Variant report

Variant	nsv1032540
Chromosome Location	chr8:35565491-35949132
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1096)
CpG islands
(count:854)
Chromatin interactive
region (count:22)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1096 , 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	ATF1	chr8:35694479-35694576	K562	blood:	n/a	n/a
2	ATF2	chr8:35718465-35718780	GM12878	blood:	n/a	n/a
3	ATF2	chr8:35718359-35718833	GM12878	blood:	n/a	n/a
4	BACH1	chr8:35817981-35818072	K562	blood:	n/a	n/a
5	BACH1	chr8:35801904-35802359	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:35874478-35874818	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr8:35767333-35767578	GM12878	blood:	n/a	n/a
8	BATF	chr8:35718466-35718742	GM12878	blood:	n/a	chr8:35718642-35718652
9	BATF	chr8:35718379-35718751	GM12878	blood:	n/a	chr8:35718642-35718652
10	BCL11A	chr8:35755403-35755668	GM12878	blood:	n/a	n/a
11	BCL11A	chr8:35718409-35718777	GM12878	blood:	n/a	n/a
12	BCL11A	chr8:35718438-35718749	GM12878	blood:	n/a	n/a
13	BHLHE40	chr8:35755372-35755653	GM12878	blood:	n/a	n/a
14	BHLHE40	chr8:35768471-35768657	GM12878	blood:	n/a	n/a
15	BRCA1	chr8:35725959-35725973	GM12878	blood:	n/a	n/a
16	BRCA1	chr8:35916503-35916505	GM12878	blood:	n/a	n/a
17	CBX3	chr8:35817194-35817452	K562	blood:	n/a	n/a
18	CEBPB	chr8:35641050-35641476	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:35910037-35910101	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr8:35643373-35643678	K562	blood:	n/a	chr8:35643499-35643510
21	CEBPB	chr8:35637870-35638208	A549	lung:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
22	CEBPB	chr8:35575000-35575611	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr8:35643368-35643653	ECC-1	luminal epithelium:	n/a	chr8:35643499-35643510
24	CEBPB	chr8:35637869-35638225	IMR90	lung:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
25	CEBPB	chr8:35802637-35802717	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:35643317-35643677	Hela-S3	cervix:	n/a	chr8:35643499-35643510
27	CEBPB	chr8:35643342-35643712	ECC-1	luminal epithelium:	n/a	chr8:35643499-35643510
28	CEBPB	chr8:35832375-35832682	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr8:35637840-35638217	H1-hESC	embryonic stem cell:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
30	CEBPB	chr8:35716391-35716548	HepG2	liver:	n/a	n/a
31	CEBPB	chr8:35893934-35894005	H1-hESC	embryonic stem cell:	n/a	chr8:35893965-35893982 chr8:35893968-35893981 chr8:35893968-35893981
32	CEBPB	chr8:35832422-35832677	A549	lung:	n/a	n/a
33	CEBPB	chr8:35587769-35588129	A549	lung:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
34	CEBPB	chr8:35637878-35638216	HepG2	liver:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
35	CEBPB	chr8:35587784-35588055	K562	blood:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
36	CEBPB	chr8:35637927-35638130	K562	blood:	n/a	chr8:35638032-35638041 chr8:35638031-35638042
37	CEBPB	chr8:35643317-35643694	A549	lung:	n/a	chr8:35643499-35643510
38	CEBPB	chr8:35643318-35643686	HepG2	liver:	n/a	chr8:35643499-35643510
39	CEBPB	chr8:35914872-35915081	HepG2	liver:	n/a	chr8:35914963-35914974 chr8:35914965-35914976 chr8:35914965-35914974
40	CEBPB	chr8:35587790-35588138	IMR90	lung:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
41	CEBPB	chr8:35587780-35588134	HepG2	liver:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
42	CEBPB	chr8:35618307-35618518	A549	lung:	n/a	chr8:35618369-35618382
43	CEBPB	chr8:35587803-35588127	H1-hESC	embryonic stem cell:	n/a	chr8:35587949-35587960 chr8:35587950-35587959 chr8:35587948-35587961 chr8:35587948-35587959
44	CEBPB	chr8:35643317-35643693	IMR90	lung:	n/a	chr8:35643499-35643510
45	CEBPB	chr8:35832368-35832711	HepG2	liver:	n/a	n/a
46	CEBPB	chr8:35602643-35602843	HepG2	liver:	n/a	chr8:35602724-35602735
47	CEBPB	chr8:35832380-35832725	IMR90	lung:	n/a	n/a
48	CEBPB	chr8:35643320-35643687	H1-hESC	embryonic stem cell:	n/a	chr8:35643499-35643510
49	CEBPB	chr8:35875286-35875292	K562	blood:	n/a	n/a
50	CEBPB	chr8:35807629-35807792	A549	lung:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:35598326-35598376	HCT-116	colon:	n/a
2	chr8:35576222-35576272	AG04450	lung:	fetal
3	chr8:35613299-35613349	PFSK-1	brain:	n/a
4	chr8:35744638-35744688	K562	blood:	n/a
5	chr8:35803167-35803217	SK-N-SH	brain:	n/a
6	chr8:35731494-35731544	PrEC	prostate:	n/a
7	chr8:35762637-35762687	AoSMC	blood vessel:	n/a
8	chr8:35731494-35731544	AoSMC	blood vessel:	n/a
9	chr8:35913614-35913664	HL-60	blood:	n/a
10	chr8:35762637-35762687	PrEC	prostate:	n/a
11	chr8:35598326-35598376	U87	brain:	n/a
