Variant report

Variant	nsv1024024
Chromosome Location	chr8:6490665-6555558
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:964)
CpG islands
(count:307)
Chromatin interactive
region (count:31)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:6498370-6498595	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:6522196-6522363	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:6505744-6505995	HepG2	liver:	n/a	n/a
4	ATF1	chr8:6539983-6540077	K562	blood:	n/a	n/a
5	ATF1	chr8:6537036-6537368	K562	blood:	n/a	chr8:6537348-6537362
6	ATF2	chr8:6502240-6502826	GM12878	blood:	n/a	n/a
7	ATF2	chr8:6502283-6502814	GM12878	blood:	n/a	n/a
8	ATF2	chr8:6547509-6548608	GM12878	blood:	n/a	n/a
9	ATF2	chr8:6522693-6523336	GM12878	blood:	n/a	n/a
10	ATF2	chr8:6522100-6523433	GM12878	blood:	n/a	n/a
11	ATF2	chr8:6547433-6548484	GM12878	blood:	n/a	n/a
12	ATF3	chr8:6506557-6506761	K562	blood:	n/a	n/a
13	ATF3	chr8:6506162-6507323	HCT-116	colon:	n/a	n/a
14	ATF3	chr8:6506143-6507310	HCT-116	colon:	n/a	n/a
15	BACH1	chr8:6515590-6515641	K562	blood:	n/a	n/a
16	BACH1	chr8:6502437-6502793	K562	blood:	n/a	n/a
17	BACH1	chr8:6506558-6506756	K562	blood:	n/a	n/a
18	BACH1	chr8:6502386-6502829	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr8:6506417-6507012	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr8:6502324-6502817	GM12878	blood:	n/a	n/a
21	BATF	chr8:6547942-6548313	GM12878	blood:	n/a	n/a
22	BATF	chr8:6502391-6502630	GM12878	blood:	n/a	n/a
23	BATF	chr8:6506343-6507039	GM12878	blood:	n/a	chr8:6506704-6506715
24	BATF	chr8:6522793-6523195	GM12878	blood:	n/a	chr8:6523060-6523071 chr8:6523007-6523018
25	BATF	chr8:6547624-6548376	GM12878	blood:	n/a	n/a
26	BATF	chr8:6522802-6523311	GM12878	blood:	n/a	chr8:6523060-6523071 chr8:6523007-6523018
27	BCL11A	chr8:6547591-6548250	GM12878	blood:	n/a	n/a
28	BCL11A	chr8:6522846-6523089	GM12878	blood:	n/a	n/a
29	BCL11A	chr8:6547523-6548351	GM12878	blood:	n/a	n/a
30	BCL11A	chr8:6502407-6502751	GM12878	blood:	n/a	n/a
31	BCL11A	chr8:6522798-6523231	GM12878	blood:	n/a	n/a
32	BCL3	chr8:6506161-6507196	GM12878	blood:	n/a	n/a
33	BCL3	chr8:6502319-6502765	GM12878	blood:	n/a	n/a
34	BCL3	chr8:6506318-6507119	GM12878	blood:	n/a	n/a
35	BCL3	chr8:6547626-6548268	GM12878	blood:	n/a	n/a
36	BCL3	chr8:6547645-6548384	GM12878	blood:	n/a	n/a
37	BCL3	chr8:6522728-6523191	GM12878	blood:	n/a	n/a
38	BCLAF1	chr8:6547611-6548417	GM12878	blood:	n/a	n/a
39	BCLAF1	chr8:6522639-6523348	GM12878	blood:	n/a	n/a
40	BCLAF1	chr8:6547480-6548465	GM12878	blood:	n/a	n/a
41	BCLAF1	chr8:6502395-6502820	GM12878	blood:	n/a	n/a
42	BHLHE40	chr8:6491102-6491413	GM12878	blood:	n/a	n/a
43	BHLHE40	chr8:6506779-6506920	GM12878	blood:	n/a	n/a
44	BHLHE40	chr8:6506487-6507068	HepG2	liver:	n/a	n/a
45	BHLHE40	chr8:6506482-6506991	K562	blood:	n/a	n/a
46	BHLHE40	chr8:6522060-6522558	GM12878	blood:	n/a	n/a
47	BHLHE40	chr8:6547542-6548394	GM12878	blood:	n/a	n/a
48	BHLHE40	chr8:6522844-6523179	GM12878	blood:	n/a	n/a
49	BRCA1	chr8:6548729-6548789	GM12878	blood:	n/a	n/a
50	BRCA1	chr8:6539818-6540283	Hela-S3	cervix:	n/a	n/a

(count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:6492556-6492606	Caco-2	colon:	n/a
2	chr8:6534897-6534947	GM12891	blood:	n/a
3	chr8:6492556-6492606	Caco-2	colon:	n/a
4	chr8:6534897-6534947	GM12891	blood:	n/a
5	chr8:6534897-6534947	HepG2	liver:	n/a
6	chr8:6501499-6501549	HNPCEpiC	eye:	n/a
7	chr8:6519110-6519160	H1-hESC	embryonic stem cell:	embryo
8	chr8:6492556-6492606	GM12892	blood:	n/a
9	chr8:6501499-6501549	GM12878	blood:	n/a
10	chr8:6501499-6501549	NHBE	bronchial:	n/a
11	chr8:6492556-6492606	BE2_C	brain:	n/a
12	chr8:6492531-6492581	RPTEC	kidney:	n/a
13	chr8:6492556-6492606	Hela-S3	cervix:	n/a
14	chr8:6534897-6534947	Jurkat	blood:	n/a
15	chr8:6534897-6534947	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:6501499-6501549	HCT-116	colon:	n/a
17	chr8:6534897-6534947	HUVEC	blood vessel:	n/a
18	chr8:6519110-6519160	Hela-S3	cervix:	n/a
19	chr8:6519110-6519160	HRPEpiC	eye:	n/a
20	chr8:6519110-6519160	HNPCEpiC	eye:	n/a
21	chr8:6534897-6534947	A549	lung:	n/a
22	chr8:6534897-6534947	BE2_C	brain:	n/a
