Variant report

Variant	nsv524527
Chromosome Location	chr14:22288841-22387318
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	chr14:22382007-22382328	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:22385887-22386446	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:22314485-22314711	HepG2	liver:	n/a	n/a
4	ATF3	chr14:22385671-22386303	A549	lung:	n/a	n/a
5	ATF3	chr14:22385683-22386371	A549	lung:	n/a	n/a
6	BCL3	chr14:22385683-22386287	A549	lung:	n/a	chr14:22386028-22386037 chr14:22386029-22386038
7	BCL3	chr14:22385601-22386437	A549	lung:	n/a	chr14:22386028-22386037 chr14:22386029-22386038
8	BHLHE40	chr14:22336665-22336765	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:22328457-22328580	HepG2	liver:	n/a	n/a
10	BHLHE40	chr14:22382000-22382307	K562	blood:	n/a	n/a
11	BHLHE40	chr14:22386172-22386257	K562	blood:	n/a	n/a
12	BHLHE40	chr14:22382030-22382321	HepG2	liver:	n/a	n/a
13	BRCA1	chr14:22320309-22320440	HepG2	liver:	n/a	n/a
14	CBX3	chr14:22314483-22314815	HCT-116	colon:	n/a	n/a
15	CEBPB	chr14:22314496-22314592	A549	lung:	n/a	n/a
16	CEBPB	chr14:22378049-22378242	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr14:22385716-22386286	A549	lung:	n/a	chr14:22386039-22386052
18	CEBPB	chr14:22331741-22331789	K562	blood:	n/a	chr14:22331764-22331775
19	CEBPB	chr14:22363762-22363787	A549	lung:	n/a	n/a
20	CEBPB	chr14:22331605-22331904	HepG2	liver:	n/a	chr14:22331764-22331775
21	CEBPB	chr14:22335185-22335344	IMR90	lung:	n/a	n/a
22	CEBPB	chr14:22331634-22331889	IMR90	lung:	n/a	chr14:22331764-22331775
23	CEBPB	chr14:22356124-22356169	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr14:22385599-22386329	A549	lung:	n/a	chr14:22386039-22386052 chr14:22385679-22385691
25	CEBPB	chr14:22331641-22331879	A549	lung:	n/a	chr14:22331764-22331775
26	CEBPB	chr14:22378015-22378341	HepG2	liver:	n/a	n/a
27	CEBPB	chr14:22358866-22359085	HepG2	liver:	n/a	chr14:22358952-22358963
28	CEBPB	chr14:22385759-22386262	A549	lung:	n/a	chr14:22386039-22386052
29	CEBPB	chr14:22378049-22378259	HepG2	liver:	n/a	n/a
30	CEBPB	chr14:22385683-22386219	MCF-7	breast:	n/a	chr14:22386039-22386052
31	CHD2	chr14:22320385-22320589	GM12878	blood:	n/a	n/a
32	CTCF	chr14:22320300-22320450	K562	blood:	n/a	n/a
33	CTCF	chr14:22386120-22386270	WERI-Rb-1	eye:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
34	CTCF	chr14:22320380-22320530	HFF	foreskin:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
35	CTCF	chr14:22336692-22336977	ECC-1	luminal epithelium:	n/a	chr14:22336811-22336829 chr14:22336812-22336828 chr14:22336813-22336834
36	CTCF	chr14:22314380-22314530	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr14:22362320-22362470	GM12872	blood:	n/a	chr14:22362424-22362442
38	CTCF	chr14:22320340-22320490	HepG2	liver:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
39	CTCF	chr14:22382160-22382310	A549	lung:	n/a	n/a
40	CTCF	chr14:22314508-22314929	GM19240	blood:	n/a	chr14:22314635-22314656 chr14:22314703-22314716 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
41	CTCF	chr14:22320328-22320558	GM12892	blood:	n/a	chr14:22320434-22320452 chr14:22320435-22320451 chr14:22320436-22320457
42	CTCF	chr14:22314540-22314690	A549	lung:	n/a	chr14:22314635-22314656 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
43	CTCF	chr14:22355846-22355934	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:22328389-22328598	GM19238	blood:	n/a	chr14:22328468-22328489 chr14:22328466-22328484 chr14:22328469-22328478 chr14:22328467-22328483 chr14:22328469-22328482
45	CTCF	chr14:22314520-22314670	MCF-7	breast:	n/a	chr14:22314635-22314656 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
46	CTCF	chr14:22314512-22314824	GM19239	blood:	n/a	chr14:22314635-22314656 chr14:22314703-22314716 chr14:22314633-22314651 chr14:22314636-22314645 chr14:22314638-22314648
47	CTCF	chr14:22370856-22371078	A549	lung:	n/a	chr14:22370957-22370975
48	CTCF	chr14:22362320-22362470	HAc	cerebellar:	n/a	chr14:22362424-22362442
49	CTCF	chr14:22386093-22386301	GM20000	blood:	n/a	chr14:22386199-22386215 chr14:22386198-22386216 chr14:22386200-22386221
50	CTCF	chr14:22382040-22382190	BJ	skin:	n/a	chr14:22382115-22382133 chr14:22382118-22382131 chr14:22382118-22382127 chr14:22382116-22382132 chr14:22382117-22382138

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:22336403-22336453	HCM	heart:	n/a
2	chr14:22336403-22336453	HCM	heart:	n/a
3	chr14:22292347-22292397	HMEC	breast:	n/a
4	chr14:22315066-22315116	LNCaP	prostate:	n/a
5	chr14:22314416-22314466	HL-60	blood:	n/a
