Variant report

Variant	nsv537882
Chromosome Location	chr5:118488501-118607405
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1279)
CpG islands
(count:918)
Chromatin interactive
region (count:92)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:3)

(count:1279 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:118565756-118565843	K562	blood:	n/a	n/a
2	ARID3A	chr5:118606863-118607063	K562	blood:	n/a	n/a
3	ARID3A	chr5:118516050-118516311	K562	blood:	n/a	n/a
4	ARID3A	chr5:118503944-118504095	K562	blood:	n/a	n/a
5	ARID3A	chr5:118505094-118505244	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:118591724-118592031	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:118554812-118555173	HepG2	liver:	n/a	n/a
8	ATF1	chr5:118603713-118604086	K562	blood:	n/a	n/a
9	ATF1	chr5:118515900-118516243	K562	blood:	n/a	n/a
10	ATF1	chr5:118604556-118605166	K562	blood:	n/a	n/a
11	ATF1	chr5:118494181-118494265	K562	blood:	n/a	n/a
12	ATF2	chr5:118603565-118604586	GM12878	blood:	n/a	n/a
13	ATF2	chr5:118556197-118556741	GM12878	blood:	n/a	n/a
14	ATF2	chr5:118556225-118556630	GM12878	blood:	n/a	n/a
15	ATF3	chr5:118604459-118604753	K562	blood:	n/a	n/a
16	ATF3	chr5:118523560-118523863	GM12878	blood:	n/a	chr5:118523740-118523749
17	BACH1	chr5:118604432-118604859	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCLAF1	chr5:118603696-118605414	GM12878	blood:	n/a	chr5:118604659-118604672 chr5:118604655-118604668 chr5:118604239-118604252
19	BCLAF1	chr5:118603942-118604715	GM12878	blood:	n/a	chr5:118604659-118604672 chr5:118604655-118604668 chr5:118604239-118604252
20	BHLHE40	chr5:118591568-118591967	HepG2	liver:	n/a	n/a
21	BHLHE40	chr5:118604935-118605354	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:118603717-118605368	K562	blood:	n/a	n/a
23	BHLHE40	chr5:118603723-118604934	HepG2	liver:	n/a	n/a
24	BHLHE40	chr5:118603661-118604624	GM12878	blood:	n/a	n/a
25	BRCA1	chr5:118603773-118604195	H1-hESC	embryonic stem cell:	n/a	n/a
26	BRCA1	chr5:118604032-118604440	GM12878	blood:	n/a	n/a
27	BRCA1	chr5:118604267-118604673	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr5:118604429-118604629	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr5:118604416-118604566	HepG2	liver:	n/a	n/a
30	CBX3	chr5:118593081-118593712	K562	blood:	n/a	n/a
31	CBX3	chr5:118603518-118605307	K562	blood:	n/a	n/a
32	CBX3	chr5:118593138-118593677	K562	blood:	n/a	n/a
33	CBX3	chr5:118591281-118592096	K562	blood:	n/a	n/a
34	CBX3	chr5:118591346-118591586	K562	blood:	n/a	n/a
35	CCNT2	chr5:118604019-118605526	K562	blood:	n/a	chr5:118604994-118605014
36	CEBPB	chr5:118604496-118604603	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr5:118586985-118587207	HepG2	liver:	n/a	chr5:118587063-118587074
38	CEBPB	chr5:118605293-118605601	K562	blood:	n/a	n/a
39	CEBPB	chr5:118526538-118526738	K562	blood:	n/a	n/a
40	CEBPB	chr5:118604861-118605078	K562	blood:	n/a	n/a
41	CEBPB	chr5:118551405-118551516	HepG2	liver:	n/a	chr5:118551454-118551465
42	CEBPB	chr5:118551438-118551493	IMR90	lung:	n/a	chr5:118551454-118551465
43	CEBPB	chr5:118604118-118605628	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr5:118533208-118533331	HepG2	liver:	n/a	chr5:118533223-118533234
45	CEBPB	chr5:118605001-118605574	HepG2	liver:	n/a	n/a
46	CEBPB	chr5:118595580-118595645	K562	blood:	n/a	n/a
47	CEBPB	chr5:118593405-118593627	K562	blood:	n/a	n/a
48	CEBPB	chr5:118579154-118579159	HepG2	liver:	n/a	n/a
49	CEBPB	chr5:118606749-118607035	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr5:118586900-118587201	IMR90	lung:	n/a	chr5:118587063-118587074

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:118603742-118603792	SKMC	muscle:	n/a
2	chr5:118603742-118603792	ECC-1	luminal epithelium:	n/a
3	chr5:118603908-118603958	AG09319	gingival:	n/a
4	chr5:118603742-118603792	SKMC	muscle:	n/a
5	chr5:118603742-118603792	ECC-1	luminal epithelium:	n/a
