Variant report

Variant	nsv613256
Chromosome Location	chr9:6750556-6859189
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2024)
CpG islands
(count:917)
Chromatin interactive
region (count:47)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2024 , 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	chr9:6779378-6780217	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:6758992-6759444	K562	blood:	n/a	n/a
3	ARID3A	chr9:6787981-6788483	HepG2	liver:	n/a	n/a
4	ARID3A	chr9:6756811-6758201	HepG2	liver:	n/a	n/a
5	ARID3A	chr9:6788815-6789003	HepG2	liver:	n/a	n/a
6	ARID3A	chr9:6819233-6819386	HepG2	liver:	n/a	n/a
7	ARID3A	chr9:6779811-6780274	K562	blood:	n/a	n/a
8	ARID3A	chr9:6845932-6846244	HepG2	liver:	n/a	n/a
9	ARID3A	chr9:6755672-6755722	K562	blood:	n/a	n/a
10	ARID3A	chr9:6781433-6781998	HepG2	liver:	n/a	n/a
11	ARID3A	chr9:6845117-6845374	HepG2	liver:	n/a	n/a
12	ARID3A	chr9:6756891-6757253	K562	blood:	n/a	n/a
13	ATF1	chr9:6753060-6753144	K562	blood:	n/a	n/a
14	ATF1	chr9:6779901-6780225	K562	blood:	n/a	n/a
15	ATF1	chr9:6756990-6758095	K562	blood:	n/a	n/a
16	ATF2	chr9:6757315-6757912	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr9:6750570-6751254	GM12878	blood:	n/a	n/a
18	ATF2	chr9:6757293-6758094	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr9:6750387-6751234	GM12878	blood:	n/a	n/a
20	ATF2	chr9:6758832-6759588	GM12878	blood:	n/a	n/a
21	ATF2	chr9:6758832-6759575	GM12878	blood:	n/a	n/a
22	ATF2	chr9:6771753-6772027	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr9:6777168-6777670	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr9:6756928-6758082	GM12878	blood:	n/a	n/a
25	ATF2	chr9:6771687-6772129	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr9:6756759-6758392	GM12878	blood:	n/a	n/a
27	ATF3	chr9:6757570-6758187	GM12878	blood:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
28	ATF3	chr9:6779898-6780160	K562	blood:	n/a	n/a
29	ATF3	chr9:6757789-6758049	GM12878	blood:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
30	ATF3	chr9:6757154-6757557	K562	blood:	n/a	n/a
31	ATF3	chr9:6757549-6758137	H1-hESC	embryonic stem cell:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
32	ATF3	chr9:6757524-6758154	A549	lung:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
33	ATF3	chr9:6757628-6758216	HepG2	liver:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
34	ATF3	chr9:6757790-6758075	K562	blood:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
35	ATF3	chr9:6757772-6758138	K562	blood:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
36	ATF3	chr9:6757652-6758141	HepG2	liver:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
37	ATF3	chr9:6757678-6758138	H1-hESC	embryonic stem cell:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
38	ATF3	chr9:6757514-6757784	K562	blood:	n/a	n/a
39	ATF3	chr9:6757468-6758055	A549	lung:	n/a	chr9:6757929-6757949 chr9:6757940-6757960 chr9:6757949-6757958 chr9:6757940-6757949 chr9:6757953-6757962
40	BACH1	chr9:6757224-6758261	H1-hESC	embryonic stem cell:	n/a	n/a
41	BACH1	chr9:6765406-6765470	H1-hESC	embryonic stem cell:	n/a	n/a
42	BACH1	chr9:6758576-6759166	H1-hESC	embryonic stem cell:	n/a	n/a
43	BACH1	chr9:6854906-6854915	H1-hESC	embryonic stem cell:	n/a	n/a
44	BACH1	chr9:6764615-6764768	H1-hESC	embryonic stem cell:	n/a	chr9:6764754-6764768
45	BATF	chr9:6816627-6816816	GM12878	blood:	n/a	n/a
46	BATF	chr9:6757171-6757975	GM12878	blood:	n/a	n/a
47	BATF	chr9:6759129-6759503	GM12878	blood:	n/a	n/a
48	BATF	chr9:6750653-6751296	GM12878	blood:	n/a	n/a
49	BCL11A	chr9:6771770-6772048	H1-hESC	embryonic stem cell:	n/a	n/a
50	BCL11A	chr9:6750696-6750991	GM12878	blood:	n/a	chr9:6750723-6750732

