Variant report

Variant	nsv1017746
Chromosome Location	chr8:8018024-8148810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3512)
CpG islands
(count:1467)
Chromatin interactive
region (count:83)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3512 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8105348-8105599	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:8101041-8101072	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8092931-8093297	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:8114109-8114421	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:8111412-8112067	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:8105314-8105669	K562	blood:	n/a	n/a
7	ARID3A	chr8:8146721-8147360	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:8127880-8128214	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:8127158-8127358	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:8102923-8103018	K562	blood:	n/a	n/a
11	ARID3A	chr8:8126032-8126609	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:8145751-8146493	HepG2	liver:	n/a	n/a
13	ARID3A	chr8:8136392-8136433	K562	blood:	n/a	n/a
14	ARID3A	chr8:8091892-8091896	HepG2	liver:	n/a	n/a
15	ARID3A	chr8:8130676-8131061	HepG2	liver:	n/a	n/a
16	ARID3A	chr8:8101412-8102391	K562	blood:	n/a	n/a
17	ARID3A	chr8:8146105-8146305	K562	blood:	n/a	n/a
18	ATF1	chr8:8144090-8144415	K562	blood:	n/a	n/a
19	ATF1	chr8:8118490-8118523	K562	blood:	n/a	n/a
20	ATF1	chr8:8101961-8102473	K562	blood:	n/a	n/a
21	ATF2	chr8:8126192-8126618	GM12878	blood:	n/a	n/a
22	ATF2	chr8:8141766-8142478	GM12878	blood:	n/a	n/a
23	ATF2	chr8:8136646-8137350	GM12878	blood:	n/a	n/a
24	ATF2	chr8:8141903-8142578	GM12878	blood:	n/a	n/a
25	ATF2	chr8:8096080-8096557	GM12878	blood:	n/a	n/a
26	ATF2	chr8:8126203-8126652	GM12878	blood:	n/a	n/a
27	ATF2	chr8:8143978-8144540	GM12878	blood:	n/a	n/a
28	ATF2	chr8:8143907-8144515	GM12878	blood:	n/a	n/a
29	ATF3	chr8:8145665-8146549	A549	lung:	n/a	n/a
30	ATF3	chr8:8145708-8146540	HCT-116	colon:	n/a	n/a
31	ATF3	chr8:8101821-8102415	K562	blood:	n/a	n/a
32	ATF3	chr8:8096172-8096477	K562	blood:	n/a	n/a
33	ATF3	chr8:8101985-8102287	K562	blood:	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	chr8:8145720-8146548	HCT-116	colon:	n/a	n/a
37	BACH1	chr8:8130683-8130937	K562	blood:	n/a	n/a
38	BATF	chr8:8086029-8086344	GM12878	blood:	n/a	n/a
39	BATF	chr8:8086780-8087231	GM12878	blood:	n/a	chr8:8086859-8086869
40	BATF	chr8:8143371-8143632	GM12878	blood:	n/a	n/a
41	BATF	chr8:8136381-8136667	GM12878	blood:	n/a	n/a
42	BATF	chr8:8086606-8086880	GM12878	blood:	n/a	chr8:8086859-8086869
43	BATF	chr8:8126297-8126540	GM12878	blood:	n/a	chr8:8126405-8126416 chr8:8126421-8126431 chr8:8126417-8126427 chr8:8126420-8126431
44	BATF	chr8:8035087-8035263	GM12878	blood:	n/a	n/a
45	BATF	chr8:8144052-8144469	GM12878	blood:	n/a	n/a
46	BATF	chr8:8025286-8025491	GM12878	blood:	n/a	n/a
47	BATF	chr8:8091245-8091594	GM12878	blood:	n/a	n/a
48	BATF	chr8:8143398-8143620	GM12878	blood:	n/a	n/a
49	BATF	chr8:8137532-8137784	GM12878	blood:	n/a	chr8:8137667-8137678 chr8:8137668-8137678
50	BATF	chr8:8141982-8142461	GM12878	blood:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8102392-8102442	ovcar-3	ovarian:	n/a
2	chr8:8131077-8131127	CMK	blood:	n/a
3	chr8:8086686-8086736	GM12892	blood:	n/a
4	chr8:8102392-8102442	ovcar-3	ovarian:	n/a
5	chr8:8131077-8131127	CMK	blood:	n/a
6	chr8:8086686-8086736	GM12892	blood:	n/a
7	chr8:8086144-8086194	RPTEC	kidney:	n/a
8	chr8:8085973-8086023	NH-A	brain:	n/a
9	chr8:8120624-8120674	SKMC	muscle:	n/a
10	chr8:8086686-8086736	GM12878	blood:	n/a
11	chr8:8131077-8131127	HCM	heart:	n/a
12	chr8:8085844-8085894	BE2_C	brain:	n/a
13	chr8:8084610-8084660	SK-N-SH_RA	brain:	n/a
14	chr8:8085946-8085996	NT2-D1	testis:	n/a
15	chr8:8085946-8085996	H1-hESC	embryonic stem cell:	embryo
16	chr8:8084126-8084176	HRPEpiC	eye:	n/a
17	chr8:8086146-8086196	SK-N-MC	brain:	n/a
18	chr8:8085503-8085553	Caco-2	colon:	n/a
19	chr8:8084974-8085024	K562	blood:	n/a
20	chr8:8090460-8090510	NH-A	brain:	n/a
21	chr8:8084610-8084660	NB4	blood:	n/a