6	chr5:118603908-118603958	AG09319	gingival:	n/a
7	chr5:118604807-118604857	HMEC	breast:	n/a
8	chr5:118604833-118604883	HPAEpiC	pulmonary alveolar:	n/a
9	chr5:118604833-118604883	Hepatocyte	liver:	n/a
10	chr5:118603908-118603958	HRPEpiC	eye:	n/a
11	chr5:118604833-118604883	AG10803	skin:	n/a
12	chr5:118603880-118603930	HRPEpiC	eye:	n/a
13	chr5:118604262-118604312	HCT-116	colon:	n/a
14	chr5:118604405-118604455	HIPEpiC	eye:	n/a
15	chr5:118603742-118603792	NHBE	bronchial:	n/a
16	chr5:118604540-118604590	NH-A	brain:	n/a
17	chr5:118604262-118604312	GM12892	blood:	n/a
18	chr5:118604833-118604883	RPTEC	kidney:	n/a
19	chr5:118502651-118502701	LNCaP	prostate:	n/a
20	chr5:118603804-118603854	Hela-S3	cervix:	n/a
21	chr5:118604405-118604455	NHBE	bronchial:	n/a
22	chr5:118603880-118603930	IMR90	lung:	fetal
23	chr5:118604943-118604993	BJ	skin:	n/a
24	chr5:118502651-118502701	HIPEpiC	eye:	n/a
25	chr5:118603880-118603930	BE2_C	brain:	n/a
26	chr5:118502651-118502701	HEK293	kidney:	embryo
27	chr5:118604833-118604883	NT2-D1	testis:	n/a
28	chr5:118584299-118584349	NT2-D1	testis:	n/a
29	chr5:118601101-118601151	HRCEpiC	kidney:	n/a
30	chr5:118502651-118502701	PFSK-1	brain:	n/a
31	chr5:118603908-118603958	PANC-1	pancreas:	n/a
32	chr5:118604405-118604455	HRPEpiC	eye:	n/a
33	chr5:118601101-118601151	RPTEC	kidney:	n/a
34	chr5:118603804-118603854	MCF10A-Er-Src	breast:	n/a
35	chr5:118604262-118604312	NT2-D1	testis:	n/a
36	chr5:118601101-118601151	GM12891	blood:	n/a
37	chr5:118601101-118601151	SK-N-SH_RA	brain:	n/a
38	chr5:118604943-118604993	A549	lung:	n/a
39	chr5:118603908-118603958	HMEC	breast:	n/a
40	chr5:118604807-118604857	LNCaP	prostate:	n/a
41	chr5:118601101-118601151	HEK293	kidney:	embryo
42	chr5:118603938-118603988	HRCEpiC	kidney:	n/a
43	chr5:118601101-118601151	NHBE	bronchial:	n/a
44	chr5:118584299-118584349	Hepatocyte	liver:	n/a
45	chr5:118584299-118584349	AoSMC	blood vessel:	n/a
46	chr5:118603742-118603792	PrEC	prostate:	n/a
47	chr5:118584299-118584349	ECC-1	luminal epithelium:	n/a
48	chr5:118584299-118584349	HCPEpiC	choroid plexus:	n/a
49	chr5:118601101-118601151	HCPEpiC	choroid plexus:	n/a
50	chr5:118603804-118603854	NT2-D1	testis:	n/a

(count:92 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:118605019..118607417-chr5:118636347..118638717,3	MCF-7	breast:
2	chr5:118603857..118604648-chr9:131709720..131710335,2	Hela-S3	cervix:
3	chr5:118583005..118584543-chr5:118587332..118589504,2	K562	blood:
4	chr5:118506899..118509414-chr5:118511277..118513937,2	MCF-7	breast:
5	chr1:33282573..33283573-chr5:118604777..118605431,2	Hela-S3	cervix:
6	chr11:64878891..64879742-chr5:118606808..118607308,2	NB4	blood:
7	chr5:118551365..118552971-chr5:118559798..118561455,2	K562	blood:
8	chr5:118560242..118562661-chr5:118578972..118580567,2	MCF-7	breast:
9	chr5:118553070..118555553-chr5:118571329..118573313,2	K562	blood:
10	chr5:118499661..118503036-chr5:118503421..118506608,3	K562	blood:
11	chr5:118586532..118588054-chr5:118602135..118604215,2	K562	blood:
12	chr5:118508746..118512101-chr5:118513302..118516471,4	K562	blood:
13	chr5:118548598..118551453-chr5:118553322..118554885,2	MCF-7	breast:
14	chr5:118581217..118584329-chr5:118602907..118604848,3	K562	blood:
15	chr5:118574799..118576857-chr5:118580303..118583195,3	K562	blood:
16	chr5:118581886..118584543-chr5:118587332..118589504,3	K562	blood:
17	chr5:118503506..118505330-chr5:118525953..118528174,2	K562	blood:
18	chr5:118486635..118489506-chr5:118495369..118497251,2	K562	blood:
19	chr5:118593519..118596091-chr5:118597746..118599406,2	K562	blood:
20	chr5:118567020..118569794-chr5:118587970..118590169,2	K562	blood:
21	chr5:118494371..118496864-chr5:118503410..118506409,2	K562	blood:
22	chr5:118599452..118601690-chr5:118601827..118605890,4	K562	blood:
23	chr5:118551365..118552971-chr5:118559798..118561455,2	K562	blood:
