Variant report

Variant	nsv834398
Chromosome Location	chr2:145659419-145830156
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1152)
CpG islands
(count:610)
Chromatin interactive
region (count:37)
LncRNA
region (count:48)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1152 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:145671824-145671903	K562	blood:	n/a	n/a
2	ATF1	chr2:145693428-145693732	K562	blood:	n/a	n/a
3	ATF3	chr2:145775756-145776640	A549	lung:	n/a	n/a
4	ATF3	chr2:145776008-145776571	A549	lung:	n/a	n/a
5	ATF3	chr2:145700236-145701206	A549	lung:	n/a	n/a
6	BACH1	chr2:145770748-145770895	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr2:145700069-145701327	A549	lung:	n/a	n/a
8	BCL3	chr2:145778097-145778750	A549	lung:	n/a	n/a
9	BCL3	chr2:145700221-145701238	A549	lung:	n/a	n/a
10	BCL3	chr2:145780286-145781082	A549	lung:	n/a	n/a
11	BCL3	chr2:145775876-145776620	A549	lung:	n/a	n/a
12	BCL3	chr2:145775711-145776533	A549	lung:	n/a	n/a
13	BHLHE40	chr2:145700446-145700751	K562	blood:	n/a	n/a
14	BHLHE40	chr2:145701660-145701823	A549	lung:	n/a	n/a
15	BHLHE40	chr2:145693371-145693761	K562	blood:	n/a	n/a
16	BHLHE40	chr2:145696027-145696243	K562	blood:	n/a	n/a
17	CBX3	chr2:145722778-145723048	K562	blood:	n/a	n/a
18	CBX3	chr2:145686237-145686553	K562	blood:	n/a	n/a
19	CBX3	chr2:145727909-145728385	K562	blood:	n/a	n/a
20	CBX3	chr2:145685801-145686582	K562	blood:	n/a	n/a
21	CBX3	chr2:145708707-145709166	HCT-116	colon:	n/a	n/a
22	CBX3	chr2:145722746-145723313	K562	blood:	n/a	n/a
23	CCNT2	chr2:145693376-145693639	K562	blood:	n/a	n/a
24	CCNT2	chr2:145764440-145764481	K562	blood:	n/a	n/a
25	CCNT2	chr2:145822065-145822195	K562	blood:	n/a	n/a
26	CEBPB	chr2:145753810-145754178	K562	blood:	n/a	chr2:145753987-145753998 chr2:145753987-145754000
27	CEBPB	chr2:145778164-145778651	A549	lung:	n/a	n/a
28	CEBPB	chr2:145780614-145780922	IMR90	lung:	n/a	n/a
29	CEBPB	chr2:145741644-145741977	HepG2	liver:	n/a	chr2:145741808-145741819
30	CEBPB	chr2:145741677-145741890	Hela-S3	cervix:	n/a	chr2:145741808-145741819
31	CEBPB	chr2:145699352-145699666	A549	lung:	n/a	n/a
32	CEBPB	chr2:145775949-145776476	A549	lung:	n/a	n/a
33	CEBPB	chr2:145753072-145753373	HepG2	liver:	n/a	chr2:145753265-145753276 chr2:145753193-145753204 chr2:145753192-145753203
34	CEBPB	chr2:145753802-145754388	Hela-S3	cervix:	n/a	chr2:145753987-145753998 chr2:145753987-145754000
35	CEBPB	chr2:145764411-145765219	IMR90	lung:	n/a	chr2:145764717-145764728 chr2:145764716-145764727 chr2:145764716-145764729 chr2:145764716-145764729
36	CEBPB	chr2:145770232-145770486	K562	blood:	n/a	chr2:145770373-145770386 chr2:145770373-145770386 chr2:145770373-145770384
37	CEBPB	chr2:145756087-145756334	A549	lung:	n/a	n/a
38	CEBPB	chr2:145704579-145704712	IMR90	lung:	n/a	n/a
39	CEBPB	chr2:145703984-145704140	K562	blood:	n/a	n/a
40	CEBPB	chr2:145793866-145794160	HepG2	liver:	n/a	chr2:145794001-145794012
41	CEBPB	chr2:145753803-145754186	A549	lung:	n/a	chr2:145753987-145753998 chr2:145753987-145754000
42	CEBPB	chr2:145753019-145753465	Hela-S3	cervix:	n/a	chr2:145753265-145753276 chr2:145753193-145753204 chr2:145753192-145753203
43	CEBPB	chr2:145703988-145704209	HepG2	liver:	n/a	n/a
44	CEBPB	chr2:145770355-145770455	HepG2	liver:	n/a	chr2:145770373-145770386 chr2:145770373-145770386 chr2:145770373-145770384
45	CEBPB	chr2:145753108-145753385	A549	lung:	n/a	chr2:145753265-145753276 chr2:145753193-145753204 chr2:145753192-145753203
46	CEBPB	chr2:145708797-145709144	A549	lung:	n/a	n/a
47	CEBPB	chr2:145708671-145709307	A549	lung:	n/a	n/a
48	CEBPB	chr2:145708872-145709175	A549	lung:	n/a	n/a
49	CEBPB	chr2:145735163-145735500	HepG2	liver:	n/a	chr2:145735338-145735349
50	CEBPB	chr2:145708659-145709278	HCT-116	colon:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:145660909-145660959	GM06990	blood:	n/a
2	chr2:145747877-145747927	AG09319	gingival:	n/a
3	chr2:145660909-145660959	GM12891	blood:	n/a
4	chr2:145764890-145764940	BE2_C	brain:	n/a
5	chr2:145764890-145764940	NB4	blood:	n/a
6	chr2:145823182-145823232	GM06990	blood:	n/a
