Variant report

Variant	nsv883269
Chromosome Location	chr5:178951106-179031595
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1795)
CpG islands
(count:2993)
Chromatin interactive
region (count:130)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1795 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178985842-178986538	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178977590-178977818	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178977115-178977357	HepG2	liver:	n/a	n/a
4	ATF2	chr5:178971353-178972009	GM12878	blood:	n/a	n/a
5	ATF2	chr5:178985934-178986763	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:178971356-178971893	GM12878	blood:	n/a	n/a
7	ATF2	chr5:178960873-178961287	GM12878	blood:	n/a	n/a
8	ATF2	chr5:178976968-178977468	GM12878	blood:	n/a	n/a
9	ATF2	chr5:178986020-178986776	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr5:178977014-178977777	GM12878	blood:	n/a	n/a
11	BACH1	chr5:178977696-178978347	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:178976363-178976432	K562	blood:	n/a	n/a
13	BACH1	chr5:178957142-178957774	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr5:178971422-178971880	GM12878	blood:	n/a	chr5:178971650-178971659
15	BCL11A	chr5:178971440-178971812	GM12878	blood:	n/a	chr5:178971650-178971659
16	BCL3	chr5:178995361-178995595	GM12878	blood:	n/a	n/a
17	BCL3	chr5:179020495-179020879	GM12878	blood:	n/a	n/a
18	BCL3	chr5:179031106-179031606	A549	lung:	n/a	n/a
19	BCL3	chr5:178985836-178986998	A549	lung:	n/a	n/a
20	BCL3	chr5:179020516-179020812	GM12878	blood:	n/a	n/a
21	BCL3	chr5:178995617-178995986	GM12878	blood:	n/a	n/a
22	BCL3	chr5:178986050-178987128	A549	lung:	n/a	n/a
23	BCL3	chr5:178999749-179000029	GM12878	blood:	n/a	n/a
24	BCLAF1	chr5:178977522-178978403	GM12878	blood:	n/a	chr5:178978060-178978073 chr5:178978272-178978285 chr5:178978064-178978077
25	BCLAF1	chr5:178971380-178972055	GM12878	blood:	n/a	chr5:178971650-178971659
26	BCLAF1	chr5:178977094-178977496	GM12878	blood:	n/a	chr5:178977430-178977439
27	BHLHE40	chr5:178977025-178978380	K562	blood:	n/a	chr5:178978066-178978082 chr5:178978012-178978028 chr5:178978259-178978275
28	BHLHE40	chr5:178971425-178971980	GM12878	blood:	n/a	n/a
29	BHLHE40	chr5:178960996-178961233	GM12878	blood:	n/a	n/a
30	BHLHE40	chr5:178977555-178978270	HepG2	liver:	n/a	chr5:178978066-178978082 chr5:178978012-178978028
31	BHLHE40	chr5:178976912-178978367	GM12878	blood:	n/a	chr5:178978066-178978082 chr5:178978012-178978028 chr5:178978259-178978275
32	BHLHE40	chr5:178967579-178967940	HepG2	liver:	n/a	n/a
33	BHLHE40	chr5:179012837-179013284	K562	blood:	n/a	n/a
34	BRCA1	chr5:178985953-178986744	H1-hESC	embryonic stem cell:	n/a	n/a
35	CBX3	chr5:178985780-178986131	K562	blood:	n/a	n/a
36	CBX3	chr5:178957621-178958014	K562	blood:	n/a	n/a
37	CCNT2	chr5:178957677-178957915	K562	blood:	n/a	n/a
38	CCNT2	chr5:178977542-178978403	K562	blood:	n/a	n/a
39	CEBPB	chr5:178978079-178978276	HepG2	liver:	n/a	n/a
40	CEBPB	chr5:178985853-178986832	A549	lung:	n/a	n/a
41	CEBPB	chr5:178980992-178981217	A549	lung:	n/a	n/a
42	CEBPB	chr5:178969704-178969985	K562	blood:	n/a	chr5:178969816-178969827
43	CEBPB	chr5:178971323-178971992	GM12878	blood:	n/a	n/a
44	CEBPB	chr5:178954009-178954592	Hela-S3	cervix:	n/a	chr5:178954195-178954204 chr5:178954195-178954204 chr5:178954166-178954178 chr5:178954194-178954205 chr5:178954195-178954204 chr5:178954193-178954204 chr5:178954195-178954204 chr5:178954193-178954206 chr5:178954193-178954206
45	CEBPB	chr5:178954151-178954257	H1-hESC	embryonic stem cell:	n/a	chr5:178954195-178954204 chr5:178954195-178954204 chr5:178954166-178954178 chr5:178954194-178954205 chr5:178954195-178954204 chr5:178954193-178954204 chr5:178954195-178954204 chr5:178954193-178954206 chr5:178954193-178954206
46	CEBPB	chr5:178969558-178970171	HCT-116	colon:	n/a	chr5:178969816-178969827
47	CEBPB	chr5:178954047-178954405	A549	lung:	n/a	chr5:178954195-178954204 chr5:178954195-178954204 chr5:178954166-178954178 chr5:178954194-178954205 chr5:178954195-178954204 chr5:178954193-178954204 chr5:178954195-178954204 chr5:178954193-178954206 chr5:178954193-178954206
