Variant report

Variant	nsv563846
Chromosome Location	chr14:20844859-20854238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:16)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:16 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr14:20853551-20853682	K562	blood:	n/a	n/a
2	FOXA1	chr14:20844292-20844890	HepG2	liver:	n/a	n/a
3	FOXA1	chr14:20844300-20844887	HepG2	liver:	n/a	n/a
4	FOXA1	chr14:20844298-20844875	HepG2	liver:	n/a	n/a
5	FOXA2	chr14:20844242-20844985	HepG2	liver:	n/a	n/a
6	HEY1	chr14:20844295-20844925	HepG2	liver:	n/a	n/a
7	JUND	chr14:20846801-20846886	HepG2	liver:	n/a	chr14:20846862-20846871 chr14:20846861-20846872 chr14:20846864-20846871 chr14:20846861-20846872
8	MAX	chr14:20844190-20844945	HepG2	liver:	n/a	n/a
9	MAX	chr14:20844292-20844871	HepG2	liver:	n/a	n/a
10	MAZ	chr14:20851696-20851722	Hela-S3	cervix:	n/a	n/a
11	POLR2A	chr14:20844338-20844876	HepG2	liver:	n/a	n/a
12	POLR2A	chr14:20848503-20848550	HUVEC	blood vessel:	n/a	n/a
13	POLR2A	chr14:20846585-20846738	K562	blood:	n/a	n/a
14	POLR2A	chr14:20847150-20847305	GM12878	blood:	n/a	n/a
15	POLR2A	chr14:20846126-20846241	GM12878	blood:	n/a	n/a
16	USF1	chr14:20844415-20844860	HepG2	liver:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:20851317-20851367	MCF-7	breast:	n/a
2	chr14:20851317-20851367	HepG2	liver:	n/a
3	chr14:20851317-20851367	GM06990	blood:	n/a
4	chr14:20851317-20851367	PANC-1	pancreas:	n/a
5	chr14:20851317-20851367	ovcar-3	ovarian:	n/a
6	chr14:20851317-20851367	BJ	skin:	n/a
7	chr14:20851317-20851367	Jurkat	blood:	n/a
8	chr14:20851317-20851367	HCF	heart:	n/a
9	chr14:20851317-20851367	BE2_C	brain:	n/a
10	chr14:20851317-20851367	HL-60	blood:	n/a
11	chr14:20851317-20851367	NH-A	brain:	n/a
12	chr14:20851317-20851367	HRCEpiC	kidney:	n/a
13	chr14:20851317-20851367	HIPEpiC	eye:	n/a
14	chr14:20851317-20851367	HCPEpiC	choroid plexus:	n/a
15	chr14:20851317-20851367	HCT-116	colon:	n/a
16	chr14:20851317-20851367	AG09309	skin:	n/a
17	chr14:20851317-20851367	ECC-1	luminal epithelium:	n/a
18	chr14:20851317-20851367	NHDF-neo	bronchial:	n/a
19	chr14:20851317-20851367	GM12892	blood:	n/a
20	chr14:20851317-20851367	HPAEpiC	pulmonary alveolar:	n/a
21	chr14:20851317-20851367	HRPEpiC	eye:	n/a
22	chr14:20851317-20851367	U87	brain:	n/a
23	chr14:20851317-20851367	LNCaP	prostate:	n/a
24	chr14:20851317-20851367	Hela-S3	cervix:	n/a
25	chr14:20851317-20851367	AG04450	lung:	fetal
26	chr14:20851317-20851367	HEEpiC	esophagus:	n/a
27	chr14:20851317-20851367	PrEC	prostate:	n/a
28	chr14:20851317-20851367	CMK	blood:	n/a
29	chr14:20851317-20851367	HAEpiC	amniotic membrane:	n/a
30	chr14:20851317-20851367	NB4	blood:	n/a
31	chr14:20851317-20851367	HNPCEpiC	eye:	n/a
32	chr14:20851317-20851367	HRE	kidney:	n/a
33	chr14:20851317-20851367	K562	blood:	n/a
34	chr14:20851317-20851367	RPTEC	kidney:	n/a
35	chr14:20851317-20851367	AG09319	gingival:	n/a
36	chr14:20851317-20851367	SK-N-SH	brain:	n/a
37	chr14:20851317-20851367	HCM	heart:	n/a
38	chr14:20851317-20851367	Caco-2	colon:	n/a
39	chr14:20851317-20851367	MCF10A-Er-Src	breast:	n/a
40	chr14:20851317-20851367	T-47D	breast:	n/a
41	chr14:20851317-20851367	NHBE	bronchial:	n/a
42	chr14:20851317-20851367	AG10803	skin:	n/a
43	chr14:20851317-20851367	PFSK-1	brain:	n/a
44	chr14:20851317-20851367	GM12891	blood:	n/a
45	chr14:20851317-20851367	SK-N-MC	brain:	n/a
46	chr14:20851317-20851367	IMR90	lung:	fetal
47	chr14:20851317-20851367	GM19239	blood:	n/a
48	chr14:20851317-20851367	HEK293	kidney:	embryo
49	chr14:20851317-20851367	SAEC	small airway:	n/a
50	chr14:20851317-20851367	HMEC	breast:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:20845933..20849347-chr14:20928261..20932601,3	MCF-7	breast:
2	chr14:20838530..20842338-chr14:20842548..20848826,6	K562	blood:
3	chr14:20846717..20848818-chr14:20880774..20883378,2	MCF-7	breast:
4	chr14:20809810..20811515-chr14:20846784..20849983,4	MCF-7	breast:
5	chr14:20848289..20849833-chr6:32935793..32938604,2	MCF-7	breast:
6	chr14:20838639..20841584-chr14:20847946..20850095,2	MCF-7	breast:
7	chr14:20795714..20797764-chr14:20850473..20853253,2	MCF-7	breast:
8	chr14:20844586..20846563-chr14:20847289..20849171,2	MCF-7	breast:
9	chr14:20846371..20847951-chr14:20850513..20852177,2	K562	blood:
10	chr14:20850017..20851995-chr14:20853636..20856576,3	MCF-7	breast:
11	chr14:20810084..20813225-chr14:20848218..20850163,3	MCF-7	breast:
12	chr14:20839458..20842686-chr14:20844361..20847884,4	MCF-7	breast:
13	chr14:20847183..20849755-chr14:20910442..20913283,2	MCF-7	breast:
14	chr14:20846371..20847951-chr14:20850513..20852177,2	K562	blood:
15	chr14:20850810..20853297-chr14:20937260..20939231,2	MCF-7	breast:

