Variant report

Variant	nsv901482
Chromosome Location	chr14:22356551-22392983
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	chr14:22385887-22386446	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:22382007-22382328	HepG2	liver:	n/a	n/a
3	ATF3	chr14:22385671-22386303	A549	lung:	n/a	n/a
4	ATF3	chr14:22385683-22386371	A549	lung:	n/a	n/a
5	BCL3	chr14:22385601-22386437	A549	lung:	n/a	chr14:22386028-22386037 chr14:22386029-22386038
6	BCL3	chr14:22385683-22386287	A549	lung:	n/a	chr14:22386028-22386037 chr14:22386029-22386038
7	BHLHE40	chr14:22386172-22386257	K562	blood:	n/a	n/a
8	BHLHE40	chr14:22382030-22382321	HepG2	liver:	n/a	n/a
9	BHLHE40	chr14:22382000-22382307	K562	blood:	n/a	n/a
10	CEBPB	chr14:22363762-22363787	A549	lung:	n/a	n/a
11	CEBPB	chr14:22385683-22386219	MCF-7	breast:	n/a	chr14:22386039-22386052
12	CEBPB	chr14:22358866-22359085	HepG2	liver:	n/a	chr14:22358952-22358963
13	CEBPB	chr14:22385759-22386262	A549	lung:	n/a	chr14:22386039-22386052
14	CEBPB	chr14:22378049-22378259	HepG2	liver:	n/a	n/a
15	CEBPB	chr14:22378049-22378242	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr14:22385716-22386286	A549	lung:	n/a	chr14:22386039-22386052
17	CEBPB	chr14:22385599-22386329	A549	lung:	n/a	chr14:22386039-22386052 chr14:22385679-22385691
18	CEBPB	chr14:22378015-22378341	HepG2	liver:	n/a	n/a
19	CTCF	chr14:22385720-22385870	HepG2	liver:	n/a	n/a
20	CTCF	chr14:22386160-22386310	GM12874	blood:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
21	CTCF	chr14:22371080-22371230	MCF-7	breast:	n/a	n/a
22	CTCF	chr14:22386032-22386309	T-47D	breast:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
23	CTCF	chr14:22362664-22362738	GM19240	blood:	n/a	n/a
24	CTCF	chr14:22385990-22386405	IMR90	lung:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
25	CTCF	chr14:22386090-22386329	HepG2	liver:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
26	CTCF	chr14:22370820-22370970	NHDF-neo	bronchial:	n/a	n/a
27	CTCF	chr14:22370926-22371055	GM12891	blood:	n/a	chr14:22370957-22370975
28	CTCF	chr14:22382020-22382170	HBMEC	blood vessel:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
29	CTCF	chr14:22386140-22386290	HMEC	breast:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
30	CTCF	chr14:22386120-22386270	AG09309	skin:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
31	CTCF	chr14:22371060-22371210	A549	lung:	n/a	n/a
32	CTCF	chr14:22371080-22371230	GM12865	blood:	n/a	n/a
33	CTCF	chr14:22370840-22370990	GM12871	blood:	n/a	chr14:22370957-22370975
34	CTCF	chr14:22370460-22370610	GM12864	blood:	n/a	n/a
35	CTCF	chr14:22370880-22371030	HepG2	liver:	n/a	chr14:22370957-22370975
36	CTCF	chr14:22362328-22362510	GM10248	blood:	n/a	chr14:22362494-22362507 chr14:22362424-22362442
37	CTCF	chr14:22386160-22386310	GM12801	blood:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
38	CTCF	chr14:22371080-22371230	GM12872	blood:	n/a	n/a
39	CTCF	chr14:22386055-22386362	ECC-1	luminal epithelium:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
40	CTCF	chr14:22382200-22382350	HAc	cerebellar:	n/a	n/a
41	CTCF	chr14:22362380-22362530	GM12865	blood:	n/a	chr14:22362494-22362507 chr14:22362424-22362442
42	CTCF	chr14:22362300-22362450	NHEK	skin:	n/a	chr14:22362424-22362442
43	CTCF	chr14:22386120-22386270	AG09319	gingival:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
44	CTCF	chr14:22381981-22382254	MCF-7	breast:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
45	CTCF	chr14:22362300-22362450	AoAF	blood vessel:	n/a	chr14:22362424-22362442
46	CTCF	chr14:22382060-22382210	HRPEpiC	eye:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
47	CTCF	chr14:22370820-22370970	GM12868	blood:	n/a	n/a
48	CTCF	chr14:22382040-22382190	GM12801	blood:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138
49	CTCF	chr14:22385943-22386457	A549	lung:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
50	CTCF	chr14:22362300-22362450	GM12873	blood:	n/a	chr14:22362424-22362442

