Variant report

Variant	nsv1002396
Chromosome Location	chr2:34581285-34993188
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1060)
CpG islands
(count:427)
Chromatin interactive
region (count:23)
LncRNA
region (count:48)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1060 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:34814574-34814687	K562	blood:	n/a	n/a
2	ATF2	chr2:34590863-34591498	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:34989249-34989315	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:34881803-34882061	GM12878	blood:	n/a	n/a
5	BATF	chr2:34626271-34626588	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
6	BATF	chr2:34902415-34902679	GM12878	blood:	n/a	n/a
7	BATF	chr2:34902921-34903226	GM12878	blood:	n/a	n/a
8	BATF	chr2:34902925-34903229	GM12878	blood:	n/a	n/a
9	BATF	chr2:34626250-34626627	GM12878	blood:	n/a	chr2:34626402-34626412 chr2:34626401-34626412
10	BCL11A	chr2:34626351-34626529	GM12878	blood:	n/a	chr2:34626400-34626409 chr2:34626401-34626410
11	BCL11A	chr2:34591088-34591422	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr2:34633212-34633509	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
13	BCL3	chr2:34633202-34633571	GM12878	blood:	n/a	chr2:34633318-34633327 chr2:34633317-34633326
14	BCL3	chr2:34803709-34804015	GM12878	blood:	n/a	n/a
15	BHLHE40	chr2:34963851-34964109	GM12878	blood:	n/a	n/a
16	BHLHE40	chr2:34891473-34891834	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:34827333-34827668	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:34930671-34930923	GM12878	blood:	n/a	n/a
19	BHLHE40	chr2:34908833-34908941	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:34795688-34795858	GM12878	blood:	n/a	n/a
21	BHLHE40	chr2:34902255-34902723	GM12878	blood:	n/a	n/a
22	BHLHE40	chr2:34633159-34633448	GM12878	blood:	n/a	n/a
23	CBX3	chr2:34744823-34745018	K562	blood:	n/a	n/a
24	CCNT2	chr2:34623370-34623530	K562	blood:	n/a	n/a
25	CEBPB	chr2:34907939-34908176	A549	lung:	n/a	chr2:34908035-34908046
26	CEBPB	chr2:34633823-34633989	A549	lung:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
27	CEBPB	chr2:34759033-34759047	HepG2	liver:	n/a	n/a
28	CEBPB	chr2:34706631-34706981	IMR90	lung:	n/a	chr2:34706794-34706805
29	CEBPB	chr2:34793002-34793270	HepG2	liver:	n/a	chr2:34793159-34793170 chr2:34793159-34793172 chr2:34793160-34793171
30	CEBPB	chr2:34637607-34637980	HepG2	liver:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
31	CEBPB	chr2:34803766-34804113	MCF-7	breast:	n/a	n/a
32	CEBPB	chr2:34637705-34637966	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
33	CEBPB	chr2:34637703-34637950	MCF-7	breast:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
34	CEBPB	chr2:34850814-34851079	HepG2	liver:	n/a	chr2:34850939-34850950 chr2:34850903-34850914
35	CEBPB	chr2:34661633-34661923	HepG2	liver:	n/a	chr2:34661857-34661869
36	CEBPB	chr2:34759886-34760188	MCF-7	breast:	n/a	chr2:34759972-34759985
37	CEBPB	chr2:34610798-34611191	HepG2	liver:	n/a	chr2:34610999-34611008 chr2:34611030-34611038 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610999-34611008 chr2:34610997-34611010 chr2:34610999-34611008 chr2:34610997-34611008 chr2:34610997-34611010 chr2:34610998-34611009 chr2:34610997-34611008
38	CEBPB	chr2:34931219-34931422	HepG2	liver:	n/a	chr2:34931302-34931313
39	CEBPB	chr2:34651788-34652080	HepG2	liver:	n/a	chr2:34651953-34651964
40	CEBPB	chr2:34651781-34652060	IMR90	lung:	n/a	chr2:34651953-34651964
41	CEBPB	chr2:34706608-34706989	HepG2	liver:	n/a	chr2:34706794-34706805
42	CEBPB	chr2:34717914-34718139	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:34960041-34960126	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr2:34637621-34637979	H1-hESC	embryonic stem cell:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
45	CEBPB	chr2:34637610-34637983	IMR90	lung:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
46	CEBPB	chr2:34706676-34706941	A549	lung:	n/a	chr2:34706794-34706805
