Variant report

Variant	esv3376001
Chromosome Location	chr14:22309888-22356663
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	chr14:22314485-22314711	HepG2	liver:	n/a	n/a
2	BHLHE40	chr14:22336665-22336765	GM12878	blood:	n/a	n/a
3	BHLHE40	chr14:22328457-22328580	HepG2	liver:	n/a	n/a
4	BRCA1	chr14:22320309-22320440	HepG2	liver:	n/a	n/a
5	CBX3	chr14:22314483-22314815	HCT-116	colon:	n/a	n/a
6	CEBPB	chr14:22335185-22335344	IMR90	lung:	n/a	n/a
7	CEBPB	chr14:22331741-22331789	K562	blood:	n/a	chr14:22331764-22331775
8	CEBPB	chr14:22356124-22356169	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr14:22331634-22331889	IMR90	lung:	n/a	chr14:22331764-22331775
10	CEBPB	chr14:22331605-22331904	HepG2	liver:	n/a	chr14:22331764-22331775
11	CEBPB	chr14:22331641-22331879	A549	lung:	n/a	chr14:22331764-22331775
12	CEBPB	chr14:22314496-22314592	A549	lung:	n/a	n/a
13	CHD2	chr14:22320385-22320589	GM12878	blood:	n/a	n/a
14	CTCF	chr14:22328420-22328570	HCFaa	heart:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
15	CTCF	chr14:22328460-22328610	BJ	skin:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
16	CTCF	chr14:22314540-22314690	HAc	cerebellar:	n/a	chr14:22314635-22314656 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
17	CTCF	chr14:22314720-22314870	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr14:22320380-22320530	HFF-Myc	foreskin:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
19	CTCF	chr14:22320340-22320490	HCFaa	heart:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
20	CTCF	chr14:22355807-22355896	Gliobla	brain:	n/a	chr14:22355841-22355862 chr14:22355840-22355856 chr14:22355839-22355857
21	CTCF	chr14:22320130-22320182	GM19240	blood:	n/a	n/a
22	CTCF	chr14:22320360-22320510	NHEK	skin:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
23	CTCF	chr14:22320337-22320563	GM20000	blood:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
24	CTCF	chr14:22336686-22336965	GM10266	blood:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
25	CTCF	chr14:22320313-22320565	NHEK	skin:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
26	CTCF	chr14:22320360-22320510	HAc	cerebellar:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
27	CTCF	chr14:22314289-22314346	NHEK	skin:	n/a	n/a
28	CTCF	chr14:22336400-22336550	AG04450	lung:	n/a	n/a
29	CTCF	chr14:22314457-22314841	H1-hESC	embryonic stem cell:	n/a	chr14:22314635-22314656 chr14:22314703-22314716 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
30	CTCF	chr14:22314460-22314610	HVMF	connective:	n/a	n/a
31	CTCF	chr14:22355839-22355928	GM19239	blood:	n/a	chr14:22355841-22355862 chr14:22355840-22355856 chr14:22355839-22355857
32	CTCF	chr14:22328380-22328530	NHEK	skin:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
33	CTCF	chr14:22355833-22355923	A549	lung:	n/a	chr14:22355841-22355862 chr14:22355840-22355856 chr14:22355839-22355857
34	CTCF	chr14:22320380-22320530	GM12867	blood:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
35	CTCF	chr14:22328400-22328550	HCPEpiC	choroid plexus:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
36	CTCF	chr14:22328380-22328530	GM12865	blood:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
37	CTCF	chr14:22328440-22328590	HFF-Myc	foreskin:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
38	CTCF	chr14:22314311-22314369	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr14:22314420-22314570	HAc	cerebellar:	n/a	n/a
40	CTCF	chr14:22320328-22320558	GM12892	blood:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
41	CTCF	chr14:22336760-22336910	BE2_C	brain:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
42	CTCF	chr14:22336740-22336890	HPF	lung:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
43	CTCF	chr14:22355780-22355930	MCF-7	breast:	n/a	chr14:22355841-22355862 chr14:22355840-22355856 chr14:22355839-22355857
44	CTCF	chr14:22314309-22315048	SK-N-SH	brain:	n/a	chr14:22314635-22314656 chr14:22314703-22314716 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
45	CTCF	chr14:22314858-22314977	MCF-7	breast:	n/a	n/a
46	CTCF	chr14:22328395-22328530	GM19239	blood:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
47	CTCF	chr14:22314508-22314775	Spleen_OC	spleen:	n/a	chr14:22314635-22314656 chr14:22314703-22314716 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
48	CTCF	chr14:22314240-22314390	GM12864	blood:	n/a	n/a
49	CTCF	chr14:22314180-22314330	NHEK	skin:	n/a	n/a
50	CTCF	chr14:22337480-22337630	HMF	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22314416-22314466	HNPCEpiC	eye:	n/a
2	chr14:22314540-22314590	SAEC	small airway:	n/a
3	chr14:22320448-22320498	SAEC	small airway:	n/a
4	chr14:22314958-22315008	HEK293	kidney:	embryo
5	chr14:22314682-22314732	HRPEpiC	eye:	n/a
6	chr14:22314416-22314466	GM06990	blood:	n/a
7	chr14:22320326-22320376	A549	lung:	n/a
8	chr14:22320326-22320376	AG09309	skin:	n/a
9	chr14:22314958-22315008	HUVEC	blood vessel:	n/a
10	chr14:22320448-22320498	AG09319	gingival:	n/a
11	chr14:22336334-22336384	HEEpiC	esophagus:	n/a
12	chr14:22314958-22315008	AoSMC	blood vessel:	n/a
13	chr14:22314958-22315008	T-47D	breast:	n/a
14	chr14:22336403-22336453	T-47D	breast:	n/a
15	chr14:22336403-22336453	AG04450	lung:	fetal
16	chr14:22336403-22336453	HL-60	blood:	n/a
17	chr14:22314540-22314590	HPAEpiC	pulmonary alveolar:	n/a
18	chr14:22314958-22315008	AG09319	gingival:	n/a
19	chr14:22314682-22314732	GM12891	blood:	n/a
20	chr14:22314416-22314466	PFSK-1	brain:	n/a
21	chr14:22314416-22314466	ProgFib	skin:	n/a
22	chr14:22314958-22315008	GM06990	blood:	n/a
23	chr14:22320448-22320498	AG04450	lung:	fetal
