Variant report

Variant	nsv432482
Chromosome Location	chr3:121364236-121629634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2751)
CpG islands
(count:2750)
Chromatin interactive
region (count:184)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2751 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:121462983-121463054	K562	blood:	n/a	n/a
2	ARID3A	chr3:121514064-121514134	K562	blood:	n/a	n/a
3	ARID3A	chr3:121468403-121468989	K562	blood:	n/a	n/a
4	ARID3A	chr3:121555327-121555897	K562	blood:	n/a	n/a
5	ARID3A	chr3:121467807-121469274	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:121602426-121602710	K562	blood:	n/a	n/a
7	ARID3A	chr3:121553892-121554340	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:121523332-121523538	K562	blood:	n/a	n/a
9	ARID3A	chr3:121602415-121602687	HepG2	liver:	n/a	n/a
10	ARID3A	chr3:121553786-121554196	K562	blood:	n/a	n/a
11	ATF1	chr3:121468484-121469028	K562	blood:	n/a	chr3:121468524-121468538
12	ATF2	chr3:121468423-121468994	H1-hESC	embryonic stem cell:	n/a	chr3:121468524-121468538
13	ATF2	chr3:121373211-121373782	GM12878	blood:	n/a	n/a
14	ATF2	chr3:121468395-121469101	GM12878	blood:	n/a	chr3:121468524-121468538
15	ATF2	chr3:121467974-121468305	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr3:121379019-121380056	GM12878	blood:	n/a	n/a
17	ATF2	chr3:121528089-121528693	GM12878	blood:	n/a	n/a
18	ATF2	chr3:121553346-121554690	GM12878	blood:	n/a	n/a
19	ATF2	chr3:121453881-121454600	GM12878	blood:	n/a	n/a
20	ATF2	chr3:121442824-121443362	GM12878	blood:	n/a	n/a
21	ATF2	chr3:121528006-121528576	GM12878	blood:	n/a	n/a
22	ATF2	chr3:121553559-121554147	GM12878	blood:	n/a	n/a
23	ATF2	chr3:121454131-121454588	GM12878	blood:	n/a	n/a
24	ATF2	chr3:121379094-121380020	GM12878	blood:	n/a	n/a
25	ATF3	chr3:121468342-121468877	A549	lung:	n/a	chr3:121468527-121468547 chr3:121468567-121468576
26	BACH1	chr3:121468537-121468931	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr3:121554053-121554074	K562	blood:	n/a	n/a
28	BACH1	chr3:121370567-121370886	H1-hESC	embryonic stem cell:	n/a	n/a
29	BACH1	chr3:121553761-121554262	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr3:121370532-121370903	K562	blood:	n/a	n/a
31	BACH1	chr3:121508656-121508683	K562	blood:	n/a	n/a
32	BATF	chr3:121553976-121554220	GM12878	blood:	n/a	n/a
33	BATF	chr3:121528186-121528478	GM12878	blood:	n/a	n/a
34	BATF	chr3:121454203-121454501	GM12878	blood:	n/a	n/a
35	BATF	chr3:121409910-121410215	GM12878	blood:	n/a	chr3:121410034-121410045
36	BATF	chr3:121528193-121528452	GM12878	blood:	n/a	n/a
37	BATF	chr3:121411145-121411408	GM12878	blood:	n/a	n/a
38	BATF	chr3:121373310-121373733	GM12878	blood:	n/a	n/a
39	BATF	chr3:121409958-121410240	GM12878	blood:	n/a	chr3:121410034-121410045
40	BATF	chr3:121454227-121454518	GM12878	blood:	n/a	n/a
41	BATF	chr3:121553884-121554288	GM12878	blood:	n/a	n/a
42	BATF	chr3:121373309-121373740	GM12878	blood:	n/a	n/a
43	BCL11A	chr3:121528141-121528529	GM12878	blood:	n/a	chr3:121528342-121528351
44	BCL11A	chr3:121454226-121454493	GM12878	blood:	n/a	n/a
45	BCL3	chr3:121486039-121486304	GM12878	blood:	n/a	n/a
46	BCL3	chr3:121468324-121469213	A549	lung:	n/a	chr3:121468829-121468838 chr3:121468566-121468575 chr3:121468400-121468413
47	BCLAF1	chr3:121373301-121373736	GM12878	blood:	n/a	n/a
48	BCLAF1	chr3:121553367-121554432	GM12878	blood:	n/a	chr3:121553872-121553885 chr3:121553949-121553958
49	BCLAF1	chr3:121379038-121380039	GM12878	blood:	n/a	n/a
50	BCLAF1	chr3:121373280-121373842	GM12878	blood:	n/a	n/a