47	CEBPB	chr2:34637613-34637978	K562	blood:	n/a	chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637786-34637795 chr2:34637784-34637797 chr2:34637785-34637796 chr2:34637786-34637795
48	CEBPB	chr2:34907924-34908188	HepG2	liver:	n/a	chr2:34908035-34908046
49	CEBPB	chr2:34633778-34633979	HepG2	liver:	n/a	chr2:34633880-34633891 chr2:34633878-34633891 chr2:34633878-34633889 chr2:34633878-34633891
50	CEBPB	chr2:34651815-34652025	H1-hESC	embryonic stem cell:	n/a	chr2:34651953-34651964

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:34633637-34633687	AG10803	skin:	n/a
2	chr2:34590591-34590641	HCM	heart:	n/a
3	chr2:34902113-34902163	NT2-D1	testis:	n/a
4	chr2:34720275-34720325	NHBE	bronchial:	n/a
5	chr2:34852273-34852323	SK-N-SH	brain:	n/a
6	chr2:34633637-34633687	T-47D	breast:	n/a
7	chr2:34902113-34902163	GM12878	blood:	n/a
8	chr2:34902113-34902163	Jurkat	blood:	n/a
9	chr2:34720275-34720325	HCT-116	colon:	n/a
10	chr2:34852273-34852323	HEEpiC	esophagus:	n/a
11	chr2:34633637-34633687	AG04449	skin:	fetal
12	chr2:34719565-34719615	ECC-1	luminal epithelium:	n/a
13	chr2:34633637-34633687	RPTEC	kidney:	n/a
14	chr2:34719719-34719769	HCPEpiC	choroid plexus:	n/a
15	chr2:34719565-34719615	GM12892	blood:	n/a
16	chr2:34852273-34852323	HNPCEpiC	eye:	n/a
17	chr2:34590591-34590641	ovcar-3	ovarian:	n/a
18	chr2:34719719-34719769	PANC-1	pancreas:	n/a
19	chr2:34720275-34720325	U87	brain:	n/a
20	chr2:34633637-34633687	HMEC	breast:	n/a
21	chr2:34852273-34852323	HIPEpiC	eye:	n/a
22	chr2:34720275-34720325	GM12892	blood:	n/a
23	chr2:34719565-34719615	Hela-S3	cervix:	n/a
24	chr2:34719719-34719769	CMK	blood:	n/a
25	chr2:34719565-34719615	HCT-116	colon:	n/a
26	chr2:34633637-34633687	AoSMC	blood vessel:	n/a
27	chr2:34902113-34902163	NB4	blood:	n/a
28	chr2:34633637-34633687	NB4	blood:	n/a
29	chr2:34852273-34852323	HCM	heart:	n/a
30	chr2:34719719-34719769	PFSK-1	brain:	n/a
31	chr2:34719565-34719615	HMEC	breast:	n/a
32	chr2:34590591-34590641	RPTEC	kidney:	n/a
33	chr2:34719719-34719769	MCF-7	breast:	n/a
34	chr2:34719719-34719769	RPTEC	kidney:	n/a
35	chr2:34902113-34902163	Hepatocyte	liver:	n/a
36	chr2:34590591-34590641	NH-A	brain:	n/a
37	chr2:34852273-34852323	LNCaP	prostate:	n/a
38	chr2:34633637-34633687	BJ	skin:	n/a
39	chr2:34633637-34633687	GM12891	blood:	n/a
40	chr2:34633637-34633687	HAEpiC	amniotic membrane:	n/a
41	chr2:34852273-34852323	PANC-1	pancreas:	n/a
42	chr2:34852273-34852323	AG10803	skin:	n/a
43	chr2:34852273-34852323	HepG2	liver:	n/a
44	chr2:34719565-34719615	HNPCEpiC	eye:	n/a
45	chr2:34719719-34719769	SK-N-MC	brain:	n/a
46	chr2:34719719-34719769	LNCaP	prostate:	n/a
47	chr2:34633637-34633687	MCF10A-Er-Src	breast:	n/a
48	chr2:34590591-34590641	PFSK-1	brain:	n/a
49	chr2:34852273-34852323	GM12891	blood:	n/a
50	chr2:34590591-34590641	MCF-7	breast:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:33906151..33906814-chr2:34795262..34796206,5	MCF-7	breast:
2	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
3	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
4	chr2:34237681..34238401-chr2:34795339..34796232,5	MCF-7	breast:
5	chr2:34321239..34322372-chr2:34772370..34773083,4	MCF-7	breast:
6	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
7	chr17:76778253..76778888-chr2:34769758..34770277,2	MCF-7	breast:
8	chr2:34929052..34931868-chr2:34933062..34935710,2	K562	blood:
9	chr2:34876891..34879240-chr2:34886043..34888561,2	K562	blood:
10	chr17:41466170..41467868-chr2:34623111..34624611,2	MCF-7	breast:
11	chr2:34237581..34238416-chr2:34963443..34964247,2	MCF-7	breast:
12	chr2:34237506..34238447-chr2:34795265..34796658,5	MCF-7	breast:
13	chr2:34321381..34322557-chr2:34795669..34796275,5	MCF-7	breast:
14	chr2:34636657..34638446-chr2:34644514..34646250,2	K562	blood:
15	chr2:34929052..34931868-chr2:34933062..34935710,2	K562	blood:
16	chr2:34624209..34626557-chr2:34688886..34690644,2	K562	blood:
17	chr12:46765173..46767943-chr2:34590937..34593382,2	MCF-7	breast:
18	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