23	chr8:6492531-6492581	HCM	heart:	n/a
24	chr8:6492531-6492581	HCPEpiC	choroid plexus:	n/a
25	chr8:6492556-6492606	SK-N-MC	brain:	n/a
26	chr8:6492556-6492606	AG09309	skin:	n/a
27	chr8:6501499-6501549	HRE	kidney:	n/a
28	chr8:6519110-6519160	ovcar-3	ovarian:	n/a
29	chr8:6501499-6501549	GM12891	blood:	n/a
30	chr8:6501499-6501549	T-47D	breast:	n/a
31	chr8:6492531-6492581	NB4	blood:	n/a
32	chr8:6501499-6501549	A549	lung:	n/a
33	chr8:6501499-6501549	NT2-D1	testis:	n/a
34	chr8:6534897-6534947	PrEC	prostate:	n/a
35	chr8:6534897-6534947	HNPCEpiC	eye:	n/a
36	chr8:6492556-6492606	HIPEpiC	eye:	n/a
37	chr8:6492556-6492606	T-47D	breast:	n/a
38	chr8:6492556-6492606	RPTEC	kidney:	n/a
39	chr8:6534897-6534947	AG04450	lung:	fetal
40	chr8:6492531-6492581	Jurkat	blood:	n/a
41	chr8:6501499-6501549	HepG2	liver:	n/a
42	chr8:6492531-6492581	SAEC	small airway:	n/a
43	chr8:6492556-6492606	HEEpiC	esophagus:	n/a
44	chr8:6519110-6519160	HCM	heart:	n/a
45	chr8:6492556-6492606	MCF10A-Er-Src	breast:	n/a
46	chr8:6519110-6519160	ProgFib	skin:	n/a
47	chr8:6492556-6492606	GM12891	blood:	n/a
48	chr8:6534897-6534947	U87	brain:	n/a
49	chr8:6534897-6534947	HEEpiC	esophagus:	n/a
50	chr8:6534897-6534947	NT2-D1	testis:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:6498880..6501314-chr8:6501971..6503524,2	K562	blood:
2	chr8:6528532..6532073-chr8:6534513..6537566,4	K562	blood:
3	chr8:6281436..6282039-chr8:6539712..6540563,2	MCF-7	breast:
4	chr8:6520749..6523640-chr8:6556573..6558187,2	K562	blood:
5	chr8:6549877..6551891-chr8:6565870..6567774,2	K562	blood:
6	chr8:6540971..6543741-chr8:6558303..6560709,2	MCF-7	breast:
7	chr8:6554514..6556156-chr8:6566360..6567887,2	MCF-7	breast:
8	chr8:6549877..6552444-chr8:6565870..6567915,3	K562	blood:
9	chr8:6532319..6534254-chr8:6544320..6546354,2	MCF-7	breast:
10	chr8:6555465..6559889-chr8:6564305..6567198,4	K562	blood:
11	chr8:6528532..6532073-chr8:6534513..6537566,4	K562	blood:
12	chr8:6545602..6548015-chr8:6631917..6634011,2	K562	blood:
13	chr8:6282250..6282973-chr8:6539904..6540599,2	MCF-7	breast:
14	chr8:6538303..6541938-chr8:6546683..6549264,3	K562	blood:
15	chr8:6519234..6520905-chr8:6522490..6524579,2	K562	blood:
16	chr8:6545858..6548126-chr8:6615946..6617987,2	K562	blood:
17	chr8:6551896..6556965-chr8:6563084..6567295,6	K562	blood:
18	chr8:6521887..6524409-chr8:6525968..6528888,2	K562	blood:
19	chr8:6538303..6541938-chr8:6546683..6549264,3	K562	blood:
20	chr8:6498880..6501314-chr8:6501971..6503524,2	K562	blood:
21	chr8:6548421..6550136-chr8:6565619..6568535,2	MCF-7	breast:
22	chr8:6519234..6520905-chr8:6522490..6524579,2	K562	blood:
23	chr8:6539663..6540421-chr8:6636961..6637870,2	MCF-7	breast:
24	chr8:6545835..6547591-chr8:6566035..6567552,2	MCF-7	breast:
25	chr8:6490982..6493435-chr8:6506576..6508778,2	K562	blood:
26	chr8:6282447..6283252-chr8:6539685..6540602,2	K562	blood:
27	chr8:6532319..6534254-chr8:6544320..6546354,2	MCF-7	breast:
28	chr8:6490982..6493435-chr8:6506576..6508778,2	K562	blood:
29	chr8:6521887..6524409-chr8:6525968..6528888,2	K562	blood:
30	chr8:6546257..6548889-chr8:6565743..6567687,2	K562	blood:
31	chr8:6541963..6544362-chr8:6557182..6559282,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPT2-1	chr8:6526843-6527761	NONHSAT124782
2	lnc-ANGPT2-1	chr8:6505804-6506328	ENSG00000249898.3
3	lnc-ANGPT2-9	chr8:6514841-6515169	l_3535_chr8:6514840-6553144_testes
4	lnc-ANGPT2-1	chr8:6492467-6492940	ENSG00000249898.3
5	lnc-MCPH1-1	chr8:6503576-6506025	ENSG00000271927.1
6	lnc-ANGPT2-1	chr8:6492363-6492940	ENSG00000249898.3
7	lnc-ANGPT2-1	chr8:6527510-6527761	ENSG00000249898.3
8	lnc-MCPH1-2	chr8:6507067-6507095	NONHSAT124781
9	lnc-ANGPT2-9	chr8:6553070-6553144	l_3535_chr8:6514840-6553144_testes
10	lnc-MCPH1-2	chr8:6506319-6506990	NONHSAT124781

No data

Variant related genes	Relation type
ENSG00000271927	TF binding region
ENSG00000249898	TF binding region
ENSG00000271927	CpG island
ENSG00000249898	CpG island
ENSG00000249898	chromatin interactions
ENSG00000155189	chromatin interactions

Extended variants
