Variant report

Variant	nsv611149
Chromosome Location	chr8:43124666-43791691
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2524)
CpG islands
(count:2934)
Chromatin interactive
region (count:13)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2524 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:43786577-43787136	K562	blood:	n/a	n/a
2	ATF1	chr8:43785555-43785668	K562	blood:	n/a	n/a
3	ATF3	chr8:43147119-43147233	K562	blood:	n/a	n/a
4	ATF3	chr8:43136024-43136278	K562	blood:	n/a	n/a
5	ATF3	chr8:43135995-43136320	GM12878	blood:	n/a	n/a
6	ATF3	chr8:43136037-43136199	HepG2	liver:	n/a	n/a
7	ATF3	chr8:43135865-43136266	HepG2	liver:	n/a	n/a
8	BACH1	chr8:43572418-43572443	K562	blood:	n/a	n/a
9	BACH1	chr8:43790059-43790248	K562	blood:	n/a	n/a
10	BACH1	chr8:43654724-43654750	K562	blood:	n/a	n/a
11	BACH1	chr8:43779446-43779599	K562	blood:	n/a	n/a
12	BACH1	chr8:43717526-43717725	K562	blood:	n/a	n/a
13	BATF	chr8:43760193-43760718	GM12878	blood:	n/a	n/a
14	BATF	chr8:43789506-43789826	GM12878	blood:	n/a	n/a
15	BATF	chr8:43772038-43772467	GM12878	blood:	n/a	n/a
16	BATF	chr8:43790975-43791219	GM12878	blood:	n/a	n/a
17	BATF	chr8:43760917-43761158	GM12878	blood:	n/a	n/a
18	BATF	chr8:43790368-43790722	GM12878	blood:	n/a	n/a
19	BATF	chr8:43761295-43761752	GM12878	blood:	n/a	n/a
20	BATF	chr8:43789506-43789769	GM12878	blood:	n/a	n/a
21	BATF	chr8:43783535-43783800	GM12878	blood:	n/a	n/a
22	BATF	chr8:43790147-43790722	GM12878	blood:	n/a	n/a
23	BATF	chr8:43776273-43776586	GM12878	blood:	n/a	n/a
24	BATF	chr8:43771212-43771629	GM12878	blood:	n/a	n/a
25	BATF	chr8:43783610-43783797	GM12878	blood:	n/a	n/a
26	BATF	chr8:43771808-43772466	GM12878	blood:	n/a	n/a
27	BATF	chr8:43770392-43770728	GM12878	blood:	n/a	n/a
28	BATF	chr8:43785488-43786069	GM12878	blood:	n/a	n/a
29	BATF	chr8:43761208-43761764	GM12878	blood:	n/a	n/a
30	BATF	chr8:43764727-43764995	GM12878	blood:	n/a	n/a
31	BATF	chr8:43771245-43771622	GM12878	blood:	n/a	n/a
32	BATF	chr8:43759902-43760143	GM12878	blood:	n/a	n/a
33	BATF	chr8:43760280-43760716	GM12878	blood:	n/a	n/a
34	BATF	chr8:43781686-43781952	GM12878	blood:	n/a	n/a
35	BATF	chr8:43778905-43779151	GM12878	blood:	n/a	n/a
36	BATF	chr8:43785460-43785804	GM12878	blood:	n/a	n/a
37	BATF	chr8:43781687-43781911	GM12878	blood:	n/a	n/a
38	BATF	chr8:43782910-43783364	GM12878	blood:	n/a	n/a
39	BCL11A	chr8:43761170-43762049	GM12878	blood:	n/a	n/a
40	BCL11A	chr8:43778827-43779220	GM12878	blood:	n/a	n/a
41	BCL11A	chr8:43771282-43771511	GM12878	blood:	n/a	n/a
42	BCL11A	chr8:43790385-43790700	GM12878	blood:	n/a	n/a
43	BCL11A	chr8:43782626-43783058	GM12878	blood:	n/a	n/a
44	BCL11A	chr8:43760155-43760933	GM12878	blood:	n/a	n/a
45	BCL11A	chr8:43789364-43789781	GM12878	blood:	n/a	n/a
46	BCL11A	chr8:43772033-43772507	GM12878	blood:	n/a	n/a
47	BCL11A	chr8:43785837-43785995	GM12878	blood:	n/a	n/a
48	BCL11A	chr8:43783550-43783791	GM12878	blood:	n/a	n/a
49	BCL11A	chr8:43783542-43783935	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:43785261-43786095	GM12878	blood:	n/a	n/a

