Variant report

Variant	esv1846460
Chromosome Location	chr1:145205845-145303090
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2601)
CpG islands
(count:672)
Chromatin interactive
region (count:42)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2601 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:145246167-145246562	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:145208929-145209290	HepG2	liver:	n/a	chr1:145209007-145209015
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	chr1:145293424-145293644	K562	blood:	n/a	n/a
7	ARID3A	chr1:145254404-145254507	K562	blood:	n/a	n/a
8	ATF1	chr1:145208937-145209133	K562	blood:	n/a	n/a
9	ATF1	chr1:145216140-145216326	K562	blood:	n/a	n/a
10	ATF1	chr1:145292274-145292564	K562	blood:	n/a	n/a
11	ATF1	chr1:145293304-145293510	K562	blood:	n/a	n/a
12	ATF1	chr1:145254447-145254481	K562	blood:	n/a	n/a
13	ATF2	chr1:145208822-145209212	GM12878	blood:	n/a	n/a
14	ATF2	chr1:145291190-145292070	GM12878	blood:	n/a	n/a
15	ATF2	chr1:145233655-145233883	GM12878	blood:	n/a	n/a
16	ATF3	chr1:145208814-145209112	A549	lung:	n/a	n/a
17	ATF3	chr1:145208827-145209217	A549	lung:	n/a	n/a
18	BACH1	chr1:145254231-145254659	K562	blood:	n/a	n/a
19	BACH1	chr1:145254230-145254652	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr1:145292365-145292516	K562	blood:	n/a	n/a
21	BACH1	chr1:145208936-145209146	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr1:145253854-145253876	K562	blood:	n/a	n/a
23	BATF	chr1:145281369-145281733	GM12878	blood:	n/a	n/a
24	BATF	chr1:145234411-145234753	GM12878	blood:	n/a	n/a
25	BATF	chr1:145212001-145212472	GM12878	blood:	n/a	n/a
26	BATF	chr1:145296892-145297102	GM12878	blood:	n/a	n/a
27	BATF	chr1:145234955-145235323	GM12878	blood:	n/a	n/a
28	BATF	chr1:145277151-145277624	GM12878	blood:	n/a	n/a
29	BATF	chr1:145285189-145285435	GM12878	blood:	n/a	n/a
30	BATF	chr1:145233198-145234079	GM12878	blood:	n/a	n/a
31	BATF	chr1:145213599-145213876	GM12878	blood:	n/a	n/a
32	BATF	chr1:145234968-145235329	GM12878	blood:	n/a	n/a
33	BATF	chr1:145208490-145209291	GM12878	blood:	n/a	chr1:145209134-145209142
34	BATF	chr1:145291523-145292252	GM12878	blood:	n/a	n/a
35	BATF	chr1:145259491-145259713	GM12878	blood:	n/a	chr1:145259620-145259631
36	BATF	chr1:145293025-145293677	GM12878	blood:	n/a	n/a
37	BATF	chr1:145210338-145210530	GM12878	blood:	n/a	n/a
38	BATF	chr1:145233237-145234045	GM12878	blood:	n/a	n/a
39	BATF	chr1:145277155-145277522	GM12878	blood:	n/a	n/a
40	BATF	chr1:145210057-145210394	GM12878	blood:	n/a	n/a
41	BATF	chr1:145210075-145210284	GM12878	blood:	n/a	n/a
42	BATF	chr1:145209382-145209998	GM12878	blood:	n/a	n/a
43	BATF	chr1:145219743-145220000	GM12878	blood:	n/a	n/a
44	BATF	chr1:145297112-145297381	GM12878	blood:	n/a	n/a
