Variant report

Variant	esv1810959
Chromosome Location	chr5:179945112-179997861
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:533)
CpG islands
(count:490)
Chromatin interactive
region (count:52)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179975587-179975877	K562	blood:	n/a	n/a
2	ARID3A	chr5:179980269-179980947	K562	blood:	n/a	n/a
3	ARID3A	chr5:179989773-179990046	K562	blood:	n/a	n/a
4	ARID3A	chr5:179982176-179983500	K562	blood:	n/a	n/a
5	ARID3A	chr5:179978584-179978636	K562	blood:	n/a	n/a
6	ATF1	chr5:179980451-179980815	K562	blood:	n/a	n/a
7	ATF1	chr5:179982258-179982960	K562	blood:	n/a	n/a
8	ATF2	chr5:179989676-179990117	GM12878	blood:	n/a	n/a
9	ATF2	chr5:179966866-179967742	GM12878	blood:	n/a	n/a
10	ATF2	chr5:179989638-179990187	GM12878	blood:	n/a	n/a
11	BACH1	chr5:179975564-179975823	K562	blood:	n/a	n/a
12	BATF	chr5:179989665-179990001	GM12878	blood:	n/a	n/a
13	BATF	chr5:179967060-179967643	GM12878	blood:	n/a	chr5:179967376-179967387
14	BATF	chr5:179967271-179967670	GM12878	blood:	n/a	chr5:179967376-179967387
15	BATF	chr5:179989718-179990055	GM12878	blood:	n/a	n/a
16	BCL11A	chr5:179967330-179967536	GM12878	blood:	n/a	n/a
17	BCL11A	chr5:179967329-179967703	GM12878	blood:	n/a	n/a
18	BCL3	chr5:179954713-179954975	GM12878	blood:	n/a	n/a
19	BCL3	chr5:179954691-179955054	GM12878	blood:	n/a	n/a
20	BCL3	chr5:179989720-179990061	GM12878	blood:	n/a	chr5:179989861-179989868
21	BCLAF1	chr5:179967270-179967735	GM12878	blood:	n/a	n/a
22	BHLHE40	chr5:179989676-179990195	GM12878	blood:	n/a	n/a
23	BHLHE40	chr5:179991026-179991295	GM12878	blood:	n/a	n/a
24	BHLHE40	chr5:179982128-179982802	K562	blood:	n/a	n/a
25	BHLHE40	chr5:179971806-179971955	K562	blood:	n/a	n/a
26	BHLHE40	chr5:179975767-179975857	K562	blood:	n/a	n/a
27	BHLHE40	chr5:179967103-179967608	GM12878	blood:	n/a	n/a
28	BHLHE40	chr5:179989714-179990142	K562	blood:	n/a	n/a
29	BHLHE40	chr5:179975467-179975475	K562	blood:	n/a	n/a
30	CBX3	chr5:179982155-179982664	K562	blood:	n/a	n/a
31	CCNT2	chr5:179980542-179980908	K562	blood:	n/a	chr5:179980612-179980632
32	CCNT2	chr5:179982238-179982594	K562	blood:	n/a	chr5:179982490-179982510
33	CCNT2	chr5:179989733-179990001	K562	blood:	n/a	n/a
34	CCNT2	chr5:179985379-179985579	K562	blood:	n/a	n/a
35	CCNT2	chr5:179975626-179975820	K562	blood:	n/a	n/a
36	CEBPB	chr5:179982676-179983046	A549	lung:	n/a	n/a
37	CEBPB	chr5:179982533-179983142	A549	lung:	n/a	n/a
38	CEBPB	chr5:179980388-179980958	K562	blood:	n/a	n/a
39	CEBPB	chr5:179946180-179946318	Hela-S3	cervix:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
40	CEBPB	chr5:179980436-179980905	K562	blood:	n/a	n/a
41	CEBPB	chr5:179982651-179982986	A549	lung:	n/a	n/a
42	CEBPB	chr5:179946221-179946350	A549	lung:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
43	CEBPB	chr5:179982676-179983049	IMR90	lung:	n/a	n/a
44	CEBPB	chr5:179982311-179982910	K562	blood:	n/a	n/a
45	CEBPB	chr5:179982173-179982883	K562	blood:	n/a	n/a
46	CEBPB	chr5:179989813-179989992	K562	blood:	n/a	n/a
47	CEBPB	chr5:179946110-179946453	IMR90	lung:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
48	CEBPB	chr5:179946168-179946373	HepG2	liver:	n/a	chr5:179946274-179946287 chr5:179946275-179946286
49	CEBPD	chr5:179989648-179990082	K562	blood:	n/a	n/a
50	CEBPD	chr5:179980482-179980861	K562	blood:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179961652-179961702	HepG2	liver:	n/a
2	chr5:179962105-179962155	RPTEC	kidney:	n/a
3	chr5:179961652-179961702	HepG2	liver:	n/a
4	chr5:179962105-179962155	RPTEC	kidney:	n/a
5	chr5:179982651-179982701	CMK	blood:	n/a
6	chr5:179987837-179987887	RPTEC	kidney:	n/a
7	chr5:179982651-179982701	RPTEC	kidney:	n/a
8	chr5:179982651-179982701	AG04450	lung:	fetal
9	chr5:179961652-179961702	CMK	blood:	n/a
10	chr5:179982651-179982701	HCPEpiC	choroid plexus:	n/a
11	chr5:179987837-179987887	A549	lung:	n/a
12	chr5:179961903-179961953	U87	brain:	n/a
13	chr5:179962105-179962155	SAEC	small airway:	n/a
14	chr5:179987837-179987887	LNCaP	prostate:	n/a
15	chr5:179958483-179958533	H1-hESC	embryonic stem cell:	embryo
16	chr5:179987837-179987887	HCM	heart:	n/a
17	chr5:179958483-179958533	ovcar-3	ovarian:	n/a
18	chr5:179958483-179958533	BE2_C	brain:	n/a
19	chr5:179958483-179958533	LNCaP	prostate:	n/a
20	chr5:179958483-179958533	HCPEpiC	choroid plexus:	n/a
21	chr5:179950726-179950776	CMK	blood:	n/a
22	chr5:179958313-179958363	HIPEpiC	eye:	n/a
23	chr5:179961652-179961702	A549	lung:	n/a
24	chr5:179961903-179961953	SKMC	muscle:	n/a
25	chr5:179982651-179982701	HNPCEpiC	eye:	n/a
