Variant report

Variant	nsv902020
Chromosome Location	chr14:64434288-64506541
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	ARID3A	chr14:64479586-64479817	HepG2	liver:	n/a	n/a
2	ATF1	chr14:64479517-64479717	K562	blood:	n/a	n/a
3	ATF2	chr14:64438881-64439493	GM12878	blood:	n/a	n/a
4	BATF	chr14:64458576-64458835	GM12878	blood:	n/a	chr14:64458723-64458734
5	CEBPB	chr14:64484676-64484961	A549	lung:	n/a	n/a
6	CEBPB	chr14:64453970-64454207	A549	lung:	n/a	n/a
7	CEBPB	chr14:64449141-64449203	HepG2	liver:	n/a	chr14:64449188-64449199
8	CEBPB	chr14:64505685-64505972	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:64453896-64454259	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr14:64493392-64493544	A549	lung:	n/a	n/a
11	CEBPB	chr14:64493389-64493627	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr14:64484654-64484966	IMR90	lung:	n/a	n/a
13	CEBPB	chr14:64493243-64493687	MCF-7	breast:	n/a	n/a
14	CEBPB	chr14:64484640-64484997	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:64449168-64449171	A549	lung:	n/a	n/a
16	CEBPB	chr14:64449143-64449323	H1-hESC	embryonic stem cell:	n/a	chr14:64449188-64449199
17	CEBPB	chr14:64449172-64449232	IMR90	lung:	n/a	chr14:64449188-64449199
18	CEBPB	chr14:64484692-64484930	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr14:64453815-64454299	IMR90	lung:	n/a	n/a
20	CTCF	chr14:64460862-64461026	MCF-7	breast:	n/a	n/a
21	CTCF	chr14:64477120-64477270	BE2_C	brain:	n/a	n/a
22	CTCF	chr14:64477232-64477390	Hela-S3	cervix:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
23	CTCF	chr14:64493400-64493550	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr14:64477260-64477410	GM12871	blood:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
25	CTCF	chr14:64478060-64478210	AG04449	skin:	n/a	n/a
26	CTCF	chr14:64460880-64461030	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr14:64461040-64461190	RPTEC	kidney:	n/a	n/a
28	CTCF	chr14:64493443-64493564	MCF-7	breast:	n/a	n/a
29	CTCF	chr14:64477120-64477270	HVMF	connective:	n/a	n/a
30	CTCF	chr14:64460680-64460830	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr14:64477240-64477390	HMEC	breast:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
32	CTCF	chr14:64460880-64461030	Caco-2	colon:	n/a	n/a
33	CTCF	chr14:64460850-64461060	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr14:64481120-64481174	GM13976	blood:	n/a	n/a
35	CTCF	chr14:64477240-64477390	Hela-S3	cervix:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
36	CTCF	chr14:64460846-64461052	IMR90	lung:	n/a	n/a
37	CTCF	chr14:64460760-64460910	HAc	cerebellar:	n/a	n/a
38	CTCF	chr14:64477300-64477450	NHDF-neo	bronchial:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
39	CTCF	chr14:64477220-64477370	HPAF	blood vessel:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
40	CTCF	chr14:64477260-64477410	AG04450	lung:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
41	CTCF	chr14:64460882-64460975	Gliobla	brain:	n/a	n/a
42	CTCF	chr14:64476800-64476950	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr14:64477228-64477393	Spleen_OC	spleen:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
44	CTCF	chr14:64460880-64461030	HL-60	blood:	n/a	n/a
45	CTCF	chr14:64476900-64477050	HCM	heart:	n/a	n/a
46	CTCF	chr14:64478040-64478190	HFF-Myc	foreskin:	n/a	chr14:64478048-64478069 chr14:64478059-64478068 chr14:64478053-64478071
47	CTCF	chr14:64460900-64461050	AG04449	skin:	n/a	n/a
48	CTCF	chr14:64506463-64506541	LNCaP	prostate:	n/a	n/a
49	CTCF	chr14:64477260-64477410	HVMF	connective:	n/a	chr14:64477312-64477328 chr14:64477313-64477334 chr14:64477311-64477329 chr14:64477315-64477322
50	CTCF	chr14:64460900-64461050	AG09319	gingival:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:64505421-64505471	RPTEC	kidney:	n/a
2	chr14:64505421-64505471	HRE	kidney:	n/a
3	chr14:64505421-64505471	AoSMC	blood vessel:	n/a
4	chr14:64505421-64505471	HCM	heart:	n/a
5	chr14:64505421-64505471	HMEC	breast:	n/a
6	chr14:64505421-64505471	GM12891	blood:	n/a
7	chr14:64505421-64505471	T-47D	breast:	n/a
8	chr14:64505421-64505471	HL-60	blood:	n/a
9	chr14:64505421-64505471	IMR90	lung:	fetal
10	chr14:64505421-64505471	AG09309	skin:	n/a
11	chr14:64505421-64505471	HEK293	kidney:	embryo
12	chr14:64505421-64505471	NT2-D1	testis:	n/a
13	chr14:64505421-64505471	PrEC	prostate:	n/a
14	chr14:64505421-64505471	HAEpiC	amniotic membrane:	n/a
15	chr14:64505421-64505471	HUVEC	blood vessel:	n/a
16	chr14:64505421-64505471	MCF-7	breast:	n/a
17	chr14:64505421-64505471	SKMC	muscle:	n/a
18	chr14:64505421-64505471	HIPEpiC	eye:	n/a
19	chr14:64505421-64505471	PFSK-1	brain:	n/a
20	chr14:64505421-64505471	CMK	blood:	n/a
21	chr14:64505421-64505471	A549	lung:	n/a
22	chr14:64505421-64505471	NHBE	bronchial:	n/a
23	chr14:64505421-64505471	HEEpiC	esophagus:	n/a
24	chr14:64505421-64505471	AG10803	skin:	n/a
25	chr14:64505421-64505471	Jurkat	blood:	n/a
26	chr14:64505421-64505471	BJ	skin:	n/a
27	chr14:64505421-64505471	ProgFib	skin:	n/a
28	chr14:64505421-64505471	K562	blood:	n/a
29	chr14:64505421-64505471	PANC-1	pancreas:	n/a
30	chr14:64505421-64505471	HNPCEpiC	eye:	n/a
31	chr14:64505421-64505471	LNCaP	prostate:	n/a
32	chr14:64505421-64505471	NB4	blood:	n/a
33	chr14:64505421-64505471	AG09319	gingival:	n/a
34	chr14:64505421-64505471	HCPEpiC	choroid plexus:	n/a
