Variant report

Variant	nsv518814
Chromosome Location	chr3:143666825-143703750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1910)
CpG islands
(count:1464)
Chromatin interactive
region (count:63)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1910 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:143693676-143695333	K562	blood:	n/a	n/a
2	ARID3A	chr3:143690276-143690865	K562	blood:	n/a	n/a
3	ARID3A	chr3:143692016-143692262	K562	blood:	n/a	n/a
4	ARID3A	chr3:143690119-143690425	HepG2	liver:	n/a	n/a
5	ATF1	chr3:143690072-143691003	K562	blood:	n/a	n/a
6	ATF1	chr3:143691998-143692250	K562	blood:	n/a	n/a
7	ATF2	chr3:143696616-143697247	GM12878	blood:	n/a	n/a
8	ATF2	chr3:143689642-143689972	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:143689985-143691159	GM12878	blood:	n/a	n/a
10	ATF2	chr3:143690239-143690706	GM12878	blood:	n/a	n/a
11	ATF2	chr3:143689913-143690495	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr3:143691190-143692375	GM12878	blood:	n/a	n/a
13	ATF2	chr3:143690518-143690969	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr3:143696796-143697225	GM12878	blood:	n/a	n/a
15	ATF2	chr3:143689986-143690694	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr3:143689546-143689945	GM12878	blood:	n/a	n/a
17	ATF3	chr3:143693632-143694035	K562	blood:	n/a	n/a
18	BACH1	chr3:143691359-143691614	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr3:143690053-143691021	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr3:143670241-143670516	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr3:143690304-143690487	K562	blood:	n/a	n/a
22	BACH1	chr3:143693737-143693998	K562	blood:	n/a	n/a
23	BACH1	chr3:143691840-143692192	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr3:143693163-143693272	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr3:143696864-143697108	GM12878	blood:	n/a	n/a
26	BATF	chr3:143690287-143690589	GM12878	blood:	n/a	n/a
27	BATF	chr3:143696837-143697130	GM12878	blood:	n/a	n/a
28	BATF	chr3:143691917-143692241	GM12878	blood:	n/a	n/a
29	BCL3	chr3:143690183-143690968	A549	lung:	n/a	chr3:143690783-143690796 chr3:143690605-143690614
30	BCL3	chr3:143690035-143691020	GM12878	blood:	n/a	chr3:143690783-143690796 chr3:143690605-143690614
31	BCL3	chr3:143696726-143697161	GM12878	blood:	n/a	n/a
32	BCL3	chr3:143689933-143690628	A549	lung:	n/a	chr3:143690605-143690614
33	BCLAF1	chr3:143691843-143692343	GM12878	blood:	n/a	n/a
34	BCLAF1	chr3:143689915-143692474	GM12878	blood:	n/a	chr3:143690783-143690796 chr3:143690605-143690614 chr3:143691047-143691056
35	BHLHE40	chr3:143692346-143692846	HepG2	liver:	n/a	n/a
36	BHLHE40	chr3:143693562-143693571	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:143691990-143692386	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:143693062-143693064	GM12878	blood:	n/a	n/a
39	BHLHE40	chr3:143689623-143691632	GM12878	blood:	n/a	chr3:143691050-143691066
40	BHLHE40	chr3:143691295-143691495	A549	lung:	n/a	n/a
41	BHLHE40	chr3:143689620-143692459	K562	blood:	n/a	chr3:143691050-143691066
42	BRCA1	chr3:143690351-143690737	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr3:143691819-143692647	Hela-S3	cervix:	n/a	n/a
44	BRCA1	chr3:143689916-143691085	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr3:143690903-143690962	HepG2	liver:	n/a	n/a
46	BRCA1	chr3:143690389-143690910	GM12878	blood:	n/a	n/a
47	BRCA1	chr3:143689791-143689815	GM12878	blood:	n/a	n/a
48	BRCA1	chr3:143691742-143691775	GM12878	blood:	n/a	n/a
49	BRCA1	chr3:143692161-143692163	GM12878	blood:	n/a	n/a
50	CBX3	chr3:143689868-143691100	K562	blood:	n/a	n/a

(count:1464 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143692087-143692137	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:143692006-143692056	CMK	blood:	n/a
3	chr3:143692255-143692305	PFSK-1	brain:	n/a
4	chr3:143691269-143691319	SK-N-MC	brain:	n/a
5	chr3:143689916-143689966	ovcar-3	ovarian:	n/a
6	chr3:143692087-143692137	MCF10A-Er-Src	breast:	n/a
7	chr3:143692785-143692835	AG09309	skin:	n/a
8	chr3:143690991-143691041	HEEpiC	esophagus:	n/a
9	chr3:143691269-143691319	ProgFib	skin:	n/a
10	chr3:143690208-143690258	U87	brain:	n/a
11	chr3:143691409-143691459	HNPCEpiC	eye:	n/a
12	chr3:143695141-143695191	AG04450	lung:	fetal
13	chr3:143691409-143691459	GM12891	blood:	n/a
14	chr3:143690495-143690545	Jurkat	blood:	n/a
15	chr3:143691269-143691319	HRE	kidney:	n/a
16	chr3:143692056-143692106	HRE	kidney:	n/a
17	chr3:143689972-143690022	GM06990	blood:	n/a
18	chr3:143692785-143692835	HPAEpiC	pulmonary alveolar:	n/a
19	chr3:143692087-143692137	RPTEC	kidney:	n/a
20	chr3:143691269-143691319	PFSK-1	brain:	n/a
21	chr3:143695141-143695191	GM12892	blood:	n/a
22	chr3:143690495-143690545	PANC-1	pancreas:	n/a
23	chr3:143690145-143690195	U87	brain:	n/a
24	chr3:143689916-143689966	NHBE	bronchial:	n/a
25	chr3:143692255-143692305	A549	lung:	n/a
