Variant report

Variant	nsv532804
Chromosome Location	chr5:45184041-45972996
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2095)
CpG islands
(count:1709)
Chromatin interactive
region (count:37)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2095 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:45779869-45779893	K562	blood:	n/a	n/a
2	ATF1	chr5:45384259-45384430	K562	blood:	n/a	n/a
3	ATF1	chr5:45520472-45520538	K562	blood:	n/a	n/a
4	ATF2	chr5:45205408-45206121	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr5:45793625-45794610	GM12878	blood:	n/a	n/a
6	ATF2	chr5:45205482-45205984	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr5:45793733-45794112	GM12878	blood:	n/a	n/a
8	BACH1	chr5:45695045-45695509	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr5:45194371-45194425	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr5:45622547-45622743	K562	blood:	n/a	n/a
11	BACH1	chr5:45622469-45623083	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr5:45694432-45694821	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr5:45696406-45696585	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr5:45793691-45794568	GM12878	blood:	n/a	n/a
15	BATF	chr5:45206930-45207199	GM12878	blood:	n/a	n/a
16	BATF	chr5:45794116-45794419	GM12878	blood:	n/a	n/a
17	BATF	chr5:45206937-45207259	GM12878	blood:	n/a	n/a
18	BATF	chr5:45793742-45794099	GM12878	blood:	n/a	n/a
19	BATF	chr5:45206365-45206599	GM12878	blood:	n/a	n/a
20	BCL11A	chr5:45205547-45205862	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL11A	chr5:45793646-45794647	GM12878	blood:	n/a	n/a
22	BCL11A	chr5:45848140-45848326	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr5:45794121-45794555	GM12878	blood:	n/a	n/a
24	BCL11A	chr5:45205512-45205912	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr5:45206949-45207174	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:45793739-45794103	GM12878	blood:	n/a	n/a
27	BHLHE40	chr5:45799491-45799496	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:45793537-45794787	GM12878	blood:	n/a	n/a
29	BRCA1	chr5:45551191-45551382	H1-hESC	embryonic stem cell:	n/a	n/a
30	BRCA1	chr5:45564807-45564864	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr5:45412229-45412265	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr5:45696466-45696687	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr5:45624018-45624277	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr5:45279148-45279663	HCT-116	colon:	n/a	n/a
35	CBX3	chr5:45385462-45386770	HCT-116	colon:	n/a	n/a
36	CBX3	chr5:45277804-45278448	HCT-116	colon:	n/a	n/a
37	CBX3	chr5:45385629-45386224	HCT-116	colon:	n/a	n/a
38	CEBPB	chr5:45199707-45199935	A549	lung:	n/a	chr5:45199846-45199859 chr5:45199847-45199858 chr5:45199856-45199869
39	CEBPB	chr5:45740115-45740413	HepG2	liver:	n/a	chr5:45740245-45740256
40	CEBPB	chr5:45405872-45406072	HepG2	liver:	n/a	chr5:45405921-45405934 chr5:45405921-45405934 chr5:45405921-45405932 chr5:45405923-45405934
41	CEBPB	chr5:45684266-45684560	HepG2	liver:	n/a	chr5:45684417-45684428 chr5:45684416-45684429 chr5:45684418-45684427 chr5:45684416-45684427 chr5:45684418-45684427 chr5:45684416-45684429 chr5:45684418-45684427 chr5:45684418-45684427
42	CEBPB	chr5:45623926-45624273	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr5:45417169-45418084	Hela-S3	cervix:	n/a	chr5:45417980-45417993
44	CEBPB	chr5:45509316-45509326	A549	lung:	n/a	n/a
45	CEBPB	chr5:45187482-45187821	Hela-S3	cervix:	n/a	chr5:45187663-45187674
46	CEBPB	chr5:45740075-45740364	A549	lung:	n/a	chr5:45740245-45740256
47	CEBPB	chr5:45338308-45338508	HepG2	liver:	n/a	chr5:45338439-45338452 chr5:45338440-45338451 chr5:45338439-45338452 chr5:45338439-45338450 chr5:45338439-45338450
48	CEBPB	chr5:45382746-45383041	IMR90	lung:	n/a	chr5:45382913-45382922 chr5:45382896-45382907 chr5:45382913-45382922
49	CEBPB	chr5:45187527-45187841	HepG2	liver:	n/a	chr5:45187663-45187674
50	CEBPB	chr5:45609832-45610172	Hela-S3	cervix:	n/a	n/a

(count:1709 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:45694523-45694573	AG04450	lung:	fetal
2	chr5:45694523-45694573	AG04450	lung:	fetal
3	chr5:45678610-45678660	SK-N-SH	brain:	n/a
4	chr5:45499395-45499445	T-47D	breast:	n/a
5	chr5:45262329-45262379	CMK	blood:	n/a
6	chr5:45695467-45695517	BE2_C	brain:	n/a
7	chr5:45695839-45695889	NHBE	bronchial:	n/a
8	chr5:45695643-45695693	HMEC	breast:	n/a
9	chr5:45696206-45696256	HIPEpiC	eye:	n/a
10	chr5:45700402-45700452	HRCEpiC	kidney:	n/a
11	chr5:45695643-45695693	SK-N-SH	brain:	n/a
12	chr5:45649048-45649098	HNPCEpiC	eye:	n/a
13	chr5:45204945-45204995	HEEpiC	esophagus:	n/a
14	chr5:45553518-45553568	HEEpiC	esophagus:	n/a
15	chr5:45696455-45696505	ECC-1	luminal epithelium:	n/a
16	chr5:45695467-45695517	PrEC	prostate:	n/a
17	chr5:45649048-45649098	NH-A	brain:	n/a