No data

Variant related genes	Relation type
TEP1	TF binding region
TEP1	CpG island
ENSG00000204257	chromatin interactions
ENSG00000100814	chromatin interactions
ENSG00000129566	chromatin interactions
ENSG00000200225	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000165782	chromatin interactions
ENSG00000198805	chromatin interactions
ENSG00000223837	chromatin interactions
ENSG00000259001	chromatin interactions
ENSG00000129484	chromatin interactions

Extended variants
information (count: 522 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:522 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1760907	chr14:20844859-20844860	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs61996761	chr14:20844877-20844878	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs4982017	chr14:20844935-20844936	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs1760906	chr14:20845018-20845019	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs542812842	chr14:20845020-20845021	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs115090941	chr14:20845077-20845078	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556568310	chr14:20845093-20845094	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs187016543	chr14:20845112-20845113	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs140581428	chr14:20845113-20845114	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs560208828	chr14:20845135-20845136	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs572222933	chr14:20845141-20845142	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs145717418	chr14:20845155-20845156	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs561063319	chr14:20845172-20845173	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs564158499	chr14:20845173-20845174	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs138349769	chr14:20845184-20845185	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531796942	chr14:20845194-20845195	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs550336416	chr14:20845230-20845231	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs142545980	chr14:20845231-20845232	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150573285	chr14:20845242-20845243	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs548838442	chr14:20845251-20845252	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs567057228	chr14:20845275-20845276	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs534087161	chr14:20845287-20845288	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs552396370	chr14:20845325-20845326	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs532426853	chr14:20845328-20845329	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs371616341	chr14:20845374-20845375	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs537977621	chr14:20845381-20845382	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs546213045	chr14:20845421-20845422	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556397357	chr14:20845464-20845465	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs375172392	chr14:20845481-20845482	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs140332121	chr14:20845501-20845502	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs2229101	chr14:20845521-20845522	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs535483591	chr14:20845557-20845558	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs138288297	chr14:20845634-20845635	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs112458527	chr14:20845635-20845636	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs201794310	chr14:20845694-20845695	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs200974138	chr14:20845714-20845715	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs372939145	chr14:20845715-20845716	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs546015654	chr14:20845716-20845717	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs370439177	chr14:20845740-20845741	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34895824	chr14:20845770-20845771	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs149326341	chr14:20845791-20845792	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs377389073	chr14:20845794-20845795	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs200869389	chr14:20845795-20845796	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs374311707	chr14:20845813-20845814	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs138722240	chr14:20845825-20845826	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs199552134	chr14:20845833-20845834	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs111442503	chr14:20845834-20845835	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs374371530	chr14:20845842-20845843	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190667354	chr14:20845879-20845880	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs370712702	chr14:20845881-20845882	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	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
