Variant report

Variant	nsv882496
Chromosome Location	chr5:101066107-101507854
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	chr5:101426566-101426872	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:101473945-101474313	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:101435321-101436198	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:101489024-101489385	HepG2	liver:	n/a	n/a
5	ATF1	chr5:101338849-101338931	K562	blood:	n/a	n/a
6	ATF1	chr5:101236378-101236518	K562	blood:	n/a	n/a
7	ATF3	chr5:101384616-101385017	HCT-116	colon:	n/a	n/a
8	BACH1	chr5:101098504-101098821	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr5:101435704-101436031	HepG2	liver:	n/a	n/a
10	BHLHE40	chr5:101473978-101474432	HepG2	liver:	n/a	n/a
11	BHLHE40	chr5:101313640-101313757	GM12878	blood:	n/a	n/a
12	BHLHE40	chr5:101435342-101436124	HepG2	liver:	n/a	n/a
13	BHLHE40	chr5:101435606-101436058	HepG2	liver:	n/a	n/a
14	CEBPB	chr5:101368294-101368640	HepG2	liver:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
15	CEBPB	chr5:101474104-101474393	HepG2	liver:	n/a	chr5:101474303-101474316 chr5:101474305-101474316 chr5:101474303-101474316 chr5:101474303-101474314 chr5:101474303-101474316
16	CEBPB	chr5:101230709-101231058	HepG2	liver:	n/a	chr5:101230870-101230879 chr5:101230868-101230881 chr5:101230868-101230881 chr5:101231019-101231031 chr5:101230870-101230879 chr5:101230870-101230879 chr5:101230869-101230880
17	CEBPB	chr5:101343099-101343242	A549	lung:	n/a	n/a
18	CEBPB	chr5:101117728-101117741	K562	blood:	n/a	n/a
19	CEBPB	chr5:101385370-101385528	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr5:101373464-101373634	HepG2	liver:	n/a	chr5:101373550-101373561
21	CEBPB	chr5:101384640-101384936	A549	lung:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
22	CEBPB	chr5:101368313-101368639	IMR90	lung:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
23	CEBPB	chr5:101240483-101240827	ECC-1	luminal epithelium:	n/a	chr5:101240645-101240654 chr5:101240643-101240656 chr5:101240645-101240654 chr5:101240645-101240654 chr5:101240644-101240655 chr5:101240645-101240654 chr5:101240643-101240656 chr5:101240643-101240656 chr5:101240643-101240654
24	CEBPB	chr5:101336311-101336608	HepG2	liver:	n/a	chr5:101336472-101336483
25	CEBPB	chr5:101459346-101459437	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr5:101431550-101431869	HepG2	liver:	n/a	chr5:101431724-101431735
27	CEBPB	chr5:101230700-101231060	IMR90	lung:	n/a	chr5:101230870-101230879 chr5:101230868-101230881 chr5:101230868-101230881 chr5:101231019-101231031 chr5:101230870-101230879 chr5:101230870-101230879 chr5:101230869-101230880
28	CEBPB	chr5:101230716-101231013	ECC-1	luminal epithelium:	n/a	chr5:101230870-101230879 chr5:101230868-101230881 chr5:101230868-101230881 chr5:101230870-101230879 chr5:101230870-101230879 chr5:101230869-101230880
29	CEBPB	chr5:101384613-101384975	HepG2	liver:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
30	CEBPB	chr5:101492747-101492947	HepG2	liver:	n/a	n/a
31	CEBPB	chr5:101165030-101165279	A549	lung:	n/a	n/a
32	CEBPB	chr5:101421009-101421457	MCF-7	breast:	n/a	n/a
33	CEBPB	chr5:101331266-101331761	MCF-7	breast:	n/a	n/a
34	CEBPB	chr5:101368296-101368559	MCF-7	breast:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
35	CEBPB	chr5:101421142-101421383	MCF-7	breast:	n/a	n/a
36	CEBPB	chr5:101081760-101081990	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr5:101440235-101440558	A549	lung:	n/a	chr5:101440390-101440401
38	CEBPB	chr5:101165091-101165242	K562	blood:	n/a	n/a
39	CEBPB	chr5:101250910-101251177	A549	lung:	n/a	chr5:101251033-101251044
40	CEBPB	chr5:101250923-101251163	HepG2	liver:	n/a	chr5:101251033-101251044
41	CEBPB	chr5:101368447-101368563	H1-hESC	embryonic stem cell:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473
42	CEBPB	chr5:101440285-101440515	H1-hESC	embryonic stem cell:	n/a	chr5:101440390-101440401
43	CEBPB	chr5:101117582-101117899	HepG2	liver:	n/a	chr5:101117734-101117745 chr5:101117735-101117744
44	CEBPB	chr5:101384652-101384939	K562	blood:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
45	CEBPB	chr5:101440224-101440561	HepG2	liver:	n/a	chr5:101440390-101440401
46	CEBPB	chr5:101310922-101310941	A549	lung:	n/a	n/a
47	CEBPB	chr5:101384615-101384959	ECC-1	luminal epithelium:	n/a	chr5:101384786-101384797 chr5:101384786-101384799
48	CEBPB	chr5:101506875-101507212	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:101307371-101307487	A549	lung:	n/a	chr5:101307466-101307477
50	CEBPB	chr5:101368316-101368637	A549	lung:	n/a	chr5:101368460-101368473 chr5:101368460-101368471 chr5:101368460-101368473 chr5:101368462-101368473