19	chr2:34876891..34879240-chr2:34886043..34888561,2	K562	blood:
20	chr2:34795663..34796225-chr8:85142407..85143298,2	MCF-7	breast:
21	chr2:34707651..34709954-chr2:34710435..34712219,2	MCF-7	breast:
22	chr2:34590795..34592507-chr2:34600278..34603033,2	K562	blood:
23	chr17:57969237..57970939-chr2:34675539..34678526,2	MCF-7	breast:

(count:48 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASGRP3-4	chr2:34938646-34938840	ENSG00000228262.4
2	lnc-RASGRP3-4	chr2:34962172-34963510	NONHSAT070051
3	lnc-RASGRP3-3	chr2:34609584-34609796	NONHSAT070034
4	lnc-RASGRP3-14	chr2:34800570-34803561	l_1807_chr2:34789043-34803561_liver
5	lnc-RASGRP3-4	chr2:34938657-34938840	ENSG00000228262
6	lnc-RASGRP3-4	chr2:34938646-34938840	ENSG00000228262.4
7	lnc-RASGRP3-14	chr2:34792150-34792344	NONHSAT070037
8	lnc-FAM98A-7	chr2:34787656-34787849	NONHSAT070038
9	lnc-RASGRP3-4	chr2:34929778-34929989	ENSG00000228262.4
10	lnc-RASGRP3-14	chr2:34792161-34792344	NONHSAT070039
11	lnc-RASGRP3-4	chr2:34960145-34960753	ENSG00000228262.4
12	lnc-RASGRP3-4	chr2:34938646-34938840	NONHSAT070045
13	lnc-RASGRP3-4	chr2:34962148-34962183	NONHSAT070048
14	lnc-FAM98A-8	chr2:34917357-34917552	ENSG00000272027.1
15	lnc-RASGRP3-4	chr2:34957515-34957624	ENSG00000228262
16	lnc-RASGRP3-3	chr2:34608855-34609276	ENSG00000226785
17	lnc-RASGRP3-4	chr2:34947066-34947580	ENSG00000228262.4
18	lnc-RASGRP3-4	chr2:34962388-34962644	ENSG00000228262.4
19	lnc-RASGRP3-4	chr2:34935519-34935571	NONHSAT070044
20	lnc-RASGRP3-4	chr2:34947066-34947188	ENSG00000228262.4
21	lnc-FAM98A-8	chr2:34919267-34919365	ENSG00000272027.1
22	lnc-RASGRP3-14	chr2:34792147-34792344	l_1807_chr2:34789043-34803561_liver
23	lnc-RASGRP3-4	chr2:34947066-34947186	ENSG00000228262.4
24	lnc-RASGRP3-4	chr2:34935518-34935580	NONHSAT070045
25	lnc-RASGRP3-4	chr2:34962388-34963298	ENSG00000228262
26	lnc-RASGRP3-4	chr2:34947066-34950118	NONHSAT070045
27	lnc-RASGRP3-4	chr2:34959627-34961285	NONHSAT070048
28	lnc-RASGRP3-3	chr2:34609584-34609636	ENSG00000226785
29	lnc-RASGRP3-4	chr2:34902711-34902994	NONHSAT070044
30	lnc-RASGRP3-13	chr2:34713820-34713911	NONHSAT070033
31	lnc-RASGRP3-3	chr2:34860316-34860407	ENSG00000226785
32	lnc-RASGRP3-4	chr2:34935519-34935580	ENSG00000228262.4
33	lnc-RASGRP3-4	chr2:34978401-34978447	NONHSAT070051
34	lnc-RASGRP3-14	chr2:34811019-34811128	NONHSAT070039
35	lnc-RASGRP3-4	chr2:34962388-34962638	ENSG00000228262.4
36	lnc-FAM98A-7	chr2:34823138-34823205	NONHSAT070038
37	lnc-FAM98A-2	chr2:34960042-34960174	ENSG00000232153
38	lnc-RASGRP3-15	chr2:34878421-34878470	NONHSAT070041
39	lnc-RASGRP3-14	chr2:34789044-34789084	l_1807_chr2:34789043-34803561_liver
40	lnc-RASGRP3-4	chr2:34956433-34956605	ENSG00000228262.4
41	lnc-RASGRP3-14	chr2:34815892-34816802	NONHSAT070039
42	lnc-RASGRP3-14	chr2:34815937-34816109	l_1807_chr2:34789043-34803561_liver
43	lnc-RASGRP3-4	chr2:34938657-34938840	ENSG00000228262.4
44	lnc-RASGRP3-4	chr2:34957515-34957624	ENSG00000228262.4
45	lnc-RASGRP3-14	chr2:34800570-34801134	NONHSAT070037
46	lnc-RASGRP3-15	chr2:34909934-34910063	NONHSAT070041
47	lnc-FAM98A-2	chr2:34962148-34962185	ENSG00000232153
48	lnc-RASGRP3-14	chr2:34756150-34756498	NONHSAT070037

No data

Variant related genes	Relation type
ENSG00000212025	TF binding region
ENSG00000226785	TF binding region
ENSG00000272027	TF binding region
ENSG00000232153	TF binding region
ENSG00000228262	TF binding region
ENSG00000212025	CpG island
ENSG00000226785	CpG island
ENSG00000272027	CpG island
ENSG00000232153	CpG island
ENSG00000228262	CpG island
ENSG00000228262	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000258096	chromatin interactions
