Variant report

Variant	esv1792376
Chromosome Location	chr14:56108007-56150151
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	ATF2	chr14:56131774-56132158	GM12878	blood:	n/a	n/a
2	BATF	chr14:56131780-56132130	GM12878	blood:	n/a	chr14:56131921-56131930
3	BATF	chr14:56131730-56132108	GM12878	blood:	n/a	chr14:56131921-56131930
4	BCL11A	chr14:56131816-56132106	GM12878	blood:	n/a	n/a
5	BHLHE40	chr14:56131219-56131251	HepG2	liver:	n/a	n/a
6	BRCA1	chr14:56113291-56113333	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr14:56113304-56113504	GM12878	blood:	n/a	n/a
8	CEBPB	chr14:56126681-56126897	HepG2	liver:	n/a	chr14:56126760-56126769 chr14:56126758-56126769
9	CEBPB	chr14:56143724-56143964	K562	blood:	n/a	chr14:56143854-56143863 chr14:56143853-56143864 chr14:56143852-56143863 chr14:56143852-56143865
10	CEBPB	chr14:56143681-56143998	IMR90	lung:	n/a	chr14:56143854-56143863 chr14:56143853-56143864 chr14:56143852-56143863 chr14:56143852-56143865
11	CEBPB	chr14:56143754-56143928	H1-hESC	embryonic stem cell:	n/a	chr14:56143854-56143863 chr14:56143853-56143864 chr14:56143852-56143863 chr14:56143852-56143865
12	CEBPB	chr14:56143792-56143983	Hela-S3	cervix:	n/a	chr14:56143854-56143863 chr14:56143853-56143864 chr14:56143852-56143863 chr14:56143852-56143865
13	CEBPB	chr14:56143716-56143976	A549	lung:	n/a	chr14:56143854-56143863 chr14:56143853-56143864 chr14:56143852-56143863 chr14:56143852-56143865
14	CEBPB	chr14:56143674-56144007	HepG2	liver:	n/a	chr14:56143854-56143863 chr14:56143853-56143864 chr14:56143852-56143863 chr14:56143852-56143865
15	CHD2	chr14:56113307-56113331	HepG2	liver:	n/a	n/a
16	CTCF	chr14:56131300-56131450	HMF	breast:	n/a	n/a
17	CTCF	chr14:56142300-56142450	HepG2	liver:	n/a	n/a
18	CTCF	chr14:56131300-56131450	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr14:56131340-56131490	A549	lung:	n/a	n/a
20	CTCF	chr14:56131332-56131503	GM12878	blood:	n/a	n/a
21	CTCF	chr14:56131180-56131330	HVMF	connective:	n/a	n/a
22	E2F4	chr14:56139878-56140199	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr14:56113810-56113934	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr14:56131882-56132029	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr14:56127145-56127413	MCF10A-Er-Src	breast:	n/a	n/a
26	EBF1	chr14:56131777-56132071	GM12878	blood:	n/a	n/a
27	EP300	chr14:56131858-56132119	GM12878	blood:	n/a	n/a
28	EP300	chr14:56130269-56130440	K562	blood:	n/a	n/a
29	EP300	chr14:56133743-56133862	K562	blood:	n/a	n/a
30	EP300	chr14:56131804-56132190	GM12878	blood:	n/a	n/a
31	EP300	chr14:56108664-56109050	H1-hESC	embryonic stem cell:	n/a	n/a
32	FAM48A	chr14:56138363-56138431	GM12878	blood:	n/a	n/a
33	FAM48A	chr14:56108769-56108951	GM12878	blood:	n/a	n/a
34	FOS	chr14:56138495-56138605	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr14:56139854-56139948	MCF10A-Er-Src	breast:	n/a	n/a
36	FOXA2	chr14:56121066-56121221	HepG2	liver:	n/a	chr14:56121110-56121122
37	FOXA2	chr14:56138405-56138716	A549	lung:	n/a	n/a
38	GATA1	chr14:56134295-56135826	PBDE	blood:	n/a	n/a
39	GATA1	chr14:56129179-56130077	PBDE	blood:	n/a	chr14:56129929-56129939 chr14:56129605-56129622 chr14:56129616-56129623 chr14:56129614-56129624
40	GATA1	chr14:56120510-56121717	PBDE	blood:	n/a	chr14:56121141-56121162 chr14:56121148-56121157 chr14:56121147-56121157 chr14:56120698-56120711 chr14:56121045-56121066
41	GATA3	chr14:56120863-56121242	MCF-7	breast:	n/a	chr14:56121141-56121162 chr14:56121148-56121157 chr14:56121147-56121157 chr14:56121045-56121066
42	GATA3	chr14:56136959-56137252	SH-SY5Y	brain:	n/a	n/a
43	GATA3	chr14:56112650-56112850	SH-SY5Y	brain:	n/a	chr14:56112765-56112772 chr14:56112761-56112774 chr14:56112775-56112782
44	GATA3	chr14:56149941-56150197	SH-SY5Y	brain:	n/a	n/a
45	GATA3	chr14:56128060-56128552	SK-N-SH	brain:	n/a	n/a
46	GATA3	chr14:56117349-56117487	SH-SY5Y	brain:	n/a	n/a
47	GTF2F1	chr14:56113306-56113333	H1-hESC	embryonic stem cell:	n/a	n/a
48	IKZF1	chr14:56131888-56132017	GM12878	blood:	n/a	n/a
49	IKZF1	chr14:56133122-56133290	GM12878	blood:	n/a	n/a
50	IRF1	chr14:56112740-56112795	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:56113692..56116512-chr14:56123800..56126287,2	MCF-7	breast:
2	chr1:144531660..144535087-chr14:56140285..56143287,3	K562	blood:
3	chr14:56120614..56122257-chr14:56126744..56128626,2	MCF-7	breast:
4	chr14:56136295..56138118-chr14:56139376..56142156,3	K562	blood:
5	chr14:56126633..56128204-chr14:56129295..56131290,2	K562	blood:
6	chr1:144533498..144535527-chr14:56140284..56141806,2	K562	blood:
7	chr14:56110772..56112668-chr14:56115971..56118185,2	K562	blood:
8	chr14:56136295..56138118-chr14:56139376..56142156,3	K562	blood:
9	chr14:56135952..56138303-chr14:56139128..56140660,2	MCF-7	breast:
10	chr14:56127727..56129684-chr14:56130205..56132063,2	MCF-7	breast:
11	chr14:56123511..56126228-chr14:56130259..56133014,2	K562	blood:
12	chr14:56135769..56139247-chr14:56140208..56143081,3	K562	blood:
13	chr14:56113692..56116512-chr14:56123800..56126287,2	MCF-7	breast:
14	chr14:56133519..56136072-chr14:56136743..56138846,2	MCF-7	breast:
15	chr14:56109854..56112064-chr14:56118999..56121625,2	K562	blood:
