Variant report

Variant	esv3487256
Chromosome Location	chr14:22323425-22376244
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	BHLHE40	chr14:22336665-22336765	GM12878	blood:	n/a	n/a
2	BHLHE40	chr14:22328457-22328580	HepG2	liver:	n/a	n/a
3	CEBPB	chr14:22363762-22363787	A549	lung:	n/a	n/a
4	CEBPB	chr14:22331634-22331889	IMR90	lung:	n/a	chr14:22331764-22331775
5	CEBPB	chr14:22331741-22331789	K562	blood:	n/a	chr14:22331764-22331775
6	CEBPB	chr14:22358866-22359085	HepG2	liver:	n/a	chr14:22358952-22358963
7	CEBPB	chr14:22335185-22335344	IMR90	lung:	n/a	n/a
8	CEBPB	chr14:22331641-22331879	A549	lung:	n/a	chr14:22331764-22331775
9	CEBPB	chr14:22331605-22331904	HepG2	liver:	n/a	chr14:22331764-22331775
10	CEBPB	chr14:22356124-22356169	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr14:22370927-22370965	LNCaP	prostate:	n/a	n/a
12	CTCF	chr14:22336740-22336890	HPF	lung:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
13	CTCF	chr14:22328400-22328550	MCF-7	breast:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
14	CTCF	chr14:22362380-22362530	SK-N-SH_RA	brain:	n/a	chr14:22362494-22362507 chr14:22362424-22362442
15	CTCF	chr14:22370820-22370970	GM12867	blood:	n/a	n/a
16	CTCF	chr14:22355720-22355870	HBMEC	blood vessel:	n/a	chr14:22355841-22355862 chr14:22355840-22355856 chr14:22355839-22355857
17	CTCF	chr14:22328575-22328601	GM19239	blood:	n/a	n/a
18	CTCF	chr14:22328263-22328756	MCF-7	breast:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
19	CTCF	chr14:22362320-22362470	HAc	cerebellar:	n/a	chr14:22362424-22362442
20	CTCF	chr14:22327378-22327399	GM13976	blood:	n/a	n/a
21	CTCF	chr14:22370874-22371122	GM12878	blood:	n/a	chr14:22370957-22370975
22	CTCF	chr14:22336740-22336890	A549	lung:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
23	CTCF	chr14:22336760-22336910	GM12867	blood:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
24	CTCF	chr14:22362268-22362583	A549	lung:	n/a	chr14:22362494-22362507 chr14:22362424-22362442
25	CTCF	chr14:22370800-22370950	AG04450	lung:	n/a	n/a
26	CTCF	chr14:22336732-22336914	A549	lung:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
27	CTCF	chr14:22370881-22371068	GM19240	blood:	n/a	chr14:22370957-22370975
28	CTCF	chr14:22362315-22362571	K562	blood:	n/a	chr14:22362494-22362507 chr14:22362424-22362442
29	CTCF	chr14:22328460-22328610	HCT-116	colon:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
30	CTCF	chr14:22355720-22355870	GM12872	blood:	n/a	chr14:22355841-22355862 chr14:22355840-22355856 chr14:22355839-22355857
31	CTCF	chr14:22336700-22336850	HL-60	blood:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
32	CTCF	chr14:22336660-22336810	NHDF-neo	bronchial:	n/a	n/a
33	CTCF	chr14:22336702-22336929	GM20000	blood:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
34	CTCF	chr14:22370800-22370950	GM12874	blood:	n/a	n/a
35	CTCF	chr14:22370820-22370970	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr14:22370840-22370990	GM12871	blood:	n/a	chr14:22370957-22370975
37	CTCF	chr14:22328440-22328590	K562	blood:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
38	CTCF	chr14:22328420-22328570	HA-sp	spinal cord:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
39	CTCF	chr14:22336740-22336890	MCF-7	breast:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
40	CTCF	chr14:22336760-22336910	GM12870	blood:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
41	CTCF	chr14:22336720-22336870	GM12864	blood:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
42	CTCF	chr14:22336740-22336890	HUVEC	blood vessel:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
43	CTCF	chr14:22336619-22337096	HCT-116	colon:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
44	CTCF	chr14:22328420-22328570	GM12867	blood:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
45	CTCF	chr14:22328400-22328550	RPTEC	kidney:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
46	CTCF	chr14:22355500-22355650	GM06990	blood:	n/a	n/a
47	CTCF	chr14:22370820-22370970	GM12869	blood:	n/a	n/a
48	CTCF	chr14:22362300-22362450	HepG2	liver:	n/a	chr14:22362424-22362442
49	CTCF	chr14:22328400-22328550	GM12874	blood:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
50	CTCF	chr14:22362300-22362450	HRPEpiC	eye:	n/a	chr14:22362424-22362442

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22362441-22362491	HMEC	breast:	n/a
2	chr14:22362441-22362491	Jurkat	blood:	n/a
3	chr14:22361282-22361332	RPTEC	kidney:	n/a
4	chr14:22336334-22336384	NB4	blood:	n/a
5	chr14:22362410-22362460	AG09319	gingival:	n/a
6	chr14:22361282-22361332	HCM	heart:	n/a
7	chr14:22362071-22362121	Hela-S3	cervix:	n/a
8	chr14:22362410-22362460	NH-A	brain:	n/a
9	chr14:22336403-22336453	GM12891	blood:	n/a
10	chr14:22362071-22362121	SAEC	small airway:	n/a
11	chr14:22362441-22362491	HEK293	kidney:	embryo
12	chr14:22370776-22370826	GM12892	blood:	n/a
13	chr14:22362071-22362121	GM12891	blood:	n/a
14	chr14:22361282-22361332	PFSK-1	brain:	n/a
15	chr14:22370776-22370826	HPAEpiC	pulmonary alveolar:	n/a
16	chr14:22336334-22336384	Caco-2	colon:	n/a
17	chr14:22362071-22362121	HCPEpiC	choroid plexus:	n/a
18	chr14:22362441-22362491	AG09319	gingival:	n/a
19	chr14:22362071-22362121	AG10803	skin:	n/a
20	chr14:22370776-22370826	NHDF-neo	bronchial:	n/a
21	chr14:22336334-22336384	NHDF-neo	bronchial:	n/a
22	chr14:22336334-22336384	K562	blood:	n/a
