Variant report

Variant	nsv591395
Chromosome Location	chr3:120970900-121501070
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3599)
CpG islands
(count:3604)
Chromatin interactive
region (count:214)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:3599 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:121293415-121293609	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:121316377-121316483	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:121361606-121361746	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:121468403-121468989	K562	blood:	n/a	n/a
5	ARID3A	chr3:121264757-121265250	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:121316361-121316430	K562	blood:	n/a	n/a
7	ARID3A	chr3:121467807-121469274	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:121265453-121265941	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:121265480-121265882	K562	blood:	n/a	n/a
10	ARID3A	chr3:121264632-121265235	K562	blood:	n/a	n/a
11	ARID3A	chr3:121293291-121293628	K562	blood:	n/a	n/a
12	ARID3A	chr3:121462983-121463054	K562	blood:	n/a	n/a
13	ATF1	chr3:121468484-121469028	K562	blood:	n/a	chr3:121468524-121468538
14	ATF1	chr3:121293341-121293636	K562	blood:	n/a	n/a
15	ATF2	chr3:121150837-121151409	GM12878	blood:	n/a	n/a
16	ATF2	chr3:121311674-121312713	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr3:121468395-121469101	GM12878	blood:	n/a	chr3:121468524-121468538
18	ATF2	chr3:121265572-121266011	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr3:121267479-121267985	GM12878	blood:	n/a	n/a
20	ATF2	chr3:121468423-121468994	H1-hESC	embryonic stem cell:	n/a	chr3:121468524-121468538
21	ATF2	chr3:121150918-121151361	GM12878	blood:	n/a	n/a
22	ATF2	chr3:121453881-121454600	GM12878	blood:	n/a	n/a
23	ATF2	chr3:121379019-121380056	GM12878	blood:	n/a	n/a
24	ATF2	chr3:121373211-121373782	GM12878	blood:	n/a	n/a
25	ATF2	chr3:121264597-121265169	GM12878	blood:	n/a	n/a
26	ATF2	chr3:121379094-121380020	GM12878	blood:	n/a	n/a
27	ATF2	chr3:121267420-121267944	GM12878	blood:	n/a	n/a
28	ATF2	chr3:121311633-121312689	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr3:121454131-121454588	GM12878	blood:	n/a	n/a
30	ATF2	chr3:121467974-121468305	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr3:121264561-121265245	GM12878	blood:	n/a	n/a
32	ATF2	chr3:121442824-121443362	GM12878	blood:	n/a	n/a
33	ATF3	chr3:121468342-121468877	A549	lung:	n/a	chr3:121468527-121468547 chr3:121468567-121468576
34	ATF3	chr3:121312116-121312453	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF3	chr3:121264594-121265142	A549	lung:	n/a	chr3:121264846-121264855
36	ATF3	chr3:121293358-121293722	K562	blood:	n/a	n/a
37	BACH1	chr3:121293357-121293710	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr3:121182712-121182826	K562	blood:	n/a	n/a
39	BACH1	chr3:121311672-121312712	H1-hESC	embryonic stem cell:	n/a	n/a
40	BACH1	chr3:121370567-121370886	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr3:121163484-121163523	K562	blood:	n/a	n/a
42	BACH1	chr3:121468537-121468931	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr3:121370532-121370903	K562	blood:	n/a	n/a
44	BATF	chr3:121267535-121267976	GM12878	blood:	n/a	n/a
45	BATF	chr3:121454227-121454518	GM12878	blood:	n/a	n/a
46	BATF	chr3:121411145-121411408	GM12878	blood:	n/a	n/a
47	BATF	chr3:121373310-121373733	GM12878	blood:	n/a	n/a
48	BATF	chr3:121454203-121454501	GM12878	blood:	n/a	n/a
49	BATF	chr3:121409910-121410215	GM12878	blood:	n/a	chr3:121410034-121410045
50	BATF	chr3:121409958-121410240	GM12878	blood:	n/a	chr3:121410034-121410045