6	chr14:22336403-22336453	LNCaP	prostate:	n/a
7	chr14:22309073-22309123	GM12878	blood:	n/a
8	chr14:22315066-22315116	PFSK-1	brain:	n/a
9	chr14:22361282-22361332	HNPCEpiC	eye:	n/a
10	chr14:22361282-22361332	HMEC	breast:	n/a
11	chr14:22362071-22362121	Jurkat	blood:	n/a
12	chr14:22320448-22320498	HEEpiC	esophagus:	n/a
13	chr14:22292347-22292397	H1-hESC	embryonic stem cell:	embryo
14	chr14:22362441-22362491	GM19239	blood:	n/a
15	chr14:22385890-22385940	AG04450	lung:	fetal
16	chr14:22292347-22292397	MCF10A-Er-Src	breast:	n/a
17	chr14:22336403-22336453	HL-60	blood:	n/a
18	chr14:22314416-22314466	HRE	kidney:	n/a
19	chr14:22370776-22370826	HMEC	breast:	n/a
20	chr14:22362071-22362121	MCF-7	breast:	n/a
21	chr14:22314682-22314732	BJ	skin:	n/a
22	chr14:22336403-22336453	SAEC	small airway:	n/a
23	chr14:22320448-22320498	HIPEpiC	eye:	n/a
24	chr14:22320326-22320376	HNPCEpiC	eye:	n/a
25	chr14:22320101-22320151	GM12878	blood:	n/a
26	chr14:22336403-22336453	HCT-116	colon:	n/a
27	chr14:22315066-22315116	AG09319	gingival:	n/a
28	chr14:22314682-22314732	SK-N-MC	brain:	n/a
29	chr14:22320101-22320151	GM12892	blood:	n/a
30	chr14:22361282-22361332	SK-N-MC	brain:	n/a
31	chr14:22314416-22314466	NT2-D1	testis:	n/a
32	chr14:22385890-22385940	ECC-1	luminal epithelium:	n/a
33	chr14:22315066-22315116	K562	blood:	n/a
34	chr14:22314958-22315008	RPTEC	kidney:	n/a
35	chr14:22320101-22320151	SAEC	small airway:	n/a
36	chr14:22292347-22292397	IMR90	lung:	fetal
37	chr14:22320448-22320498	BJ	skin:	n/a
38	chr14:22292347-22292397	HCF	heart:	n/a
39	chr14:22385791-22385841	MCF-7	breast:	n/a
40	chr14:22314540-22314590	NHBE	bronchial:	n/a
41	chr14:22315066-22315116	NHBE	bronchial:	n/a
42	chr14:22320101-22320151	HCM	heart:	n/a
43	chr14:22385791-22385841	HRE	kidney:	n/a
44	chr14:22320448-22320498	GM06990	blood:	n/a
45	chr14:22314540-22314590	HRCEpiC	kidney:	n/a
46	chr14:22314682-22314732	HIPEpiC	eye:	n/a
47	chr14:22320326-22320376	AG04450	lung:	fetal
48	chr14:22314958-22315008	LNCaP	prostate:	n/a
49	chr14:22320448-22320498	HL-60	blood:	n/a
50	chr14:22314416-22314466	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:122491977..122492787-chr14:22328270..22328892,2	MCF-7	breast:
2	chr14:22295303..22297076-chr14:22298582..22300710,2	K562	blood:
3	chr14:22217192..22217714-chr14:22336654..22337322,2	MCF-7	breast:
4	chr14:22381710..22382649-chr14:22401797..22402492,3	MCF-7	breast:
5	chr14:22381747..22382682-chr14:22568612..22569505,2	MCF-7	breast:
6	chr14:22314728..22316376-chr14:22332070..22334330,2	MCF-7	breast:
7	chr14:22361725..22364403-chr14:22372418..22374806,2	MCF-7	breast:
8	chr14:22310665..22312480-chr14:22315447..22317872,2	MCF-7	breast:
9	chr14:22319959..22320920-chr14:22368475..22369126,2	MCF-7	breast:
10	chr14:22310665..22312480-chr14:22315447..22317872,2	MCF-7	breast:
11	chr14:22327903..22328851-chr14:22336403..22337266,2	MCF-7	breast:
12	chr14:22384435..22387181-chr14:22391820..22393820,2	MCF-7	breast:
13	chr14:22381561..22382521-chr14:22456003..22456911,2	MCF-7	breast:
14	chr14:22295303..22297076-chr14:22298582..22300710,2	K562	blood:
15	chr14:22386659..22388626-chr14:22391599..22394453,2	K562	blood:
16	chr14:22319960..22320506-chr14:22370012..22371430,7	MCF-7	breast:
17	chr14:22314728..22316376-chr14:22332070..22334330,2	MCF-7	breast:
18	chr14:22359585..22361948-chr14:22361972..22363588,2	MCF-7	breast:
19	chr14:22293105..22294016-chr14:22319903..22320481,2	MCF-7	breast:
20	chr14:22381656..22382465-chr5:35444689..35445277,2	MCF-7	breast:
21	chr14:22355742..22356307-chr14:22381815..22382504,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AE000662.92.1-10	chr14:22386642-22386919	NONHSAT035712
2	lnc-AE000662.92.1-10	chr14:22386669-22386931	NONHSAT035714
3	lnc-OR4E2-2	chr14:22297692-22297743	NONHSAT035707
4	lnc-AE000662.92.1-10	chr14:22386431-22386481	NONHSAT035712
5	lnc-OR10G2-5	chr14:22320548-22320780	NONHSAT035708
6	lnc-AE000662.92.1-10	chr14:22386653-22386919	NONHSAT035713
7	lnc-AE000662.92.1-10	chr14:22386378-22386481	NONHSAT035711
8	lnc-OR4E2-2	chr14:22297937-22298223	NONHSAT035707
9	lnc-OR10G2-5	chr14:22320890-22321003	NONHSAT035708
10	lnc-AE000662.92.1-10	chr14:22337290-22337543	NONHSAT035709
11	lnc-AE000662.92.1-10	chr14:22386642-22386928	NONHSAT035711

Variant related genes	Relation type
TRAV13-1	TF binding region
TRAV8-2	TF binding region
TRAV8-4	TF binding region
TRAV10	TF binding region
TRAV11	TF binding region
TRAV13-2	TF binding region
TRAV14DV4	TF binding region
TRAV12-1	TF binding region
TRAV8-5	TF binding region
TRAV12-2	TF binding region
TRAV8-3	TF binding region