16	chr14:56149406..56151839-chr14:56154721..56157088,2	K562	blood:
17	chr14:56120266..56122635-chr14:56124757..56126273,2	K562	blood:
18	chr14:56135769..56139247-chr14:56140208..56143081,3	K562	blood:
19	chr14:56120266..56122635-chr14:56124757..56126273,2	K562	blood:
20	chr14:56118646..56123000-chr14:56124614..56127350,4	MCF-7	breast:
21	chr14:56133519..56136072-chr14:56136743..56138846,2	MCF-7	breast:
22	chr14:56046884..56048461-chr14:56110849..56113567,2	K562	blood:
23	chr14:56126633..56128204-chr14:56129295..56131290,2	K562	blood:
24	chr14:56135952..56138303-chr14:56139128..56140660,2	MCF-7	breast:
25	chr14:56110772..56112668-chr14:56115971..56118185,2	K562	blood:
26	chr14:56123511..56126228-chr14:56130259..56133014,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO34-2	chr14:56125264-56125332	NONHSAT037019
2	lnc-FBXO34-2	chr14:56122760-56123065	NONHSAT037017
3	lnc-FBXO34-2	chr14:56128240-56128575	NONHSAT037019
4	lnc-FBXO34-2	chr14:56120277-56120314	NONHSAT037017
5	lnc-FBXO34-2	chr14:56118608-56118645	NONHSAT037017
6	lnc-FBXO34-2	chr14:56119568-56119658	NONHSAT037017
7	lnc-FBXO34-2	chr14:56139647-56141022	NONHSAT037020
8	lnc-FBXO34-2	chr14:56139348-56139419	NONHSAT037020
9	lnc-FBXO34-2	chr14:56122818-56122850	NONHSAT037019
10	lnc-FBXO34-2	chr14:56119735-56119803	NONHSAT037017
11	lnc-FBXO34-2	chr14:56138580-56138595	NONHSAT037020
12	lnc-FBXO34-2	chr14:56126384-56126421	NONHSAT037019
13	lnc-FBXO34-2	chr14:56117353-56117355	NONHSAT037017

Variant related genes	Relation type
KTN1	TF binding region
ENSG00000200742	TF binding region
ENSG00000201699	chromatin interactions
ENSG00000126777	chromatin interactions

Extended variants
information (count: 1828 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1828 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10483649	chr14:56108007-56108008	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs115810209	chr14:56108012-56108013	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569270370	chr14:56108025-56108026	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs2341890	chr14:56108033-56108034	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs558594682	chr14:56108048-56108049	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs570434828	chr14:56108098-56108099	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs79807559	chr14:56108117-56108118	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	mRNA abundance
8	rs553591999	chr14:56108145-56108146	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs374102155	chr14:56108181-56108182	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs367961876	chr14:56108182-56108183	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs542493299	chr14:56108186-56108187	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs557399775	chr14:56108196-56108197	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs145902784	chr14:56108201-56108202	Genic enhancers Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs546002805	chr14:56108229-56108230	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192212040	chr14:56108232-56108233	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs138455932	chr14:56108234-56108235	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575555042	chr14:56108259-56108260	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs142958036	chr14:56108289-56108290	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529948487	chr14:56108301-56108302	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150678811	chr14:56108308-56108309	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs548048056	chr14:56108378-56108379	Genic enhancers Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569334261	chr14:56108410-56108411	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs140464911	chr14:56108429-56108430	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs145880665	chr14:56108430-56108431	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs368227576	chr14:56108476-56108477	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs139871872	chr14:56108482-56108483	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs149280320	chr14:56108515-56108516	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs1951890	chr14:56108520-56108521	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs184276581	chr14:56108529-56108530	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs553605962	chr14:56108539-56108540	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568627789	chr14:56108566-56108567	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs45599941	chr14:56108586-56108587	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs144484283	chr14:56108599-56108600	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115879375	chr14:56108616-56108617	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548107579	chr14:56108642-56108643	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577872608	chr14:56108708-56108709	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs557864713	chr14:56108742-56108743	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs573291295	chr14:56108743-56108744	