35	chr14:64505421-64505471	GM12892	blood:	n/a
36	chr14:64505421-64505471	ovcar-3	ovarian:	n/a
37	chr14:64505421-64505471	Hela-S3	cervix:	n/a
38	chr14:64505421-64505471	BE2_C	brain:	n/a
39	chr14:64505421-64505471	HCT-116	colon:	n/a
40	chr14:64505421-64505471	AG04449	skin:	fetal
41	chr14:64505421-64505471	SK-N-SH_RA	brain:	n/a
42	chr14:64505421-64505471	HRCEpiC	kidney:	n/a
43	chr14:64505421-64505471	Hepatocyte	liver:	n/a
44	chr14:64505421-64505471	NH-A	brain:	n/a
45	chr14:64505421-64505471	HRPEpiC	eye:	n/a
46	chr14:64505421-64505471	HCF	heart:	n/a
47	chr14:64505421-64505471	AG04450	lung:	fetal
48	chr14:64505421-64505471	U87	brain:	n/a
49	chr14:64505421-64505471	Caco-2	colon:	n/a
50	chr14:64505421-64505471	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:64490181..64492007-chr14:64498703..64500791,2	MCF-7	breast:
2	chr14:64265952..64266822-chr14:64460521..64461407,3	MCF-7	breast:
3	chr14:64459939..64462358-chr14:64466934..64469220,2	MCF-7	breast:
4	chr14:64318653..64321289-chr14:64441036..64444017,2	MCF-7	breast:
5	chr14:64490181..64492007-chr14:64498703..64500791,2	MCF-7	breast:
6	chr14:64457255..64458823-chr14:64462869..64464742,2	K562	blood:
7	chr14:64483143..64485630-chr14:64487133..64489542,2	MCF-7	breast:
8	chr14:64479160..64481857-chr14:64484574..64486419,2	MCF-7	breast:
9	chr14:64319797..64321605-chr14:64466270..64468504,2	MCF-7	breast:
10	chr14:64476776..64478688-chr14:64505226..64506868,2	MCF-7	breast:
11	chr14:64479160..64481857-chr14:64484574..64486419,2	MCF-7	breast:
12	chr14:64459939..64462358-chr14:64466934..64469220,2	MCF-7	breast:
13	chr14:64476776..64478688-chr14:64505226..64506868,2	MCF-7	breast:
14	chr14:64457255..64458823-chr14:64462869..64464742,2	K562	blood:
15	chr14:64483143..64485630-chr14:64487133..64489542,2	MCF-7	breast:
16	chr14:64319515..64320345-chr14:64460464..64461475,3	MCF-7	breast:
17	chr14:64477263..64477827-chr14:64761253..64761994,2	K562	blood:
18	chr14:64477325..64478067-chr14:64761385..64762337,2	MCF-7	breast:

Variant related genes	Relation type
SYNE2	TF binding region
SYNE2	CpG island
ENSG00000054654	chromatin interactions

Extended variants
information (count: 2889 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:2889 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12884607	chr14:64434288-64434289	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs377284737	chr14:64434312-64434313	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545948917	chr14:64434331-64434332	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs76505252	chr14:64434339-64434340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370726266	chr14:64434358-64434359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148644895	chr14:64434364-64434365	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs77445320	chr14:64434399-64434400	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376253539	chr14:64434414-64434415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531679716	chr14:64434429-64434430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs370697495	chr14:64434434-64434435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374073818	chr14:64434496-64434497	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs368015444	chr14:64434503-64434504	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs550699600	chr14:64434542-64434543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371916462	chr14:64434556-64434557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570522489	chr14:64434616-64434617	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1255891	chr14:64434652-64434653	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs150728672	chr14:64434661-64434662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113102885	chr14:64434691-64434692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs1255892	chr14:64434701-64434702	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535779186	chr14:64434714-64434715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs190422326	chr14:64434719-64434720	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568486834	chr14:64434740-64434741	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs537000409	chr14:64434773-64434774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs541428813	chr14:64434785-64434786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561685389	chr14:64434830-64434831	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557042308	chr14:64434831-64434832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370168327	chr14:64434835-64434836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78067424	chr14:64434881-64434882	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576890880	chr14:64434883-64434884	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192116960	chr14:64434909-64434910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553558182	chr14:64434926-64434927	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573340953	chr14:64434930-64434931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144927139	chr14:64434949-64434950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544143029	chr14:64434954-64434955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs563812234	