(count:917 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:6758853-6758903	AG04449	skin:	fetal
2	chr9:6758683-6758733	GM06990	blood:	n/a
3	chr9:6758853-6758903	AG04449	skin:	fetal
4	chr9:6758683-6758733	GM06990	blood:	n/a
5	chr9:6758683-6758733	HIPEpiC	eye:	n/a
6	chr9:6758935-6758985	HCPEpiC	choroid plexus:	n/a
7	chr9:6758546-6758596	HL-60	blood:	n/a
8	chr9:6779450-6779500	MCF-7	breast:	n/a
9	chr9:6757347-6757397	GM06990	blood:	n/a
10	chr9:6757912-6757962	PrEC	prostate:	n/a
11	chr9:6757781-6757831	GM12891	blood:	n/a
12	chr9:6779450-6779500	LNCaP	prostate:	n/a
13	chr9:6761072-6761122	SK-N-MC	brain:	n/a
14	chr9:6757826-6757876	PFSK-1	brain:	n/a
15	chr9:6758853-6758903	HEK293	kidney:	embryo
16	chr9:6758546-6758596	HCT-116	colon:	n/a
17	chr9:6835001-6835051	IMR90	lung:	fetal
18	chr9:6758683-6758733	HEEpiC	esophagus:	n/a
19	chr9:6755109-6755159	RPTEC	kidney:	n/a
20	chr9:6779450-6779500	AG09319	gingival:	n/a
21	chr9:6758683-6758733	LNCaP	prostate:	n/a
22	chr9:6836634-6836684	HCF	heart:	n/a
23	chr9:6757781-6757831	HCT-116	colon:	n/a
24	chr9:6757347-6757397	PFSK-1	brain:	n/a
25	chr9:6758683-6758733	HMEC	breast:	n/a
26	chr9:6835001-6835051	AG04449	skin:	fetal
27	chr9:6757912-6757962	CMK	blood:	n/a
28	chr9:6835001-6835051	SK-N-MC	brain:	n/a
29	chr9:6757146-6757196	SK-N-SH	brain:	n/a
30	chr9:6757781-6757831	Jurkat	blood:	n/a
31	chr9:6758140-6758190	A549	lung:	n/a
32	chr9:6758935-6758985	AG04449	skin:	fetal
33	chr9:6758140-6758190	HCM	heart:	n/a
34	chr9:6757781-6757831	HUVEC	blood vessel:	n/a
35	chr9:6758546-6758596	MCF-7	breast:	n/a
36	chr9:6836634-6836684	HAEpiC	amniotic membrane:	n/a
37	chr9:6761072-6761122	HCPEpiC	choroid plexus:	n/a
38	chr9:6758683-6758733	IMR90	lung:	fetal
39	chr9:6758853-6758903	RPTEC	kidney:	n/a
40	chr9:6758853-6758903	HRCEpiC	kidney:	n/a
41	chr9:6761072-6761122	K562	blood:	n/a
42	chr9:6761072-6761122	Hela-S3	cervix:	n/a
43	chr9:6758683-6758733	PANC-1	pancreas:	n/a
44	chr9:6779450-6779500	HIPEpiC	eye:	n/a
45	chr9:6836634-6836684	HCPEpiC	choroid plexus:	n/a
46	chr9:6758546-6758596	BE2_C	brain:	n/a
47	chr9:6755109-6755159	PFSK-1	brain:	n/a
48	chr9:6758546-6758596	A549	lung:	n/a
49	chr9:6779450-6779500	NH-A	brain:	n/a
50	chr9:6836634-6836684	HepG2	liver:	n/a

