Variant report

Variant	nsv1016780
Chromosome Location	chr8:7972326-8148289
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3962)
CpG islands
(count:1468)
Chromatin interactive
region (count:82)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3962 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8126032-8126609	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8127880-8128214	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8101412-8102391	K562	blood:	n/a	n/a
4	ARID3A	chr8:8130676-8131061	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:8092931-8093297	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:8146721-8147360	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:8101041-8101072	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:8114109-8114421	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:8136392-8136433	K562	blood:	n/a	n/a
10	ARID3A	chr8:8105348-8105599	HepG2	liver:	n/a	n/a
11	ARID3A	chr8:8102923-8103018	K562	blood:	n/a	n/a
12	ARID3A	chr8:8145751-8146493	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:8111412-8112067	HepG2	liver:	n/a	n/a
14	ARID3A	chr8:8127158-8127358	HepG2	liver:	n/a	n/a
15	ARID3A	chr8:8146105-8146305	K562	blood:	n/a	n/a
16	ARID3A	chr8:8105314-8105669	K562	blood:	n/a	n/a
17	ARID3A	chr8:8091892-8091896	HepG2	liver:	n/a	n/a
18	ATF1	chr8:8101961-8102473	K562	blood:	n/a	n/a
19	ATF1	chr8:8118490-8118523	K562	blood:	n/a	n/a
20	ATF1	chr8:8144090-8144415	K562	blood:	n/a	n/a
21	ATF2	chr8:8143978-8144540	GM12878	blood:	n/a	n/a
22	ATF2	chr8:8141903-8142578	GM12878	blood:	n/a	n/a
23	ATF2	chr8:8126203-8126652	GM12878	blood:	n/a	n/a
24	ATF2	chr8:8126192-8126618	GM12878	blood:	n/a	n/a
25	ATF2	chr8:8096080-8096557	GM12878	blood:	n/a	n/a
26	ATF2	chr8:8143907-8144515	GM12878	blood:	n/a	n/a
27	ATF2	chr8:8136646-8137350	GM12878	blood:	n/a	n/a
28	ATF2	chr8:8141766-8142478	GM12878	blood:	n/a	n/a
29	ATF3	chr8:8145708-8146540	HCT-116	colon:	n/a	n/a
30	ATF3	chr8:8101985-8102287	K562	blood:	n/a	n/a
31	ATF3	chr8:8145665-8146549	A549	lung:	n/a	n/a
32	ATF3	chr8:8101821-8102415	K562	blood:	n/a	n/a
33	ATF3	chr8:8145720-8146548	HCT-116	colon:	n/a	n/a
34	ATF3	chr8:8145728-8146513	A549	lung:	n/a	n/a
35	ATF3	chr8:8127796-8128282	A549	lung:	n/a	n/a
36	ATF3	chr8:8096172-8096477	K562	blood:	n/a	n/a
37	BACH1	chr8:8130683-8130937	K562	blood:	n/a	n/a
38	BATF	chr8:8144052-8144469	GM12878	blood:	n/a	n/a
39	BATF	chr8:8095764-8096661	GM12878	blood:	n/a	n/a
40	BATF	chr8:8091245-8091594	GM12878	blood:	n/a	n/a
41	BATF	chr8:8005702-8005954	GM12878	blood:	n/a	n/a
42	BATF	chr8:8007429-8007921	GM12878	blood:	n/a	chr8:8007742-8007750
43	BATF	chr8:8005100-8005302	GM12878	blood:	n/a	n/a
44	BATF	chr8:8126185-8126638	GM12878	blood:	n/a	chr8:8126405-8126416 chr8:8126421-8126431 chr8:8126417-8126427 chr8:8126420-8126431
45	BATF	chr8:8086780-8087231	GM12878	blood:	n/a	chr8:8086859-8086869
46	BATF	chr8:8143371-8143632	GM12878	blood:	n/a	n/a
47	BATF	chr8:8143398-8143620	GM12878	blood:	n/a	n/a
48	BATF	chr8:7994763-7995094	GM12878	blood:	n/a	n/a
49	BATF	chr8:8136381-8136667	GM12878	blood:	n/a	n/a
50	BATF	chr8:8000576-8001188	GM12878	blood:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8086146-8086196	GM12891	blood:	n/a
2	chr8:8131077-8131127	Hepatocyte	liver:	n/a
3	chr8:8085532-8085582	A549	lung:	n/a
4	chr8:8084126-8084176	ProgFib	skin:	n/a
5	chr8:8086146-8086196	GM12891	blood:	n/a
6	chr8:8131077-8131127	Hepatocyte	liver:	n/a
7	chr8:8085532-8085582	A549	lung:	n/a
8	chr8:8084126-8084176	ProgFib	skin:	n/a
9	chr8:8034763-8034813	Hepatocyte	liver:	n/a
10	chr8:8085544-8085594	GM12878	blood:	n/a
11	chr8:8146129-8146179	HRPEpiC	eye:	n/a
12	chr8:8085503-8085553	MCF10A-Er-Src	breast:	n/a
13	chr8:8085973-8086023	BE2_C	brain:	n/a
14	chr8:8085532-8085582	AG09319	gingival:	n/a
15	chr8:8032031-8032081	HCT-116	colon:	n/a
16	chr8:8085844-8085894	AG09309	skin:	n/a
17	chr8:8085496-8085546	ProgFib	skin:	n/a
18	chr8:8102392-8102442	K562	blood:	n/a
19	chr8:8082819-8082869	MCF10A-Er-Src	breast:	n/a
20	chr8:8034763-8034813	AG04449	skin:	fetal
21	chr8:8082819-8082869	AG09319	gingival:	n/a
22	chr8:8131077-8131127	BE2_C	brain:	n/a
23	chr8:8085496-8085546	Caco-2	colon:	n/a
24	chr8:8082819-8082869	ProgFib	skin:	n/a
25	chr8:8034602-8034652	AG09319	gingival:	n/a
26	chr8:8090460-8090510	NT2-D1	testis:	n/a
27	chr8:8034602-8034652	AG04450	lung:	fetal
28	chr8:8032031-8032081	MCF-7	breast:	n/a
29	chr8:8084974-8085024	IMR90	lung:	fetal