45	BATF	chr1:145231709-145232035	GM12878	blood:	n/a	n/a
46	BATF	chr1:145260188-145260447	GM12878	blood:	n/a	n/a
47	BATF	chr1:145218967-145219192	GM12878	blood:	n/a	chr1:145218977-145218990
48	BATF	chr1:145212132-145212476	GM12878	blood:	n/a	n/a
49	BATF	chr1:145291553-145291993	GM12878	blood:	n/a	n/a
50	BATF	chr1:145296560-145296816	GM12878	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145207943-145207993	GM12892	blood:	n/a
2	chr1:145207943-145207993	GM12892	blood:	n/a
3	chr1:145210014-145210064	SAEC	small airway:	n/a
4	chr1:145208980-145209030	BE2_C	brain:	n/a
5	chr1:145301948-145301998	HEK293	kidney:	embryo
6	chr1:145210014-145210064	Hela-S3	cervix:	n/a
7	chr1:145209236-145209286	HCM	heart:	n/a
8	chr1:145209830-145209880	LNCaP	prostate:	n/a
9	chr1:145210014-145210064	Hepatocyte	liver:	n/a
10	chr1:145210014-145210064	HUVEC	blood vessel:	n/a
11	chr1:145210014-145210064	H1-hESC	embryonic stem cell:	embryo
12	chr1:145301948-145301998	HCPEpiC	choroid plexus:	n/a
13	chr1:145209236-145209286	HEK293	kidney:	embryo
14	chr1:145213338-145213388	BJ	skin:	n/a
15	chr1:145301948-145301998	HUVEC	blood vessel:	n/a
16	chr1:145302551-145302601	SK-N-SH	brain:	n/a
17	chr1:145209236-145209286	AG04449	skin:	fetal
18	chr1:145209830-145209880	SK-N-SH_RA	brain:	n/a
19	chr1:145209236-145209286	HIPEpiC	eye:	n/a
20	chr1:145301948-145301998	GM12892	blood:	n/a
21	chr1:145213338-145213388	HAEpiC	amniotic membrane:	n/a
22	chr1:145210014-145210064	AG04449	skin:	fetal
23	chr1:145210014-145210064	AG10803	skin:	n/a
24	chr1:145302551-145302601	AG10803	skin:	n/a
25	chr1:145301948-145301998	SKMC	muscle:	n/a
26	chr1:145211389-145211439	AG09309	skin:	n/a
27	chr1:145209930-145209980	NB4	blood:	n/a
28	chr1:145250914-145250964	HEK293	kidney:	embryo
29	chr1:145209930-145209980	MCF10A-Er-Src	breast:	n/a
30	chr1:145213338-145213388	Caco-2	colon:	n/a
31	chr1:145213338-145213388	GM12891	blood:	n/a
32	chr1:145207943-145207993	HPAEpiC	pulmonary alveolar:	n/a
33	chr1:145302551-145302601	CMK	blood:	n/a
34	chr1:145209236-145209286	BJ	skin:	n/a
35	chr1:145209236-145209286	SK-N-SH	brain:	n/a
36	chr1:145210014-145210064	HCT-116	colon:	n/a
37	chr1:145211389-145211439	SK-N-MC	brain:	n/a
38	chr1:145209930-145209980	HCPEpiC	choroid plexus:	n/a
39	chr1:145209830-145209880	AG10803	skin:	n/a
40	chr1:145210014-145210064	ovcar-3	ovarian:	n/a
41	chr1:145209236-145209286	AG10803	skin:	n/a
42	chr1:145208980-145209030	GM06990	blood:	n/a
43	chr1:145211389-145211439	LNCaP	prostate:	n/a
44	chr1:145209236-145209286	GM06990	blood:	n/a
45	chr1:145210014-145210064	ProgFib	skin:	n/a
46	chr1:145209830-145209880	U87	brain:	n/a
47	chr1:145208980-145209030	RPTEC	kidney:	n/a
48	chr1:145213338-145213388	HCM	heart:	n/a
49	chr1:145302551-145302601	HCF	heart:	n/a
50	chr1:145211389-145211439	AG10803	skin:	n/a