(count:2934 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:43404458-43404508	MCF10A-Er-Src	breast:	n/a
2	chr8:43401874-43401924	NHDF-neo	bronchial:	n/a
3	chr8:43131535-43131585	U87	brain:	n/a
4	chr8:43406411-43406461	HPAEpiC	pulmonary alveolar:	n/a
5	chr8:43401874-43401924	AG10803	skin:	n/a
6	chr8:43129374-43129424	HIPEpiC	eye:	n/a
7	chr8:43404458-43404508	MCF10A-Er-Src	breast:	n/a
8	chr8:43401874-43401924	NHDF-neo	bronchial:	n/a
9	chr8:43131535-43131585	U87	brain:	n/a
10	chr8:43406411-43406461	HPAEpiC	pulmonary alveolar:	n/a
11	chr8:43401874-43401924	AG10803	skin:	n/a
12	chr8:43129374-43129424	HIPEpiC	eye:	n/a
13	chr8:43402930-43402980	SK-N-MC	brain:	n/a
14	chr8:43131260-43131310	HCF	heart:	n/a
15	chr8:43129374-43129424	PANC-1	pancreas:	n/a
16	chr8:43147602-43147652	A549	lung:	n/a
17	chr8:43136162-43136212	ProgFib	skin:	n/a
18	chr8:43417291-43417341	LNCaP	prostate:	n/a
19	chr8:43406144-43406194	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:43405687-43405737	HCT-116	colon:	n/a
21	chr8:43404458-43404508	U87	brain:	n/a
22	chr8:43136162-43136212	CMK	blood:	n/a
23	chr8:43406314-43406364	A549	lung:	n/a
24	chr8:43406411-43406461	NH-A	brain:	n/a
25	chr8:43406314-43406364	HUVEC	blood vessel:	n/a
26	chr8:43132125-43132175	NH-A	brain:	n/a
27	chr8:43129374-43129424	SK-N-SH	brain:	n/a
28	chr8:43127238-43127288	H1-hESC	embryonic stem cell:	embryo
29	chr8:43136162-43136212	HCF	heart:	n/a
30	chr8:43403277-43403327	PrEC	prostate:	n/a
31	chr8:43127072-43127122	Jurkat	blood:	n/a
32	chr8:43131656-43131706	SKMC	muscle:	n/a
33	chr8:43157775-43157825	K562	blood:	n/a
34	chr8:43147564-43147614	HCF	heart:	n/a
35	chr8:43213875-43213925	BE2_C	brain:	n/a
36	chr8:43157775-43157825	AG10803	skin:	n/a
37	chr8:43136162-43136212	HCPEpiC	choroid plexus:	n/a
38	chr8:43146894-43146944	ECC-1	luminal epithelium:	n/a
39	chr8:43418406-43418456	U87	brain:	n/a
40	chr8:43278783-43278833	NH-A	brain:	n/a
41	chr8:43146388-43146438	NH-A	brain:	n/a
42	chr8:43405687-43405737	ovcar-3	ovarian:	n/a
43	chr8:43405739-43405789	NH-A	brain:	n/a
44	chr8:43131353-43131403	Caco-2	colon:	n/a
45	chr8:43147211-43147261	HCPEpiC	choroid plexus:	n/a
46	chr8:43131535-43131585	ProgFib	skin:	n/a
47	chr8:43147564-43147614	BJ	skin:	n/a
48	chr8:43213875-43213925	GM19239	blood:	n/a
49	chr8:43136445-43136495	K562	blood:	n/a
50	chr8:43132256-43132306	Caco-2	colon:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:42947579..42949100-chr8:43300446..43303387,2	MCF-7	breast:
2	chr8:42948115..42950146-chr8:43255758..43258426,2	K562	blood:
3	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:
4	chr8:43370024..43372377-chr8:43374871..43376951,2	K562	blood:
5	chr8:43143648..43145525-chr8:43156290..43158603,2	MCF-7	breast:
6	chr8:42947110..42950521-chr8:43131245..43133918,5	K562	blood:
7	chr8:42948083..42948640-chr8:43285913..43286769,2	MCF-7	breast:
8	chr8:43395245..43397661-chr8:43402500..43405220,3	K562	blood:
9	chr5:82184309..82184963-chr8:43234719..43235395,2	MCF-7	breast:
10	chr15:63385860..63386443-chr8:43553599..43554374,2	MCF-7	breast:
11	chr8:42947421..42949412-chr8:43129646..43132331,3	K562	blood:
12	chr8:43394978..43396738-chr8:43399115..43401110,2	K562	blood:
13	chr8:42948202..42949138-chr8:43130975..43131934,4	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HGSNAT-7	chr8:43307943-43308055	NONHSAT126356
2	lnc-HGSNAT-7	chr8:43306599-43306780	NONHSAT126356
3	lnc-HGSNAT-10	chr8:43394280-43394615	NONHSAT126362
4	lnc-RNF170-9	chr8:43529413-43529734	NONHSAT126368
5	lnc-HGSNAT-12	chr8:43527966-43528218	NONHSAT126367
6	lnc-HGSNAT-6	chr8:43236787-43237091	NONHSAT126355
7	lnc-HGSNAT-5	chr8:43233441-43233652	NONHSAT126354
8	lnc-HGSNAT-8	chr8:43349080-43349905	NONHSAT126357
9	lnc-HGSNAT-7	chr8:43298045-43298224	NONHSAT126356
10	lnc-HGSNAT-7	chr8:43299491-43299558	NONHSAT126356
11	lnc-HGSNAT-4	chr8:43169091-43169343	NONHSAT126351
12	lnc-HGSNAT-9	chr8:43368786-43369564	NONHSAT126361
13	lnc-RNF170-8	chr8:43366963-43367176	NONHSAT126358
14	lnc-HGSNAT-7	chr8:43303948-43304047	NONHSAT126356