7	chr2:145660909-145660959	HMEC	breast:	n/a
8	chr2:145770038-145770088	BJ	skin:	n/a
9	chr2:145701813-145701863	HEK293	kidney:	embryo
10	chr2:145780010-145780060	BE2_C	brain:	n/a
11	chr2:145701813-145701863	HCPEpiC	choroid plexus:	n/a
12	chr2:145660909-145660959	T-47D	breast:	n/a
13	chr2:145779560-145779610	GM12891	blood:	n/a
14	chr2:145764890-145764940	AG09319	gingival:	n/a
15	chr2:145770038-145770088	MCF-7	breast:	n/a
16	chr2:145753993-145754043	ECC-1	luminal epithelium:	n/a
17	chr2:145823182-145823232	RPTEC	kidney:	n/a
18	chr2:145753993-145754043	NH-A	brain:	n/a
19	chr2:145660909-145660959	HepG2	liver:	n/a
20	chr2:145823182-145823232	H1-hESC	embryonic stem cell:	embryo
21	chr2:145660909-145660959	U87	brain:	n/a
22	chr2:145823182-145823232	SK-N-MC	brain:	n/a
23	chr2:145795797-145795847	HRCEpiC	kidney:	n/a
24	chr2:145747877-145747927	HEK293	kidney:	embryo
25	chr2:145823182-145823232	SKMC	muscle:	n/a
26	chr2:145753993-145754043	Caco-2	colon:	n/a
27	chr2:145701813-145701863	HL-60	blood:	n/a
28	chr2:145780010-145780060	AG04450	lung:	fetal
29	chr2:145753993-145754043	CMK	blood:	n/a
30	chr2:145780010-145780060	H1-hESC	embryonic stem cell:	embryo
31	chr2:145770038-145770088	HCF	heart:	n/a
32	chr2:145823182-145823232	AG04449	skin:	fetal
33	chr2:145660909-145660959	MCF10A-Er-Src	breast:	n/a
34	chr2:145823182-145823232	CMK	blood:	n/a
35	chr2:145753993-145754043	NB4	blood:	n/a
36	chr2:145753993-145754043	ovcar-3	ovarian:	n/a
37	chr2:145795797-145795847	GM12891	blood:	n/a
38	chr2:145795797-145795847	GM19239	blood:	n/a
39	chr2:145764890-145764940	HUVEC	blood vessel:	n/a
40	chr2:145701813-145701863	SK-N-MC	brain:	n/a
41	chr2:145660909-145660959	ProgFib	skin:	n/a
42	chr2:145764890-145764940	Hela-S3	cervix:	n/a
43	chr2:145764890-145764940	NHBE	bronchial:	n/a
44	chr2:145779560-145779610	BE2_C	brain:	n/a
45	chr2:145780010-145780060	GM06990	blood:	n/a
46	chr2:145753993-145754043	RPTEC	kidney:	n/a
47	chr2:145779560-145779610	MCF-7	breast:	n/a
48	chr2:145779560-145779610	RPTEC	kidney:	n/a
49	chr2:145753993-145754043	GM06990	blood:	n/a
50	chr2:145701813-145701863	CMK	blood:	n/a

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:145692575..145694209-chr2:145694723..145697330,2	K562	blood:
2	chr2:145675431..145677342-chr2:145678479..145680168,2	K562	blood:
3	chr2:145785797..145788281-chr2:145794965..145797267,2	K562	blood:
4	chr2:145766027..145767852-chr2:145771285..145773781,2	K562	blood:
5	chr2:145701982..145703622-chr2:145707217..145709192,2	K562	blood:
6	chr2:145737683..145739757-chr2:145742970..145744798,2	K562	blood:
7	chr2:145687133..145689183-chr2:145693172..145695781,2	K562	blood:
8	chr2:145687133..145689183-chr2:145693172..145695781,2	K562	blood:
9	chr2:145701982..145703622-chr2:145707217..145709192,2	K562	blood:
10	chr2:145696000..145699095-chr2:145703578..145707289,3	K562	blood:
11	chr2:145737683..145739757-chr2:145742970..145744798,2	K562	blood:
12	chr2:145692796..145697382-chr2:145698219..145701649,5	K562	blood:
13	chr2:145706300..145709031-chr2:145712643..145714364,2	K562	blood:
14	chr2:145638931..145641686-chr2:145711451..145713690,2	K562	blood:
15	chr2:145734658..145736993-chr2:145739662..145742200,2	K562	blood:
16	chr2:145696000..145699095-chr2:145703578..145707289,3	K562	blood:
17	chr2:145676567..145679523-chr2:145696189..145700342,3	K562	blood:
18	chr2:145785797..145788281-chr2:145794965..145797267,2	K562	blood:
19	chr2:145713732..145715600-chr2:145728396..145731039,2	K562	blood:
20	chr2:145692796..145697382-chr2:145698219..145701649,5	K562	blood:
21	chr2:145672621..145674786-chr2:145681190..145683817,2	K562	blood:
22	chr2:145766027..145767852-chr2:145771285..145773781,2	K562	blood:
23	chr2:145713732..145715600-chr2:145728396..145731039,2	K562	blood:
24	chr2:145662568..145665486-chr2:145667581..145669789,3	K562	blood:
25	chr2:145676567..145679523-chr2:145696189..145700342,3	K562	blood:
26	chr2:145706300..145709031-chr2:145712643..145714364,2	K562	blood:
27	chr2:145692575..145694209-chr2:145694723..145697330,2	K562	blood:
28	chr2:145662568..145665486-chr2:145667581..145669789,3	K562	blood:
