Variant report

Variant	nsv1035158
Chromosome Location	chr14:55638386-55684228
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:896)
CpG islands
(count:610)
Chromatin interactive
region (count:35)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:896 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:55658149-55658306	K562	blood:	n/a	n/a
2	ARID3A	chr14:55658164-55658525	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:55679767-55680127	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:55679809-55680088	K562	blood:	n/a	n/a
5	ATF2	chr14:55657956-55658453	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr14:55658066-55658590	GM12878	blood:	n/a	n/a
7	ATF2	chr14:55657811-55658690	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr14:55646911-55647760	GM12878	blood:	n/a	n/a
9	ATF2	chr14:55667894-55668260	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr14:55647068-55647696	GM12878	blood:	n/a	n/a
11	ATF2	chr14:55679782-55680187	GM12878	blood:	n/a	n/a
12	BACH1	chr14:55658236-55658711	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr14:55647125-55647568	GM12878	blood:	n/a	n/a
14	BATF	chr14:55679889-55680152	GM12878	blood:	n/a	n/a
15	BCL3	chr14:55647147-55647664	GM12878	blood:	n/a	n/a
16	BCL3	chr14:55647236-55647577	GM12878	blood:	n/a	n/a
17	BCLAF1	chr14:55657972-55658763	GM12878	blood:	n/a	chr14:55658341-55658350
18	BCLAF1	chr14:55647026-55647533	GM12878	blood:	n/a	n/a
19	BHLHE40	chr14:55658193-55658737	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:55658119-55658864	K562	blood:	n/a	n/a
21	BRCA1	chr14:55658218-55658573	GM12878	blood:	n/a	n/a
22	BRCA1	chr14:55658188-55658482	HepG2	liver:	n/a	n/a
23	BRCA1	chr14:55657534-55658576	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr14:55679822-55680189	K562	blood:	n/a	n/a
25	CBX3	chr14:55657846-55658606	K562	blood:	n/a	n/a
26	CCNT2	chr14:55657913-55658651	K562	blood:	n/a	n/a
27	CEBPB	chr14:55665506-55665826	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr14:55679925-55680358	K562	blood:	n/a	chr14:55680193-55680204
29	CEBPB	chr14:55663946-55664110	K562	blood:	n/a	chr14:55664040-55664053 chr14:55664042-55664053 chr14:55664040-55664053 chr14:55663983-55663994
30	CEBPB	chr14:55665488-55665854	IMR90	lung:	n/a	n/a
31	CEBPB	chr14:55665573-55665724	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr14:55665488-55665848	HepG2	liver:	n/a	n/a
33	CEBPB	chr14:55669654-55669727	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:55672319-55672373	K562	blood:	n/a	chr14:55672339-55672350
35	CEBPB	chr14:55679904-55680314	A549	lung:	n/a	chr14:55680193-55680204
36	CEBPB	chr14:55665527-55665851	A549	lung:	n/a	n/a
37	CEBPB	chr14:55680159-55680351	HepG2	liver:	n/a	chr14:55680193-55680204
38	CEBPB	chr14:55672203-55672476	A549	lung:	n/a	chr14:55672339-55672350
39	CEBPB	chr14:55639748-55639928	A549	lung:	n/a	chr14:55639769-55639782 chr14:55639769-55639780 chr14:55639769-55639782
40	CEBPB	chr14:55672258-55672422	HepG2	liver:	n/a	chr14:55672339-55672350
41	CEBPB	chr14:55665497-55665828	K562	blood:	n/a	n/a
42	CEBPB	chr14:55679916-55680333	IMR90	lung:	n/a	chr14:55680193-55680204
43	CEBPB	chr14:55665441-55665808	MCF-7	breast:	n/a	n/a
44	CEBPB	chr14:55679872-55680256	Hela-S3	cervix:	n/a	chr14:55680193-55680204
45	CEBPB	chr14:55639748-55639818	HepG2	liver:	n/a	chr14:55639769-55639782 chr14:55639769-55639780 chr14:55639769-55639782
46	CEBPB	chr14:55669584-55669764	K562	blood:	n/a	n/a
47	CEBPB	chr14:55665516-55665757	K562	blood:	n/a	n/a
48	CEBPB	chr14:55665550-55665895	MCF-7	breast:	n/a	n/a
49	CEBPD	chr14:55658056-55658296	HepG2	liver:	n/a	n/a
50	CEBPZ	chr14:55658368-55658487	HepG2	liver:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:55658290-55658340	ovcar-3	ovarian:	n/a
2	chr14:55658249-55658299	ECC-1	luminal epithelium:	n/a
3	chr14:55657967-55658017	NHDF-neo	bronchial:	n/a
4	chr14:55658093-55658143	GM12892	blood:	n/a
5	chr14:55658290-55658340	NHDF-neo	bronchial:	n/a
6	chr14:55661413-55661463	H1-hESC	embryonic stem cell:	embryo
7	chr14:55647471-55647521	GM12891	blood:	n/a
8	chr14:55668446-55668496	MCF-7	breast:	n/a
9	chr14:55659715-55659765	AG04450	lung:	fetal
10	chr14:55658290-55658340	H1-hESC	embryonic stem cell:	embryo
11	chr14:55661413-55661463	AG04449	skin:	fetal
12	chr14:55659715-55659765	GM12892	blood:	n/a
13	chr14:55657967-55658017	U87	brain:	n/a
14	chr14:55658398-55658448	LNCaP	prostate:	n/a