30	chr8:8085946-8085996	NH-A	brain:	n/a
31	chr8:8084610-8084660	HIPEpiC	eye:	n/a
32	chr8:8146129-8146179	PANC-1	pancreas:	n/a
33	chr8:8084610-8084660	HCPEpiC	choroid plexus:	n/a
34	chr8:8084126-8084176	ovcar-3	ovarian:	n/a
35	chr8:8102392-8102442	NB4	blood:	n/a
36	chr8:8146129-8146179	Hepatocyte	liver:	n/a
37	chr8:8085946-8085996	PFSK-1	brain:	n/a
38	chr8:8102392-8102442	BJ	skin:	n/a
39	chr8:8032031-8032081	PANC-1	pancreas:	n/a
40	chr8:8082819-8082869	GM12892	blood:	n/a
41	chr8:8084610-8084660	Hela-S3	cervix:	n/a
42	chr8:8131077-8131127	HRPEpiC	eye:	n/a
43	chr8:8082819-8082869	NB4	blood:	n/a
44	chr8:8034602-8034652	RPTEC	kidney:	n/a
45	chr8:8131077-8131127	NH-A	brain:	n/a
46	chr8:8084974-8085024	ovcar-3	ovarian:	n/a
47	chr8:8086146-8086196	HEEpiC	esophagus:	n/a
48	chr8:8102121-8102171	CMK	blood:	n/a
49	chr8:8131077-8131127	GM19239	blood:	n/a
50	chr8:8085844-8085894	Hepatocyte	liver:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:8145925..8147772-chr8:8172599..8174671,2	MCF-7	breast:
2	chr8:8146386..8147240-chr8:8365579..8366086,2	MCF-7	breast:
3	chr8:8134812..8136654-chr8:8146118..8147961,3	K562	blood:
4	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
5	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
6	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
7	chr8:8147966..8148515-chr8:8336160..8336710,2	MCF-7	breast:
8	chr8:8134812..8136654-chr8:8146118..8147961,3	K562	blood:
9	chr8:8140760..8143388-chr8:8146728..8148425,2	K562	blood:
10	chr8:8126556..8131624-chr8:8143035..8148399,10	MCF-7	breast:
11	chr8:8126193..8127836-chr8:8129384..8131743,2	MCF-7	breast:
12	chr8:8101157..8102709-chr8:8124508..8126459,2	MCF-7	breast:
13	chr3:129829770..129830533-chr8:8085798..8086673,3	Hela-S3	cervix:
14	chr8:8146134..8147870-chr8:8228066..8231062,2	MCF-7	breast:
15	chr8:8142616..8145069-chr8:8226333..8228141,2	MCF-7	breast:
16	chr8:8147573..8150272-chr8:8166843..8168780,2	MCF-7	breast:
17	chr8:8094096..8094629-chr8:8147947..8148540,2	MCF-7	breast:
18	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
19	chr15:59062813..59063449-chr8:8085838..8086625,2	Hela-S3	cervix:
20	chr8:8104258..8105835-chr8:8243426..8245376,2	MCF-7	breast:
21	chr8:8147577..8148479-chr8:8171987..8172936,6	MCF-7	breast:
22	chr8:8086683..8088508-chr8:8193858..8196209,2	MCF-7	breast:
23	chr8:8134161..8136694-chr8:8559309..8560894,2	MCF-7	breast:
24	chr8:8147508..8148471-chr8:8365206..8366162,5	MCF-7	breast:
25	chr8:8147577..8148485-chr8:8171987..8172936,5	MCF-7	breast:
26	chr8:8105578..8107200-chr8:8525517..8527239,2	MCF-7	breast:
27	chr8:8105059..8106011-chr8:8526943..8527953,6	MCF-7	breast:
28	chr8:8140760..8143388-chr8:8146728..8148425,2	K562	blood:
29	chr8:8141970..8144276-chr8:8242374..8245136,3	MCF-7	breast:
30	chr8:8145045..8147805-chr8:8168275..8170393,2	MCF-7	breast:
31	chr5:40835342..40835901-chr8:8146133..8146693,2	Hela-S3	cervix:
32	chr8:8138288..8140321-chr8:8142532..8144155,2	MCF-7	breast:
33	chr8:8094104..8094693-chr8:8146401..8147333,2	MCF-7	breast:
34	chr8:8142878..8144520-chr8:8146399..8149197,2	MCF-7	breast:
35	chr8:8146402..8147201-chr8:8172122..8172875,3	MCF-7	breast:
36	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
37	chr8:8147727..8148466-chr8:8172098..8172982,3	MCF-7	breast:
38	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
39	chr8:8146302..8147264-chr8:8365295..8366108,2	MCF-7	breast:
40	chr8:8144375..8149679-chr8:8240479..8246459,10	MCF-7	breast:
41	chr8:8108549..8111183-chr8:8240516..8242778,2	MCF-7	breast:
42	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
43	chr8:8145815..8148362-chr8:8152420..8155525,4	MCF-7	breast:
44	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
45	chr8:8131655..8133179-chr8:8135431..8137292,2	MCF-7	breast:
46	chr8:8142878..8144520-chr8:8146399..8149197,2	MCF-7	breast:
47	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
48	chr8:8101610..8104492-chr8:8112542..8114092,2	K562	blood:
49	chr8:8105365..8106008-chr8:8526894..8527465,2	K562	blood:
50	chr8:8094104..8094693-chr8:8146401..8147333,2	MCF-7	breast:

(count:36 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
FAM86B3P	TF binding region
FAM85B	TF binding region
ENPP7P1	TF binding region
ENSG00000268955	TF binding region
ENSG00000221027	TF binding region
ENSG00000254311	TF binding region
ALG1L13P	TF binding region
FAM86B3P	CpG island
FAM85B	CpG island
ENPP7P1	CpG island
ENSG00000268955	CpG island
