Variant report

Variant	nsv874156
Chromosome Location	chr2:55474026-55636351
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2008)
CpG islands
(count:1893)
Chromatin interactive
region (count:151)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2008 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55509163-55509804	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:55496079-55496648	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:55569819-55570013	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:55592432-55592822	K562	blood:	n/a	n/a
5	ARID3A	chr2:55618268-55619692	K562	blood:	n/a	n/a
6	ATF1	chr2:55592548-55592774	K562	blood:	n/a	n/a
7	ATF2	chr2:55496074-55496639	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr2:55509172-55509997	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr2:55523473-55523953	GM12878	blood:	n/a	n/a
10	ATF2	chr2:55496023-55496744	GM12878	blood:	n/a	n/a
11	ATF2	chr2:55509103-55509930	GM12878	blood:	n/a	n/a
12	ATF2	chr2:55538284-55539073	GM12878	blood:	n/a	n/a
13	ATF2	chr2:55496025-55496883	GM12878	blood:	n/a	n/a
14	ATF2	chr2:55529274-55529855	GM12878	blood:	n/a	n/a
15	ATF2	chr2:55523307-55523927	GM12878	blood:	n/a	n/a
16	ATF2	chr2:55496054-55496589	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:55538318-55539135	GM12878	blood:	n/a	n/a
18	ATF2	chr2:55529331-55529829	GM12878	blood:	n/a	n/a
19	ATF3	chr2:55495727-55496643	A549	lung:	n/a	n/a
20	ATF3	chr2:55509128-55509706	A549	lung:	n/a	n/a
21	ATF3	chr2:55495945-55496752	A549	lung:	n/a	n/a
22	BACH1	chr2:55507233-55507574	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr2:55495852-55496650	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr2:55509167-55509605	H1-hESC	embryonic stem cell:	n/a	n/a
25	BATF	chr2:55496203-55496583	GM12878	blood:	n/a	n/a
26	BATF	chr2:55538437-55539121	GM12878	blood:	n/a	n/a
27	BATF	chr2:55529422-55529698	GM12878	blood:	n/a	n/a
28	BATF	chr2:55542020-55542394	GM12878	blood:	n/a	chr2:55542211-55542221 chr2:55542210-55542221
29	BATF	chr2:55538455-55539013	GM12878	blood:	n/a	n/a
30	BATF	chr2:55623002-55623354	GM12878	blood:	n/a	n/a
31	BATF	chr2:55529332-55529717	GM12878	blood:	n/a	n/a
32	BATF	chr2:55523487-55523919	GM12878	blood:	n/a	n/a
33	BCL11A	chr2:55542063-55542391	GM12878	blood:	n/a	chr2:55542210-55542219
34	BCL11A	chr2:55496170-55496563	GM12878	blood:	n/a	n/a
35	BCL11A	chr2:55529336-55529669	GM12878	blood:	n/a	chr2:55529597-55529606
36	BCL11A	chr2:55529282-55529766	GM12878	blood:	n/a	chr2:55529597-55529606
37	BCL11A	chr2:55523450-55523911	GM12878	blood:	n/a	n/a
38	BCL11A	chr2:55538483-55539067	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:55538417-55539027	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:55523485-55523768	GM12878	blood:	n/a	n/a
41	BCL3	chr2:55509056-55509740	GM12878	blood:	n/a	chr2:55509245-55509258 chr2:55509239-55509248
42	BCL3	chr2:55495510-55496662	A549	lung:	n/a	chr2:55496096-55496109
43	BCL3	chr2:55495902-55496848	A549	lung:	n/a	chr2:55496096-55496109
44	BCL3	chr2:55509009-55510047	A549	lung:	n/a	chr2:55509245-55509258 chr2:55509239-55509248
45	BCL3	chr2:55538496-55539033	GM12878	blood:	n/a	n/a
46	BCL3	chr2:55508957-55510111	A549	lung:	n/a	chr2:55509245-55509258 chr2:55509239-55509248
47	BCL3	chr2:55496202-55496581	GM12878	blood:	n/a	n/a
48	BCLAF1	chr2:55523368-55523864	GM12878	blood:	n/a	n/a
49	BCLAF1	chr2:55495967-55496768	K562	blood:	n/a	chr2:55496096-55496109
50	BCLAF1	chr2:55495968-55496709	GM12878	blood:	n/a	chr2:55496096-55496109

(count:1893 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55509253-55509303	AoSMC	blood vessel:	n/a
2	chr2:55496004-55496054	HRPEpiC	eye:	n/a
3	chr2:55509253-55509303	AoSMC	blood vessel:	n/a
4	chr2:55496004-55496054	HRPEpiC	eye:	n/a
5	chr2:55496144-55496194	HL-60	blood:	n/a
6	chr2:55556195-55556245	HCPEpiC	choroid plexus:	n/a