29	chr2:145282963..145285154-chr2:145751784..145754718,2	K562	blood:
30	chr2:145675431..145677342-chr2:145678479..145680168,2	K562	blood:
31	chr2:145761619..145763555-chr2:145780660..145782291,2	MCF-7	breast:
32	chr2:145672621..145674786-chr2:145681190..145683817,2	K562	blood:
33	chr2:145691983..145697033-chr2:145697956..145702108,6	K562	blood:
34	chr2:145774729..145777688-chr2:145783583..145786278,2	K562	blood:
35	chr2:145691983..145697033-chr2:145697956..145702108,6	K562	blood:
36	chr2:145734658..145736993-chr2:145739662..145742200,2	K562	blood:
37	chr2:145774729..145777688-chr2:145783583..145786278,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP15-6	chr2:145780725-145780840	ENSG00000226674
2	lnc-ARHGAP15-6	chr2:145780739-145780840	ENSG00000226674.4
3	lnc-ARHGAP15-6	chr2:145698425-145698512	ENSG00000226674.4
4	lnc-ARHGAP15-6	chr2:145830091-145830713	ENSG00000226674.4
5	lnc-ARHGAP15-6	chr2:145830091-145830402	NONHSAT074827
6	lnc-ARHGAP15-6	chr2:145828387-145828508	NONHSAT074787
7	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
8	lnc-ARHGAP15-6	chr2:145780799-145780840	ENSG00000226674.4
9	lnc-ZEB2-17	chr2:145768315-145768444	NONHSAT074814
10	lnc-ARHGAP15-6	chr2:145698425-145698512	ENSG00000226674.4
11	lnc-ARHGAP15-6	chr2:145815256-145815295	NONHSAT074827
12	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
13	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
14	lnc-ARHGAP15-6	chr2:145815218-145815777	ENSG00000226674.4
15	lnc-ARHGAP15-6	chr2:145661233-145661370	NONHSAT074787
16	lnc-ARHGAP15-6	chr2:145830091-145834296	ENSG00000226674
17	lnc-ARHGAP15-6	chr2:145815218-145815295	ENSG00000226674.4
18	lnc-ARHGAP15-6	chr2:145661233-145661370	ENSG00000226674.4
19	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
20	lnc-ARHGAP15-6	chr2:145801454-145801634	ENSG00000226674
21	lnc-ARHGAP15-6	chr2:145661233-145661370	ENSG00000226674.4
22	lnc-ZEB2-17	chr2:145799444-145799477	NONHSAT074814
23	lnc-ARHGAP15-6	chr2:145780739-145780840	ENSG00000226674.4
24	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
25	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
26	lnc-ARHGAP15-6	chr2:145815218-145815295	ENSG00000226674.4
27	lnc-ZEB2-17	chr2:145804735-145804784	NONHSAT074814
28	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
29	lnc-ARHGAP15-6	chr2:145815218-145815295	ENSG00000226674.4
30	lnc-ARHGAP15-6	chr2:145828387-145828508	ENSG00000226674
31	lnc-ARHGAP15-6	chr2:145830091-145831662	ENSG00000226674
32	lnc-ARHGAP15-6	chr2:145780754-145780840	ENSG00000226674
33	lnc-ARHGAP15-6	chr2:145828387-145828508	ENSG00000226674
34	lnc-ARHGAP15-6	chr2:145801933-145802010	ENSG00000226674
35	lnc-ZEB2-17	chr2:145805844-145805885	NONHSAT074814
36	lnc-ARHGAP15-6	chr2:145661233-145661370	ENSG00000226674
37	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
38	lnc-ARHGAP15-6	chr2:145830091-145834291	NONHSAT074787
39	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
40	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
41	lnc-ARHGAP15-6	chr2:145801193-145801512	ENSG00000226674.4
42	lnc-ZEB2-17	chr2:145769135-145769226	NONHSAT074814
43	lnc-ARHGAP15-6	chr2:145780795-145780840	ENSG00000226674.4
44	lnc-ARHGAP15-6	chr2:145830091-145830221	ENSG00000226674
45	lnc-ARHGAP15-6	chr2:145815381-145815472	ENSG00000226674.4
46	lnc-ARHGAP15-6	chr2:145661233-145661370	ENSG00000226674.4
47	lnc-ARHGAP15-6	chr2:145780662-145780840	ENSG00000226674
48	lnc-ARHGAP15-6	chr2:145692924-145693050	ENSG00000226674.4

No data

Variant related genes	Relation type
TEX41	TF binding region
TEX41	CpG island
ENSG00000226674	chromatin interactions
ENSG00000268580	chromatin interactions

Extended variants
information (count: 5487 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:5487 , 50 per page) page: 1 2 3 4 5 6 7 ... 110

