Variant report

Variant	nsv874232
Chromosome Location	chr2:62758044-62906084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1362)
CpG islands
(count:1042)
Chromatin interactive
region (count:31)
LncRNA
region (count:60)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1362 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:62794907-62795517	HepG2	liver:	n/a	chr2:62795435-62795451
2	ARID3A	chr2:62817057-62817459	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:62805120-62806370	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:62792371-62792922	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:62795969-62798122	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:62880772-62881775	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:62767386-62768109	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:62869353-62870394	HepG2	liver:	n/a	n/a
9	ARID3A	chr2:62899728-62900427	HepG2	liver:	n/a	n/a
10	ATF1	chr2:62814171-62814501	K562	blood:	n/a	n/a
11	ATF2	chr2:62825956-62826272	GM12878	blood:	n/a	n/a
12	ATF2	chr2:62825831-62826320	GM12878	blood:	n/a	n/a
13	ATF2	chr2:62899787-62900210	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr2:62804843-62805812	HCT-116	colon:	n/a	n/a
15	ATF3	chr2:62796473-62797820	A549	lung:	n/a	n/a
16	ATF3	chr2:62804903-62806678	A549	lung:	n/a	n/a
17	ATF3	chr2:62804747-62806787	A549	lung:	n/a	n/a
18	ATF3	chr2:62796945-62797930	A549	lung:	n/a	n/a
19	BACH1	chr2:62798211-62798463	H1-hESC	embryonic stem cell:	n/a	chr2:62798385-62798399
20	BACH1	chr2:62797394-62797489	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr2:62899808-62900287	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr2:62831421-62831702	GM12878	blood:	n/a	n/a
23	BATF	chr2:62831417-62831739	GM12878	blood:	n/a	n/a
24	BATF	chr2:62887859-62888254	GM12878	blood:	n/a	chr2:62888061-62888072
25	BATF	chr2:62825661-62825845	GM12878	blood:	n/a	n/a
26	BCL3	chr2:62804577-62807004	A549	lung:	n/a	n/a
27	BCL3	chr2:62804749-62806984	A549	lung:	n/a	n/a
28	BCL3	chr2:62796374-62798026	A549	lung:	n/a	chr2:62797896-62797909
29	BCL3	chr2:62880798-62881857	A549	lung:	n/a	n/a
30	BCL3	chr2:62796345-62798363	A549	lung:	n/a	chr2:62797896-62797909
31	BCLAF1	chr2:62887071-62887719	GM12878	blood:	n/a	n/a
32	BHLHE40	chr2:62797227-62797503	A549	lung:	n/a	n/a
33	BHLHE40	chr2:62798272-62798471	K562	blood:	n/a	n/a
34	BHLHE40	chr2:62797189-62797527	HepG2	liver:	n/a	n/a
35	BHLHE40	chr2:62797130-62797700	HepG2	liver:	n/a	n/a
36	BHLHE40	chr2:62814204-62814370	GM12878	blood:	n/a	n/a
37	BHLHE40	chr2:62796783-62797824	HepG2	liver:	n/a	n/a
38	BHLHE40	chr2:62842761-62842897	K562	blood:	n/a	n/a
39	BRCA1	chr2:62884441-62884529	GM12878	blood:	n/a	n/a
40	CBX3	chr2:62804868-62808039	HCT-116	colon:	n/a	n/a
41	CBX3	chr2:62804937-62806981	HCT-116	colon:	n/a	n/a
42	CEBPB	chr2:62764015-62764538	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:62814159-62814459	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:62805999-62806422	MCF-7	breast:	n/a	chr2:62806192-62806203
45	CEBPB	chr2:62797006-62797921	HepG2	liver:	n/a	n/a
46	CEBPB	chr2:62788769-62789037	HepG2	liver:	n/a	chr2:62788941-62788952
47	CEBPB	chr2:62788781-62789024	HepG2	liver:	n/a	chr2:62788941-62788952
48	CEBPB	chr2:62852042-62852399	IMR90	lung:	n/a	n/a
49	CEBPB	chr2:62880913-62882093	A549	lung:	n/a	n/a
50	CEBPB	chr2:62881061-62881502	HepG2	liver:	n/a	n/a

(count:1042 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:62901175-62901225	ovcar-3	ovarian:	n/a
2	chr2:62824045-62824095	HCPEpiC	choroid plexus:	n/a
3	chr2:62805851-62805901	HCF	heart:	n/a
4	chr2:62824045-62824095	GM12892	blood:	n/a
5	chr2:62797865-62797915	SK-N-SH_RA	brain:	n/a
6	chr2:62901175-62901225	ovcar-3	ovarian:	n/a
7	chr2:62824045-62824095	HCPEpiC	choroid plexus:	n/a
8	chr2:62805851-62805901	HCF	heart:	n/a