ENSG00000221027	CpG island
ENSG00000254311	CpG island
ALG1L13P	CpG island
ENSG00000145592	chromatin interactions
ENSG00000128923	chromatin interactions
ENSG00000253958	chromatin interactions
ENSG00000245975	chromatin interactions
ENSG00000182319	chromatin interactions
ENSG00000253540	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000176305	chromatin interactions
ENSG00000254153	chromatin interactions
ENSG00000253981	chromatin interactions
ENSG00000173295	chromatin interactions
ENSG00000124693	chromatin interactions
UBQLN1	miRNA target sites

Extended variants
information (count: 6174 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:6174 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530461805	chr8:7974274-7974275	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs546859549	chr8:7974282-7974283	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs567078455	chr8:7974383-7974384	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs538726218	chr8:7974447-7974448	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs552263746	chr8:7974457-7974458	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs568866633	chr8:7974471-7974472	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs575455760	chr8:7974899-7974900	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs558824691	chr8:7975662-7975663	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs575391914	chr8:7975668-7975669	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs544348058	chr8:7975721-7975722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs574385033	chr8:7975967-7975968	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs540524898	chr8:7976015-7976016	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs201862891	chr8:7976018-7976019	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs200015008	chr8:7976037-7976038	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs113655427	chr8:7976771-7976772	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs547517727	chr8:7976784-7976785	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs377399865	chr8:7976799-7976800	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551814205	chr8:7976817-7976818	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs371014646	chr8:7976820-7976821	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs185731839	chr8:7978174-7978175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs202197247	chr8:7978189-7978190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs186362509	chr8:7978220-7978221	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs189585305	chr8:7978224-7978225	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs200239885	chr8:7978245-7978246	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs538036801	chr8:7978269-7978270	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs190196809	chr8:7978301-7978302	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs375870573	chr8:7978315-7978316	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs79559273	chr8:7978361-7978362	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs183836078	chr8:7978390-7978391	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs112574115	chr8:7978395-7978396	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs199741838	chr8:7978410-7978411	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs200586246	chr8:7978485-7978486	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs186674656	chr8:7978533-7978534	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs201235803	chr8:7978545-7978546	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs568132932	chr8:7978553-7978554	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs112196606	chr8:7991253-7991254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs374749079	chr8:7991319-7991320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200856124	chr8:7991355-7991356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369108038	chr8:7991382-7991383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371753276	chr8:7991433-7991434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2933987	chr8:7991444-7991445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369874542	chr8:7991445-7991446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs3103865	chr8:7991492-7991493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62496707	chr8:7991513-7991514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377277969	chr8:7991519-7991520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202228285	chr8:7991544-7991545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3989472	chr8:7991546-7991547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201167182	chr8:7991555-7991556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548680500	chr8:7991568-7991569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs565693141	chr8:7991592-7991593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Williams Syndrome	20824207	CNVD