15	chr14:55659715-55659765	Hepatocyte	liver:	n/a
16	chr14:55657967-55658017	SK-N-SH	brain:	n/a
17	chr14:55657967-55658017	GM06990	blood:	n/a
18	chr14:55658093-55658143	HRE	kidney:	n/a
19	chr14:55658686-55658736	BJ	skin:	n/a
20	chr14:55668446-55668496	HCM	heart:	n/a
21	chr14:55659715-55659765	MCF-7	breast:	n/a
22	chr14:55658249-55658299	HepG2	liver:	n/a
23	chr14:55658249-55658299	PFSK-1	brain:	n/a
24	chr14:55658686-55658736	HCT-116	colon:	n/a
25	chr14:55647471-55647521	AG09309	skin:	n/a
26	chr14:55661413-55661463	NT2-D1	testis:	n/a
27	chr14:55647471-55647521	Hela-S3	cervix:	n/a
28	chr14:55658686-55658736	IMR90	lung:	fetal
29	chr14:55658290-55658340	AG04450	lung:	fetal
30	chr14:55668446-55668496	NH-A	brain:	n/a
31	chr14:55658093-55658143	ProgFib	skin:	n/a
32	chr14:55647471-55647521	PFSK-1	brain:	n/a
33	chr14:55659715-55659765	HCPEpiC	choroid plexus:	n/a
34	chr14:55658290-55658340	NH-A	brain:	n/a
35	chr14:55659715-55659765	NHBE	bronchial:	n/a
36	chr14:55647471-55647521	HepG2	liver:	n/a
37	chr14:55658249-55658299	SK-N-MC	brain:	n/a
38	chr14:55658398-55658448	HEK293	kidney:	embryo
39	chr14:55658398-55658448	HepG2	liver:	n/a
40	chr14:55661413-55661463	U87	brain:	n/a
41	chr14:55658290-55658340	NHBE	bronchial:	n/a
42	chr14:55657967-55658017	BJ	skin:	n/a
43	chr14:55658093-55658143	Caco-2	colon:	n/a
44	chr14:55668446-55668496	ECC-1	luminal epithelium:	n/a
45	chr14:55647471-55647521	GM06990	blood:	n/a
46	chr14:55658290-55658340	BJ	skin:	n/a
47	chr14:55658398-55658448	PFSK-1	brain:	n/a
48	chr14:55647471-55647521	NB4	blood:	n/a
49	chr14:55658249-55658299	AG09319	gingival:	n/a
50	chr14:55647471-55647521	IMR90	lung:	fetal

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:55648717..55651069-chr14:55656824..55659113,2	K562	blood:
2	chr14:55516908..55519746-chr14:55654326..55658338,3	K562	blood:
3	chr14:55645788..55648762-chr14:55649731..55651963,3	K562	blood:
4	chr14:55662245..55664403-chr14:55736553..55739431,2	K562	blood:
5	chr14:55643693..55646676-chr14:55654219..55656043,3	K562	blood:
6	chr14:55653901..55655851-chr14:55656440..55658540,2	MCF-7	breast:
7	chr14:55665869..55668002-chr14:55685179..55686916,2	MCF-7	breast:
8	chr14:55679230..55681659-chr14:55700930..55702648,2	MCF-7	breast:
9	chr14:55679501..55680006-chr14:55737665..55738471,2	MCF-7	breast:
10	chr14:55643693..55646676-chr14:55654219..55656043,3	K562	blood:
11	chr14:55634555..55636876-chr14:55655010..55657376,2	K562	blood:
12	chr14:55638690..55641240-chr14:55642123..55643920,2	K562	blood:
13	chr14:55678554..55682853-chr14:55737022..55740091,3	K562	blood:
14	chr14:55517066..55519736-chr14:55644348..55646551,3	MCF-7	breast:
15	chr14:55641769..55647288-chr14:55647379..55651271,6	K562	blood:
16	chr14:55664630..55666911-chr14:55737863..55740088,2	K562	blood:
17	chr14:55678786..55680522-chr14:55737916..55739440,2	MCF-7	breast:
18	chr14:55648437..55651811-chr14:55651962..55655981,4	K562	blood:
19	chr14:55638690..55641240-chr14:55642123..55643920,2	K562	blood:
20	chr14:55657344..55659337-chr14:55662940..55664641,2	K562	blood:
21	chr14:55517345..55520488-chr14:55656247..55658381,3	K562	blood:
22	chr14:55658532..55660880-chr14:55663249..55664893,2	MCF-7	breast:
23	chr14:55648437..55651811-chr14:55651962..55655981,4	K562	blood:
24	chr14:55570108..55572293-chr14:55641654..55643309,2	K562	blood:
25	chr14:55608162..55610995-chr14:55649616..55651209,2	K562	blood:
26	chr14:55654827..55657243-chr14:55881202..55883542,2	K562	blood:
27	chr14:55658532..55660880-chr14:55663249..55664893,2	MCF-7	breast:
28	chr14:55678337..55681530-chr14:55738296..55741228,5	K562	blood:
29	chr14:55645788..55648762-chr14:55649731..55651963,3	K562	blood:
30	chr14:55641769..55647288-chr14:55647379..55651271,6	K562	blood:
31	chr14:55679455..55680007-chr14:55821048..55821633,3	K562	blood:
32	chr14:55657821..55660879-chr14:55735073..55739609,4	K562	blood:
33	chr14:55679464..55680429-chr14:55912644..55913465,2	K562	blood:
34	chr14:55647150..55649562-chr14:55656835..55658830,2	MCF-7	breast:
35	chr14:55679463..55680489-chr14:55896488..55897538,5	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DLGAP5-1	chr14:55663445-55663846	ENSG00000258050
2	lnc-LGALS3-1	chr14:55658458-55658520	XLOC_010837
3	lnc-LGALS3-1	chr14:55661507-55661716	XLOC_010837
4	lnc-DLGAP5-1	chr14:55665566-55665731	ENSG00000258050

No data

