Variant report

Variant	nsv1026506
Chromosome Location	chr8:9258997-9338042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:529)
CpG islands
(count:183)
Chromatin interactive
region (count:4)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:529 , 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	chr8:9334453-9334756	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:9306103-9306534	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:9318207-9318547	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:9278878-9279410	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:9308180-9309361	HepG2	liver:	n/a	chr8:9309163-9309179
6	ARID3A	chr8:9291262-9291958	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:9278102-9278582	HepG2	liver:	n/a	n/a
8	ATF1	chr8:9278166-9278351	K562	blood:	n/a	n/a
9	ATF2	chr8:9321110-9321873	GM12878	blood:	n/a	n/a
10	ATF2	chr8:9321026-9321933	GM12878	blood:	n/a	n/a
11	ATF3	chr8:9273451-9273572	K562	blood:	n/a	n/a
12	BACH1	chr8:9269856-9270069	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr8:9268141-9268184	K562	blood:	n/a	n/a
14	BACH1	chr8:9271926-9271967	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr8:9273684-9273878	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr8:9259998-9260555	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr8:9273578-9273842	K562	blood:	n/a	n/a
18	BATF	chr8:9321011-9321638	GM12878	blood:	n/a	chr8:9321598-9321608
19	BATF	chr8:9321035-9321493	GM12878	blood:	n/a	n/a
20	BATF	chr8:9268145-9268417	GM12878	blood:	n/a	n/a
21	BCL11A	chr8:9321269-9321587	GM12878	blood:	n/a	n/a
22	BCL11A	chr8:9321156-9321595	GM12878	blood:	n/a	n/a
23	BCLAF1	chr8:9321068-9321564	GM12878	blood:	n/a	n/a
24	BCLAF1	chr8:9321061-9321689	GM12878	blood:	n/a	chr8:9321596-9321605 chr8:9321597-9321606
25	BHLHE40	chr8:9308226-9308311	K562	blood:	n/a	n/a
26	BHLHE40	chr8:9259888-9259949	HepG2	liver:	n/a	chr8:9259912-9259933 chr8:9259916-9259929
27	BHLHE40	chr8:9259868-9260006	K562	blood:	n/a	chr8:9259912-9259933 chr8:9259916-9259929
28	BHLHE40	chr8:9334452-9334719	HepG2	liver:	n/a	n/a
29	BHLHE40	chr8:9261373-9261581	K562	blood:	n/a	n/a
30	BHLHE40	chr8:9308092-9309235	HepG2	liver:	n/a	n/a
31	BHLHE40	chr8:9279045-9279235	HepG2	liver:	n/a	n/a
32	BHLHE40	chr8:9273206-9273409	K562	blood:	n/a	chr8:9273312-9273321
33	BHLHE40	chr8:9321148-9321624	GM12878	blood:	n/a	n/a
34	CEBPB	chr8:9278951-9279158	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:9295186-9295259	K562	blood:	n/a	n/a
36	CEBPB	chr8:9306032-9306545	Hela-S3	cervix:	n/a	chr8:9306316-9306329 chr8:9306317-9306328 chr8:9306316-9306329
37	CEBPB	chr8:9315795-9315900	HepG2	liver:	n/a	chr8:9315855-9315866 chr8:9315855-9315868
38	CEBPB	chr8:9276732-9277128	A549	lung:	n/a	n/a
39	CEBPB	chr8:9264102-9264210	K562	blood:	n/a	n/a
40	CEBPB	chr8:9305456-9305613	K562	blood:	n/a	n/a
41	CEBPB	chr8:9305442-9305641	HepG2	liver:	n/a	n/a
42	CEBPB	chr8:9308169-9308892	HepG2	liver:	n/a	chr8:9308281-9308294 chr8:9308700-9308711
43	CEBPB	chr8:9306037-9306510	MCF-7	breast:	n/a	chr8:9306316-9306329 chr8:9306317-9306328 chr8:9306316-9306329
44	CEBPB	chr8:9305412-9305667	A549	lung:	n/a	n/a
45	CEBPB	chr8:9306127-9306456	HepG2	liver:	n/a	chr8:9306316-9306329 chr8:9306317-9306328 chr8:9306316-9306329
46	CEBPB	chr8:9278151-9278358	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:9318173-9318511	HepG2	liver:	n/a	n/a
48	CEBPB	chr8:9278120-9278416	K562	blood:	n/a	n/a
49	CEBPB	chr8:9306033-9306515	A549	lung:	n/a	chr8:9306316-9306329 chr8:9306317-9306328 chr8:9306316-9306329
50	CEBPB	chr8:9293602-9293928	HepG2	liver:	n/a	chr8:9293763-9293774