(count:2750 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:121554169-121554219	SAEC	small airway:	n/a
2	chr3:121380236-121380286	ProgFib	skin:	n/a
3	chr3:121553821-121553871	HNPCEpiC	eye:	n/a
4	chr3:121379791-121379841	NH-A	brain:	n/a
5	chr3:121554094-121554144	HL-60	blood:	n/a
6	chr3:121554169-121554219	SAEC	small airway:	n/a
7	chr3:121380236-121380286	ProgFib	skin:	n/a
8	chr3:121553821-121553871	HNPCEpiC	eye:	n/a
9	chr3:121379791-121379841	NH-A	brain:	n/a
10	chr3:121554094-121554144	HL-60	blood:	n/a
11	chr3:121379791-121379841	HCF	heart:	n/a
12	chr3:121380236-121380286	HRE	kidney:	n/a
13	chr3:121554019-121554069	GM12892	blood:	n/a
14	chr3:121612956-121613006	IMR90	lung:	fetal
15	chr3:121468093-121468143	A549	lung:	n/a
16	chr3:121379745-121379795	HCPEpiC	choroid plexus:	n/a
17	chr3:121613703-121613753	HRPEpiC	eye:	n/a
18	chr3:121553721-121553771	SK-N-MC	brain:	n/a
19	chr3:121468260-121468310	BJ	skin:	n/a
20	chr3:121554019-121554069	HEK293	kidney:	embryo
21	chr3:121468645-121468695	NT2-D1	testis:	n/a
22	chr3:121468027-121468077	ProgFib	skin:	n/a
23	chr3:121468945-121468995	RPTEC	kidney:	n/a
24	chr3:121469168-121469218	ProgFib	skin:	n/a
25	chr3:121379745-121379795	PFSK-1	brain:	n/a
26	chr3:121554019-121554069	T-47D	breast:	n/a
27	chr3:121453622-121453672	PANC-1	pancreas:	n/a
28	chr3:121553821-121553871	NB4	blood:	n/a
29	chr3:121612991-121613041	AG09309	skin:	n/a
30	chr3:121380533-121380583	AoSMC	blood vessel:	n/a
31	chr3:121468720-121468770	MCF-7	breast:	n/a
32	chr3:121453622-121453672	HRE	kidney:	n/a
33	chr3:121553992-121554042	SK-N-SH	brain:	n/a
34	chr3:121491382-121491432	RPTEC	kidney:	n/a
35	chr3:121472567-121472617	H1-hESC	embryonic stem cell:	embryo
36	chr3:121553721-121553771	SK-N-SH_RA	brain:	n/a
37	chr3:121468706-121468756	HMEC	breast:	n/a
38	chr3:121379777-121379827	HL-60	blood:	n/a
39	chr3:121553361-121553411	PANC-1	pancreas:	n/a
40	chr3:121553361-121553411	ProgFib	skin:	n/a
41	chr3:121553992-121554042	HEEpiC	esophagus:	n/a
42	chr3:121553586-121553636	HIPEpiC	eye:	n/a
43	chr3:121468984-121469034	Caco-2	colon:	n/a
44	chr3:121553940-121553990	HL-60	blood:	n/a
45	chr3:121553361-121553411	HAEpiC	amniotic membrane:	n/a
46	chr3:121613703-121613753	ProgFib	skin:	n/a
47	chr3:121553586-121553636	Caco-2	colon:	n/a
48	chr3:121468984-121469034	CMK	blood:	n/a
49	chr3:121553992-121554042	AG10803	skin:	n/a
50	chr3:121613703-121613753	AG04449	skin:	fetal