Variant related genes	Relation type
DLGAP5	TF binding region
ENSG00000258050	TF binding region
DLGAP5	CpG island
ENSG00000258050	CpG island
ENSG00000258413	chromatin interactions
ENSG00000168175	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000126787	chromatin interactions

Extended variants
information (count: 1754 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1754 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115885957	chr14:55638397-55638398	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs114411034	chr14:55638531-55638532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs534005858	chr14:55638533-55638534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549472449	chr14:55638537-55638538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs190794066	chr14:55638572-55638573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535616213	chr14:55638612-55638613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs11845848	chr14:55638701-55638702	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575155654	chr14:55638735-55638736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572281180	chr14:55638762-55638763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs539352185	chr14:55638768-55638769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs557303479	chr14:55638789-55638790	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373000379	chr14:55638792-55638793	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572814626	chr14:55638809-55638810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs542562412	chr14:55638850-55638851	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376765357	chr14:55638885-55638886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs35259527	chr14:55638898-55638899	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61975417	chr14:55638917-55638918	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566076925	chr14:55638924-55638925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561802077	chr14:55638981-55638982	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573703573	chr14:55638992-55638993	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544808354	chr14:55638995-55638996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376522635	chr14:55639008-55639009	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563081073	chr14:55639009-55639010	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs533618094	chr14:55639027-55639028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377275530	chr14:55639056-55639057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4271526	chr14:55639057-55639058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552121725	chr14:55639070-55639071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116788799	chr14:55639080-55639081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs527669830	chr14:55639105-55639106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540801633	chr14:55639160-55639161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs549136687	chr14:55639172-55639173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139345252	chr14:55639179-55639180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369629466	chr14:55639181-55639182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs114732546	chr14:55639200-55639201	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554361671	chr14:55639231-55639232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548683243	chr14:55639267-55639268	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs537963115	chr14:55639296-55639297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181797295	chr14:55639310-55639311	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186106210	chr14:55639400-55639401	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539315273	chr14:55639411-55639412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537671624	chr14:55639423-55639424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs557224989	chr14:55639425-55639426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs557618287	chr14:55639430-55639431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573085940	chr14:55639452-55639453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533781778	chr14:55639476-55639477	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs113065061	chr14:55639486-55639487	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73271796	chr14:55639512-55639513	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs188936757	chr14:55639517-55639518	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544325409	chr14:55639525-55639526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556763264	chr14:55639526-55639527	Weak transcription Strong transcription	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
