Variant report

Variant	nsv1007118
Chromosome Location	chr2:57562051-58147588
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3575)
CpG islands
(count:612)
Chromatin interactive
region (count:107)
LncRNA
region (count:31)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3575 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:57743893-57744250	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:58120865-58121650	HepG2	liver:	n/a	chr2:58120933-58120949
3	ARID3A	chr2:58133318-58133560	K562	blood:	n/a	n/a
4	ARID3A	chr2:58004102-58004565	K562	blood:	n/a	n/a
5	ARID3A	chr2:57987011-57987296	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:58110241-58110306	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:57743917-57744232	K562	blood:	n/a	n/a
8	ARID3A	chr2:58109239-58109431	HepG2	liver:	n/a	n/a
9	ATF1	chr2:57903557-57903607	K562	blood:	n/a	n/a
10	ATF2	chr2:58135565-58136257	GM12878	blood:	n/a	n/a
11	ATF2	chr2:58023548-58024173	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr2:57677308-57677677	GM12878	blood:	n/a	n/a
13	ATF2	chr2:58119903-58120465	GM12878	blood:	n/a	n/a
14	ATF2	chr2:57776638-57777346	GM12878	blood:	n/a	n/a
15	ATF2	chr2:57743819-57744269	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr2:57928447-57928865	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:57743479-57744326	GM12878	blood:	n/a	n/a
18	ATF2	chr2:58117511-58118049	GM12878	blood:	n/a	n/a
19	ATF2	chr2:58119765-58120524	GM12878	blood:	n/a	n/a
20	ATF2	chr2:58023643-58024051	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF2	chr2:58135724-58136260	GM12878	blood:	n/a	n/a
22	ATF2	chr2:58036301-58036756	GM12878	blood:	n/a	n/a
23	ATF2	chr2:57763704-57764026	GM12878	blood:	n/a	n/a
24	ATF2	chr2:57677283-57677736	GM12878	blood:	n/a	n/a
25	ATF2	chr2:57763687-57764134	GM12878	blood:	n/a	n/a
26	ATF2	chr2:58036295-58036793	GM12878	blood:	n/a	n/a
27	ATF2	chr2:57743726-57744291	GM12878	blood:	n/a	n/a
28	ATF2	chr2:58103420-58103903	GM12878	blood:	n/a	n/a
29	ATF2	chr2:57987004-57987361	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF2	chr2:57743836-57744261	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr2:57776792-57777231	GM12878	blood:	n/a	n/a
32	ATF3	chr2:58108949-58109883	A549	lung:	n/a	n/a
33	ATF3	chr2:58108826-58109957	A549	lung:	n/a	n/a
34	ATF3	chr2:58113432-58113668	K562	blood:	n/a	n/a
35	ATF3	chr2:57986897-57987440	A549	lung:	n/a	n/a
36	ATF3	chr2:57743851-57744153	K562	blood:	n/a	n/a
37	ATF3	chr2:57600561-57601162	HCT-116	colon:	n/a	n/a
38	BACH1	chr2:57623493-57623938	H1-hESC	embryonic stem cell:	n/a	n/a
39	BATF	chr2:57987544-57987875	GM12878	blood:	n/a	n/a
40	BATF	chr2:57677301-57677735	GM12878	blood:	n/a	n/a
41	BATF	chr2:58119946-58120342	GM12878	blood:	n/a	n/a
42	BATF	chr2:57776752-57777212	GM12878	blood:	n/a	n/a
43	BATF	chr2:57677353-57677672	GM12878	blood:	n/a	n/a
44	BATF	chr2:57987600-57987899	GM12878	blood:	n/a	n/a
45	BATF	chr2:57987032-57987313	GM12878	blood:	n/a	n/a
46	BATF	chr2:58103513-58103804	GM12878	blood:	n/a	n/a
47	BATF	chr2:58119970-58120390	GM12878	blood:	n/a	n/a
48	BATF	chr2:57763704-57763928	GM12878	blood:	n/a	n/a
49	BATF	chr2:58117578-58117969	GM12878	blood:	n/a	chr2:58117780-58117791
50	BATF	chr2:58109338-58109594	GM12878	blood:	n/a	chr2:58109489-58109500

(count:612 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:58023996-58024046	GM19239	blood:	n/a
2	chr2:57987263-57987313	PANC-1	pancreas:	n/a
3	chr2:58023996-58024046	GM19239	blood:	n/a
4	chr2:57987263-57987313	PANC-1	pancreas:	n/a
5	chr2:58029503-58029553	ovcar-3	ovarian:	n/a
6	chr2:58029565-58029615	SK-N-SH_RA	brain:	n/a
7	chr2:58130074-58130124	HRCEpiC	kidney:	n/a
8	chr2:57938135-57938185	BE2_C	brain:	n/a
9	chr2:58029565-58029615	ECC-1	luminal epithelium:	n/a
10	chr2:58133858-58133908	AoSMC	blood vessel:	n/a
11	chr2:58029503-58029553	AG04450	lung:	fetal