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9260335-9260385	NH-A	brain:	n/a
2	chr8:9278742-9278792	SKMC	muscle:	n/a
3	chr8:9278742-9278792	PANC-1	pancreas:	n/a
4	chr8:9278742-9278792	HRE	kidney:	n/a
5	chr8:9278742-9278792	U87	brain:	n/a
6	chr8:9260354-9260404	BE2_C	brain:	n/a
7	chr8:9278742-9278792	SK-N-MC	brain:	n/a
8	chr8:9260335-9260385	HAEpiC	amniotic membrane:	n/a
9	chr8:9260354-9260404	HEEpiC	esophagus:	n/a
10	chr8:9260354-9260404	HAEpiC	amniotic membrane:	n/a
11	chr8:9260354-9260404	AG04449	skin:	fetal
12	chr8:9260335-9260385	SK-N-SH_RA	brain:	n/a
13	chr8:9278742-9278792	MCF10A-Er-Src	breast:	n/a
14	chr8:9278742-9278792	H1-hESC	embryonic stem cell:	embryo
15	chr8:9260354-9260404	ovcar-3	ovarian:	n/a
16	chr8:9260335-9260385	AG04450	lung:	fetal
17	chr8:9260335-9260385	SK-N-SH	brain:	n/a
18	chr8:9278742-9278792	BE2_C	brain:	n/a
19	chr8:9260335-9260385	AG10803	skin:	n/a
20	chr8:9260335-9260385	HEK293	kidney:	embryo
21	chr8:9260354-9260404	HCF	heart:	n/a
22	chr8:9260335-9260385	Caco-2	colon:	n/a
23	chr8:9278742-9278792	HL-60	blood:	n/a
24	chr8:9278742-9278792	AG09319	gingival:	n/a
25	chr8:9278742-9278792	ProgFib	skin:	n/a
26	chr8:9278742-9278792	AG04449	skin:	fetal
27	chr8:9260335-9260385	GM12878	blood:	n/a
28	chr8:9260335-9260385	NHBE	bronchial:	n/a
29	chr8:9260335-9260385	BJ	skin:	n/a
30	chr8:9260335-9260385	HUVEC	blood vessel:	n/a
31	chr8:9278742-9278792	HepG2	liver:	n/a
32	chr8:9278742-9278792	K562	blood:	n/a
33	chr8:9260335-9260385	H1-hESC	embryonic stem cell:	embryo
34	chr8:9260354-9260404	AG09319	gingival:	n/a
35	chr8:9278742-9278792	HCF	heart:	n/a
36	chr8:9260354-9260404	HPAEpiC	pulmonary alveolar:	n/a
37	chr8:9278742-9278792	HCT-116	colon:	n/a
38	chr8:9260335-9260385	ProgFib	skin:	n/a
39	chr8:9278742-9278792	T-47D	breast:	n/a
40	chr8:9260335-9260385	AG04449	skin:	fetal
41	chr8:9260354-9260404	U87	brain:	n/a