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
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	16397240	CNVD
Breast cancer	21633010	CNVD
Breast cancer	22032731	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:55598600-55656600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:55605200-55656000	Strong transcription	HUES64 Cell Line	embryonic stem cell
3	chr14:55605400-55657000	Weak transcription	Fetal Kidney	kidney
4	chr14:55606600-55656000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr14:55607000-55656000	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr14:55607200-55652200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
7	chr14:55607600-55651800	Strong transcription	H1 Cell Line	embryonic stem cell
8	chr14:55607600-55655200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
9	chr14:55610600-55651600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr14:55610600-55655400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr14:55610600-55655600	Strong transcription	Dnd41	blood
12	chr14:55610800-55656000	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr14:55611000-55656000	Weak transcription	Fetal Heart	heart
14	chr14:55611200-55643400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr14:55611600-55656600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr14:55613400-55639200	Weak transcription	Fetal Intestine Small	intestine
17	chr14:55613400-55657800	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr14:55619200-55646800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr14:55619600-55643800	Weak transcription	NHDF-Ad	bronchial
20	chr14:55619800-55647400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr14:55621400-55643800	Weak transcription	NH-A	brain
22	chr14:55621800-55646200	Weak transcription	NHEK	skin
23	chr14:55622600-55649000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
24	chr14:55623600-55657000	Weak transcription	Fetal Muscle Leg	muscle
25	chr14:55624800-55644200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr14:55629000-55650400	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr14:55629200-55639000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr14:55629200-55655600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr14:55629400-55650600	Strong transcription	Primary monocytes fromperipheralblood	blood
30	chr14:55629400-55652000	Strong transcription	Monocytes-CD14+_RO01746	blood
31	chr14:55630200-55656600	Weak transcription	Fetal Brain Female	brain
32	chr14:55631200-55645800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr14:55631200-55649400	Weak transcription	Duodenum Mucosa	Duodenum
34	chr14:55631200-55650400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr14:55632400-55656200	Weak transcription	HSMM	muscle
36	chr14:55632600-55646800	Weak transcription	Osteobl	bone
37	chr14:55632600-55647000	Weak transcription	NHLF	lung
38	chr14:55634200-55655400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr14:55634400-55638800	Weak transcription	Fetal Stomach	stomach
40	chr14:55634400-55639800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr14:55634400-55640200	Strong transcription	Hela-S3	cervix
42	chr14:55634400-55656200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr14:55634600-55638800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr14:55634600-55646000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr14:55634800-55641600	Weak transcription	Fetal Muscle Trunk	muscle
46	chr14:55635000-55639800	Weak transcription	Thymus	Thymus
47	chr14:55635000-55644800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr14:55635000-55647200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr14:55635200-55638400	Strong transcription	HUVEC	blood vessel
50	chr14:55635400-55646800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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