Variant report

Variant	esv1817820
Chromosome Location	chr1:145184155-145291431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2192)
CpG islands
(count:611)
Chromatin interactive
region (count:42)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2192 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145289928-145289938	K562	blood:	n/a	n/a
2	ARID3A	chr1:145254404-145254507	K562	blood:	n/a	n/a
3	ARID3A	chr1:145253698-145253898	K562	blood:	n/a	n/a
4	ARID3A	chr1:145208951-145209121	K562	blood:	n/a	chr1:145209007-145209015
5	ARID3A	chr1:145246167-145246562	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:145208929-145209290	HepG2	liver:	n/a	chr1:145209007-145209015
7	ATF1	chr1:145195978-145196042	K562	blood:	n/a	n/a
8	ATF1	chr1:145216140-145216326	K562	blood:	n/a	n/a
9	ATF1	chr1:145208937-145209133	K562	blood:	n/a	n/a
10	ATF1	chr1:145254447-145254481	K562	blood:	n/a	n/a
11	ATF2	chr1:145208822-145209212	GM12878	blood:	n/a	n/a
12	ATF2	chr1:145233655-145233883	GM12878	blood:	n/a	n/a
13	ATF2	chr1:145291190-145292070	GM12878	blood:	n/a	n/a
14	ATF3	chr1:145208814-145209112	A549	lung:	n/a	n/a
15	ATF3	chr1:145208827-145209217	A549	lung:	n/a	n/a
16	BACH1	chr1:145254231-145254659	K562	blood:	n/a	n/a
17	BACH1	chr1:145253854-145253876	K562	blood:	n/a	n/a
18	BACH1	chr1:145254230-145254652	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr1:145208936-145209146	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr1:145210338-145210530	GM12878	blood:	n/a	n/a
21	BATF	chr1:145209382-145209998	GM12878	blood:	n/a	n/a
22	BATF	chr1:145277151-145277624	GM12878	blood:	n/a	n/a
23	BATF	chr1:145233198-145234079	GM12878	blood:	n/a	n/a
24	BATF	chr1:145277155-145277522	GM12878	blood:	n/a	n/a
25	BATF	chr1:145210075-145210284	GM12878	blood:	n/a	n/a
26	BATF	chr1:145285189-145285435	GM12878	blood:	n/a	n/a
27	BATF	chr1:145233237-145234045	GM12878	blood:	n/a	n/a
28	BATF	chr1:145213599-145213876	GM12878	blood:	n/a	n/a
29	BATF	chr1:145212001-145212472	GM12878	blood:	n/a	n/a
30	BATF	chr1:145281369-145281733	GM12878	blood:	n/a	n/a
31	BATF	chr1:145195914-145196301	GM12878	blood:	n/a	n/a
32	BATF	chr1:145234968-145235329	GM12878	blood:	n/a	n/a
33	BATF	chr1:145290357-145290900	GM12878	blood:	n/a	n/a
34	BATF	chr1:145231709-145232035	GM12878	blood:	n/a	n/a
35	BATF	chr1:145210057-145210394	GM12878	blood:	n/a	n/a
36	BATF	chr1:145234411-145234753	GM12878	blood:	n/a	n/a
37	BATF	chr1:145212132-145212476	GM12878	blood:	n/a	n/a
38	BATF	chr1:145208490-145209291	GM12878	blood:	n/a	chr1:145209134-145209142
39	BATF	chr1:145259491-145259713	GM12878	blood:	n/a	chr1:145259620-145259631
40	BATF	chr1:145219743-145220000	GM12878	blood:	n/a	n/a
41	BATF	chr1:145234955-145235323	GM12878	blood:	n/a	n/a
42	BATF	chr1:145218967-145219192	GM12878	blood:	n/a	chr1:145218977-145218990
43	BATF	chr1:145189103-145189407	GM12878	blood:	n/a	n/a
44	BATF	chr1:145260188-145260447	GM12878	blood:	n/a	n/a
45	BCL11A	chr1:145228759-145228989	GM12878	blood:	n/a	n/a
46	BCL11A	chr1:145219707-145219881	GM12878	blood:	n/a	n/a
47	BCL11A	chr1:145208542-145209895	GM12878	blood:	n/a	chr1:145209027-145209040 chr1:145209689-145209702 chr1:145209045-145209058 chr1:145209538-145209551 chr1:145209041-145209054 chr1:145209454-145209462 chr1:145209010-145209019
48	BCL11A	chr1:145208600-145209261	GM12878	blood:	n/a	chr1:145209027-145209040 chr1:145209045-145209058 chr1:145209041-145209054 chr1:145209010-145209019
49	BCL11A	chr1:145253572-145253790	GM12878	blood:	n/a	n/a
50	BCL11A	chr1:145195841-145196148	GM12878	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145210014-145210064	H1-hESC	embryonic stem cell:	embryo
2	chr1:145210014-145210064	H1-hESC	embryonic stem cell:	embryo
3	chr1:145205174-145205224	NHBE	bronchial:	n/a
4	chr1:145209930-145209980	PrEC	prostate:	n/a
5	chr1:145208980-145209030	SK-N-MC	brain:	n/a
6	chr1:145208980-145209030	H1-hESC	embryonic stem cell:	embryo
7	chr1:145205174-145205224	GM12892	blood:	n/a
8	chr1:145211389-145211439	HRE	kidney:	n/a
9	chr1:145209930-145209980	NT2-D1	testis:	n/a
10	chr1:145208980-145209030	SAEC	small airway:	n/a
11	chr1:145213338-145213388	H1-hESC	embryonic stem cell:	embryo
12	chr1:145209236-145209286	NHDF-neo	bronchial:	n/a
13	chr1:145209830-145209880	HCF	heart:	n/a
14	chr1:145210014-145210064	SAEC	small airway:	n/a
15	chr1:145209930-145209980	NHBE	bronchial:	n/a
16	chr1:145210014-145210064	HL-60	blood:	n/a
17	chr1:145213338-145213388	GM12891	blood:	n/a
18	chr1:145209236-145209286	HMEC	breast:	n/a
19	chr1:145208980-145209030	GM12878	blood:	n/a
20	chr1:145213338-145213388	HRPEpiC	eye:	n/a
21	chr1:145213338-145213388	HCPEpiC	choroid plexus:	n/a
22	chr1:145205174-145205224	ovcar-3	ovarian:	n/a
23	chr1:145207943-145207993	SK-N-SH	brain:	n/a