ENSG00000108669	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 7351 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:7351 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560152946	chr2:34581622-34581623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs190954893	chr2:34581663-34581664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542169339	chr2:34581692-34581693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562192777	chr2:34581794-34581795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs563099851	chr2:34581842-34581843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116648444	chr2:34581864-34581865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551222927	chr2:34581866-34581867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183145660	chr2:34581871-34581872	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188328643	chr2:34581953-34581954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs200929506	chr2:34581959-34581960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547189045	chr2:34581966-34581967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190136951	chr2:34581978-34581979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs567565572	chr2:34584225-34584226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200856497	chr2:34584226-34584227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs10176072	chr2:34584271-34584272	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs534962787	chr2:34584292-34584293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs66838605	chr2:34584310-34584311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370306177	chr2:34584312-34584313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs113797663	chr2:34584325-34584326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187334611	chr2:34584334-34584335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568097039	chr2:34584339-34584340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs377624835	chr2:34584347-34584348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139494840	chr2:34584348-34584349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376120524	chr2:34584355-34584356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs556991795	chr2:34584395-34584396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs576881688	chr2:34584403-34584404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539184146	chr2:34584415-34584416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191852277	chr2:34584427-34584428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145286032	chr2:34584450-34584451	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541367879	chr2:34584515-34584516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554531328	chr2:34584536-34584537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs13011348	chr2:34584541-34584542	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs147647704	chr2:34584549-34584550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs180992497	chr2:34584567-34584568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs532501259	chr2:34584572-34584573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs549063143	chr2:34584611-34584612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140470081	chr2:34584628-34584629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs559323823	chr2:34584629-34584630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149722130	chr2:34584641-34584642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548530571	chr2:34584659-34584660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145223119	chr2:34584674-34584675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs376269793	chr2:34584718-34584719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530483501	chr2:34584726-34584727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550316236	chr2:34584729-34584730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185129468	chr2:34584750-34584751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs149164213	chr2:34584754-34584755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35963420	chr2:34584799-34584800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541431317	chr2:34587410-34587411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185062897	chr2:34587468-34587469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1368937	chr2:34587470-34587471	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Incontinentia Pigmenti	22033527	CNVD