48	CEBPB	chr5:178977303-178977503	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:178986395-178987118	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:178973964-178974161	HepG2	liver:	n/a	chr5:178974017-178974028

(count:2993 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178986726-178986776	PrEC	prostate:	n/a
2	chr5:178986728-178986778	HNPCEpiC	eye:	n/a
3	chr5:178986620-178986670	HAEpiC	amniotic membrane:	n/a
4	chr5:178980927-178980977	HUVEC	blood vessel:	n/a
5	chr5:178986726-178986776	PrEC	prostate:	n/a
6	chr5:178986728-178986778	HNPCEpiC	eye:	n/a
7	chr5:178986620-178986670	HAEpiC	amniotic membrane:	n/a
8	chr5:178980927-178980977	HUVEC	blood vessel:	n/a
9	chr5:178956931-178956981	PFSK-1	brain:	n/a
10	chr5:178977377-178977427	T-47D	breast:	n/a
11	chr5:178977326-178977376	PFSK-1	brain:	n/a
12	chr5:178956073-178956123	HEEpiC	esophagus:	n/a
13	chr5:178990055-178990105	SAEC	small airway:	n/a
14	chr5:178957930-178957980	GM12892	blood:	n/a
15	chr5:178957930-178957980	SK-N-SH	brain:	n/a
16	chr5:178973820-178973870	GM12892	blood:	n/a
17	chr5:178957344-178957394	HNPCEpiC	eye:	n/a
18	chr5:179004535-179004585	RPTEC	kidney:	n/a
19	chr5:178977326-178977376	AG04450	lung:	fetal
20	chr5:178977394-178977444	HMEC	breast:	n/a
21	chr5:178977123-178977173	ProgFib	skin:	n/a
22	chr5:178978460-178978510	LNCaP	prostate:	n/a
23	chr5:178982556-178982606	PFSK-1	brain:	n/a
24	chr5:178977236-178977286	H1-hESC	embryonic stem cell:	embryo
25	chr5:178953596-178953646	AG10803	skin:	n/a
26	chr5:178957880-178957930	LNCaP	prostate:	n/a
27	chr5:178986830-178986880	HCF	heart:	n/a
28	chr5:179029719-179029769	HCF	heart:	n/a
29	chr5:178986291-178986341	GM19239	blood:	n/a
30	chr5:178977398-178977448	HIPEpiC	eye:	n/a
31	chr5:178977326-178977376	NH-A	brain:	n/a
32	chr5:178973820-178973870	HEEpiC	esophagus:	n/a
33	chr5:179008603-179008653	BE2_C	brain:	n/a
34	chr5:178977394-178977444	RPTEC	kidney:	n/a
35	chr5:179004757-179004807	BE2_C	brain:	n/a
36	chr5:178982556-178982606	NT2-D1	testis:	n/a
37	chr5:178986404-178986454	HUVEC	blood vessel:	n/a
38	chr5:179004707-179004757	H1-hESC	embryonic stem cell:	embryo
39	chr5:178977375-178977425	NHDF-neo	bronchial:	n/a
40	chr5:178957930-178957980	PFSK-1	brain:	n/a
41	chr5:178977375-178977425	BE2_C	brain:	n/a
42	chr5:179006403-179006453	AG09309	skin:	n/a
43	chr5:179002268-179002318	SK-N-MC	brain:	n/a
44	chr5:178957880-178957930	SAEC	small airway:	n/a
45	chr5:178956838-178956888	ovcar-3	ovarian:	n/a
46	chr5:178986728-178986778	HPAEpiC	pulmonary alveolar:	n/a
47	chr5:178986726-178986776	HEK293	kidney:	embryo
48	chr5:178973820-178973870	NH-A	brain:	n/a
49	chr5:179029719-179029769	NHDF-neo	bronchial:	n/a
50	chr5:178977406-178977456	A549	lung:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:178975871..178983601-chr5:179047224..179052413,15	K562	blood:
2	chr5:178985192..178988541-chr5:179048594..179052191,5	MCF-7	breast:
3	chr5:178977341..178979490-chr5:179011302..179013107,2	MCF-7	breast:
4	chr5:178975751..178978306-chr5:178993914..178996502,2	MCF-7	breast:
5	chr12:50135028..50135993-chr5:178977449..178978052,2	Hela-S3	cervix:
6	chr5:178958919..178961962-chr5:178962607..178965657,3	K562	blood:
7	chr1:110881782..110882370-chr5:178977392..178978012,2	Hela-S3	cervix:
8	chr5:178978852..178982589-chr5:179047122..179052388,6	MCF-7	breast:
9	chr5:178955819..178957353-chr5:179123603..179125281,2	MCF-7	breast:
10	chr5:178984558..178987542-chr5:178988263..178990973,3	K562	blood:
11	chr5:178951884..178954426-chr5:179031332..179033126,2	MCF-7	breast:
12	chr5:178976850..178979581-chr5:179125172..179127163,2	K562	blood:
13	chr5:178972500..178975262-chr5:178977445..178979874,2	K562	blood:
14	chr5:178976288..178979908-chr5:179158372..179161228,3	MCF-7	breast:
15	chr5:178979685..178981544-chr5:178981841..178984975,3	K562	blood:
16	chr5:178969062..178971266-chr5:178976850..178979130,2	K562	blood:
17	chr5:178986726..178988892-chr5:179104044..179106638,2	K562	blood:
18	chr5:178979256..178982161-chr5:178989561..178991785,2	K562	blood:
19	chr5:178967564..178969306-chr5:178978047..178979581,2	K562	blood:
20	chr5:178964185..178968820-chr5:178974807..178977846,4	K562	blood:
21	chr5:178972300..178975805-chr5:178975972..178979443,5	MCF-7	breast:
22	chr5:178977295..178978049-chrX:153718720..153719639,2	Hela-S3	cervix:
23	chr5:178967564..178969306-chr5:178978047..178979581,2	K562	blood:
24	chr5:178993088..178996882-chr5:179048174..179052059,4	K562	blood:
25	chr5:178961944..178964885-chr5:178975318..178977306,2	MCF-7	breast:
26	chr5:178976299..178979036-chr5:178987617..178989903,2	K562	blood:
27	chr5:178976299..178979036-chr5:178987617..178989903,2	K562	blood:
28	chr5:178976757..178979190-chr5:180687275..180690244,2	K562	blood:
29	chr5:178997303..179000137-chr5:179000501..179003984,3	MCF-7	breast:
30	chr5:178989647..178992005-chr5:179000001..179001767,2	K562	blood:
31	chr5:178953283..178956112-chr5:178976067..178979094,3	MCF-7	breast:
32	chr5:178947804..178950473-chr5:178974779..178977233,2	MCF-7	breast:
33	chr5:178975690..178977861-chr5:179029775..179032308,2	K562	blood:
34	chr5:178986818..178988892-chr5:179105129..179106638,2	K562	blood:
35	chr5:179011616..179013589-chr5:179034982..179036835,2	K562	blood:
36	chr5:178981782..178983559-chr5:178998257..179000519,2	K562	blood:
37	chr5:178958919..178961962-chr5:178962607..178965657,3	K562	blood:
38	chr5:178959529..178962397-chr5:178966368..178968696,2	K562	blood:
39	chr5:179023883..179026184-chr5:179031149..179032775,2	MCF-7	breast:
40	chr5:178998693..179001088-chr5:179125400..179127599,2	K562	blood:
41	chr5:178967183..178969964-chr5:178976742..178979184,3	MCF-7	breast:
42	chr5:179023716..179025532-chr5:179027753..179029789,2	K562	blood:
43	chr5:179001067..179003316-chr5:179026144..179027789,2	MCF-7	breast:
44	chr5:179001067..179003316-chr5:179026144..179027789,2	MCF-7	breast:
45	chr5:178999030..179001028-chr5:179028298..179031172,2	MCF-7	breast:
46	chr5:178975801..178977799-chr5:178987617..178990258,3	K562	blood:
47	chr5:178973738..178976008-chr5:178976265..178978073,2	K562	blood:
48	chr5:178996663..178999644-chr5:179000508..179002723,3	K562	blood:
49	chr5:178979685..178981544-chr5:178981841..178984975,3	K562	blood:
50	chr5:178981570..178984338-chr5:178984530..178988621,4	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RUFY1-4	chr5:178951021-178952136	NONHSAT105587
2	lnc-HNRNPH1-1	chr5:179026269-179026390	ENSG00000244945.1
3	lnc-HNRNPH1-1	chr5:179027074-179027099	ENSG00000244945.1
4	lnc-HNRNPH1-1	chr5:179025254-179025356	ENSG00000244945.1
5	lnc-HNRNPH1-1	chr5:179029065-179029267	ENSG00000244945.1
6	lnc-AC136604.1-5	chr5:178999157-178999742	NONHSAT105590
7	lnc-HNRNPH1-4	chr5:178975273-178975507	expReg_chr5_10798_-
8	lnc-HNRNPH1-1	chr5:179029378-179029773	ENSG00000244945.1
9	lnc-HNRNPH1-1	chr5:179023823-179023962	ENSG00000244945.1
10	lnc-HNRNPH1-1	chr5:179026486-179026636	ENSG00000244945.1
11	lnc-HNRNPH1-1	chr5:179022905-179023594	ENSG00000244945.1
12	lnc-HNRNPH1-1	chr5:179030608-179030742	ENSG00000244945.1
13	lnc-HNRNPH1-2	chr5:178951450-178952173	ENSG00000251657
14	lnc-RUFY1-4	chr5:178951021-178952136	NONHSAT105586
15	lnc-RUFY1-3	chr5:178971224-178972983	NONHSAT105589

No data

Variant related genes	Relation type
PRDX2P3	TF binding region
ENSG00000244945	TF binding region
ENSG00000253520	TF binding region
RUFY1	TF binding region
PRDX2P3	CpG island
ENSG00000244945	CpG island
ENSG00000253520	CpG island
RUFY1	CpG island
ENSG00000183718	chromatin interactions
ENSG00000162775	chromatin interactions
ENSG00000253520	chromatin interactions
ENSG00000161021	chromatin interactions
ENSG00000251545	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000221394	chromatin interactions
ENSG00000139644	chromatin interactions
ENSG00000126903	chromatin interactions
ENSG00000153575	chromatin interactions
ENSG00000186594	chromatin interactions
ENSG00000131876	chromatin interactions
ENSG00000244945	chromatin interactions
ENSG00000161011	chromatin interactions
ENSG00000227963	chromatin interactions
ENSG00000127022	chromatin interactions
ENSG00000176783	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000259172	chromatin interactions
ENSG00000225051	chromatin interactions
ENSG00000249140	chromatin interactions
ENSG00000248275	chromatin interactions
ENSG00000167716	chromatin interactions
PIGU	miRNA target sites

Extended variants