26	chr5:179962105-179962155	NHBE	bronchial:	n/a
27	chr5:179950726-179950776	K562	blood:	n/a
28	chr5:179962105-179962155	CMK	blood:	n/a
29	chr5:179962105-179962155	NB4	blood:	n/a
30	chr5:179961903-179961953	SK-N-SH_RA	brain:	n/a
31	chr5:179958313-179958363	HEEpiC	esophagus:	n/a
32	chr5:179950726-179950776	NB4	blood:	n/a
33	chr5:179961903-179961953	HL-60	blood:	n/a
34	chr5:179962105-179962155	PrEC	prostate:	n/a
35	chr5:179982651-179982701	HAEpiC	amniotic membrane:	n/a
36	chr5:179958313-179958363	MCF-7	breast:	n/a
37	chr5:179961903-179961953	GM12892	blood:	n/a
38	chr5:179961903-179961953	NT2-D1	testis:	n/a
39	chr5:179961652-179961702	AG04450	lung:	fetal
40	chr5:179958313-179958363	HRCEpiC	kidney:	n/a
41	chr5:179987837-179987887	Hela-S3	cervix:	n/a
42	chr5:179958483-179958533	SAEC	small airway:	n/a
43	chr5:179987837-179987887	NHBE	bronchial:	n/a
44	chr5:179958483-179958533	A549	lung:	n/a
45	chr5:179982651-179982701	GM12891	blood:	n/a
46	chr5:179961652-179961702	MCF10A-Er-Src	breast:	n/a
47	chr5:179987837-179987887	NHDF-neo	bronchial:	n/a
48	chr5:179982651-179982701	SK-N-MC	brain:	n/a
49	chr5:179987837-179987887	MCF-7	breast:	n/a
50	chr5:179961652-179961702	HUVEC	blood vessel:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr5:179935454..179937135-chr5:179951603..179954291,2	MCF-7	breast:
2	chr5:179919729..179922158-chr5:179992133..179994057,2	MCF-7	breast:
3	chr5:179971098..179973715-chr5:179974219..179975941,2	MCF-7	breast:
4	chr5:179919689..179923000-chr5:179977820..179981821,3	K562	blood:
5	chr5:179982448..179984121-chr5:179987078..179988868,3	K562	blood:
6	chr5:179975334..179978058-chr5:179994170..179996114,2	MCF-7	breast:
7	chr5:179992805..179995123-chr5:179996913..179999172,2	K562	blood:
8	chr5:179977718..179980387-chr5:179982082..179983928,2	MCF-7	breast:
9	chr5:179923854..179927597-chr5:179974532..179977818,3	MCF-7	breast:
10	chr5:179982448..179984121-chr5:179987078..179988868,3	K562	blood:
11	chr5:179982621..179985082-chr5:179986194..179988848,3	K562	blood:
12	chr5:179944903..179947278-chr5:179974741..179976598,2	MCF-7	breast:
13	chr5:179987845..179991399-chr5:179992538..179995326,4	K562	blood:
14	chr5:179946293..179947943-chr5:179949478..179951199,2	MCF-7	breast:
15	chr5:179991328..179993518-chr5:179994470..179996881,2	K562	blood:
16	chr5:179943961..179945573-chr5:179952586..179955313,2	MCF-7	breast:
17	chr5:179987248..179989879-chr5:180004376..180006674,2	MCF-7	breast:
18	chr5:179978847..179981539-chr5:179988349..179990200,2	K562	blood:
19	chr5:179919703..179922578-chr5:179977796..179980500,2	MCF-7	breast:
20	chr5:179951354..179953735-chr5:179973821..179976240,2	K562	blood:
21	chr5:179985555..179987224-chr5:179991936..179994332,2	MCF-7	breast:
22	chr5:179944903..179947278-chr5:179974741..179976598,2	MCF-7	breast:
23	chr5:179951729..179953788-chr5:179957919..179959696,2	MCF-7	breast:
24	chr5:179982621..179985082-chr5:179986194..179988848,3	K562	blood:
25	chr5:179978847..179981539-chr5:179988349..179990200,2	K562	blood:
26	chr5:179992805..179995123-chr5:179996913..179999172,2	K562	blood:
27	chr5:179991328..179993518-chr5:179994470..179996881,2	K562	blood:
28	chr5:179921441..179923328-chr5:179994530..179996709,2	MCF-7	breast:
29	chr5:179975222..179976782-chr5:179978271..179981266,2	K562	blood:
30	chr5:179986356..179988734-chr5:179996759..179998539,2	K562	blood:
31	chr5:179975222..179976782-chr5:179978271..179981266,2	K562	blood:
32	chr5:179986356..179988734-chr5:179996759..179998539,2	K562	blood:
33	chr5:179951729..179953788-chr5:179957919..179959696,2	MCF-7	breast:
34	chr5:179951354..179953735-chr5:179973821..179976240,2	K562	blood:
35	chr5:179996392..179998893-chr5:180054015..180056843,2	K562	blood:
36	chr5:179954302..179955834-chr5:179973302..179975583,2	K562	blood:
37	chr5:179971098..179973715-chr5:179974219..179975941,2	MCF-7	breast:
38	chr5:179921323..179924030-chr5:179984115..179985925,2	K562	blood:
39	chr5:179990995..179993150-chr5:180017683..180019570,2	K562	blood:
40	chr5:179910027..179911879-chr5:179947833..179949549,2	MCF-7	breast:
41	chr5:179949366..179951227-chr5:180284274..180286708,2	K562	blood:
42	chr5:179943961..179945573-chr5:179952586..179955313,2	MCF-7	breast:
43	chr5:179977718..179980387-chr5:179982082..179983928,2	MCF-7	breast:
44	chr3:158973363..158973863-chr5:179971569..179972230,2	MCF-7	breast:
45	chr5:179725066..179727186-chr5:179974697..179977225,2	K562	blood:
46	chr5:179987845..179991399-chr5:179992538..179995326,4	K562	blood:
47	chr5:179985555..179987224-chr5:179991936..179994332,2	MCF-7	breast:
48	chr5:179920138..179923580-chr5:179954774..179958751,3	MCF-7	breast:
49	chr5:179946293..179947943-chr5:179949478..179951199,2	MCF-7	breast:
50	chr5:179975334..179978058-chr5:179994170..179996114,2	MCF-7	breast:

No data

Variant related genes	Relation type
CNOT6	TF binding region
ENSG00000250749	TF binding region
CNOT6	CpG island
ENSG00000250749	CpG island
ENSG00000113300	chromatin interactions
ENSG00000161055	chromatin interactions
ENSG00000037280	chromatin interactions

Extended variants
information (count: 2267 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2267 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548270134	chr5:179945166-179945167	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568167847	chr5:179945190-179945191	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs377692313	chr5:179945202-179945203	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533722409	chr5:179945223-179945224	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs115321308	chr5:179945251-179945252	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138333110	chr5:179945259-179945260	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs386695773	chr5:179945334-179945335	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs6899301	chr5:179945336-179945337	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs62405526	chr5:179945337-179945338	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs149638388	chr5:179945365-179945366	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368095691	chr5:179945379-179945380	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146137217	chr5:179945390-179945391	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371660704	chr5:179945405-179945406	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572222276	chr5:179945415-179945416	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs541248310	chr5:179945476-179945477	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs548193430	chr5:179945497-179945498	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs199537604	chr5:179945504-179945505	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576599916	chr5:179945506-179945507	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377228627	chr5:179945648-179945649	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542004033	chr5:179945680-179945681	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563980669	chr5:179945720-179945721	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140118786	chr5:179945801-179945802	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs59207572	chr5:179945805-179945806	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs17080384	chr5:179945827-179945828	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs200072918	chr5:179945865-179945866	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs568129726	chr5:179945892-179945893	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs541420846	chr5:179945902-179945903	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs527417081	chr5:179945915-179945916	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs11742141	chr5:179945933-179945934	Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs11949203	chr5:179946059-179946060	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs72811164	chr5:179946077-179946078	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs375457648	chr5:179946107-179946108	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs72811166	chr5:179946108-179946109	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs371867742	chr5:179946125-179946126	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs568246172	chr5:179946184-179946185	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs569635795	chr5:179946187-179946188	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs535422799	chr5:179946203-179946204	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555374828	chr5:179946240-179946241	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374871714	chr5:179946242-179946243	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs144063538	chr5:179946262-179946263	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs72811168	chr5:179946289-179946290	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs551747393	chr5:179946298-179946299	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs558059194	chr5:179946307-179946308	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72812928	chr5:179946311-179946312	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs180707847	chr5:179946320-179946321	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs145975155	chr5:179946409-179946410	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570929570	chr5:179946469-179946470	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs148631057	chr5:179946496-179946497	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs80326979	chr5:179946505-179946506	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550259250	chr5:179946553-179946554	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