18	chr5:45569042-45569092	K562	blood:	n/a
19	chr5:45225802-45225852	AG04450	lung:	fetal
20	chr5:45693264-45693314	HCT-116	colon:	n/a
21	chr5:45262329-45262379	IMR90	lung:	fetal
22	chr5:45204945-45204995	GM12878	blood:	n/a
23	chr5:45695241-45695291	SKMC	muscle:	n/a
24	chr5:45696465-45696515	HEEpiC	esophagus:	n/a
25	chr5:45696465-45696515	SK-N-MC	brain:	n/a
26	chr5:45262268-45262318	HIPEpiC	eye:	n/a
27	chr5:45678610-45678660	HCPEpiC	choroid plexus:	n/a
28	chr5:45225802-45225852	SK-N-SH_RA	brain:	n/a
29	chr5:45724903-45724953	HMEC	breast:	n/a
30	chr5:45262268-45262318	AoSMC	blood vessel:	n/a
31	chr5:45499395-45499445	AG09319	gingival:	n/a
32	chr5:45696592-45696642	HIPEpiC	eye:	n/a
33	chr5:45553518-45553568	ProgFib	skin:	n/a
34	chr5:45695467-45695517	GM12891	blood:	n/a
35	chr5:45225802-45225852	H1-hESC	embryonic stem cell:	embryo
36	chr5:45695922-45695972	BE2_C	brain:	n/a
37	chr5:45724903-45724953	PFSK-1	brain:	n/a
38	chr5:45499395-45499445	ProgFib	skin:	n/a
39	chr5:45696491-45696541	AG10803	skin:	n/a
40	chr5:45696465-45696515	GM12878	blood:	n/a
41	chr5:45695922-45695972	SK-N-MC	brain:	n/a
42	chr5:45260623-45260673	HepG2	liver:	n/a
43	chr5:45696592-45696642	HUVEC	blood vessel:	n/a
44	chr5:45192536-45192586	CMK	blood:	n/a
45	chr5:45678610-45678660	HUVEC	blood vessel:	n/a
46	chr5:45262329-45262379	GM12892	blood:	n/a
47	chr5:45262443-45262493	NH-A	brain:	n/a
48	chr5:45695643-45695693	AG09319	gingival:	n/a
49	chr5:45696465-45696515	MCF10A-Er-Src	breast:	n/a
50	chr5:45696592-45696642	HCF	heart:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:45292372..45295265-chr5:45301198..45304020,2	MCF-7	breast:
2	chr5:45189744..45191464-chr5:45191625..45193258,2	MCF-7	breast:
3	chr5:45292372..45295265-chr5:45301198..45304020,2	MCF-7	breast:
4	chr5:45635537..45637341-chr5:45642108..45644494,2	K562	blood:
5	chr5:45189744..45191464-chr5:45191625..45193258,2	MCF-7	breast:
6	chr5:45423533..45425292-chr5:45434104..45435924,2	MCF-7	breast:
7	chr5:45435601..45437646-chr5:45441992..45444757,2	K562	blood:
8	chr5:45487505..45488239-chr6:10695353..10695968,2	MCF-7	breast:
9	chr5:45232284..45234490-chr5:45416046..45418115,2	MCF-7	breast:
10	chr5:44952326..44952886-chr5:45639183..45639775,2	MCF-7	breast:
11	chr5:45259723..45261348-chr5:45262944..45264451,2	K562	blood:
12	chr16:3076387..3078714-chr5:45193841..45195630,2	MCF-7	breast:
13	chr5:45700474..45703420-chr5:45719507..45722171,2	MCF-7	breast:
14	chr5:45228553..45229390-chr6:23065553..23066212,2	MCF-7	breast:
15	chr5:45389967..45392520-chr5:45393920..45396887,2	K562	blood:
16	chr5:45688826..45690382-chr5:45691879..45693420,2	K562	blood:
17	chr13:55537336..55537947-chr5:45562607..45563107,2	MCF-7	breast:
18	chr5:44952200..44952811-chr5:45521283..45521849,2	MCF-7	breast:
19	chr1:205318512..205319277-chr5:45469628..45470349,2	MCF-7	breast:
20	chr5:45688826..45690382-chr5:45691879..45693420,2	K562	blood:
21	chr5:45435601..45437646-chr5:45441992..45444757,2	K562	blood:
22	chr5:45423533..45425292-chr5:45434104..45435924,2	MCF-7	breast:
23	chr5:45232284..45234490-chr5:45416046..45418115,2	MCF-7	breast:
24	chr3:104438340..104439030-chr5:45401914..45402431,2	MCF-7	breast:
25	chr5:45389967..45392520-chr5:45393920..45396887,2	K562	blood:
26	chr5:44356260..44358499-chr5:45223439..45226183,2	K562	blood:
27	chr15:66571588..66572090-chr5:45541388..45542303,2	MCF-7	breast:
28	chr5:45038409..45039119-chr5:45520902..45521831,4	MCF-7	breast:
29	chr5:45635537..45637341-chr5:45642108..45644494,2	K562	blood:
30	chr5:45038244..45038751-chr5:45773997..45774955,2	MCF-7	breast:
31	chr5:45468898..45471467-chr5:45477657..45479826,2	MCF-7	breast:
32	chr5:45259723..45261348-chr5:45262944..45264451,2	K562	blood:
33	chr11:62608627..62609151-chr5:45773998..45774657,2	MCF-7	breast:
34	chr5:44952363..44953098-chr5:45773975..45774930,2	MCF-7	breast:
35	chr5:45468898..45471467-chr5:45477657..45479826,2	MCF-7	breast:
36	chr5:45700474..45703420-chr5:45719507..45722171,2	MCF-7	breast:
37	chr17:56742322..56745282-chr5:45859385..45861280,2	MCF-7	breast:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MRPS30-14	chr5:45753168-45753300	NONHSAT101363
2	lnc-MRPS30-4	chr5:45227480-45227662	XLOC_004375
3	lnc-MRPS30-14	chr5:45752904-45753159	NONHSAT101363
4	lnc-MRPS30-14	chr5:45749057-45749335	NONHSAT101363
5	lnc-MRPS30-13	chr5:45574692-45576714	NONHSAT101361
6	lnc-MRPS30-4	chr5:45228193-45228451	XLOC_004375
7	lnc-MRPS30-12	chr5:45558021-45560088	NONHSAT101360
8	lnc-MRPS30-11	chr5:45212601-45212751	NONHSAT101357
9	lnc-MRPS30-11	chr5:45214560-45217161	NONHSAT101357
10	lnc-FGF10-4	chr5:45267793-45268115	ENSG00000251117.1
11	lnc-FGF10-4	chr5:45266826-45266920	ENSG00000251117.1

No data

Variant related genes	Relation type
ENSG00000250122	TF binding region
HCN1	TF binding region
ENSG00000250017	TF binding region