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:6765179..6766927-chr9:6770237..6771845,2	K562	blood:
2	chr12:49245554..49246083-chr9:6757387..6757976,2	Hela-S3	cervix:
3	chr22:39077394..39078187-chr9:6757291..6757887,2	HCT-116	colon:
4	chr9:6757938..6759489-chr9:6817335..6820629,3	MCF-7	breast:
5	chr9:6749158..6750730-chr9:6754623..6757370,3	K562	blood:
6	chr9:6711589..6718151-chr9:6755774..6759657,12	MCF-7	breast:
7	chr6:26216402..26217347-chr9:6757097..6757962,2	Hela-S3	cervix:
8	chr9:6702391..6705446-chr9:6756717..6760058,5	MCF-7	breast:
9	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:
10	chr11:57102959..57103791-chr9:6757018..6757636,2	NB4	blood:
11	chr1:24117621..24118528-chr9:6757285..6757921,2	Hela-S3	cervix:
12	chr9:6751286..6753075-chr9:6755508..6757503,2	MCF-7	breast:
13	chr9:6765179..6766927-chr9:6770237..6771845,2	K562	blood:
14	chr17:45727006..45727831-chr9:6757854..6758764,2	HCT-116	colon:
15	chr9:6680103..6682666-chr9:6784102..6786978,2	K562	blood:
16	chr9:6757388..6759261-chr9:6764601..6766785,2	MCF-7	breast:
17	chr9:6757988..6759532-chr9:6768470..6771009,2	K562	blood:
18	chr17:4458410..4459064-chr9:6757173..6757817,2	NB4	blood:
19	chr11:88070952..88071704-chr9:6757255..6758140,2	NB4	blood:
20	chr9:6756506..6759336-chr9:6761694..6766158,6	MCF-7	breast:
21	chr9:6766833..6770674-chr9:6780008..6783723,3	K562	blood:
22	chr9:6845574..6847293-chr9:6858590..6860659,2	K562	blood:
23	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:
24	chr9:6714844..6717578-chr9:6754943..6759087,4	MCF-7	breast:
25	chr9:6749197..6752825-chr9:6755235..6757236,4	K562	blood:
26	chr9:6747740..6749345-chr9:6756036..6758918,2	MCF-7	breast:
27	chr9:6706468..6709007-chr9:6764056..6766511,2	MCF-7	breast:
28	chr1:201979647..201980421-chr9:6757390..6758317,2	HCT-116	colon:
29	chr9:6411580..6414419-chr9:6755713..6757647,2	K562	blood:
30	chr9:6766833..6770674-chr9:6780008..6783723,3	K562	blood:
31	chr9:6842488..6845236-chr9:6852172..6854079,2	MCF-7	breast:
32	chr9:6751679..6753304-chr9:6755614..6757783,2	MCF-7	breast:
33	chr1:78469866..78470559-chr9:6757407..6758029,2	NB4	blood:
34	chr9:6749197..6752825-chr9:6755235..6757236,4	K562	blood:
35	chr9:6722888..6726785-chr9:6754807..6757177,3	K562	blood:
36	chr9:6413251..6414875-chr9:6756450..6759044,2	K562	blood:
37	chr9:6842488..6845236-chr9:6852172..6854079,2	MCF-7	breast:
38	chr9:6831771..6833427-chr9:6836426..6839172,2	K562	blood:
39	chr2:219187766..219188395-chr9:6757084..6757687,2	NB4	blood:
40	chr9:6757021..6759532-chr9:6768470..6771017,3	K562	blood:
41	chr1:63833144..63833741-chr9:6757006..6757570,2	NB4	blood:
42	chr9:6845574..6847293-chr9:6858590..6860659,2	K562	blood:
43	chr9:6749158..6750730-chr9:6754623..6757370,3	K562	blood:
44	chr7:86781908..86782653-chr9:6757524..6758733,3	Hela-S3	cervix:
45	chr9:6751286..6753075-chr9:6755508..6757503,2	MCF-7	breast:
46	chr9:6668807..6671531-chr9:6755488..6757060,2	K562	blood:
47	chr9:6826110..6829506-chr9:6834474..6836178,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UHRF2-1	chr9:6780333-6780490	ENSG00000236563.1
2	lnc-UHRF2-1	chr9:6785601-6785929	ENSG00000236563.1

No data

Variant related genes	Relation type
ENSG00000230581	TF binding region
SNRPEP2	TF binding region
KDM4C	TF binding region
ENSG00000230581	CpG island
SNRPEP2	CpG island
KDM4C	CpG island
ENSG00000011009	chromatin interactions
ENSG00000107077	chromatin interactions
ENSG00000088035	chromatin interactions
ENSG00000109861	chromatin interactions
ENSG00000100216	chromatin interactions
ENSG00000174243	chromatin interactions
ENSG00000135164	chromatin interactions
ENSG00000132382	chromatin interactions
ENSG00000149136	chromatin interactions
ENSG00000225489	chromatin interactions
ENSG00000228274	chromatin interactions
ENSG00000231381	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000162616	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000256968	chromatin interactions
ENSG00000229611	chromatin interactions
ENSG00000147854	chromatin interactions
ENSG00000127838	chromatin interactions
ENSG00000273338	chromatin interactions

