Variant report

Variant	nsv834332
Chromosome Location	chr2:112197703-112403360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3255)
CpG islands
(count:366)
Chromatin interactive
region (count:40)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3255 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:112376535-112377049	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:112279969-112280556	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:112377103-112377411	K562	blood:	n/a	n/a
4	ARID3A	chr2:112374864-112376031	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:112400566-112400827	K562	blood:	n/a	n/a
6	ARID3A	chr2:112286629-112286892	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:112382440-112382785	K562	blood:	n/a	n/a
8	ARID3A	chr2:112383691-112384719	K562	blood:	n/a	n/a
9	ARID3A	chr2:112221794-112221988	HepG2	liver:	n/a	n/a
10	ATF1	chr2:112382410-112382671	K562	blood:	n/a	n/a
11	ATF1	chr2:112391689-112391967	K562	blood:	n/a	n/a
12	ATF1	chr2:112252616-112252812	K562	blood:	n/a	n/a
13	ATF1	chr2:112400419-112400917	K562	blood:	n/a	n/a
14	ATF1	chr2:112383432-112384030	K562	blood:	n/a	n/a
15	ATF1	chr2:112251003-112251203	K562	blood:	n/a	n/a
16	ATF2	chr2:112390137-112390517	GM12878	blood:	n/a	n/a
17	ATF2	chr2:112390081-112390607	GM12878	blood:	n/a	n/a
18	ATF2	chr2:112236677-112236938	GM12878	blood:	n/a	n/a
19	ATF3	chr2:112292952-112293475	HepG2	liver:	n/a	chr2:112293252-112293272 chr2:112293263-112293272
20	ATF3	chr2:112383692-112384042	K562	blood:	n/a	n/a
21	BACH1	chr2:112251425-112251440	K562	blood:	n/a	n/a
22	BACH1	chr2:112400397-112400730	K562	blood:	n/a	n/a
23	BATF	chr2:112285351-112285619	GM12878	blood:	n/a	n/a
24	BATF	chr2:112250963-112251779	GM12878	blood:	n/a	chr2:112251535-112251545 chr2:112251573-112251582
25	BATF	chr2:112248607-112249357	GM12878	blood:	n/a	n/a
26	BATF	chr2:112251972-112252940	GM12878	blood:	n/a	chr2:112252692-112252702 chr2:112252678-112252688
27	BATF	chr2:112282643-112283006	GM12878	blood:	n/a	n/a
28	BATF	chr2:112305421-112305663	GM12878	blood:	n/a	chr2:112305590-112305600 chr2:112305586-112305596
29	BATF	chr2:112221408-112221914	GM12878	blood:	n/a	n/a
30	BATF	chr2:112327815-112328182	GM12878	blood:	n/a	n/a
31	BATF	chr2:112303348-112304091	GM12878	blood:	n/a	chr2:112303735-112303744
32	BATF	chr2:112220893-112221142	GM12878	blood:	n/a	n/a
33	BATF	chr2:112236417-112237152	GM12878	blood:	n/a	n/a
34	BATF	chr2:112238764-112238956	GM12878	blood:	n/a	n/a
35	BATF	chr2:112209629-112210364	GM12878	blood:	n/a	n/a
36	BATF	chr2:112206432-112206650	GM12878	blood:	n/a	n/a
37	BATF	chr2:112209363-112210356	GM12878	blood:	n/a	n/a
38	BATF	chr2:112221520-112221892	GM12878	blood:	n/a	n/a
39	BATF	chr2:112303521-112304031	GM12878	blood:	n/a	chr2:112303735-112303744
40	BATF	chr2:112211973-112212259	GM12878	blood:	n/a	n/a
41	BATF	chr2:112248667-112249139	GM12878	blood:	n/a	n/a
42	BATF	chr2:112285289-112285637	GM12878	blood:	n/a	n/a
43	BATF	chr2:112251368-112251781	GM12878	blood:	n/a	chr2:112251535-112251545 chr2:112251573-112251582
44	BATF	chr2:112258184-112258454	GM12878	blood:	n/a	n/a
45	BATF	chr2:112290692-112291073	GM12878	blood:	n/a	chr2:112290906-112290916 chr2:112290905-112290916
46	BATF	chr2:112211976-112212278	GM12878	blood:	n/a	n/a
47	BATF	chr2:112264445-112264864	GM12878	blood:	n/a	n/a
48	BATF	chr2:112240605-112241034	GM12878	blood:	n/a	chr2:112240788-112240798
49	BATF	chr2:112198041-112198360	GM12878	blood:	n/a	n/a
50	BATF	chr2:112264388-112264857	GM12878	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:112252254-112252304	HNPCEpiC	eye:	n/a
2	chr2:112375854-112375904	HEEpiC	esophagus:	n/a
3	chr2:112252254-112252304	Caco-2	colon:	n/a
4	chr2:112280286-112280336	HUVEC	blood vessel:	n/a
5	chr2:112252254-112252304	HUVEC	blood vessel:	n/a
6	chr2:112375854-112375904	Hela-S3	cervix:	n/a
7	chr2:112383396-112383446	PFSK-1	brain:	n/a
8	chr2:112391213-112391263	AG09319	gingival:	n/a
9	chr2:112383396-112383446	HUVEC	blood vessel:	n/a
