Variant report

Variant	nsv610099
Chromosome Location	chr8:7631008-8101641
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3834)
CpG islands
(count:4095)
Chromatin interactive
region (count:18)
LncRNA
region (count:40)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:3834 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8091892-8091896	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8092931-8093297	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8101412-8102391	K562	blood:	n/a	n/a
4	ARID3A	chr8:8101041-8101072	HepG2	liver:	n/a	n/a
5	ATF1	chr8:7771027-7771432	K562	blood:	n/a	n/a
6	ATF1	chr8:7694221-7694565	K562	blood:	n/a	n/a
7	ATF2	chr8:8096080-8096557	GM12878	blood:	n/a	n/a
8	ATF3	chr8:8096172-8096477	K562	blood:	n/a	n/a
9	BACH1	chr8:7771106-7771311	K562	blood:	n/a	n/a
10	BATF	chr8:7922797-7923045	GM12878	blood:	n/a	n/a
11	BATF	chr8:8005726-8005964	GM12878	blood:	n/a	n/a
12	BATF	chr8:8029997-8030427	GM12878	blood:	n/a	n/a
13	BATF	chr8:7809497-7809672	GM12878	blood:	n/a	chr8:7809580-7809591
14	BATF	chr8:8086957-8087326	GM12878	blood:	n/a	n/a
15	BATF	chr8:8035087-8035263	GM12878	blood:	n/a	n/a
16	BATF	chr8:8005100-8005302	GM12878	blood:	n/a	n/a
17	BATF	chr8:8000698-8001151	GM12878	blood:	n/a	n/a
18	BATF	chr8:7896196-7896603	GM12878	blood:	n/a	n/a
19	BATF	chr8:7936786-7937116	GM12878	blood:	n/a	chr8:7936968-7936979
20	BATF	chr8:7994763-7995094	GM12878	blood:	n/a	n/a
21	BATF	chr8:8007429-8007921	GM12878	blood:	n/a	chr8:8007742-8007750
22	BATF	chr8:8030089-8030387	GM12878	blood:	n/a	n/a
23	BATF	chr8:8091245-8091594	GM12878	blood:	n/a	n/a
24	BATF	chr8:8000576-8001188	GM12878	blood:	n/a	n/a
25	BATF	chr8:7994136-7994338	GM12878	blood:	n/a	n/a
26	BATF	chr8:7949085-7949285	GM12878	blood:	n/a	n/a
27	BATF	chr8:8086029-8086344	GM12878	blood:	n/a	n/a
28	BATF	chr8:7896260-7896568	GM12878	blood:	n/a	n/a
29	BATF	chr8:8085189-8085406	GM12878	blood:	n/a	n/a
30	BATF	chr8:8004195-8004622	GM12878	blood:	n/a	n/a
31	BATF	chr8:7804596-7805021	GM12878	blood:	n/a	n/a
32	BATF	chr8:8096176-8096555	GM12878	blood:	n/a	n/a
33	BATF	chr8:8043601-8043892	GM12878	blood:	n/a	n/a
34	BATF	chr8:7812383-7812672	GM12878	blood:	n/a	n/a
35	BATF	chr8:8095764-8096661	GM12878	blood:	n/a	n/a
36	BATF	chr8:8025286-8025491	GM12878	blood:	n/a	n/a
37	BATF	chr8:8005702-8005954	GM12878	blood:	n/a	n/a
38	BATF	chr8:8056483-8056771	GM12878	blood:	n/a	n/a
39	BATF	chr8:8086606-8086880	GM12878	blood:	n/a	chr8:8086859-8086869
40	BATF	chr8:8056440-8056802	GM12878	blood:	n/a	n/a
41	BATF	chr8:8000024-8000529	GM12878	blood:	n/a	n/a
42	BATF	chr8:7936788-7937244	GM12878	blood:	n/a	chr8:7936968-7936979
43	BATF	chr8:8004193-8004724	GM12878	blood:	n/a	n/a
44	BATF	chr8:8025297-8025584	GM12878	blood:	n/a	n/a
45	BATF	chr8:8086780-8087231	GM12878	blood:	n/a	chr8:8086859-8086869
46	BATF	chr8:7744485-7744737	GM12878	blood:	n/a	n/a
47	BATF	chr8:7809440-7809731	GM12878	blood:	n/a	chr8:7809580-7809591
48	BATF	chr8:8007454-8008025	GM12878	blood:	n/a	chr8:8007742-8007750
49	BCL11A	chr8:8023210-8023461	GM12878	blood:	n/a	n/a
50	BCL11A	chr8:8007410-8007710	GM12878	blood:	n/a	chr8:8007656-8007665