12	chr2:58023996-58024046	HMEC	breast:	n/a
13	chr2:58130074-58130124	ovcar-3	ovarian:	n/a
14	chr2:58023996-58024046	HL-60	blood:	n/a
15	chr2:58029503-58029553	NH-A	brain:	n/a
16	chr2:58133858-58133908	NT2-D1	testis:	n/a
17	chr2:58023996-58024046	PANC-1	pancreas:	n/a
18	chr2:57986550-57986600	SKMC	muscle:	n/a
19	chr2:57986550-57986600	HEEpiC	esophagus:	n/a
20	chr2:57938135-57938185	HMEC	breast:	n/a
21	chr2:57987263-57987313	HRE	kidney:	n/a
22	chr2:58130074-58130124	AG09319	gingival:	n/a
23	chr2:57765322-57765372	HL-60	blood:	n/a
24	chr2:57938135-57938185	PFSK-1	brain:	n/a
25	chr2:58130074-58130124	BE2_C	brain:	n/a
26	chr2:57765322-57765372	HNPCEpiC	eye:	n/a
27	chr2:57986550-57986600	HepG2	liver:	n/a
28	chr2:57987263-57987313	BE2_C	brain:	n/a
29	chr2:57634837-57634887	PrEC	prostate:	n/a
30	chr2:58130074-58130124	SK-N-SH_RA	brain:	n/a
31	chr2:57987263-57987313	NB4	blood:	n/a
32	chr2:57987263-57987313	AG04449	skin:	fetal
33	chr2:57938135-57938185	AG04449	skin:	fetal
34	chr2:57634837-57634887	HAEpiC	amniotic membrane:	n/a
35	chr2:57986550-57986600	U87	brain:	n/a
36	chr2:57986550-57986600	HL-60	blood:	n/a
37	chr2:58023996-58024046	PFSK-1	brain:	n/a
38	chr2:57986550-57986600	HMEC	breast:	n/a
39	chr2:57938135-57938185	Hepatocyte	liver:	n/a
40	chr2:58130074-58130124	CMK	blood:	n/a
41	chr2:57765322-57765372	Hepatocyte	liver:	n/a
42	chr2:57634837-57634887	PFSK-1	brain:	n/a
43	chr2:58029565-58029615	HMEC	breast:	n/a
44	chr2:57938135-57938185	A549	lung:	n/a
45	chr2:57938135-57938185	IMR90	lung:	fetal
46	chr2:58029565-58029615	RPTEC	kidney:	n/a
47	chr2:57765322-57765372	HCPEpiC	choroid plexus:	n/a
48	chr2:58133858-58133908	PFSK-1	brain:	n/a
49	chr2:58133858-58133908	Hepatocyte	liver:	n/a
50	chr2:57765322-57765372	SAEC	small airway:	n/a

(count:107 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:56410841..56411352-chr2:57724378..57725263,2	K562	blood:
2	chr2:57925926..57927856-chr2:57928524..57930468,2	K562	blood:
3	chr2:57726879..57729165-chr2:57731131..57733736,2	K562	blood:
4	chr2:57940740..57942738-chr2:57945191..57947948,2	K562	blood:
5	chr2:57800058..57801669-chr2:57807424..57809542,2	K562	blood:
6	chr2:57695038..57697832-chr2:57697917..57700071,2	MCF-7	breast:
7	chr2:58133863..58138456-chr2:58272095..58275151,4	MCF-7	breast:
8	chr2:57705830..57708555-chr2:57710659..57712382,2	MCF-7	breast:
9	chr2:57726879..57729165-chr2:57731131..57733736,2	K562	blood:
10	chr2:58094285..58096431-chr2:58101485..58103642,2	MCF-7	breast:
11	chr2:57986735..57987942-chr2:58674900..58675939,5	MCF-7	breast:
12	chr2:57988184..57990505-chr2:57993308..57996155,2	K562	blood:
13	chr2:57724780..57726357-chr2:57726897..57728575,2	MCF-7	breast:
14	chr2:57669021..57671005-chr2:57673900..57675904,2	K562	blood:
15	chr2:57726830..57729165-chr2:57729921..57733736,3	K562	blood:
16	chr2:57686552..57689405-chr2:57735534..57737911,2	K562	blood:
17	chr2:57603852..57604740-chr2:57724321..57725273,3	MCF-7	breast:
18	chr2:58109065..58111032-chr2:58113088..58114709,2	MCF-7	breast:
19	chr2:57748644..57750664-chr2:57753276..57755750,2	K562	blood:
20	chr2:58090841..58093056-chr2:58096618..58098915,2	K562	blood:
21	chr2:58097977..58100316-chr2:58105031..58107914,3	K562	blood:
22	chr2:57967586..57970326-chr2:57972561..57975358,2	K562	blood:
23	chr2:57794327..57795954-chr2:57796915..57799788,2	K562	blood:
24	chr2:57940740..57942738-chr2:57945191..57947948,2	K562	blood:
25	chr2:57923440..57925046-chr2:57926940..57929497,2	K562	blood:
26	chr2:56357220..56358069-chr2:57743520..57744164,2	MCF-7	breast:
27	chr2:58131028..58133565-chr2:58275828..58277987,2	MCF-7	breast:
28	chr2:57835362..57837031-chr2:57842743..57844296,2	MCF-7	breast:
29	chr2:58025264..58027443-chr2:58030430..58032051,2	MCF-7	breast:
30	chr2:58133383..58133906-chr2:58674883..58675813,3	K562	blood:
31	chr2:57719207..57721496-chr2:57722799..57725075,2	MCF-7	breast:
32	chr2:58096956..58099985-chr2:58100360..58105173,5	K562	blood:
33	chr2:57794327..57795954-chr2:57796915..57799788,2	K562	blood:
34	chr2:58109065..58111032-chr2:58113088..58114709,2	MCF-7	breast:
35	chr2:57584628..57586577-chr2:57587736..57590174,2	K562	blood:
36	chr2:58108798..58111320-chr2:58112288..58115523,3	K562	blood:
37	chr2:57947786..57948883-chr2:58675068..58675903,3	MCF-7	breast:
38	chr2:58085320..58088148-chr2:58088783..58090766,2	K562	blood:
39	chr2:57680802..57681722-chr2:57724395..57725159,3	MCF-7	breast:
40	chr2:58003897..58005970-chr2:58009303..58012151,2	K562	blood:
41	chr2:57967586..57970326-chr2:57972561..57975358,2	K562	blood:
42	chr2:58035263..58037581-chr2:58040221..58042453,2	K562	blood:
43	chr2:57923440..57925046-chr2:57926940..57929497,2	K562	blood:
44	chr2:57603431..57604465-chr2:57724481..57725285,5	MCF-7	breast:
45	chr2:58118375..58121623-chr2:58123563..58127574,4	K562	blood:
46	chr2:58137881..58138419-chr2:58675132..58675784,2	MCF-7	breast:
47	chr2:57800058..57801669-chr2:57807424..57809542,2	K562	blood:
48	chr2:57705830..57708555-chr2:57710659..57712382,2	MCF-7	breast:
49	chr2:57719207..57721496-chr2:57722799..57725075,2	MCF-7	breast:
50	chr2:57986795..57987623-chr2:58674835..58675860,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VRK2-13	chr2:57806334-57806788	l_1838_chr2:57801423-57806788_testes
2	lnc-FANCL-7	chr2:57826063-57826269	uc_51_-
3	lnc-VRK2-3	chr2:57928210-57928749	NONHSAT070836
4	lnc-VRK2-3	chr2:57928667-57928926	NONHSAT070838
5	lnc-VRK2-3	chr2:57933558-57933718	XLOC_001483
6	lnc-VRK2-13	chr2:57801424-57801615	l_1838_chr2:57801423-57806788_testes
7	lnc-VRK2-10	chr2:57991847-57992345	NONHSAT070842
8	lnc-VRK2-10	chr2:57982563-57982922	NONHSAT070842
9	lnc-VRK2-3	chr2:57928888-57928926	XLOC_001483
10	lnc-VRK2-13	chr2:57803525-57803591	l_1838_chr2:57801423-57806788_testes
11	lnc-VRK2-3	chr2:57940102-57940235	NONHSAT070838
12	lnc-VRK2-12	chr2:57826063-57826269	uc_51_+
13	lnc-VRK2-2	chr2:57950063-57950087	XLOC_001484
14	lnc-VRK2-3	chr2:57933557-57933718	NONHSAT070836
15	lnc-VRK2-3	chr2:57940102-57940316	XLOC_001483
16	lnc-VRK2-3	chr2:57940101-57940316	NONHSAT070836
17	lnc-FANCL-8	chr2:57656683-57656947	NONHSAT070833
18	lnc-CCDC85A-6	chr2:58134791-58134974	NONHSAT070844
19	lnc-VRK2-3	chr2:57933558-57933718	XLOC_001483
20	lnc-FANCL-8	chr2:57657275-57657340	NONHSAT070833
21	lnc-VRK2-2	chr2:57952830-57953284	XLOC_001484
22	lnc-VRK2-11	chr2:57972558-57972765	NONHSAT147090
23	lnc-VRK2-3	chr2:57940102-57940273	XLOC_001483
24	lnc-CCDC85A-6	chr2:58134787-58134974	NONHSAT070843
25	lnc-VRK2-15	chr2:57793606-57793820	l_1837_chr2:57781955-57793820_testes
26	lnc-VRK2-15	chr2:57787062-57787228	l_1837_chr2:57781955-57793820_testes
27	lnc-FANCL-8	chr2:57657781-57657828	NONHSAT070833
28	lnc-VRK2-3	chr2:57928211-57928749	XLOC_001483
29	lnc-VRK2-15	chr2:57781956-57782430	l_1837_chr2:57781955-57793820_testes
30	lnc-VRK2-16	chr2:57672949-57673194	NONHSAT070834
31	lnc-VRK2-16	chr2:57659475-57659520	NONHSAT070834

No data

Variant related genes	Relation type
VRK2	TF binding region
ENSG00000271615	TF binding region
ENSG00000212168	TF binding region
ENSG00000270569	TF binding region
VRK2	CpG island
ENSG00000271615	CpG island
ENSG00000212168	CpG island
ENSG00000270569	CpG island
ENSG00000055813	chromatin interactions
ENSG00000028116	chromatin interactions
ENSG00000271615	chromatin interactions
ENSG00000233251	chromatin interactions
ENSG00000124226	chromatin interactions

Extended variants
information (count: 13332 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:13332 , 50 per page) page: 1 2 3 4 5 6 7 ... 267

