Variant report

Variant	nsv1028498
Chromosome Location	chr5:80712364-80860430
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1217)
CpG islands
(count:123)
Chromatin interactive
region (count:81)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1217 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:80809841-80810204	K562	blood:	n/a	chr5:80809992-80810008
2	ARID3A	chr5:80849720-80849942	K562	blood:	n/a	n/a
3	ARID3A	chr5:80716144-80716203	HepG2	liver:	n/a	n/a
4	ARID3A	chr5:80802828-80803058	HepG2	liver:	n/a	n/a
5	ARID3A	chr5:80718482-80718934	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:80802753-80803141	K562	blood:	n/a	n/a
7	ARID3A	chr5:80812066-80812259	K562	blood:	n/a	n/a
8	ARID3A	chr5:80746498-80747192	HepG2	liver:	n/a	n/a
9	ARID3A	chr5:80849397-80849518	K562	blood:	n/a	n/a
10	ATF1	chr5:80821520-80821929	K562	blood:	n/a	n/a
11	ATF1	chr5:80714391-80714547	K562	blood:	n/a	n/a
12	ATF1	chr5:80716043-80716427	K562	blood:	n/a	n/a
13	ATF1	chr5:80802729-80803123	K562	blood:	n/a	n/a
14	ATF2	chr5:80802576-80803228	GM12878	blood:	n/a	n/a
15	ATF2	chr5:80802609-80803210	GM12878	blood:	n/a	n/a
16	ATF3	chr5:80802692-80803102	K562	blood:	n/a	n/a
17	ATF3	chr5:80718570-80718885	HepG2	liver:	n/a	n/a
18	BACH1	chr5:80721454-80721479	K562	blood:	n/a	n/a
19	BATF	chr5:80802740-80803008	GM12878	blood:	n/a	n/a
20	BATF	chr5:80802740-80803045	GM12878	blood:	n/a	n/a
21	BCLAF1	chr5:80802704-80803227	GM12878	blood:	n/a	chr5:80802820-80802829
22	BHLHE40	chr5:80802713-80803136	GM12878	blood:	n/a	n/a
23	BRCA1	chr5:80718528-80718912	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr5:80802759-80803143	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr5:80761651-80761655	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr5:80721332-80721798	Hela-S3	cervix:	n/a	n/a
27	CBX3	chr5:80797844-80798248	K562	blood:	n/a	n/a
28	CBX3	chr5:80715883-80716581	HCT-116	colon:	n/a	n/a
29	CCNT2	chr5:80721416-80721514	K562	blood:	n/a	n/a
30	CEBPB	chr5:80746753-80747110	H1-hESC	embryonic stem cell:	n/a	chr5:80747018-80747029
31	CEBPB	chr5:80746808-80747137	A549	lung:	n/a	chr5:80747018-80747029
32	CEBPB	chr5:80844961-80845312	IMR90	lung:	n/a	chr5:80845124-80845135
33	CEBPB	chr5:80802690-80803127	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr5:80813331-80813618	IMR90	lung:	n/a	n/a
35	CEBPB	chr5:80759917-80760181	HepG2	liver:	n/a	chr5:80760077-80760089 chr5:80760014-80760025
36	CEBPB	chr5:80777469-80777501	K562	blood:	n/a	n/a
37	CEBPB	chr5:80718433-80718900	IMR90	lung:	n/a	chr5:80718658-80718671
38	CEBPB	chr5:80802725-80803082	K562	blood:	n/a	n/a
39	CEBPB	chr5:80802715-80803088	IMR90	lung:	n/a	n/a
40	CEBPB	chr5:80718474-80718869	HepG2	liver:	n/a	chr5:80718658-80718671
41	CEBPB	chr5:80718582-80718713	HepG2	liver:	n/a	chr5:80718658-80718671
42	CEBPB	chr5:80746893-80747132	MCF-7	breast:	n/a	chr5:80747018-80747029
43	CEBPB	chr5:80746783-80747186	HepG2	liver:	n/a	chr5:80747018-80747029
44	CEBPB	chr5:80712877-80713415	HCT-116	colon:	n/a	n/a
45	CEBPB	chr5:80844983-80845292	A549	lung:	n/a	chr5:80845124-80845135
46	CEBPB	chr5:80718511-80718949	A549	lung:	n/a	chr5:80718658-80718671
47	CEBPB	chr5:80746331-80747194	HepG2	liver:	n/a	chr5:80747018-80747029
48	CEBPB	chr5:80845000-80845220	MCF-7	breast:	n/a	chr5:80845124-80845135
49	CEBPB	chr5:80813343-80813611	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:80802733-80803067	A549	lung:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:80795179-80795229	CMK	blood:	n/a
2	chr5:80795179-80795229	CMK	blood:	n/a
3	chr5:80795179-80795229	HEEpiC	esophagus:	n/a
4	chr5:80716263-80716313	Hela-S3	cervix:	n/a
5	chr5:80716263-80716313	GM06990	blood:	n/a
6	chr5:80795179-80795229	PANC-1	pancreas:	n/a
7	chr5:80795179-80795229	GM12892	blood:	n/a
8	chr5:80716263-80716313	HAEpiC	amniotic membrane:	n/a
9	chr5:80795179-80795229	HNPCEpiC	eye:	n/a
10	chr5:80716263-80716313	SK-N-SH	brain:	n/a
11	chr5:80716263-80716313	HEK293	kidney:	embryo
12	chr5:80795179-80795229	ProgFib	skin:	n/a
13	chr5:80795179-80795229	IMR90	lung:	fetal
14	chr5:80795179-80795229	NH-A	brain:	n/a
15	chr5:80716263-80716313	Caco-2	colon:	n/a
16	chr5:80795179-80795229	ECC-1	luminal epithelium:	n/a
17	chr5:80795179-80795229	U87	brain:	n/a
18	chr5:80716263-80716313	HCPEpiC	choroid plexus:	n/a
19	chr5:80716263-80716313	MCF10A-Er-Src	breast:	n/a
20	chr5:80716263-80716313	AG09319	gingival:	n/a
21	chr5:80795179-80795229	NHDF-neo	bronchial:	n/a
22	chr5:80795179-80795229	AoSMC	blood vessel:	n/a
23	chr5:80795179-80795229	HepG2	liver:	n/a