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:101119084-101119134	GM12891	blood:	n/a
2	chr5:101279502-101279552	CMK	blood:	n/a
3	chr5:101119084-101119134	GM12891	blood:	n/a
4	chr5:101279502-101279552	CMK	blood:	n/a
5	chr5:101119420-101119470	NT2-D1	testis:	n/a
6	chr5:101279502-101279552	BJ	skin:	n/a
7	chr5:101297137-101297187	U87	brain:	n/a
8	chr5:101425870-101425920	T-47D	breast:	n/a
9	chr5:101297174-101297224	NH-A	brain:	n/a
10	chr5:101425870-101425920	Hepatocyte	liver:	n/a
11	chr5:101119084-101119134	RPTEC	kidney:	n/a
12	chr5:101279502-101279552	SK-N-SH_RA	brain:	n/a
13	chr5:101119128-101119178	AG09309	skin:	n/a
14	chr5:101119084-101119134	SKMC	muscle:	n/a
15	chr5:101297137-101297187	HCF	heart:	n/a
16	chr5:101119084-101119134	SK-N-MC	brain:	n/a
17	chr5:101297137-101297187	HUVEC	blood vessel:	n/a
18	chr5:101297137-101297187	NT2-D1	testis:	n/a
19	chr5:101119084-101119134	AG04450	lung:	fetal
20	chr5:101119566-101119616	NT2-D1	testis:	n/a
21	chr5:101297137-101297187	HIPEpiC	eye:	n/a
22	chr5:101297174-101297224	NT2-D1	testis:	n/a
23	chr5:101279502-101279552	LNCaP	prostate:	n/a
24	chr5:101119766-101119816	NB4	blood:	n/a
25	chr5:101425870-101425920	PFSK-1	brain:	n/a
26	chr5:101119566-101119616	HCF	heart:	n/a
27	chr5:101297174-101297224	MCF-7	breast:	n/a
28	chr5:101297174-101297224	PANC-1	pancreas:	n/a
29	chr5:101119766-101119816	NT2-D1	testis:	n/a
30	chr5:101119128-101119178	SKMC	muscle:	n/a
31	chr5:101119566-101119616	MCF10A-Er-Src	breast:	n/a
32	chr5:101425870-101425920	NH-A	brain:	n/a
33	chr5:101279502-101279552	A549	lung:	n/a
34	chr5:101119128-101119178	A549	lung:	n/a
35	chr5:101279502-101279552	SKMC	muscle:	n/a
36	chr5:101119128-101119178	HRPEpiC	eye:	n/a
37	chr5:101119766-101119816	HRE	kidney:	n/a
38	chr5:101279502-101279552	HCM	heart:	n/a
39	chr5:101297174-101297224	MCF10A-Er-Src	breast:	n/a
40	chr5:101119566-101119616	HEK293	kidney:	embryo
41	chr5:101119084-101119134	SK-N-SH	brain:	n/a
42	chr5:101119084-101119134	HCM	heart:	n/a
43	chr5:101119128-101119178	ProgFib	skin:	n/a
44	chr5:101119084-101119134	HepG2	liver:	n/a
45	chr5:101119420-101119470	HPAEpiC	pulmonary alveolar:	n/a
46	chr5:101119566-101119616	AG04449	skin:	fetal
47	chr5:101119420-101119470	IMR90	lung:	fetal
48	chr5:101119084-101119134	Hela-S3	cervix:	n/a
49	chr5:101119128-101119178	GM12892	blood:	n/a
50	chr5:101425870-101425920	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr5:101137073..101139756-chr5:101141662..101143533,2	MCF-7	breast:
2	chr5:101435579..101437280-chr5:101437849..101439350,2	MCF-7	breast:
3	chr5:101312840..101313801-chr5:101426237..101427126,3	MCF-7	breast:
4	chr17:27716905..27717691-chr5:101351042..101351795,2	MCF-7	breast:
5	chr5:101277581..101278499-chr5:101426192..101427059,2	MCF-7	breast:
6	chr5:101341869..101344693-chr5:101345059..101347272,2	MCF-7	breast:
7	chr5:101341869..101344693-chr5:101345059..101347272,2	MCF-7	breast:
8	chr5:101432287..101434879-chr5:101435908..101438270,2	K562	blood:
9	chr5:101476598..101478204-chr5:101481147..101483100,2	MCF-7	breast:
10	chr5:101277636..101278379-chr5:101489093..101489664,2	MCF-7	breast:
11	chr5:101361879..101363839-chr5:101365059..101366576,2	MCF-7	breast:
12	chr5:101326987..101328842-chr5:101335717..101338180,2	MCF-7	breast:
13	chr5:101432287..101434879-chr5:101435908..101438270,2	K562	blood:
14	chr5:101078843..101080982-chr5:101098462..101100344,2	MCF-7	breast:
15	chr5:101277790..101278635-chr5:101488732..101489585,4	MCF-7	breast:
16	chr5:101216484..101218050-chr5:101219554..101221470,2	MCF-7	breast:
17	chr5:101137073..101139756-chr5:101141662..101143533,2	MCF-7	breast:
18	chr5:101277790..101278635-chr5:101488732..101489585,4	MCF-7	breast:
19	chr5:101277703..101278961-chr5:101426537..101427100,3	MCF-7	breast:
20	chr5:101209236..101211408-chr5:101214038..101216724,2	K562	blood:
21	chr5:101006866..101009211-chr5:101203107..101204677,2	MCF-7	breast:
22	chr5:101277636..101278379-chr5:101489093..101489664,2	MCF-7	breast:
23	chr5:101475498..101477506-chr5:101479656..101481283,2	K562	blood:
24	chr10:68291165..68291817-chr5:101132057..101132805,2	MCF-7	breast:
25	chr5:101326987..101328842-chr5:101335717..101338180,2	MCF-7	breast:
26	chr5:101435579..101437280-chr5:101437849..101439350,2	MCF-7	breast:
27	chr5:101216484..101218050-chr5:101219554..101221470,2	MCF-7	breast:
28	chr5:101277581..101278499-chr5:101426192..101427059,2	MCF-7	breast:
29	chr5:101476598..101478204-chr5:101481147..101483100,2	MCF-7	breast:
30	chr5:101078843..101080982-chr5:101098462..101100344,2	MCF-7	breast:
31	chr5:100977296..100978177-chr5:101426469..101427113,2	MCF-7	breast:
32	chr5:101277703..101278961-chr5:101426537..101427100,3	MCF-7	breast:
33	chr5:101361879..101363839-chr5:101365059..101366576,2	MCF-7	breast:
34	chr5:101312840..101313801-chr5:101426237..101427126,3	MCF-7	breast:
35	chr5:101209236..101211408-chr5:101214038..101216724,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PAM-5	chr5:101482018-101482276	NONHSAT103022
2	lnc-PAM-8	chr5:101312000-101312502	NONHSAT103019
3	lnc-PAM-5	chr5:101479780-101479847	NONHSAT103022
4	lnc-PAM-5	chr5:101482019-101482276	XLOC_004491
5	lnc-PAM-5	chr5:101479781-101479847	XLOC_004491

Variant related genes	Relation type
ENSG00000248261	TF binding region
OR7H2P	TF binding region
ENSG00000249495	TF binding region
RNA5SP188	TF binding region
ENSG00000248261	CpG island
OR7H2P	CpG island
ENSG00000249495	CpG island
RNA5SP188	CpG island
ENSG00000248261	chromatin interactions
ENSG00000160551	chromatin interactions
ENSG00000263719	chromatin interactions

Extended variants
information (count: 4911 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:4911 , 50 per page) page: 1 2 3 4 5 6 7 ... 99

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190341353	chr5:101081429-101081430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573263487	chr5:101081454-101081455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138689541	chr5:101081490-101081491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559314192	chr5:101081495-101081496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs565331999	chr5:101081502-101081503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532226326	chr5:101081504-101081505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs550714727	chr5:101081505-101081506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562530210	chr5:101081593-101081594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372128735	chr5:101081640-101081641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529968405	chr5:101081650-101081651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548077287	chr5:101081680-101081681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78326549	chr5:101081819-101081820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367991130	chr5:101081856-101081857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs193298906	chr5:101081881-101081882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533506293	chr5:101081937-101081938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551989352	chr5:101081955-101081956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185078629	chr5:101081967-101081968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149379985	chr5:101081993-101081994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76303078	chr5:101081995-101081996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs13157830	chr5:101090812-101090813	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs77254259	chr5:101090832-101090833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs186267689	chr5:101090854-101090855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs530270220	chr5:101090855-101090856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs548883581	chr5:101090858-101090859	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs143667708	chr5:101090873-101090874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566012535	chr5:101090877-101090878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs534492946	chr5:101090879-101090880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs552318290	chr5:101090898-101090899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116284952	chr5:101090904-101090905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs537992164	chr5:101090924-101090925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556201348	chr5:101090974-101090975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73777562	chr5:101091036-101091037	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs533577808	chr5:101091038-101091039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs148077652	chr5:101091070-101091071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs190155946	chr5:101091074-101091075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572276898	chr5:101091100-101091101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs377295769	chr5:101091129-101091130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs546073382	chr5:101091181-101091182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs557824429	chr5:101091194-101091195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs553723029	chr5:101091215-101091216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34807592	