information (count: 3541 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:3541 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4701187	chr5:178951106-178951107	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561701770	chr5:178951127-178951128	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
3	rs573573834	chr5:178951147-178951148	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs542484015	chr5:178951180-178951181	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
5	rs577208952	chr5:178951182-178951183	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
6	rs200202475	chr5:178951183-178951184	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs527841573	chr5:178951229-178951230	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs552343532	chr5:178951235-178951236	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs564386789	chr5:178951269-178951270	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs545976521	chr5:178951302-178951303	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs549894885	chr5:178951325-178951326	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
12	rs568406385	chr5:178951326-178951327	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs145029017	chr5:178951351-178951352	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs138816614	chr5:178951365-178951366	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs565845228	chr5:178951386-178951387	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs189271397	chr5:178951413-178951414	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs557979858	chr5:178951414-178951415	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs181597595	chr5:178951420-178951421	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs537110093	chr5:178951422-178951423	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs555192962	chr5:178951453-178951454	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs147878913	chr5:178951462-178951463	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs114689634	chr5:178951463-178951464	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs540679601	chr5:178951464-178951465	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs200383528	chr5:178951506-178951507	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs572406086	chr5:178951515-178951516	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs546118896	chr5:178951517-178951518	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs201058960	chr5:178951548-178951549	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs199521634	chr5:178951551-178951552	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs543868863	chr5:178951560-178951561	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs562042738	chr5:178951563-178951564	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs529243354	chr5:178951574-178951575	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs185182857	chr5:178951588-178951589	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs4701188	chr5:178951598-178951599	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533241311	chr5:178951603-178951604	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs189583930	chr5:178951618-178951619	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs551732846	chr5:178951619-178951620	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
37	rs569839803	chr5:178951637-178951638	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
38	rs181126029	chr5:178951658-178951659	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
39	rs537246668	chr5:178951661-178951662	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs201987065	chr5:178951695-178951696	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs199784161	chr5:178951697-178951698	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs200558640	chr5:178951698-178951699	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
43	rs201720896	chr5:178951699-178951700	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