24	chr5:80795179-80795229	NT2-D1	testis:	n/a
25	chr5:80716263-80716313	SK-N-SH_RA	brain:	n/a
26	chr5:80716263-80716313	NHBE	bronchial:	n/a
27	chr5:80716263-80716313	NH-A	brain:	n/a
28	chr5:80795179-80795229	PrEC	prostate:	n/a
29	chr5:80716263-80716313	PANC-1	pancreas:	n/a
30	chr5:80716263-80716313	ECC-1	luminal epithelium:	n/a
31	chr5:80795179-80795229	HRPEpiC	eye:	n/a
32	chr5:80795179-80795229	SK-N-SH	brain:	n/a
33	chr5:80716263-80716313	RPTEC	kidney:	n/a
34	chr5:80795179-80795229	HUVEC	blood vessel:	n/a
35	chr5:80716263-80716313	PrEC	prostate:	n/a
36	chr5:80795179-80795229	HEK293	kidney:	embryo
37	chr5:80716263-80716313	AG04450	lung:	fetal
38	chr5:80716263-80716313	IMR90	lung:	fetal
39	chr5:80795179-80795229	BE2_C	brain:	n/a
40	chr5:80716263-80716313	A549	lung:	n/a
41	chr5:80716263-80716313	H1-hESC	embryonic stem cell:	embryo
42	chr5:80716263-80716313	AG10803	skin:	n/a
43	chr5:80795179-80795229	SKMC	muscle:	n/a
44	chr5:80795179-80795229	NHBE	bronchial:	n/a
45	chr5:80716263-80716313	HUVEC	blood vessel:	n/a
46	chr5:80716263-80716313	HCF	heart:	n/a
47	chr5:80716263-80716313	AG09309	skin:	n/a
48	chr5:80795179-80795229	Hepatocyte	liver:	n/a
49	chr5:80716263-80716313	HPAEpiC	pulmonary alveolar:	n/a
50	chr5:80795179-80795229	LNCaP	prostate:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:80755024..80758673-chr5:80763976..80766268,3	K562	blood:
2	chr5:80789170..80791164-chr5:80794505..80797059,2	K562	blood:
3	chr5:80754955..80756530-chr5:80760992..80762774,2	K562	blood:
4	chr5:80804010..80805576-chr5:80828120..80830137,2	K562	blood:
5	chr5:80807758..80809776-chr5:80812780..80814946,2	K562	blood:
6	chr5:80763988..80765693-chr5:80769242..80771448,2	K562	blood:
7	chr5:80804010..80805576-chr5:80828120..80830137,2	K562	blood:
8	chr5:80755024..80758673-chr5:80763976..80766268,3	K562	blood:
9	chr5:80797821..80800021-chr5:80804544..80806893,2	K562	blood:
10	chr5:80705493..80708422-chr5:80713834..80715686,2	K562	blood:
11	chr5:80713886..80715612-chr5:80719927..80721805,2	K562	blood:
12	chr5:80809463..80812209-chr5:80829247..80831979,2	K562	blood:
13	chr5:80808501..80811000-chr5:81045914..81048051,2	MCF-7	breast:
14	chr5:80848254..80852026-chr5:80853882..80857592,4	K562	blood:
15	chr5:80705376..80707322-chr5:80721977..80724375,2	K562	blood:
16	chr5:80842997..80845139-chr5:81045840..81047643,2	MCF-7	breast:
17	chr5:80810187..80812295-chr5:80817394..80821079,3	K562	blood:
18	chr5:80802610..80803123-chr5:81461507..81462444,2	MCF-7	breast:
19	chr5:80721205..80721977-chr5:81461493..81462401,2	K562	blood:
20	chr5:80768944..80770618-chr5:80775514..80777278,2	K562	blood:
21	chr5:80760814..80762946-chr5:80766170..80768156,2	MCF-7	breast:
22	chr5:80764193..80766521-chr5:80769242..80771330,2	K562	blood:
23	chr5:80810187..80812295-chr5:80817394..80821079,3	K562	blood:
24	chr5:80809576..80810094-chr5:81044225..81044774,2	MCF-7	breast:
25	chr5:80784791..80786688-chr5:80790192..80793142,3	K562	blood:
26	chr5:80810454..80812112-chr5:80812984..80815281,2	K562	blood:
27	chr5:80721446..80723519-chr5:80723791..80726002,2	MCF-7	breast:
28	chr5:80803472..80805493-chr5:81046109..81048770,2	K562	blood:
29	chr5:80725023..80728216-chr5:80731290..80736124,4	MCF-7	breast:
30	chr5:80764193..80766521-chr5:80769242..80771330,2	K562	blood:
31	chr5:80848254..80852026-chr5:80853882..80857592,4	K562	blood:
32	chr5:80853359..80856106-chr5:80858395..80860848,2	K562	blood:
33	chr5:80818037..80820072-chr5:80821098..80823290,2	K562	blood:
34	chr5:80812937..80815009-chr5:80816402..80819126,2	MCF-7	breast:
35	chr5:80721034..80721965-chr5:81134326..81134999,2	K562	blood:
36	chr5:80757422..80759303-chr5:80761432..80763460,2	K562	blood:
37	chr5:80846060..80848703-chr5:80848977..80851148,2	MCF-7	breast:
38	chr5:80810454..80812112-chr5:80812984..80815281,2	K562	blood:
39	chr5:80818057..80820183-chr5:80829963..80832323,2	K562	blood:
40	chr5:80784791..80786688-chr5:80790192..80793142,3	K562	blood:
41	chr5:80818037..80820072-chr5:80821098..80823290,2	K562	blood:
42	chr5:80763988..80765693-chr5:80769242..80771448,2	K562	blood:
43	chr5:80787085..80790084-chr5:80793682..80796599,2	MCF-7	breast:
44	chr5:80846060..80848703-chr5:80848977..80851148,2	MCF-7	breast:
45	chr5:80802774..80803458-chr5:81044304..81045045,2	MCF-7	breast:
46	chr5:80812504..80815105-chr5:80816670..80818298,2	K562	blood:
47	chr5:80793049..80793949-chr8:127349056..127349904,2	MCF-7	breast:
48	chr5:80723383..80725570-chr5:80725878..80728362,2	K562	blood:
49	chr5:80757299..80759638-chr5:80770497..80773294,2	MCF-7	breast:
50	chr5:80819955..80822161-chr5:80822941..80824763,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ACOT12-9	chr5:80813191-80815724	NONHSAT102466

No data

Variant related genes	Relation type
SSBP2	TF binding region
SSBP2	CpG island
ENSG00000145687	chromatin interactions

Extended variants
information (count: 4798 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:4798 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549815400	chr5:80712366-80712367	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs569884263	chr5:80712368-80712369	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs535312113	chr5:80712415-80712416	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139211667	chr5:80712424-80712425	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs190660059	chr5:80712463-80712464	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534389623	chr5:80712527-80712528	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557804821	chr5:80712550-80712551	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs115982186	chr5:80712566-80712567	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs180897815	chr5:80712571-80712572	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187011158	chr5:80712576-80712577	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs532421331	chr5:80712597-80712598	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547494841	chr5:80712602-80712603	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192465462	chr5:80712750-80712751	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs563046707	chr5:80712783-80712784	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576808583	chr5:80712811-80712812	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542483238	chr5:80712824-80712825	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562252137	chr5:80712829-80712830	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182871962	chr5:80712885-80712886	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537487912	chr5:80712911-80712912	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34161096	chr5:80712943-80712944	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs564562624	chr5:80712977-80712978	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533174863	chr5:80713000-80713001	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550146061	chr5:80713006-80713007	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117620086	chr5:80713033-80713034	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs11949697	chr5:80713096-80713097	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs548792320	chr5:80713112-80713113	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565558008	chr5:80713148-80713149	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534478251	chr5:80713181-80713182	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186005668	chr5:80713293-80713294	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs78668688	chr5:80713305-80713306	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs371829064	chr5:80713335-80713336	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1054799	chr5:80713340-80713341	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116580567	chr5:80713365-80713366	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs144910826	chr5:80713390-80713391	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79280665	chr5:80713440-80713441	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542520148	chr5:80713457-80713458	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562341659	chr5:80713573-80713574	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs190566119	chr5:80713587-80713588	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541565931	chr5:80713628-80713629	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182434693	chr5:80713630-80713631	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs535947297	chr5:80713634-80713635	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533456070	chr5:80713724-80713725	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs549938329	chr5:80713776-80713777	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563317834	chr5:80713777-80713778	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs76020813	chr5:80713854-80713855	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570362781	chr5:80713855-80713856	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs146698071	chr5:80713875-80713876	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs528279096	chr5:80714031-80714032	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs76153773	chr5:80714048-80714049	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs571298049	chr5:80714093-80714094	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Prostate cancer	21965145	CNVD