7	chr2:55496384-55496434	GM12878	blood:	n/a
8	chr2:55496004-55496054	HUVEC	blood vessel:	n/a
9	chr2:55509779-55509829	CMK	blood:	n/a
10	chr2:55511435-55511485	HepG2	liver:	n/a
11	chr2:55507730-55507780	HEEpiC	esophagus:	n/a
12	chr2:55563533-55563583	HRE	kidney:	n/a
13	chr2:55496144-55496194	PFSK-1	brain:	n/a
14	chr2:55497012-55497062	BE2_C	brain:	n/a
15	chr2:55509150-55509200	HCM	heart:	n/a
16	chr2:55509334-55509384	AG04450	lung:	fetal
17	chr2:55515029-55515079	SKMC	muscle:	n/a
18	chr2:55496144-55496194	U87	brain:	n/a
19	chr2:55477848-55477898	GM19239	blood:	n/a
20	chr2:55509523-55509573	A549	lung:	n/a
21	chr2:55556201-55556251	A549	lung:	n/a
22	chr2:55496390-55496440	HIPEpiC	eye:	n/a
23	chr2:55617438-55617488	GM19239	blood:	n/a
24	chr2:55515029-55515079	AG09309	skin:	n/a
25	chr2:55496495-55496545	NB4	blood:	n/a
26	chr2:55563533-55563583	Hela-S3	cervix:	n/a
27	chr2:55512437-55512487	BE2_C	brain:	n/a
28	chr2:55496371-55496421	Caco-2	colon:	n/a
29	chr2:55566679-55566729	AG04450	lung:	fetal
30	chr2:55496144-55496194	GM06990	blood:	n/a
31	chr2:55493212-55493262	GM12892	blood:	n/a
32	chr2:55617438-55617488	PANC-1	pancreas:	n/a
33	chr2:55496232-55496282	HMEC	breast:	n/a
34	chr2:55556195-55556245	NB4	blood:	n/a
35	chr2:55496552-55496602	HRE	kidney:	n/a
36	chr2:55496462-55496512	SK-N-SH_RA	brain:	n/a
37	chr2:55477848-55477898	GM12892	blood:	n/a
38	chr2:55496144-55496194	Jurkat	blood:	n/a
39	chr2:55497012-55497062	PFSK-1	brain:	n/a
40	chr2:55500061-55500111	HL-60	blood:	n/a
41	chr2:55500061-55500111	NT2-D1	testis:	n/a
42	chr2:55509334-55509384	HUVEC	blood vessel:	n/a
43	chr2:55556195-55556245	HRE	kidney:	n/a
44	chr2:55496384-55496434	GM12891	blood:	n/a
45	chr2:55496462-55496512	PANC-1	pancreas:	n/a
46	chr2:55496552-55496602	AoSMC	blood vessel:	n/a
47	chr2:55509334-55509384	PrEC	prostate:	n/a
48	chr2:55496232-55496282	Caco-2	colon:	n/a
49	chr2:55509258-55509308	HEEpiC	esophagus:	n/a
50	chr2:55496144-55496194	AG04449	skin:	fetal

(count:151 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr2:55629189..55632200-chr2:55632234..55637417,4	K562	blood:
2	chr2:55586524..55588974-chr2:55589647..55593883,3	K562	blood:
3	chr2:55540693..55542535-chr2:55543595..55545823,2	K562	blood:
4	chr2:55481797..55485521-chr2:55489463..55492846,3	K562	blood:
5	chr2:55592018..55593531-chr2:55595519..55597043,2	K562	blood:
6	chr2:55499045..55500751-chr2:55505359..55507052,2	MCF-7	breast:
7	chr2:55554925..55556673-chr2:55560073..55562213,2	K562	blood:
8	chr2:55633136..55639027-chr2:55639441..55643745,9	K562	blood:
9	chr2:55496544..55498355-chr2:55643954..55646229,2	K562	blood:
10	chr2:55579484..55581776-chr2:55584319..55586422,2	K562	blood:
11	chr2:55597784..55600046-chr2:55608046..55611475,3	K562	blood:
12	chr2:55540921..55542713-chr2:55544726..55547576,2	MCF-7	breast:
13	chr2:55528159..55530005-chr2:55532153..55533845,2	MCF-7	breast:
14	chr2:55494963..55498122-chr2:55498179..55500707,3	K562	blood:
15	chr2:55570093..55571972-chr2:55587892..55590606,2	K562	blood:
16	chr2:55599888..55601639-chr2:55606569..55609062,2	K562	blood:
17	chr2:55495879..55496701-chr7:143598878..143599680,2	HCT-116	colon:
18	chr2:55618745..55621738-chr2:55622062..55625126,3	K562	blood:
19	chr2:55274992..55277411-chr2:55494676..55497816,3	K562	blood:
20	chr2:55494928..55498059-chr2:55506695..55512310,8	K562	blood:
21	chr2:55617949..55620712-chr2:55634436..55637353,2	K562	blood:
22	chr2:55629328..55632200-chr2:55634808..55637417,2	K562	blood:
23	chr2:55584108..55586165-chr2:55591531..55593375,2	K562	blood:
24	chr2:55458633..55461619-chr2:55478405..55481835,3	K562	blood:
25	chr2:55510957..55512657-chr2:55520415..55521941,2	MCF-7	breast:
26	chr2:55507639..55510296-chr2:55843126..55844712,2	K562	blood:
27	chr2:55543117..55545665-chr2:55550405..55552133,2	K562	blood:
28	chr2:55546328..55548637-chr2:55556115..55557896,2	K562	blood:
29	chr2:55494631..55497013-chr2:55842868..55845390,2	MCF-7	breast:
30	chr2:55514301..55516151-chr2:55518959..55520928,3	MCF-7	breast:
31	chr2:55501428..55503229-chr2:55507740..55510366,2	MCF-7	breast:
32	chr2:55494750..55497639-chr2:55510154..55512422,2	MCF-7	breast:
33	chr2:55599888..55601639-chr2:55606569..55609062,2	K562	blood:
34	chr2:55458256..55461079-chr2:55494634..55496499,3	K562	blood:
35	chr2:55476363..55477867-chr2:55478489..55480345,2	MCF-7	breast:
36	chr2:55545711..55548722-chr2:55552487..55555212,4	K562	blood:
37	chr2:55546328..55548637-chr2:55556115..55557896,2	K562	blood:
38	chr2:55570093..55571972-chr2:55587892..55590606,2	K562	blood:
39	chr2:55509212..55512081-chr2:55556525..55559325,2	MCF-7	breast:
40	chr2:55536648..55539597-chr2:55541310..55544144,3	K562	blood:
41	chr2:55596421..55599307-chr2:55605325..55607627,2	MCF-7	breast:
42	chr2:55627338..55628874-chr2:55629453..55631312,2	MCF-7	breast:
43	chr2:55555173..55557100-chr2:55560073..55561601,2	K562	blood:
44	chr2:55592018..55593531-chr2:55595519..55597043,2	K562	blood:
45	chr2:55481770..55484795-chr2:55484832..55488632,4	K562	blood:
46	chr2:55545183..55549012-chr2:55745098..55746778,3	MCF-7	breast:
47	chr2:55589556..55591958-chr2:55592375..55594974,2	MCF-7	breast:
48	chr2:55596421..55599307-chr2:55605325..55607627,2	MCF-7	breast:
49	chr2:55635517..55637604-chr2:55646032..55648354,3	K562	blood:
50	chr2:55555173..55557100-chr2:55560073..55561601,2	K562	blood:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RPS27A-1	chr2:55556558-55556655	ENSG00000240401.4
2	lnc-RPS27A-1	chr2:55541218-55541387	ENSG00000240401.4
3	lnc-RPS27A-1	chr2:55535628-55536063	ENSG00000240401.4
4	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4
5	lnc-RPS27A-1	chr2:55556558-55556849	ENSG00000240401.4
6	lnc-RPS27A-1	chr2:55566639-55566931	ENSG00000240401.4
7	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4
8	lnc-RPS27A-1	chr2:55541124-55541797	ENSG00000240401.4
9	lnc-RPS27A-1	chr2:55541298-55541387	ENSG00000240401.4
10	lnc-RPS27A-1	chr2:55541124-55541797	ENSG00000240401.2
11	lnc-MTIF2-4	chr2:55628085-55628362	expReg_chr2_4282_-
12	lnc-RPS27A-1	chr2:55535967-55536063	ENSG00000240401.2
13	lnc-RPS27A-1	chr2:55566639-55567304	ENSG00000240401.4
14	lnc-RPS27A-1	chr2:55566639-55567446	ENSG00000240401.4
15	lnc-RPS27A-1	chr2:55572493-55573185	ENSG00000240401.4

No data

Variant related genes	Relation type
PRORSD1P	TF binding region
ENSG00000240401	TF binding region
CCDC88A	TF binding region
MTIF2	TF binding region
ENSG00000206964	TF binding region
PRORSD1P	CpG island
ENSG00000240401	CpG island
CCDC88A	CpG island
MTIF2	CpG island
ENSG00000206964	CpG island
ENSG00000162994	chromatin interactions
ENSG00000085760	chromatin interactions
ENSG00000138041	chromatin interactions
ENSG00000272606	chromatin interactions
ENSG00000227799	chromatin interactions
ENSG00000066027	chromatin interactions
ENSG00000162997	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000115310	chromatin interactions
ENSG00000115355	chromatin interactions
ENSG00000198420	chromatin interactions
ENSG00000206964	chromatin interactions
ENSG00000240401	chromatin interactions
ENSG00000163001	chromatin interactions
ENSG00000143947	chromatin interactions

Extended variants
information (count: 6762 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:6762 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17432234	chr2:55474026-55474027	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs146325493	chr2:55474115-55474116	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs138150189	chr2:55474132-55474133	Weak transcription Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs187097759	chr2:55474213-55474214	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs535457033	chr2:55474218-55474219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373080815	chr2:55474228-55474229	