26	chr3:143690145-143690195	HCT-116	colon:	n/a
27	chr3:143690928-143690978	NT2-D1	testis:	n/a
28	chr3:143690246-143690296	NHDF-neo	bronchial:	n/a
29	chr3:143692320-143692370	RPTEC	kidney:	n/a
30	chr3:143690991-143691041	SAEC	small airway:	n/a
31	chr3:143692056-143692106	Hela-S3	cervix:	n/a
32	chr3:143690493-143690543	SKMC	muscle:	n/a
33	chr3:143690741-143690791	HNPCEpiC	eye:	n/a
34	chr3:143692146-143692196	SK-N-SH	brain:	n/a
35	chr3:143689916-143689966	H1-hESC	embryonic stem cell:	embryo
36	chr3:143692255-143692305	T-47D	breast:	n/a
37	chr3:143692146-143692196	Hepatocyte	liver:	n/a
38	chr3:143692134-143692184	SK-N-SH_RA	brain:	n/a
39	chr3:143692056-143692106	T-47D	breast:	n/a
40	chr3:143690493-143690543	NB4	blood:	n/a
41	chr3:143690991-143691041	HCM	heart:	n/a
42	chr3:143695141-143695191	HCPEpiC	choroid plexus:	n/a
43	chr3:143690208-143690258	AG10803	skin:	n/a
44	chr3:143690208-143690258	PFSK-1	brain:	n/a
45	chr3:143689810-143689860	U87	brain:	n/a
46	chr3:143690145-143690195	MCF10A-Er-Src	breast:	n/a
47	chr3:143692785-143692835	GM12891	blood:	n/a
48	chr3:143690404-143690454	Caco-2	colon:	n/a
49	chr3:143689584-143689634	LNCaP	prostate:	n/a
50	chr3:143692087-143692137	HCT-116	colon:	n/a

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:143694158..143694846-chr3:143996996..143997942,2	MCF-7	breast:
2	chr11:65625345..65626177-chr3:143690525..143691289,2	Hela-S3	cervix:
3	chr3:143689763..143690371-chr7:23510326..23510860,2	Hela-S3	cervix:
4	chr3:143614293..143615305-chr3:143670036..143670705,3	MCF-7	breast:
5	chr3:143674139..143676355-chr3:143690634..143693638,3	K562	blood:
6	chr3:143689777..143690496-chr6:26055384..26056279,2	Hela-S3	cervix:
7	chr3:143665779..143667511-chr3:143689617..143691914,2	MCF-7	breast:
8	chr3:143566553..143569042-chr3:143690803..143692633,2	MCF-7	breast:
9	chr3:143689459..143694662-chr3:143702114..143706390,7	K562	blood:
10	chr12:12956339..12957122-chr3:143689535..143690489,2	Hela-S3	cervix:
11	chr3:143514332..143514918-chr3:143670242..143670855,2	MCF-7	breast:
12	chr3:143614737..143615277-chr3:143670652..143671460,2	MCF-7	breast:
13	chr3:143684124..143687534-chr3:143688769..143693859,7	MCF-7	breast:
14	chr10:98592013..98592977-chr3:143690256..143690764,2	Hela-S3	cervix:
15	chr3:143679544..143684036-chr3:143688020..143692535,7	MCF-7	breast:
16	chr3:143701901..143703424-chr3:143714628..143717411,2	K562	blood:
17	chr3:143692106..143692865-chr7:112090373..112091302,2	Hela-S3	cervix:
18	chr3:143687536..143689056-chr3:143689809..143691733,2	MCF-7	breast:
19	chr3:143693440..143695168-chr3:143824981..143826507,2	K562	blood:
20	chr12:16064190..16064741-chr3:143690280..143690998,2	Hela-S3	cervix:
21	chr3:143674855..143677233-chr3:143692138..143694491,2	K562	blood:
22	chr3:143694211..143696611-chr3:143698183..143700521,4	K562	blood:
23	chr3:143680103..143683758-chr3:143690045..143692584,4	MCF-7	breast:
24	chr3:143665083..143667441-chr3:143670165..143673071,2	K562	blood:
25	chr11:17097769..17100478-chr3:143690055..143692307,2	MCF-7	breast:
26	chr16:88876624..88878169-chr3:143691035..143693133,2	MCF-7	breast:
27	chr3:143694211..143696611-chr3:143698183..143700521,4	K562	blood:
28	chr12:92539191..92539985-chr3:143690264..143691024,2	Hela-S3	cervix:
29	chr3:143695787..143698743-chr3:143748690..143750623,2	K562	blood:
30	chr3:143604403..143605317-chr3:143669942..143670478,2	K562	blood:
31	chr17:57914617..57916585-chr3:143689584..143691332,2	MCF-7	breast:
32	chr3:143688929..143690453-chr9:116724811..116727064,2	MCF-7	breast:
33	chr3:143669131..143673434-chr3:143689474..143692408,5	MCF-7	breast:
34	chr22:19418740..19420583-chr3:143689830..143691587,2	MCF-7	breast:
35	chr3:143677587..143679390-chr3:143686141..143687965,2	MCF-7	breast:
36	chr3:143690723..143691617-chr6:74230015..74230752,2	Hela-S3	cervix:
37	chr3:143604467..143605336-chr3:143669926..143671031,5	MCF-7	breast:
38	chr3:143694108..143696591-chr3:143721286..143722845,2	K562	blood:
39	chr19:57831383..57832246-chr3:143690551..143691404,2	NB4	blood:
40	chr3:143677587..143679390-chr3:143686141..143687965,2	MCF-7	breast:
41	chr16:28857621..28858218-chr3:143690524..143691094,2	Hela-S3	cervix:
42	chr3:143695188..143697980-chr3:143701408..143704204,2	MCF-7	breast:
43	chr3:112280243..112281155-chr3:143690900..143691448,2	Hela-S3	cervix:
44	chr3:143695188..143697980-chr3:143701408..143704204,2	MCF-7	breast:
45	chr3:143676919..143679412-chr3:143688995..143692223,3	MCF-7	breast:
46	chr2:88315349..88316190-chr3:143690878..143691682,2	HCT-116	colon:
47	chr3:143689958..143690542-chr6:44224790..44225315,2	Hela-S3	cervix:
48	chr3:143690729..143691347-chr6:35656198..35657113,2	Hela-S3	cervix:
49	chr3:143668700..143672507-chr3:143690640..143693277,4	K562	blood:
50	chr3:143694586..143698442-chr3:143710768..143713586,3	K562	blood:

No data

Variant related genes	Relation type
C3orf58	TF binding region
