Variant report

Variant	esv3429846
Chromosome Location	chr1:144007818-144094735
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:862)
CpG islands
(count:183)
Chromatin interactive
region (count:17)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:862 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:144009537-144010228	HepG2	liver:	n/a	n/a
2	ATF1	chr1:144007354-144008520	K562	blood:	n/a	n/a
3	ATF3	chr1:144009987-144010286	HepG2	liver:	n/a	n/a
4	BATF	chr1:144036890-144037115	GM12878	blood:	n/a	n/a
5	BATF	chr1:144091634-144091915	GM12878	blood:	n/a	n/a
6	BATF	chr1:144068682-144069090	GM12878	blood:	n/a	chr1:144068921-144068932
7	BATF	chr1:144067068-144067372	GM12878	blood:	n/a	chr1:144067195-144067206
8	BATF	chr1:144067020-144067334	GM12878	blood:	n/a	chr1:144067195-144067206
9	BATF	chr1:144078682-144078883	GM12878	blood:	n/a	n/a
10	BATF	chr1:144094411-144095211	GM12878	blood:	n/a	chr1:144094595-144094605
11	BATF	chr1:144068660-144069151	GM12878	blood:	n/a	chr1:144068921-144068932
12	BCL11A	chr1:144068737-144068972	GM12878	blood:	n/a	chr1:144068891-144068900
13	BCL11A	chr1:144068678-144069120	GM12878	blood:	n/a	chr1:144068891-144068900
14	BCL11A	chr1:144067064-144067392	GM12878	blood:	n/a	chr1:144067198-144067207 chr1:144067199-144067208
15	BDP1	chr1:144010720-144011204	Hela-S3	cervix:	n/a	n/a
16	BDP1	chr1:144015729-144016250	Hela-S3	cervix:	n/a	n/a
17	BDP1	chr1:144012483-144012705	Hela-S3	cervix:	n/a	n/a
18	BDP1	chr1:144009584-144010066	Hela-S3	cervix:	n/a	n/a
19	BDP1	chr1:144014544-144014784	Hela-S3	cervix:	n/a	n/a
20	BHLHE40	chr1:144007605-144007908	HepG2	liver:	n/a	n/a
21	BHLHE40	chr1:144008888-144009019	K562	blood:	n/a	n/a
22	BHLHE40	chr1:144062267-144062414	HepG2	liver:	n/a	n/a
23	BHLHE40	chr1:144009665-144010383	HepG2	liver:	n/a	n/a
24	BHLHE40	chr1:144007856-144008633	K562	blood:	n/a	n/a
25	BRCA1	chr1:144010246-144010408	GM12878	blood:	n/a	n/a
26	BRCA1	chr1:144011162-144011413	GM12878	blood:	n/a	n/a
27	BRCA1	chr1:144013982-144014002	GM12878	blood:	n/a	n/a
28	BRCA1	chr1:144009811-144010169	HepG2	liver:	n/a	n/a
29	BRF1	chr1:144007903-144008287	Hela-S3	cervix:	n/a	n/a
30	BRF1	chr1:144015830-144016214	Hela-S3	cervix:	n/a	n/a
31	BRF1	chr1:144012739-144013432	Hela-S3	cervix:	n/a	n/a
32	CBX3	chr1:144081214-144081820	K562	blood:	n/a	n/a
33	CBX3	chr1:144090319-144090853	K562	blood:	n/a	n/a
34	CBX3	chr1:144081243-144081797	K562	blood:	n/a	n/a
35	CBX3	chr1:144090933-144092074	K562	blood:	n/a	n/a
36	CCNT2	chr1:144007578-144008686	K562	blood:	n/a	n/a
37	CEBPB	chr1:144091003-144091512	K562	blood:	n/a	n/a
38	CEBPB	chr1:144015895-144016153	IMR90	lung:	n/a	n/a
39	CEBPB	chr1:144010716-144011177	IMR90	lung:	n/a	n/a
40	CEBPB	chr1:144091576-144091974	K562	blood:	n/a	n/a
41	CEBPB	chr1:144090439-144090823	K562	blood:	n/a	n/a
42	CEBPB	chr1:144010898-144011226	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr1:144012658-144013264	A549	lung:	n/a	n/a
44	CEBPB	chr1:144012668-144013207	HepG2	liver:	n/a	n/a
45	CEBPB	chr1:144012633-144013313	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:144009099-144009299	K562	blood:	n/a	n/a
47	CEBPB	chr1:144010915-144011222	A549	lung:	n/a	n/a
48	CEBPB	chr1:144091669-144091905	K562	blood:	n/a	n/a
49	CEBPB	chr1:144090475-144090778	K562	blood:	n/a	n/a
50	CEBPB	chr1:144012626-144013828	Hela-S3	cervix:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144015221-144015271	HPAEpiC	pulmonary alveolar:	n/a
2	chr1:144044138-144044188	NT2-D1	testis:	n/a
3	chr1:144044138-144044188	GM12892	blood:	n/a
4	chr1:144008937-144008987	NHBE	bronchial:	n/a
5	chr1:144008937-144008987	MCF-7	breast:	n/a
6	chr1:144015221-144015271	K562	blood:	n/a
7	chr1:144044138-144044188	AG09309	skin:	n/a
8	chr1:144008937-144008987	HIPEpiC	eye:	n/a
9	chr1:144008937-144008987	HL-60	blood:	n/a
10	chr1:144015221-144015271	SK-N-SH_RA	brain:	n/a
11	chr1:144044138-144044188	HCF	heart:	n/a
12	chr1:144044138-144044188	BE2_C	brain:	n/a
13	chr1:144015221-144015271	BJ	skin:	n/a
14	chr1:144015221-144015271	PFSK-1	brain:	n/a
15	chr1:144008937-144008987	HUVEC	blood vessel:	n/a
16	chr1:144015221-144015271	AG04449	skin:	fetal
17	chr1:144008937-144008987	U87	brain:	n/a