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73941263	chr2:57562100-57562101	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533624308	chr2:57562107-57562108	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs72933520	chr2:57562114-57562115	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs140668813	chr2:57593612-57593613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72935538	chr2:57593623-57593624	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs180979029	chr2:57593628-57593629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs138476340	chr2:57593719-57593720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559737880	chr2:57593742-57593743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs143000256	chr2:57593754-57593755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541471062	chr2:57593758-57593759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs548032083	chr2:57593792-57593793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561654027	chr2:57593860-57593861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184110323	chr2:57593874-57593875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs550773901	chr2:57593894-57593895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs113887084	chr2:57593954-57593955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570430803	chr2:57593967-57593968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs539552321	chr2:57593995-57593996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188537506	chr2:57594015-57594016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75169641	chr2:57594022-57594023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74934462	chr2:57594035-57594036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs555261273	chr2:57594040-57594041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs13389238	chr2:57594051-57594052	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs147468726	chr2:57594130-57594131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74680021	chr2:57594150-57594151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557562243	chr2:57594159-57594160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577253427	chr2:57594220-57594221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546322573	chr2:57594248-57594249	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139965010	chr2:57594266-57594267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139941529	chr2:57594296-57594297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79186641	chr2:57594307-57594308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541834560	chr2:57594328-57594329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs181349617	chr2:57594329-57594330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530741357	chr2:57594359-57594360	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544060898	chr2:57594360-57594361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs13398603	chr2:57594369-57594370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs186778154	chr2:57594489-57594490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546628872	chr2:57594571-57594572	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191606089	chr2:57594654-57594655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376093945	chr2:57594675-57594676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114820769	chr2:57594684-57594685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541849145	chr2:57594689-57594690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549023522	chr2:57594702-57594703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs565597400	chr2:57594728-57594729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376242219	chr2:57594735-57594736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs77902302	chr2:57594786-57594787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145552136	chr2:57594813-57594814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148459982	chr2:57594845-57594846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs13399155	chr2:57594882-57594883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539652557	chr2:57594888-57594889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200902334	chr2:57594889-57594890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