9	chr2:62824045-62824095	GM12892	blood:	n/a
10	chr2:62797865-62797915	SK-N-SH_RA	brain:	n/a
11	chr2:62888566-62888616	IMR90	lung:	fetal
12	chr2:62797901-62797951	HIPEpiC	eye:	n/a
13	chr2:62824045-62824095	HCF	heart:	n/a
14	chr2:62857522-62857572	HEEpiC	esophagus:	n/a
15	chr2:62798365-62798415	SK-N-MC	brain:	n/a
16	chr2:62816860-62816910	NHBE	bronchial:	n/a
17	chr2:62767922-62767972	Hela-S3	cervix:	n/a
18	chr2:62900312-62900362	AG04450	lung:	fetal
19	chr2:62797901-62797951	AG09319	gingival:	n/a
20	chr2:62901049-62901099	U87	brain:	n/a
21	chr2:62788813-62788863	NHDF-neo	bronchial:	n/a
22	chr2:62899546-62899596	MCF10A-Er-Src	breast:	n/a
23	chr2:62857522-62857572	H1-hESC	embryonic stem cell:	embryo
24	chr2:62816860-62816910	ProgFib	skin:	n/a
25	chr2:62767922-62767972	K562	blood:	n/a
26	chr2:62900312-62900362	NB4	blood:	n/a
27	chr2:62857522-62857572	GM12891	blood:	n/a
28	chr2:62797865-62797915	IMR90	lung:	fetal
29	chr2:62797865-62797915	RPTEC	kidney:	n/a
30	chr2:62797901-62797951	GM12891	blood:	n/a
31	chr2:62824045-62824095	HAEpiC	amniotic membrane:	n/a
32	chr2:62798448-62798498	NH-A	brain:	n/a
33	chr2:62857522-62857572	SKMC	muscle:	n/a
34	chr2:62899546-62899596	ProgFib	skin:	n/a
35	chr2:62798365-62798415	SK-N-SH	brain:	n/a
36	chr2:62798448-62798498	AG09309	skin:	n/a
37	chr2:62901049-62901099	HCPEpiC	choroid plexus:	n/a
38	chr2:62798365-62798415	AG04449	skin:	fetal
39	chr2:62788813-62788863	ProgFib	skin:	n/a
40	chr2:62900312-62900362	SK-N-SH	brain:	n/a
41	chr2:62798365-62798415	NHBE	bronchial:	n/a
42	chr2:62797926-62797976	AoSMC	blood vessel:	n/a
43	chr2:62901175-62901225	MCF-7	breast:	n/a
44	chr2:62788813-62788863	PANC-1	pancreas:	n/a
45	chr2:62797865-62797915	HCM	heart:	n/a
46	chr2:62797865-62797915	HCPEpiC	choroid plexus:	n/a
47	chr2:62767922-62767972	HEK293	kidney:	embryo
48	chr2:62805851-62805901	HepG2	liver:	n/a
49	chr2:62901175-62901225	SK-N-MC	brain:	n/a
50	chr2:62901175-62901225	AG09309	skin:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:62781352..62783656-chr2:62789677..62792468,2	K562	blood:
2	chr2:62774741..62777496-chr2:62784442..62786163,2	K562	blood:
3	chr2:62219244..62222236-chr2:62763935..62766858,2	K562	blood:
4	chr2:62883737..62887558-chr2:62889986..62892467,3	K562	blood:
5	chr2:62883289..62885199-chr2:62932148..62934917,2	K562	blood:
6	chr2:62805472..62807401-chr2:62822491..62825176,2	MCF-7	breast:
7	chr2:62866392..62868630-chr2:62870444..62872522,2	MCF-7	breast:
8	chr2:62682086..62684850-chr2:62901715..62904268,2	K562	blood:
9	chr2:62789959..62792774-chr2:62932258..62934992,3	MCF-7	breast:
10	chr2:62732443..62734653-chr2:62900758..62903078,2	MCF-7	breast:
11	chr2:62781352..62783656-chr2:62789677..62792468,2	K562	blood:
12	chr2:62815568..62818395-chr2:62989644..62992050,2	K562	blood:
13	chr2:62883737..62887558-chr2:62889986..62892467,3	K562	blood:
14	chr2:62801914..62804670-chr2:62805943..62809053,3	K562	blood:
15	chr2:62803038..62805318-chr2:62807553..62809617,2	K562	blood:
16	chr2:62750475..62752947-chr2:62754435..62758816,4	MCF-7	breast:
17	chr2:62801914..62804670-chr2:62805943..62809053,3	K562	blood:
18	chr2:62805472..62807401-chr2:62822491..62825176,2	MCF-7	breast:
19	chr2:62905588..62907868-chr2:62914672..62916535,2	K562	blood:
20	chr2:62796756..62798416-chr2:62803232..62804863,2	MCF-7	breast:
21	chr2:62868727..62871605-chr2:62931209..62933790,2	MCF-7	breast:
22	chr2:62796756..62798416-chr2:62803232..62804863,2	MCF-7	breast:
23	chr2:62886240..62888184-chr2:62910280..62913021,2	K562	blood:
24	chr2:62774741..62777496-chr2:62784442..62786163,2	K562	blood:
25	chr2:62825643..62826253-chr5:138713570..138714131,2	MCF-7	breast:
26	chr2:62899645..62902423-chr2:62906045..62908750,2	K562	blood:
27	chr2:62886383..62889324-chr2:62914421..62916883,2	K562	blood:
28	chr2:62889688..62892538-chr2:62898649..62900381,2	K562	blood:
29	chr2:62803038..62805318-chr2:62807553..62809617,2	K562	blood:
30	chr2:62866392..62868630-chr2:62870444..62872522,2	MCF-7	breast:
31	chr2:62897067..62900392-chr2:62900736..62904878,3	K562	blood:

(count:60 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM17-2	chr2:62889743-62889929	XLOC_002117
2	lnc-EHBP1-2	chr2:62839450-62839526	NONHSAT071024
3	lnc-TMEM17-2	chr2:62817636-62817712	NONHSAT071022
4	lnc-EHBP1-2	chr2:62840740-62841281	NONHSAT071024
5	lnc-EHBP1-2	chr2:62889742-62889927	NONHSAT071024
6	lnc-TMEM17-2	chr2:62840741-62840837	XLOC_002117
7	lnc-TMEM17-2	chr2:62858537-62858701	XLOC_002117
8	lnc-TMEM17-5	chr2:62788193-62788558	NONHSAT071020
9	lnc-TMEM17-2	chr2:62839451-62839526	XLOC_002117
10	lnc-TMEM17-2	chr2:62889743-62889929	XLOC_002117
11	lnc-TMEM17-2	chr2:62852102-62852146	NONHSAT071032
12	lnc-TMEM17-2	chr2:62858537-62858700	XLOC_002117
13	lnc-TMEM17-2	chr2:62838524-62839358	XLOC_002117
14	lnc-TMEM17-2	chr2:62817636-62817712	XLOC_002117
15	lnc-TMEM17-2	chr2:62839451-62839526	XLOC_002117
16	lnc-TMEM17-2	chr2:62817390-62817712	XLOC_002117
17	lnc-TMEM17-2	chr2:62838915-62839358	XLOC_002117
18	lnc-TMEM17-2	chr2:62889743-62889763	XLOC_002117
19	lnc-TMEM17-2	chr2:62838524-62839358	XLOC_002117
20	lnc-TMEM17-2	chr2:62839007-62839358	XLOC_002117
21	lnc-TMEM17-2	chr2:62852262-62852355	NONHSAT071032
22	lnc-TMEM17-2	chr2:62858537-62858700	XLOC_002117
23	lnc-EHBP1-2	chr2:62889029-62889089	NONHSAT071024
24	lnc-TMEM17-2	chr2:62889743-62889927	XLOC_002117
25	lnc-EHBP1-2	chr2:62858536-62858700	NONHSAT071024
26	lnc-TMEM17-2	chr2:62839451-62839526	XLOC_002117
27	lnc-TMEM17-2	chr2:62815940-62816078	NONHSAT071023
28	lnc-TMEM17-2	chr2:62856488-62856579	XLOC_002117
29	lnc-TMEM17-2	chr2:62889743-62889789	XLOC_002117
30	lnc-TMEM17-2	chr2:62858537-62858700	XLOC_002117
31	lnc-TMEM17-2	chr2:62858537-62858700	XLOC_002117
32	lnc-TMEM17-2	chr2:62856488-62856611	XLOC_002117
33	lnc-TMEM17-2	chr2:62814590-62815055	NONHSAT071023
34	lnc-TMEM17-2	chr2:62889030-62889068	XLOC_002117
35	lnc-EHBP1-2	chr2:62817389-62817712	NONHSAT071024
36	lnc-TMEM17-2	chr2:62856488-62856595	NONHSAT071032
37	lnc-TMEM17-2	chr2:62858537-62858697	NONHSAT071022
38	lnc-TMEM17-4	chr2:62779598-62780569	NONHSAT071019
39	lnc-TMEM17-2	chr2:62889743-62889751	XLOC_002117
40	lnc-TMEM17-2	chr2:62852088-62852146	XLOC_002117
41	lnc-TMEM17-2	chr2:62839451-62839526	XLOC_002117
42	lnc-EHBP1-2	chr2:62838914-62839358	NONHSAT071024
43	lnc-TMEM17-2	chr2:62838524-62839358	XLOC_002117
44	lnc-TMEM17-2	chr2:62858537-62858700	XLOC_002117
45	lnc-TMEM17-2	chr2:62889030-62889068	XLOC_002117
46	lnc-TMEM17-2	chr2:62839451-62839526	XLOC_002117
47	lnc-EHBP1-2	chr2:62852087-62852146	NONHSAT071024
48	lnc-TMEM17-2	chr2:62889030-62889068	XLOC_002117
49	lnc-TMEM17-2	chr2:62839451-62839526	XLOC_002117
50	lnc-TMEM17-2	chr2:62852088-62852146	XLOC_002117

No data

Variant related genes	Relation type
ENSG00000226622	TF binding region
EHBP1	TF binding region
PSAT1P2	TF binding region
ENSG00000229503	TF binding region
RSL24D1P2	TF binding region
ENSG00000226622	CpG island
EHBP1	CpG island
PSAT1P2	CpG island
ENSG00000229503	CpG island
RSL24D1P2	CpG island
ENSG00000226622	chromatin interactions
ENSG00000115504	chromatin interactions
ENSG00000186889	chromatin interactions
MITF	miRNA target sites
LIMS1	miRNA target sites
MYH10	miRNA target sites
TIMP3	miRNA target sites
FSTL1	miRNA target sites
GNAI2	miRNA target sites
PALLD	miRNA target sites
MKNK2	miRNA target sites
CCDC99	miRNA target sites
MKLN1	miRNA target sites
MKRN1	miRNA target sites

Extended variants