24	chr5:118580319..118581889-chr5:118587199..118590009,2	K562	blood:
25	chr5:118542220..118543849-chr5:118544632..118547228,2	K562	blood:
26	chr5:118508746..118512101-chr5:118513302..118516471,4	K562	blood:
27	chr5:118604371..118606788-chr5:118640818..118642448,2	K562	blood:
28	chr5:118510458..118512160-chr5:118512976..118516180,3	K562	blood:
29	chr5:118607071..118610754-chr5:118620607..118623123,4	K562	blood:
30	chr5:118415616..118417740-chr5:118600067..118602902,2	MCF-7	breast:
31	chr5:118503506..118505330-chr5:118525953..118528174,2	K562	blood:
32	chr5:118605299..118606814-chr5:118613006..118614761,2	K562	blood:
33	chr5:118405445..118408256-chr5:118508657..118510829,2	MCF-7	breast:
34	chr5:118565495..118568249-chr5:118569908..118571816,2	K562	blood:
35	chr5:118580319..118581889-chr5:118587199..118590009,2	K562	blood:
36	chr3:48342633..48343492-chr5:118604190..118604719,2	HCT-116	colon:
37	chr13:111367305..111368155-chr5:118604250..118604937,2	NB4	blood:
38	chr5:118579079..118581230-chr5:118604088..118605942,2	MCF-7	breast:
39	chr5:118571373..118573245-chr5:118582858..118585572,2	K562	blood:
40	chr5:118604371..118606578-chr5:118640818..118642432,2	K562	blood:
41	chr5:118547822..118550227-chr5:118558352..118560676,2	K562	blood:
42	chr5:118583032..118585646-chr5:118590465..118591965,2	K562	blood:
43	chr5:118606735..118608940-chr5:118610555..118612827,2	MCF-7	breast:
44	chr5:118586532..118588054-chr5:118602135..118604215,2	K562	blood:
45	chr5:118573504..118576319-chr5:118580787..118583650,2	K562	blood:
46	chr2:105654308..105655008-chr5:118603902..118604609,2	HCT-116	colon:
47	chr5:118573504..118576319-chr5:118580787..118583650,2	K562	blood:
48	chr5:118597056..118599082-chr5:118600428..118603358,2	K562	blood:
49	chr5:118564790..118566564-chr5:118567290..118569739,2	MCF-7	breast:
50	chr5:118581886..118584543-chr5:118587332..118589504,3	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5706	chr5:118490341-118490362	MIMAT0022500

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	DMXL1	hsa-miR-92a-3p	chr5:118584515-118584522
2	DMXL1	hsa-miR-92a-3p	chr5:118584501-118584522
3	DMXL1	hsa-miR-9-5p	chr5:118584038-118584059

Variant related genes	Relation type
ENSG00000266587	TF binding region
TNFAIP8	TF binding region
MIR5706	TF binding region
DMXL1	TF binding region
ENSG00000266587	CpG island
TNFAIP8	CpG island
MIR5706	CpG island
DMXL1	CpG island
ENSG00000224509	chromatin interactions
ENSG00000172113	chromatin interactions
ENSG00000145779	chromatin interactions
ENSG00000172869	chromatin interactions
ENSG00000175283	chromatin interactions
ENSG00000266587	chromatin interactions
ENSG00000169570	chromatin interactions
ENSG00000095319	chromatin interactions
ENSG00000197956	chromatin interactions
ENSG00000249494	chromatin interactions
ENSG00000254501	chromatin interactions
ENSG00000134684	chromatin interactions
ENSG00000102007	chromatin interactions
ENSG00000149809	chromatin interactions
ENSG00000243333	chromatin interactions
ENSG00000116497	chromatin interactions
ENSG00000135972	chromatin interactions
ENSG00000173653	chromatin interactions
ENSG00000153487	chromatin interactions

Extended variants
information (count: 4725 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4725 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs367633409	chr5:118488506-118488507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531901149	chr5:118488512-118488513	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577319699	chr5:118488532-118488533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs545628294	chr5:118488598-118488599	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565339304	chr5:118488693-118488694	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140764679	chr5:118488712-118488713	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs547530300	chr5:118488742-118488743	