Variant report

Variant	nsv8091
Chromosome Location	chr1:145189119-145372647
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3214)
CpG islands
(count:856)
Chromatin interactive
region (count:43)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3214 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

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	chr1:145289928-145289938	K562	blood:	n/a	n/a
3	ARID3A	chr1:145208951-145209121	K562	blood:	n/a	chr1:145209007-145209015
4	ARID3A	chr1:145254404-145254507	K562	blood:	n/a	n/a
5	ARID3A	chr1:145208929-145209290	HepG2	liver:	n/a	chr1:145209007-145209015
6	ARID3A	chr1:145253698-145253898	K562	blood:	n/a	n/a
7	ARID3A	chr1:145293424-145293644	K562	blood:	n/a	n/a
8	ATF1	chr1:145293304-145293510	K562	blood:	n/a	n/a
9	ATF1	chr1:145195978-145196042	K562	blood:	n/a	n/a
10	ATF1	chr1:145208937-145209133	K562	blood:	n/a	n/a
11	ATF1	chr1:145292274-145292564	K562	blood:	n/a	n/a
12	ATF1	chr1:145254447-145254481	K562	blood:	n/a	n/a
13	ATF1	chr1:145216140-145216326	K562	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	ATF2	chr1:145208822-145209212	GM12878	blood:	n/a	n/a
17	ATF3	chr1:145208827-145209217	A549	lung:	n/a	n/a
18	ATF3	chr1:145208814-145209112	A549	lung:	n/a	n/a
19	BACH1	chr1:145292365-145292516	K562	blood:	n/a	n/a
20	BACH1	chr1:145254230-145254652	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr1:145253854-145253876	K562	blood:	n/a	n/a
22	BACH1	chr1:145208936-145209146	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr1:145254231-145254659	K562	blood:	n/a	n/a
24	BATF	chr1:145277151-145277624	GM12878	blood:	n/a	n/a
25	BATF	chr1:145234968-145235329	GM12878	blood:	n/a	n/a
26	BATF	chr1:145369205-145369460	GM12878	blood:	n/a	n/a
27	BATF	chr1:145297112-145297381	GM12878	blood:	n/a	n/a
28	BATF	chr1:145234955-145235323	GM12878	blood:	n/a	n/a
29	BATF	chr1:145299644-145300057	GM12878	blood:	n/a	n/a
30	BATF	chr1:145337454-145337613	GM12878	blood:	n/a	n/a
31	BATF	chr1:145208490-145209291	GM12878	blood:	n/a	chr1:145209134-145209142
32	BATF	chr1:145293193-145293698	GM12878	blood:	n/a	n/a
33	BATF	chr1:145260188-145260447	GM12878	blood:	n/a	n/a
34	BATF	chr1:145296560-145296816	GM12878	blood:	n/a	n/a
35	BATF	chr1:145234411-145234753	GM12878	blood:	n/a	n/a
36	BATF	chr1:145259491-145259713	GM12878	blood:	n/a	chr1:145259620-145259631
37	BATF	chr1:145323297-145323456	GM12878	blood:	n/a	n/a
38	BATF	chr1:145195914-145196301	GM12878	blood:	n/a	n/a
39	BATF	chr1:145189103-145189407	GM12878	blood:	n/a	n/a
40	BATF	chr1:145212001-145212472	GM12878	blood:	n/a	n/a
41	BATF	chr1:145210057-145210394	GM12878	blood:	n/a	n/a
42	BATF	chr1:145310440-145310923	GM12878	blood:	n/a	chr1:145310669-145310677
43	BATF	chr1:145277155-145277522	GM12878	blood:	n/a	n/a
44	BATF	chr1:145233198-145234079	GM12878	blood:	n/a	n/a
45	BATF	chr1:145362622-145362781	GM12878	blood:	n/a	n/a
46	BATF	chr1:145342174-145342333	GM12878	blood:	n/a	n/a
47	BATF	chr1:145210075-145210284	GM12878	blood:	n/a	n/a
48	BATF	chr1:145291523-145292252	GM12878	blood:	n/a	n/a
49	BATF	chr1:145351628-145351787	GM12878	blood:	n/a	n/a
50	BATF	chr1:145369080-145369247	GM12878	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:145301948-145301998	NHBE	bronchial:	n/a
2	chr1:145209930-145209980	HepG2	liver:	n/a
3	chr1:145301948-145301998	NHBE	bronchial:	n/a
4	chr1:145209930-145209980	HepG2	liver:	n/a
5	chr1:145207943-145207993	AG09319	gingival:	n/a
6	chr1:145250914-145250964	GM19239	blood:	n/a
7	chr1:145366536-145366586	LNCaP	prostate:	n/a
8	chr1:145301948-145301998	HRCEpiC	kidney:	n/a
9	chr1:145207943-145207993	HCT-116	colon:	n/a
10	chr1:145208980-145209030	BE2_C	brain:	n/a
11	chr1:145205174-145205224	HPAEpiC	pulmonary alveolar:	n/a
12	chr1:145213338-145213388	PFSK-1	brain:	n/a
13	chr1:145213338-145213388	GM19239	blood:	n/a
14	chr1:145207943-145207993	MCF10A-Er-Src	breast:	n/a
15	chr1:145302551-145302601	HEK293	kidney:	embryo
16	chr1:145250914-145250964	Hela-S3	cervix:	n/a
17	chr1:145366524-145366574	Caco-2	colon:	n/a
18	chr1:145209930-145209980	HCT-116	colon:	n/a
19	chr1:145209830-145209880	MCF-7	breast:	n/a
20	chr1:145366524-145366574	CMK	blood:	n/a
21	chr1:145209236-145209286	HAEpiC	amniotic membrane:	n/a
22	chr1:145209830-145209880	K562	blood:	n/a
23	chr1:145213338-145213388	T-47D	breast:	n/a
24	chr1:145211389-145211439	ProgFib	skin:	n/a
25	chr1:145213338-145213388	Caco-2	colon:	n/a
26	chr1:145209930-145209980	NHDF-neo	bronchial:	n/a
27	chr1:145366536-145366586	RPTEC	kidney:	n/a
28	chr1:145207943-145207993	A549	lung:	n/a
29	chr1:145366536-145366586	HRPEpiC	eye:	n/a
30	chr1:145366524-145366574	GM12891	blood:	n/a
31	chr1:145209236-145209286	NHBE	bronchial:	n/a
32	chr1:145211389-145211439	ovcar-3	ovarian:	n/a
33	chr1:145366524-145366574	A549	lung:	n/a
34	chr1:145213338-145213388	K562	blood:	n/a
35	chr1:145209930-145209980	AG04449	skin:	fetal
36	chr1:145250914-145250964	HUVEC	blood vessel:	n/a
37	chr1:145209830-145209880	NB4	blood:	n/a
38	chr1:145211389-145211439	GM12878	blood:	n/a
39	chr1:145209830-145209880	HRE	kidney:	n/a
40	chr1:145366536-145366586	HCF	heart:	n/a
41	chr1:145209930-145209980	HUVEC	blood vessel:	n/a
42	chr1:145208980-145209030	ProgFib	skin:	n/a
43	chr1:145366536-145366586	HIPEpiC	eye:	n/a
44	chr1:145209236-145209286	GM12878	blood:	n/a
45	chr1:145301948-145301998	HRE	kidney:	n/a
46	chr1:145209930-145209980	GM12891	blood:	n/a
47	chr1:145213338-145213388	SK-N-MC	brain:	n/a
48	chr1:145301948-145301998	SK-N-SH_RA	brain:	n/a
49	chr1:145207943-145207993	CMK	blood:	n/a
50	chr1:145366536-145366586	PrEC	prostate:	n/a