information (count: 3975 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:3975 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2912065	chr8:6490665-6490666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531245547	chr8:6490700-6490701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547336788	chr8:6490735-6490736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139510791	chr8:6490743-6490744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs544461762	chr8:6490760-6490761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561556234	chr8:6490779-6490780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528973259	chr8:6490787-6490788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549024482	chr8:6490802-6490803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs565443023	chr8:6490817-6490818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146400986	chr8:6490860-6490861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139769358	chr8:6490933-6490934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191377911	chr8:6490951-6490952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs537380030	chr8:6490965-6490966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2515561	chr8:6490975-6490976	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs144361845	chr8:6490999-6491000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146608817	chr8:6491000-6491001	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553384441	chr8:6491003-6491004	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117986542	chr8:6491013-6491014	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs564123309	chr8:6491026-6491027	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2911974	chr8:6491035-6491036	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs559023438	chr8:6491121-6491122	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377064155	chr8:6491122-6491123	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62496954	chr8:6491130-6491131	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs1834451	chr8:6491181-6491182	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs1648114	chr8:6491187-6491188	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148743692	chr8:6491209-6491210	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536126089	chr8:6491221-6491222	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561434374	chr8:6491236-6491237	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs142373756	chr8:6491256-6491257	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540494502	chr8:6491259-6491260	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558992222	chr8:6491260-6491261	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs528207206	chr8:6491281-6491282	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550941192	chr8:6491319-6491320	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs570957783	chr8:6491323-6491324	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs71525746	chr8:6491368-6491369	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183189108	chr8:6491390-6491391	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs113614508	chr8:6491408-6491409	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186808233	chr8:6491411-6491412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs546831926	chr8:6491412-6491413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141832946	chr8:6491440-6491441	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs566952469	chr8:6491441-6491442	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372909532	chr8:6491443-6491444	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs190517869	chr8:6491445-6491446	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112918670	chr8:6491467-6491468	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140461536	chr8:6491477-6491478	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537857049	chr8:6491489-6491490	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535740108	chr8:6491490-6491491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575049314	chr8:6491501-6491502	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557935603	chr8:6491529-6491530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs71525747	chr8:6491553-6491554	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:139)

