Variant report

Variant	esv3386885
Chromosome Location	chr11:46140826-46145624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1071)
CpG islands
(count:612)
Chromatin interactive
region (count:29)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1071 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46143897-46144099	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:46144336-46144766	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:46144371-46144871	K562	blood:	n/a	n/a
4	ARID3A	chr11:46140655-46141090	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:46143322-46143585	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:46142914-46143059	K562	blood:	n/a	n/a
7	ATF3	chr11:46142430-46143127	A549	lung:	n/a	n/a
8	BCL3	chr11:46142399-46143143	A549	lung:	n/a	chr11:46143007-46143016
9	BCL3	chr11:46142338-46142949	A549	lung:	n/a	n/a
10	BCLAF1	chr11:46142792-46143216	GM12878	blood:	n/a	chr11:46143007-46143016
11	BCLAF1	chr11:46140890-46141820	GM12878	blood:	n/a	chr11:46141629-46141638
12	BHLHE40	chr11:46140847-46141745	GM12878	blood:	n/a	chr11:46141718-46141734
13	BHLHE40	chr11:46141001-46141298	K562	blood:	n/a	n/a
14	BHLHE40	chr11:46142369-46143089	K562	blood:	n/a	chr11:46142991-46143007
15	BHLHE40	chr11:46143380-46143851	K562	blood:	n/a	chr11:46143696-46143712 chr11:46143642-46143658
16	BHLHE40	chr11:46142573-46143793	GM12878	blood:	n/a	chr11:46143696-46143712 chr11:46142991-46143007 chr11:46143642-46143658
17	BRCA1	chr11:46142854-46143074	GM12878	blood:	n/a	n/a
18	BRCA1	chr11:46140741-46141369	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr11:46143978-46144218	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr11:46142870-46143067	H1-hESC	embryonic stem cell:	n/a	n/a
21	BRCA1	chr11:46142320-46142919	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr11:46142905-46143053	HepG2	liver:	n/a	n/a
23	BRCA1	chr11:46143369-46143533	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr11:46142793-46143064	K562	blood:	n/a	n/a
25	CCNT2	chr11:46142347-46143802	K562	blood:	n/a	chr11:46142804-46142813 chr11:46142789-46142798
26	CCNT2	chr11:46141220-46141710	K562	blood:	n/a	chr11:46141239-46141248
27	CEBPB	chr11:46144992-46145257	A549	lung:	n/a	n/a
28	CEBPB	chr11:46140751-46141502	A549	lung:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
29	CEBPB	chr11:46143770-46143889	IMR90	lung:	n/a	n/a
30	CEBPB	chr11:46144633-46144718	HepG2	liver:	n/a	n/a
31	CEBPB	chr11:46140844-46141222	K562	blood:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
32	CEBPB	chr11:46142890-46143074	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:46140707-46141233	HepG2	liver:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
34	CEBPB	chr11:46140783-46141245	IMR90	lung:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
35	CEBPB	chr11:46140796-46141146	HepG2	liver:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
36	CEBPB	chr11:46143283-46144052	A549	lung:	n/a	chr11:46143931-46143943
37	CEBPB	chr11:46143768-46143876	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:46140777-46141219	K562	blood:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
39	CEBPB	chr11:46140331-46141693	Hela-S3	cervix:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
40	CEBPB	chr11:46142895-46143034	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr11:46142319-46144272	Hela-S3	cervix:	n/a	chr11:46143931-46143943
42	CEBPB	chr11:46140857-46141210	MCF-7	breast:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
43	CEBPB	chr11:46140868-46141109	K562	blood:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
44	CEBPB	chr11:46140814-46141286	A549	lung:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
45	CEBPB	chr11:46140738-46141163	HepG2	liver:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
46	CEBPB	chr11:46140819-46141366	A549	lung:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
47	CEBPB	chr11:46140828-46141245	HepG2	liver:	n/a	chr11:46141016-46141027 chr11:46141016-46141029
48	CEBPD	chr11:46141337-46141612	HepG2	liver:	n/a	n/a
49	CEBPD	chr11:46142274-46142549	HepG2	liver:	n/a	n/a
50	CEBPD	chr11:46143080-46143825	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46141207-46141257	NB4	blood:	n/a
2	chr11:46143993-46144043	ovcar-3	ovarian:	n/a
3	chr11:46141207-46141257	NB4	blood:	n/a
4	chr11:46143993-46144043	ovcar-3	ovarian:	n/a
5	chr11:46142000-46142050	GM12878	blood:	n/a
6	chr11:46143011-46143061	U87	brain:	n/a