12	chr8:35803167-35803217	HRPEpiC	eye:	n/a
13	chr8:35762637-35762687	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:35598326-35598376	LNCaP	prostate:	n/a
15	chr8:35613299-35613349	SK-N-SH_RA	brain:	n/a
16	chr8:35744638-35744688	NHDF-neo	bronchial:	n/a
17	chr8:35598326-35598376	AoSMC	blood vessel:	n/a
18	chr8:35731494-35731544	HRCEpiC	kidney:	n/a
19	chr8:35580432-35580482	SK-N-MC	brain:	n/a
20	chr8:35913614-35913664	Caco-2	colon:	n/a
21	chr8:35731609-35731659	NB4	blood:	n/a
22	chr8:35731494-35731544	HEEpiC	esophagus:	n/a
23	chr8:35580715-35580765	HPAEpiC	pulmonary alveolar:	n/a
24	chr8:35685207-35685257	MCF-7	breast:	n/a
25	chr8:35581526-35581576	HUVEC	blood vessel:	n/a
26	chr8:35913614-35913664	HNPCEpiC	eye:	n/a
27	chr8:35581526-35581576	HAEpiC	amniotic membrane:	n/a
28	chr8:35744638-35744688	SKMC	muscle:	n/a
29	chr8:35803167-35803217	HEK293	kidney:	embryo
30	chr8:35731494-35731544	GM06990	blood:	n/a
31	chr8:35731494-35731544	IMR90	lung:	fetal
32	chr8:35744638-35744688	H1-hESC	embryonic stem cell:	embryo
33	chr8:35580432-35580482	SAEC	small airway:	n/a
34	chr8:35744638-35744688	AoSMC	blood vessel:	n/a
35	chr8:35762637-35762687	GM12891	blood:	n/a
36	chr8:35576222-35576272	U87	brain:	n/a
37	chr8:35649016-35649066	PANC-1	pancreas:	n/a
38	chr8:35598326-35598376	AG04450	lung:	fetal
39	chr8:35580715-35580765	ECC-1	luminal epithelium:	n/a
40	chr8:35803167-35803217	GM12878	blood:	n/a
41	chr8:35762637-35762687	PFSK-1	brain:	n/a
42	chr8:35762637-35762687	HEEpiC	esophagus:	n/a
43	chr8:35731609-35731659	HRCEpiC	kidney:	n/a
44	chr8:35803167-35803217	PrEC	prostate:	n/a
45	chr8:35649016-35649066	HCPEpiC	choroid plexus:	n/a
46	chr8:35685207-35685257	HCT-116	colon:	n/a
47	chr8:35581526-35581576	BE2_C	brain:	n/a
48	chr8:35685207-35685257	HCF	heart:	n/a
49	chr8:35731494-35731544	HMEC	breast:	n/a
50	chr8:35598326-35598376	CMK	blood:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:35899435..35901974-chr8:35902766..35905726,2	K562	blood:
2	chr8:35596968..35598886-chr8:35604620..35606278,2	K562	blood:
3	chr8:33663430..33663957-chr8:35744542..35745198,2	MCF-7	breast:
4	chr8:35638386..35640452-chr8:35642289..35644463,2	K562	blood:
5	chr17:41463858..41466219-chr8:35678069..35679569,3	K562	blood:
6	chr3:73159093..73162068-chr8:35678068..35679569,2	MCF-7	breast:
7	chr8:35620195..35622822-chr8:35626883..35629554,2	K562	blood:
8	chr8:35787657..35788212-chr8:35806131..35807030,2	MCF-7	breast:
9	chr17:41399296..41402359-chr8:35678068..35681088,3	MCF-7	breast:
10	chr3:73158515..73160568-chr8:35679569..35681069,2	K562	blood:
11	chr8:35744346..35744912-chr8:35998590..35999359,2	MCF-7	breast:
12	chr8:35899435..35901974-chr8:35902766..35905726,2	K562	blood:
13	chr17:41401117..41402640-chr8:35678068..35679569,2	K562	blood:
14	chr8:35596968..35598886-chr8:35604620..35606278,2	K562	blood:
15	chr17:41464397..41466335-chr8:35678069..35679588,3	K562	blood:
16	chr17:41400768..41402617-chr8:35678068..35679569,3	K562	blood:
17	chr8:35787657..35788212-chr8:35806131..35807030,2	MCF-7	breast:
18	chr8:35620195..35622822-chr8:35626883..35629554,2	K562	blood:
19	chr8:35638386..35640452-chr8:35642289..35644463,2	K562	blood:
20	chr8:35497530..35499054-chr8:35564853..35566842,2	K562	blood:
21	chr17:41380631..41382205-chr8:35678068..35679588,2	MCF-7	breast:
22	chr17:41398363..41402584-chr8:35679569..35681089,3	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC5D-2	chr8:35750072-35750201	ENSG00000253452
2	lnc-UNC5D-2	chr8:35801762-35801920	ENSG00000253452
3	lnc-UNC5D-2	chr8:35757901-35758022	ENSG00000253452
4	lnc-RP11-419C23.1.1-4	chr8:35892385-35892466	ENSG00000253524
5	lnc-RP11-419C23.1.1-4	chr8:35861834-35862110	ENSG00000253524
6	lnc-RP11-419C23.1.1-4	chr8:35861838-35862110	ENSG00000253524
7	lnc-UNC5D-2	chr8:35750072-35750201	ENSG00000253452
8	lnc-UNC5D-2	chr8:35720027-35720138	ENSG00000253452
9	lnc-UNC5D-2	chr8:35783552-35783638	ENSG00000253452
10	lnc-UNC5D-2	chr8:35720025-35720138	ENSG00000253452
11	lnc-UNC5D-2	chr8:35788183-35788228	ENSG00000253452
12	lnc-UNC5D-2	chr8:35787238-35787275	ENSG00000253452
13	lnc-UNC5D-2	chr8:35719641-35719668	ENSG00000253452
14	lnc-UNC5D-2	chr8:35757901-35758022	ENSG00000253452
15	lnc-UNC5D-2	chr8:35828131-35828183	ENSG00000253452

No data

Variant related genes	Relation type
UNC5D	TF binding region
ENSG00000253452	TF binding region
ENSG00000233863	TF binding region
UNC5D	CpG island
ENSG00000253452	CpG island
ENSG00000233863	CpG island
ENSG00000223247	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 8466 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:8466 , 50 per page) page: 1 2 3 4 5 6 7 ... 170