(count:3604 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121468984-121469034	GM06990	blood:	n/a
2	chr3:121363104-121363154	NHBE	bronchial:	n/a
3	chr3:121264278-121264328	SK-N-SH_RA	brain:	n/a
4	chr3:121264844-121264894	NHDF-neo	bronchial:	n/a
5	chr3:121264819-121264869	AoSMC	blood vessel:	n/a
6	chr3:121468984-121469034	GM06990	blood:	n/a
7	chr3:121363104-121363154	NHBE	bronchial:	n/a
8	chr3:121264278-121264328	SK-N-SH_RA	brain:	n/a
9	chr3:121264844-121264894	NHDF-neo	bronchial:	n/a
10	chr3:121264819-121264869	AoSMC	blood vessel:	n/a
11	chr3:121380233-121380283	HRPEpiC	eye:	n/a
12	chr3:121468093-121468143	PrEC	prostate:	n/a
13	chr3:121264849-121264899	AG09309	skin:	n/a
14	chr3:121264819-121264869	GM06990	blood:	n/a
15	chr3:121265395-121265445	HRE	kidney:	n/a
16	chr3:121264923-121264973	PFSK-1	brain:	n/a
17	chr3:121286820-121286870	Hela-S3	cervix:	n/a
18	chr3:121379791-121379841	A549	lung:	n/a
19	chr3:121468552-121468602	CMK	blood:	n/a
20	chr3:121264929-121264979	HCT-116	colon:	n/a
21	chr3:121264538-121264588	HMEC	breast:	n/a
22	chr3:121379777-121379827	HRPEpiC	eye:	n/a
23	chr3:121264942-121264992	GM12892	blood:	n/a
24	chr3:121262243-121262293	HMEC	breast:	n/a
25	chr3:121286354-121286404	ProgFib	skin:	n/a
26	chr3:121468720-121468770	HRPEpiC	eye:	n/a
27	chr3:121380236-121380286	HMEC	breast:	n/a
28	chr3:121264538-121264588	HEEpiC	esophagus:	n/a
29	chr3:121310923-121310973	HCM	heart:	n/a
30	chr3:121286563-121286613	GM12878	blood:	n/a
31	chr3:121264693-121264743	HRE	kidney:	n/a
32	chr3:121468645-121468695	HRE	kidney:	n/a
33	chr3:121307887-121307937	AG04450	lung:	fetal
34	chr3:121468706-121468756	HRCEpiC	kidney:	n/a
35	chr3:121142525-121142575	K562	blood:	n/a
36	chr3:121286354-121286404	T-47D	breast:	n/a
37	chr3:121311075-121311125	U87	brain:	n/a
38	chr3:121468607-121468657	NH-A	brain:	n/a
39	chr3:121264942-121264992	Hepatocyte	liver:	n/a
40	chr3:121264278-121264328	K562	blood:	n/a
41	chr3:121307887-121307937	HIPEpiC	eye:	n/a
42	chr3:121468628-121468678	HCM	heart:	n/a
43	chr3:121380236-121380286	HCT-116	colon:	n/a
44	chr3:121264929-121264979	HNPCEpiC	eye:	n/a
45	chr3:121312241-121312291	U87	brain:	n/a
46	chr3:121265395-121265445	SK-N-SH_RA	brain:	n/a
47	chr3:121196810-121196860	NHBE	bronchial:	n/a
48	chr3:121469168-121469218	SAEC	small airway:	n/a
49	chr3:121468093-121468143	HCT-116	colon:	n/a
50	chr3:121142525-121142575	NH-A	brain:	n/a