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
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1792 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179923400-179946000	Weak transcription	Primary B cells from peripheral blood	blood
2	chr5:179923600-179949800	Weak transcription	Gastric	stomach
3	chr5:179923600-179949800	Weak transcription	Psoas Muscle	Psoas
4	chr5:179923600-179957000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr5:179924000-179948000	Weak transcription	A549	lung
6	chr5:179924000-179949800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr5:179924200-179949200	Weak transcription	Pancreas	Pancrea
8	chr5:179924200-179949600	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr5:179924200-179950000	Weak transcription	Brain Angular Gyrus	brain
10	chr5:179924600-179949800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr5:179924600-179957000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr5:179925600-179945600	Weak transcription	Lung	lung
13	chr5:179925800-179949200	Weak transcription	Left Ventricle	heart
14	chr5:179926000-179947600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr5:179926800-179948600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr5:179927000-179946000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr5:179927000-179947800	Weak transcription	NHEK	skin
18	chr5:179927000-179948000	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr5:179927000-179954400	Weak transcription	Hela-S3	cervix
20	chr5:179927400-179945800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr5:179927400-179948200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr5:179927400-179948200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr5:179927400-179949200	Weak transcription	H1 Cell Line	embryonic stem cell
24	chr5:179927400-179949200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr5:179927400-179949600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr5:179928600-179945800	Weak transcription	Monocytes-CD14+_RO01746	blood
27	chr5:179929000-179959200	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr5:179929200-179945800	Weak transcription	Fetal Brain Female	brain
29	chr5:179931400-179946000	Weak transcription	Osteobl	bone
30	chr5:179933800-179950000	Weak transcription	Colon Smooth Muscle	Colon
31	chr5:179933800-179959000	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr5:179934200-179948400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr5:179934200-179949600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr5:179934200-179956600	Weak transcription	Rectal Smooth Muscle	rectum
35	chr5:179935000-179951000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr5:179935200-179951400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr5:179935400-179946000	Weak transcription	Primary hematopoietic stem cells	blood
38	chr5:179935400-179948000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
39	chr5:179935400-179948200	Weak transcription	Primary T cells from cord blood	blood
40	chr5:179935800-179945600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr5:179936800-179949200	Weak transcription	Thymus	Thymus
42	chr5:179936800-179949600	Weak transcription	Fetal Muscle Leg	muscle
43	chr5:179936800-179950000	Weak transcription	Fetal Stomach	stomach
44	chr5:179936800-179956200	Weak transcription	Fetal Muscle Trunk	muscle
45	chr5:179937400-179945600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr5:179937400-179948200	Weak transcription	Brain Anterior Caudate	brain
47	chr5:179938800-179956600	Weak transcription	HSMM	muscle
48	chr5:179939200-179948600	Weak transcription	Fetal Thymus	thymus
49	chr5:179939400-179947800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr5:179939600-179946000	Weak transcription	Primary B cells from cord blood	blood

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