24	chr14:22314958-22315008	HCPEpiC	choroid plexus:	n/a
25	chr14:22314682-22314732	NHBE	bronchial:	n/a
26	chr14:22320101-22320151	BJ	skin:	n/a
27	chr14:22314682-22314732	HCT-116	colon:	n/a
28	chr14:22314682-22314732	SKMC	muscle:	n/a
29	chr14:22320326-22320376	Jurkat	blood:	n/a
30	chr14:22320448-22320498	LNCaP	prostate:	n/a
31	chr14:22336334-22336384	HAEpiC	amniotic membrane:	n/a
32	chr14:22320101-22320151	HIPEpiC	eye:	n/a
33	chr14:22320326-22320376	ovcar-3	ovarian:	n/a
34	chr14:22314958-22315008	NB4	blood:	n/a
35	chr14:22315066-22315116	HRCEpiC	kidney:	n/a
36	chr14:22314958-22315008	HIPEpiC	eye:	n/a
37	chr14:22336403-22336453	IMR90	lung:	fetal
38	chr14:22336334-22336384	Caco-2	colon:	n/a
39	chr14:22320326-22320376	GM12891	blood:	n/a
40	chr14:22314682-22314732	AG10803	skin:	n/a
41	chr14:22314958-22315008	CMK	blood:	n/a
42	chr14:22314958-22315008	AG10803	skin:	n/a
43	chr14:22336334-22336384	HUVEC	blood vessel:	n/a
44	chr14:22320101-22320151	HEK293	kidney:	embryo
45	chr14:22336334-22336384	AG04449	skin:	fetal
46	chr14:22320326-22320376	HNPCEpiC	eye:	n/a
47	chr14:22314682-22314732	GM12878	blood:	n/a
48	chr14:22336403-22336453	HCM	heart:	n/a
49	chr14:22336334-22336384	AG04450	lung:	fetal
50	chr14:22320448-22320498	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:22217192..22217714-chr14:22336654..22337322,2	MCF-7	breast:
2	chr14:22310665..22312480-chr14:22315447..22317872,2	MCF-7	breast:
3	chr14:22314728..22316376-chr14:22332070..22334330,2	MCF-7	breast:
4	chr14:22319960..22320506-chr14:22370012..22371430,7	MCF-7	breast:
5	chr14:22310665..22312480-chr14:22315447..22317872,2	MCF-7	breast:
6	chr14:22293105..22294016-chr14:22319903..22320481,2	MCF-7	breast:
7	chr12:122491977..122492787-chr14:22328270..22328892,2	MCF-7	breast:
8	chr14:22327903..22328851-chr14:22336403..22337266,2	MCF-7	breast:
9	chr14:22314728..22316376-chr14:22332070..22334330,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR10G2-5	chr14:22320548-22320780	NONHSAT035708
2	lnc-AE000662.92.1-10	chr14:22337290-22337543	NONHSAT035709
3	lnc-OR10G2-5	chr14:22320890-22321003	NONHSAT035708

Variant related genes	Relation type
TRAV8-2	TF binding region
TRAV13-1	TF binding region
TRAV12-2	TF binding region
TRAV8-3	TF binding region
TRAV8-2	CpG island
TRAV13-1	CpG island
TRAV12-2	CpG island
TRAV8-3	CpG island
ENSG00000256379	chromatin interactions
ENSG00000211788	chromatin interactions
ENSG00000211784	chromatin interactions
ENSG00000211779	chromatin interactions

Extended variants
information (count: 1935 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1935 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537042131	chr14:22309900-22309901	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs372096973	chr14:22309911-22309912	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs573975477	chr14:22309918-22309919	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs374536823	chr14:22309932-22309933	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs117539068	chr14:22309937-22309938	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs559638451	chr14:22309938-22309939	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs142171935	chr14:22309942-22309943	Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs61742979	chr14:22309948-22309949	Active TSS Bivalent/Poised TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs369215572	chr14:22309956-22309957	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs564020016	chr14:22309966-22309967	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs117289173	chr14:22309967-22309968	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs549494212	chr14:22309979-22309980	Active TSS Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs117751126	chr14:22310003-22310004	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs192219588	chr14:22310009-22310010	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs117872947	chr14:22310020-22310021	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs565983847	chr14:22310023-22310024	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs528270920	chr14:22310030-22310031	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551594213	chr14:22310065-22310066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76998161	chr14:22310068-22310069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374312304	chr14:22310098-22310099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs537581629	chr14:22310116-22310117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183935409	chr14:22310161-22310162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145913168	chr14:22310167-22310168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs118131982	chr14:22310189-22310190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs57469310	chr14:22310200-22310201	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs370924714	chr14:22310207-22310208	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs373961306	chr14:22310251-22310252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs539595743	chr14:22310261-22310262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs61181417	chr14:22310294-22310295	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs559139165	chr14:22310343-22310344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577642304	chr14:22310348-22310349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190002291	chr14:22310366-22310367	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs563386856	chr14:22310380-22310381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140417676	