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

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

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NOTCH2NL-2	chr1:145320511-145320619	NR_104217
2	lnc-NOTCH2NL-2	chr1:145303910-145303982	NR_104217
3	lnc-NOTCH2NL-2	chr1:145290781-145290850	NONHSAT005883
4	lnc-NOTCH2NL-2	chr1:145302649-145302868	NR_104217
5	lnc-NOTCH2NL-2	chr1:145311103-145311154	NR_104217
6	lnc-NOTCH2NL-2	chr1:145369718-145370303	NR_104217
7	lnc-NOTCH2NL-2	chr1:145318054-145318226	NR_104217
8	lnc-NOTCH2NL-2	chr1:145293371-145293580	NR_104217
9	lnc-NOTCH2NL-2	chr1:145301720-145301817	NR_104217
10	lnc-NOTCH2NL-2	chr1:145368441-145369446	NR_104217
11	lnc-NOTCH2NL-2	chr1:145290429-145290511	NR_104217
12	lnc-NBPF10-1	chr1:145213108-145213374	expReg_chr1_15650_+
13	lnc-POLR3GL-1	chr1:145372088-145373798	NONHSAT005886
14	lnc-NOTCH2NL-2	chr1:145318936-145318987	NR_104217
15	lnc-NOTCH2NL-2	chr1:145304447-145304652	NR_104217
16	lnc-NOTCH2NL-2	chr1:145317406-145317457	NR_104217
17	lnc-NOTCH2NL-2	chr1:145319624-145319796	NR_104217
18	lnc-NOTCH2NL-2	chr1:145291855-145291972	NONHSAT005883
19	lnc-NOTCH2NL-2	chr1:145305945-145305996	NR_104217
20	lnc-NOTCH2NL-2	chr1:145316512-145316684	NR_104217
21	lnc-PDE4DIP-6	chr1:145200338-145200891	ENSG00000272709.1
22	lnc-NOTCH2NL-2	chr1:145309900-145310063	NR_104217
23	lnc-NOTCH2NL-2	chr1:145289770-145289906	NR_104217
24	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
ENSG00000213240	chromatin interactions
ENSG00000163386	chromatin interactions
ENSG00000255168	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000252211	chromatin interactions
ENSG00000134250	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000162377	chromatin interactions

