Variant report

Variant	esv1826082
Chromosome Location	chr1:145191306-145292994
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2256)
CpG islands
(count:613)
Chromatin interactive
region (count:43)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2256 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145254404-145254507	K562	blood:	n/a	n/a
2	ARID3A	chr1:145246167-145246562	HepG2	liver:	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	chr1:145289928-145289938	K562	blood:	n/a	n/a
6	ARID3A	chr1:145208929-145209290	HepG2	liver:	n/a	chr1:145209007-145209015
7	ATF1	chr1:145208937-145209133	K562	blood:	n/a	n/a
8	ATF1	chr1:145195978-145196042	K562	blood:	n/a	n/a
9	ATF1	chr1:145292274-145292564	K562	blood:	n/a	n/a
10	ATF1	chr1:145254447-145254481	K562	blood:	n/a	n/a
11	ATF1	chr1:145216140-145216326	K562	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	ATF2	chr1:145208822-145209212	GM12878	blood:	n/a	n/a
15	ATF3	chr1:145208827-145209217	A549	lung:	n/a	n/a
16	ATF3	chr1:145208814-145209112	A549	lung:	n/a	n/a
17	BACH1	chr1:145254230-145254652	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr1:145292365-145292516	K562	blood:	n/a	n/a
19	BACH1	chr1:145208936-145209146	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr1:145253854-145253876	K562	blood:	n/a	n/a
21	BACH1	chr1:145254231-145254659	K562	blood:	n/a	n/a
22	BATF	chr1:145291523-145292252	GM12878	blood:	n/a	n/a
23	BATF	chr1:145260188-145260447	GM12878	blood:	n/a	n/a
24	BATF	chr1:145210075-145210284	GM12878	blood:	n/a	n/a
25	BATF	chr1:145290357-145290900	GM12878	blood:	n/a	n/a
26	BATF	chr1:145233237-145234045	GM12878	blood:	n/a	n/a
27	BATF	chr1:145212001-145212472	GM12878	blood:	n/a	n/a
28	BATF	chr1:145219743-145220000	GM12878	blood:	n/a	n/a
29	BATF	chr1:145231709-145232035	GM12878	blood:	n/a	n/a
30	BATF	chr1:145234411-145234753	GM12878	blood:	n/a	n/a
31	BATF	chr1:145277151-145277624	GM12878	blood:	n/a	n/a
32	BATF	chr1:145285189-145285435	GM12878	blood:	n/a	n/a
33	BATF	chr1:145208490-145209291	GM12878	blood:	n/a	chr1:145209134-145209142
34	BATF	chr1:145233198-145234079	GM12878	blood:	n/a	n/a
35	BATF	chr1:145195914-145196301	GM12878	blood:	n/a	n/a
36	BATF	chr1:145210338-145210530	GM12878	blood:	n/a	n/a
37	BATF	chr1:145212132-145212476	GM12878	blood:	n/a	n/a
38	BATF	chr1:145281369-145281733	GM12878	blood:	n/a	n/a
39	BATF	chr1:145259491-145259713	GM12878	blood:	n/a	chr1:145259620-145259631
40	BATF	chr1:145218967-145219192	GM12878	blood:	n/a	chr1:145218977-145218990
41	BATF	chr1:145234955-145235323	GM12878	blood:	n/a	n/a
42	BATF	chr1:145213599-145213876	GM12878	blood:	n/a	n/a
43	BATF	chr1:145291553-145291993	GM12878	blood:	n/a	n/a
44	BATF	chr1:145277155-145277522	GM12878	blood:	n/a	n/a
45	BATF	chr1:145234968-145235329	GM12878	blood:	n/a	n/a
46	BATF	chr1:145209382-145209998	GM12878	blood:	n/a	n/a
47	BATF	chr1:145210057-145210394	GM12878	blood:	n/a	n/a
48	BCL11A	chr1:145291532-145292185	GM12878	blood:	n/a	n/a
49	BCL11A	chr1:145208329-145208557	GM12878	blood:	n/a	n/a
50	BCL11A	chr1:145234388-145234726	GM12878	blood:	n/a	n/a

(count:613 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145213338-145213388	NHBE	bronchial:	n/a
2	chr1:145213338-145213388	SAEC	small airway:	n/a
3	chr1:145211389-145211439	SK-N-SH	brain:	n/a
4	chr1:145213338-145213388	NHBE	bronchial:	n/a
5	chr1:145213338-145213388	SAEC	small airway:	n/a
6	chr1:145211389-145211439	SK-N-SH	brain:	n/a
7	chr1:145207943-145207993	PFSK-1	brain:	n/a
8	chr1:145209236-145209286	H1-hESC	embryonic stem cell:	embryo
9	chr1:145209930-145209980	HRPEpiC	eye:	n/a
10	chr1:145210014-145210064	MCF10A-Er-Src	breast:	n/a
11	chr1:145209236-145209286	ECC-1	luminal epithelium:	n/a
12	chr1:145210014-145210064	K562	blood:	n/a
13	chr1:145250914-145250964	IMR90	lung:	fetal
14	chr1:145209930-145209980	U87	brain:	n/a
15	chr1:145210014-145210064	HAEpiC	amniotic membrane:	n/a
16	chr1:145209930-145209980	AG09319	gingival:	n/a
17	chr1:145209236-145209286	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:145250914-145250964	AG09319	gingival:	n/a
19	chr1:145207943-145207993	SK-N-MC	brain:	n/a
20	chr1:145205174-145205224	GM12892	blood:	n/a
21	chr1:145207943-145207993	HCM	heart:	n/a
22	chr1:145209930-145209980	BE2_C	brain:	n/a
23	chr1:145210014-145210064	Caco-2	colon:	n/a
24	chr1:145209830-145209880	AG04449	skin:	fetal
25	chr1:145208980-145209030	BE2_C	brain:	n/a
26	chr1:145209830-145209880	HEK293	kidney:	embryo
27	chr1:145211389-145211439	GM12878	blood:	n/a
