Variant report

Variant	nsv1036997
Chromosome Location	chr11:5243698-5287790
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:632)
CpG islands
(count:1283)
Chromatin interactive
region (count:53)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:5264837-5265363	K562	blood:	n/a	n/a
2	ARID3A	chr11:5249644-5249844	K562	blood:	n/a	n/a
3	ARID3A	chr11:5276151-5276402	K562	blood:	n/a	n/a
4	ARID3A	chr11:5257576-5257774	K562	blood:	n/a	n/a
5	ARID3A	chr11:5245587-5246192	K562	blood:	n/a	n/a
6	ARID3A	chr11:5271239-5271565	K562	blood:	n/a	n/a
7	ARID3A	chr11:5268316-5269020	K562	blood:	n/a	n/a
8	ARID3A	chr11:5272954-5273932	K562	blood:	n/a	n/a
9	ARID3A	chr11:5261872-5262055	K562	blood:	n/a	n/a
10	ARID3A	chr11:5265713-5266219	K562	blood:	n/a	n/a
11	ARID3A	chr11:5260276-5260613	K562	blood:	n/a	n/a
12	ARID3A	chr11:5246856-5247135	K562	blood:	n/a	n/a
13	ARID3A	chr11:5255679-5256104	K562	blood:	n/a	n/a
14	ARID3A	chr11:5267239-5267293	K562	blood:	n/a	n/a
15	ATF1	chr11:5279847-5280189	K562	blood:	n/a	n/a
16	ATF1	chr11:5264167-5265053	K562	blood:	n/a	n/a
17	ATF1	chr11:5245779-5246154	K562	blood:	n/a	n/a
18	ATF1	chr11:5268522-5269044	K562	blood:	n/a	n/a
19	ATF1	chr11:5255603-5256048	K562	blood:	n/a	n/a
20	ATF2	chr11:5278483-5278915	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr11:5278495-5278943	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF3	chr11:5279833-5280095	K562	blood:	n/a	n/a
23	BACH1	chr11:5268459-5268512	K562	blood:	n/a	n/a
24	BACH1	chr11:5264322-5264867	K562	blood:	n/a	n/a
25	BCLAF1	chr11:5264168-5265450	K562	blood:	n/a	n/a
26	BHLHE40	chr11:5265777-5266337	K562	blood:	n/a	n/a
27	BHLHE40	chr11:5274846-5275018	K562	blood:	n/a	n/a
28	BHLHE40	chr11:5264205-5264494	GM12878	blood:	n/a	n/a
29	BHLHE40	chr11:5264141-5265268	K562	blood:	n/a	n/a
30	BHLHE40	chr11:5255546-5256047	K562	blood:	n/a	n/a
31	BHLHE40	chr11:5278607-5278864	K562	blood:	n/a	n/a
32	BHLHE40	chr11:5279730-5280390	K562	blood:	n/a	n/a
33	BHLHE40	chr11:5246783-5247124	K562	blood:	n/a	n/a
34	BHLHE40	chr11:5268500-5268516	K562	blood:	n/a	n/a
35	BHLHE40	chr11:5268754-5269061	K562	blood:	n/a	n/a
36	BHLHE40	chr11:5273446-5273968	K562	blood:	n/a	n/a
37	CBX3	chr11:5275620-5276341	K562	blood:	n/a	n/a
38	CBX3	chr11:5270739-5271346	K562	blood:	n/a	n/a
39	CBX3	chr11:5279666-5280299	K562	blood:	n/a	n/a
40	CBX3	chr11:5280809-5281099	K562	blood:	n/a	n/a
41	CBX3	chr11:5255529-5256122	K562	blood:	n/a	n/a
42	CCNT2	chr11:5264236-5265372	K562	blood:	n/a	chr11:5264966-5264975 chr11:5264792-5264812
43	CCNT2	chr11:5272987-5273828	K562	blood:	n/a	n/a
44	CCNT2	chr11:5263465-5263811	K562	blood:	n/a	n/a
45	CCNT2	chr11:5267900-5269339	K562	blood:	n/a	chr11:5268321-5268341
46	CCNT2	chr11:5265622-5266433	K562	blood:	n/a	n/a
47	CCNT2	chr11:5255609-5256050	K562	blood:	n/a	n/a
48	CEBPB	chr11:5273972-5274132	K562	blood:	n/a	n/a
49	CEBPB	chr11:5270882-5271768	K562	blood:	n/a	chr11:5271513-5271524 chr11:5271513-5271526
50	CEBPB	chr11:5248361-5248384	K562	blood:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:5274883-5274933	HNPCEpiC	eye:	n/a
2	chr11:5272039-5272089	HNPCEpiC	eye:	n/a
3	chr11:5274883-5274933	HNPCEpiC	eye:	n/a
4	chr11:5272039-5272089	HNPCEpiC	eye:	n/a
5	chr11:5275217-5275267	GM12891	blood:	n/a
6	chr11:5257253-5257303	NB4	blood:	n/a
7	chr11:5279386-5279436	Hepatocyte	liver:	n/a
8	chr11:5270556-5270606	Jurkat	blood:	n/a
9	chr11:5276490-5276540	AG04450	lung:	fetal
10	chr11:5265008-5265058	HepG2	liver:	n/a
11	chr11:5279386-5279436	PFSK-1	brain:	n/a
12	chr11:5263432-5263482	Jurkat	blood:	n/a
13	chr11:5255926-5255976	Hela-S3	cervix:	n/a
14	chr11:5265992-5266042	MCF-7	breast:	n/a
15	chr11:5275217-5275267	Hepatocyte	liver:	n/a
16	chr11:5247586-5247636	ovcar-3	ovarian:	n/a
17	chr11:5255926-5255976	NH-A	brain:	n/a
18	chr11:5248218-5248268	HMEC	breast:	n/a
19	chr11:5265992-5266042	Hepatocyte	liver:	n/a
20	chr11:5274883-5274933	AG09309	skin:	n/a
21	chr11:5263432-5263482	IMR90	lung:	fetal
22	chr11:5279386-5279436	SK-N-SH	brain:	n/a
23	chr11:5255926-5255976	HCPEpiC	choroid plexus:	n/a
24	chr11:5248566-5248616	HEK293	kidney:	embryo
25	chr11:5265992-5266042	A549	lung:	n/a
26	chr11:5276490-5276540	SK-N-SH_RA	brain:	n/a
27	chr11:5275217-5275267	SK-N-SH	brain:	n/a
28	chr11:5279386-5279436	T-47D	breast:	n/a
29	chr11:5248426-5248476	MCF-7	breast:	n/a
30	chr11:5249528-5249578	ovcar-3	ovarian:	n/a
31	chr11:5274883-5274933	HCF	heart:	n/a
32	chr11:5265008-5265058	GM12892	blood:	n/a