chr14:22310381-22310382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180841297	chr14:22310391-22310392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571465329	chr14:22310395-22310396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs118052845	chr14:22310409-22310410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs539146514	chr14:22310436-22310437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76414414	chr14:22310447-22310448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551267555	chr14:22310460-22310461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs77806131	chr14:22310503-22310504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs80248429	chr14:22310505-22310506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs150370274	chr14:22310515-22310516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35023171	chr14:22310555-22310556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs117340468	chr14:22310556-22310557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190222111	chr14:22310564-22310565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs79938555	chr14:22310602-22310603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs74404264	chr14:22310607-22310608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs12100515	chr14:22310633-22310634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549630907	chr14:22310655-22310656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Barrett''s syndrome	19417022	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lysinuric protein intolerance	18716612	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22309200-22310000	Active TSS	Primary T cells fromperipheralblood	blood
2	chr14:22309400-22310000	Bivalent/Poised TSS	Primary T killer naive cells fromperipheralblood	blood
3	chr14:22309400-22310000	Active TSS	Thymus	Thymus
4	chr14:22309600-22310000	Active TSS	Primary T cells from cord blood	blood
5	chr14:22309600-22310000	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
6	chr14:22309800-22310000	Active TSS	Fetal Thymus	thymus
7	chr14:22310000-22314000	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr14:22311200-22311400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
9	chr14:22313000-22313200	Enhancers	Primary T helper cells fromperipheralblood	blood
10	chr14:22313600-22314400	Weak transcription	Primary T helper cells fromperipheralblood	blood
11	chr14:22314200-22314400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr14:22314200-22314600	Enhancers	Primary T helper naive cells from peripheral blood	blood
13	chr14:22314200-22316400	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
14	chr14:22314400-22314600	Enhancers	Primary T helper cells fromperipheralblood	blood
15	chr14:22314400-22314600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
16	chr14:22314400-22314800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr14:22314600-22314800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
18	chr14:22314600-22314800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr14:22314600-22315000	Bivalent/Poised TSS	Primary T helper 17 cells PMA-I stimulated	--
20	chr14:22314600-22315000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
21	chr14:22314600-22317000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
22	chr14:22314600-22317200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
23	chr14:22314600-22318000	Active TSS	Primary T helper cells PMA-I stimulated	--
24	chr14:22314600-22318400	Active TSS	Thymus	Thymus
25	chr14:22314600-22318800	Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr14:22314600-22326600	Active TSS	Primary T cells from cord blood	blood
27	chr14:22314800-22315000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr14:22314800-22315000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr14:22314800-22315000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
30	chr14:22314800-22315000	Bivalent Enhancer	A549	lung
31	chr14:22314800-22315200	Active TSS	Primary T helper naive cells from peripheral blood	blood
32	chr14:22314800-22315200	Bivalent/Poised TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr14:22314800-22315200	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
34	chr14:22314800-22315200	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr14:22314800-22315200	Flanking Active TSS	Fetal Thymus	thymus
36	chr14:22314800-22315400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
37	chr14:22314800-22315400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
38	chr14:22314800-22317000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr14:22315000-22315200	Bivalent/Poised TSS	Primary T cells fromperipheralblood	blood
40	chr14:22315000-22315200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
41	chr14:22315200-22317400	Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr14:22315200-22318200	Active TSS	Fetal Thymus	thymus
43	chr14:22315200-22319400	Active TSS	Primary T cells fromperipheralblood	blood
44	chr14:22315400-22316200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr14:22315400-22317200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr14:22316200-22316400	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
47	chr14:22316400-22316800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
48	chr14:22316400-22317000	Active TSS	Primary T helper naive cells from peripheral blood	blood
49	chr14:22316400-22318200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
50	chr14:22316800-22317000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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