C3orf58	CpG island
ENSG00000144848	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000109046	chromatin interactions
ENSG00000100084	chromatin interactions
ENSG00000178229	chromatin interactions
ENSG00000181744	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000006652	chromatin interactions
ENSG00000140941	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000178952	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000181804	chromatin interactions
ENSG00000023697	chromatin interactions
ENSG00000105771	chromatin interactions
ENSG00000196233	chromatin interactions
ENSG00000138459	chromatin interactions
ENSG00000096060	chromatin interactions
ENSG00000123416	chromatin interactions
ENSG00000198931	chromatin interactions
ENSG00000172757	chromatin interactions
ENSG00000174749	chromatin interactions
ENSG00000221983	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000137504	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000178188	chromatin interactions
ENSG00000185608	chromatin interactions
ENSG00000157593	chromatin interactions

Extended variants
information (count: 1430 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1430 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11917772	chr3:143666825-143666826	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114221681	chr3:143666874-143666875	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs146330800	chr3:143666892-143666893	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs559286737	chr3:143666898-143666899	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532926714	chr3:143666916-143666917	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551057982	chr3:143666995-143666996	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs569518473	chr3:143667004-143667005	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs377163350	chr3:143667005-143667006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs138733964	chr3:143667042-143667043	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs193055499	chr3:143667051-143667052	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528416722	chr3:143667071-143667072	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs11914522	chr3:143667176-143667177	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs140394634	chr3:143667222-143667223	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs553911042	chr3:143667256-143667257	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs1436629	chr3:143667262-143667263	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs539983232	chr3:143667296-143667297	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs373366671	chr3:143667297-143667298	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs150414784	chr3:143667322-143667323	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs576729134	chr3:143667357-143667358	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs138131406	chr3:143667372-143667373	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs62267456	chr3:143667403-143667404	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs6768153	chr3:143667429-143667430	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34341235	chr3:143667434-143667435	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149597116	chr3:143667467-143667468	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541702428	chr3:143667474-143667475	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs185766511	chr3:143667484-143667485	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs1354495	chr3:143668854-143668855	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570057595	chr3:143668868-143668869	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs77618596	chr3:143668877-143668878	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs541884155	chr3:143668897-143668898	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs555784161	chr3:143668968-143668969	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs143161805	chr3:143668969-143668970	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535183786	chr3:143669027-143669028	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs7643008	chr3:143669057-143669058	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs147508606	chr3:143669064-143669065	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545279495	chr3:143669088-143669089	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs185892846	chr3:143669131-143669132	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs556577153	chr3:143669179-143669180	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574888800	chr3:143669193-143669194	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs189572927	chr3:143669199-143669200	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs115071446	chr3:143669247-143669248	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs1550141	