33	chr11:5279386-5279436	CMK	blood:	n/a
34	chr11:5275217-5275267	GM06990	blood:	n/a
35	chr11:5277210-5277260	GM12878	blood:	n/a
36	chr11:5265155-5265205	LNCaP	prostate:	n/a
37	chr11:5265008-5265058	MCF10A-Er-Src	breast:	n/a
38	chr11:5265155-5265205	A549	lung:	n/a
39	chr11:5276490-5276540	HepG2	liver:	n/a
40	chr11:5270556-5270606	T-47D	breast:	n/a
41	chr11:5265215-5265265	K562	blood:	n/a
42	chr11:5248218-5248268	PrEC	prostate:	n/a
43	chr11:5263432-5263482	HUVEC	blood vessel:	n/a
44	chr11:5265008-5265058	GM19239	blood:	n/a
45	chr11:5265155-5265205	HL-60	blood:	n/a
46	chr11:5270556-5270606	HRCEpiC	kidney:	n/a
47	chr11:5247586-5247636	NHDF-neo	bronchial:	n/a
48	chr11:5265992-5266042	NHBE	bronchial:	n/a
49	chr11:5275217-5275267	NH-A	brain:	n/a
50	chr11:5275217-5275267	NHBE	bronchial:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:5277602..5279692-chr11:5306290..5308679,2	K562	blood:
2	chr11:5220556..5223187-chr11:5263121..5265697,2	K562	blood:
3	chr11:5227943..5230443-chr11:5260953..5263248,2	K562	blood:
4	chr11:5263207..5265743-chr11:5278391..5279965,2	K562	blood:
5	chr11:5252860..5257215-chr11:5269390..5273074,4	K562	blood:
6	11:5281513-5288772..11:5721056-5732713	K562	blood:
7	chr11:5258087..5259967-chr11:5277201..5279069,2	K562	blood:
8	11:5281513-5288772..11:5505728-5514500	K562	blood:
9	chr11:5267593..5269501-chr11:5620817..5623766,2	K562	blood:
10	chr11:5257329..5260096-chr11:5307374..5309530,2	K562	blood:
11	11:4988858-5002113..11:5250847-5268367	Hela-S3	cervix:
12	11:5281513-5288772..11:5533869-5541626	K562	blood:
13	chr11:5149389..5153211-chr11:5272377..5275357,4	K562	blood:
14	11:5281513-5288772..11:5714465-5718134	K562	blood:
15	chr11:5260030..5265620-chr11:5286872..5292555,7	K562	blood:
16	chr11:5271867..5274635-chr11:5288575..5290959,2	K562	blood:
17	chr11:5286597..5289777-chr11:5309468..5312767,3	K562	blood:
18	chr11:5270253..5272815-chr11:5288791..5291580,2	K562	blood:
19	chr11:5273135..5283072-chr11:5287409..5292550,13	K562	blood:
20	chr11:5216338..5218129-chr11:5279337..5280949,2	K562	blood:
21	11:5272427-5273151..11:5616559-5618985	K562	blood:
22	11:5250847-5268367..11:5571131-5578892	K562	blood:
23	chr11:5265929..5269608-chr11:5311418..5314048,3	K562	blood:
24	11:5093737-5099374..11:5250847-5268367	Hela-S3	cervix:
25	chr11:5274899..5283703-chr11:5287409..5292802,11	K562	blood:
26	chr11:5151728..5155807-chr11:5263615..5268276,6	K562	blood:
27	chr11:5246037..5247818-chr11:5310743..5312829,2	K562	blood:
28	chr11:5261877..5263572-chr11:5273707..5276513,2	K562	blood:
29	chr11:5271864..5275702-chr11:5276083..5279926,6	K562	blood:
30	11:5243048-5250847..11:5268367-5269120	K562	blood:
31	11:5033143-5038367..11:5243048-5250847	Hela-S3	cervix:
32	chr11:5150718..5153704-chr11:5259366..5262458,3	K562	blood:
33	11:5033143-5038367..11:5250847-5268367	Hela-S3	cervix:
34	11:5243048-5250847..11:5349791-5355747	GM12878	blood:
35	chr11:5252860..5257215-chr11:5269390..5273074,4	K562	blood:
36	chr11:5271864..5275702-chr11:5276083..5279926,6	K562	blood:
37	chr11:5278168..5280291-chr11:5317279..5319861,2	K562	blood:
38	chr11:5274899..5283703-chr11:5287409..5292802,11	K562	blood:
39	chr11:5245072..5246710-chr11:5271824..5273616,2	K562	blood:
40	11:5243048-5250847..11:5272427-5273151	K562	blood:
41	11:5281513-5288772..11:5700314-5707362	K562	blood:
42	11:5250847-5268367..11:5380014-5384338	H1-hESC	embryonic stem cell:	embryo
43	11:4988858-5002113..11:5243048-5250847	Hela-S3	cervix:
44	chr11:5258087..5259967-chr11:5277201..5279069,2	K562	blood:
45	11:5146608-5154908..11:5281513-5288772	K562	blood:
46	11:5243048-5250847..11:5281513-5288772	K562	blood:
47	chr11:5260030..5265620-chr11:5286872..5292555,7	K562	blood:
48	chr11:5271470..5273351-chr11:5300652..5303323,2	K562	blood:
49	11:5250847-5268367..11:5281513-5288772	K562	blood:
50	chr11:5253263..5255348-chr11:5314463..5316756,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HBG1-1	chr11:5265784-5266777	ENSG00000260629.1

No data

Variant related genes	Relation type
HBG1	TF binding region
HBBP1	TF binding region
HBD	TF binding region
HBB	TF binding region
ENSG00000221031	TF binding region
ENSG00000260629	TF binding region
HBG2	TF binding region
HBG1	CpG island
HBBP1	CpG island
HBD	CpG island
HBB	CpG island
ENSG00000221031	CpG island
ENSG00000260629	CpG island
HBG2	CpG island
ENSG00000236248	chromatin interactions
ENSG00000237354	chromatin interactions
ENSG00000183251	chromatin interactions