Disease	PMID	Source
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
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
Epilepsy	22083797	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
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	21364760	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Osteosarcoma	21215367	CNVD
Cognitive impairment	21505072	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:789 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:6458000-6498400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:6474200-6505200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:6474800-6498400	Weak transcription	HSMM	muscle
4	chr8:6476400-6499000	Weak transcription	Brain Angular Gyrus	brain
5	chr8:6476400-6502800	Weak transcription	Colonic Mucosa	Colon
6	chr8:6478200-6494600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr8:6478400-6498400	Weak transcription	HMEC	breast
8	chr8:6479600-6499800	Weak transcription	Aorta	Aorta
9	chr8:6480000-6502000	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr8:6480200-6501800	Weak transcription	NHEK	skin
11	chr8:6480200-6502000	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr8:6480200-6502600	Weak transcription	Gastric	stomach
13	chr8:6480200-6523800	Weak transcription	Fetal Brain Female	brain
14	chr8:6480400-6491400	Weak transcription	Rectal Smooth Muscle	rectum
15	chr8:6480400-6498400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr8:6480400-6499600	Weak transcription	Brain Anterior Caudate	brain
17	chr8:6480400-6499800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:6480400-6499800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:6480400-6499800	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr8:6480400-6502200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:6480400-6505400	Weak transcription	Lung	lung
22	chr8:6480800-6499600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr8:6481800-6501800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr8:6482000-6501800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:6482000-6503600	Weak transcription	Esophagus	oesophagus
26	chr8:6482200-6501200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr8:6483200-6496200	Weak transcription	Pancreas	Pancrea
28	chr8:6483800-6504400	Weak transcription	Liver	Liver
29	chr8:6484000-6500200	Weak transcription	Primary T cells fromperipheralblood	blood
30	chr8:6484000-6502000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr8:6484000-6502200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:6484400-6499800	Weak transcription	Brain Hippocampus Middle	brain
33	chr8:6484400-6502400	Weak transcription	Stomach Smooth Muscle	stomach
34	chr8:6484400-6503000	Weak transcription	Spleen	Spleen
35	chr8:6484400-6503400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr8:6484800-6491800	Weak transcription	Primary T cells from cord blood	blood
37	chr8:6484800-6496400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr8:6484800-6505200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
39	chr8:6485000-6499800	Weak transcription	Fetal Muscle Leg	muscle
40	chr8:6485000-6500400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr8:6485000-6502800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr8:6485000-6504400	Weak transcription	Fetal Intestine Large	intestine
43	chr8:6485200-6494000	Weak transcription	Thymus	Thymus
44	chr8:6485200-6502000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr8:6485400-6494800	Weak transcription	Dnd41	blood
46	chr8:6485400-6499000	Weak transcription	Placenta	Placenta
47	chr8:6485400-6499800	Weak transcription	Fetal Muscle Trunk	muscle
48	chr8:6485400-6501400	Weak transcription	Fetal Intestine Small	intestine
49	chr8:6485400-6503800	Weak transcription	Fetal Stomach	stomach
50	chr8:6486800-6491800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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