28	chr1:145211389-145211439	PFSK-1	brain:	n/a
29	chr1:145250914-145250964	HAEpiC	amniotic membrane:	n/a
30	chr1:145207943-145207993	PrEC	prostate:	n/a
31	chr1:145250914-145250964	CMK	blood:	n/a
32	chr1:145210014-145210064	HCPEpiC	choroid plexus:	n/a
33	chr1:145207943-145207993	BE2_C	brain:	n/a
34	chr1:145208980-145209030	LNCaP	prostate:	n/a
35	chr1:145209236-145209286	HMEC	breast:	n/a
36	chr1:145209830-145209880	ProgFib	skin:	n/a
37	chr1:145210014-145210064	GM12878	blood:	n/a
38	chr1:145210014-145210064	AG10803	skin:	n/a
39	chr1:145207943-145207993	IMR90	lung:	fetal
40	chr1:145209830-145209880	Hela-S3	cervix:	n/a
41	chr1:145209930-145209980	HIPEpiC	eye:	n/a
42	chr1:145211389-145211439	LNCaP	prostate:	n/a
43	chr1:145250914-145250964	PrEC	prostate:	n/a
44	chr1:145209930-145209980	SAEC	small airway:	n/a
45	chr1:145213338-145213388	HMEC	breast:	n/a
46	chr1:145205174-145205224	K562	blood:	n/a
47	chr1:145209930-145209980	HCPEpiC	choroid plexus:	n/a
48	chr1:145207943-145207993	LNCaP	prostate:	n/a
49	chr1:145207943-145207993	AG04449	skin:	fetal
50	chr1:145209930-145209980	PFSK-1	brain:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:120573750..120576750-chr1:145244417..145247281,4	MCF-7	breast:
2	chr1:145289699..145292602-chr1:149222944..149224949,3	MCF-7	breast:
3	chr1:120565033..120566748-chr1:145252742..145255259,2	MCF-7	breast:
4	chr1:120610094..120613669-chr1:145207447..145211087,11	MCF-7	breast:
5	chr1:145257082..145259251-chr1:145260108..145261925,2	MCF-7	breast:
6	chr1:145193254..145195284-chr1:145382712..145384267,2	MCF-7	breast:
7	chr1:145208214..145210170-chr1:145381446..145384467,3	MCF-7	breast:
8	chr1:145209435..145210070-chr1:145293272..145293941,2	MCF-7	breast:
9	chr1:145209133..145210911-chr1:145213297..145216185,2	MCF-7	breast:
10	chr1:120611958..120612515-chr1:145208972..145209639,2	NB4	blood:
11	chr1:145287740..145289244-chr18:67226861..67228381,2	MCF-7	breast:
12	chr1:145258606..145260477-chr1:145381662..145384269,2	MCF-7	breast:
13	chr1:145210633..145213326-chr1:149222498..149224954,2	MCF-7	breast:
14	chr1:145238836..145241577-chr1:145243504..145245771,2	K562	blood:
15	chr1:145257082..145259251-chr1:145260108..145261925,2	MCF-7	breast:
16	chr1:120611825..120612753-chr1:145208933..145209629,3	Hela-S3	cervix:
17	chr1:145110521..145113203-chr1:145271699..145274224,2	MCF-7	breast:
18	chr1:120561821..120563990-chr1:145256491..145258504,4	MCF-7	breast:
19	chr1:120610124..120613523-chr1:145208226..145211226,7	MCF-7	breast:
20	chr1:145238836..145241577-chr1:145243504..145245771,2	K562	blood:
21	chr1:120574754..120575346-chr1:145245858..145246575,2	MCF-7	breast:
22	chr1:145130093..145132779-chr1:145291052..145292604,2	K562	blood:
23	chr1:120611803..120612535-chr1:145208972..145209627,6	MCF-7	breast:
24	chr1:145209779..145211659-chr1:145381647..145384503,2	MCF-7	breast:
25	chr1:145209931..145210445-chr19:58874333..58874839,2	Hela-S3	cervix:
26	chr1:145208945..145211572-chr1:145290799..145293780,3	MCF-7	breast:
27	chr1:120555279..120557791-chr1:145264672..145267612,3	K562	blood:
28	chr1:120611941..120612674-chr1:145209107..145209637,6	MCF-7	breast:
29	chr1:145207909..145210605-chr1:145214441..145216644,2	MCF-7	breast:
30	chr1:145208945..145211572-chr1:145290799..145293780,3	MCF-7	breast:
31	chr1:145291510..145293949-chr1:149222418..149224230,2	K562	blood:
32	chr1:145288943..145293306-chr1:149221737..149224658,6	MCF-7	breast:
33	chr1:120576520..120578439-chr1:145242059..145244929,2	MCF-7	breast:
34	chr1:120533140..120534660-chr1:145287386..145288888,2	MCF-7	breast:
35	chr1:120606120..120607638-chr1:145207438..145208952,2	MCF-7	breast:
36	chr1:120602747..120604407-chr1:145216153..145218112,2	MCF-7	breast:
37	chr1:145209043..145210611-chr1:149222292..149224968,3	MCF-7	breast:
38	chr1:120562041..120564945-chr1:145257130..145258905,2	K562	blood:
39	chr1:145246366..145248846-chr1:149222454..149225152,2	MCF-7	breast:
40	chr1:145290091..145292740-chr1:145382337..145384639,2	MCF-7	breast:
41	chr1:53163301..53163992-chr1:145209547..145210339,2	Hela-S3	cervix:
42	chr1:145264618..145267295-chr1:145381743..145384010,2	K562	blood:
43	chr1:120562393..120564845-chr1:145256114..145258582,3	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOTCH2NL-2	chr1:145290429-145290511	NR_104217
2	lnc-PDE4DIP-6	chr1:145200338-145200891	ENSG00000272709.1
3	lnc-NOTCH2NL-2	chr1:145290422-145290511	NONHSAT005883
4	lnc-NOTCH2NL-2	chr1:145290781-145290850	NONHSAT005883