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22362441-22362491	HCF	heart:	n/a
2	chr14:22370776-22370826	GM12892	blood:	n/a
3	chr14:22370776-22370826	NHDF-neo	bronchial:	n/a
4	chr14:22361282-22361332	MCF-7	breast:	n/a
5	chr14:22361282-22361332	GM12878	blood:	n/a
6	chr14:22392573-22392623	AG09309	skin:	n/a
7	chr14:22385791-22385841	GM06990	blood:	n/a
8	chr14:22370643-22370693	HEK293	kidney:	embryo
9	chr14:22385890-22385940	HAEpiC	amniotic membrane:	n/a
10	chr14:22362071-22362121	AG10803	skin:	n/a
11	chr14:22362071-22362121	HRE	kidney:	n/a
12	chr14:22385791-22385841	Jurkat	blood:	n/a
13	chr14:22362441-22362491	AG10803	skin:	n/a
14	chr14:22362441-22362491	T-47D	breast:	n/a
15	chr14:22385890-22385940	Hela-S3	cervix:	n/a
16	chr14:22362071-22362121	SAEC	small airway:	n/a
17	chr14:22385890-22385940	NT2-D1	testis:	n/a
18	chr14:22362071-22362121	ovcar-3	ovarian:	n/a
19	chr14:22392573-22392623	HAEpiC	amniotic membrane:	n/a
20	chr14:22362441-22362491	HCPEpiC	choroid plexus:	n/a
21	chr14:22385791-22385841	AG09319	gingival:	n/a
22	chr14:22362071-22362121	BJ	skin:	n/a
23	chr14:22361282-22361332	A549	lung:	n/a
24	chr14:22370643-22370693	HUVEC	blood vessel:	n/a
25	chr14:22370776-22370826	K562	blood:	n/a
26	chr14:22370776-22370826	HIPEpiC	eye:	n/a
27	chr14:22385890-22385940	SK-N-SH_RA	brain:	n/a
28	chr14:22362071-22362121	T-47D	breast:	n/a
29	chr14:22370643-22370693	ProgFib	skin:	n/a
30	chr14:22362410-22362460	HMEC	breast:	n/a
31	chr14:22385791-22385841	PFSK-1	brain:	n/a
32	chr14:22362071-22362121	HAEpiC	amniotic membrane:	n/a
33	chr14:22392573-22392623	Jurkat	blood:	n/a
34	chr14:22362441-22362491	SK-N-SH_RA	brain:	n/a
35	chr14:22385890-22385940	K562	blood:	n/a
36	chr14:22362071-22362121	NHDF-neo	bronchial:	n/a
37	chr14:22385890-22385940	LNCaP	prostate:	n/a
38	chr14:22392573-22392623	HRCEpiC	kidney:	n/a
39	chr14:22385890-22385940	PANC-1	pancreas:	n/a
40	chr14:22362071-22362121	HL-60	blood:	n/a
41	chr14:22362071-22362121	GM19239	blood:	n/a
42	chr14:22392573-22392623	HL-60	blood:	n/a
43	chr14:22370643-22370693	Caco-2	colon:	n/a
44	chr14:22370643-22370693	NH-A	brain:	n/a
45	chr14:22385791-22385841	NHBE	bronchial:	n/a
46	chr14:22385890-22385940	ECC-1	luminal epithelium:	n/a
47	chr14:22362071-22362121	GM06990	blood:	n/a
48	chr14:22385791-22385841	ProgFib	skin:	n/a
49	chr14:22361282-22361332	GM12892	blood:	n/a
50	chr14:22370643-22370693	HCPEpiC	choroid plexus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:22361725..22364403-chr14:22372418..22374806,2	MCF-7	breast:
2	chr14:22381561..22382521-chr14:22456003..22456911,2	MCF-7	breast:
3	chr14:22381710..22382649-chr14:22401797..22402492,3	MCF-7	breast:
4	chr14:22381747..22382682-chr14:22568612..22569505,2	MCF-7	breast:
5	chr14:22386659..22388626-chr14:22391599..22394453,2	K562	blood:
6	chr14:22359585..22361948-chr14:22361972..22363588,2	MCF-7	breast:
7	chr14:22384435..22387181-chr14:22391820..22393820,2	MCF-7	breast:
8	chr14:22381656..22382465-chr5:35444689..35445277,2	MCF-7	breast:
9	chr14:22388102..22388976-chr14:22401807..22402500,2	MCF-7	breast:
10	chr14:22384435..22387181-chr14:22391820..22393820,2	MCF-7	breast:
11	chr14:22319959..22320920-chr14:22368475..22369126,2	MCF-7	breast:
12	chr14:22355742..22356307-chr14:22381815..22382504,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AE000662.92.1-10	chr14:22386431-22386481	NONHSAT035712
2	lnc-AE000662.92.1-10	chr14:22386653-22386919	NONHSAT035713
3	lnc-AE000662.92.1-10	chr14:22386642-22386919	NONHSAT035712
4	lnc-AE000662.92.1-10	chr14:22392662-22392811	NONHSAT035718
5	lnc-AE000662.92.1-10	chr14:22392607-22392811	NONHSAT035715
6	lnc-AE000662.92.1-10	chr14:22386669-22386931	NONHSAT035714
7	lnc-AE000662.92.1-10	chr14:22386642-22386928	NONHSAT035711
8	lnc-AE000662.92.1-10	chr14:22392628-22392831	NONHSAT035716
9	lnc-AE000662.92.1-10	chr14:22392658-22392811	NONHSAT035717
10	lnc-AE000662.92.1-10	chr14:22386378-22386481	NONHSAT035711