24	chr1:145208980-145209030	Caco-2	colon:	n/a
25	chr1:145209236-145209286	MCF-7	breast:	n/a
26	chr1:145211389-145211439	HUVEC	blood vessel:	n/a
27	chr1:145209830-145209880	GM12891	blood:	n/a
28	chr1:145209930-145209980	Caco-2	colon:	n/a
29	chr1:145209830-145209880	IMR90	lung:	fetal
30	chr1:145209930-145209980	SAEC	small airway:	n/a
31	chr1:145209930-145209980	GM19239	blood:	n/a
32	chr1:145209830-145209880	NH-A	brain:	n/a
33	chr1:145209930-145209980	ProgFib	skin:	n/a
34	chr1:145213338-145213388	HL-60	blood:	n/a
35	chr1:145210014-145210064	PANC-1	pancreas:	n/a
36	chr1:145210014-145210064	U87	brain:	n/a
37	chr1:145250914-145250964	PrEC	prostate:	n/a
38	chr1:145209830-145209880	PrEC	prostate:	n/a
39	chr1:145209930-145209980	HCF	heart:	n/a
40	chr1:145211389-145211439	NHBE	bronchial:	n/a
41	chr1:145209236-145209286	H1-hESC	embryonic stem cell:	embryo
42	chr1:145211389-145211439	RPTEC	kidney:	n/a
43	chr1:145209236-145209286	CMK	blood:	n/a
44	chr1:145209236-145209286	HRPEpiC	eye:	n/a
45	chr1:145213338-145213388	GM19239	blood:	n/a
46	chr1:145211389-145211439	GM12892	blood:	n/a
47	chr1:145211389-145211439	HRCEpiC	kidney:	n/a
48	chr1:145209830-145209880	GM19239	blood:	n/a
49	chr1:145211389-145211439	SAEC	small airway:	n/a
50	chr1:145209236-145209286	SK-N-MC	brain:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:145209779..145211659-chr1:145381647..145384503,2	MCF-7	breast:
2	chr1:120610094..120613669-chr1:145207447..145211087,11	MCF-7	breast:
3	chr1:145246366..145248846-chr1:149222454..149225152,2	MCF-7	breast:
4	chr1:120610124..120613523-chr1:145208226..145211226,7	MCF-7	breast:
5	chr1:145257082..145259251-chr1:145260108..145261925,2	MCF-7	breast:
6	chr1:120602747..120604407-chr1:145216153..145218112,2	MCF-7	breast:
7	chr1:145110521..145113203-chr1:145271699..145274224,2	MCF-7	breast:
8	chr1:120562393..120564845-chr1:145256114..145258582,3	MCF-7	breast:
9	chr1:120611803..120612535-chr1:145208972..145209627,6	MCF-7	breast:
10	chr1:145207909..145210605-chr1:145214441..145216644,2	MCF-7	breast:
11	chr1:120611941..120612674-chr1:145209107..145209637,6	MCF-7	breast:
12	chr1:120611958..120612515-chr1:145208972..145209639,2	NB4	blood:
13	chr1:145209931..145210445-chr19:58874333..58874839,2	Hela-S3	cervix:
14	chr1:145264618..145267295-chr1:145381743..145384010,2	K562	blood:
15	chr1:145209043..145210611-chr1:149222292..149224968,3	MCF-7	breast:
16	chr1:120611825..120612753-chr1:145208933..145209629,3	Hela-S3	cervix:
17	chr1:120574754..120575346-chr1:145245858..145246575,2	MCF-7	breast:
18	chr1:145208945..145211572-chr1:145290799..145293780,3	MCF-7	breast:
19	chr1:120565033..120566748-chr1:145252742..145255259,2	MCF-7	breast:
20	chr1:145287740..145289244-chr18:67226861..67228381,2	MCF-7	breast:
21	chr1:120555279..120557791-chr1:145264672..145267612,3	K562	blood:
22	chr1:120573750..120576750-chr1:145244417..145247281,4	MCF-7	breast:
23	chr1:120561821..120563990-chr1:145256491..145258504,4	MCF-7	breast:
24	chr1:53163301..53163992-chr1:145209547..145210339,2	Hela-S3	cervix:
25	chr1:145258606..145260477-chr1:145381662..145384269,2	MCF-7	breast:
26	chr1:145288943..145293306-chr1:149221737..149224658,6	MCF-7	breast:
27	chr1:145289699..145292602-chr1:149222944..149224949,3	MCF-7	breast:
28	chr1:120562041..120564945-chr1:145257130..145258905,2	K562	blood:
29	chr1:145210633..145213326-chr1:149222498..149224954,2	MCF-7	breast:
30	chr1:145209435..145210070-chr1:145293272..145293941,2	MCF-7	breast:
31	chr1:145257082..145259251-chr1:145260108..145261925,2	MCF-7	breast:
32	chr1:145130093..145132779-chr1:145291052..145292604,2	K562	blood:
33	chr1:120533140..120534660-chr1:145287386..145288888,2	MCF-7	breast:
34	chr1:120606120..120607638-chr1:145207438..145208952,2	MCF-7	breast:
35	chr1:145238836..145241577-chr1:145243504..145245771,2	K562	blood:
36	chr1:145290091..145292740-chr1:145382337..145384639,2	MCF-7	breast:
37	chr1:145238836..145241577-chr1:145243504..145245771,2	K562	blood:
38	chr1:145208945..145211572-chr1:145290799..145293780,3	MCF-7	breast:
39	chr1:145209133..145210911-chr1:145213297..145216185,2	MCF-7	breast:
40	chr1:145208214..145210170-chr1:145381446..145384467,3	MCF-7	breast:
41	chr1:145193254..145195284-chr1:145382712..145384267,2	MCF-7	breast:
42	chr1:120576520..120578439-chr1:145242059..145244929,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBPF10-1	chr1:145213108-145213374	expReg_chr1_15650_+
2	lnc-PDE4DIP-6	chr1:145200338-145200891	ENSG00000272709.1
3	lnc-NOTCH2NL-2	chr1:145290429-145290511	NR_104217
4	lnc-NOTCH2NL-2	chr1:145289770-145289906	NR_104217
5	lnc-NOTCH2NL-2	chr1:145290781-145290850	NONHSAT005883
6	lnc-NOTCH2NL-2	chr1:145290422-145290511	NONHSAT005883

No data

Variant related genes	Relation type
ENSG00000272709	TF binding region