10	chr2:112383396-112383446	HEK293	kidney:	embryo
11	chr2:112280286-112280336	ProgFib	skin:	n/a
12	chr2:112252254-112252304	NB4	blood:	n/a
13	chr2:112383396-112383446	HMEC	breast:	n/a
14	chr2:112252254-112252304	ovcar-3	ovarian:	n/a
15	chr2:112383396-112383446	ECC-1	luminal epithelium:	n/a
16	chr2:112280286-112280336	NH-A	brain:	n/a
17	chr2:112375854-112375904	Hepatocyte	liver:	n/a
18	chr2:112252254-112252304	HIPEpiC	eye:	n/a
19	chr2:112293267-112293317	GM12892	blood:	n/a
20	chr2:112280286-112280336	T-47D	breast:	n/a
21	chr2:112375854-112375904	CMK	blood:	n/a
22	chr2:112391213-112391263	MCF-7	breast:	n/a
23	chr2:112391213-112391263	AG04450	lung:	fetal
24	chr2:112252254-112252304	GM12892	blood:	n/a
25	chr2:112383396-112383446	A549	lung:	n/a
26	chr2:112280286-112280336	HCM	heart:	n/a
27	chr2:112375854-112375904	ECC-1	luminal epithelium:	n/a
28	chr2:112252254-112252304	CMK	blood:	n/a
29	chr2:112383396-112383446	GM12891	blood:	n/a
30	chr2:112375854-112375904	Caco-2	colon:	n/a
31	chr2:112252254-112252304	NH-A	brain:	n/a
32	chr2:112375854-112375904	HL-60	blood:	n/a
33	chr2:112375854-112375904	HIPEpiC	eye:	n/a
34	chr2:112383396-112383446	AG09309	skin:	n/a
35	chr2:112280286-112280336	GM06990	blood:	n/a
36	chr2:112252254-112252304	GM12878	blood:	n/a
37	chr2:112375854-112375904	AG09309	skin:	n/a
38	chr2:112280286-112280336	GM12892	blood:	n/a
39	chr2:112280286-112280336	AG10803	skin:	n/a
40	chr2:112252254-112252304	LNCaP	prostate:	n/a
41	chr2:112252254-112252304	SKMC	muscle:	n/a
42	chr2:112391213-112391263	NB4	blood:	n/a
43	chr2:112293267-112293317	NB4	blood:	n/a
44	chr2:112375854-112375904	HCF	heart:	n/a
45	chr2:112293267-112293317	HRPEpiC	eye:	n/a
46	chr2:112293267-112293317	HCF	heart:	n/a
47	chr2:112280286-112280336	NHDF-neo	bronchial:	n/a
48	chr2:112391213-112391263	HNPCEpiC	eye:	n/a
49	chr2:112280286-112280336	HepG2	liver:	n/a
50	chr2:112375854-112375904	SK-N-SH	brain:	n/a

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:112381593..112384142-chr2:112386347..112388792,2	MCF-7	breast:
2	chr2:112376832..112377622-chr2:112493675..112494396,3	MCF-7	breast:
3	chr2:112395623..112398484-chr2:112400861..112402821,2	K562	blood:
4	chr2:111877393..111879713-chr2:112235053..112237981,2	K562	blood:
5	chr2:112374742..112377562-chr2:112458693..112461036,2	MCF-7	breast:
6	chr2:112377013..112378994-chr2:112455600..112458086,2	K562	blood:
7	chr2:112390933..112393569-chr2:112395712..112398433,3	K562	blood:
8	chr2:112392219..112395501-chr2:112398954..112401482,3	K562	blood:
9	chr2:112376815..112377394-chr2:112421087..112421873,3	MCF-7	breast:
10	chr2:112374024..112376697-chr2:112377578..112380485,2	K562	blood:
11	chr2:112390933..112393569-chr2:112395712..112398433,3	K562	blood:
12	chr2:112391627..112394097-chr2:112402013..112403917,2	K562	blood:
13	chr2:112389816..112391811-chr2:112392544..112394680,2	MCF-7	breast:
14	chr2:112397541..112399746-chr2:112416589..112418149,2	MCF-7	breast:
15	chr2:112391627..112394432-chr2:112401597..112404973,3	K562	blood:
16	chr1:182808366..182808884-chr2:112383326..112383826,2	NB4	blood:
17	chr2:112374024..112376697-chr2:112377578..112380485,2	K562	blood:
18	chr2:112382780..112385327-chr2:112409728..112411247,2	MCF-7	breast:
19	chr2:112391627..112394097-chr2:112402013..112403917,2	K562	blood:
20	chr1:144533941..144534634-chr2:112378543..112379544,3	HCT-116	colon:
21	chr2:112239413..112241217-chr2:112461159..112463413,2	MCF-7	breast:
22	chr2:112375556..112378419-chr2:112378851..112380695,2	MCF-7	breast:
23	chr2:112391627..112394432-chr2:112401597..112404973,3	K562	blood:
24	chr2:111876869..111879041-chr2:112387692..112389774,2	MCF-7	breast:
25	chr2:112395813..112398635-chr2:112411801..112413497,2	MCF-7	breast:
26	chr2:112381593..112384142-chr2:112386347..112388792,2	MCF-7	breast:
27	chr2:112395623..112398484-chr2:112400861..112402821,2	K562	blood:
28	chr2:112395688..112397342-chr2:112404915..112406866,2	K562	blood:
29	chr2:112374717..112376877-chr2:112415569..112417178,2	MCF-7	breast:
30	chr2:112402711..112405515-chr2:112410229..112412374,2	K562	blood:
31	chr2:111878764..111880387-chr2:112231090..112233888,2	MCF-7	breast:
32	chr2:112402419..112406237-chr2:112407904..112411161,4	MCF-7	breast:
33	chr2:111877705..111880008-chr2:112211679..112213711,2	MCF-7	breast:
34	chr2:112376861..112378670-chr2:112458387..112460460,2	K562	blood:
35	chr2:112392219..112395501-chr2:112398954..112401482,3	K562	blood:
36	chr2:112377497..112380123-chr2:112459340..112461483,2	MCF-7	breast:
37	chr2:112377428..112379190-chr2:112425946..112427813,2	MCF-7	breast:
38	chr2:112375556..112378419-chr2:112378851..112380695,2	MCF-7	breast:
39	chr2:112376956..112377705-chr2:112424491..112425897,3	MCF-7	breast:
40	chr2:112389816..112391811-chr2:112392544..112394680,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC108463.1-3	chr2:112227364-112227564	ENSG00000172965.6
2	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073622
3	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
4	lnc-AC108463.1-3	chr2:112252462-112252611	ENSG00000172965.6
5	lnc-MERTK-1	chr2:112365418-112365592	XLOC_001626
6	lnc-AC108463.1-3	chr2:112227095-112227564	ENSG00000172965.6
7	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073640
8	lnc-AC108463.1-3	chr2:112227364-112227376	NONHSAT073639
9	lnc-AC108463.1-3	chr2:112227215-112227564	ENSG00000172965.6
10	lnc-AC108463.1-3	chr2:112252462-112252610	ENSG00000172965.6
11	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
12	lnc-MERTK-1	chr2:112365277-112365592	NONHSAT073660
13	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073654
14	lnc-ANAPC1-3	chr2:112315990-112317514	NONHSAT073659
15	lnc-AC108463.1-2	chr2:112249520-112250145	ENSG00000224959
16	lnc-BCL2L11-3	chr2:112268201-112268567	XLOC_001625
17	lnc-BCL2L11-3	chr2:112248850-112249239	XLOC_001625
18	lnc-AC108463.1-3	chr2:112252462-112252677	ENSG00000172965.6
19	lnc-BCL2L11-3	chr2:112249107-112249838	NONHSAT073656
20	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
21	lnc-MERTK-1	chr2:112369479-112369982	NONHSAT073660
22	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073658
23	lnc-AC108463.1-3	chr2:112199085-112199198	ENSG00000172965.6
24	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6
25	lnc-AC108463.1-3	chr2:112227180-112227564	ENSG00000172965.6
26	lnc-AC108463.1-3	chr2:112252462-112252692	NONHSAT073642
27	lnc-AC108463.1-3	chr2:112252462-112252540	NONHSAT073639
28	lnc-BCL2L11-3	chr2:112257365-112258585	NONHSAT073656
29	lnc-AC108463.1-3	chr2:112237484-112237657	NONHSAT073639
30	lnc-AC108463.1-3	chr2:112252462-112252631	ENSG00000172965.6
31	lnc-AC108463.1-3	chr2:112237484-112237638	ENSG00000172965.6
32	lnc-AC108463.1-3	chr2:112237746-112237838	ENSG00000172965.6
33	lnc-AC108463.1-3	chr2:112252462-112252597	ENSG00000172965.6
34	lnc-AC108463.1-3	chr2:112252462-112252625	ENSG00000172965.6
35	lnc-MERTK-1	chr2:112369479-112370095	XLOC_001626
36	lnc-AC108463.1-2	chr2:112252134-112252388	ENSG00000224959
37	lnc-AC108463.1-3	chr2:112252462-112252602	ENSG00000172965.6
38	lnc-AC108463.1-3	chr2:112229566-112229674	ENSG00000172965.6

No data

Variant related genes	Relation type
MIR4435-1HG	TF binding region
ENSG00000271635	TF binding region
ENSG00000240350	TF binding region
ENSG00000224959	TF binding region
ENSG00000225744	TF binding region
MIR4435-1HG	CpG island
ENSG00000271635	CpG island
ENSG00000240350	CpG island
ENSG00000224959	CpG island
ENSG00000225744	CpG island
ENSG00000201699	chromatin interactions
ENSG00000153094	chromatin interactions
ENSG00000135829	chromatin interactions

Extended variants
