Variant report

Variant	nsv1028236
Chromosome Location	chr5:178962087-179019981
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1325)
CpG islands
(count:2203)
Chromatin interactive
region (count:108)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1325 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:178977590-178977818	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:178977115-178977357	HepG2	liver:	n/a	n/a
3	ARID3A	chr5:178985842-178986538	HepG2	liver:	n/a	n/a
4	ATF2	chr5:178985934-178986763	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:178986020-178986776	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr5:178977014-178977777	GM12878	blood:	n/a	n/a
7	ATF2	chr5:178971356-178971893	GM12878	blood:	n/a	n/a
8	ATF2	chr5:178971353-178972009	GM12878	blood:	n/a	n/a
9	ATF2	chr5:178976968-178977468	GM12878	blood:	n/a	n/a
10	BACH1	chr5:178976363-178976432	K562	blood:	n/a	n/a
11	BACH1	chr5:178977696-178978347	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr5:178971422-178971880	GM12878	blood:	n/a	chr5:178971650-178971659
13	BCL11A	chr5:178971440-178971812	GM12878	blood:	n/a	chr5:178971650-178971659
14	BCL3	chr5:178995361-178995595	GM12878	blood:	n/a	n/a
15	BCL3	chr5:178986050-178987128	A549	lung:	n/a	n/a
16	BCL3	chr5:178999749-179000029	GM12878	blood:	n/a	n/a
17	BCL3	chr5:178995617-178995986	GM12878	blood:	n/a	n/a
18	BCL3	chr5:178985836-178986998	A549	lung:	n/a	n/a
19	BCLAF1	chr5:178977522-178978403	GM12878	blood:	n/a	chr5:178978060-178978073 chr5:178978272-178978285 chr5:178978064-178978077
20	BCLAF1	chr5:178977094-178977496	GM12878	blood:	n/a	chr5:178977430-178977439
21	BCLAF1	chr5:178971380-178972055	GM12878	blood:	n/a	chr5:178971650-178971659
22	BHLHE40	chr5:179012837-179013284	K562	blood:	n/a	n/a
23	BHLHE40	chr5:178977555-178978270	HepG2	liver:	n/a	chr5:178978066-178978082 chr5:178978012-178978028
24	BHLHE40	chr5:178971425-178971980	GM12878	blood:	n/a	n/a
25	BHLHE40	chr5:178967579-178967940	HepG2	liver:	n/a	n/a
26	BHLHE40	chr5:178976912-178978367	GM12878	blood:	n/a	chr5:178978066-178978082 chr5:178978012-178978028 chr5:178978259-178978275
27	BHLHE40	chr5:178977025-178978380	K562	blood:	n/a	chr5:178978066-178978082 chr5:178978012-178978028 chr5:178978259-178978275
28	BRCA1	chr5:178985953-178986744	H1-hESC	embryonic stem cell:	n/a	n/a
29	CBX3	chr5:178985780-178986131	K562	blood:	n/a	n/a
30	CCNT2	chr5:178977542-178978403	K562	blood:	n/a	n/a
31	CEBPB	chr5:178986608-178986863	HepG2	liver:	n/a	n/a
32	CEBPB	chr5:178983477-178983608	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr5:179016185-179016305	HepG2	liver:	n/a	n/a
34	CEBPB	chr5:178969712-178969909	HepG2	liver:	n/a	chr5:178969816-178969827
35	CEBPB	chr5:179010195-179010334	IMR90	lung:	n/a	n/a
36	CEBPB	chr5:178985390-178985674	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr5:178976139-178976344	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr5:178977303-178977503	HepG2	liver:	n/a	n/a
39	CEBPB	chr5:178985906-178986047	K562	blood:	n/a	n/a
40	CEBPB	chr5:178969707-178969953	K562	blood:	n/a	chr5:178969816-178969827
41	CEBPB	chr5:178977272-178977473	K562	blood:	n/a	n/a
42	CEBPB	chr5:178980904-178981262	IMR90	lung:	n/a	n/a
43	CEBPB	chr5:178975670-178975842	H1-hESC	embryonic stem cell:	n/a	chr5:178975778-178975789
44	CEBPB	chr5:178971323-178971992	GM12878	blood:	n/a	n/a
45	CEBPB	chr5:178981094-178981104	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:178973964-178974161	HepG2	liver:	n/a	chr5:178974017-178974028
47	CEBPB	chr5:178973974-178974068	H1-hESC	embryonic stem cell:	n/a	chr5:178974017-178974028
48	CEBPB	chr5:178976200-178976292	K562	blood:	n/a	n/a
49	CEBPB	chr5:178986657-178987112	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr5:178969707-178969931	A549	lung:	n/a	chr5:178969816-178969827

(count:2203 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:178977181-178977231	HRPEpiC	eye:	n/a
2	chr5:179004535-179004585	K562	blood:	n/a
3	chr5:179004757-179004807	PFSK-1	brain:	n/a
4	chr5:178973820-178973870	U87	brain:	n/a
5	chr5:179003843-179003893	T-47D	breast:	n/a
6	chr5:179004739-179004789	ECC-1	luminal epithelium:	n/a
7	chr5:178987429-178987479	CMK	blood:	n/a
8	chr5:178977181-178977231	HRPEpiC	eye:	n/a
9	chr5:179004535-179004585	K562	blood:	n/a
10	chr5:179004757-179004807	PFSK-1	brain:	n/a
11	chr5:178973820-178973870	U87	brain:	n/a
12	chr5:179003843-179003893	T-47D	breast:	n/a
13	chr5:179004739-179004789	ECC-1	luminal epithelium:	n/a
14	chr5:178987429-178987479	CMK	blood:	n/a
15	chr5:178986906-178986956	LNCaP	prostate:	n/a
16	chr5:178982556-178982606	Caco-2	colon:	n/a