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558067334	chr2:55474282-55474283	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571949913	chr2:55474283-55474284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555763732	chr2:55474302-55474303	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs529563226	chr2:55474321-55474322	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs534206765	chr2:55474337-55474338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553380640	chr2:55474355-55474356	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191551011	chr2:55474366-55474367	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs183659533	chr2:55474393-55474394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs2920965	chr2:55474420-55474421	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs149552446	chr2:55474421-55474422	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374078921	chr2:55474425-55474426	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs144229887	chr2:55474452-55474453	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs148810122	chr2:55474463-55474464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189433380	chr2:55474480-55474481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545234106	chr2:55474490-55474491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs564920619	chr2:55474520-55474521	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs544268737	chr2:55474526-55474527	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572337032	chr2:55474531-55474532	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144906210	chr2:55474532-55474533	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs560495274	chr2:55474533-55474534	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs529266717	chr2:55474587-55474588	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549504882	chr2:55474603-55474604	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs1821832	chr2:55474604-55474605	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs531704355	chr2:55474645-55474646	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551985799	chr2:55474701-55474702	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571728132	chr2:55474729-55474730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182287882	chr2:55474730-55474731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2589080	chr2:55474735-55474736	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs73936964	chr2:55474892-55474893	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs140048855	chr2:55474963-55474964	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs144328147	chr2:55474982-55474983	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576127279	chr2:55475083-55475084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538337478	chr2:55475139-55475140	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79693341	chr2:55475146-55475147	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
41	rs559385867	chr2:55475165-55475166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34693232	chr2:55475190-55475191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572239985	chr2:55475214-55475215	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541350704	chr2:55475274-55475275	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185618622	chr2:55475277-55475278	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528415562	chr2:55475316-55475317	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs543086740	chr2:55475317-55475318	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs547861527	chr2:55475344-55475345	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs190094112	chr2:55475393-55475394	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530522759	chr2:55475468-55475469	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Williams Syndrome	20824207	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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:4208 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55461400-55477600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:55461600-55477000	Strong transcription	Fetal Muscle Leg	muscle