Extended variants
information (count: 5890 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5890 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10117618	chr9:6750556-6750557	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556608842	chr9:6750678-6750679	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs575063864	chr9:6750698-6750699	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs535743367	chr9:6750714-6750715	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs554162020	chr9:6750756-6750757	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs572428113	chr9:6750813-6750814	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs546357865	chr9:6750821-6750822	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs150927537	chr9:6750825-6750826	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs72699607	chr9:6750828-6750829	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs562508730	chr9:6750952-6750953	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs558219314	chr9:6750972-6750973	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs140632545	chr9:6750980-6750981	Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs140671833	chr9:6751028-6751029	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs113506607	chr9:6751047-6751048	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs541555254	chr9:6751056-6751057	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs150094121	chr9:6751059-6751060	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs527282338	chr9:6751066-6751067	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs551900611	chr9:6751081-6751082	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs190683080	chr9:6751082-6751083	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs564545744	chr9:6751121-6751122	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs531847141	chr9:6751144-6751145	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs533441922	chr9:6751175-6751176	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs138419344	chr9:6751221-6751222	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs369660487	chr9:6751293-6751294	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs140295587	chr9:6751326-6751327	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs200879065	chr9:6751411-6751412	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs376445652	chr9:6751425-6751426	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs536152707	chr9:6751432-6751433	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs199532641	chr9:6751451-6751452	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs554493712	chr9:6751466-6751467	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs57845144	chr9:6751467-6751468	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs566123833	chr9:6751486-6751487	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs10975819	chr9:6751506-6751507	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs558315606	chr9:6751540-6751541	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs576495484	chr9:6751601-6751602	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs543522945	chr9:6751624-6751625	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs556327017	chr9:6751635-6751636	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs574506489	chr9:6751636-6751637	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs192811815	chr9:6751639-6751640	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs531678913	chr9:6751642-6751643	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs548137078	chr9:6751654-6751655	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs12347059	chr9:6751664-6751665	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs545380135	chr9:6751695-6751696	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555776197	chr9:6751704-6751705	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563705664	chr9:6751735-6751736	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs375609580	chr9:6751792-6751793	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs533712900	chr9:6751801-6751802	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs530009912	chr9:6751802-6751803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550321977	chr9:6751854-6751855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs35982799	chr9:6751865-6751866	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Intracranial aneurysm	16715129	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Disorders of sex development	22290220	CNVD
Glioblastoma multiforme	21080181	CNVD
Sudden cardiac death	19188705	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	21952639	CNVD
Disorders of sex development	21048976	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
abnormal development	18461090	CNVD
Honadal dysgenesis	21048976	CNVD
Medulloblastoma	21979893	CNVD
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Developmental delay	21147756	CNVD
Lung cancer	18438408	CNVD
XY gonadal dysgenesis	20685758	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Metastatic melanoma	18483359	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Medullary thyroid carcinoma	18765511	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD

Chromatin state (count:3159 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6750000-6750600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr9:6750000-6751000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr9:6750000-6751200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr9:6750200-6750600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
5	chr9:6750200-6751000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
6	chr9:6750200-6751000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr9:6750200-6751000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
8	chr9:6750200-6751000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr9:6750200-6751200	Enhancers	Primary monocytes fromperipheralblood	blood
10	chr9:6750200-6751200	Flanking Active TSS	Primary B cells from cord blood	blood
11	chr9:6750200-6751200	Flanking Active TSS	Primary B cells from peripheral blood	blood
12	chr9:6750200-6751400	Enhancers	Fetal Thymus	thymus
13	chr9:6750400-6750600	Flanking Active TSS	Primary hematopoietic stem cells	blood
14	chr9:6750400-6750600	Active TSS	Primary T helper naive cells from peripheral blood	blood
15	chr9:6750400-6750600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
16	chr9:6750400-6750800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
17	chr9:6750400-6750800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
18	chr9:6750400-6750800	Active TSS	GM12878-XiMat	blood
19	chr9:6750400-6751000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
20	chr9:6750400-6751000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr9:6750400-6751000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr9:6750400-6751000	Active TSS	Primary T killer memory cells from peripheral blood	blood
23	chr9:6750400-6751000	Active TSS	Rectal Mucosa Donor 29	rectum
24	chr9:6750400-6751000	Enhancers	HMEC	breast
25	chr9:6750400-6751000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr9:6750400-6751200	Enhancers	Primary T cells from cord blood	blood
27	chr9:6750400-6751200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
28	chr9:6750600-6750800	Active TSS	Primary hematopoietic stem cells	blood
29	chr9:6750600-6750800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr9:6750600-6751000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
31	chr9:6750600-6751000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr9:6750600-6751000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr9:6750600-6751000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr9:6750600-6751000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
35	chr9:6750600-6751000	Active TSS	Duodenum Mucosa	Duodenum
36	chr9:6750600-6751200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr9:6750600-6751200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
38	chr9:6750600-6751200	Enhancers	Dnd41	blood
39	chr9:6750800-6751000	Flanking Active TSS	Primary hematopoietic stem cells	blood
40	chr9:6750800-6751000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
41	chr9:6750800-6751200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
42	chr9:6750800-6751800	Flanking Active TSS	GM12878-XiMat	blood
43	chr9:6751000-6751200	Enhancers	Primary hematopoietic stem cells	blood
44	chr9:6751000-6751200	Active TSS	Primary T helper cells PMA-I stimulated	--
45	chr9:6751000-6751200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:6751000-6751200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:6751000-6751200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
48	chr9:6751000-6751200	Active TSS	Monocytes-CD14+_RO01746	blood
49	chr9:6751000-6751400	Enhancers	Primary T cells fromperipheralblood	blood
50	chr9:6751000-6751400	Enhancers	Primary T helper cells fromperipheralblood	blood

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