5	lnc-NOTCH2NL-2	chr1:145289770-145289906	NR_104217
6	lnc-NOTCH2NL-2	chr1:145291855-145291972	NONHSAT005883
7	lnc-NBPF10-1	chr1:145213108-145213374	expReg_chr1_15650_+

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
ENSG00000163386	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000134250	chromatin interactions
ENSG00000162377	chromatin interactions
ENSG00000255168	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000213240	chromatin interactions
ENSG00000252211	chromatin interactions

Extended variants
information (count: 2725 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:2725 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs587748013	chr1:145191326-145191327	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs587655947	chr1:145191396-145191397	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs374883338	chr1:145191417-145191418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368130170	chr1:145191462-145191463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs4649535	chr1:145191531-145191532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374285032	chr1:145191551-145191552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368828499	chr1:145191556-145191557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs587711489	chr1:145191565-145191566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76865315	chr1:145191608-145191609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs587765036	chr1:145191611-145191612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201188057	chr1:145191615-145191616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12138004	chr1:145191672-145191673	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs367604456	chr1:145191746-145191747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113877965	chr1:145191795-145191796	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201899104	chr1:145191832-145191833	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587621943	chr1:145191842-145191843	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs199977985	chr1:145191846-145191847	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587695381	chr1:145191903-145191904	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs3010126	chr1:145192045-145192046	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs75550726	chr1:145192054-145192055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs79616874	chr1:145192061-145192062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376784700	chr1:145192162-145192163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373198080	chr1:145192174-145192175	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs369959932	chr1:145192180-145192181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2982627	chr1:145192189-145192190	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs587710420	chr1:145192204-145192205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs587755928	chr1:145192417-145192418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs201749461	chr1:145192463-145192464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201860290	chr1:145192546-145192547	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs587652888	chr1:145192560-145192561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200449249	chr1:145192566-145192567	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs587708012	chr1:145192567-145192568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs371729358	chr1:145192615-145192616	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375059621	chr1:145192616-145192617	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs150715251	chr1:145192617-145192618	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs587601973	chr1:145192678-145192679	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs374606490	chr1:145192745-145192746	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs587638286	chr1:145192795-145192796	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs113155759	chr1:145192807-145192808	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs587709901	chr1:145192831-145192832	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs587594320	chr1:145192839-145192840	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs587701019	chr1:145192840-145192841	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs377365525	chr1:145192858-145192859	