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371232001	chr5:118488772-118488773	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149800279	chr5:118488775-118488776	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs144753521	chr5:118488796-118488797	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148454139	chr5:118488809-118488810	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569511341	chr5:118488814-118488815	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs573246464	chr5:118488840-118488841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs538562618	chr5:118488897-118488898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541642400	chr5:118488911-118488912	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs565557760	chr5:118488912-118488913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534484058	chr5:118488916-118488917	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs374991449	chr5:118488919-118488920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs373782389	chr5:118488924-118488925	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536689439	chr5:118488953-118488954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535436565	chr5:118488954-118488955	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576338782	chr5:118488984-118488985	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs80031024	chr5:118489029-118489030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs565544014	chr5:118489042-118489043	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs146512527	chr5:118489057-118489058	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182520192	chr5:118489070-118489071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186652914	chr5:118489082-118489083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190416435	chr5:118489086-118489087	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs367878450	chr5:118489126-118489127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs181235958	chr5:118489168-118489169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555673366	chr5:118489174-118489175	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113322253	chr5:118489216-118489217	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532100579	chr5:118489225-118489226	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs62374141	chr5:118489244-118489245	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs78411387	chr5:118489359-118489360	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs534539169	chr5:118489373-118489374	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs141128758	chr5:118489403-118489404	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs76956245	chr5:118489424-118489425	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs567465535	chr5:118489427-118489428	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs536349044	chr5:118489444-118489445	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs556578771	chr5:118489459-118489460	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs143134005	chr5:118489470-118489471	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs376707243	chr5:118489491-118489492	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs530830129	chr5:118489534-118489535	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs185533180	chr5:118489563-118489564	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs190245445	chr5:118489576-118489577	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs182174878	chr5:118489580-118489581	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs572766798	chr5:118489587-118489588	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs541694493	chr5:118489591-118489592	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs146666600	chr5:118489598-118489599	Strong transcription Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20531469	CNVD