7	chr11:46143461-46143511	PFSK-1	brain:	n/a
8	chr11:46141386-46141436	HCM	heart:	n/a
9	chr11:46143011-46143061	AG04449	skin:	fetal
10	chr11:46142000-46142050	IMR90	lung:	fetal
11	chr11:46143434-46143484	HCPEpiC	choroid plexus:	n/a
12	chr11:46142000-46142050	MCF10A-Er-Src	breast:	n/a
13	chr11:46142000-46142050	GM12891	blood:	n/a
14	chr11:46141207-46141257	SK-N-MC	brain:	n/a
15	chr11:46142000-46142050	HNPCEpiC	eye:	n/a
16	chr11:46143993-46144043	GM06990	blood:	n/a
17	chr11:46143000-46143050	HCF	heart:	n/a
18	chr11:46141172-46141222	A549	lung:	n/a
19	chr11:46141172-46141222	MCF10A-Er-Src	breast:	n/a
20	chr11:46143461-46143511	HUVEC	blood vessel:	n/a
21	chr11:46141207-46141257	SK-N-SH_RA	brain:	n/a
22	chr11:46143993-46144043	PANC-1	pancreas:	n/a
23	chr11:46143993-46144043	SKMC	muscle:	n/a
24	chr11:46142000-46142050	ProgFib	skin:	n/a
25	chr11:46143014-46143064	HUVEC	blood vessel:	n/a
26	chr11:46143011-46143061	PrEC	prostate:	n/a
27	chr11:46141386-46141436	HRCEpiC	kidney:	n/a
28	chr11:46141172-46141222	ECC-1	luminal epithelium:	n/a
29	chr11:46141207-46141257	AG04449	skin:	fetal
30	chr11:46143011-46143061	AG04450	lung:	fetal
31	chr11:46143434-46143484	AG04449	skin:	fetal
32	chr11:46143993-46144043	NHDF-neo	bronchial:	n/a
33	chr11:46143014-46143064	GM06990	blood:	n/a
34	chr11:46141207-46141257	HRE	kidney:	n/a
35	chr11:46143993-46144043	AG09319	gingival:	n/a
36	chr11:46141207-46141257	MCF-7	breast:	n/a
37	chr11:46143993-46144043	Hela-S3	cervix:	n/a
38	chr11:46141386-46141436	Hepatocyte	liver:	n/a
39	chr11:46143461-46143511	RPTEC	kidney:	n/a
40	chr11:46143461-46143511	ProgFib	skin:	n/a
41	chr11:46141172-46141222	HL-60	blood:	n/a
42	chr11:46142000-46142050	HIPEpiC	eye:	n/a
43	chr11:46143011-46143061	SK-N-SH	brain:	n/a
44	chr11:46141172-46141222	PANC-1	pancreas:	n/a
45	chr11:46143000-46143050	Caco-2	colon:	n/a
46	chr11:46142000-46142050	HCPEpiC	choroid plexus:	n/a
47	chr11:46141207-46141257	SK-N-SH	brain:	n/a
48	chr11:46142000-46142050	SK-N-MC	brain:	n/a
49	chr11:46143434-46143484	H1-hESC	embryonic stem cell:	embryo
50	chr11:46141207-46141257	Hepatocyte	liver:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:46142872..46144744-chr11:46382813..46385236,2	MCF-7	breast:
2	chr11:46143681..46146343-chr11:46159365..46161019,2	K562	blood:
3	chr11:46013966..46016594-chr11:46138214..46140856,2	K562	blood:
4	chr11:46136566..46145134-chr11:46256772..46268048,26	K562	blood:
5	chr11:46140775..46145022-chr11:46256711..46262008,9	MCF-7	breast:
6	chr11:46143507..46145451-chr11:46333298..46335406,2	K562	blood:
7	chr11:46141780..46143612-chr11:46331038..46333172,2	MCF-7	breast:
8	chr11:46028036..46029889-chr11:46143429..46146254,2	K562	blood:
9	chr11:46125754..46127349-chr11:46143825..46145810,2	MCF-7	breast:
10	chr11:45986176..45988319-chr11:46143475..46145056,2	MCF-7	breast:
11	chr11:45942020..45943576-chr11:46141975..46144467,2	MCF-7	breast:
12	chr11:46141950..46143787-chr11:46718847..46721759,2	K562	blood:
13	chr11:46141914..46143962-chr11:46401995..46404790,2	K562	blood:
14	chr11:46140376..46142887-chr11:46639092..46640615,2	MCF-7	breast:
15	chr11:46141504..46142447-chr19:8386292..8386834,2	NB4	blood:
16	chr11:45939411..45941074-chr11:46142423..46143961,2	MCF-7	breast:
17	chr11:46139740..46148810-chr11:46253862..46264263,27	K562	blood:
18	chr11:45942684..45944705-chr11:46141351..46143147,2	K562	blood:
19	chr11:45920093..45922965-chr11:46143378..46145105,2	K562	blood:
20	chr1:28286209..28286793-chr11:46142913..46143431,2	Hela-S3	cervix:
21	chr11:46141272..46145852-chr11:46256882..46262702,15	MCF-7	breast:
22	chr11:45867136..45869190-chr11:46140608..46142204,2	K562	blood:
23	chr1:27985504..27986010-chr11:46141635..46142214,2	Hela-S3	cervix:
24	chr11:46141379..46143279-chr11:46237350..46239276,2	MCF-7	breast:
25	chr11:46143580..46145236-chr11:46369479..46372129,2	MCF-7	breast:
26	chr11:46092605..46094562-chr11:46143473..46145813,3	K562	blood:
27	chr11:46143224..46145220-chr11:46317344..46319023,2	K562	blood:
28	chr11:46142486..46143034-chr5:64064158..64064978,2	Hela-S3	cervix:
29	chr11:45867179..45868974-chr11:46142893..46144558,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PEX16-4	chr11:46141275-46141378	NONHSAT021153

No data

Variant related genes	Relation type
PHF21A	TF binding region
PHF21A	CpG island
ENSG00000180423	chromatin interactions
ENSG00000227050	chromatin interactions
ENSG00000121680	chromatin interactions
ENSG00000175220	chromatin interactions