chr5:101091221-101091222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576066597	chr5:101091235-101091236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs80094176	chr5:101091267-101091268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs570230980	chr5:101091334-101091335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561737657	chr5:101091350-101091351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs573703831	chr5:101091369-101091370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs530330200	chr5:101091410-101091411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542093705	chr5:101091472-101091473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs6869060	chr5:101091513-101091514	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs528023207	chr5:101091515-101091516	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Merkel cell carcinoma	19020549	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	21509527	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:101081400-101082000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr5:101090800-101092200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr5:101093800-101094000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:101093800-101094200	Enhancers	Pancreas	Pancrea
5	chr5:101094200-101095200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr5:101095200-101096200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr5:101095200-101096200	Enhancers	Adipose Nuclei	Adipose
8	chr5:101117000-101117200	Enhancers	Colon Smooth Muscle	Colon
9	chr5:101117200-101119000	Weak transcription	Colon Smooth Muscle	Colon
10	chr5:101117800-101119800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr5:101118200-101118400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr5:101118200-101118600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr5:101118400-101118600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr5:101118400-101118800	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr5:101118400-101119600	Active TSS	A549	lung
16	chr5:101118600-101118800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chr5:101118600-101119000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr5:101118600-101119600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
19	chr5:101118600-101119600	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr5:101118800-101119000	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
21	chr5:101118800-101119000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr5:101118800-101119000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
23	chr5:101118800-101119200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
24	chr5:101118800-101119200	Active TSS	Stomach Mucosa	stomach
25	chr5:101118800-101119400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr5:101118800-101119600	Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr5:101118800-101119600	Active TSS	Brain Angular Gyrus	brain
28	chr5:101118800-101119600	Active TSS	Brain Anterior Caudate	brain
29	chr5:101118800-101119600	Active TSS	NH-A	brain
30	chr5:101118800-101119800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr5:101118800-101119800	Active TSS	Brain Germinal Matrix	brain
32	chr5:101118800-101119800	Active TSS	Brain Hippocampus Middle	brain
33	chr5:101118800-101119800	Active TSS	Brain Substantia Nigra	brain
34	chr5:101118800-101119800	Active TSS	Fetal Brain Female	brain
35	chr5:101118800-101119800	Active TSS	NHDF-Ad	bronchial
36	chr5:101119000-101119200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr5:101119000-101119200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr5:101119000-101119200	Enhancers	Lung	lung
39	chr5:101119000-101119400	Active TSS	Primary hematopoietic stem cells	blood
40	chr5:101119000-101119400	Active TSS	HSMM	muscle
41	chr5:101119000-101119600	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
42	chr5:101119000-101119600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
43	chr5:101119000-101119600	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr5:101119000-101119600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr5:101119000-101119600	Active TSS	Adipose Nuclei	Adipose
46	chr5:101119000-101119600	Active TSS	Brain Inferior Temporal Lobe	brain
47	chr5:101119000-101119600	Active TSS	Fetal Intestine Large	intestine
48	chr5:101119000-101119600	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
49	chr5:101119000-101119600	Active TSS	Fetal Muscle Trunk	muscle
50	chr5:101119000-101119600	Active TSS	Fetal Muscle Leg	muscle

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