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
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1558 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:57593600-57601000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:57595200-57595800	Enhancers	HMEC	breast
3	chr2:57595400-57595800	Enhancers	NHEK	skin
4	chr2:57595800-57599600	Weak transcription	NHEK	skin
5	chr2:57595800-57600000	Weak transcription	HMEC	breast
6	chr2:57596200-57596800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:57598000-57598400	Enhancers	HSMMtube	muscle
8	chr2:57598200-57598400	Enhancers	HSMM	muscle
9	chr2:57598400-57599800	Weak transcription	HSMMtube	muscle
10	chr2:57598400-57602000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr2:57598600-57599600	Weak transcription	HSMM	muscle
12	chr2:57599000-57601400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr2:57599400-57601400	Enhancers	HUVEC	blood vessel
14	chr2:57599600-57600200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr2:57599600-57601400	Enhancers	NHEK	skin
16	chr2:57599600-57601800	Enhancers	HSMM	muscle
17	chr2:57599600-57601800	Enhancers	NHDF-Ad	bronchial
18	chr2:57599800-57600000	Active TSS	A549	lung
19	chr2:57599800-57601400	Enhancers	HSMMtube	muscle
20	chr2:57600000-57600200	Flanking Active TSS	A549	lung
21	chr2:57600000-57601000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr2:57600000-57601200	Enhancers	NH-A	brain
23	chr2:57600000-57601400	Enhancers	HMEC	breast
24	chr2:57600200-57601800	Enhancers	A549	lung
25	chr2:57601000-57601200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr2:57605600-57606400	Active TSS	ES-I3 Cell Line	embryonic stem cell
27	chr2:57613400-57614000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr2:57623200-57624000	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr2:57623400-57623800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:57623400-57624000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr2:57623400-57624200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr2:57623400-57624200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr2:57623400-57624200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr2:57623400-57624200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr2:57623400-57624200	Enhancers	A549	lung
36	chr2:57623400-57624200	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr2:57623400-57624400	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr2:57623600-57624000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr2:57623800-57624000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:57623800-57625000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr2:57623800-57625200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr2:57624000-57624200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
43	chr2:57624000-57634800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr2:57624200-57624800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr2:57624800-57625400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:57625000-57625200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr2:57629000-57629400	Enhancers	Fetal Brain Female	brain
48	chr2:57629000-57630400	Enhancers	Fetal Lung	lung
49	chr2:57633400-57633600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr2:57633400-57636000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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