(count:4095 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:7881548-7881598	ECC-1	luminal epithelium:	n/a
2	chr8:7888738-7888788	H1-hESC	embryonic stem cell:	embryo
3	chr8:7886076-7886126	ovcar-3	ovarian:	n/a
4	chr8:7885761-7885811	ProgFib	skin:	n/a
5	chr8:7706073-7706123	PANC-1	pancreas:	n/a
6	chr8:7880727-7880777	HNPCEpiC	eye:	n/a
7	chr8:8085532-8085582	PrEC	prostate:	n/a
8	chr8:7880088-7880138	Caco-2	colon:	n/a
9	chr8:7881548-7881598	ECC-1	luminal epithelium:	n/a
10	chr8:7888738-7888788	H1-hESC	embryonic stem cell:	embryo
11	chr8:7886076-7886126	ovcar-3	ovarian:	n/a
12	chr8:7885761-7885811	ProgFib	skin:	n/a
13	chr8:7706073-7706123	PANC-1	pancreas:	n/a
14	chr8:7880727-7880777	HNPCEpiC	eye:	n/a
15	chr8:8085532-8085582	PrEC	prostate:	n/a
16	chr8:7880088-7880138	Caco-2	colon:	n/a
17	chr8:8086144-8086194	GM12878	blood:	n/a
18	chr8:8085544-8085594	ovcar-3	ovarian:	n/a
19	chr8:7884052-7884102	HMEC	breast:	n/a
20	chr8:7721128-7721178	HRE	kidney:	n/a
21	chr8:7886076-7886126	NB4	blood:	n/a
22	chr8:8085973-8086023	GM12892	blood:	n/a
23	chr8:7651924-7651974	GM06990	blood:	n/a
24	chr8:7651924-7651974	HIPEpiC	eye:	n/a
25	chr8:7686204-7686254	IMR90	lung:	fetal
26	chr8:8085496-8085546	NB4	blood:	n/a
27	chr8:7631923-7631973	AG09309	skin:	n/a
28	chr8:7631469-7631519	ProgFib	skin:	n/a
29	chr8:8085496-8085546	AG09309	skin:	n/a
30	chr8:8085496-8085546	AG09319	gingival:	n/a
31	chr8:7706073-7706123	HRPEpiC	eye:	n/a
32	chr8:8084610-8084660	HMEC	breast:	n/a
33	chr8:7881548-7881598	HCM	heart:	n/a
34	chr8:8085532-8085582	NH-A	brain:	n/a
35	chr8:8086686-8086736	GM12892	blood:	n/a
36	chr8:7754234-7754284	HRCEpiC	kidney:	n/a
37	chr8:8084974-8085024	ECC-1	luminal epithelium:	n/a
38	chr8:7650102-7650152	HCT-116	colon:	n/a
39	chr8:7923629-7923679	HCPEpiC	choroid plexus:	n/a
40	chr8:8085544-8085594	HEK293	kidney:	embryo
41	chr8:7888738-7888788	HRE	kidney:	n/a
42	chr8:7867451-7867501	A549	lung:	n/a
43	chr8:7753688-7753738	CMK	blood:	n/a
44	chr8:7873837-7873887	HCF	heart:	n/a
45	chr8:8034602-8034652	HCPEpiC	choroid plexus:	n/a
46	chr8:7885901-7885951	Jurkat	blood:	n/a
47	chr8:7671497-7671547	HL-60	blood:	n/a
48	chr8:7671497-7671547	PANC-1	pancreas:	n/a
49	chr8:7885761-7885811	Hela-S3	cervix:	n/a
50	chr8:7639801-7639851	ProgFib	skin:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
2	chr6:26031709..26032614-chr8:8085130..8085961,2	Hela-S3	cervix:
3	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
4	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
5	chr15:59062813..59063449-chr8:8085838..8086625,2	Hela-S3	cervix:
6	chr8:8086683..8088508-chr8:8193858..8196209,2	MCF-7	breast:
7	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
8	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
9	chr11:3443497..3444149-chr8:8085706..8086350,2	HCT-116	colon:
10	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
11	chr8:8094096..8094629-chr8:8147947..8148540,2	MCF-7	breast:
12	chr8:8094104..8094693-chr8:8146401..8147333,2	MCF-7	breast:
13	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
14	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
15	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
16	chr3:129829770..129830533-chr8:8085798..8086673,3	Hela-S3	cervix:
17	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
18	chr8:7255181..7256067-chr8:7770740..7771265,2	MCF-7	breast:

(count:40 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRAGMIN.1-7	chr8:8097017-8097128	NONHSAT124860
2	lnc-PRAGMIN.1-3	chr8:8077566-8077704	ENSG00000253893.2
3	lnc-PRAGMIN.1-7	chr8:8095696-8095860	NONHSAT124863
4	lnc-PRAGMIN.1-7	chr8:8097728-8097835	NONHSAT124863
5	lnc-PRAGMIN.1-3	chr8:8084256-8084265	XLOC_006994
6	lnc-PRAGMIN.1-3	chr8:8081348-8081432	XLOC_006993
7	lnc-PRAGMIN.1-3	chr8:8081348-8081409	ENSG00000253893.1
8	lnc-PRAGMIN.1-3	chr8:7992174-7992262	ENSG00000253893.1
9	lnc-AC068020.1-1	chr8:8098797-8099202	NONHSAT124867
10	lnc-AC068020.1-1	chr8:8099150-8099484	NONHSAT124868
11	lnc-AC068020.1-1	chr8:8094730-8094797	NONHSAT124861
12	lnc-PRAGMIN.1-7	chr8:8097960-8098070	NONHSAT124863
13	lnc-PRAGMIN.1-3	chr8:8077586-8077704	XLOC_006993
14	lnc-PRAGMIN.1-7	chr8:8097015-8097098	NONHSAT124863
15	lnc-DEFB105A-4	chr8:7854986-7855043	NONHSAT124844
16	lnc-AC068020.1-1	chr8:8101621-8101684	NONHSAT124868
17	lnc-PRAGMIN.1-3	chr8:8077566-8077704	ENSG00000253893.1
18	lnc-AC068020.1-1	chr8:8101621-8102385	NONHSAT124866
19	lnc-PRAGMIN.1-3	chr8:8025339-8025605	ENSG00000253893.1
20	lnc-PRAGMIN.1-3	chr8:8084842-8085129	XLOC_006994
21	lnc-PRAGMIN.1-3	chr8:8083918-8084136	ENSG00000253893.2
22	lnc-PRAGMIN.1-7	chr8:8093525-8093885	NONHSAT124858
23	lnc-PRAGMIN.1-3	chr8:8042248-8042354	ENSG00000253893.2
24	lnc-PRAGMIN.1-7	chr8:8094648-8095823	NONHSAT124860
25	lnc-PRAGMIN.1-3	chr8:8042248-8042354	ENSG00000253893.1
26	lnc-PRAGMIN.1-7	chr8:8095713-8095872	NONHSAT124858
27	lnc-AC068020.1-2	chr8:7996388-7996558	NONHSAT124852
28	lnc-PRAGMIN.1-10	chr8:7974267-7974471	NONHSAT124849
29	lnc-DEFB105A-4	chr8:7847937-7848142	NONHSAT124844
30	lnc-PRAGMIN.1-3	chr8:8083918-8084265	ENSG00000253893.1
31	lnc-DEFB105A-1	chr8:7748525-7750077	NONHSAT124838
32	lnc-PRAGMIN.1-11	chr8:7943544-7944287	NONHSAT124847
33	lnc-PRAGMIN.1-3	chr8:8081348-8081409	ENSG00000253893.2
34	lnc-AC068020.1-2	chr8:7997454-7997523	NONHSAT124852
35	lnc-AC068020.1-1	chr8:8101621-8101707	NONHSAT124867
36	lnc-PRAGMIN.1-7	chr8:8098818-8098933	NONHSAT124863
37	lnc-AC068020.1-1	chr8:8097891-8099954	NONHSAT124866
38	lnc-PRAGMIN.1-3	chr8:8084720-8085385	ENSG00000253893.1
39	lnc-PRAGMIN.1-3	chr8:8025341-8025605	ENSG00000253893.2
40	lnc-AC068020.1-1	chr8:8095815-8096448	NONHSAT124861