3	chr2:55461600-55481600	Strong transcription	Fetal Thymus	thymus
4	chr2:55461600-55495400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr2:55461600-55495400	Weak transcription	Stomach Mucosa	stomach
6	chr2:55461800-55474400	Strong transcription	Primary T cells fromperipheralblood	blood
7	chr2:55461800-55493400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr2:55461800-55495000	Weak transcription	Fetal Brain Male	brain
9	chr2:55462000-55493200	Strong transcription	Duodenum Mucosa	Duodenum
10	chr2:55462200-55490200	Weak transcription	Small Intestine	intestine
11	chr2:55462400-55476800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr2:55462400-55476800	Strong transcription	Rectal Mucosa Donor 29	rectum
13	chr2:55462600-55485800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr2:55463000-55477600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
15	chr2:55463000-55480200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr2:55463000-55481000	Weak transcription	Placenta Amnion	Placenta Amnion
17	chr2:55463000-55495400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr2:55463200-55481000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr2:55463400-55474200	Weak transcription	Aorta	Aorta
20	chr2:55463400-55475800	Weak transcription	Spleen	Spleen
21	chr2:55463400-55488200	Weak transcription	Pancreas	Pancrea
22	chr2:55463600-55474800	Weak transcription	Thymus	Thymus
23	chr2:55463600-55483800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr2:55463800-55475400	Weak transcription	Esophagus	oesophagus
25	chr2:55463800-55479600	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr2:55463800-55486200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr2:55463800-55490400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr2:55463800-55494800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr2:55463800-55495600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:55464000-55476200	Weak transcription	Fetal Kidney	kidney
31	chr2:55464400-55476200	Weak transcription	Brain Angular Gyrus	brain
32	chr2:55464400-55479600	Weak transcription	NHLF	lung
33	chr2:55464600-55475600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr2:55464600-55476200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr2:55464600-55476200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr2:55464600-55479400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr2:55464600-55495800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
38	chr2:55465400-55490600	Weak transcription	Brain Germinal Matrix	brain
39	chr2:55465600-55486000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
40	chr2:55465600-55494400	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr2:55465800-55476400	Strong transcription	Primary B cells from peripheral blood	blood
42	chr2:55465800-55477600	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr2:55466000-55493200	Strong transcription	Rectal Mucosa Donor 31	rectum
44	chr2:55466200-55476600	Strong transcription	Fetal Lung	lung
45	chr2:55466600-55475000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
46	chr2:55467400-55474600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr2:55468000-55477600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr2:55468200-55493400	Strong transcription	Monocytes-CD14+_RO01746	blood
49	chr2:55468400-55493200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr2:55468400-55494400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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