Variant report

Variant	nsv1013532
Chromosome Location	chr3:20172889-20305612
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1336)
CpG islands
(count:1221)
Chromatin interactive
region (count:104)
LncRNA
region (count:13)
Mature miRNA
region (count: 1)
miRNA target
sites (count:14)

(count:1336 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:20267278-20267600	K562	blood:	n/a	n/a
2	ARID3A	chr3:20227329-20228186	K562	blood:	n/a	n/a
3	ARID3A	chr3:20227487-20228388	HepG2	liver:	n/a	n/a
4	ATF1	chr3:20226994-20228147	K562	blood:	n/a	n/a
5	ATF2	chr3:20227207-20228211	GM12878	blood:	n/a	n/a
6	ATF2	chr3:20288074-20288600	GM12878	blood:	n/a	n/a
7	ATF2	chr3:20288131-20288515	GM12878	blood:	n/a	n/a
8	ATF2	chr3:20227637-20228238	GM12878	blood:	n/a	n/a
9	ATF3	chr3:20227527-20228058	GM12878	blood:	n/a	n/a
10	ATF3	chr3:20227535-20227966	K562	blood:	n/a	n/a
11	ATF3	chr3:20227605-20227903	HepG2	liver:	n/a	n/a
12	ATF3	chr3:20227425-20228037	HepG2	liver:	n/a	n/a
13	ATF3	chr3:20227448-20228043	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr3:20227575-20227873	GM12878	blood:	n/a	n/a
15	ATF3	chr3:20227505-20227918	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr3:20227585-20227975	K562	blood:	n/a	n/a
17	BACH1	chr3:20197358-20197428	K562	blood:	n/a	n/a
18	BATF	chr3:20288158-20288422	GM12878	blood:	n/a	chr3:20288290-20288301
19	BATF	chr3:20288183-20288438	GM12878	blood:	n/a	chr3:20288290-20288301
20	BATF	chr3:20277379-20277647	GM12878	blood:	n/a	n/a
21	BATF	chr3:20277377-20277645	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:20288193-20288461	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:20288232-20288418	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:20263779-20264109	H1-hESC	embryonic stem cell:	n/a	n/a
25	BCL11A	chr3:20263785-20264058	H1-hESC	embryonic stem cell:	n/a	n/a
26	BCL3	chr3:20227304-20227885	A549	lung:	n/a	n/a
27	BCLAF1	chr3:20227146-20228169	GM12878	blood:	n/a	n/a
28	BCLAF1	chr3:20227123-20228281	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:20188531-20188551	GM12878	blood:	n/a	n/a
30	BHLHE40	chr3:20227454-20228139	HepG2	liver:	n/a	n/a
31	BHLHE40	chr3:20227167-20228366	GM12878	blood:	n/a	n/a
32	BHLHE40	chr3:20226943-20228838	K562	blood:	n/a	n/a
33	BHLHE40	chr3:20227627-20227958	A549	lung:	n/a	n/a
34	BRCA1	chr3:20227654-20228038	HepG2	liver:	n/a	n/a
35	BRCA1	chr3:20227548-20228269	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr3:20239197-20239673	HCT-116	colon:	n/a	n/a
37	CBX3	chr3:20226778-20228315	K562	blood:	n/a	n/a
38	CBX3	chr3:20227437-20228131	K562	blood:	n/a	n/a
39	CCNT2	chr3:20227443-20228238	K562	blood:	n/a	n/a
40	CEBPB	chr3:20203127-20203582	HepG2	liver:	n/a	chr3:20203398-20203409
41	CEBPB	chr3:20268310-20268510	HepG2	liver:	n/a	chr3:20268446-20268457
42	CEBPB	chr3:20243180-20243265	K562	blood:	n/a	n/a
43	CEBPB	chr3:20268370-20268487	K562	blood:	n/a	chr3:20268446-20268457
44	CEBPB	chr3:20203174-20203569	IMR90	lung:	n/a	chr3:20203398-20203409
45	CEBPB	chr3:20208029-20208263	Hela-S3	cervix:	n/a	chr3:20208153-20208164
46	CEBPB	chr3:20227521-20227532	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:20203224-20203542	A549	lung:	n/a	chr3:20203398-20203409
48	CEBPB	chr3:20298924-20299012	K562	blood:	n/a	chr3:20298947-20298958
49	CEBPB	chr3:20195623-20195949	HepG2	liver:	n/a	chr3:20195761-20195772
50	CEBPB	chr3:20208038-20208329	MCF-7	breast:	n/a	chr3:20208153-20208164

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:20227809-20227859	HCT-116	colon:	n/a
2	chr3:20227809-20227859	HCT-116	colon:	n/a
3	chr3:20228976-20229026	AoSMC	blood vessel:	n/a
4	chr3:20195067-20195117	GM12892	blood:	n/a
5	chr3:20227801-20227851	AG04450	lung:	fetal
6	chr3:20227059-20227109	ProgFib	skin:	n/a
7	chr3:20227670-20227720	GM19239	blood:	n/a
8	chr3:20227059-20227109	BE2_C	brain:	n/a
9	chr3:20227663-20227713	NB4	blood:	n/a
10	chr3:20227809-20227859	CMK	blood:	n/a
11	chr3:20227940-20227990	HCPEpiC	choroid plexus:	n/a