ENSG00000149091	chromatin interactions
ENSG00000121671	chromatin interactions
ENSG00000165905	chromatin interactions
ENSG00000175224	chromatin interactions
ENSG00000157613	chromatin interactions
ENSG00000254639	chromatin interactions
ENSG00000153006	chromatin interactions
ENSG00000135365	chromatin interactions
ENSG00000110492	chromatin interactions
ENSG00000233927	chromatin interactions
ENSG00000153015	chromatin interactions
ENSG00000255269	chromatin interactions

Extended variants
information (count: 141 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:141 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192668534	chr11:46140894-46140895	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs570658680	chr11:46140911-46140912	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs1132657	chr11:46140922-46140923	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs4281461	chr11:46140935-46140936	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs114728305	chr11:46140960-46140961	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs77205953	chr11:46140964-46140965	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs185618979	chr11:46141010-46141011	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs541557747	chr11:46141024-46141025	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs564461132	chr11:46141036-46141037	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs201635943	chr11:46141108-46141109	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs371365529	chr11:46141112-46141113	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs533395868	chr11:46141133-46141134	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs144146541	chr11:46141134-46141135	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs190092193	chr11:46141158-46141159	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs192835366	chr11:46141180-46141181	Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs529600830	chr11:46141243-46141244	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs549263759	chr11:46141248-46141249	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs61884080	chr11:46141292-46141293	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
19	rs185376348	chr11:46141295-46141296	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs397803889	chr11:46141309-46141310	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs190203499	chr11:46141310-46141311	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs566309959	chr11:46141312-46141313	Active TSS Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs533640819	chr11:46141358-46141359	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
24	rs563438457	chr11:46141373-46141374	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
25	rs193174046	chr11:46141391-46141392	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs148683230	chr11:46141422-46141423	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs55722202	chr11:46141440-46141441	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs539017408	chr11:46141450-46141451	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs555754158	chr11:46141511-46141512	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs575889317	chr11:46141569-46141570	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs535741318	chr11:46141584-46141585	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs555266199	chr11:46141594-46141595	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs572240947	chr11:46141624-46141625	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs541146453	chr11:46141629-46141630	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs374773338	chr11:46141769-46141770	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs558256455	chr11:46141797-46141798	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs578156087	chr11:46141798-46141799	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
38	rs74366855	chr11:46141823-46141824	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