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544214028	chr2:145660227-145660228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs372697121	chr2:145660228-145660229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529808772	chr2:145660236-145660237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377266893	chr2:145660248-145660249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369498393	chr2:145660260-145660261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547970938	chr2:145660318-145660319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567119372	chr2:145660328-145660329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527867351	chr2:145660373-145660374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572634524	chr2:145660399-145660400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542928958	chr2:145660422-145660423	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs555264696	chr2:145660430-145660431	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs538129314	chr2:145660441-145660442	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs556529641	chr2:145660454-145660455	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs568354385	chr2:145660467-145660468	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs372399910	chr2:145660468-145660469	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs200182936	chr2:145660470-145660471	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs539578265	chr2:145660477-145660478	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs201617897	chr2:145660483-145660484	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs553826766	chr2:145660502-145660503	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs786275	chr2:145660509-145660510	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs375142101	chr2:145660510-145660511	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs572733759	chr2:145660511-145660512	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs146359491	chr2:145660513-145660514	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs142047833	chr2:145660517-145660518	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs540051507	chr2:145660531-145660532	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs786276	chr2:145660537-145660538	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs558299646	chr2:145660626-145660627	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs577067764	chr2:145660627-145660628	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs786277	chr2:145660645-145660646	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs786278	chr2:145660670-145660671	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs529656499	chr2:145660698-145660699	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs376926230	chr2:145660719-145660720	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs541976717	chr2:145660727-145660728	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs369039781	chr2:145660735-145660736	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs560274285	chr2:145660750-145660751	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs373322025	chr2:145660752-145660753	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs527346946	chr2:145660756-145660757	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs376478555	chr2:145660779-145660780	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs552827777	chr2:145660798-145660799	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs370596451	chr2:145660800-145660801	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs559270866	chr2:145660803-145660804	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs190558072	chr2:145660810-145660811	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs532070695	chr2:145660811-145660812	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs182329442	chr2:145660812-145660813	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs367749118	chr2:145660817-145660818	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs535465105	chr2:145660828-145660829	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs553712646	chr2:145660833-145660834	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs786279	chr2:145660840-145660841	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs539499424	chr2:145660861-145660862	Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs59001323	chr2:145660874-145660875	Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Mental retardation	22214275	CNVD