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79101690	chr8:35565520-35565521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372600619	chr8:35565529-35565530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs3824287	chr8:35565565-35565566	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs551495820	chr8:35565576-35565577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs570316690	chr8:35565579-35565580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs368194846	chr8:35565649-35565650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145134535	chr8:35565660-35565661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570444608	chr8:35565676-35565677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534641176	chr8:35565733-35565734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188247225	chr8:35565741-35565742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568185977	chr8:35565752-35565753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192539877	chr8:35565755-35565756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556762192	chr8:35565769-35565770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575163616	chr8:35565806-35565807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs545678672	chr8:35565808-35565809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139010978	chr8:35565815-35565816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs577166476	chr8:35565823-35565824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs183310430	chr8:35565825-35565826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187485527	chr8:35565827-35565828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530213622	chr8:35565868-35565869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78267044	chr8:35565884-35565885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115814269	chr8:35565885-35565886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs142284188	chr8:35565905-35565906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73583060	chr8:35565941-35565942	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs191369957	chr8:35565947-35565948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7837786	chr8:35565977-35565978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs528062617	chr8:35566021-35566022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs369804964	chr8:35566040-35566041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7837943	chr8:35566080-35566081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374207552	chr8:35566122-35566123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546581995	chr8:35566131-35566132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs370184146	chr8:35566142-35566143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145627682	chr8:35566159-35566160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs7815563	chr8:35566203-35566204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs535555573	chr8:35566204-35566205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7819182	chr8:35566235-35566236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144517927	chr8:35566248-35566249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566610904	chr8:35566284-35566285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377610905	chr8:35566302-35566303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7820182	chr8:35566315-35566316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs568692212	chr8:35566341-35566342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184631890	chr8:35566357-35566358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573219026	chr8:35566360-35566361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557620771	chr8:35566438-35566439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs138163029	chr8:35566510-35566511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116444152	chr8:35566514-35566515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574803860	chr8:35566582-35566583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542325984	chr8:35566599-35566600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7820599	chr8:35566614-35566615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563799301	chr8:35566653-35566654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
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
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
Acute lymphoblastic leukemia	21248843	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