Ovarian cancer	20844748	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
Oral cancer	21386901	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	19602461	CNVD
Esophageal adenocarcinoma	18519675	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
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
lymphocytic leukemia	21291569	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Testicular cancer	18059402	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Tetralogy of Fallot	22912587	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:80693400-80721600	Weak transcription	Fetal Brain Male	brain
2	chr5:80693800-80714600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr5:80694800-80722400	Weak transcription	Aorta	Aorta
4	chr5:80695400-80716000	Weak transcription	Brain Angular Gyrus	brain
5	chr5:80697200-80739600	Weak transcription	Left Ventricle	heart
6	chr5:80697400-80716000	Weak transcription	Fetal Muscle Trunk	muscle
7	chr5:80698200-80716000	Weak transcription	Thymus	Thymus
8	chr5:80700200-80715000	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr5:80700400-80712400	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr5:80701600-80715800	Weak transcription	Brain Anterior Caudate	brain
11	chr5:80701600-80715800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr5:80701800-80722000	Weak transcription	Ovary	ovary
13	chr5:80702000-80716000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr5:80702200-80733600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr5:80702400-80715800	Weak transcription	Stomach Smooth Muscle	stomach
16	chr5:80703200-80714000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr5:80703200-80714000	Weak transcription	Primary B cells from peripheral blood	blood
18	chr5:80703200-80779200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr5:80703400-80716000	Weak transcription	Fetal Brain Female	brain
20	chr5:80704000-80716800	Weak transcription	Colon Smooth Muscle	Colon
21	chr5:80704400-80721600	Weak transcription	Fetal Stomach	stomach
22	chr5:80704400-80747600	Weak transcription	Placenta	Placenta
23	chr5:80704600-80721600	Weak transcription	Fetal Kidney	kidney
24	chr5:80704800-80712400	Weak transcription	Primary hematopoietic stem cells	blood
25	chr5:80705200-80712400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:80705200-80713000	Weak transcription	Adipose Nuclei	Adipose
27	chr5:80705400-80713000	Weak transcription	NHDF-Ad	bronchial
28	chr5:80705600-80722000	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr5:80706400-80713000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr5:80706400-80715600	Weak transcription	NHLF	lung
31	chr5:80706400-80715800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr5:80706600-80715600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr5:80706600-80716000	Weak transcription	Fetal Muscle Leg	muscle
34	chr5:80707200-80714000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
35	chr5:80707200-80715600	Weak transcription	HSMM	muscle
36	chr5:80707400-80748400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr5:80708000-80722400	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr5:80708000-80729400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr5:80708200-80721600	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr5:80708600-80714200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr5:80708800-80714200	Weak transcription	Fetal Lung	lung
42	chr5:80709000-80715000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr5:80709200-80715000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr5:80709200-80755200	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr5:80709400-80715200	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr5:80710400-80718400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr5:80710400-80721600	Strong transcription	Fetal Thymus	thymus
48	chr5:80710600-80721600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr5:80711000-80716000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr5:80711200-80713800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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