12	chr3:20227801-20227851	HRE	kidney:	n/a
13	chr3:20227801-20227851	MCF-7	breast:	n/a
14	chr3:20227091-20227141	IMR90	lung:	fetal
15	chr3:20226994-20227044	AG09319	gingival:	n/a
16	chr3:20202403-20202453	CMK	blood:	n/a
17	chr3:20202403-20202453	Caco-2	colon:	n/a
18	chr3:20223923-20223973	Hepatocyte	liver:	n/a
19	chr3:20227809-20227859	H1-hESC	embryonic stem cell:	embryo
20	chr3:20227059-20227109	HRCEpiC	kidney:	n/a
21	chr3:20231061-20231111	Jurkat	blood:	n/a
22	chr3:20227397-20227447	CMK	blood:	n/a
23	chr3:20227059-20227109	HCF	heart:	n/a
24	chr3:20227940-20227990	AG04449	skin:	fetal
25	chr3:20227809-20227859	SKMC	muscle:	n/a
26	chr3:20195067-20195117	HCF	heart:	n/a
27	chr3:20227940-20227990	GM12891	blood:	n/a
28	chr3:20227516-20227566	AG09319	gingival:	n/a
29	chr3:20228976-20229026	A549	lung:	n/a
30	chr3:20227822-20227872	GM12891	blood:	n/a
31	chr3:20227059-20227109	MCF-7	breast:	n/a
32	chr3:20226964-20227014	HRE	kidney:	n/a
33	chr3:20227663-20227713	AG04449	skin:	fetal
34	chr3:20183665-20183715	HCPEpiC	choroid plexus:	n/a
35	chr3:20183665-20183715	T-47D	breast:	n/a
36	chr3:20223923-20223973	HEK293	kidney:	embryo
37	chr3:20227801-20227851	K562	blood:	n/a
38	chr3:20226964-20227014	BJ	skin:	n/a
39	chr3:20223923-20223973	NH-A	brain:	n/a
40	chr3:20227809-20227859	K562	blood:	n/a
41	chr3:20231061-20231111	HEEpiC	esophagus:	n/a
42	chr3:20183665-20183715	MCF-7	breast:	n/a
43	chr3:20227516-20227566	HRE	kidney:	n/a
44	chr3:20226994-20227044	K562	blood:	n/a
45	chr3:20226994-20227044	Hela-S3	cervix:	n/a
46	chr3:20227925-20227975	T-47D	breast:	n/a
47	chr3:20227663-20227713	GM19239	blood:	n/a
48	chr3:20226994-20227044	Caco-2	colon:	n/a
49	chr3:20227397-20227447	HIPEpiC	eye:	n/a
50	chr3:20195067-20195117	Hela-S3	cervix:	n/a

(count:104 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:20026744..20028391-chr3:20179736..20182279,2	MCF-7	breast:
2	chr3:20227937..20230614-chr3:20238703..20240365,2	K562	blood:
3	chr2:97426251..97427245-chr3:20227662..20228331,2	Hela-S3	cervix:
4	chr3:20195965..20199003-chr3:20200424..20204373,5	K562	blood:
5	chr3:20219250..20222131-chr3:20228592..20230370,2	K562	blood:
6	chr3:20079527..20082964-chr3:20226742..20229620,4	K562	blood:
7	chr15:42565172..42565968-chr3:20227231..20227766,2	Hela-S3	cervix:
8	chr3:20210669..20212300-chr3:20217697..20220649,2	K562	blood:
9	chr3:20080757..20082677-chr3:20192981..20195193,2	K562	blood:
10	chr3:20212661..20217850-chr3:20224065..20229766,9	K562	blood:
11	chr3:20195965..20199003-chr3:20200424..20204373,5	K562	blood:
12	chr3:20195318..20197314-chr3:20202622..20204510,2	MCF-7	breast:
13	chr3:20208211..20212087-chr3:20224920..20227676,5	K562	blood:
14	chr3:20201533..20203572-chr3:20204589..20206739,2	K562	blood:
15	chr3:20029851..20032501-chr3:20180308..20182516,2	K562	blood:
16	chr3:20201533..20203572-chr3:20204589..20206739,2	K562	blood:
17	chr3:20213813..20216501-chr3:20227432..20229116,2	MCF-7	breast:
18	chr1:211431812..211432720-chr3:20227589..20228353,2	Hela-S3	cervix:
19	chr3:20191414..20193219-chr3:20194880..20197331,2	K562	blood:
20	chr3:20080195..20082473-chr3:20238022..20239548,2	MCF-7	breast:
21	chr3:19986817..19988952-chr3:20217097..20219211,2	K562	blood:
22	chr3:19991248..19993079-chr3:20225987..20227552,2	MCF-7	breast:
23	chr3:20239141..20242093-chr3:20243237..20245367,3	K562	blood:
24	chr3:20269133..20272394-chr3:20272728..20275710,3	K562	blood:
25	chr3:20081214..20082103-chr3:20196180..20196782,3	MCF-7	breast:
26	chr3:20177373..20179838-chr3:20195136..20197383,2	K562	blood:
27	chr3:20079993..20081743-chr3:20205055..20207823,2	MCF-7	breast:
28	chr3:20240283..20242142-chr3:20254913..20256935,2	K562	blood:
29	chr3:20212661..20217850-chr3:20224065..20229766,9	K562	blood:
30	chr3:20080018..20082340-chr3:20176608..20178833,2	K562	blood:
31	chr3:20197127..20199080-chr3:20208900..20210840,2	MCF-7	breast:
32	chr3:20219250..20222131-chr3:20228592..20230370,2	K562	blood:
33	chr3:20226448..20228980-chr3:20231144..20234755,4	MCF-7	breast:
34	chr3:20186107..20188316-chr3:20191004..20193087,2	MCF-7	breast:
35	chr3:20255206..20257186-chr3:20272224..20273896,2	K562	blood:
36	chr3:20223638..20225446-chr3:20225885..20227918,2	MCF-7	breast:
37	chr3:20225377..20229978-chr3:20232761..20235716,5	K562	blood:
38	chr3:20228018..20229588-chr3:20240700..20242261,2	K562	blood:
39	chr3:19985145..19990136-chr3:20225418..20228312,6	K562	blood:
40	chr3:20197490..20199260-chr3:20227955..20230018,2	K562	blood:
41	chr3:20202636..20204189-chr3:20204811..20206613,2	MCF-7	breast:
42	chr3:20212391..20215096-chr3:20215867..20218986,3	K562	blood:
43	chr3:20188319..20191715-chr3:20218902..20221810,3	K562	blood:
44	chr3:20216479..20218064-chr3:20218704..20221260,2	K562	blood:
45	chr3:20225377..20229978-chr3:20232761..20235716,5	K562	blood:
46	chr3:20191414..20193219-chr3:20194880..20197331,2	K562	blood:
47	chr3:20185698..20188649-chr3:20188952..20191423,4	K562	blood:
48	chr3:20240283..20242142-chr3:20254913..20256935,2	K562	blood:
49	chr3:20188934..20192869-chr3:20226143..20228338,3	MCF-7	breast:
50	chr13:113841278..113842020-chr3:20226671..20227468,2	Hela-S3	cervix:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KAT2B-1	chr3:20216227-20216310	ENSG00000237485.1
2	lnc-KAT2B-5	chr3:20210846-20210905	l_2328_chr3:20202875-20210905_testes
3	lnc-KAT2B-1	chr3:20215736-20216017	ENSG00000237485.1
4	lnc-KAT2B-1	chr3:20227726-20230848	NONHSAT088617
5	lnc-KAT2B-1	chr3:20218709-20218742	ENSG00000237485.1
6	lnc-PP2D1-2	chr3:20212535-20212759	NONHSAT088614
7	lnc-KAT2B-1	chr3:20227467-20227607	ENSG00000237485.1
8	lnc-PP2D1-2	chr3:20211553-20212307	NONHSAT088614
9	lnc-KAT2B-1	chr3:20216227-20216310	ENSG00000237485.1
10	lnc-KAT2B-1	chr3:20215778-20216017	ENSG00000237485.1
11	lnc-KAT2B-6	chr3:20286533-20287951	NONHSAT088619
12	lnc-KAT2B-5	chr3:20202876-20203154	l_2328_chr3:20202875-20210905_testes
13	lnc-KAT2B-1	chr3:20227467-20227919	ENSG00000237485.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-3135a	chr3:20179066-20179087	MIMAT0015001

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	KAT2B	hsa-miR-93-5p	chr3:20194121-20194144
2	KAT2B	hsa-miR-106b-5p	chr3:20195703-20195723
3	KAT2B	hsa-miR-106b-5p	chr3:20194137-20194143
4	KAT2B	hsa-miR-93-5p	chr3:20195701-20195723
5	KAT2B	hsa-miR-32-5p	chr3:20195765-20195772
6	KAT2B	hsa-miR-106b-5p	chr3:20194123-20194144
7	KAT2B	hsa-miR-25-3p	chr3:20195765-20195772
8	KAT2B	hsa-miR-92a-3p	chr3:20195765-20195772
9	KAT2B	hsa-miR-181b-5p	chr3:20194367-20194390
10	KAT2B	hsa-miR-93-5p	chr3:20194137-20194143
11	KAT2B	hsa-miR-25-3p	chr3:20195750-20195772
12	KAT2B	hsa-miR-181a-5p	chr3:20194367-20194390
13	KAT2B	hsa-miR-32-5p	chr3:20195750-20195772
14	KAT2B	hsa-miR-92a-3p	chr3:20195750-20195772

Variant related genes	Relation type
KAT2B	TF binding region
MIR3135A	TF binding region
RNY4P22	TF binding region
SGOL1-AS1	TF binding region
SGOL1	TF binding region
KAT2B	CpG island
MIR3135A	CpG island
RNY4P22	CpG island
SGOL1-AS1	CpG island
SGOL1	CpG island
ENSG00000163576	chromatin interactions
ENSG00000214013	chromatin interactions
ENSG00000126226	chromatin interactions
ENSG00000114166	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000144566	chromatin interactions
ENSG00000129810	chromatin interactions
ENSG00000234779	chromatin interactions
ENSG00000237485	chromatin interactions
ENSG00000103978	chromatin interactions
ENSG00000117625	chromatin interactions
ENSG00000266745	chromatin interactions
ENSG00000229468	chromatin interactions
ENSG00000158158	chromatin interactions
ENSG00000252442	chromatin interactions

Extended variants