42	chr8:9260335-9260385	HNPCEpiC	eye:	n/a
43	chr8:9278742-9278792	GM12892	blood:	n/a
44	chr8:9260335-9260385	HRCEpiC	kidney:	n/a
45	chr8:9260354-9260404	NT2-D1	testis:	n/a
46	chr8:9278742-9278792	HMEC	breast:	n/a
47	chr8:9278742-9278792	NB4	blood:	n/a
48	chr8:9278742-9278792	RPTEC	kidney:	n/a
49	chr8:9260354-9260404	HNPCEpiC	eye:	n/a
50	chr8:9260335-9260385	RPTEC	kidney:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:9268719..9271294-chr8:9413214..9415247,2	MCF-7	breast:
2	chr8:9322565..9324066-chr8:9347698..9350401,2	K562	blood:
3	chr8:9239070..9241481-chr8:9260327..9263090,2	MCF-7	breast:
4	chr8:9048939..9051745-chr8:9268709..9271649,2	K562	blood:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP1R3B-7	chr8:9267774-9268026	l_3547_chr8:9260263-9270085_testes
2	lnc-PPP1R3B-8	chr8:9282245-9282386	NONHSAT124954
3	lnc-PPP1R3B-8	chr8:9280338-9281391	NONHSAT124954
4	lnc-PPP1R3B-7	chr8:9269854-9270085	l_3547_chr8:9260263-9270085_testes
5	lnc-RP11-10A14.4.1-4	chr8:9271159-9271386	NONHSAT124948
6	lnc-PPP1R3B-9	chr8:9304981-9305257	NONHSAT124955
7	lnc-TNKS-5	chr8:9311815-9312409	NONHSAT124956
8	lnc-PPP1R3B-8	chr8:9279664-9279765	NONHSAT124954
9	lnc-TNKS-5	chr8:9314677-9314928	NONHSAT124956
10	lnc-PPP1R3B-7	chr8:9266473-9267064	l_3547_chr8:9260263-9270085_testes
11	lnc-TNKS-5	chr8:9311208-9311467	NONHSAT124956
12	lnc-TNKS-4	chr8:9318958-9319950	NONHSAT124957
13	lnc-TNKS-4	chr8:9318958-9319950	FPKM1_group_30860_transcript_4
14	lnc-PPP1R3B-7	chr8:9260264-9260351	l_3547_chr8:9260263-9270085_testes
15	lnc-PPP1R3B-4	chr8:9273386-9273450	ENSG00000254237
16	lnc-TNKS-5	chr8:9313405-9314332	NONHSAT124956
17	lnc-PPP1R3B-4	chr8:9261455-9261554	ENSG00000254237
18	lnc-PPP1R3B-9	chr8:9299027-9299099	NONHSAT124955
19	lnc-PPP1R3B-4	chr8:9293542-9293715	ENSG00000254237
20	lnc-TNKS-4	chr8:9320538-9320752	NONHSAT124957
21	lnc-TNKS-4	chr8:9319116-9319330	FPKM1_group_30860_transcript_4