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs187164897	chr14:56108750-56108751	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs559140032	chr14:56108758-56108759	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs574267269	chr14:56108769-56108770	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs540491945	chr14:56108778-56108779	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs373370711	chr14:56108780-56108781	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs541604824	chr14:56108843-56108844	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs563637064	chr14:56108870-56108871	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs530702652	chr14:56108910-56108911	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs559515546	chr14:56108919-56108920	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs377060730	chr14:56108930-56108931	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs35855971	chr14:56108955-56108956	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs552194665	chr14:56108966-56108967	Enhancers Weak transcription Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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	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
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	21163964	CNVD
Cancer	20164919	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1147 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:56078600-56148600	Weak transcription	Stomach Mucosa	stomach
2	chr14:56079800-56111400	Strong transcription	Rectal Mucosa Donor 29	rectum
3	chr14:56080800-56110800	Strong transcription	Primary T helper cells PMA-I stimulated	--
4	chr14:56087400-56111800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr14:56087400-56112200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
6	chr14:56087400-56132200	Strong transcription	Dnd41	blood
7	chr14:56087600-56110000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:56087600-56145200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr14:56088200-56108600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr14:56088200-56129400	Weak transcription	Spleen	Spleen
11	chr14:56088200-56132200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr14:56088400-56121600	Weak transcription	Aorta	Aorta
13	chr14:56088400-56121800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:56088400-56153200	Weak transcription	Gastric	stomach
15	chr14:56092800-56135400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr14:56093200-56110000	Strong transcription	Rectal Mucosa Donor 31	rectum
17	chr14:56093800-56110000	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr14:56094200-56110000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr14:56094200-56110200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr14:56094400-56109800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr14:56094400-56113000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
22	chr14:56094400-56132600	Strong transcription	HSMM	muscle
23	chr14:56094600-56110000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr14:56094600-56110200	Strong transcription	Liver	Liver
25	chr14:56095000-56142200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr14:56096200-56112000	Strong transcription	Primary T helper cells fromperipheralblood	blood
27	chr14:56096600-56109400	Strong transcription	GM12878-XiMat	blood
28	chr14:56097600-56115600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr14:56097600-56145200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr14:56097600-56155400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr14:56098600-56121600	Weak transcription	Small Intestine	intestine
32	chr14:56099000-56128000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr14:56099400-56118600	Strong transcription	Hela-S3	cervix
34	chr14:56099800-56110000	Strong transcription	Fetal Thymus	thymus
35	chr14:56100000-56109000	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr14:56100200-56131000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
37	chr14:56100400-56109800	Strong transcription	Placenta	Placenta
38	chr14:56100400-56110200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr14:56100400-56112600	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr14:56100800-56109800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr14:56100800-56109800	Strong transcription	A549	lung
42	chr14:56100800-56112200	Strong transcription	Duodenum Mucosa	Duodenum
43	chr14:56101000-56132800	Strong transcription	Primary B cells from peripheral blood	blood
44	chr14:56101400-56112800	Strong transcription	Primary B cells from cord blood	blood
45	chr14:56101800-56109200	Strong transcription	NHDF-Ad	bronchial
46	chr14:56101800-56118200	Weak transcription	Fetal Brain Female	brain
47	chr14:56101800-56121600	Weak transcription	Pancreas	Pancrea
48	chr14:56101800-56123200	Weak transcription	Fetal Intestine Small	intestine
49	chr14:56101800-56128800	Weak transcription	Fetal Stomach	stomach
50	chr14:56101800-56162800	Weak transcription	Brain Germinal Matrix	brain

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