information (count: 4955 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4955 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535849652	chr3:20172976-20172977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557358600	chr3:20173103-20173104	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs368635967	chr3:20173111-20173112	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187373789	chr3:20173113-20173114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148473980	chr3:20173128-20173129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557962613	chr3:20173144-20173145	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150042375	chr3:20173153-20173154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573116916	chr3:20173252-20173253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs371046808	chr3:20173270-20173271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs192095565	chr3:20173305-20173306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552653308	chr3:20173308-20173309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374464691	chr3:20173352-20173353	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs557516137	chr3:20173365-20173366	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574312292	chr3:20173423-20173424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541851556	chr3:20173424-20173425	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563433728	chr3:20173493-20173494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs142623636	chr3:20173527-20173528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150557507	chr3:20173534-20173535	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540927159	chr3:20173538-20173539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs564241660	chr3:20173566-20173567	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528294887	chr3:20173594-20173595	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547072879	chr3:20173606-20173607	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568578552	chr3:20173609-20173610	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529252731	chr3:20173638-20173639	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs13313945	chr3:20173642-20173643	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs13317632	chr3:20173656-20173657	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs540086356	chr3:20173691-20173692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368172380	chr3:20173743-20173744	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs182234333	chr3:20173752-20173753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs534139521	chr3:20173753-20173754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573487039	chr3:20173759-20173760	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377096260	chr3:20173768-20173769	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs11705766	chr3:20173805-20173806	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs558308911	chr3:20173848-20173849	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs574501976	chr3:20174126-20174127	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs535099385	chr3:20174158-20174159	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs577060994	chr3:20174199-20174200	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs556954909	chr3:20174209-20174210	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs575138195	chr3:20174221-20174222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112927228	chr3:20174294-20174295	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2686313	chr3:20174337-20174338	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs9851303	chr3:20174355-20174356	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs4858768	chr3:20174369-20174370	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs17797581	chr3:20174396-20174397	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs530554132	chr3:20174414-20174415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4858769	chr3:20174426-20174427	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs189914689	chr3:20174542-20174543	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs369824634	chr3:20174570-20174571	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs562854757	chr3:20174640-20174641	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs533177720	chr3:20174655-20174656	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1570 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:20116400-20194800	Weak transcription	NHDF-Ad	bronchial