No data

Variant related genes	Relation type
ENSG00000253195	TF binding region
ENSG00000254145	TF binding region
ENSG00000250637	TF binding region
ENSG00000201329	TF binding region
AFG3L2P1	TF binding region
ENSG00000254342	TF binding region
RN7SKP41	TF binding region
ENSG00000253486	TF binding region
ENSG00000253707	TF binding region
ENSG00000264094	TF binding region
ENSG00000234713	TF binding region
CYP4F44P	TF binding region
ENSG00000221295	TF binding region
ENSG00000253845	TF binding region
ENSG00000255497	TF binding region
ENSG00000253198	TF binding region
POTEA	TF binding region
ENSG00000253319	TF binding region
RNU6-104P	TF binding region
SNX18P27	TF binding region
ENSG00000254069	TF binding region
ENSG00000253195	CpG island
ENSG00000254145	CpG island
ENSG00000250637	CpG island
ENSG00000201329	CpG island
AFG3L2P1	CpG island
ENSG00000254342	CpG island
RN7SKP41	CpG island
ENSG00000253486	CpG island
ENSG00000253707	CpG island
ENSG00000264094	CpG island
ENSG00000234713	CpG island
CYP4F44P	CpG island
ENSG00000221295	CpG island
ENSG00000253845	CpG island
ENSG00000255497	CpG island
ENSG00000253198	CpG island
POTEA	CpG island
ENSG00000253319	CpG island
RNU6-104P	CpG island
SNX18P27	CpG island
ENSG00000254069	CpG island
ENSG00000185900	chromatin interactions
ENSG00000253748	chromatin interactions
ENSG00000238509	chromatin interactions
ENSG00000253195	chromatin interactions

Extended variants
information (count: 27053 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:27053 , 50 per page) page: 1 2 3 4 5 6 7 ... 542