18	chr1:144044138-144044188	U87	brain:	n/a
19	chr1:144044138-144044188	HEEpiC	esophagus:	n/a
20	chr1:144044138-144044188	SK-N-SH_RA	brain:	n/a
21	chr1:144008937-144008987	SKMC	muscle:	n/a
22	chr1:144008937-144008987	GM06990	blood:	n/a
23	chr1:144015221-144015271	GM12892	blood:	n/a
24	chr1:144008937-144008987	ProgFib	skin:	n/a
25	chr1:144008937-144008987	HRCEpiC	kidney:	n/a
26	chr1:144015221-144015271	HRPEpiC	eye:	n/a
27	chr1:144008937-144008987	ECC-1	luminal epithelium:	n/a
28	chr1:144044138-144044188	H1-hESC	embryonic stem cell:	embryo
29	chr1:144015221-144015271	Hela-S3	cervix:	n/a
30	chr1:144015221-144015271	CMK	blood:	n/a
31	chr1:144015221-144015271	HCM	heart:	n/a
32	chr1:144044138-144044188	GM06990	blood:	n/a
33	chr1:144008937-144008987	SK-N-SH	brain:	n/a
34	chr1:144008937-144008987	CMK	blood:	n/a
35	chr1:144015221-144015271	HCF	heart:	n/a
36	chr1:144008937-144008987	H1-hESC	embryonic stem cell:	embryo
37	chr1:144015221-144015271	GM19239	blood:	n/a
38	chr1:144044138-144044188	HIPEpiC	eye:	n/a
39	chr1:144008937-144008987	LNCaP	prostate:	n/a
40	chr1:144008937-144008987	NHDF-neo	bronchial:	n/a
41	chr1:144008937-144008987	BJ	skin:	n/a
42	chr1:144044138-144044188	HCM	heart:	n/a
43	chr1:144015221-144015271	AG04450	lung:	fetal
44	chr1:144008937-144008987	NB4	blood:	n/a
45	chr1:144008937-144008987	NT2-D1	testis:	n/a
46	chr1:144015221-144015271	A549	lung:	n/a
47	chr1:144044138-144044188	HepG2	liver:	n/a
48	chr1:144015221-144015271	HMEC	breast:	n/a
49	chr1:144044138-144044188	GM12891	blood:	n/a
50	chr1:144008937-144008987	A549	lung:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:144006261..144009396-chr1:144011579..144015331,3	MCF-7	breast:
2	chr1:144005794..144008523-chr1:144009105..144010733,2	K562	blood:
3	chr1:144008498..144010730-chr1:144011056..144012625,2	MCF-7	breast:
4	chr1:144010495..144012548-chr1:144014486..144017526,3	MCF-7	breast:
5	chr1:144005391..144007992-chr1:144016509..144019128,2	MCF-7	breast:
6	chr1:144011179..144012723-chr1:144016173..144018871,2	MCF-7	breast:
7	chr1:144005391..144007992-chr1:144016509..144019128,2	MCF-7	breast:
8	chr1:144008498..144010730-chr1:144011056..144012625,2	MCF-7	breast:
9	chr1:144005794..144008523-chr1:144009105..144010733,2	K562	blood:
10	chr1:144010824..144012800-chr12:56121573..56123817,2	MCF-7	breast:
11	chr1:144019336..144020898-chr1:206481705..206484114,2	MCF-7	breast:
12	chr1:144011179..144012723-chr1:144016173..144018871,2	MCF-7	breast:
13	chr1:144003920..144006822-chr1:144010130..144014545,4	K562	blood:
14	chr1:144006261..144009396-chr1:144011579..144015331,3	MCF-7	breast:
15	chr1:144010495..144012548-chr1:144014486..144017526,3	MCF-7	breast:
16	chr1:144007296..144010001-chr1:144014414..144016453,2	K562	blood:
17	chr1:144007296..144010001-chr1:144014414..144016453,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM72D-1	chr1:144091810-144091946	ENSG00000224363
2	lnc-FAM72D-1	chr1:144088423-144088668	NONHSAT005767
3	lnc-FAM72D-3	chr1:144084411-144084864	NONHSAT005763
4	lnc-FAM72D-3	chr1:144086700-144086911	NONHSAT005763
5	lnc-FAM72D-1	chr1:144088374-144088668	NONHSAT005765
6	lnc-FAM72D-1	chr1:144089214-144091251	ENSG00000224363
7	lnc-FAM72D-1	chr1:144093413-144093719	NONHSAT005766
8	lnc-FAM72D-1	chr1:144089281-144089406	NONHSAT005767
9	lnc-FAM72D-1	chr1:144088374-144088668	NONHSAT005766
10	lnc-FAM72D-1	chr1:144087482-144087804	NONHSAT005764
11	lnc-FAM72D-1	chr1:144087524-144087804	NONHSAT005765
12	lnc-FAM72D-1	chr1:144087684-144087804	NONHSAT005766
13	lnc-FAM72D-1	chr1:144089058-144089129	NONHSAT005765
14	lnc-FAM72D-1	chr1:144087901-144088049	NONHSAT005764
15	lnc-FAM72D-1	chr1:144087901-144088049	NONHSAT005766
16	lnc-FAM72D-1	chr1:144093413-144093754	NONHSAT005764
17	lnc-FAM72D-3	chr1:144083445-144085155	ucscGeneNc_uc001eng_1
18	lnc-FAM72D-2	chr1:144085156-144086051	ucscGeneNc_uc001enh_1

No data

Variant related genes	Relation type
ENSG00000224363	TF binding region
ENSG00000271644	TF binding region
ENSG00000224363	CpG island
ENSG00000271644	CpG island
ENSG00000258056	chromatin interactions
ENSG00000135404	chromatin interactions

Extended variants