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr8:7946552-7946573	MIMAT0005935_2

No data

Variant related genes	Relation type
OR7E96P	TF binding region
FAM90A12P	TF binding region
DEFB107A	TF binding region
FAM90A11P	TF binding region
ENSG00000253881	TF binding region
FAM90A24P	TF binding region
FAM66E	TF binding region
FAM86B3P	TF binding region
FAM85B	TF binding region
ENSG00000254776	TF binding region
DEFB105A	TF binding region
ENPP7P1	TF binding region
MIR548I3	TF binding region
HSPD1P2	TF binding region
ZNF705B	TF binding region
PRR23D2	TF binding region
ENSG00000255459	TF binding region
DEFB4A	TF binding region
USP17L8	TF binding region
SPAG11A	TF binding region
USP17L3	TF binding region
ENSG00000268955	TF binding region
ENSG00000244427	TF binding region
ENSG00000221027	TF binding region
DEFB103A	TF binding region
ENSG00000254311	TF binding region
DEFB104A	TF binding region
ENSG00000215977	TF binding region
DEFB108P1	TF binding region
ENSG00000255211	TF binding region
ALG1L13P	TF binding region
ENSG00000205989	TF binding region
DEFB106A	TF binding region
OR7E96P	CpG island
FAM90A12P	CpG island
DEFB107A	CpG island
FAM90A11P	CpG island
ENSG00000253881	CpG island
FAM90A24P	CpG island
FAM66E	CpG island
FAM86B3P	CpG island
FAM85B	CpG island
ENSG00000254776	CpG island
DEFB105A	CpG island
ENPP7P1	CpG island
MIR548I3	CpG island
HSPD1P2	CpG island
ZNF705B	CpG island
PRR23D2	CpG island
ENSG00000255459	CpG island
DEFB4A	CpG island
USP17L8	CpG island
SPAG11A	CpG island
USP17L3	CpG island
ENSG00000268955	CpG island
ENSG00000244427	CpG island
ENSG00000221027	CpG island
DEFB103A	CpG island
ENSG00000254311	CpG island
DEFB104A	CpG island
ENSG00000215977	CpG island
DEFB108P1	CpG island
ENSG00000255211	CpG island
ALG1L13P	CpG island
ENSG00000205989	CpG island
DEFB106A	CpG island
ENSG00000124693	chromatin interactions
ENSG00000253981	chromatin interactions
ENSG00000173295	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000253540	chromatin interactions
ENSG00000245975	chromatin interactions
UBQLN1	miRNA target sites

Extended variants
information (count: 5688 )
Associated
traits (count: 156 )