ENSG00000250422	TF binding region
ENSG00000250122	CpG island
HCN1	CpG island
ENSG00000250017	CpG island
ENSG00000250422	CpG island
ENSG00000199426	chromatin interactions

Extended variants
information (count: 13627 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:13627 , 50 per page) page: 1 2 3 4 5 6 7 ... 273

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575689738	chr5:45184117-45184118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184290095	chr5:45184130-45184131	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555586139	chr5:45184296-45184297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34386652	chr5:45184300-45184301	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149246466	chr5:45184325-45184326	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374662986	chr5:45184360-45184361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564769519	chr5:45184361-45184362	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs533196760	chr5:45184380-45184381	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372255360	chr5:45184381-45184382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146920840	chr5:45184397-45184398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563783428	chr5:45184434-45184435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs75904534	chr5:45184440-45184441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551509933	chr5:45184462-45184463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190738351	chr5:45184480-45184481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376553538	chr5:45184484-45184485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71616283	chr5:45184485-45184486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs555240140	chr5:45184507-45184508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182082992	chr5:45184559-45184560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138030706	chr5:45184593-45184594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs113954698	chr5:45184605-45184606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs539069876	chr5:45184606-45184607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs184637406	chr5:45184610-45184611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569305380	chr5:45184629-45184630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535199930	chr5:45184694-45184695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374302189	chr5:45184695-45184696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555025823	chr5:45184702-45184703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540814150	chr5:45184709-45184710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377486194	chr5:45184716-45184717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs541588756	chr5:45184746-45184747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558173506	chr5:45184790-45184791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs578167683	chr5:45184865-45184866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs543750691	chr5:45184883-45184884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs563721215	chr5:45184974-45184975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189203640	chr5:45185027-45185028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs147200141	chr5:45185072-45185073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543179561	chr5:45185081-45185082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559856263	chr5:45185086-45185087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs527496170	chr5:45185123-45185124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs547528935	chr5:45185137-45185138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs73099407	chr5:45185172-45185173	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs140489612	chr5:45185200-45185201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549782783	chr5:45185313-45185314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371158686	chr5:45185322-45185323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569345172	chr5:45185327-45185328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs535047449	chr5:45185350-45185351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548692077	chr5:45185370-45185371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373674422	chr5:45185377-45185378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs180680351	chr5:45185381-45185382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534918735	chr5:45185388-45185389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141386616	chr5:45185417-45185418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Thyroid cancer	19087340	CNVD