information (count: 5374 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:5374 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562873708	chr2:112197711-112197712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs71260660	chr2:112197722-112197723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs62160704	chr2:112197745-112197746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs201880027	chr2:112197750-112197751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368343021	chr2:112197751-112197752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs71385809	chr2:112197775-112197776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140383632	chr2:112197792-112197793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs550545083	chr2:112197832-112197833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs570375569	chr2:112197879-112197880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs376827957	chr2:112198030-112198031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546160431	chr2:112198031-112198032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566577032	chr2:112198038-112198039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566147144	chr2:112198052-112198053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs535141503	chr2:112198058-112198059	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs368954570	chr2:112198111-112198112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs555420325	chr2:112198120-112198121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568904445	chr2:112198466-112198467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs538423154	chr2:112198483-112198484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs558075376	chr2:112198485-112198486	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181473170	chr2:112198491-112198492	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540949234	chr2:112198499-112198500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554174610	chr2:112198523-112198524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574066929	chr2:112198670-112198671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs186599101	chr2:112198786-112198787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs551901487	chr2:112198803-112198804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs562991210	chr2:112198825-112198826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531722144	chr2:112198885-112198886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544349098	chr2:112198887-112198888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563961594	chr2:112198907-112198908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533026564	chr2:112198920-112198921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546476316	chr2:112198981-112198982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560046197	chr2:112199013-112199014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528879935	chr2:112199024-112199025	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs999334	chr2:112199034-112199035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548742763	chr2:112199045-112199046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs568891729	chr2:112199046-112199047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537544856	chr2:112199077-112199078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs551972658	chr2:112199086-112199087	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs568807766	chr2:112199176-112199177	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs1004117	chr2:112199177-112199178	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
41	rs571885454	chr2:112199181-112199182	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
42	rs554883716	chr2:112199183-112199184	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
43	rs568009288	chr2:112199193-112199194	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
44	rs554483373	chr2:112199206-112199207	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs574298048	chr2:112199248-112199249	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs536608432	chr2:112199347-112199348	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs533741325	chr2:112199350-112199351	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs576454430	chr2:112199371-112199372	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs545190359	chr2:112199459-112199460	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs191910485	chr2:112199468-112199469	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	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
