Variant report

Variant	nsv429859
Chromosome Location	chr8:8069131-8145931
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2647)
CpG islands
(count:1220)
Chromatin interactive
region (count:59)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2647 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:8136392-8136433	K562	blood:	n/a	n/a
2	ARID3A	chr8:8092931-8093297	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:8127880-8128214	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:8130676-8131061	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:8127158-8127358	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:8111412-8112067	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	chr8:8145751-8146493	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:8105314-8105669	K562	blood:	n/a	n/a
11	ARID3A	chr8:8126032-8126609	HepG2	liver:	n/a	n/a
12	ARID3A	chr8:8101412-8102391	K562	blood:	n/a	n/a
13	ARID3A	chr8:8091892-8091896	HepG2	liver:	n/a	n/a
14	ARID3A	chr8:8105348-8105599	HepG2	liver:	n/a	n/a
15	ARID3A	chr8:8102923-8103018	K562	blood:	n/a	n/a
16	ATF1	chr8:8101961-8102473	K562	blood:	n/a	n/a
17	ATF1	chr8:8144090-8144415	K562	blood:	n/a	n/a
18	ATF1	chr8:8118490-8118523	K562	blood:	n/a	n/a
19	ATF2	chr8:8143907-8144515	GM12878	blood:	n/a	n/a
20	ATF2	chr8:8126203-8126652	GM12878	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	chr8:8141766-8142478	GM12878	blood:	n/a	n/a
24	ATF2	chr8:8126192-8126618	GM12878	blood:	n/a	n/a
25	ATF2	chr8:8136646-8137350	GM12878	blood:	n/a	n/a
26	ATF2	chr8:8096080-8096557	GM12878	blood:	n/a	n/a
27	ATF3	chr8:8145728-8146513	A549	lung:	n/a	n/a
28	ATF3	chr8:8127796-8128282	A549	lung:	n/a	n/a
29	ATF3	chr8:8145665-8146549	A549	lung:	n/a	n/a
30	ATF3	chr8:8096172-8096477	K562	blood:	n/a	n/a
31	ATF3	chr8:8145720-8146548	HCT-116	colon:	n/a	n/a
32	ATF3	chr8:8145708-8146540	HCT-116	colon:	n/a	n/a
33	ATF3	chr8:8101821-8102415	K562	blood:	n/a	n/a
34	ATF3	chr8:8101985-8102287	K562	blood:	n/a	n/a
35	BACH1	chr8:8130683-8130937	K562	blood:	n/a	n/a
36	BATF	chr8:8144052-8144469	GM12878	blood:	n/a	n/a
37	BATF	chr8:8143398-8143620	GM12878	blood:	n/a	n/a
38	BATF	chr8:8086957-8087326	GM12878	blood:	n/a	n/a
39	BATF	chr8:8143371-8143632	GM12878	blood:	n/a	n/a
40	BATF	chr8:8137532-8137784	GM12878	blood:	n/a	chr8:8137667-8137678 chr8:8137668-8137678
41	BATF	chr8:8126297-8126540	GM12878	blood:	n/a	chr8:8126405-8126416 chr8:8126421-8126431 chr8:8126417-8126427 chr8:8126420-8126431
42	BATF	chr8:8086780-8087231	GM12878	blood:	n/a	chr8:8086859-8086869
43	BATF	chr8:8141982-8142461	GM12878	blood:	n/a	n/a
44	BATF	chr8:8086606-8086880	GM12878	blood:	n/a	chr8:8086859-8086869
45	BATF	chr8:8085189-8085406	GM12878	blood:	n/a	n/a
46	BATF	chr8:8091245-8091594	GM12878	blood:	n/a	n/a
47	BATF	chr8:8096176-8096555	GM12878	blood:	n/a	n/a
48	BATF	chr8:8144007-8144450	GM12878	blood:	n/a	n/a
49	BATF	chr8:8136381-8136667	GM12878	blood:	n/a	n/a
50	BATF	chr8:8126185-8126638	GM12878	blood:	n/a	chr8:8126405-8126416 chr8:8126421-8126431 chr8:8126417-8126427 chr8:8126420-8126431

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:8085973-8086023	HAEpiC	amniotic membrane:	n/a
2	chr8:8085503-8085553	HL-60	blood:	n/a
3	chr8:8084126-8084176	MCF10A-Er-Src	breast:	n/a
4	chr8:8102392-8102442	U87	brain:	n/a
5	chr8:8085844-8085894	SKMC	muscle:	n/a
6	chr8:8084126-8084176	HEEpiC	esophagus:	n/a
7	chr8:8085544-8085594	NHBE	bronchial:	n/a
8	chr8:8086146-8086196	HRCEpiC	kidney:	n/a
9	chr8:8085503-8085553	K562	blood:	n/a
10	chr8:8086607-8086657	CMK	blood:	n/a
11	chr8:8102121-8102171	HepG2	liver:	n/a
12	chr8:8120624-8120674	GM12891	blood:	n/a
13	chr8:8102392-8102442	IMR90	lung:	fetal
14	chr8:8086607-8086657	HAEpiC	amniotic membrane:	n/a
15	chr8:8085532-8085582	ovcar-3	ovarian:	n/a
16	chr8:8085503-8085553	BE2_C	brain:	n/a
17	chr8:8085503-8085553	AoSMC	blood vessel:	n/a
18	chr8:8085844-8085894	A549	lung:	n/a
19	chr8:8084974-8085024	ECC-1	luminal epithelium:	n/a
20	chr8:8085496-8085546	BJ	skin:	n/a
21	chr8:8084126-8084176	AG10803	skin:	n/a
22	chr8:8085532-8085582	HRE	kidney:	n/a
23	chr8:8085503-8085553	T-47D	breast:	n/a