Variant overlapped rSNPs/rCNVs (count:5688 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201910128	chr8:7640939-7640940	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs200534249	chr8:7641022-7641023	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs201423419	chr8:7641033-7641034	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs202164484	chr8:7641089-7641090	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200525847	chr8:7641128-7641129	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs201423313	chr8:7641190-7641191	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs548695709	chr8:7641345-7641346	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs565419946	chr8:7641372-7641373	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs576970852	chr8:7641382-7641383	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs377084098	chr8:7641404-7641405	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs557952166	chr8:7641428-7641429	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs571702718	chr8:7641477-7641478	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs375926640	chr8:7641574-7641575	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs537788754	chr8:7641598-7641599	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs557366674	chr8:7641754-7641755	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs185146342	chr8:7641765-7641766	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs2954330	chr8:7657047-7657048	Inactive region	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
18	rs200882271	chr8:7675478-7675479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs554684538	chr8:7680894-7680895	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs200147309	chr8:7682178-7682179	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
21	rs574497755	chr8:7684269-7684270	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs541543635	chr8:7685640-7685641	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570475597	chr8:7686208-7686209	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs539098974	chr8:7686211-7686212	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs150372518	chr8:7686216-7686217	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs556344742	chr8:7686228-7686229	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
27	rs569903827	chr8:7686236-7686237	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
28	rs535791008	chr8:7686250-7686251	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
29	rs538700855	chr8:7690490-7690491	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs551171989	chr8:7690534-7690535	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs571101140	chr8:7690561-7690562	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs201923598	chr8:7690709-7690710	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs536998581	chr8:7690724-7690725	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs9773211	chr8:7692059-7692060	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs565182133	chr8:7692140-7692141	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs561279721	chr8:7692154-7692155	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs200823870	chr8:7692161-7692162	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs575088402	chr8:7692277-7692278	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs540561793	chr8:7692298-7692299	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs185967614	chr8:7693516-7693517	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs148826727	chr8:7693542-7693543	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs532399771	chr8:7693547-7693548	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs60249228	chr8:7693605-7693606	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs147561244	chr8:7693618-7693619	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs2740691	chr8:7693670-7693671	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs376178791	chr8:7693682-7693683	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs534148564	chr8:7693690-7693691	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs553922227	chr8:7693709-7693710	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs577125808	chr8:7693725-7693726	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs546076264	chr8:7693734-7693735	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:156)

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
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
Colorectal cancer	16774939	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
Cognitive impairment	21505072	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	20369283	CNVD
Urothelial carcinoma	21177765	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	21364760	CNVD
Developmental disorder	20461109	CNVD
Crohn''s disease	17953491	CNVD
Immune disease	21076436	CNVD
Crohn''s disease	21956041	CNVD
Autism	21865298	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	22302058	CNVD
Schizophrenia	23813976	CNVD
Schizophrenia	21346763	CNVD

Chromatin state (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:7641200-7641600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr8:7641200-7641600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:7641200-7641600	Active TSS	Primary T cells fromperipheralblood	blood
4	chr8:7641200-7641600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:7641200-7641600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr8:7641200-7641600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr8:7641200-7641600	Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr8:7641200-7641600	Active TSS	Stomach Smooth Muscle	stomach
9	chr8:7693600-7693800	Bivalent Enhancer	Duodenum Mucosa	Duodenum
10	chr8:7694200-7694400	Enhancers	Brain Anterior Caudate	brain
11	chr8:7720200-7721000	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:7721000-7721200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr8:7721000-7721200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:7721000-7721200	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr8:7721000-7721200	Enhancers	HSMM	muscle
16	chr8:7721000-7721200	Enhancers	HSMMtube	muscle
17	chr8:7721000-7721400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr8:7721000-7721400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr8:7721000-7721400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:7721000-7721400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:7721000-7721400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr8:7721000-7721400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr8:7721000-7721400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr8:7721000-7721400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr8:7721000-7721400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr8:7721000-7721400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr8:7721000-7721400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr8:7721000-7721400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr8:7721000-7721400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr8:7721000-7721400	Enhancers	NHEK	skin
31	chr8:7721000-7721400	Enhancers	Osteobl	bone
32	chr8:7731200-7731600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr8:7731400-7731800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr8:7731400-7732400	Enhancers	Muscle Satellite Cultured Cells	--
35	chr8:7731800-7732200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr8:7732200-7732400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:7732400-7736400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr8:7736400-7736800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr8:7746200-7746600	Enhancers	Dnd41	blood
40	chr8:7746600-7746800	Weak transcription	Dnd41	blood
41	chr8:7746800-7747200	Enhancers	Dnd41	blood
42	chr8:7747200-7752000	Weak transcription	Dnd41	blood
43	chr8:7750000-7750800	Enhancers	Stomach Mucosa	stomach
44	chr8:7752000-7752400	Enhancers	Dnd41	blood
45	chr8:7759600-7760000	Enhancers	Osteobl	bone
46	chr8:7770200-7770400	Enhancers	Muscle Satellite Cultured Cells	--
47	chr8:7770200-7771200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr8:7770200-7771200	Enhancers	Osteobl	bone
49	chr8:7770200-7771400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr8:7770400-7770600	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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