39	rs563676499	chr11:46141867-46141868	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs200621220	chr11:46141886-46141887	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs545259668	chr11:46141888-46141889	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs376281870	chr11:46141889-46141890	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs201588912	chr11:46141893-46141894	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs529558339	chr11:46141902-46141903	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs552058237	chr11:46141910-46141911	Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs543346610	chr11:46141950-46141951	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs559675326	chr11:46142027-46142028	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs528711676	chr11:46142115-46142116	Active TSS Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs75796602	chr11:46142254-46142255	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs551579880	chr11:46142261-46142262	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21364760	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46138200-46144200	Active TSS	Ovary	ovary
2	chr11:46138600-46141000	Weak transcription	Spleen	Spleen
3	chr11:46138800-46141400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr11:46138800-46141400	Flanking Active TSS	Dnd41	blood
5	chr11:46138800-46144600	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr11:46138800-46144800	Active TSS	ES-I3 Cell Line	embryonic stem cell
7	chr11:46139000-46141000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
8	chr11:46139000-46144400	Active TSS	GM12878-XiMat	blood
9	chr11:46139200-46141200	Flanking Active TSS	Primary B cells from cord blood	blood
10	chr11:46139200-46144200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr11:46139400-46141200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
12	chr11:46139400-46141200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
13	chr11:46139400-46141200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr11:46139400-46141400	Flanking Active TSS	Primary hematopoietic stem cells	blood
15	chr11:46139400-46141400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr11:46139400-46144600	Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr11:46139600-46142400	Active TSS	Right Atrium	heart
18	chr11:46139600-46144000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr11:46139600-46144400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:46139600-46145000	Active TSS	H1 Cell Line	embryonic stem cell
21	chr11:46139800-46141200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
22	chr11:46139800-46144600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:46139800-46144600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr11:46139800-46144600	Active TSS	K562	blood
25	chr11:46140000-46141000	Flanking Active TSS	Brain Anterior Caudate	brain
26	chr11:46140000-46141800	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
27	chr11:46140200-46141000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
28	chr11:46140200-46141000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr11:46140200-46141000	Flanking Active TSS	Brain Hippocampus Middle	brain
30	chr11:46140200-46141000	Flanking Active TSS	Duodenum Mucosa	Duodenum
31	chr11:46140200-46141200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr11:46140200-46141200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:46140200-46141400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
34	chr11:46140200-46141800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
35	chr11:46140200-46143800	Active TSS	Primary T cells fromperipheralblood	blood
36	chr11:46140200-46144400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr11:46140200-46144400	Active TSS	Rectal Mucosa Donor 29	rectum
38	chr11:46140200-46144400	Active TSS	NHLF	lung
39	chr11:46140200-46144600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr11:46140200-46144600	Active TSS	HUES6 Cell Line	embryonic stem cell
41	chr11:46140200-46144600	Active TSS	Brain Germinal Matrix	brain
42	chr11:46140400-46141000	Flanking Active TSS	Primary T cells from cord blood	blood
43	chr11:46140400-46141000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr11:46140400-46141000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
45	chr11:46140400-46141000	Flanking Active TSS	Fetal Intestine Small	intestine
46	chr11:46140400-46141000	Flanking Active TSS	Fetal Muscle Leg	muscle
47	chr11:46140400-46141000	Flanking Active TSS	HMEC	breast
48	chr11:46140400-46141200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
49	chr11:46140400-46141200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr11:46140400-46141200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood

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