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	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
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Ependymoma	20639864	CNVD
Cone-rod dystrophy	22138850	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:209 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20812400-20880200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr14:20812600-20845600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:20813200-20869200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr14:20825200-20863200	Weak transcription	Fetal Heart	heart
5	chr14:20825800-20846600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:20826400-20847800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr14:20829000-20855800	Strong transcription	Monocytes-CD14+_RO01746	blood
8	chr14:20829200-20877000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr14:20829400-20855800	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr14:20829400-20876800	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr14:20829600-20876800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
12	chr14:20829800-20864800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr14:20829800-20877400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr14:20830400-20869000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr14:20830400-20876800	Strong transcription	Fetal Stomach	stomach
16	chr14:20830400-20877200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr14:20831000-20860800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr14:20831000-20860800	Strong transcription	Primary T cells from cord blood	blood
19	chr14:20831000-20868200	Strong transcription	Placenta	Placenta
20	chr14:20831200-20859200	Strong transcription	Skeletal Muscle Female	skeletal muscle
21	chr14:20831200-20867800	Strong transcription	Duodenum Smooth Muscle	Duodenum
22	chr14:20831400-20855800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr14:20831400-20877000	Strong transcription	Primary T cells fromperipheralblood	blood
24	chr14:20832000-20873600	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr14:20832200-20855000	Strong transcription	HSMM	muscle
26	chr14:20832200-20855800	Strong transcription	Primary B cells from peripheral blood	blood
27	chr14:20832200-20876800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr14:20832400-20860200	Strong transcription	Lung	lung
29	chr14:20832400-20865400	Strong transcription	Primary B cells from cord blood	blood
30	chr14:20832600-20877000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr14:20833000-20860800	Strong transcription	Left Ventricle	heart
32	chr14:20833800-20861400	Strong transcription	Osteobl	bone
33	chr14:20833800-20869200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr14:20834000-20845600	Strong transcription	HUVEC	blood vessel
35	chr14:20834000-20860800	Strong transcription	HSMMtube	muscle
36	chr14:20834000-20865800	Strong transcription	Colon Smooth Muscle	Colon
37	chr14:20834000-20867800	Strong transcription	Stomach Smooth Muscle	stomach
38	chr14:20834000-20868200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr14:20834000-20868400	Strong transcription	Primary T helper cells PMA-I stimulated	--
40	chr14:20834000-20870000	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr14:20834000-20876800	Strong transcription	Adipose Nuclei	Adipose
42	chr14:20834200-20856200	Strong transcription	HUES6 Cell Line	embryonic stem cell
43	chr14:20834200-20860200	Strong transcription	Fetal Thymus	thymus
44	chr14:20834200-20860400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr14:20834200-20860800	Strong transcription	Brain Anterior Caudate	brain
46	chr14:20834200-20860800	Strong transcription	Dnd41	blood
47	chr14:20834200-20865400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr14:20834200-20876200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr14:20834200-20876600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr14:20834200-20876800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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