood:
12	chr14:81834534..81837450-chr14:81839716..81841468,3	K562	blood:
13	chr14:81875040..81877398-chr14:81879695..81881536,2	K562	blood:
14	chr14:81686697..81688459-chr14:81858395..81860078,2	MCF-7	breast:
15	chr14:81834534..81837450-chr14:81839716..81841468,3	K562	blood:
16	chr14:81810357..81812474-chr14:81820150..81822566,2	K562	blood:
17	chr14:81684503..81687134-chr14:81866673..81870053,4	K562	blood:
18	chr14:81855959..81858905-chr14:81901728..81904527,2	K562	blood:
19	chr14:81870339..81872408-chr14:81882068..81884278,2	K562	blood:
20	chr14:81866040..81868691-chr14:81870203..81872674,2	K562	blood:
21	chr14:81848326..81851225-chr14:81856125..81857650,2	K562	blood:
22	chr14:81857190..81860023-chr14:81897316..81899061,2	K562	blood:
23	chr14:81847233..81850100-chr14:81861547..81864501,2	MCF-7	breast:
24	chr14:81847525..81850212-chr14:81854009..81856380,2	MCF-7	breast:
25	chr14:81806925..81809248-chr14:81809834..81812689,2	MCF-7	breast:
26	chr14:81686224..81688353-chr14:81839920..81841889,2	K562	blood:
27	chr14:81852266..81853780-chr14:81865825..81868508,2	K562	blood:
28	chr14:81685500..81688239-chr14:81854042..81856248,2	K562	blood:
29	chr14:81828038..81830813-chr14:81831805..81834058,2	K562	blood:
30	chr14:81867077..81868960-chr14:81900756..81902701,2	K562	blood:
31	chr14:81870453..81872408-chr14:81882778..81884349,2	K562	blood:
32	chr14:81837694..81839198-chr14:81840938..81842642,2	MCF-7	breast:
33	chr14:81816404..81818224-chr14:81820646..81822876,2	MCF-7	breast:
34	chr14:81862798..81865439-chr14:81880673..81882798,2	K562	blood:
35	chr14:81817681..81819808-chr14:81839825..81842521,2	MCF-7	breast:
36	chr14:81816404..81818224-chr14:81820646..81822876,2	MCF-7	breast:
37	chr14:81847233..81850100-chr14:81861547..81864501,2	MCF-7	breast:
38	chr14:81839869..81841648-chr14:81852139..81854142,2	K562	blood:
39	chr14:81867994..81870092-chr14:81876125..81877918,2	K562	blood:
40	chr14:81787114..81788758-chr14:81816249..81818905,2	K562	blood:
41	chr14:81875040..81877398-chr14:81879695..81881536,2	K562	blood:
42	chr14:81816828..81818366-chr14:81868014..81870055,2	K562	blood:
43	chr14:81866040..81868691-chr14:81870203..81872674,2	K562	blood:
44	chr14:81871493..81873378-chr14:81876007..81877708,2	K562	blood:
45	chr14:81859822..81862537-chr14:81898596..81900276,2	K562	blood:
46	chr14:81865470..81868504-chr14:81891136..81896392,5	K562	blood:
47	chr14:81684469..81687360-chr14:81875537..81877645,3	K562	blood:
48	chr14:81684359..81686133-chr14:81846262..81848030,2	K562	blood:
49	chr14:81817681..81819808-chr14:81839825..81842521,2	MCF-7	breast:
50	chr14:81876702..81879078-chr14:81892366..81894170,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SEL1L-11	chr14:81881291-81881385	NONHSAT038064

No data

Variant related genes	Relation type
ENSG00000258605	TF binding region
STON2	TF binding region
ENSG00000258605	CpG island
STON2	CpG island
ENSG00000140022	chromatin interactions
ENSG00000165417	chromatin interactions