23	chr14:22362441-22362491	AoSMC	blood vessel:	n/a
24	chr14:22362441-22362491	GM06990	blood:	n/a
25	chr14:22361282-22361332	NHBE	bronchial:	n/a
26	chr14:22370643-22370693	HUVEC	blood vessel:	n/a
27	chr14:22336403-22336453	HEK293	kidney:	embryo
28	chr14:22336334-22336384	GM19239	blood:	n/a
29	chr14:22370776-22370826	BE2_C	brain:	n/a
30	chr14:22336403-22336453	GM12892	blood:	n/a
31	chr14:22370643-22370693	PrEC	prostate:	n/a
32	chr14:22370643-22370693	Caco-2	colon:	n/a
33	chr14:22362410-22362460	AG10803	skin:	n/a
34	chr14:22370643-22370693	AG09319	gingival:	n/a
35	chr14:22336334-22336384	HRE	kidney:	n/a
36	chr14:22370643-22370693	MCF10A-Er-Src	breast:	n/a
37	chr14:22336403-22336453	GM19239	blood:	n/a
38	chr14:22361282-22361332	NT2-D1	testis:	n/a
39	chr14:22370643-22370693	IMR90	lung:	fetal
40	chr14:22362441-22362491	HCF	heart:	n/a
41	chr14:22370776-22370826	HCT-116	colon:	n/a
42	chr14:22370643-22370693	NHDF-neo	bronchial:	n/a
43	chr14:22361282-22361332	MCF-7	breast:	n/a
44	chr14:22362441-22362491	GM19239	blood:	n/a
45	chr14:22336403-22336453	HCPEpiC	choroid plexus:	n/a
46	chr14:22370643-22370693	AoSMC	blood vessel:	n/a
47	chr14:22362441-22362491	HRCEpiC	kidney:	n/a
48	chr14:22361282-22361332	HRCEpiC	kidney:	n/a
49	chr14:22336334-22336384	NH-A	brain:	n/a
50	chr14:22336403-22336453	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:122491977..122492787-chr14:22328270..22328892,2	MCF-7	breast:
2	chr14:22359585..22361948-chr14:22361972..22363588,2	MCF-7	breast:
3	chr14:22314728..22316376-chr14:22332070..22334330,2	MCF-7	breast:
4	chr14:22217192..22217714-chr14:22336654..22337322,2	MCF-7	breast:
5	chr14:22361725..22364403-chr14:22372418..22374806,2	MCF-7	breast:
6	chr14:22327903..22328851-chr14:22336403..22337266,2	MCF-7	breast:
7	chr14:22319959..22320920-chr14:22368475..22369126,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AE000662.92.1-10	chr14:22337290-22337543	NONHSAT035709

Variant related genes	Relation type
TRAV13-1	TF binding region
TRAV8-4	TF binding region
TRAV8-5	TF binding region
TRAV12-2	TF binding region
TRAV13-1	CpG island
TRAV8-4	CpG island
TRAV8-5	CpG island
TRAV12-2	CpG island
ENSG00000211787	chromatin interactions
ENSG00000211788	chromatin interactions
ENSG00000211790	chromatin interactions
ENSG00000211779	chromatin interactions

Extended variants
information (count: 2242 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:2242 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546304253	chr14:22323430-22323431	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566092406	chr14:22323462-22323463	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531985618	chr14:22323472-22323473	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552185623	chr14:22323490-22323491	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184127960	chr14:22323568-22323569	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537632138	chr14:22323571-22323572	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188877681	chr14:22323635-22323636	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs191763983	chr14:22323692-22323693	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534253506	chr14:22323839-22323840	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs8015464	chr14:22323859-22323860	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs8019485	chr14:22323876-22323877	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35018902	chr14:22323892-22323893	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571464150	chr14:22323932-22323933	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546257904	chr14:22323963-22323964	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs8013555	chr14:22323965-22323966	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs150412755	chr14:22324077-22324078	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138134439	chr14:22324105-22324106	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs545645637	chr14:22324115-22324116	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554142013	chr14:22324129-22324130	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2204936	chr14:22324143-22324144	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs2204937	chr14:22324164-22324165	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs149598336	chr14:22324210-22324211	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs559862005	chr14:22324224-22324225	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10136014	chr14:22324231-22324232	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2204938	chr14:22324237-22324238	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs569038132	chr14:22324242-22324243	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531607218	chr14:22324243-22324244	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550988552	chr14:22324279-22324280	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs148197424	chr14:22324284-22324285	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183591862	chr14:22324310-22324311	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs386775443	chr14:22324369-22324370	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs115479569	chr14:22324370-22324371	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146082140	chr14:22324430-22324431	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2222917	chr14:22324460-22324461	