Variant related genes	Relation type
TRAV8-5	TF binding region
TRAV8-4	TF binding region
TRAV13-2	TF binding region
TRAV14DV4	TF binding region
TRAV8-5	CpG island
TRAV8-4	CpG island
TRAV13-2	CpG island
TRAV14DV4	CpG island
ENSG00000211789	chromatin interactions
ENSG00000211792	chromatin interactions
ENSG00000211790	chromatin interactions
ENSG00000211791	chromatin interactions
ENSG00000211787	chromatin interactions

Extended variants
information (count: 1686 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1686 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10483261	chr14:22356551-22356552	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370272700	chr14:22356569-22356570	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs61744739	chr14:22356571-22356572	Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs368917143	chr14:22356600-22356601	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371159445	chr14:22356635-22356636	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs555477268	chr14:22356684-22356685	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs375047844	chr14:22356685-22356686	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146508905	chr14:22356698-22356699	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371857554	chr14:22356719-22356720	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534684598	chr14:22356759-22356760	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs10483262	chr14:22356791-22356792	Flanking Active TSS Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs578151226	chr14:22356823-22356824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs117984926	chr14:22356866-22356867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117719993	chr14:22356897-22356898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs76599966	chr14:22356900-22356901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs541929758	chr14:22356948-22356949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186542110	chr14:22356964-22356965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs527402547	chr14:22356993-22356994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370018329	chr14:22357016-22357017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75445746	chr14:22357030-22357031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540622723	chr14:22357052-22357053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191196458	chr14:22357086-22357087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs75204741	chr14:22357127-22357128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs78534470	chr14:22357129-22357130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs115140935	chr14:22357188-22357189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529022737	chr14:22357251-22357252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548790216	chr14:22357277-22357278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs565995490	chr14:22357347-22357348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374647367	chr14:22357381-22357382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs202199459	chr14:22357382-22357383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569042399	chr14:22357395-22357396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs397853301	chr14:22357397-22357398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11331123	chr14:22357398-22357399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs180703706	chr14:22357420-22357421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs386775445	chr14:22357441-22357442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs8012426	chr14:22357443-22357444	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs571049621	chr14:22357455-22357456	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs8012435	chr14:22357466-22357467	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs557719983	chr14:22357471-22357472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs553624581	chr14:22357483-22357484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568632249	chr14:22357491-22357492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185149913	chr14:22357506-22357507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190791894	chr14:22357516-22357517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543214490	chr14:22357525-22357526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562583469	chr14:22357540-22357541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78495407	chr14:22357578-22357579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536384894	chr14:22357619-22357620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183171496	chr14:22357633-22357634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533027790	chr14:22357635-22357636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371515532	chr14:22357636-22357637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Barrett''s syndrome	19417022	CNVD
Lysinuric protein intolerance	18716612	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22354800-22356600	Enhancers	HUVEC	blood vessel
2	chr14:22355200-22356800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr14:22355400-22356600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr14:22355400-22356800	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr14:22355400-22356800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
6	chr14:22355400-22356800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr14:22355600-22356800	Enhancers	Primary T helper naive cells from peripheral blood	blood
8	chr14:22355800-22356800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr14:22355800-22356800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr14:22356000-22356800	Flanking Active TSS	Primary T cells from cord blood	blood
11	chr14:22356000-22356800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
12	chr14:22356000-22356800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr14:22356000-22356800	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr14:22356000-22356800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
15	chr14:22356000-22356800	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr14:22356000-22356800	Enhancers	Fetal Thymus	thymus
17	chr14:22356200-22356800	Enhancers	Primary T cells fromperipheralblood	blood
18	chr14:22356200-22356800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr14:22356400-22356800	Flanking Active TSS	Thymus	Thymus
20	chr14:22356600-22357800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr14:22356600-22359000	Weak transcription	HUVEC	blood vessel
22	chr14:22356800-22360200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr14:22356800-22360200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr14:22356800-22362000	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr14:22356800-22362200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr14:22356800-22362600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:22356800-22362600	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr14:22357000-22357600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
29	chr14:22359000-22361000	Enhancers	HUVEC	blood vessel
30	chr14:22360200-22360600	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr14:22360200-22360600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr14:22360200-22360800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr14:22360600-22362600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr14:22361000-22362000	Weak transcription	HUVEC	blood vessel
35	chr14:22361000-22362200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr14:22361600-22362400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr14:22362000-22362200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr14:22362000-22362400	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr14:22362000-22362400	Enhancers	HUVEC	blood vessel
40	chr14:22362200-22362600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr14:22362200-22362800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chr14:22362200-22362800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr14:22362200-22371200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr14:22362400-22362600	Enhancers	Primary T cells fromperipheralblood	blood
45	chr14:22362400-22362600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr14:22362400-22362600	Enhancers	Fetal Thymus	thymus
47	chr14:22362400-22362800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr14:22362400-22363000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
49	chr14:22362400-22363400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
50	chr14:22362400-22364000	Active TSS	Thymus	Thymus

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