Variant report

Variant	nsv995040
Chromosome Location	chr8:43110494-43528350
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1075)
CpG islands
(count:2993)
Chromatin interactive
region (count:12)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1075 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr8:43147119-43147233	K562	blood:	n/a	n/a
2	ATF3	chr8:43136024-43136278	K562	blood:	n/a	n/a
3	ATF3	chr8:43135865-43136266	HepG2	liver:	n/a	n/a
4	ATF3	chr8:43136037-43136199	HepG2	liver:	n/a	n/a
5	ATF3	chr8:43135995-43136320	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:43135956-43136341	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:43135956-43136331	K562	blood:	n/a	n/a
8	BHLHE40	chr8:43135971-43136325	HepG2	liver:	n/a	n/a
9	BHLHE40	chr8:43147157-43147318	K562	blood:	n/a	chr8:43147193-43147202
10	BRCA1	chr8:43519669-43520216	Hela-S3	cervix:	n/a	n/a
11	CBX3	chr8:43420572-43420906	K562	blood:	n/a	n/a
12	CBX3	chr8:43136043-43136239	K562	blood:	n/a	n/a
13	CBX3	chr8:43135925-43136324	K562	blood:	n/a	n/a
14	CCNT2	chr8:43136064-43136182	K562	blood:	n/a	n/a
15	CEBPB	chr8:43221416-43221477	A549	lung:	n/a	n/a
16	CEBPB	chr8:43198145-43198345	HepG2	liver:	n/a	chr8:43198226-43198237
17	CEBPB	chr8:43145377-43145724	ECC-1	luminal epithelium:	n/a	chr8:43145521-43145532 chr8:43145523-43145532
18	CEBPB	chr8:43414546-43414811	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr8:43373700-43374000	HepG2	liver:	n/a	chr8:43373832-43373843
20	CEBPB	chr8:43306501-43306786	IMR90	lung:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
21	CEBPB	chr8:43373683-43374020	IMR90	lung:	n/a	chr8:43373832-43373843
22	CEBPB	chr8:43151840-43151928	A549	lung:	n/a	n/a
23	CEBPB	chr8:43222991-43222998	HepG2	liver:	n/a	n/a
24	CEBPB	chr8:43414610-43414720	HepG2	liver:	n/a	n/a
25	CEBPB	chr8:43306476-43306804	HepG2	liver:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
26	CEBPB	chr8:43145445-43145645	HepG2	liver:	n/a	chr8:43145521-43145532 chr8:43145523-43145532
27	CEBPB	chr8:43221409-43221449	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:43303234-43303525	HepG2	liver:	n/a	chr8:43303409-43303422 chr8:43303410-43303421
29	CEBPB	chr8:43145440-43145639	ECC-1	luminal epithelium:	n/a	chr8:43145521-43145532 chr8:43145523-43145532
30	CEBPB	chr8:43352248-43352856	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr8:43302895-43303465	A549	lung:	n/a	chr8:43303409-43303422 chr8:43303410-43303421
32	CEBPB	chr8:43306612-43306676	K562	blood:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
33	CEBPB	chr8:43317791-43318030	A549	lung:	n/a	chr8:43317903-43317914 chr8:43317902-43317915
34	CEBPB	chr8:43373772-43373988	A549	lung:	n/a	chr8:43373832-43373843
35	CEBPB	chr8:43306491-43306829	A549	lung:	n/a	chr8:43306646-43306657 chr8:43306657-43306668
36	CEBPB	chr8:43352224-43352840	A549	lung:	n/a	n/a
37	CEBPB	chr8:43359811-43360200	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr8:43317774-43318025	HepG2	liver:	n/a	chr8:43317903-43317914 chr8:43317902-43317915
39	CHD2	chr8:43519669-43520389	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr8:43136015-43136318	A549	lung:	n/a	n/a
41	CTCF	chr8:43131400-43131550	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr8:43136038-43136191	Kidney_OC	kidney:	n/a	chr8:43136108-43136121
43	CTCF	chr8:43131394-43131577	GM12892	blood:	n/a	n/a
44	CTCF	chr8:43265020-43265170	HEK293	kidney:	n/a	n/a
45	CTCF	chr8:43303248-43303403	GM12878	blood:	n/a	n/a
46	CTCF	chr8:43131420-43131570	GM12875	blood:	n/a	n/a
47	CTCF	chr8:43291280-43291430	HepG2	liver:	n/a	n/a
48	CTCF	chr8:43291200-43291350	AG04450	lung:	n/a	n/a
49	CTCF	chr8:43131440-43131590	GM12871	blood:	n/a	n/a
50	CTCF	chr8:43135967-43136259	K562	blood:	n/a	chr8:43136108-43136121