NOTCH2NL	TF binding region
ENSG00000255168	TF binding region
NBPF10	TF binding region
ENSG00000272709	CpG island
NOTCH2NL	CpG island
ENSG00000255168	CpG island
NBPF10	CpG island
ENSG00000201558	chromatin interactions
ENSG00000163386	chromatin interactions
ENSG00000162377	chromatin interactions
ENSG00000255168	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000213240	chromatin interactions
ENSG00000134250	chromatin interactions
ENSG00000252211	chromatin interactions

Extended variants
information (count: 2910 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:2910 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587739004	chr1:145184172-145184173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs587608737	chr1:145184174-145184175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs61812726	chr1:145184223-145184224	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs587692603	chr1:145184250-145184251	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs111665064	chr1:145184260-145184261	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs587746564	chr1:145184316-145184317	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs189517620	chr1:145184318-145184319	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs587705280	chr1:145184319-145184320	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs2793885	chr1:145184324-145184325	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs587774821	chr1:145184361-145184362	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs587673168	chr1:145184385-145184386	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs369475446	chr1:145184482-145184483	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs2793884	chr1:145184483-145184484	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs76212446	chr1:145184486-145184487	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs587731632	chr1:145184499-145184500	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs78171312	chr1:145184519-145184520	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs373094772	chr1:145184564-145184565	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs202117542	chr1:145184565-145184566	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs587629324	chr1:145184591-145184592	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs587637131	chr1:145184594-145184595	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs61812728	chr1:145184603-145184604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587723119	chr1:145184616-145184617	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs587599443	chr1:145184718-145184719	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587679880	chr1:145184743-145184744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376260597	chr1:145184786-145184787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138287189	chr1:145184791-145184792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs386635208	chr1:145184802-145184803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200389637	chr1:145184805-145184806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587605013	chr1:145184817-145184818	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs587659288	chr1:145184826-145184827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4649530	chr1:145184875-145184876	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587740762	chr1:145184900-145184901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs56984759	chr1:145184901-145184902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs60186535	chr1:145184911-145184912	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs587615607	chr1:145184981-145184982	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs57942976	chr1:145185020-145185021	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs587729281	chr1:145185023-145185024	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs374590347	chr1:145185122-145185123	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs587621070	chr1:145185168-145185169	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs587707214	chr1:145185169-145185170	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28461460	chr1:145185223-145185224	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs28558988	chr1:145185241-145185242	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs55792242	chr1:145185287-145185288	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs57924818	chr1:145185333-145185334	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs61812731	chr1:145185343-145185344	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587772176	chr1:145185350-145185351	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs373121895	chr1:145185426-145185427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs587651803	chr1:145185463-145185464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587709269	chr1:145185486-145185487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56042618	chr1:145185500-145185501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:170)