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs587758418	chr1:145192867-145192868	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs587631308	chr1:145192882-145192883	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs587688706	chr1:145192888-145192889	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587745380	chr1:145192914-145192915	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs587614527	chr1:145193025-145193026	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587698322	chr1:145193030-145193031	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs587728127	chr1:145193050-145193051	Weak transcription Strong 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:4107 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145177600-145191800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:145186600-145195800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr1:145187400-145195600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:145187400-145195600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:145187600-145194600	Weak transcription	Osteobl	bone
6	chr1:145188200-145195800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr1:145188800-145191400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
8	chr1:145189000-145191400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
9	chr1:145189200-145191400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
10	chr1:145189200-145192000	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr1:145189400-145192200	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr1:145189400-145194800	Weak transcription	Dnd41	blood
13	chr1:145189400-145195600	Weak transcription	Primary T helper cells fromperipheralblood	blood
14	chr1:145189400-145195600	Weak transcription	HMEC	breast
15	chr1:145189400-145195600	Weak transcription	NHDF-Ad	bronchial
16	chr1:145189400-145197200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr1:145189400-145199600	Weak transcription	Primary T cells from cord blood	blood
18	chr1:145190000-145204000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:145190400-145192200	Enhancers	Primary B cells from cord blood	blood
20	chr1:145190600-145192000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr1:145190800-145192200	Enhancers	Primary B cells from peripheral blood	blood
22	chr1:145190800-145192200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr1:145190800-145195200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr1:145191000-145192000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr1:145191200-145191400	Enhancers	Spleen	Spleen
26	chr1:145191200-145192000	Enhancers	Primary hematopoietic stem cells	blood
27	chr1:145191200-145192000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr1:145191200-145192000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr1:145191200-145192000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:145191200-145192000	Enhancers	Fetal Lung	lung
31	chr1:145191200-145192000	Enhancers	Fetal Thymus	thymus
32	chr1:145191400-145195800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
33	chr1:145191400-145197200	Weak transcription	Spleen	Spleen
34	chr1:145192000-145193000	Enhancers	Liver	Liver
35	chr1:145192000-145193000	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr1:145192000-145194800	Weak transcription	Fetal Lung	lung
37	chr1:145192000-145195600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr1:145192000-145195600	Weak transcription	Muscle Satellite Cultured Cells	--
39	chr1:145192000-145195600	Weak transcription	Fetal Thymus	thymus
40	chr1:145192000-145195800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr1:145192000-145208800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr1:145192200-145192600	Weak transcription	Primary B cells from peripheral blood	blood
43	chr1:145192200-145195600	Weak transcription	Primary monocytes fromperipheralblood	blood
44	chr1:145192200-145198000	Weak transcription	Primary B cells from cord blood	blood
45	chr1:145192600-145195800	Strong transcription	Primary B cells from peripheral blood	blood
46	chr1:145193000-145194800	Strong transcription	Monocytes-CD14+_RO01746	blood
47	chr1:145194600-145195600	Enhancers	Osteobl	bone
48	chr1:145194800-145195000	Enhancers	Fetal Lung	lung
49	chr1:145194800-145195600	Enhancers	Dnd41	blood
50	chr1:145194800-145196000	Genic enhancers	Monocytes-CD14+_RO01746	blood

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