24	chr8:8090460-8090510	BJ	skin:	n/a
25	chr8:8085532-8085582	MCF-7	breast:	n/a
26	chr8:8085946-8085996	GM19239	blood:	n/a
27	chr8:8102392-8102442	AG10803	skin:	n/a
28	chr8:8084126-8084176	PANC-1	pancreas:	n/a
29	chr8:8085532-8085582	AG04450	lung:	fetal
30	chr8:8084610-8084660	HRE	kidney:	n/a
31	chr8:8131077-8131127	NHBE	bronchial:	n/a
32	chr8:8120624-8120674	SK-N-SH	brain:	n/a
33	chr8:8086146-8086196	NT2-D1	testis:	n/a
34	chr8:8082819-8082869	GM06990	blood:	n/a
35	chr8:8084610-8084660	IMR90	lung:	fetal
36	chr8:8086686-8086736	SKMC	muscle:	n/a
37	chr8:8086146-8086196	AG10803	skin:	n/a
38	chr8:8082819-8082869	AG09309	skin:	n/a
39	chr8:8085973-8086023	Jurkat	blood:	n/a
40	chr8:8085973-8086023	PANC-1	pancreas:	n/a
41	chr8:8085532-8085582	RPTEC	kidney:	n/a
42	chr8:8102121-8102171	BJ	skin:	n/a
43	chr8:8085844-8085894	Hepatocyte	liver:	n/a
44	chr8:8086144-8086194	GM12892	blood:	n/a
45	chr8:8086146-8086196	NB4	blood:	n/a
46	chr8:8085946-8085996	SK-N-MC	brain:	n/a
47	chr8:8085844-8085894	HRCEpiC	kidney:	n/a
48	chr8:8086144-8086194	ECC-1	luminal epithelium:	n/a
49	chr8:8086146-8086196	A549	lung:	n/a
50	chr8:8102121-8102171	MCF-7	breast:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:8108549..8111183-chr8:8240516..8242778,2	MCF-7	breast:
2	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
3	chr8:8140760..8143388-chr8:8146728..8148425,2	K562	blood:
4	chr8:8126193..8127836-chr8:8129384..8131743,2	MCF-7	breast:
5	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
6	chr8:8101610..8104492-chr8:8112542..8114092,2	K562	blood:
7	chr8:8130511..8132438-chr8:8135661..8137544,2	K562	blood:
8	chr8:8105365..8106008-chr8:8526894..8527465,2	K562	blood:
9	chr8:8101610..8104279-chr8:8111391..8114092,2	K562	blood:
10	chr8:8134812..8136654-chr8:8146118..8147961,3	K562	blood:
11	chr8:8126193..8127836-chr8:8129384..8131743,2	MCF-7	breast:
12	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
13	chr8:8145815..8148362-chr8:8152420..8155525,4	MCF-7	breast:
14	chr8:8130421..8131300-chr8:8175825..8176932,3	K562	blood:
15	chr8:8126556..8131624-chr8:8143035..8148399,10	MCF-7	breast:
16	chr8:8145045..8147805-chr8:8168275..8170393,2	MCF-7	breast:
17	chr8:8105059..8106011-chr8:8526943..8527953,6	MCF-7	breast:
18	chr3:129829770..129830533-chr8:8085798..8086673,3	Hela-S3	cervix:
19	chr8:8130322..8131342-chr8:8527334..8528198,3	MCF-7	breast:
20	chr8:8134161..8136694-chr8:8559309..8560894,2	MCF-7	breast:
21	chr8:8138288..8140321-chr8:8142532..8144155,2	MCF-7	breast:
22	chr8:8145925..8147772-chr8:8172599..8174671,2	MCF-7	breast:
23	chr8:8142878..8144520-chr8:8146399..8149197,2	MCF-7	breast:
24	chr8:8094104..8094693-chr8:8146401..8147333,2	MCF-7	breast:
25	chr8:8125550..8129443-chr8:8243752..8245349,3	MCF-7	breast:
26	chr8:8128010..8130864-chr8:8317877..8319814,2	MCF-7	breast:
27	chr8:8145200..8147453-chr8:8312155..8314860,2	MCF-7	breast:
28	chr8:8131655..8133179-chr8:8135431..8137292,2	MCF-7	breast:
29	chr8:8084641..8087551-chr8:8098301..8100358,2	K562	blood:
30	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
31	chr8:8144375..8149679-chr8:8240479..8246459,10	MCF-7	breast:
32	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
33	chr6:26031709..26032614-chr8:8085130..8085961,2	Hela-S3	cervix:
34	chr8:8104258..8105835-chr8:8243426..8245376,2	MCF-7	breast:
35	chr8:8131655..8133179-chr8:8135431..8137292,2	MCF-7	breast:
36	chr8:8126556..8131624-chr8:8143035..8148399,10	MCF-7	breast:
37	chr8:8141970..8144276-chr8:8242374..8245136,3	MCF-7	breast:
38	chr8:8142616..8145069-chr8:8226333..8228141,2	MCF-7	breast:
39	chr15:59062813..59063449-chr8:8085838..8086625,2	Hela-S3	cervix:
40	chr8:8092255..8094353-chr8:8097556..8100076,2	K562	blood:
41	chr8:8098254..8100230-chr8:8106571..8108592,2	K562	blood:
42	chr8:8101157..8102709-chr8:8124508..8126459,2	MCF-7	breast:
43	chr8:8118434..8122893-chr8:8123384..8125953,5	MCF-7	breast:
44	chr8:8093979..8097330-chr8:8100546..8105094,4	K562	blood:
45	chr8:8128833..8131355-chr8:8136442..8139093,2	MCF-7	breast:
46	chr8:8138288..8140321-chr8:8142532..8144155,2	MCF-7	breast:
47	chr8:8094651..8097727-chr8:8099626..8103713,3	MCF-7	breast:
48	chr8:8093979..8096897-chr8:8099466..8105094,8	K562	blood:
49	chr8:8086683..8088508-chr8:8193858..8196209,2	MCF-7	breast:
50	chr8:8129344..8132133-chr8:8525629..8527896,2	MCF-7	breast:

(count:28 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 4555 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:4555 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1969388	chr8:8069131-8069132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538352141	chr8:8069158-8069159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557532225	chr8:8069165-8069166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs793733	chr8:8069180-8069181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs111474057	chr8:8069223-8069224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs573939512	chr8:8069237-8069238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2955574	chr8:8069253-8069254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370165702	chr8:8069257-8069258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542700696	chr8:8069268-8069269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559453684	chr8:8069285-8069286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572879578	chr8:8069290-8069291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79904365	chr8:8069293-8069294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs60343426	chr8:8069301-8069302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201134482	chr8:8069312-8069313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs77744396	chr8:8069323-8069324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77137898	chr8:8069326-8069327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564189565	chr8:8069329-8069330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78116745	chr8:8069330-8069331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2955575	chr8:8069362-8069363	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs549663933	chr8:8069363-8069364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs563494701	chr8:8069371-8069372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs112735118	chr8:8069397-8069398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10046719	chr8:8069410-8069411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs10046760	chr8:8069482-8069483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs61378754	chr8:8069493-8069494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60912866	chr8:8069515-8069516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs61561267	chr8:8069526-8069527	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529142580	chr8:8069529-8069530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10046642	chr8:8069540-8069541	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs549086727	chr8:8069548-8069549	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs565811764	chr8:8069559-8069560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10046643	chr8:8069564-8069565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534574722	chr8:8069588-8069589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551364240	chr8:8069590-8069591	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs59785162	chr8:8069591-8069592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs59983264	chr8:8069661-8069662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62495066	chr8:8069669-8069670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs58777857	chr8:8069688-8069689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs10106480	chr8:8069695-8069696	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs10046660	chr8:8069710-8069711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs571799729	chr8:8069727-8069728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375338406	chr8:8069739-8069740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10095509	chr8:8069750-8069751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557407030	chr8:8069759-8069760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs10046612	chr8:8069781-8069782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10046661	chr8:8069788-8069789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs10046613	chr8:8069839-8069840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573879633	chr8:8069844-8069845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188779426	chr8:8069905-8069906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536475539	chr8:8069918-8069919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Incontinentia Pigmenti	22033527	CNVD