information (count: 2372 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:2372 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6694902	chr1:144007842-144007843	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs587646107	chr1:144007862-144007863	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs587703154	chr1:144007919-144007920	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs587775864	chr1:144007927-144007928	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs587644365	chr1:144008019-144008020	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs587697542	chr1:144008068-144008069	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs587759112	chr1:144008099-144008100	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376534471	chr1:144008114-144008115	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544462419	chr1:144008117-144008118	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6600705	chr1:144008119-144008120	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs587710918	chr1:144008179-144008180	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs587610954	chr1:144008205-144008206	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587651086	chr1:144008224-144008225	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587708151	chr1:144008321-144008322	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377651580	chr1:144008323-144008324	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs587662877	chr1:144008328-144008329	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs587734160	chr1:144008357-144008358	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs587594143	chr1:144008433-144008434	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587665756	chr1:144008445-144008446	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs7547126	chr1:144008458-144008459	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587749951	chr1:144008479-144008480	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs1884149	chr1:144008509-144008510	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7547106	chr1:144008512-144008513	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587653954	chr1:144008594-144008595	Enhancers Genic enhancers Flanking Active TSS Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587686899	chr1:144008600-144008601	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs7536026	chr1:144008611-144008612	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12127414	chr1:144008618-144008619	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12127397	chr1:144008658-144008659	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs6600704	chr1:144008672-144008673	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587769602	chr1:144008745-144008746	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs587616489	chr1:144008849-144008850	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587698373	chr1:144008854-144008855	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs587750542	chr1:144008869-144008870	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs587632252	chr1:144008887-144008888	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587689757	chr1:144008903-144008904	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs587755552	chr1:144008920-144008921	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587650959	chr1:144008936-144008937	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587710227	chr1:144008940-144008941	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587765255	chr1:144008957-144008958	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587629243	chr1:144008961-144008962	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587714907	chr1:144009008-144009009	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs6691358	chr1:144009009-144009010	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs587595652	chr1:144009011-144009012	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs587670627	chr1:144009031-144009032	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs12033165	chr1:144009053-144009054	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587733870	chr1:144009065-144009066	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs6698999	chr1:144009118-144009119	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201779728	chr1:144009132-144009133	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6695951	chr1:144009150-144009151	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12034007	chr1:144009172-144009173	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:160)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Williams Syndrome	20824207	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	23813976	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	20729466	CNVD