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

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

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOTCH2NL-2	chr1:145289770-145289906	NR_104217
2	lnc-NOTCH2NL-2	chr1:145302649-145302868	NR_104217
3	lnc-NOTCH2NL-2	chr1:145290429-145290511	NR_104217
4	lnc-NOTCH2NL-2	chr1:145291855-145291972	NONHSAT005883
5	lnc-NOTCH2NL-2	chr1:145290422-145290511	NONHSAT005883
6	lnc-NBPF10-1	chr1:145213108-145213374	expReg_chr1_15650_+
7	lnc-NOTCH2NL-2	chr1:145301720-145301817	NR_104217
8	lnc-NOTCH2NL-2	chr1:145293371-145293580	NR_104217
9	lnc-NOTCH2NL-2	chr1:145290781-145290850	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
ENSG00000163386	chromatin interactions
ENSG00000255168	chromatin interactions
ENSG00000252211	chromatin interactions
ENSG00000213240	chromatin interactions
ENSG00000162377	chromatin interactions
ENSG00000134250	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000201558	chromatin interactions

Extended variants
information (count: 2997 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:2997 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79892690	chr1:145205846-145205847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs2799260	chr1:145205933-145205934	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs112247984	chr1:145205934-145205935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78034397	chr1:145205935-145205936	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12046179	chr1:145206073-145206074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs369861883	chr1:145206079-145206080	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2260701	chr1:145206080-145206081	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs587693473	chr1:145206137-145206138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs587757587	chr1:145206175-145206176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2794171	chr1:145206216-145206217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370161414	chr1:145206263-145206264	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs200409996	chr1:145206282-145206283	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs375730293	chr1:145206289-145206290	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs71077256	chr1:145206293-145206294	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs112451230	chr1:145206294-145206295	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs367944644	chr1:145206309-145206310	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs372153703	chr1:145206310-145206311	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs12046250	chr1:145206311-145206312	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs373267782	chr1:145206344-145206345	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs587655270	chr1:145206388-145206389	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs587689714	chr1:145206405-145206406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs376343825	chr1:145206513-145206514	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs140275284	chr1:145206515-145206516	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs374256875	chr1:145206564-145206565	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs377395594	chr1:145206583-145206584	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs370973503	chr1:145206584-145206585	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs587755519	chr1:145206638-145206639	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs374329497	chr1:145206727-145206728	Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs374483292	chr1:145206924-145206925	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs77340893	chr1:145206967-145206968	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs587643471	chr1:145206998-145206999	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs56307323	chr1:145207021-145207022	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs587706836	chr1:145207069-145207070	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs201577294	chr1:145207145-145207146	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs374358574	chr1:145207164-145207165	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs587603759	chr1:145207379-145207380	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs199671331	chr1:145207380-145207381	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs368055298	chr1:145207428-145207429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs199589282	chr1:145207515-145207516	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs149373468	chr1:145207564-145207565	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587736022	chr1:145207656-145207657	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs200806847	chr1:145207708-145207709	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs67888009	chr1:145207728-145207729	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs587594896	chr1:145207746-145207747	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs587692744	chr1:145207749-145207750	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs587758065	chr1:145207832-145207833	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2794169	chr1:145207922-145207923	Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs587612320	chr1:145207943-145207944	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs587663570	chr1:145207944-145207945	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs201089037	chr1:145207957-145207958	Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	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:4375 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:145192000-145208800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr1:145196200-145207400	Weak transcription	NHDF-Ad	bronchial
3	chr1:145196600-145207000	Weak transcription	Osteobl	bone
4	chr1:145196600-145207800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:145200600-145208800	Weak transcription	Thymus	Thymus
6	chr1:145201800-145208800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr1:145203400-145208800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:145203600-145206200	Strong transcription	Monocytes-CD14+_RO01746	blood
9	chr1:145203800-145206000	Strong transcription	Primary monocytes fromperipheralblood	blood
10	chr1:145204200-145208800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr1:145205000-145209000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:145205400-145208800	Weak transcription	K562	blood
13	chr1:145205600-145208800	Weak transcription	Primary B cells from cord blood	blood
14	chr1:145205800-145208800	Weak transcription	Primary B cells from peripheral blood	blood
15	chr1:145206000-145207600	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr1:145206200-145207600	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr1:145206800-145207000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr1:145206800-145208000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr1:145206800-145208200	Enhancers	HepG2	liver
20	chr1:145207000-145207200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr1:145207000-145207600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:145207000-145207800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr1:145207000-145207800	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr1:145207000-145207800	Enhancers	Osteobl	bone
25	chr1:145207000-145208800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr1:145207200-145208800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr1:145207400-145207800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr1:145207400-145207800	Enhancers	HMEC	breast
29	chr1:145207400-145208000	Enhancers	NHDF-Ad	bronchial
30	chr1:145207600-145208000	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr1:145207600-145208200	Enhancers	Primary monocytes fromperipheralblood	blood
32	chr1:145207600-145208200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
33	chr1:145207600-145208800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr1:145207800-145208000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:145207800-145208000	Enhancers	Fetal Kidney	kidney
36	chr1:145207800-145208000	Enhancers	Dnd41	blood
37	chr1:145207800-145208800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr1:145207800-145208800	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr1:145207800-145208800	Weak transcription	HMEC	breast
40	chr1:145207800-145208800	Weak transcription	Osteobl	bone
41	chr1:145207800-145209000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr1:145208000-145208200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr1:145208000-145208800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:145208000-145208800	Weak transcription	Monocytes-CD14+_RO01746	blood
45	chr1:145208000-145209200	Weak transcription	NHDF-Ad	bronchial
46	chr1:145208000-145211200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr1:145208200-145208600	Enhancers	Liver	Liver
48	chr1:145208200-145208800	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr1:145208200-145208800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr1:145208200-145208800	Weak transcription	HepG2	liver

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