Williams Syndrome	20824207	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
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Glioblastoma multiforme	21138945	CNVD

Chromatin state (count:1057 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8068200-8076200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:8068400-8069400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr8:8069400-8069600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr8:8076200-8076800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:8080400-8080600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr8:8080600-8080800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr8:8080800-8081600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr8:8081600-8081800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr8:8081600-8082000	Enhancers	NHLF	lung
10	chr8:8081600-8082400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr8:8081600-8082400	Enhancers	Muscle Satellite Cultured Cells	--
12	chr8:8081800-8084600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr8:8082000-8082400	Enhancers	Hela-S3	cervix
14	chr8:8082000-8082400	Weak transcription	NHLF	lung
15	chr8:8082000-8084800	Weak transcription	Stomach Mucosa	stomach
16	chr8:8082200-8084000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr8:8082400-8082600	Enhancers	NHLF	lung
18	chr8:8082400-8084000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr8:8082400-8084000	Weak transcription	Hela-S3	cervix
20	chr8:8082400-8084800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr8:8082600-8084800	Weak transcription	NHLF	lung
22	chr8:8084000-8084200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr8:8084000-8084200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr8:8084000-8084200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr8:8084000-8084200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr8:8084000-8084200	Enhancers	Hela-S3	cervix
27	chr8:8084000-8084600	Enhancers	Fetal Intestine Large	intestine
28	chr8:8084000-8084800	Enhancers	Liver	Liver
29	chr8:8084200-8084400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr8:8084200-8084400	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr8:8084200-8084400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr8:8084200-8084600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr8:8084200-8084600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:8084200-8084600	Weak transcription	Hela-S3	cervix
35	chr8:8084200-8085200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
36	chr8:8084200-8086800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr8:8084200-8087200	Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr8:8084400-8084600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr8:8084400-8086800	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr8:8084400-8086800	Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr8:8084400-8087000	Active TSS	iPS-15b Cell Line	embryonic stem cell
42	chr8:8084400-8087000	Active TSS	iPS-18 Cell Line	embryonic stem cell
43	chr8:8084600-8084800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr8:8084600-8084800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr8:8084600-8084800	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr8:8084600-8084800	Enhancers	Colonic Mucosa	Colon
47	chr8:8084600-8084800	Enhancers	Duodenum Mucosa	Duodenum
48	chr8:8084600-8084800	Flanking Active TSS	Fetal Intestine Large	intestine
49	chr8:8084600-8084800	Enhancers	Placenta	Placenta
50	chr8:8084600-8084800	Enhancers	Dnd41	blood

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