44	rs200061507	chr5:178951700-178951701	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs563748407	chr5:178951701-178951702	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs377043384	chr5:178951705-178951706	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs552674190	chr5:178951716-178951717	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs577254318	chr5:178951717-178951718	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs534498404	chr5:178951719-178951720	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs200716035	chr5:178951729-178951730	Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	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
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
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2956 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178947000-178952600	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr5:178949400-178956600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr5:178951000-178957000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:178953200-178956600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
5	chr5:178953600-178954800	Enhancers	Hela-S3	cervix
6	chr5:178953600-178956400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:178953600-178956600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr5:178954200-178954600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr5:178954200-178954800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr5:178954400-178954600	Enhancers	Primary hematopoietic stem cells	blood
11	chr5:178954400-178954600	Enhancers	Spleen	Spleen
12	chr5:178954600-178954800	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr5:178954600-178954800	Enhancers	Thymus	Thymus
14	chr5:178954600-178956600	Weak transcription	Primary hematopoietic stem cells	blood
15	chr5:178954600-178956800	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr5:178954600-178957200	Weak transcription	Spleen	Spleen
17	chr5:178954800-178955000	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr5:178954800-178956600	Weak transcription	Brain Inferior Temporal Lobe	brain
19	chr5:178954800-178956600	Weak transcription	Thymus	Thymus
20	chr5:178954800-178957400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr5:178955000-178955200	Enhancers	Dnd41	blood
22	chr5:178955000-178956800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr5:178955200-178955400	Enhancers	Colon Smooth Muscle	Colon
24	chr5:178955200-178956600	Weak transcription	Dnd41	blood
25	chr5:178955400-178956600	Weak transcription	Colon Smooth Muscle	Colon
26	chr5:178955800-178956400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr5:178956400-178958800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr5:178956600-178956800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr5:178956600-178956800	Enhancers	Adipose Nuclei	Adipose
30	chr5:178956600-178956800	Enhancers	Duodenum Mucosa	Duodenum
31	chr5:178956600-178957000	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr5:178956600-178957000	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr5:178956600-178957000	Enhancers	Colon Smooth Muscle	Colon
34	chr5:178956600-178957000	Enhancers	Thymus	Thymus
35	chr5:178956600-178957400	Flanking Active TSS	Primary hematopoietic stem cells	blood
36	chr5:178956600-178957400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr5:178956600-178957800	Active TSS	iPS-15b Cell Line	embryonic stem cell
38	chr5:178956600-178958200	Active TSS	GM12878-XiMat	blood
39	chr5:178956600-178958800	Flanking Active TSS	Dnd41	blood
40	chr5:178956800-178957000	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr5:178956800-178957000	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr5:178956800-178957000	Enhancers	Primary B cells from peripheral blood	blood
43	chr5:178956800-178957000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr5:178956800-178957000	Enhancers	Fetal Thymus	thymus
45	chr5:178956800-178957000	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr5:178956800-178957200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr5:178956800-178957200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr5:178956800-178957200	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
49	chr5:178956800-178957400	Flanking Active TSS	Duodenum Mucosa	Duodenum
50	chr5:178956800-178957800	Flanking Active TSS	Adipose Nuclei	Adipose

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