Chromatin state (count:1363 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:143999200-144013800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr1:143999200-144013800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr1:143999200-144013800	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr1:143999200-144013800	Weak transcription	Dnd41	blood
5	chr1:143999200-144014000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr1:144001600-144009600	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr1:144002800-144013600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr1:144003200-144008000	Weak transcription	Liver	Liver
9	chr1:144003800-144013800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr1:144005000-144008800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr1:144005200-144008600	Strong transcription	Primary B cells from cord blood	blood
12	chr1:144005600-144008200	Weak transcription	Esophagus	oesophagus
13	chr1:144005600-144010400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr1:144005800-144008800	Weak transcription	Fetal Intestine Small	intestine
15	chr1:144005800-144009600	Weak transcription	Fetal Intestine Large	intestine
16	chr1:144006400-144015600	Genic enhancers	Fetal Muscle Leg	muscle
17	chr1:144006400-144019400	Strong transcription	Primary T cells from cord blood	blood
18	chr1:144006600-144008000	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:144006600-144008000	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr1:144006600-144008200	Genic enhancers	HepG2	liver
21	chr1:144006600-144008600	Enhancers	Brain Germinal Matrix	brain
22	chr1:144006600-144009200	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr1:144006600-144010200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr1:144006600-144010600	Enhancers	Placenta	Placenta
25	chr1:144006600-144011400	Enhancers	Left Ventricle	heart
26	chr1:144006600-144011400	Enhancers	Ovary	ovary
27	chr1:144006600-144013200	Enhancers	Spleen	Spleen
28	chr1:144006600-144014200	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr1:144006800-144008000	Enhancers	Brain Anterior Caudate	brain
30	chr1:144006800-144008200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:144006800-144008200	Enhancers	NHDF-Ad	bronchial
32	chr1:144006800-144008400	Enhancers	Fetal Brain Female	brain
33	chr1:144006800-144009000	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr1:144006800-144009600	Enhancers	Brain Cingulate Gyrus	brain
35	chr1:144006800-144009600	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr1:144006800-144009800	Enhancers	NHLF	lung
37	chr1:144006800-144010400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr1:144006800-144011000	Enhancers	K562	blood
39	chr1:144006800-144011400	Enhancers	Lung	lung
40	chr1:144006800-144012200	Enhancers	HUVEC	blood vessel
41	chr1:144006800-144013200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:144006800-144013600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr1:144006800-144013800	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr1:144006800-144014000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr1:144006800-144015200	Enhancers	Right Atrium	heart
46	chr1:144007000-144008000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:144007000-144008200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr1:144007000-144009000	Enhancers	Fetal Muscle Trunk	muscle
49	chr1:144007200-144008200	Weak transcription	Pancreas	Pancrea
50	chr1:144007200-144008400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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