Endometrioid adenocarcinoma	16974079	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
Multiple myeloma	16616336	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	21806811	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	20459607	CNVD
Renal cell carcinoma	18765545	CNVD
Colorectal cancer	16912164	CNVD
Neuroticism	17667963	CNVD
Non-muscle invasive bladder neoplasm	19445696	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
Urothelial carcinoma	18382360	CNVD
Ductal carcinoma	18381933	CNVD
Breast cancer	21328542	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Intellectual disability	22045946	CNVD
Lung cancer	17925434	CNVD
Uveal melanoma	20484589	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21364760	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21785460	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Renal cell carcinoma	21215367	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1232 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:35531000-35579600	Weak transcription	Fetal Brain Female	brain
2	chr8:35538000-35575200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr8:35547400-35579800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr8:35564000-35573400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr8:35564800-35573400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr8:35565000-35573400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr8:35565200-35573600	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr8:35565200-35573800	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr8:35565400-35576200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:35570000-35570400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr8:35570000-35570400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr8:35570400-35575200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr8:35570400-35575200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:35572800-35573000	Enhancers	Stomach Mucosa	stomach
15	chr8:35573400-35576600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr8:35573400-35577000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr8:35573400-35577000	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr8:35573400-35577800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr8:35573600-35574600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr8:35573600-35577200	Enhancers	H1 Cell Line	embryonic stem cell
21	chr8:35573800-35577000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr8:35573800-35577000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr8:35573800-35578000	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr8:35574200-35575000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
25	chr8:35574200-35577000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr8:35574200-35577200	Enhancers	Fetal Lung	lung
27	chr8:35574600-35575200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr8:35575000-35587400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
29	chr8:35575000-35600200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:35575200-35575400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr8:35575200-35576200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr8:35575200-35576600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr8:35575200-35577000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr8:35575200-35579200	Enhancers	Stomach Mucosa	stomach
35	chr8:35575400-35575600	Enhancers	Small Intestine	intestine
36	chr8:35575400-35579800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr8:35575600-35577600	Weak transcription	Small Intestine	intestine
38	chr8:35575600-35579800	Enhancers	Duodenum Mucosa	Duodenum
39	chr8:35575800-35576000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:35576000-35631600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr8:35576200-35576400	Enhancers	Gastric	stomach
42	chr8:35576200-35577400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr8:35576200-35583400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr8:35576600-35577600	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr8:35576600-35586000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr8:35577000-35578000	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr8:35577000-35579000	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr8:35577000-35579200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr8:35577000-35579800	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr8:35577000-35587800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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