ENSG00000224300	chromatin interactions
ENSG00000175518	chromatin interactions
ENSG00000260629	chromatin interactions
ENSG00000213931	chromatin interactions
ENSG00000213934	chromatin interactions
ENSG00000229093	chromatin interactions
ENSG00000196565	chromatin interactions
ENSG00000258588	chromatin interactions
ENSG00000176742	chromatin interactions
ENSG00000221031	chromatin interactions
ENSG00000132274	chromatin interactions
ENSG00000229988	chromatin interactions
ENSG00000225003	chromatin interactions
ENSG00000181609	chromatin interactions
ENSG00000121236	chromatin interactions
ENSG00000236359	chromatin interactions
ENSG00000223609	chromatin interactions
ENSG00000248553	chromatin interactions
ENSG00000132256	chromatin interactions
ENSG00000244734	chromatin interactions
ENSG00000171944	chromatin interactions

Extended variants
information (count: 2884 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:2884 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559486952	chr11:5243718-5243719	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs190291103	chr11:5243732-5243733	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs374717960	chr11:5243733-5243734	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs7930833	chr11:5243757-5243758	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs563789306	chr11:5243759-5243760	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs527724656	chr11:5243779-5243780	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs530696674	chr11:5243783-5243784	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs111847305	chr11:5243788-5243789	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs570659180	chr11:5243792-5243793	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs113184763	chr11:5243825-5243826	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs546920115	chr11:5243854-5243855	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs567914906	chr11:5243859-5243860	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs183991229	chr11:5243898-5243899	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs556304466	chr11:5243908-5243909	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs112317789	chr11:5243917-5243918	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs113850170	chr11:5243936-5243937	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs552130663	chr11:5243950-5243951	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs558876766	chr11:5243989-5243990	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs113956879	chr11:5244074-5244075	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs570643472	chr11:5244076-5244077	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs553639297	chr11:5244099-5244100	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs112884104	chr11:5244107-5244108	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs188124316	chr11:5244141-5244142	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs12364872	chr11:5244144-5244145	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs142104438	chr11:5244163-5244164	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs564988793	chr11:5244176-5244177	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs575791401	chr11:5244235-5244236	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs572008918	chr11:5244291-5244292	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs10837626	chr11:5244299-5244300	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs560129585	chr11:5244325-5244326	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs529330207	chr11:5244378-5244379	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs181024015	chr11:5244383-5244384	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs531656822	chr11:5244402-5244403	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs10837628	chr11:5244404-5244405	Inactive region	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs186182418	chr11:5244427-5244428	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs192086695	chr11:5244467-5244468	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs370293446	chr11:5244491-5244492	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs561661826	chr11:5244501-5244502	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs528829525	chr11:5244520-5244521	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs550147495	chr11:5244539-5244540	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs568555372	