(count:184 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr3:121465799..121468529-chr3:121552939..121555166,2	MCF-7	breast:
2	chr3:121602683..121606791-chr3:121612031..121615875,3	MCF-7	breast:
3	chr3:121470646..121472980-chr3:121473144..121475007,2	MCF-7	breast:
4	chr3:121538956..121540532-chr3:121552640..121554149,2	MCF-7	breast:
5	chr13:111365321..111365930-chr3:121468002..121468980,2	Hela-S3	cervix:
6	chr3:121467372..121472022-chr3:121479274..121484300,4	K562	blood:
7	chr3:121468842..121470508-chr3:121478422..121481372,2	MCF-7	breast:
8	chr3:121442790..121445405-chr3:121448638..121450630,2	K562	blood:
9	chr3:121445585..121448189-chr3:121448345..121450193,2	K562	blood:
10	chr3:121466668..121468934-chr3:121518860..121521865,3	MCF-7	breast:
11	chr3:121594806..121597719-chr3:121598676..121600747,2	K562	blood:
12	chr3:121468307..121470189-chr3:121481888..121483548,2	MCF-7	breast:
13	chr3:121462008..121465920-chr3:121468429..121472755,5	MCF-7	breast:
14	chr3:121535928..121538474-chr3:121548099..121550812,2	K562	blood:
15	chr3:121466883..121469866-chr3:121509905..121511763,2	MCF-7	breast:
16	chr3:121448663..121450267-chr3:121453001..121454799,2	K562	blood:
17	chr3:121544640..121546526-chr3:121557877..121559785,2	MCF-7	breast:
18	chr3:121451393..121453533-chr3:121465182..121467129,2	K562	blood:
19	chr3:121466769..121469107-chr3:121494508..121496191,2	MCF-7	breast:
20	chr3:121498622..121501358-chr3:121516478..121520165,3	K562	blood:
21	chr3:121573144..121575640-chr3:121713880..121715602,2	MCF-7	breast:
22	chr3:121374281..121376977-chr3:121381116..121385045,3	MCF-7	breast:
23	chr3:121469866..121471508-chr3:121475985..121477623,2	K562	blood:
24	chr3:121417372..121420493-chr3:121467097..121470141,4	K562	blood:
25	chr3:121480892..121483629-chr3:121486983..121489016,2	K562	blood:
26	chr3:121552093..121553677-chr3:122102440..122104911,2	K562	blood:
27	chr3:121449098..121450770-chr3:121467330..121469547,2	MCF-7	breast:
28	chr15:32907073..32907588-chr3:121468161..121469013,2	NB4	blood:
29	chr3:121442817..121449533-chr3:121463247..121470201,7	K562	blood:
30	chr3:121384342..121386908-chr3:121387953..121390169,2	K562	blood:
31	chr3:121557805..121560130-chr3:121563669..121566331,2	MCF-7	breast:
32	chr3:121566038..121567568-chr3:121569275..121571033,2	K562	blood:
33	chr3:121466624..121468797-chr3:121553319..121555550,2	MCF-7	breast:
34	chr3:121361933..121363730-chr3:121367165..121368759,2	K562	blood:
35	chr3:121553807..121555677-chr3:121556073..121558919,2	K562	blood:
36	chr3:121463605..121466506-chr3:121466686..121468331,2	MCF-7	breast:
37	chr3:121552259..121553812-chr3:121688554..121691121,2	MCF-7	breast:
38	chr3:121603643..121605566-chr3:121656266..121657891,2	MCF-7	breast:
39	chr3:121503081..121505086-chr3:121506757..121508419,2	MCF-7	breast:
40	chr3:121506516..121509256-chr3:121552587..121555250,2	MCF-7	breast:
41	chr3:121456187..121459032-chr3:121465141..121468523,4	MCF-7	breast:
42	chr3:121377179..121379153-chr3:121573085..121574882,2	MCF-7	breast:
43	chr3:121479199..121481654-chr3:121483529..121486442,3	K562	blood:
44	chr3:121381533..121383209-chr3:121385289..121388100,2	MCF-7	breast:
45	chr3:121541912..121545321-chr3:121545405..121548683,3	MCF-7	breast:
46	chr3:121420842..121422524-chr3:121426480..121428817,2	MCF-7	breast:
47	chr3:121557805..121560130-chr3:121563669..121566331,2	MCF-7	breast:
48	chr3:121461219..121463948-chr3:121466247..121469994,3	K562	blood:
49	chr3:121465792..121467849-chr3:121506947..121509810,2	MCF-7	breast:
50	chr3:121422713..121424587-chr3:121439673..121442209,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOLGB1-2	chr3:121372843-121373143	NONHSAT091474
2	lnc-EAF2-2	chr3:121489799-121490825	l_2448_chr3:121487690-121490825_testes
3	lnc-EAF2-3	chr3:121468132-121470030	NONHSAT091480
4	lnc-GOLGB1-3	chr3:121553813-121553839	NONHSAT091482
5	lnc-EAF2-2	chr3:121487691-121488674	l_2448_chr3:121487690-121490825_testes
6	lnc-GOLGB1-1	chr3:121376829-121377194	NONHSAT091478
7	lnc-GOLGB1-3	chr3:121552783-121553326	NONHSAT091482
8	lnc-GOLGB1-1	chr3:121379667-121379750	NONHSAT091478