TRAV13-1	CpG island
TRAV8-2	CpG island
TRAV8-4	CpG island
TRAV10	CpG island
TRAV11	CpG island
TRAV13-2	CpG island
TRAV14DV4	CpG island
TRAV12-1	CpG island
TRAV8-5	CpG island
TRAV12-2	CpG island
TRAV8-3	CpG island
ENSG00000211788	chromatin interactions
ENSG00000211787	chromatin interactions
ENSG00000211779	chromatin interactions
ENSG00000211789	chromatin interactions
ENSG00000211784	chromatin interactions
ENSG00000211790	chromatin interactions
ENSG00000211792	chromatin interactions
ENSG00000256379	chromatin interactions

Extended variants
information (count: 3680 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3680 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12050401	chr14:22288841-22288842	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571835993	chr14:22288863-22288864	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs574579028	chr14:22288887-22288888	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs539991828	chr14:22288915-22288916	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs560074086	chr14:22288916-22288917	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531986249	chr14:22288954-22288955	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs180821956	chr14:22288973-22288974	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs535399623	chr14:22288976-22288977	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs531505923	chr14:22289003-22289004	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs547978879	chr14:22289014-22289015	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs568468979	chr14:22289049-22289050	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs534283373	chr14:22289065-22289066	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs547601908	chr14:22289066-22289067	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs112445445	chr14:22289080-22289081	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557559480	chr14:22289084-22289085	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573434227	chr14:22289123-22289124	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs145516750	chr14:22289138-22289139	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs148860490	chr14:22289148-22289149	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs556603739	chr14:22289154-22289155	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs540451310	chr14:22289170-22289171	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs35915477	chr14:22289178-22289179	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs576760191	chr14:22289179-22289180	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs536197549	chr14:22289199-22289200	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs555983857	chr14:22289215-22289216	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs146955903	chr14:22289220-22289221	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs538825731	chr14:22289252-22289253	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs139270144	chr14:22289272-22289273	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs559960193	chr14:22289349-22289350	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs7155867	chr14:22289359-22289360	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs376851021	chr14:22289363-22289364	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs545437083	chr14:22289371-22289372	Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs368969191	chr14:22289421-22289422	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs185080167	chr14:22289452-22289453	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs531493492	chr14:22289457-22289458	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs191815001	chr14:22289464-22289465	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs141731914	chr14:22289466-22289467	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs527465577	chr14:22289525-22289526	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs547584326	chr14:22289538-22289539	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs570815095	chr14:22289540-22289541	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs147120582	chr14:22289541-22289542	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs116816548	chr14:22289542-22289543	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs367761517	chr14:22289554-22289555	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs73590403	chr14:22289570-22289571	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs12897433	chr14:22289606-22289607	