22	chr8:8034763-8034813	CMK	blood:	n/a
23	chr8:8085532-8085582	AG09319	gingival:	n/a
24	chr8:8085946-8085996	BJ	skin:	n/a
25	chr8:8120624-8120674	AG10803	skin:	n/a
26	chr8:8085496-8085546	SKMC	muscle:	n/a
27	chr8:8085946-8085996	AG04449	skin:	fetal
28	chr8:8131077-8131127	GM19239	blood:	n/a
29	chr8:8102392-8102442	HEK293	kidney:	embryo
30	chr8:8085946-8085996	HCT-116	colon:	n/a
31	chr8:8086686-8086736	T-47D	breast:	n/a
32	chr8:8085844-8085894	Hela-S3	cervix:	n/a
33	chr8:8085946-8085996	AG09309	skin:	n/a
34	chr8:8085532-8085582	SAEC	small airway:	n/a
35	chr8:8085973-8086023	BJ	skin:	n/a
36	chr8:8034763-8034813	Hela-S3	cervix:	n/a
37	chr8:8086146-8086196	PANC-1	pancreas:	n/a
38	chr8:8086144-8086194	ovcar-3	ovarian:	n/a
39	chr8:8084126-8084176	CMK	blood:	n/a
40	chr8:8084610-8084660	Caco-2	colon:	n/a
41	chr8:8146129-8146179	HL-60	blood:	n/a
42	chr8:8102392-8102442	HUVEC	blood vessel:	n/a
43	chr8:8102121-8102171	HMEC	breast:	n/a
44	chr8:8085973-8086023	GM12891	blood:	n/a
45	chr8:8120624-8120674	HCT-116	colon:	n/a
46	chr8:8082819-8082869	GM12878	blood:	n/a
47	chr8:8102121-8102171	SK-N-SH	brain:	n/a
48	chr8:8085496-8085546	NB4	blood:	n/a
49	chr8:8086144-8086194	GM12878	blood:	n/a
50	chr8:8086144-8086194	HIPEpiC	eye:	n/a

(count:83 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:8128010..8130864-chr8:8317877..8319814,2	MCF-7	breast:
2	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
3	chr8:8146324..8147133-chr8:8168152..8168656,2	MCF-7	breast:
4	chr8:8147727..8148466-chr8:8172098..8172982,3	MCF-7	breast:
5	chr8:8147089..8149132-chr8:8190153..8192051,2	MCF-7	breast:
6	chr8:8146657..8147172-chr8:8172119..8172832,2	MCF-7	breast:
7	chr8:8141970..8144276-chr8:8242374..8245136,3	MCF-7	breast:
8	chr5:40835342..40835901-chr8:8146133..8146693,2	Hela-S3	cervix:
9	chr8:8134812..8136654-chr8:8146118..8147961,3	K562	blood:
10	chr8:8105578..8107200-chr8:8525517..8527239,2	MCF-7	breast:
11	chr15:59062813..59063449-chr8:8085838..8086625,2	Hela-S3	cervix:
12	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
13	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
14	chr8:8146386..8147240-chr8:8365579..8366086,2	MCF-7	breast:
15	chr8:8094096..8095019-chr8:8147506..8148540,3	MCF-7	breast:
16	chr8:8126193..8127836-chr8:8129384..8131743,2	MCF-7	breast:
17	chr8:8130384..8131365-chr8:8526780..8528280,9	K562	blood:
18	chr8:8130322..8131342-chr8:8527334..8528198,3	MCF-7	breast:
19	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
20	chr8:8145200..8147453-chr8:8312155..8314860,2	MCF-7	breast:
21	chr8:8138288..8140321-chr8:8142532..8144155,2	MCF-7	breast:
22	chr8:8094096..8094629-chr8:8147947..8148540,2	MCF-7	breast:
23	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
24	chr8:8130421..8131300-chr8:8175825..8176932,3	K562	blood:
25	chr8:8146274..8147281-chr8:8365228..8366135,6	MCF-7	breast:
26	chr8:8101610..8104279-chr8:8111391..8114092,2	K562	blood:
27	chr8:8145045..8147805-chr8:8168275..8170393,2	MCF-7	breast:
28	chr8:8131655..8133179-chr8:8135431..8137292,2	MCF-7	breast:
29	chr8:8134161..8136694-chr8:8559309..8560894,2	MCF-7	breast:
30	chr8:8142878..8144520-chr8:8146399..8149197,2	MCF-7	breast:
31	chr8:8148672..8150547-chr8:8158525..8160965,2	MCF-7	breast:
32	chr8:8126556..8131624-chr8:8143035..8148399,10	MCF-7	breast:
33	chr8:8134812..8136654-chr8:8146118..8147961,3	K562	blood:
34	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
35	chr8:8129344..8132133-chr8:8525629..8527896,2	MCF-7	breast:
36	chr8:8105059..8106011-chr8:8526943..8527953,6	MCF-7	breast:
37	chr8:8094104..8094693-chr8:8146401..8147333,2	MCF-7	breast:
38	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
39	chr8:8101157..8102709-chr8:8124508..8126459,2	MCF-7	breast:
40	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
41	chr8:8147966..8148515-chr8:8336160..8336710,2	MCF-7	breast:
42	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
43	chr6:26031709..26032614-chr8:8085130..8085961,2	Hela-S3	cervix:
44	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
45	chr8:8146402..8147201-chr8:8172122..8172875,3	MCF-7	breast:
46	chr8:8094104..8095024-chr8:8146401..8147333,3	MCF-7	breast:
47	chr8:8094096..8094629-chr8:8147947..8148540,2	MCF-7	breast:
48	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
49	chr8:8105365..8106008-chr8:8526894..8527465,2	K562	blood:
50	chr8:8144670..8146200-chr8:8236707..8239376,2	MCF-7	breast:

(count:32 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 5488 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:5488 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537428978	chr8:8018116-8018117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2728865	chr8:8018124-8018125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368344311	chr8:8018194-8018195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202022666	chr8:8018245-8018246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200355403	chr8:8018303-8018304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554173584	chr8:8018335-8018336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs151221014	chr8:8018351-8018352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2728867	chr8:8018357-8018358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs200802772	chr8:8018397-8018398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs71217278	chr8:8018399-8018400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200260281	chr8:8018484-8018485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs111478565	chr8:8018571-8018572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371722104	chr8:8018671-8018672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112122729	chr8:8018675-8018676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs374999666	chr8:8018687-8018688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs201254758	chr8:8018725-8018726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150501132	chr8:8018749-8018750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568389237	chr8:8018759-8018760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs200808284	chr8:8018854-8018855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs534239241	chr8:8018918-8018919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs113813497	chr8:8018978-8018979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28576496	chr8:8019009-8019010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs199632571	chr8:8019064-8019065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371860474	chr8:8019072-8019073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544197244	chr8:8019081-8019082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374462819	chr8:8019082-8019083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370014169	chr8:8019083-8019084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs71217279	chr8:8019084-8019085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553910234	chr8:8019101-8019102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577371327	chr8:8019115-8019116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201838432	chr8:8019141-8019142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546422239	chr8:8019148-8019149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs113606513	chr8:8019192-8019193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9773367	chr8:8019252-8019253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs9772451	chr8:8019261-8019262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200789410	chr8:8019343-8019344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556370574	chr8:8019443-8019444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542219739	chr8:8019463-8019464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200067145	chr8:8019478-8019479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113087655	chr8:8019539-8019540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562085307	chr8:8019892-8019893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529980233	chr8:8019913-8019914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs200849453	chr8:8019930-8019931	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201595178	