Extended variants
information (count: 5134 )
Associated
traits (count: 173 )

Variant overlapped rSNPs/rCNVs (count:5134 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369239977	chr1:145189149-145189150	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs199959741	chr1:145189168-145189169	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs587669101	chr1:145189170-145189171	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs373118517	chr1:145189193-145189194	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs587725688	chr1:145189194-145189195	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs587621534	chr1:145189251-145189252	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs587646506	chr1:145189257-145189258	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs200085374	chr1:145189310-145189311	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs587720038	chr1:145189320-145189321	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79367527	chr1:145189331-145189332	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs587602551	chr1:145189336-145189337	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201993888	chr1:145189354-145189355	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148446555	chr1:145189409-145189410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs372962939	chr1:145189431-145189432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs587672004	chr1:145189438-145189439	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs587712453	chr1:145189449-145189450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs587610956	chr1:145189451-145189452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs587665372	chr1:145189499-145189500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370178279	chr1:145189501-145189502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375609633	chr1:145189531-145189532	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs200109420	chr1:145189561-145189562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs587744973	chr1:145189626-145189627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs587622843	chr1:145189651-145189652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs587662624	chr1:145189657-145189658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs201079476	chr1:145189715-145189716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs587736138	chr1:145189734-145189735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs201997042	chr1:145189759-145189760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs61814460	chr1:145189765-145189766	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs587615627	chr1:145189819-145189820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2603997	chr1:145189904-145189905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs201286880	chr1:145189953-145189954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201697806	chr1:145190029-145190030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs587689099	chr1:145190046-145190047	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs200276465	chr1:145190211-145190212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs368640353	chr1:145190282-145190283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs375164467	chr1:145190322-145190323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs587770734	chr1:145190329-145190330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs201187239	chr1:145190356-145190357	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs587644000	chr1:145190411-145190412	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200168136	chr1:145190415-145190416	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs79896053	chr1:145190419-145190420	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2924832	chr1:145190435-145190436	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs199748277	chr1:145190472-145190473	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs61814481	chr1:145190614-145190615	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112810156	chr1:145190622-145190623	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs58567136	chr1:145190636-145190637	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs587776067	chr1:145190637-145190638	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs61814482	chr1:145190643-145190644	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs587637387	chr1:145190690-145190691	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372933823	chr1:145190704-145190705	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:173)

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
Autism	22102821	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:5161 , 50 per page) page: 1 2 3 4 5 6 7 ... 104

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	chr1:145186600-145195800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr1:145187400-145189200	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr1:145187400-145195600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:145187400-145195600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr1:145187600-145189200	Weak transcription	Primary B cells from peripheral blood	blood
8	chr1:145187600-145191200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr1:145187600-145194600	Weak transcription	Osteobl	bone
10	chr1:145187800-145189200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr1:145188200-145195800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr1:145188800-145189400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:145188800-145189400	Genic enhancers	Primary monocytes fromperipheralblood	blood
14	chr1:145188800-145189400	Enhancers	Small Intestine	intestine
15	chr1:145188800-145189400	Enhancers	HMEC	breast
16	chr1:145188800-145189400	Enhancers	HSMM	muscle
17	chr1:145188800-145190000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr1:145188800-145191400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
19	chr1:145189000-145189200	Enhancers	Primary B cells from cord blood	blood
20	chr1:145189000-145189400	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr1:145189000-145189400	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr1:145189000-145189400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr1:145189000-145189400	Enhancers	Muscle Satellite Cultured Cells	--
24	chr1:145189000-145189400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr1:145189000-145189400	Enhancers	Dnd41	blood
26	chr1:145189000-145189400	Enhancers	NHDF-Ad	bronchial
27	chr1:145189000-145189400	Enhancers	NHEK	skin
28	chr1:145189000-145189600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr1:145189000-145190000	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr1:145189000-145190600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr1:145189000-145191400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
32	chr1:145189200-145189400	Enhancers	Primary B cells from peripheral blood	blood
33	chr1:145189200-145189400	Enhancers	Primary T cells from cord blood	blood
34	chr1:145189200-145189400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
35	chr1:145189200-145189400	Enhancers	Fetal Thymus	thymus
36	chr1:145189200-145190000	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr1:145189200-145190000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr1:145189200-145190400	Weak transcription	Primary B cells from cord blood	blood
39	chr1:145189200-145190600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
40	chr1:145189200-145191400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
41	chr1:145189200-145192000	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr1:145189400-145190400	Weak transcription	Primary B cells from peripheral blood	blood
43	chr1:145189400-145190400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
44	chr1:145189400-145191200	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr1:145189400-145191200	Weak transcription	Fetal Thymus	thymus
46	chr1:145189400-145192200	Enhancers	Primary monocytes fromperipheralblood	blood
47	chr1:145189400-145194800	Weak transcription	Dnd41	blood
48	chr1:145189400-145195600	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr1:145189400-145195600	Weak transcription	HMEC	breast
50	chr1:145189400-145195600	Weak transcription	NHDF-Ad	bronchial

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