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs67766188	chr14:22324504-22324505	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs564809105	chr14:22324525-22324526	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139931749	chr14:22324574-22324575	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs371724333	chr14:22324589-22324590	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539429242	chr14:22324591-22324592	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556492735	chr14:22324598-22324599	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34654962	chr14:22324629-22324630	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs187136893	chr14:22324631-22324632	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs555790462	chr14:22324669-22324670	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs572302794	chr14:22324677-22324678	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs541267690	chr14:22324697-22324698	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs367941191	chr14:22324727-22324728	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs10483259	chr14:22324776-22324777	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs374795040	chr14:22324793-22324794	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs532106023	chr14:22324799-22324800	Active TSS Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs534956519	chr14:22324812-22324813	Active TSS 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
Lysinuric protein intolerance	18716612	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22314600-22326600	Active TSS	Primary T cells from cord blood	blood
2	chr14:22320000-22324600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
3	chr14:22320200-22325200	Active TSS	Primary T cells fromperipheralblood	blood
4	chr14:22321000-22324600	Active TSS	Primary T helper cells fromperipheralblood	blood
5	chr14:22321000-22330000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr14:22321400-22340800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr14:22323200-22324000	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr14:22323200-22337000	Weak transcription	Fetal Thymus	thymus
9	chr14:22323400-22324200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr14:22323400-22324200	Weak transcription	Thymus	Thymus
11	chr14:22324000-22324800	Active TSS	Primary T helper cells PMA-I stimulated	--
12	chr14:22324200-22324800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
13	chr14:22324200-22324800	Active TSS	Thymus	Thymus
14	chr14:22324600-22324800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
15	chr14:22324800-22326000	Weak transcription	Thymus	Thymus
16	chr14:22325200-22328600	Weak transcription	Primary T cells fromperipheralblood	blood
17	chr14:22326000-22326400	Active TSS	Primary T helper cells PMA-I stimulated	--
18	chr14:22326000-22326600	Active TSS	Thymus	Thymus
19	chr14:22326400-22328400	Weak transcription	Primary T helper cells PMA-I stimulated	--
20	chr14:22326600-22326800	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
21	chr14:22326600-22326800	Flanking Active TSS	Thymus	Thymus
22	chr14:22326600-22328600	Weak transcription	Primary T cells from cord blood	blood
23	chr14:22326800-22331600	Weak transcription	Thymus	Thymus
24	chr14:22328200-22328400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr14:22328200-22328400	Flanking Active TSS	HUVEC	blood vessel
26	chr14:22328400-22328800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr14:22328400-22328800	Enhancers	HUVEC	blood vessel
28	chr14:22328400-22329600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr14:22328400-22333400	Active TSS	Primary T helper cells PMA-I stimulated	--
30	chr14:22328600-22332400	Active TSS	Primary T cells from cord blood	blood
31	chr14:22328600-22332600	Active TSS	Primary T cells fromperipheralblood	blood
32	chr14:22328800-22329000	Active TSS	Primary T helper cells fromperipheralblood	blood
33	chr14:22328800-22329600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr14:22328800-22334000	Weak transcription	HUVEC	blood vessel
35	chr14:22329000-22329400	Enhancers	Primary T helper cells fromperipheralblood	blood
36	chr14:22329400-22330400	Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr14:22329400-22330400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr14:22329600-22330400	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
39	chr14:22329600-22331800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
40	chr14:22329800-22330000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr14:22330000-22331200	Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr14:22330400-22332000	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr14:22330800-22331200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr14:22331200-22332200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr14:22331200-22336400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
46	chr14:22331600-22334200	Enhancers	Thymus	Thymus
47	chr14:22331800-22332600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr14:22332000-22332600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
49	chr14:22332000-22332600	Enhancers	Primary T helper cells fromperipheralblood	blood
50	chr14:22332200-22332600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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