Variant report

Variant	nsv564178
Chromosome Location	chr14:31386426-31417816
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:136)
CpG islands
(count:183)
Chromatin interactive
region (count:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:136 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:31390557-31390875	K562	blood:	n/a	chr14:31390697-31390708
2	CEBPB	chr14:31390506-31390821	K562	blood:	n/a	chr14:31390697-31390708
3	CEBPB	chr14:31407864-31408203	K562	blood:	n/a	chr14:31408020-31408031
4	CEBPB	chr14:31407861-31408215	A549	lung:	n/a	chr14:31408020-31408031
5	CEBPB	chr14:31407849-31408190	H1-hESC	embryonic stem cell:	n/a	chr14:31408020-31408031
6	CEBPB	chr14:31390567-31390856	HepG2	liver:	n/a	chr14:31390697-31390708
7	CEBPB	chr14:31407850-31408210	HepG2	liver:	n/a	chr14:31408020-31408031
8	CEBPB	chr14:31407827-31408269	A549	lung:	n/a	chr14:31408020-31408031
9	CEBPB	chr14:31407822-31408276	MCF-7	breast:	n/a	chr14:31408020-31408031
10	CEBPB	chr14:31390531-31390873	Hela-S3	cervix:	n/a	chr14:31390697-31390708
11	CEBPB	chr14:31397272-31397408	HepG2	liver:	n/a	chr14:31397379-31397390
12	CEBPB	chr14:31407843-31408215	IMR90	lung:	n/a	chr14:31408020-31408031
13	CEBPB	chr14:31390541-31390863	IMR90	lung:	n/a	chr14:31390697-31390708
14	CEBPB	chr14:31407840-31408130	MCF-7	breast:	n/a	chr14:31408020-31408031
15	CEBPB	chr14:31407859-31408202	Hela-S3	cervix:	n/a	chr14:31408020-31408031
16	CTCF	chr14:31412000-31412150	MCF-7	breast:	n/a	n/a
17	CTCF	chr14:31412500-31412650	HepG2	liver:	n/a	n/a
18	CTCF	chr14:31391080-31391230	HepG2	liver:	n/a	n/a
19	CTCF	chr14:31391640-31391790	HepG2	liver:	n/a	n/a
20	CTCF	chr14:31393940-31393994	GM10248	blood:	n/a	n/a
21	E2F4	chr14:31390564-31390847	MCF10A-Er-Src	breast:	n/a	chr14:31390731-31390748 chr14:31390734-31390745
22	ELK1	chr14:31399850-31399858	GM12878	blood:	n/a	n/a
23	EP300	chr14:31390561-31390807	Hela-S3	cervix:	n/a	chr14:31390694-31390708
24	EP300	chr14:31390259-31390420	K562	blood:	n/a	n/a
25	FAM48A	chr14:31407910-31408034	GM12878	blood:	n/a	n/a
26	FAM48A	chr14:31412676-31412850	GM12878	blood:	n/a	n/a
27	FOS	chr14:31390531-31390856	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr14:31404712-31404893	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr14:31404730-31404846	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr14:31404773-31404973	HUVEC	blood vessel:	n/a	n/a
31	FOS	chr14:31390577-31390853	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr14:31390563-31390854	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr14:31390543-31390860	MCF10A-Er-Src	breast:	n/a	n/a
34	GATA2	chr14:31404630-31404983	HUVEC	blood vessel:	n/a	n/a
35	GATA3	chr14:31404600-31405041	MCF-7	breast:	n/a	n/a
36	GATA3	chr14:31404506-31405144	SK-N-SH	brain:	n/a	n/a
37	GATA3	chr14:31404486-31405143	SK-N-SH	brain:	n/a	n/a
38	GATA3	chr14:31389636-31390347	SH-SY5Y	brain:	n/a	chr14:31390316-31390323 chr14:31390315-31390325
39	GATA3	chr14:31400694-31401259	SK-N-SH	brain:	n/a	chr14:31400832-31400845
40	IRF1	chr14:31395264-31395370	K562	blood:	n/a	n/a
41	IRF1	chr14:31390340-31390428	K562	blood:	n/a	n/a
42	JUN	chr14:31390557-31390879	HUVEC	blood vessel:	n/a	n/a
43	JUN	chr14:31393268-31393333	HepG2	liver:	n/a	n/a
44	JUN	chr14:31409000-31409285	HUVEC	blood vessel:	n/a	n/a
45	JUND	chr14:31390613-31390839	K562	blood:	n/a	n/a
46	JUND	chr14:31393200-31393327	HepG2	liver:	n/a	n/a
47	MAFF	chr14:31402134-31402264	HepG2	liver:	n/a	chr14:31402188-31402206
48	MAFF	chr14:31399888-31400095	HepG2	liver:	n/a	chr14:31399959-31399977
49	MAFK	chr14:31399215-31399375	HepG2	liver:	n/a	chr14:31399290-31399306
50	MAFK	chr14:31399813-31400055	HepG2	liver:	n/a	chr14:31399962-31399982

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31389792-31389842	Hela-S3	cervix:	n/a
2	chr14:31389792-31389842	HRPEpiC	eye:	n/a
3	chr14:31398430-31398480	BJ	skin:	n/a
4	chr14:31398430-31398480	PANC-1	pancreas:	n/a
5	chr14:31408344-31408394	NB4	blood:	n/a
6	chr14:31408344-31408394	SK-N-MC	brain:	n/a