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs570782601	chr8:43127130-43127131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs544934022	chr8:43127145-43127146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116677851	chr8:43127187-43127188	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs188002564	chr8:43127190-43127191	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs62516805	chr8:43127200-43127201	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs560199171	chr8:43127218-43127219	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs529373787	chr8:43127238-43127239	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
8	rs549085280	chr8:43127239-43127240	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs144256728	chr8:43127240-43127241	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs531737410	chr8:43127246-43127247	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs531604620	chr8:43128051-43128052	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs151320435	chr8:43128493-43128494	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs545405830	chr8:43128588-43128589	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs567820906	chr8:43128611-43128612	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs536842146	chr8:43128634-43128635	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs549610644	chr8:43128699-43128700	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs545789259	chr8:43128784-43128785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs538243234	chr8:43128801-43128802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs527696771	chr8:43129215-43129216	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs112760346	chr8:43129230-43129231	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs141352595	chr8:43129270-43129271	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs377763300	chr8:43129308-43129309	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs561617996	chr8:43129312-43129313	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs530309754	chr8:43129353-43129354	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs550386309	chr8:43129374-43129375	Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs564086889	chr8:43129404-43129405	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs6987171	chr8:43129405-43129406	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs541011578	chr8:43129413-43129414	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs565294497	chr8:43129428-43129429	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs373262035	chr8:43129445-43129446	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs7012007	chr8:43129447-43129448	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs7012014	chr8:43129466-43129467	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs574432713	chr8:43129486-43129487	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs536828572	chr8:43129490-43129491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs145034281	chr8:43129501-43129502	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7008122	chr8:43129576-43129577	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs184136944	chr8:43129607-43129608	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs6987505	chr8:43129647-43129648	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs572468332	chr8:43129669-43129670	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs6988652	chr8:43129677-43129678	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs6992507	chr8:43129700-43129701	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs530453816	chr8:43129701-43129702	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs543784027	chr8:43129720-43129721	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs563869486	chr8:43129755-43129756	Inactive region	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs532605406	chr8:43129804-43129805	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs138882316	chr8:43129806-43129807	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565481857	chr8:43129828-43129829	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs528066533	chr8:43129829-43129830	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs532806837	chr8:43129880-43129881	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs114586916	chr8:43129903-43129904	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Seminomas	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
Rhabdomyosarcoma	16790082	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Breast cancer	21045282	CNVD
Lung cancer	17925434	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
abnormal development	18461090	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Mental retardation	17124404	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	20967226	CNVD
Bipolar disorder	19214233	CNVD

Chromatin state (count:760 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43129200-43129400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:43130600-43130800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr8:43130600-43132600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:43130800-43131000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
5	chr8:43130800-43131200	Bivalent/Poised TSS	HepG2	liver
6	chr8:43130800-43131200	Enhancers	K562	blood
7	chr8:43130800-43131400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr8:43131000-43131200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
9	chr8:43131000-43131400	Enhancers	GM12878-XiMat	blood
10	chr8:43131000-43131800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr8:43131000-43131800	Bivalent Enhancer	Placenta	Placenta
12	chr8:43131000-43132200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr8:43131400-43131600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr8:43131600-43131800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
15	chr8:43131600-43132200	Active TSS	GM12878-XiMat	blood
16	chr8:43131800-43132400	Flanking Bivalent TSS/Enh	Placenta	Placenta
17	chr8:43131800-43132600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr8:43132000-43132200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr8:43132000-43132200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
20	chr8:43132000-43132200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr8:43132000-43132200	Enhancers	Fetal Heart	heart
22	chr8:43132000-43132200	Bivalent Enhancer	Fetal Muscle Leg	muscle
23	chr8:43132000-43132200	Bivalent Enhancer	Thymus	Thymus
24	chr8:43132000-43132200	Flanking Bivalent TSS/Enh	Spleen	Spleen
25	chr8:43132000-43132200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
26	chr8:43132000-43132400	Bivalent Enhancer	Lung	lung
27	chr8:43132000-43132600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr8:43132000-43132600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:43132000-43134000	Weak transcription	Right Atrium	heart
30	chr8:43132200-43132400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:43132200-43132400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr8:43132200-43132400	Bivalent Enhancer	Spleen	Spleen
33	chr8:43132200-43132600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr8:43132200-43132600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr8:43132600-43133000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:43134000-43134200	Active TSS	Right Atrium	heart
37	chr8:43135600-43136200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:43136000-43136200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
39	chr8:43136000-43136400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
40	chr8:43136000-43136400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
41	chr8:43136000-43136400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:43136000-43136400	Bivalent Enhancer	Brain Anterior Caudate	brain
43	chr8:43136000-43136800	Bivalent Enhancer	HepG2	liver
44	chr8:43136200-43136400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
45	chr8:43136200-43136400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:43136200-43136400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
47	chr8:43136200-43136400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr8:43136200-43136400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr8:43136200-43136400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr8:43136200-43136400	Bivalent Enhancer	Liver	Liver

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