Glioblastoma	21080181	CNVD
Non-syndromic sensorineural hearing loss	20456320	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1451 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:145660200-145660400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr2:145660400-145660600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr2:145660600-145660800	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr2:145660600-145661400	Active TSS	H1 Cell Line	embryonic stem cell
5	chr2:145660600-145661600	Active TSS	H9 Cell Line	embryonic stem cell
6	chr2:145660600-145661600	Active TSS	HUES48 Cell Line	embryonic stem cell
7	chr2:145660600-145662000	Active TSS	iPS-15b Cell Line	embryonic stem cell
8	chr2:145660600-145663600	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr2:145660800-145661000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr2:145660800-145661800	Active TSS	HUES64 Cell Line	embryonic stem cell
11	chr2:145661000-145661200	Active TSS	HUES6 Cell Line	embryonic stem cell
12	chr2:145661200-145661400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:145661200-145661600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr2:145661200-145661600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr2:145661600-145662200	Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr2:145661600-145664400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
17	chr2:145662000-145662400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:145663600-145663800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr2:145668800-145695600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr2:145671800-145673600	Enhancers	Dnd41	blood
21	chr2:145672000-145672400	Enhancers	Ovary	ovary
22	chr2:145672000-145672400	Enhancers	HMEC	breast
23	chr2:145672000-145672800	Enhancers	NHDF-Ad	bronchial
24	chr2:145672000-145673000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr2:145672000-145673000	Enhancers	HSMM	muscle
26	chr2:145672200-145672800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr2:145672400-145672800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr2:145672400-145672800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr2:145672400-145673000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr2:145672600-145673000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr2:145672600-145673000	Enhancers	Fetal Kidney	kidney
32	chr2:145672600-145673000	Enhancers	Fetal Lung	lung
33	chr2:145675800-145676000	Enhancers	Gastric	stomach
34	chr2:145677000-145677400	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr2:145677000-145677600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr2:145677200-145677600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr2:145677600-145678000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:145678000-145680000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr2:145678200-145678600	Enhancers	Cortex derived primary cultured neurospheres	brain
40	chr2:145678400-145678800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:145678400-145678800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr2:145678400-145678800	Enhancers	Brain Germinal Matrix	brain
43	chr2:145678400-145679600	Enhancers	HSMMtube	muscle
44	chr2:145678400-145679800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr2:145678800-145682600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr2:145680200-145680600	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr2:145680200-145680600	Enhancers	Primary B cells from peripheral blood	blood
48	chr2:145682000-145684000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:145682600-145682800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr2:145682800-145683400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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