7	chr14:31389792-31389842	MCF-7	breast:	n/a
8	chr14:31408344-31408394	BJ	skin:	n/a
9	chr14:31389792-31389842	GM19239	blood:	n/a
10	chr14:31408344-31408394	ovcar-3	ovarian:	n/a
11	chr14:31389792-31389842	PrEC	prostate:	n/a
12	chr14:31389792-31389842	HMEC	breast:	n/a
13	chr14:31389792-31389842	RPTEC	kidney:	n/a
14	chr14:31389792-31389842	T-47D	breast:	n/a
15	chr14:31408344-31408394	HepG2	liver:	n/a
16	chr14:31408344-31408394	Hela-S3	cervix:	n/a
17	chr14:31408344-31408394	NT2-D1	testis:	n/a
18	chr14:31398430-31398480	AG09319	gingival:	n/a
19	chr14:31398430-31398480	PrEC	prostate:	n/a
20	chr14:31389792-31389842	K562	blood:	n/a
21	chr14:31398430-31398480	HCPEpiC	choroid plexus:	n/a
22	chr14:31398430-31398480	ProgFib	skin:	n/a
23	chr14:31408344-31408394	K562	blood:	n/a
24	chr14:31408344-31408394	HEEpiC	esophagus:	n/a
25	chr14:31398430-31398480	GM19239	blood:	n/a
26	chr14:31408344-31408394	CMK	blood:	n/a
27	chr14:31408344-31408394	SK-N-SH_RA	brain:	n/a
28	chr14:31398430-31398480	NH-A	brain:	n/a
29	chr14:31398430-31398480	HMEC	breast:	n/a
30	chr14:31389792-31389842	SK-N-MC	brain:	n/a
31	chr14:31398430-31398480	CMK	blood:	n/a
32	chr14:31389792-31389842	NB4	blood:	n/a
33	chr14:31389792-31389842	GM06990	blood:	n/a
34	chr14:31398430-31398480	NHDF-neo	bronchial:	n/a
35	chr14:31398430-31398480	Hepatocyte	liver:	n/a
36	chr14:31408344-31408394	GM19239	blood:	n/a
37	chr14:31398430-31398480	HEK293	kidney:	embryo
38	chr14:31398430-31398480	Jurkat	blood:	n/a
39	chr14:31398430-31398480	SK-N-SH_RA	brain:	n/a
40	chr14:31389792-31389842	AG04450	lung:	fetal
41	chr14:31398430-31398480	HAEpiC	amniotic membrane:	n/a
42	chr14:31398430-31398480	K562	blood:	n/a
43	chr14:31389792-31389842	GM12878	blood:	n/a
44	chr14:31408344-31408394	PANC-1	pancreas:	n/a
45	chr14:31398430-31398480	ECC-1	luminal epithelium:	n/a
46	chr14:31398430-31398480	HRE	kidney:	n/a
47	chr14:31408344-31408394	SK-N-SH	brain:	n/a
48	chr14:31398430-31398480	Caco-2	colon:	n/a
49	chr14:31398430-31398480	HPAEpiC	pulmonary alveolar:	n/a
50	chr14:31408344-31408394	HIPEpiC	eye:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:31400245..31402113-chr14:31403843..31406707,2	MCF-7	breast:
2	chr14:31390350..31392275-chr14:31395263..31396767,2	K562	blood:
3	chr14:31385492..31389361-chr14:31390065..31392327,4	K562	blood:
4	chr14:31385237..31388114-chr14:31390780..31394488,3	MCF-7	breast:
5	chr14:31412013..31413799-chr14:31413815..31415852,2	MCF-7	breast:
6	chr14:31412013..31413799-chr14:31413815..31415852,2	MCF-7	breast:
7	chr14:31400245..31402113-chr14:31403843..31406707,2	MCF-7	breast:
8	chr14:31387011..31389077-chr14:31394255..31396560,2	K562	blood:
9	chr14:31398507..31401730-chr14:31402844..31406226,4	K562	blood:
10	chr14:31402683..31406428-chr14:31407313..31410233,6	K562	blood:
11	chr14:31406134..31408433-chr14:31516211..31518078,2	K562	blood:
12	chr14:31398507..31401730-chr14:31402844..31406226,4	K562	blood:
13	chr14:31385492..31389361-chr14:31390065..31392327,4	K562	blood:
14	chr14:31397468..31399701-chr14:31410285..31412729,2	MCF-7	breast:
15	chr14:31412377..31414525-chr14:31418622..31420542,2	MCF-7	breast:
16	chr14:31387011..31389077-chr14:31394255..31396560,2	K562	blood:
17	chr14:31390350..31392275-chr14:31395263..31396767,2	K562	blood:
18	chr14:31397468..31399701-chr14:31410285..31412729,2	MCF-7	breast:
19	chr14:31376657..31378769-chr14:31384602..31386523,2	MCF-7	breast:
20	chr14:31404383..31406657-chr14:31409869..31411808,3	MCF-7	breast:
21	chr14:31385237..31388114-chr14:31390780..31394488,3	MCF-7	breast:

No data

Variant related genes	Relation type
STRN3	TF binding region
STRN3	CpG island
ENSG00000196792	chromatin interactions

Extended variants