(count:2993 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:43147397-43147447	NB4	blood:	n/a
2	chr8:43147564-43147614	Hepatocyte	liver:	n/a
3	chr8:43405739-43405789	GM12891	blood:	n/a
4	chr8:43417291-43417341	SK-N-SH	brain:	n/a
5	chr8:43147397-43147447	NB4	blood:	n/a
6	chr8:43147564-43147614	Hepatocyte	liver:	n/a
7	chr8:43405739-43405789	GM12891	blood:	n/a
8	chr8:43417291-43417341	SK-N-SH	brain:	n/a
9	chr8:43125995-43126045	Hela-S3	cervix:	n/a
10	chr8:43278783-43278833	HAEpiC	amniotic membrane:	n/a
11	chr8:43132451-43132501	SK-N-SH	brain:	n/a
12	chr8:43147602-43147652	AG10803	skin:	n/a
13	chr8:43147439-43147489	HepG2	liver:	n/a
14	chr8:43147741-43147791	CMK	blood:	n/a
15	chr8:43146894-43146944	GM12878	blood:	n/a
16	chr8:43275453-43275503	NT2-D1	testis:	n/a
17	chr8:43406144-43406194	SK-N-MC	brain:	n/a
18	chr8:43405687-43405737	NH-A	brain:	n/a
19	chr8:43147581-43147631	PrEC	prostate:	n/a
20	chr8:43132125-43132175	IMR90	lung:	fetal
21	chr8:43131535-43131585	AoSMC	blood vessel:	n/a
22	chr8:43405739-43405789	AG09319	gingival:	n/a
23	chr8:43404214-43404264	A549	lung:	n/a
24	chr8:43405687-43405737	NHDF-neo	bronchial:	n/a
25	chr8:43147581-43147631	HCT-116	colon:	n/a
26	chr8:43124515-43124565	HEK293	kidney:	embryo
27	chr8:43129726-43129776	AG09309	skin:	n/a
28	chr8:43146388-43146438	SKMC	muscle:	n/a
29	chr8:43132507-43132557	CMK	blood:	n/a
30	chr8:43124515-43124565	HMEC	breast:	n/a
31	chr8:43124515-43124565	Jurkat	blood:	n/a
32	chr8:43417291-43417341	HAEpiC	amniotic membrane:	n/a
33	chr8:43147439-43147489	HCM	heart:	n/a
34	chr8:43127072-43127122	NT2-D1	testis:	n/a
35	chr8:43125995-43126045	NHDF-neo	bronchial:	n/a
36	chr8:43136327-43136377	HEEpiC	esophagus:	n/a
37	chr8:43131431-43131481	HRCEpiC	kidney:	n/a
38	chr8:43146218-43146268	SKMC	muscle:	n/a
39	chr8:43132507-43132557	AG09309	skin:	n/a
40	chr8:43417050-43417100	HCF	heart:	n/a
41	chr8:43131260-43131310	HRPEpiC	eye:	n/a
42	chr8:43275453-43275503	HL-60	blood:	n/a
43	chr8:43147741-43147791	HL-60	blood:	n/a
44	chr8:43147741-43147791	PANC-1	pancreas:	n/a
45	chr8:43405739-43405789	HepG2	liver:	n/a
46	chr8:43406314-43406364	HCM	heart:	n/a
47	chr8:43146388-43146438	AG10803	skin:	n/a
48	chr8:43147564-43147614	IMR90	lung:	fetal
49	chr8:43417291-43417341	GM19239	blood:	n/a
50	chr8:43213875-43213925	Caco-2	colon:	n/a

(count:12 , 50 per page) page: 1

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

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

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

No data

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

Extended variants
information (count: 11082 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:11082 , 50 per page) page: 1 2 3 4 5 6 7 ... 222