Liposarcoma	21253554	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cervical Cancer	21857958	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Oral cancer	21386901	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Ewing''s sarcoma	17952124	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cervical cancer	18559093	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	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
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Breast cancer	16608533	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Cervical squamous cell carcinoma	21590768	CNVD
Prostate cancer	21965145	CNVD
Cancer	21183584	CNVD
Ovarian cancer	20844748	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	22286061	CNVD
Lung cancer	18438408	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Breast cancer	17393978	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Hirschsprung''s Disease	21712996	CNVD
Intellectual disability	21811512	CNVD
Lung adenocarcinoma	21935476	CNVD
Myelofibrosis	22110671	CNVD
Intracranial aneurysm	16715129	CNVD
Multiple myeloma	16616336	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:853 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:45182400-45192400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr5:45184000-45184400	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr5:45184400-45192600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr5:45189200-45189400	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr5:45189600-45190000	Enhancers	Liver	Liver
6	chr5:45192400-45193200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr5:45192400-45193400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr5:45192400-45193400	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr5:45192600-45193400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr5:45195000-45195800	Enhancers	Brain Germinal Matrix	brain
11	chr5:45195200-45195600	Enhancers	Fetal Brain Female	brain
12	chr5:45200000-45205600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr5:45204000-45204400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr5:45204200-45204400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr5:45204400-45204600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr5:45204400-45204600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
17	chr5:45204600-45204800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr5:45204600-45205400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr5:45204600-45205600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr5:45204800-45205000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr5:45204800-45205600	Enhancers	H9 Cell Line	embryonic stem cell
22	chr5:45204800-45205800	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr5:45205000-45206600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr5:45205400-45205600	Enhancers	H1 Cell Line	embryonic stem cell
25	chr5:45205400-45205600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr5:45205400-45206200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr5:45205400-45206600	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr5:45205600-45206000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr5:45205600-45206200	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr5:45205600-45206400	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr5:45205600-45206600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr5:45205800-45206200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr5:45206200-45206800	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr5:45206200-45207200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr5:45206200-45207400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr5:45206400-45207200	Enhancers	H9 Cell Line	embryonic stem cell
37	chr5:45206600-45206800	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr5:45206600-45207000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr5:45206600-45207200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr5:45206600-45207800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
41	chr5:45206800-45207000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr5:45206800-45207400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
43	chr5:45207000-45207200	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr5:45207000-45207200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
45	chr5:45207000-45209800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr5:45207200-45208400	Weak transcription	H1 Cell Line	embryonic stem cell
47	chr5:45207200-45211000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr5:45207200-45216600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr5:45207800-45210000	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr5:45208400-45208800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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