information (count: 5851 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:5851 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4399711	chr2:62758044-62758045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs181694602	chr2:62758054-62758055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149300921	chr2:62758065-62758066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs527785578	chr2:62758084-62758085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575190680	chr2:62758085-62758086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs552208536	chr2:62758088-62758089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564151456	chr2:62758089-62758090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185109225	chr2:62758101-62758102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550086573	chr2:62758117-62758118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6708322	chr2:62758232-62758233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs17575420	chr2:62758283-62758284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs547966773	chr2:62758292-62758293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs566093875	chr2:62758312-62758313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539546693	chr2:62758335-62758336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542780054	chr2:62758372-62758373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs146232910	chr2:62758426-62758427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs537022747	chr2:62758450-62758451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139434449	chr2:62758457-62758458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369037299	chr2:62758558-62758559	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573870690	chr2:62758596-62758597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540917636	chr2:62758611-62758612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs6752833	chr2:62758620-62758621	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs577378594	chr2:62758646-62758647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs545910073	chr2:62758658-62758659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144138769	chr2:62758754-62758755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs6708968	chr2:62758756-62758757	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs140781388	chr2:62758795-62758796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs527620527	chr2:62758865-62758866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs562288670	chr2:62758918-62758919	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529594562	chr2:62758919-62758920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs146433913	chr2:62758922-62758923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs6753189	chr2:62758933-62758934	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs533539075	chr2:62758964-62758965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551530391	chr2:62759024-62759025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370608059	chr2:62759042-62759043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs113633126	chr2:62759059-62759060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs569753493	chr2:62759089-62759090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529231986	chr2:62759098-62759099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549071384	chr2:62759160-62759161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537084053	chr2:62759172-62759173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555342412	chr2:62759175-62759176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs148610613	chr2:62759339-62759340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62178039	chr2:62759353-62759354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569352952	chr2:62759387-62759388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534928678	chr2:62759420-62759421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs552960073	chr2:62759473-62759474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377722394	chr2:62759482-62759483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370179927	chr2:62759490-62759491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149968752	chr2:62759501-62759502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs574033521	chr2:62759526-62759527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Chronic lymphocytic leukemia	20421269	CNVD