(count:214 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr3:121469866..121471508-chr3:121475985..121477623,2	K562	blood:
2	chr3:121468029..121468701-chr9:33025084..33025810,2	NB4	blood:
3	chr3:121361933..121363730-chr3:121367165..121368759,2	K562	blood:
4	chr3:121134688..121138349-chr3:121139086..121141700,5	K562	blood:
5	chr3:121265697..121266207-chr3:122977401..122978341,2	K562	blood:
6	chr3:121199222..121201861-chr3:121202113..121203793,2	K562	blood:
7	chr3:121325183..121326691-chr3:121327746..121330379,2	K562	blood:
8	chr1:151043136..151043657-chr3:121379199..121379950,2	NB4	blood:
9	chr21:40177696..40178382-chr3:121467811..121468789,2	Hela-S3	cervix:
10	chr3:121417372..121420493-chr3:121467097..121470141,4	K562	blood:
11	chr3:121047561..121048621-chr3:121247919..121248785,3	MCF-7	breast:
12	chr3:121263491..121265604-chr3:121269317..121270972,2	K562	blood:
13	chr3:121465799..121468529-chr3:121552939..121555166,2	MCF-7	breast:
14	chr16:771045..771967-chr3:121468441..121468974,2	NB4	blood:
15	chr3:121476185..121478583-chr3:121487333..121489088,3	K562	blood:
16	chr3:121344119..121346108-chr3:121348732..121350963,2	K562	blood:
17	chr3:121466624..121468797-chr3:121553319..121555550,2	MCF-7	breast:
18	chr3:121221546..121223153-chr3:121223525..121225297,2	K562	blood:
19	chr13:111365321..111365930-chr3:121468002..121468980,2	Hela-S3	cervix:
20	chr3:121468824..121470576-chr3:121473102..121475078,2	K562	blood:
21	chr3:121183395..121185152-chr3:121186567..121189009,2	MCF-7	breast:
22	chr3:121457664..121460185-chr3:121469014..121471399,2	MCF-7	breast:
23	chr3:121185944..121189270-chr3:121190973..121193182,3	K562	blood:
24	chr3:121265303..121265930-chr3:121811130..121811872,2	MCF-7	breast:
25	chr3:121190756..121192749-chr3:121194520..121196467,2	K562	blood:
26	chr3:121004364..121006948-chr3:121012227..121014018,2	MCF-7	breast:
27	chr3:121439769..121441731-chr3:121445734..121447295,2	MCF-7	breast:
28	chr3:121498622..121501358-chr3:121516478..121520165,3	K562	blood:
29	chr3:121420842..121422524-chr3:121426480..121428817,2	MCF-7	breast:
30	chr3:121122561..121125182-chr3:121127949..121129748,3	K562	blood:
31	chr3:121264895..121265445-chr3:121468081..121468931,2	HCT-116	colon:
32	chr3:121205722..121207237-chr3:121210537..121212477,2	K562	blood:
33	chr3:121125400..121127225-chr3:121128769..121131952,3	K562	blood:
34	chr3:121422713..121424587-chr3:121439673..121442209,2	MCF-7	breast:
35	chr3:121447927..121450060-chr3:121456793..121458393,2	K562	blood:
36	chr3:121150437..121151324-chr3:121212003..121212905,2	MCF-7	breast:
37	chr3:121256672..121259266-chr3:121264172..121266746,4	K562	blood:
38	chr3:121206534..121207799-chr3:121247617..121248857,4	MCF-7	breast:
39	chr3:121469093..121470860-chr3:121480115..121482218,2	K562	blood:
40	chr3:121138259..121140292-chr3:121185745..121188174,2	K562	blood:
41	chr3:14484971..14485574-chr3:121207352..121208108,2	MCF-7	breast:
42	chr3:121122561..121125182-chr3:121127949..121129748,3	K562	blood:
43	chr3:121181463..121184397-chr3:121190122..121192546,2	K562	blood:
44	chr3:121465792..121467849-chr3:121506947..121509810,2	MCF-7	breast:
45	chr3:121442790..121445405-chr3:121448638..121450630,2	K562	blood:
46	chr3:121457664..121460185-chr3:121469014..121471399,2	MCF-7	breast:
47	chr3:121206957..121207672-chr3:121248079..121248871,2	MCF-7	breast:
48	chr3:121206957..121207672-chr3:121248079..121248871,2	MCF-7	breast:
49	chr20:17868453..17869206-chr3:121103732..121104423,2	MCF-7	breast:
50	chr3:121221546..121223153-chr3:121223525..121225297,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGB1-1	chr3:121376829-121377194	NONHSAT091478
2	lnc-EAF2-2	chr3:121489799-121490825	l_2448_chr3:121487690-121490825_testes
3	lnc-GOLGB1-1	chr3:121379667-121379750	NONHSAT091478
4	lnc-EAF2-3	chr3:121468132-121470030	NONHSAT091480
5	lnc-GOLGB1-2	chr3:121372843-121373143	NONHSAT091474
6	lnc-POLQ-1	chr3:121295924-121296127	expReg_chr3_8545_-
7	lnc-ARGFX-1	chr3:121075838-121076787	NONHSAT091471
8	lnc-EAF2-2	chr3:121487691-121488674	l_2448_chr3:121487690-121490825_testes