Extended variants
information (count: 2832 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2832 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2012796	chr14:81810945-81810946	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs574304972	chr14:81810959-81810960	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs34860812	chr14:81810976-81810977	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564767169	chr14:81810988-81810989	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573479764	chr14:81811062-81811063	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs150272200	chr14:81811063-81811064	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562126466	chr14:81811064-81811065	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs529549773	chr14:81811133-81811134	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs548299984	chr14:81811139-81811140	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs72701735	chr14:81811142-81811143	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs530474730	chr14:81811216-81811217	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185652435	chr14:81811243-81811244	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570699489	chr14:81811268-81811269	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs190455426	chr14:81811307-81811308	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs577644670	chr14:81811308-81811309	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546908043	chr14:81811326-81811327	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs1570007	chr14:81811374-81811375	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs543123176	chr14:81811388-81811389	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs182736366	chr14:81811437-81811438	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563131153	chr14:81811498-81811499	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74066416	chr14:81811526-81811527	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs186759010	chr14:81811537-81811538	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138923582	chr14:81811538-81811539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544754550	chr14:81811637-81811638	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs573223683	chr14:81811642-81811643	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373672000	chr14:81811648-81811649	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs75041757	chr14:81811712-81811713	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149354709	chr14:81811817-81811818	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574236335	chr14:81811818-81811819	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144663382	chr14:81811825-81811826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561189503	chr14:81811968-81811969	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139499841	chr14:81812045-81812046	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142894267	chr14:81812081-81812082	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs559936244	chr14:81812188-81812189	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs376170134	chr14:81812204-81812205	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114485495	chr14:81812214-81812215	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563913393	chr14:81812229-81812230	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192162121	chr14:81812231-81812232	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs144438322	chr14:81812294-81812295	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs546575198	chr14:81812354-81812355	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568349292	chr14:81812404-81812405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs529014832	chr14:81812440-81812441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs550382554	chr14:81812455-81812456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183958253	chr14:81812522-81812523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs187816925	chr14:81812630-81812631	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs72701736	chr14:81812739-81812740	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs73339726	chr14:81812743-81812744	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs566747017	chr14:81812750-81812751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534198445	chr14:81812759-81812760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs75703233	chr14:81812760-81812761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	17053054	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	21922591	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16608533	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Glioblastoma	21080181	CNVD
Gastric cancer	16891809	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD

Chromatin state (count:1190 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81803800-81832200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr14:81804200-81820000	Weak transcription	K562	blood
3	chr14:81804800-81814200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr14:81805800-81814000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr14:81806000-81814200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr14:81808000-81811600	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chr14:81808000-81820600	Weak transcription	Fetal Kidney	kidney
8	chr14:81808400-81829200	Weak transcription	HMEC	breast
9	chr14:81808600-81811800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:81808600-81820200	Weak transcription	NHEK	skin
11	chr14:81808800-81830200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr14:81809000-81813000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr14:81809400-81811800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr14:81809400-81817600	Weak transcription	Brain Anterior Caudate	brain
15	chr14:81809600-81812200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr14:81809800-81811600	Weak transcription	Psoas Muscle	Psoas
17	chr14:81809800-81812600	Weak transcription	Ovary	ovary
18	chr14:81810200-81811400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr14:81810400-81811400	Weak transcription	Adipose Nuclei	Adipose
20	chr14:81810400-81811600	Weak transcription	Fetal Muscle Leg	muscle
21	chr14:81810400-81811600	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr14:81810400-81814200	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr14:81810800-81811800	Strong transcription	Primary hematopoietic stem cells	blood
24	chr14:81811400-81811600	Enhancers	Adipose Nuclei	Adipose
25	chr14:81811400-81812600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr14:81811600-81811800	Enhancers	Skeletal Muscle Female	skeletal muscle
27	chr14:81811600-81812200	Enhancers	Psoas Muscle	Psoas
28	chr14:81811600-81812400	Weak transcription	Skeletal Muscle Male	skeletal muscle
29	chr14:81811600-81812800	Enhancers	Fetal Muscle Leg	muscle
30	chr14:81811800-81812000	Enhancers	Fetal Muscle Trunk	muscle
31	chr14:81811800-81812400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr14:81811800-81818800	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr14:81811800-81821000	Weak transcription	Primary hematopoietic stem cells	blood
34	chr14:81812200-81813000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr14:81812200-81820000	Weak transcription	Psoas Muscle	Psoas
36	chr14:81812400-81812600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr14:81812400-81812600	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr14:81812600-81813400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr14:81813000-81815800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr14:81813400-81829800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr14:81814000-81814800	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr14:81814200-81814600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr14:81814200-81814800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr14:81814200-81815000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr14:81814400-81814600	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr14:81814600-81815000	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr14:81814600-81815200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr14:81814600-81816600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr14:81814600-81821200	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr14:81814800-81820200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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