chr8:8019933-8019934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs201478573	chr8:8019952-8019953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374443794	chr8:8020036-8020037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs540542090	chr8:8020050-8020051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199920631	chr8:8020058-8020059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560246392	chr8:8020084-8020085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201023119	chr8:8020103-8020104	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:1254 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8014600-8034400	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr8:8016000-8027000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:8016800-8024800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr8:8017200-8022200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr8:8017200-8022200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr8:8021000-8023200	Weak transcription	Fetal Intestine Small	intestine
7	chr8:8022200-8022400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:8022200-8022400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:8022200-8022400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr8:8022200-8022400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
11	chr8:8022400-8023000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr8:8024800-8025200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr8:8034400-8035000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr8:8034600-8034800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr8:8034600-8034800	Enhancers	NHEK	skin
16	chr8:8034600-8035000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:8034600-8035000	Active TSS	Esophagus	oesophagus
18	chr8:8034800-8035400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr8:8035000-8035400	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr8:8035400-8035600	Enhancers	H1 Cell Line	embryonic stem cell
21	chr8:8035400-8035600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr8:8035600-8038400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr8:8035600-8038400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:8037200-8037400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr8:8037400-8038400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:8037800-8039600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr8:8038400-8038600	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr8:8038400-8038600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr8:8038400-8039200	Enhancers	H1 Cell Line	embryonic stem cell
30	chr8:8038400-8039200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:8038400-8039600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr8:8038400-8039600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:8038600-8038800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr8:8038800-8039200	Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr8:8039200-8039400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr8:8039200-8039400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
37	chr8:8056000-8056800	Active TSS	Breast Myoepithelial Primary Cells	Breast
38	chr8:8056200-8056600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr8:8056200-8056600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr8:8056200-8056600	Enhancers	Adipose Nuclei	Adipose
41	chr8:8056200-8056600	Active TSS	Ovary	ovary
42	chr8:8056200-8056600	Active TSS	Right Ventricle	heart
43	chr8:8056200-8056600	Active TSS	A549	lung
44	chr8:8056200-8056600	Active TSS	HMEC	breast
45	chr8:8067400-8068200	Active TSS	Stomach Smooth Muscle	stomach
46	chr8:8067600-8068000	Enhancers	Left Ventricle	heart
47	chr8:8067600-8068000	Enhancers	Right Ventricle	heart
48	chr8:8067600-8068000	Enhancers	Hela-S3	cervix
49	chr8:8067600-8068200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr8:8068000-8068400	Enhancers	H1 Cell Line	embryonic stem cell

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