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	GOLGB1	hsa-miR-197-3p	chr3:121382796-121382817
2	IQCB1	hsa-miR-98-5p	chr3:121489033-121489056
3	GOLGB1	hsa-miR-197-3p	chr3:121382120-121382141
4	IQCB1	hsa-miR-98-5p	chr3:121489039-121489033

Variant related genes	Relation type
ENSG00000238670	TF binding region
RNU4-62P	TF binding region
RN7SL172P	TF binding region
POLQ	TF binding region
RPL7AP11	TF binding region
ENSG00000242103	TF binding region
HCLS1	TF binding region
GOLGB1	TF binding region
ARGFX	TF binding region
FBXO40	TF binding region
ENSG00000238670	CpG island
RNU4-62P	CpG island
RN7SL172P	CpG island
POLQ	CpG island
RPL7AP11	CpG island
ENSG00000242103	CpG island
HCLS1	CpG island
GOLGB1	CpG island
ARGFX	CpG island
FBXO40	CpG island
ENSG00000086061	chromatin interactions
ENSG00000180353	chromatin interactions
ENSG00000183208	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000184786	chromatin interactions
ENSG00000137074	chromatin interactions
ENSG00000163840	chromatin interactions
ENSG00000051341	chromatin interactions
ENSG00000160124	chromatin interactions
ENSG00000173230	chromatin interactions
ENSG00000138496	chromatin interactions
ENSG00000103254	chromatin interactions
ENSG00000070269	chromatin interactions
ENSG00000173226	chromatin interactions
ENSG00000179933	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000069424	chromatin interactions
ENSG00000198826	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000171861	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000225697	chromatin interactions
ENSG00000167632	chromatin interactions
ENSG00000185043	chromatin interactions
ENSG00000152291	chromatin interactions
ENSG00000163755	chromatin interactions
ENSG00000145088	chromatin interactions
ENSG00000167699	chromatin interactions
ENSG00000186103	chromatin interactions
ENSG00000130023	chromatin interactions
ENSG00000259802	chromatin interactions
ENSG00000243544	chromatin interactions
ENSG00000114023	chromatin interactions
ENSG00000233625	chromatin interactions
ENSG00000222057	chromatin interactions
ENSG00000157557	chromatin interactions
ENSG00000173193	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000262728	chromatin interactions
ENSG00000145495	chromatin interactions
ENSG00000132002	chromatin interactions
ENSG00000100813	chromatin interactions

Extended variants
information (count: 17752 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:17752 , 50 per page) page: 1 2 3 4 5 6 7 ... 356

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs338999	chr3:120970900-120970901	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373693099	chr3:120970980-120970981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs193105745	chr3:120971084-120971085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566769957	chr3:120971140-120971141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184171582	chr3:120971177-120971178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373574332	chr3:120971228-120971229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369035489	chr3:120971229-120971230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs386397759	chr3:120971236-120971237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35454737	chr3:120971251-120971252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552373008	chr3:120971252-120971253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs188916648	chr3:120971282-120971283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs538026585	chr3:120971393-120971394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370416706	chr3:120971436-120971437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555126318	chr3:120971472-120971473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181660888	chr3:120971483-120971484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534236354	chr3:120971519-120971520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553838643	chr3:120971558-120971559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs546946806	chr3:120971617-120971618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138433578	chr3:120971636-120971637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs546150739	chr3:120971638-120971639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148834479	chr3:120971642-120971643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs185422421	chr3:120971656-120971657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs143442716	chr3:120971700-120971701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs189715941	chr3:120971710-120971711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529715824	chr3:120971794-120971795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs546579866	chr3:120971857-120971858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559867112	chr3:120971859-120971860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532454360	chr3:120971918-120971919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552542526	chr3:120972009-120972010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569153888	chr3:120972017-120972018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538082002	chr3:120972027-120972028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148388400	chr3:120972101-120972102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74508775	chr3:120972103-120972104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548393323	chr3:120972115-120972116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs75405916	chr3:120972200-120972201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs115732915	chr3:120972247-120972248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72968036	chr3:120972288-120972289	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs554157982	chr3:120972304-120972305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs143070299	chr3:120972325-120972326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs373861850	chr3:120972343-120972344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146142731	chr3:120972383-120972384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs551223216	chr3:120972428-120972429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548469728	chr3:120972450-120972451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs338998	chr3:120972618-120972619	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs373767147	chr3:120972645-120972646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs74434277	chr3:120972656-120972657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7429411	chr3:120972657-120972658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs7431446	chr3:120972658-120972659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34678687	chr3:120972673-120972674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs168118	chr3:120972675-120972676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Developmental delay	22180640	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
lymphocytic leukemia	21291569	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Autism	22241247	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	17953491	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Glioma	20126413	CNVD