Chromatin state (count:2608 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:118412200-118522800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr5:118450400-118496800	Weak transcription	Stomach Mucosa	stomach
3	chr5:118451200-118533400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr5:118453800-118522800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr5:118470000-118503200	Weak transcription	NH-A	brain
6	chr5:118472800-118504000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr5:118472800-118505000	Weak transcription	HepG2	liver
8	chr5:118473000-118497000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr5:118473400-118489200	Weak transcription	K562	blood
10	chr5:118473400-118496800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:118473800-118505000	Weak transcription	A549	lung
12	chr5:118478800-118491400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:118479000-118526000	Weak transcription	Fetal Brain Male	brain
14	chr5:118480000-118493000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:118480200-118490600	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr5:118480600-118489800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr5:118481600-118492800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr5:118481800-118488800	Strong transcription	HUES64 Cell Line	embryonic stem cell
19	chr5:118481800-118493200	Strong transcription	Monocytes-CD14+_RO01746	blood
20	chr5:118482000-118491400	Strong transcription	HUES48 Cell Line	embryonic stem cell
21	chr5:118482000-118492400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr5:118482200-118491600	Strong transcription	Primary B cells from peripheral blood	blood
23	chr5:118482400-118489000	Strong transcription	Placenta	Placenta
24	chr5:118482400-118490200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr5:118482400-118490600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr5:118482400-118491600	Strong transcription	Duodenum Smooth Muscle	Duodenum
27	chr5:118482400-118491600	Strong transcription	Fetal Intestine Large	intestine
28	chr5:118482400-118492000	Strong transcription	Rectal Mucosa Donor 29	rectum
29	chr5:118482600-118490800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr5:118482600-118491600	Strong transcription	HUES6 Cell Line	embryonic stem cell
31	chr5:118482600-118492000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr5:118483000-118541400	Weak transcription	NHEK	skin
33	chr5:118484000-118490000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr5:118484800-118506400	Weak transcription	Fetal Heart	heart
35	chr5:118485200-118503800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
36	chr5:118485400-118489000	Weak transcription	Fetal Kidney	kidney
37	chr5:118485400-118500200	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr5:118485400-118506600	Weak transcription	HSMMtube	muscle
39	chr5:118485400-118522800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr5:118485600-118496800	Weak transcription	Gastric	stomach
41	chr5:118485600-118496800	Weak transcription	Spleen	Spleen
42	chr5:118485600-118500200	Weak transcription	HSMM	muscle
43	chr5:118485600-118515800	Weak transcription	Hela-S3	cervix
44	chr5:118485800-118489200	Weak transcription	Primary T cells from cord blood	blood
45	chr5:118485800-118489600	Weak transcription	Fetal Brain Female	brain
46	chr5:118485800-118489600	Weak transcription	Rectal Smooth Muscle	rectum
47	chr5:118485800-118489800	Weak transcription	Brain Cingulate Gyrus	brain
48	chr5:118485800-118490000	Weak transcription	Esophagus	oesophagus
49	chr5:118485800-118494200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr5:118485800-118496800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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