17	chr5:178978234-178978284	MCF-7	breast:	n/a
18	chr5:179006403-179006453	LNCaP	prostate:	n/a
19	chr5:179004757-179004807	U87	brain:	n/a
20	chr5:178986906-178986956	HNPCEpiC	eye:	n/a
21	chr5:179004757-179004807	HEEpiC	esophagus:	n/a
22	chr5:179004707-179004757	GM12878	blood:	n/a
23	chr5:178977521-178977571	Hela-S3	cervix:	n/a
24	chr5:179004707-179004757	PrEC	prostate:	n/a
25	chr5:179004707-179004757	RPTEC	kidney:	n/a
26	chr5:178977398-178977448	HUVEC	blood vessel:	n/a
27	chr5:178986412-178986462	NT2-D1	testis:	n/a
28	chr5:179006403-179006453	HNPCEpiC	eye:	n/a
29	chr5:178987429-178987479	HCT-116	colon:	n/a
30	chr5:178977641-178977691	NB4	blood:	n/a
31	chr5:178977375-178977425	AG09309	skin:	n/a
32	chr5:179004757-179004807	HRPEpiC	eye:	n/a
33	chr5:178977398-178977448	HRCEpiC	kidney:	n/a
34	chr5:179004739-179004789	AoSMC	blood vessel:	n/a
35	chr5:178977181-178977231	NB4	blood:	n/a
36	chr5:178977641-178977691	HRE	kidney:	n/a
37	chr5:178982556-178982606	HRE	kidney:	n/a
38	chr5:178977375-178977425	NB4	blood:	n/a
39	chr5:179003843-179003893	GM12892	blood:	n/a
40	chr5:179004739-179004789	HAEpiC	amniotic membrane:	n/a
41	chr5:178977406-178977456	Hepatocyte	liver:	n/a
42	chr5:178986412-178986462	BE2_C	brain:	n/a
43	chr5:178977375-178977425	T-47D	breast:	n/a
44	chr5:178990055-178990105	MCF10A-Er-Src	breast:	n/a
45	chr5:178977377-178977427	MCF-7	breast:	n/a
46	chr5:178986412-178986462	HRPEpiC	eye:	n/a
47	chr5:178986404-178986454	NHDF-neo	bronchial:	n/a
48	chr5:178978234-178978284	PANC-1	pancreas:	n/a
49	chr5:178986412-178986462	GM12892	blood:	n/a
50	chr5:178986726-178986776	LNCaP	prostate:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr5:178976288..178979908-chr5:179158372..179161228,3	MCF-7	breast:
2	chr5:178967564..178969306-chr5:178978047..178979581,2	K562	blood:
3	chr5:178979685..178981544-chr5:178981841..178984975,3	K562	blood:
4	chr5:179011326..179015421-chr5:179015501..179018945,4	MCF-7	breast:
5	chr5:178980836..178983768-chr5:179095589..179098241,2	MCF-7	breast:
6	chr5:178976464..178979366-chr5:179003151..179005535,3	MCF-7	breast:
7	chr5:178998693..179001088-chr5:179125400..179127599,2	K562	blood:
8	chr5:178976299..178979036-chr5:178987617..178989903,2	K562	blood:
9	chr5:178990186..178992537-chr5:178996461..178998253,2	K562	blood:
10	chr5:178979685..178981490-chr5:178983248..178984975,2	K562	blood:
11	chr5:178958501..178962397-chr5:178966368..178969379,3	K562	blood:
12	chr5:178966233..178969209-chr5:178970782..178972509,2	MCF-7	breast:
13	chr5:178993088..178996882-chr5:179048174..179052059,4	K562	blood:
14	chr15:22833249..22833980-chr5:178977502..178978069,2	Hela-S3	cervix:
15	chr5:178977809..178978321-chr5:178985908..178986661,2	MCF-7	breast:
16	chr5:179012467..179014455-chr5:179037577..179039741,2	K562	blood:
17	chr5:178984205..178987569-chr5:178988108..178992792,6	MCF-7	breast:
18	chr5:178976811..178980871-chr5:179039605..179043375,3	K562	blood:
19	chr5:177630883..177632521-chr5:178985029..178986804,2	MCF-7	breast:
20	chr5:178976299..178979036-chr5:178987617..178989903,2	K562	blood:
21	chr5:178971437..178973246-chr5:178974311..178976700,2	K562	blood:
22	chr5:178966269..178968602-chr5:178984458..178986550,2	MCF-7	breast:
23	chr5:178981570..178984338-chr5:178984530..178988621,4	K562	blood:
24	chr5:178990186..178992537-chr5:178996461..178998253,2	K562	blood:
25	chr5:178964680..178966401-chr5:178977965..178979894,2	K562	blood:
26	chr5:178975834..178978833-chr5:179245271..179247079,2	K562	blood:
27	chr5:178982934..178985451-chr5:179036566..179039640,3	K562	blood:
28	chr5:178958501..178962397-chr5:178966368..178969379,3	K562	blood:
29	chr5:178961944..178964885-chr5:178975318..178977306,2	MCF-7	breast:
30	chr5:178976329..178981059-chr5:179123787..179127407,6	K562	blood:
31	chr5:178984119..178986610-chr5:178999493..179002273,3	K562	blood:
32	chr5:178953283..178956112-chr5:178976067..178979094,3	MCF-7	breast:
33	chr1:110881782..110882370-chr5:178977392..178978012,2	Hela-S3	cervix:
34	chr5:178989647..178992005-chr5:179000001..179001767,2	K562	blood:
35	chr5:178977295..178978049-chrX:153718720..153719639,2	Hela-S3	cervix:
36	chr5:179001067..179003316-chr5:179026144..179027789,2	MCF-7	breast:
37	chr5:178967183..178969964-chr5:178976742..178979184,3	MCF-7	breast:
38	chr5:178979685..178981544-chr5:178981841..178984975,3	K562	blood:
39	chr5:178984896..178986468-chr5:179223868..179225684,2	MCF-7	breast:
40	chr5:178976591..178978128-chr5:179049452..179051597,2	MCF-7	breast:
41	chr5:178960272..178962115-chr5:178969166..178970829,2	MCF-7	breast:
42	chr5:178958919..178961962-chr5:178962607..178965657,3	K562	blood:
43	chr5:178984558..178987542-chr5:178988263..178990973,3	K562	blood:
44	chr5:178975751..178978306-chr5:178993914..178996502,2	MCF-7	breast:
45	chr5:178985192..178988541-chr5:179048594..179052191,5	MCF-7	breast:
46	chr5:178975871..178983601-chr5:179047224..179052413,15	K562	blood:
47	chr5:179004969..179007855-chr5:179049122..179050815,2	MCF-7	breast:
48	chr5:178997303..179000137-chr5:179000501..179003984,3	MCF-7	breast:
49	chr15:101835145..101835812-chr5:178986003..178986591,2	HCT-116	colon:
50	chr5:178960272..178962115-chr5:178969166..178970829,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC136604.1-5	chr5:178999157-178999742	NONHSAT105590
2	lnc-HNRNPH1-4	chr5:178975273-178975507	expReg_chr5_10798_-
3	lnc-RUFY1-3	chr5:178971224-178972983	NONHSAT105589

No data

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

Extended variants
information (count: 2483 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2483 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144894515	chr5:178962139-178962140	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs547335533	chr5:178962161-178962162	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs149025647	chr5:178962162-178962163	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs138332951	chr5:178962198-178962199	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs201408932	chr5:178962199-178962200	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs200874940	chr5:178962201-178962202	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs146194084	chr5:178962221-178962222	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs551835986	chr5:178962228-178962229	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs138963143	chr5:178962254-178962255	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs141413749	chr5:178962289-178962290	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs375910433	chr5:178962292-178962293	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs114244469	chr5:178962301-178962302	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs566559701	chr5:178962303-178962304	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs533801361	chr5:178962448-178962449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558600891	chr5:178962512-178962513	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs371327649	chr5:178962527-178962528	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577633043	chr5:178962568-178962569	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188457468	chr5:178962569-178962570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs180776624	chr5:178962570-178962571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs6601044	chr5:178962595-178962596	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs533565270	chr5:178962601-178962602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs574564284	chr5:178962661-178962662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541982864	chr5:178962692-178962693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs539590605	chr5:178962705-178962706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553770741	chr5:178962715-178962716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs200888410	chr5:178962722-178962723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs386695643	chr5:178962753-178962754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540871977	chr5:178962779-178962780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs565446407	chr5:178962782-178962783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs532878548	chr5:178962847-178962848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148031009	chr5:178962858-178962859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372244818	chr5:178962880-178962881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs9885443	chr5:178962918-178962919	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs535745365	chr5:178962933-178962934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs575829623	chr5:178962945-178962946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141895050	chr5:178962955-178962956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548291150	chr5:178962964-178962965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187607880	chr5:178962978-178962979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568304820	chr5:178963004-178963005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs527689046	chr5:178963018-178963019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs552582114	