Disease	PMID	Source
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
Wilms tumour	21544195	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
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
Tetralogy of Fallot	22912587	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Autism	22543975	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD
Developmental delay	20808231	CNVD
Obesity	20808231	CNVD
Autism	20808228	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4097 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145177600-145191800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:145178200-145190600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
3	chr1:145178600-145189000	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chr1:145178800-145188800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr1:145180600-145185400	Enhancers	Primary B cells from cord blood	blood
6	chr1:145182400-145185000	Enhancers	Primary B cells from peripheral blood	blood
7	chr1:145183400-145184200	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr1:145183400-145185400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr1:145184000-145184200	Enhancers	GM12878-XiMat	blood
10	chr1:145184000-145185200	Enhancers	Liver	Liver
11	chr1:145184000-145186600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr1:145184200-145184600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
13	chr1:145184200-145185000	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr1:145184600-145185400	Enhancers	Monocytes-CD14+_RO01746	blood
15	chr1:145185000-145185400	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr1:145185000-145185400	Genic enhancers	Primary B cells from peripheral blood	blood
17	chr1:145185200-145185400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr1:145185400-145186400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr1:145185400-145186400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr1:145185400-145186400	Weak transcription	Monocytes-CD14+_RO01746	blood
21	chr1:145185400-145186600	Weak transcription	Primary B cells from peripheral blood	blood
22	chr1:145185400-145188800	Weak transcription	Primary B cells from cord blood	blood
23	chr1:145186400-145186600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr1:145186400-145187400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr1:145186400-145187400	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr1:145186400-145188000	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr1:145186400-145188200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr1:145186600-145187000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr1:145186600-145187400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr1:145186600-145187600	Enhancers	Primary B cells from peripheral blood	blood
31	chr1:145186600-145195800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr1:145186800-145187600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:145186800-145187600	Enhancers	Osteobl	bone
34	chr1:145187000-145187200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:145187200-145187400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr1:145187400-145187600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr1:145187400-145189000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr1:145187400-145189200	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr1:145187400-145195600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr1:145187400-145195600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr1:145187600-145189200	Weak transcription	Primary B cells from peripheral blood	blood
42	chr1:145187600-145191200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:145187600-145194600	Weak transcription	Osteobl	bone
44	chr1:145187800-145189200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr1:145188000-145188800	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chr1:145188200-145195800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr1:145188600-145188800	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr1:145188800-145189000	Genic enhancers	Primary B cells from cord blood	blood
49	chr1:145188800-145189000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
50	chr1:145188800-145189400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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