chr3:143669321-143669322	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140244099	chr3:143669323-143669324	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs142964725	chr3:143669354-143669355	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs532490548	chr3:143669497-143669498	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs181963745	chr3:143669526-143669527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs573210496	chr3:143669532-143669533	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139001880	chr3:143669534-143669535	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs1550142	chr3:143669556-143669557	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs549224797	chr3:143669667-143669668	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
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
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	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
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21509527	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:876 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143673000-143673800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr3:143673000-143673800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr3:143673400-143674000	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr3:143673800-143675400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr3:143673800-143675800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr3:143674000-143676400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr3:143675200-143676400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr3:143675400-143676400	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr3:143675400-143676600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr3:143675400-143676600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:143675600-143676400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
12	chr3:143675800-143676400	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr3:143675800-143676800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr3:143676000-143676400	Enhancers	Primary T helper cells PMA-I stimulated	--
15	chr3:143676000-143677000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr3:143676000-143677200	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr3:143676200-143676600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr3:143676400-143677000	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr3:143680400-143689600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr3:143681800-143682000	Bivalent Enhancer	Left Ventricle	heart
21	chr3:143682000-143682200	Enhancers	H9 Cell Line	embryonic stem cell
22	chr3:143682200-143682800	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr3:143682200-143683800	Weak transcription	Pancreas	Pancrea
24	chr3:143682400-143683000	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:143682400-143683400	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr3:143682400-143683400	Enhancers	Monocytes-CD14+_RO01746	blood
27	chr3:143682600-143683200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:143682600-143685000	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr3:143682800-143688800	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr3:143683400-143689200	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr3:143683600-143684000	Enhancers	Osteobl	bone
32	chr3:143683800-143684000	ZNF genes & repeats	Pancreas	Pancrea
33	chr3:143683800-143689400	Weak transcription	Brain Substantia Nigra	brain
34	chr3:143684000-143689600	Weak transcription	Pancreas	Pancrea
35	chr3:143685000-143685200	Enhancers	H9 Cell Line	embryonic stem cell
36	chr3:143685000-143685600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr3:143685200-143685400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr3:143685200-143685400	Enhancers	HSMMtube	muscle
39	chr3:143685200-143689600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr3:143685600-143688800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr3:143685600-143689000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr3:143687600-143689400	Weak transcription	Right Atrium	heart
43	chr3:143687800-143688000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr3:143688000-143689600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:143688800-143689000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr3:143688800-143689000	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr3:143688800-143689000	Bivalent Enhancer	Dnd41	blood
48	chr3:143688800-143689200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:143688800-143689200	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr3:143688800-143689200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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