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22314128	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:2192 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:112176000-112199000	Weak transcription	NH-A	brain
2	chr2:112179400-112199000	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr2:112183200-112207200	Weak transcription	HUVEC	blood vessel
4	chr2:112185400-112199800	Weak transcription	HSMM	muscle
5	chr2:112185400-112220200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:112187000-112199600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr2:112187800-112199400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr2:112189600-112199400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr2:112191200-112198800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr2:112191800-112199400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:112191800-112202200	Weak transcription	Monocytes-CD14+_RO01746	blood
12	chr2:112192400-112207000	Weak transcription	K562	blood
13	chr2:112193400-112199800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:112195000-112199600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr2:112195000-112211000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr2:112195400-112199600	Weak transcription	A549	lung
17	chr2:112196800-112201600	Enhancers	Dnd41	blood
18	chr2:112197000-112197800	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr2:112197000-112197800	Enhancers	Primary B cells from peripheral blood	blood
20	chr2:112197200-112197800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr2:112197400-112197800	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr2:112197400-112197800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr2:112197400-112197800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr2:112197400-112197800	Enhancers	Osteobl	bone
25	chr2:112197400-112199600	Weak transcription	Primary T helper cells PMA-I stimulated	--
26	chr2:112197600-112197800	Enhancers	HepG2	liver
27	chr2:112197600-112198200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr2:112197600-112201600	Enhancers	Fetal Thymus	thymus
29	chr2:112197600-112209800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:112197800-112199000	Weak transcription	Osteobl	bone
31	chr2:112197800-112199600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr2:112197800-112200400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr2:112197800-112201400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:112197800-112202200	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr2:112197800-112202600	Weak transcription	Primary neutrophils fromperipheralblood	blood
36	chr2:112198200-112209800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr2:112198800-112200200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr2:112199000-112199600	Enhancers	Muscle Satellite Cultured Cells	--
39	chr2:112199000-112199600	Enhancers	NH-A	brain
40	chr2:112199000-112200800	Enhancers	Osteobl	bone
41	chr2:112199400-112200000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr2:112199400-112200200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr2:112199400-112200200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr2:112199400-112200200	Enhancers	Primary T cells fromperipheralblood	blood
45	chr2:112199600-112199800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:112199600-112199800	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr2:112199600-112199800	Enhancers	A549	lung
48	chr2:112199600-112200000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr2:112199600-112200000	Enhancers	Pancreatic Islets	Pancreatic Islet
50	chr2:112199600-112200200	Enhancers	NHDF-Ad	bronchial

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