information (count: 1205 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1205 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9322866	chr14:31386426-31386427	Weak transcription Strong transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs192304482	chr14:31386438-31386439	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs183741364	chr14:31386442-31386443	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs17097524	chr14:31386529-31386530	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs75623270	chr14:31386531-31386532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568397322	chr14:31386545-31386546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs76941922	chr14:31386569-31386570	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs557256734	chr14:31386586-31386587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs575132627	chr14:31386598-31386599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552999296	chr14:31386620-31386621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141401562	chr14:31386628-31386629	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs572900785	chr14:31386632-31386633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs72668349	chr14:31386635-31386636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540401364	chr14:31386641-31386642	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561898356	chr14:31386645-31386646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147018802	chr14:31386669-31386670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs17097526	chr14:31386678-31386679	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs187929662	chr14:31386730-31386731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs77879389	chr14:31386761-31386762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376376757	chr14:31386802-31386803	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115498283	chr14:31386813-31386814	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528609680	chr14:31386833-31386834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532316926	chr14:31386885-31386886	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74040947	chr14:31386911-31386912	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs11396931	chr14:31386916-31386917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184279805	chr14:31386923-31386924	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs397782810	chr14:31386924-31386925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9635154	chr14:31386929-31386930	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs187173810	chr14:31386993-31386994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs10483358	chr14:31386994-31386995	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs201135362	chr14:31386997-31386998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192326065	chr14:31387085-31387086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149151119	chr14:31387099-31387100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs143284779	chr14:31387113-31387114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73257912	chr14:31387175-31387176	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs185330322	chr14:31387227-31387228	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555522574	chr14:31387461-31387462	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148314557	chr14:31387467-31387468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544458781	chr14:31387483-31387484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141471961	chr14:31387511-31387512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs189867335	chr14:31387568-31387569	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182438944	chr14:31387571-31387572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543529324	chr14:31387622-31387623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs564286176	chr14:31387652-31387653	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373611203	chr14:31387663-31387664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs528505292	chr14:31387667-31387668	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540285899	chr14:31387677-31387678	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1997904	chr14:31387693-31387694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529438533	chr14:31387709-31387710	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201506527	chr14:31387719-31387720	Weak transcription Strong transcription	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