No data

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

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

Variant related genes	Relation type
HCLS1	TF binding region
GOLGB1	TF binding region
RNU4-62P	TF binding region
RN7SL172P	TF binding region
SLC15A2	TF binding region
IQCB1	TF binding region
EAF2	TF binding region
HCLS1	CpG island
GOLGB1	CpG island
RNU4-62P	CpG island
RN7SL172P	CpG island
SLC15A2	CpG island
IQCB1	CpG island
EAF2	CpG island
ENSG00000137074	chromatin interactions
ENSG00000222057	chromatin interactions
ENSG00000173226	chromatin interactions
ENSG00000130023	chromatin interactions
ENSG00000243544	chromatin interactions
ENSG00000262728	chromatin interactions
ENSG00000206652	chromatin interactions
ENSG00000152291	chromatin interactions
ENSG00000134905	chromatin interactions
ENSG00000163755	chromatin interactions
ENSG00000185043	chromatin interactions
ENSG00000259802	chromatin interactions
ENSG00000183208	chromatin interactions
ENSG00000143458	chromatin interactions
ENSG00000157557	chromatin interactions
ENSG00000083845	chromatin interactions
ENSG00000184786	chromatin interactions
ENSG00000086061	chromatin interactions
ENSG00000225697	chromatin interactions
ENSG00000171861	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000132002	chromatin interactions
ENSG00000051341	chromatin interactions
ENSG00000163406	chromatin interactions
ENSG00000103254	chromatin interactions
ENSG00000160124	chromatin interactions
ENSG00000114023	chromatin interactions
ENSG00000266640	chromatin interactions
ENSG00000069424	chromatin interactions
ENSG00000100813	chromatin interactions
ENSG00000167699	chromatin interactions
ENSG00000179933	chromatin interactions
ENSG00000145088	chromatin interactions
ENSG00000198826	chromatin interactions
ENSG00000070269	chromatin interactions
ENSG00000221869	chromatin interactions
ENSG00000180353	chromatin interactions
ENSG00000145495	chromatin interactions
ENSG00000173230	chromatin interactions

Extended variants
information (count: 9302 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:9302 , 50 per page) page: 1 2 3 4 5 6 7 ... 187

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9873644	chr3:121364236-121364237	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs9873648	chr3:121364251-121364252	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs200000017	chr3:121364299-121364300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs34917887	chr3:121364311-121364312	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573199755	chr3:121364333-121364334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs148442474	chr3:121364336-121364337	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564883421	chr3:121364360-121364361	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530569246	chr3:121364444-121364445	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543970193	chr3:121364446-121364447	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547389142	chr3:121364462-121364463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530198200	chr3:121364463-121364464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7429247	chr3:121364487-121364488	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs566776576	chr3:121364525-121364526	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568984183	chr3:121364604-121364605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532675527	chr3:121364612-121364613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552489208	chr3:121364616-121364617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7427165	chr3:121364624-121364625	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs369453761	chr3:121364656-121364657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185763548	chr3:121364675-121364676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554751479	chr3:121364697-121364698	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs564350192	chr3:121364761-121364762	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs13090660	chr3:121364780-121364781	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs10677529	chr3:121364998-121364999	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs35691635	chr3:121364999-121365000	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs59424510	chr3:121365003-121365004	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs370446441	chr3:121365004-121365005	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs372783966	chr3:121365005-121365006	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs375975877	chr3:121365013-121365014	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs188960129	chr3:121365119-121365120	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs61720711	chr3:121365198-121365199	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs370624675	chr3:121365199-121365200	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs61720712	chr3:121365201-121365202	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs374263565	chr3:121365206-121365207	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs372065267	chr3:121365209-121365210	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs61724320	chr3:121365211-121365212	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs376015693	chr3:121365213-121365214	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs56651751	chr3:121365214-121365215	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs61720713	chr3:121365218-121365219	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs546867872	chr3:121365219-121365220	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs61720714	chr3:121365225-121365226	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs377471422	chr3:121365234-121365235	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs369880530	chr3:121365239-121365240	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs374314261	chr3:121365242-121365243	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs181062543	chr3:121365261-121365262	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs200350490	chr3:121365263-121365264	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs111215344	chr3:121365327-121365328	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs111215436	chr3:121365336-121365337	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs549153501	chr3:121365410-121365411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573134499	chr3:121365444-121365445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs376961306	chr3:121365536-121365537	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:6838 , 50 per page) page: 1 2 3 4 5 6 7 ... 137