Chromatin state (count:1459 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:62749200-62760400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:62754200-62758400	Weak transcription	Pancreas	Pancrea
3	chr2:62754200-62766800	Weak transcription	Ovary	ovary
4	chr2:62758400-62759000	Enhancers	Pancreas	Pancrea
5	chr2:62759000-62766600	Weak transcription	Pancreas	Pancrea
6	chr2:62760400-62760800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:62762200-62762800	Enhancers	HepG2	liver
8	chr2:62762400-62762600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr2:62762400-62762600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr2:62762400-62762600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:62762600-62763800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr2:62762600-62764000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr2:62762800-62763200	Weak transcription	HepG2	liver
14	chr2:62763200-62763400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:62763200-62767400	Enhancers	HepG2	liver
16	chr2:62763400-62772800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr2:62763800-62764800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr2:62763800-62765200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr2:62763800-62765200	Enhancers	NHEK	skin
20	chr2:62764000-62765000	Enhancers	Gastric	stomach
21	chr2:62764000-62765600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:62764000-62770200	Enhancers	Fetal Intestine Small	intestine
23	chr2:62764200-62764600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr2:62764200-62764600	Enhancers	Stomach Mucosa	stomach
25	chr2:62764200-62765600	Enhancers	Fetal Intestine Large	intestine
26	chr2:62764600-62766800	Weak transcription	Stomach Mucosa	stomach
27	chr2:62764600-62767000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:62764800-62772000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:62765000-62767600	Weak transcription	Gastric	stomach
30	chr2:62765200-62766000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr2:62765200-62766600	Weak transcription	NHEK	skin
32	chr2:62765400-62765600	Enhancers	Small Intestine	intestine
33	chr2:62765600-62766000	Weak transcription	Fetal Intestine Large	intestine
34	chr2:62765600-62766800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:62766000-62767800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr2:62766000-62768800	Enhancers	Duodenum Mucosa	Duodenum
37	chr2:62766000-62769400	Enhancers	Fetal Intestine Large	intestine
38	chr2:62766600-62767200	Enhancers	Pancreas	Pancrea
39	chr2:62766600-62767600	Enhancers	NHEK	skin
40	chr2:62766600-62768600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr2:62766600-62769400	Enhancers	Liver	Liver
42	chr2:62766800-62767000	Enhancers	A549	lung
43	chr2:62766800-62767600	Enhancers	NHDF-Ad	bronchial
44	chr2:62766800-62767800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr2:62766800-62768600	Enhancers	Ovary	ovary
46	chr2:62766800-62769000	Enhancers	Pancreatic Islets	Pancreatic Islet
47	chr2:62766800-62769200	Enhancers	Stomach Mucosa	stomach
48	chr2:62767000-62767200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr2:62767000-62767800	Flanking Active TSS	A549	lung
50	chr2:62767000-62767800	Enhancers	HMEC	breast

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