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs11157248	chr14:22289663-22289664	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs74355796	chr14:22289689-22289690	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs377616452	chr14:22289717-22289718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs558334117	chr14:22289726-22289727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577803847	chr14:22289731-22289732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs545556328	chr14:22289742-22289743	Weak transcription Enhancers	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Lysinuric protein intolerance	18716612	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:22288000-22290400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr14:22288200-22289000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr14:22288200-22290000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr14:22288600-22289800	Enhancers	Primary hematopoietic stem cells	blood
5	chr14:22288600-22291000	Enhancers	HMEC	breast
6	chr14:22288800-22289600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:22288800-22290400	Enhancers	NHEK	skin
8	chr14:22289000-22289400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr14:22289400-22290400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr14:22289600-22290800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr14:22290800-22291000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr14:22293400-22294000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
13	chr14:22293600-22293800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
14	chr14:22293600-22294000	Active TSS	Primary T cells fromperipheralblood	blood
15	chr14:22293600-22294000	Active TSS	Primary T helper cells PMA-I stimulated	--
16	chr14:22293600-22294600	Active TSS	Thymus	Thymus
17	chr14:22293800-22294200	Active TSS	Primary T helper cells fromperipheralblood	blood
18	chr14:22293800-22294200	Active TSS	Fetal Thymus	thymus
19	chr14:22293800-22294400	Active TSS	Primary T cells from cord blood	blood
20	chr14:22302200-22302800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr14:22302800-22303200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr14:22304000-22304200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr14:22309200-22310000	Active TSS	Primary T cells fromperipheralblood	blood
24	chr14:22309400-22310000	Bivalent/Poised TSS	Primary T killer naive cells fromperipheralblood	blood
25	chr14:22309400-22310000	Active TSS	Thymus	Thymus
26	chr14:22309600-22309800	Flanking Active TSS	Fetal Thymus	thymus
27	chr14:22309600-22310000	Active TSS	Primary T cells from cord blood	blood
28	chr14:22309600-22310000	Bivalent/Poised TSS	Primary T regulatory cells fromperipheralblood	blood
29	chr14:22309800-22310000	Active TSS	Fetal Thymus	thymus
30	chr14:22310000-22314000	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr14:22311200-22311400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr14:22313000-22313200	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr14:22313600-22314400	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr14:22314200-22314400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
35	chr14:22314200-22314600	Enhancers	Primary T helper naive cells from peripheral blood	blood
36	chr14:22314200-22316400	Bivalent/Poised TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr14:22314400-22314600	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr14:22314400-22314600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
39	chr14:22314400-22314800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr14:22314600-22314800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
41	chr14:22314600-22314800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
42	chr14:22314600-22315000	Bivalent/Poised TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr14:22314600-22315000	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
44	chr14:22314600-22317000	Active TSS	Primary T killer naive cells fromperipheralblood	blood
45	chr14:22314600-22317200	Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr14:22314600-22318000	Active TSS	Primary T helper cells PMA-I stimulated	--
47	chr14:22314600-22318400	Active TSS	Thymus	Thymus
48	chr14:22314600-22318800	Active TSS	Primary T helper cells fromperipheralblood	blood
49	chr14:22314600-22326600	Active TSS	Primary T cells from cord blood	blood
50	chr14:22314800-22315000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell

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