Schizophrenia	20967226	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
Developmental disorder	20461109	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	21346763	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	21138945	CNVD

Chromatin state (count:1272 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:7991200-7999400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr8:7992600-7992800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
3	chr8:7992800-8009000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr8:7993000-7993400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr8:7993400-7993800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
6	chr8:7993800-8016200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr8:7997800-7998200	Enhancers	Fetal Thymus	thymus
8	chr8:7998200-8000600	Weak transcription	Fetal Thymus	thymus
9	chr8:7998400-7998600	Enhancers	Primary T cells from cord blood	blood
10	chr8:7999200-7999400	Enhancers	Primary T cells from cord blood	blood
11	chr8:7999200-7999400	Enhancers	Fetal Intestine Large	intestine
12	chr8:7999200-7999600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr8:7999400-7999600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:8000600-8000800	Enhancers	Fetal Thymus	thymus
15	chr8:8001400-8001800	Enhancers	Rectal Mucosa Donor 31	rectum
16	chr8:8003200-8003600	Enhancers	K562	blood
17	chr8:8008600-8011000	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr8:8009000-8009400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
19	chr8:8009400-8014200	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr8:8014200-8014600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
21	chr8:8014600-8034400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr8:8016000-8027000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr8:8016800-8024800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr8:8017200-8022200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr8:8017200-8022200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr8:8021000-8023200	Weak transcription	Fetal Intestine Small	intestine
27	chr8:8022200-8022400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:8022200-8022400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:8022200-8022400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:8022200-8022400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
31	chr8:8022400-8023000	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr8:8024800-8025200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr8:8034400-8035000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr8:8034600-8034800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr8:8034600-8034800	Enhancers	NHEK	skin
36	chr8:8034600-8035000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:8034600-8035000	Active TSS	Esophagus	oesophagus
38	chr8:8034800-8035400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr8:8035000-8035400	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr8:8035400-8035600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr8:8035400-8035600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr8:8035600-8038400	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr8:8035600-8038400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr8:8037200-8037400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr8:8037400-8038400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr8:8037800-8039600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr8:8038400-8038600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr8:8038400-8038600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr8:8038400-8039200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr8:8038400-8039200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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