2	chr3:20128200-20175800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:20135200-20173800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:20141200-20222400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:20142600-20189400	Weak transcription	Fetal Brain Male	brain
6	chr3:20147600-20194200	Weak transcription	Dnd41	blood
7	chr3:20151000-20196800	Weak transcription	Stomach Mucosa	stomach
8	chr3:20151200-20179000	Weak transcription	Fetal Kidney	kidney
9	chr3:20151600-20175800	Strong transcription	Primary T helper cells fromperipheralblood	blood
10	chr3:20152000-20182800	Weak transcription	Colonic Mucosa	Colon
11	chr3:20152600-20175200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr3:20152800-20175000	Strong transcription	Primary T cells fromperipheralblood	blood
13	chr3:20152800-20176200	Strong transcription	Primary T helper cells PMA-I stimulated	--
14	chr3:20154000-20178400	Weak transcription	Psoas Muscle	Psoas
15	chr3:20157000-20178800	Weak transcription	HUVEC	blood vessel
16	chr3:20159200-20201400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr3:20160400-20182000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:20160600-20175400	Strong transcription	Liver	Liver
19	chr3:20160600-20176000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr3:20161000-20173400	Strong transcription	Fetal Thymus	thymus
21	chr3:20162200-20183400	Weak transcription	Gastric	stomach
22	chr3:20162200-20184000	Weak transcription	Right Ventricle	heart
23	chr3:20162800-20183000	Weak transcription	Fetal Heart	heart
24	chr3:20162800-20198200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr3:20164000-20176200	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr3:20164400-20204400	Weak transcription	Small Intestine	intestine
27	chr3:20164800-20181600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr3:20164800-20181600	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr3:20164800-20211400	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr3:20165000-20178400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
31	chr3:20165800-20173400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr3:20166200-20178400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr3:20167800-20174000	Weak transcription	Placenta	Placenta
34	chr3:20167800-20181800	Weak transcription	Lung	lung
35	chr3:20167800-20196600	Weak transcription	K562	blood
36	chr3:20167800-20226000	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr3:20168000-20183600	Weak transcription	Primary hematopoietic stem cells	blood
38	chr3:20168600-20182800	Strong transcription	Monocytes-CD14+_RO01746	blood
39	chr3:20168800-20200800	Weak transcription	GM12878-XiMat	blood
40	chr3:20169400-20180800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr3:20169400-20184400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
42	chr3:20169600-20174000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:20169600-20174400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr3:20169600-20178400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
45	chr3:20169600-20179000	Weak transcription	Esophagus	oesophagus
46	chr3:20169600-20181800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr3:20169600-20181800	Weak transcription	Ovary	ovary
48	chr3:20169600-20182000	Weak transcription	Fetal Intestine Small	intestine
49	chr3:20169600-20182000	Weak transcription	Spleen	Spleen
50	chr3:20169600-20182400	Weak transcription	Brain Hippocampus Middle	brain

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