No data

Variant related genes	Relation type
ENSG00000249050	TF binding region
ENSG00000254237	TF binding region
ENSG00000249050	CpG island
ENSG00000254237	CpG island
ENSG00000173273	chromatin interactions
ENSG00000272267	chromatin interactions

Extended variants
information (count: 2918 )
Associated
traits (count: 137 )

Variant overlapped rSNPs/rCNVs (count:2918 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574747069	chr8:9259008-9259009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540241420	chr8:9259019-9259020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77599947	chr8:9259037-9259038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543112581	chr8:9259078-9259079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563439522	chr8:9259110-9259111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532685250	chr8:9259132-9259133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80036201	chr8:9259149-9259150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546010122	chr8:9259181-9259182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201705995	chr8:9259206-9259207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs142468263	chr8:9259220-9259221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75784254	chr8:9259234-9259235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs548280173	chr8:9259249-9259250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189982536	chr8:9259282-9259283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533925269	chr8:9259283-9259284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183331819	chr8:9259309-9259310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570470832	chr8:9259319-9259320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs376392851	chr8:9259330-9259331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529657493	chr8:9259358-9259359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546197060	chr8:9259379-9259380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs375519622	chr8:9259380-9259381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147888988	chr8:9259432-9259433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115574310	chr8:9259434-9259435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191995777	chr8:9259500-9259501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574821405	chr8:9259525-9259526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs185236743	chr8:9259546-9259547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560240595	chr8:9259557-9259558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200904049	chr8:9259566-9259567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9329197	chr8:9259568-9259569	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
29	rs188152780	chr8:9259601-9259602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs192639981	chr8:9259604-9259605	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs185031118	chr8:9259605-9259606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs548786953	chr8:9259634-9259635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs188128364	chr8:9259637-9259638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs377571235	chr8:9259666-9259667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141533821	chr8:9259669-9259670	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191472512	chr8:9259695-9259696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10091991	chr8:9259727-9259728	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs539432448	chr8:9259746-9259747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs61194615	chr8:9259792-9259793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374968944	chr8:9259797-9259798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs117144006	chr8:9259829-9259830	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs569591986	chr8:9259863-9259864	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs535393160	chr8:9259909-9259910	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs555132947	chr8:9259937-9259938	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs143634976	chr8:9259947-9259948	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs148061646	chr8:9259951-9259952	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs530410761	chr8:9259968-9259969	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs141772190	chr8:9259974-9259975	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs566468034	chr8:9259982-9259983	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs150144870	chr8:9259991-9259992	Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:137)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	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
Oral cancer	21386901	CNVD
Prostate cancer	21088497	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
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
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:291 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9248000-9260000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr8:9259600-9259800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr8:9259600-9259800	Enhancers	Brain Germinal Matrix	brain
4	chr8:9259600-9259800	Enhancers	Brain Hippocampus Middle	brain
5	chr8:9259600-9259800	Enhancers	Brain Inferior Temporal Lobe	brain
6	chr8:9259600-9259800	Enhancers	Brain Substantia Nigra	brain
7	chr8:9259800-9260000	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr8:9259800-9260000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
9	chr8:9259800-9260000	Enhancers	Cortex derived primary cultured neurospheres	brain
10	chr8:9259800-9260000	Flanking Active TSS	Brain Angular Gyrus	brain
11	chr8:9259800-9260000	Flanking Active TSS	Brain Hippocampus Middle	brain
12	chr8:9259800-9260000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
13	chr8:9259800-9260000	Flanking Active TSS	Brain Substantia Nigra	brain
14	chr8:9259800-9260000	Enhancers	Fetal Brain Male	brain
15	chr8:9259800-9260000	Enhancers	HSMM	muscle
16	chr8:9259800-9260200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr8:9259800-9260200	Enhancers	Fetal Muscle Leg	muscle
18	chr8:9259800-9260200	Active TSS	Psoas Muscle	Psoas
19	chr8:9259800-9260200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
20	chr8:9259800-9260400	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr8:9259800-9260400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
22	chr8:9259800-9260600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr8:9259800-9260600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr8:9259800-9260600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr8:9259800-9260600	Active TSS	Brain Anterior Caudate	brain
26	chr8:9259800-9260600	Active TSS	Brain Cingulate Gyrus	brain
27	chr8:9259800-9260600	Flanking Active TSS	Brain Germinal Matrix	brain
28	chr8:9259800-9260600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
29	chr8:9260000-9260200	Enhancers	Fetal Muscle Trunk	muscle
30	chr8:9260000-9260200	Bivalent Enhancer	Placenta	Placenta
31	chr8:9260000-9260200	Flanking Active TSS	HSMMtube	muscle
32	chr8:9260000-9260400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:9260000-9260400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
34	chr8:9260000-9260400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
35	chr8:9260000-9260400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr8:9260000-9260400	Enhancers	Adipose Nuclei	Adipose
37	chr8:9260000-9260400	Active TSS	Brain Angular Gyrus	brain
38	chr8:9260000-9260400	Active TSS	Brain Hippocampus Middle	brain
39	chr8:9260000-9260400	Flanking Active TSS	Fetal Brain Male	brain
40	chr8:9260000-9260400	Active TSS	HSMM	muscle
41	chr8:9260000-9260600	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr8:9260000-9260600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr8:9260000-9260600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr8:9260000-9260600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
45	chr8:9260000-9260600	Active TSS	Brain Inferior Temporal Lobe	brain
46	chr8:9260000-9260600	Active TSS	Brain Substantia Nigra	brain
47	chr8:9260000-9260600	Active TSS	Fetal Brain Female	brain
48	chr8:9260200-9260400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr8:9260200-9260400	Flanking Active TSS	Fetal Muscle Leg	muscle
50	chr8:9260200-9260400	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle

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