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:723 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31345000-31435400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr14:31347000-31394800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr14:31355800-31414400	Weak transcription	Spleen	Spleen
4	chr14:31356200-31412800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
5	chr14:31358000-31428200	Weak transcription	Small Intestine	intestine
6	chr14:31360200-31435600	Weak transcription	Gastric	stomach
7	chr14:31361800-31394200	Weak transcription	Fetal Brain Male	brain
8	chr14:31362200-31414400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr14:31362400-31435400	Weak transcription	Colonic Mucosa	Colon
10	chr14:31363000-31394400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr14:31363000-31430600	Weak transcription	Brain Angular Gyrus	brain
12	chr14:31363000-31435200	Weak transcription	Esophagus	oesophagus
13	chr14:31364400-31415400	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr14:31364800-31393200	Weak transcription	Brain Substantia Nigra	brain
15	chr14:31365800-31402200	Weak transcription	Thymus	Thymus
16	chr14:31365800-31414200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr14:31365800-31435600	Weak transcription	Right Ventricle	heart
18	chr14:31370000-31393600	Weak transcription	Lung	lung
19	chr14:31370000-31414400	Weak transcription	Pancreas	Pancrea
20	chr14:31372400-31414400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr14:31375600-31390000	Weak transcription	Pancreatic Islets	Pancreatic Islet
22	chr14:31376200-31403000	Weak transcription	Hela-S3	cervix
23	chr14:31377800-31435600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr14:31378000-31414400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr14:31378000-31439000	Weak transcription	Psoas Muscle	Psoas
26	chr14:31378800-31435200	Weak transcription	Aorta	Aorta
27	chr14:31378800-31435400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr14:31379000-31391000	Weak transcription	Fetal Stomach	stomach
29	chr14:31379000-31393600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr14:31379000-31393600	Weak transcription	Fetal Intestine Small	intestine
31	chr14:31379000-31413800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr14:31379400-31390000	Weak transcription	NHEK	skin
33	chr14:31379400-31404200	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr14:31379600-31402800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
35	chr14:31379600-31403400	Weak transcription	Cortex derived primary cultured neurospheres	brain
36	chr14:31379600-31404000	Weak transcription	Colon Smooth Muscle	Colon
37	chr14:31379600-31405000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr14:31379800-31391400	Weak transcription	Primary hematopoietic stem cells	blood
39	chr14:31379800-31403600	Weak transcription	Fetal Heart	heart
40	chr14:31379800-31412400	Weak transcription	Brain Hippocampus Middle	brain
41	chr14:31380400-31415400	Weak transcription	Brain Germinal Matrix	brain
42	chr14:31380600-31402600	Weak transcription	HMEC	breast
43	chr14:31380800-31391400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr14:31380800-31403200	Weak transcription	Fetal Muscle Leg	muscle
45	chr14:31380800-31405800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr14:31381200-31388000	Weak transcription	A549	lung
47	chr14:31381200-31393800	Weak transcription	Fetal Lung	lung
48	chr14:31381200-31414400	Weak transcription	Fetal Brain Female	brain
49	chr14:31381400-31387400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr14:31381400-31388000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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