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377169144	chr8:43115042-43115043	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs187994831	chr8:43115066-43115067	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs376953349	chr8:43115076-43115077	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs559142083	chr8:43115081-43115082	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs368870710	chr8:43115091-43115092	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs547468474	chr8:43115116-43115117	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs567693529	chr8:43115149-43115150	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs536645984	chr8:43115171-43115172	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs549909793	chr8:43115183-43115184	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs373057351	chr8:43115209-43115210	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs193048249	chr8:43115224-43115225	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs377228583	chr8:43115229-43115230	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs539356916	chr8:43115241-43115242	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs145569591	chr8:43115258-43115259	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs572657063	chr8:43115277-43115278	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs35272956	chr8:43115319-43115320	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs537076571	chr8:43115333-43115334	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs574498108	chr8:43115407-43115408	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs73675493	chr8:43115426-43115427	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs147263766	chr8:43115462-43115463	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs576695603	chr8:43115506-43115507	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs34452244	chr8:43115536-43115537	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs570782601	chr8:43127130-43127131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs544934022	chr8:43127145-43127146	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs116677851	chr8:43127187-43127188	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs188002564	chr8:43127190-43127191	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs62516805	chr8:43127200-43127201	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs560199171	chr8:43127218-43127219	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs529373787	chr8:43127238-43127239	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs549085280	chr8:43127239-43127240	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs144256728	chr8:43127240-43127241	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs531737410	chr8:43127246-43127247	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs531604620	chr8:43128051-43128052	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs151320435	chr8:43128493-43128494	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs545405830	chr8:43128588-43128589	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs567820906	chr8:43128611-43128612	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs536842146	chr8:43128634-43128635	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs549610644	chr8:43128699-43128700	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs545789259	chr8:43128784-43128785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs538243234	chr8:43128801-43128802	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs527696771	chr8:43129215-43129216	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs112760346	chr8:43129230-43129231	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs141352595	chr8:43129270-43129271	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs377763300	chr8:43129308-43129309	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs561617996	chr8:43129312-43129313	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs530309754	chr8:43129353-43129354	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs550386309	chr8:43129374-43129375	Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs564086889	chr8:43129404-43129405	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs6987171	chr8:43129405-43129406	Inactive region	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs541011578	chr8:43129413-43129414	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

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

Chromatin state (count:229 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:43115000-43115600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:43129200-43129400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:43130600-43130800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr8:43130600-43132600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:43130800-43131000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
6	chr8:43130800-43131200	Bivalent/Poised TSS	HepG2	liver
7	chr8:43130800-43131200	Enhancers	K562	blood
8	chr8:43130800-43131400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr8:43131000-43131200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
10	chr8:43131000-43131400	Enhancers	GM12878-XiMat	blood
11	chr8:43131000-43131800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:43131000-43131800	Bivalent Enhancer	Placenta	Placenta
13	chr8:43131000-43132200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr8:43131400-43131600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr8:43131600-43131800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr8:43131600-43132200	Active TSS	GM12878-XiMat	blood
17	chr8:43131800-43132400	Flanking Bivalent TSS/Enh	Placenta	Placenta
18	chr8:43131800-43132600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr8:43132000-43132200	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr8:43132000-43132200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
21	chr8:43132000-43132200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr8:43132000-43132200	Enhancers	Fetal Heart	heart
23	chr8:43132000-43132200	Bivalent Enhancer	Fetal Muscle Leg	muscle
24	chr8:43132000-43132200	Bivalent Enhancer	Thymus	Thymus
25	chr8:43132000-43132200	Flanking Bivalent TSS/Enh	Spleen	Spleen
26	chr8:43132000-43132200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
27	chr8:43132000-43132400	Bivalent Enhancer	Lung	lung
28	chr8:43132000-43132600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr8:43132000-43132600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:43132000-43134000	Weak transcription	Right Atrium	heart
31	chr8:43132200-43132400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr8:43132200-43132400	Bivalent/Poised TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr8:43132200-43132400	Bivalent Enhancer	Spleen	Spleen
34	chr8:43132200-43132600	Bivalent/Poised TSS	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr8:43132200-43132600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr8:43132600-43133000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr8:43134000-43134200	Active TSS	Right Atrium	heart
38	chr8:43135600-43136200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:43136000-43136200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
40	chr8:43136000-43136400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
41	chr8:43136000-43136400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
42	chr8:43136000-43136400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr8:43136000-43136400	Bivalent Enhancer	Brain Anterior Caudate	brain
44	chr8:43136000-43136800	Bivalent Enhancer	HepG2	liver
45	chr8:43136200-43136400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
46	chr8:43136200-43136400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr8:43136200-43136400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
48	chr8:43136200-43136400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr8:43136200-43136400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr8:43136200-43136400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin

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