chr5:178963019-178963020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570654391	chr5:178963026-178963027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538169935	chr5:178963051-178963052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs202069740	chr5:178963053-178963054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs568279947	chr5:178963067-178963068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535517238	chr5:178963101-178963102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553911562	chr5:178963129-178963130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190256887	chr5:178963161-178963162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545470102	chr5:178963172-178963173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114664492	chr5:178963198-178963199	Weak transcription	n/a	n/a	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:2448 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:178957600-178962400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:178958000-178962200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:178958000-178962200	Weak transcription	Spleen	Spleen
4	chr5:178958000-178962400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr5:178958000-178976800	Weak transcription	Fetal Intestine Small	intestine
6	chr5:178958000-178977000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:178958200-178963200	Weak transcription	Osteobl	bone
8	chr5:178960200-178962400	Enhancers	Primary hematopoietic stem cells	blood
9	chr5:178960400-178962400	Enhancers	Primary B cells from cord blood	blood
10	chr5:178960600-178963400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr5:178961000-178962200	Flanking Active TSS	GM12878-XiMat	blood
12	chr5:178961000-178962400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr5:178961200-178962400	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr5:178961200-178962400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr5:178961400-178962200	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr5:178961400-178962200	Enhancers	Stomach Mucosa	stomach
17	chr5:178961400-178962600	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr5:178961600-178962200	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr5:178961600-178962200	Enhancers	Primary T helper naive cells from peripheral blood	blood
20	chr5:178961800-178962200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr5:178961800-178962200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr5:178961800-178962200	Enhancers	Thymus	Thymus
23	chr5:178961800-178962400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr5:178961800-178962400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr5:178961800-178962400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
26	chr5:178961800-178962400	Enhancers	HepG2	liver
27	chr5:178962000-178962400	Enhancers	Primary B cells from peripheral blood	blood
28	chr5:178962200-178962400	Enhancers	GM12878-XiMat	blood
29	chr5:178962200-178962600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr5:178962200-178962600	Enhancers	Spleen	Spleen
31	chr5:178962400-178962600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr5:178962400-178962800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr5:178962400-178970600	Weak transcription	Primary B cells from cord blood	blood
34	chr5:178962400-178971800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr5:178962600-178971400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr5:178962800-178971400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr5:178963200-178963600	Enhancers	Osteobl	bone
38	chr5:178963200-178963800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr5:178963400-178963600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr5:178963600-178976400	Weak transcription	Osteobl	bone
41	chr5:178963800-178964000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr5:178964000-178964200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr5:178964200-178967600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr5:178966800-178967600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr5:178967200-178967600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:178969200-178969400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr5:178969200-178969600	Enhancers	NHDF-Ad	bronchial
48	chr5:178969200-178970400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr5:178969200-178970400	Enhancers	Hela-S3	cervix
50	chr5:178969400-178975000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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