Alcoholism	22295116	CNVD
small cell lung cancer	20016488	CNVD
Medulloblastoma	21163964	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:386 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:34581600-34582000	Enhancers	Fetal Heart	heart
2	chr2:34584200-34584800	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr2:34587400-34591400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:34587800-34590000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr2:34587800-34590800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:34588000-34588600	Enhancers	Fetal Kidney	kidney
7	chr2:34588000-34590600	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:34588000-34590800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr2:34588200-34588400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:34588200-34590800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:34588400-34589200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:34588600-34589000	Weak transcription	Fetal Kidney	kidney
13	chr2:34588800-34589000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:34588800-34589400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr2:34588800-34590800	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr2:34589000-34589200	Enhancers	Fetal Kidney	kidney
17	chr2:34589000-34589600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:34589000-34589800	Enhancers	Colon Smooth Muscle	Colon
19	chr2:34589000-34590200	Enhancers	H1 Cell Line	embryonic stem cell
20	chr2:34589000-34590800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr2:34589000-34592400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:34589200-34589400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr2:34589200-34589400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr2:34589200-34589600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:34589200-34590800	Weak transcription	Fetal Kidney	kidney
26	chr2:34589200-34591200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr2:34589400-34590800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr2:34589400-34590800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr2:34589600-34590000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:34589600-34590400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:34589600-34590800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr2:34590000-34590400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr2:34590000-34592600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:34590200-34591400	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr2:34590400-34590800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:34590400-34592200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr2:34590600-34590800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
38	chr2:34590800-34591000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr2:34590800-34591000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr2:34590800-34591000	Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr2:34590800-34591200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr2:34590800-34591200	Enhancers	Fetal Intestine Small	intestine
43	chr2:34590800-34591400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr2:34590800-34591600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
45	chr2:34590800-34591600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr2:34590800-34591800	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr2:34590800-34592000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
48	chr2:34590800-34592200	Enhancers	Fetal Kidney	kidney
49	chr2:34591000-34591200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:34591000-34591200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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