chr14:64434967-64434968	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184704577	chr14:64435021-64435022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532767210	chr14:64435056-64435057	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs544194674	chr14:64435083-64435084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs564194356	chr14:64435100-64435101	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs59569783	chr14:64435137-64435138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147919136	chr14:64435165-64435166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373593486	chr14:64435166-64435167	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs376031695	chr14:64435196-64435197	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs188578699	chr14:64435226-64435227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529073266	chr14:64435252-64435253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549260257	chr14:64435257-64435258	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs569015575	chr14:64435304-64435305	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537061163	chr14:64435339-64435340	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547264739	chr14:64435346-64435347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368515471	chr14:64435349-64435350	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Leukemia	18688285	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
abnormal development	18461090	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1365 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64395000-64491000	Weak transcription	Psoas Muscle	Psoas
2	chr14:64406200-64434400	Weak transcription	Hela-S3	cervix
3	chr14:64414400-64439600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr14:64415400-64435800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr14:64415600-64439000	Weak transcription	Stomach Smooth Muscle	stomach
6	chr14:64416800-64458600	Weak transcription	Gastric	stomach
7	chr14:64417000-64459200	Weak transcription	NHEK	skin
8	chr14:64417000-64466000	Weak transcription	Colon Smooth Muscle	Colon
9	chr14:64417200-64458600	Weak transcription	Esophagus	oesophagus
10	chr14:64417400-64466200	Weak transcription	Right Ventricle	heart
11	chr14:64417600-64459200	Weak transcription	Pancreas	Pancrea
12	chr14:64418000-64435000	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr14:64418000-64463000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:64418200-64450800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr14:64418400-64458600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr14:64419000-64463000	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr14:64419200-64438800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr14:64419200-64489000	Weak transcription	Small Intestine	intestine
19	chr14:64419400-64448200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr14:64419400-64459000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr14:64419400-64459200	Weak transcription	HMEC	breast
22	chr14:64420000-64458000	Weak transcription	Colonic Mucosa	Colon
23	chr14:64420200-64442400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr14:64420200-64459000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr14:64420600-64462600	Weak transcription	HUVEC	blood vessel
26	chr14:64421600-64466000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr14:64423400-64444400	Weak transcription	Liver	Liver
28	chr14:64423800-64444400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr14:64423800-64463000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr14:64426800-64440000	Strong transcription	Placenta	Placenta
31	chr14:64427400-64435400	Strong transcription	Primary T cells fromperipheralblood	blood
32	chr14:64427400-64435800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr14:64427800-64436000	Strong transcription	Primary neutrophils fromperipheralblood	blood
34	chr14:64427800-64436000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
35	chr14:64428400-64434800	Weak transcription	Primary T cells from cord blood	blood
36	chr14:64428400-64442200	Weak transcription	Primary B cells from cord blood	blood
37	chr14:64428400-64459400	Weak transcription	Aorta	Aorta
38	chr14:64429600-64458000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr14:64430400-64438400	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr14:64430400-64439000	Weak transcription	Rectal Smooth Muscle	rectum
41	chr14:64431000-64443200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr14:64431000-64444600	Weak transcription	Fetal Lung	lung
43	chr14:64431000-64458200	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr14:64431200-64434400	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr14:64431200-64463800	Weak transcription	H1 Cell Line	embryonic stem cell
46	chr14:64431200-64464800	Weak transcription	Stomach Mucosa	stomach
47	chr14:64431600-64435400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr14:64431600-64436000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr14:64431600-64436200	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr14:64431800-64434600	Strong transcription	Ovary	ovary

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