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:121345600-121376800	Weak transcription	Esophagus	oesophagus
2	chr3:121347000-121378000	Weak transcription	Right Ventricle	heart
3	chr3:121347200-121364400	Strong transcription	Primary B cells from cord blood	blood
4	chr3:121347400-121367200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr3:121347600-121364600	Strong transcription	Primary neutrophils fromperipheralblood	blood
6	chr3:121347600-121364600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr3:121347600-121364600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr3:121347800-121364600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr3:121348000-121364600	Strong transcription	Primary B cells from peripheral blood	blood
10	chr3:121348000-121364600	Strong transcription	Primary T cells fromperipheralblood	blood
11	chr3:121348000-121381800	Weak transcription	Aorta	Aorta
12	chr3:121348200-121364600	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr3:121348400-121364600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr3:121348400-121364600	Strong transcription	Monocytes-CD14+_RO01746	blood
15	chr3:121348800-121364400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr3:121348800-121367200	Weak transcription	Pancreas	Pancrea
17	chr3:121349000-121364600	Strong transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr3:121349000-121364600	Strong transcription	Dnd41	blood
19	chr3:121349000-121378000	Weak transcription	Fetal Stomach	stomach
20	chr3:121349400-121364600	Strong transcription	Primary T helper cells fromperipheralblood	blood
21	chr3:121349400-121367000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr3:121349600-121364600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr3:121349800-121367000	Weak transcription	Skeletal Muscle Female	skeletal muscle
24	chr3:121350000-121364600	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr3:121350000-121364600	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr3:121351000-121364600	Strong transcription	GM12878-XiMat	blood
27	chr3:121351000-121382800	Weak transcription	Small Intestine	intestine
28	chr3:121351400-121381400	Weak transcription	Gastric	stomach
29	chr3:121351800-121370400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr3:121353400-121364400	Strong transcription	Fetal Thymus	thymus
31	chr3:121353400-121376000	Weak transcription	Lung	lung
32	chr3:121354000-121381000	Weak transcription	Fetal Intestine Small	intestine
33	chr3:121355600-121367000	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr3:121356000-121370200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr3:121356200-121378200	Weak transcription	Colonic Mucosa	Colon
36	chr3:121356800-121379200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr3:121360200-121364600	Strong transcription	Primary T helper cells PMA-I stimulated	--
38	chr3:121360200-121364600	Strong transcription	Placenta	Placenta
39	chr3:121360600-121364600	Strong transcription	Primary T helper naive cells from peripheral blood	blood
40	chr3:121361200-121364600	Strong transcription	Primary T cells from cord blood	blood
41	chr3:121361200-121364600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
42	chr3:121361400-121364600	Strong transcription	Primary hematopoietic stem cells	blood
43	chr3:121361600-121364600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr3:121361800-121364600	Strong transcription	Primary T killer memory cells from peripheral blood	blood
45	chr3:121361800-121364600	Strong transcription	HUVEC	blood vessel
46	chr3:121362200-121366200	Weak transcription	Fetal Heart	heart
47	chr3:121362200-121379400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr3:121362600-121379600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr3:121364000-121377000	Weak transcription	Rectal Mucosa Donor 29	rectum
50	chr3:121364200-121366200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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