chr11:5244540-5244541	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs182450050	chr11:5244587-5244588	Inactive region	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs531773536	chr11:5244641-5244642	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs141845179	chr11:5244665-5244666	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs570917087	chr11:5244672-5244673	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs186639330	chr11:5244713-5244714	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs553363511	chr11:5244721-5244722	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs112395357	chr11:5244725-5244726	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs575166155	chr11:5244730-5244731	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs145391788	chr11:5244748-5244749	Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:5244600-5245200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr11:5244800-5248200	Weak transcription	Gastric	stomach
3	chr11:5245000-5245800	Enhancers	K562	blood
4	chr11:5245200-5254200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr11:5245600-5245800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr11:5245600-5246000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:5245800-5246000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:5245800-5246200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr11:5245800-5246400	Flanking Active TSS	K562	blood
10	chr11:5246000-5246200	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
11	chr11:5246000-5246200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr11:5246000-5246400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:5246000-5246800	Enhancers	Primary hematopoietic stem cells	blood
14	chr11:5246000-5247000	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr11:5246000-5247200	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
16	chr11:5246200-5246400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:5246200-5246600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:5246200-5247400	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
19	chr11:5246400-5246800	Enhancers	K562	blood
20	chr11:5246600-5247000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr11:5246800-5247200	Flanking Active TSS	K562	blood
22	chr11:5246800-5253600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr11:5247000-5247400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr11:5247000-5252800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr11:5247200-5247400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
26	chr11:5247200-5249600	Enhancers	K562	blood
27	chr11:5247400-5247600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
28	chr11:5247400-5248000	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr11:5247400-5248000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr11:5247600-5248000	Transcr. at gene 5' and 3'	Primary T regulatory cells fromperipheralblood	blood
31	chr11:5247800-5248400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr11:5248200-5248400	Enhancers	Gastric	stomach
33	chr11:5249600-5253400	Weak transcription	K562	blood
34	chr11:5250600-5251000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:5252400-5253800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:5252400-5255200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr11:5252800-5253000	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr11:5253000-5253400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr11:5253400-5254600	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr11:5253400-5254600	Genic enhancers	K562	blood
41	chr11:5253600-5253800	Enhancers	Primary hematopoietic stem cells	blood
42	chr11:5253800-5254800	Weak transcription	Primary hematopoietic stem cells	blood
43	chr11:5253800-5254800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr11:5254200-5254400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr11:5254400-5255200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr11:5254600-5255000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
47	chr11:5254600-5255400	Enhancers	K562	blood
48	chr11:5254800-5255400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:5254800-5256600	Enhancers	Primary hematopoietic stem cells	blood
50	chr11:5255000-5255200	Enhancers	Primary hematopoietic stem cells short term culture	blood

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