Chromatin state (count:6917 , 50 per page) page: 1 2 3 4 5 6 7 ... 139

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:120962000-120993000	Weak transcription	Ovary	ovary
2	chr3:120980400-120982800	Weak transcription	Brain Germinal Matrix	brain
3	chr3:120993000-120993600	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
4	chr3:120993000-120993800	ZNF genes & repeats	Ovary	ovary
5	chr3:120993200-120993600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr3:120993200-120993800	ZNF genes & repeats	Pancreas	Pancrea
7	chr3:120993400-120993800	ZNF genes & repeats	Gastric	stomach
8	chr3:120993800-120996600	Weak transcription	Ovary	ovary
9	chr3:120996600-120997200	Strong transcription	Ovary	ovary
10	chr3:120997200-121015600	Weak transcription	Ovary	ovary
11	chr3:121011800-121015600	Enhancers	HUVEC	blood vessel
12	chr3:121013000-121015800	Enhancers	Hela-S3	cervix
13	chr3:121014000-121015600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr3:121023600-121024400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr3:121023800-121024200	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr3:121023800-121024400	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr3:121033600-121052200	Weak transcription	Pancreatic Islets	Pancreatic Islet
18	chr3:121043000-121043200	Enhancers	Ovary	ovary
19	chr3:121043200-121049000	Weak transcription	Ovary	ovary
20	chr3:121048400-121049400	Enhancers	Fetal Heart	heart
21	chr3:121049000-121050000	Strong transcription	Ovary	ovary
22	chr3:121049000-121050000	Enhancers	HSMMtube	muscle
23	chr3:121049400-121049600	Flanking Active TSS	Fetal Heart	heart
24	chr3:121049600-121049800	Enhancers	Fetal Heart	heart
25	chr3:121049600-121050000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
26	chr3:121049800-121050000	Flanking Active TSS	Fetal Heart	heart
27	chr3:121050000-121050600	Enhancers	Fetal Heart	heart
28	chr3:121050000-121051600	Weak transcription	Ovary	ovary
29	chr3:121051600-121052000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr3:121075800-121076200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
31	chr3:121081200-121081800	Enhancers	Hela-S3	cervix
32	chr3:121087600-121087800	Weak transcription	Ovary	ovary
33	chr3:121087600-121087800	Bivalent/Poised TSS	Right Atrium	heart
34	chr3:121087800-121088000	ZNF genes & repeats	Ovary	ovary
35	chr3:121088000-121092200	Weak transcription	Ovary	ovary
36	chr3:121088200-121099000	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr3:121089400-121091600	Weak transcription	Brain Cingulate Gyrus	brain
38	chr3:121090200-121090800	ZNF genes & repeats	Brain Hippocampus Middle	brain
39	chr3:121090200-121090800	ZNF genes & repeats	Pancreas	Pancrea
40	chr3:121090200-121091000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr3:121090800-121094200	Weak transcription	Brain Hippocampus Middle	brain
42	chr3:121091400-121092800	Weak transcription	Brain Anterior Caudate	brain
43	chr3:121092200-121093000	Strong transcription	Ovary	ovary
44	chr3:121092600-121093000	ZNF genes & repeats	Gastric	stomach
45	chr3:121093000-121117000	Weak transcription	Ovary	ovary
46	chr3:121099200-121099400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:121099400-121099800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr3:121099400-121102800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:121099800-121101800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr3:121102800-121103000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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