Variant report

Variant	nsv1006891
Chromosome Location	chr1:46189258-46408032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2993)
CpG islands
(count:1648)
Chromatin interactive
region (count:238)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2993 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:46275452-46275617	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:46336921-46338303	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:46212733-46212803	K562	blood:	n/a	n/a
4	ARID3A	chr1:46379137-46379290	K562	blood:	n/a	n/a
5	ARID3A	chr1:46216049-46216745	K562	blood:	n/a	n/a
6	ARID3A	chr1:46350455-46350607	K562	blood:	n/a	n/a
7	ARID3A	chr1:46396414-46396789	K562	blood:	n/a	n/a
8	ARID3A	chr1:46334608-46334873	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:46268499-46269278	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:46350498-46350690	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:46217849-46218734	HepG2	liver:	n/a	n/a
12	ARID3A	chr1:46216078-46216749	HepG2	liver:	n/a	n/a
13	ARID3A	chr1:46358025-46358337	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:46288374-46288666	HepG2	liver:	n/a	n/a
15	ARID3A	chr1:46268405-46269160	K562	blood:	n/a	n/a
16	ARID3A	chr1:46219186-46219590	K562	blood:	n/a	n/a
17	ARID3A	chr1:46218650-46218651	K562	blood:	n/a	n/a
18	ARID3A	chr1:46188741-46189313	K562	blood:	n/a	n/a
19	ARID3A	chr1:46347288-46347573	HepG2	liver:	n/a	n/a
20	ATF1	chr1:46268403-46269065	K562	blood:	n/a	n/a
21	ATF1	chr1:46219179-46219477	K562	blood:	n/a	n/a
22	ATF1	chr1:46252905-46252920	K562	blood:	n/a	n/a
23	ATF1	chr1:46395037-46395359	K562	blood:	n/a	n/a
24	ATF1	chr1:46309326-46309534	K562	blood:	n/a	n/a
25	ATF1	chr1:46215975-46216656	K562	blood:	n/a	n/a
26	ATF1	chr1:46241660-46241827	K562	blood:	n/a	n/a
27	ATF1	chr1:46390439-46390744	K562	blood:	n/a	n/a
28	ATF1	chr1:46379051-46379278	K562	blood:	n/a	n/a
29	ATF2	chr1:46268393-46268945	GM12878	blood:	n/a	n/a
30	ATF2	chr1:46216149-46216697	GM12878	blood:	n/a	n/a
31	ATF2	chr1:46215714-46216734	GM12878	blood:	n/a	n/a
32	ATF2	chr1:46306272-46306830	GM12878	blood:	n/a	n/a
33	ATF2	chr1:46268428-46268979	H1-hESC	embryonic stem cell:	n/a	n/a
34	ATF2	chr1:46216108-46216795	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr1:46268462-46268881	GM12878	blood:	n/a	n/a
36	ATF2	chr1:46378895-46379457	GM12878	blood:	n/a	n/a
37	ATF2	chr1:46268444-46268793	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr1:46216159-46216812	H1-hESC	embryonic stem cell:	n/a	n/a
39	ATF3	chr1:46268962-46269408	K562	blood:	n/a	n/a
40	ATF3	chr1:46337783-46338146	A549	lung:	n/a	n/a
41	ATF3	chr1:46268279-46268864	K562	blood:	n/a	n/a
42	ATF3	chr1:46216207-46216693	A549	lung:	n/a	n/a
43	ATF3	chr1:46215909-46216646	K562	blood:	n/a	n/a
44	BACH1	chr1:46214815-46214916	K562	blood:	n/a	n/a
45	BACH1	chr1:46269744-46269925	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr1:46269216-46269229	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr1:46232313-46232331	K562	blood:	n/a	n/a
48	BACH1	chr1:46215889-46216589	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr1:46216255-46216359	K562	blood:	n/a	n/a
50	BACH1	chr1:46391484-46391522	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1648 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:46269788-46269838	HCF	heart:	n/a
2	chr1:46269788-46269838	HCF	heart:	n/a
3	chr1:46269788-46269838	PrEC	prostate:	n/a
4	chr1:46196138-46196188	HCM	heart:	n/a
5	chr1:46273758-46273808	HIPEpiC	eye:	n/a
6	chr1:46268207-46268257	SK-N-MC	brain:	n/a
7	chr1:46216195-46216245	GM06990	blood:	n/a
8	chr1:46267883-46267933	K562	blood:	n/a
9	chr1:46196138-46196188	NHDF-neo	bronchial:	n/a
10	chr1:46268207-46268257	GM06990	blood:	n/a
11	chr1:46216399-46216449	HEEpiC	esophagus:	n/a
12	chr1:46269120-46269170	BE2_C	brain:	n/a
13	chr1:46216195-46216245	HMEC	breast:	n/a
14	chr1:46269120-46269170	T-47D	breast:	n/a
15	chr1:46268979-46269029	AoSMC	blood vessel:	n/a
16	chr1:46216195-46216245	K562	blood:	n/a
17	chr1:46265164-46265214	ProgFib	skin:	n/a
18	chr1:46215957-46216007	MCF-7	breast:	n/a
19	chr1:46391567-46391617	AG04449	skin:	fetal
20	chr1:46378857-46378907	AG09309	skin:	n/a
21	chr1:46220388-46220438	AG04450	lung:	fetal
22	chr1:46268158-46268208	SK-N-MC	brain:	n/a
23	chr1:46215879-46215929	NHDF-neo	bronchial:	n/a
24	chr1:46265164-46265214	Hepatocyte	liver:	n/a
25	chr1:46216513-46216563	BE2_C	brain:	n/a
26	chr1:46265164-46265214	Caco-2	colon:	n/a
27	chr1:46269324-46269374	HRCEpiC	kidney:	n/a
28	chr1:46269397-46269447	HCPEpiC	choroid plexus:	n/a
29	chr1:46196138-46196188	NHBE	bronchial:	n/a
30	chr1:46273758-46273808	NHBE	bronchial:	n/a
31	chr1:46215879-46215929	GM12892	blood:	n/a
32	chr1:46216737-46216787	ovcar-3	ovarian:	n/a
33	chr1:46268158-46268208	HCT-116	colon:	n/a
34	chr1:46268207-46268257	HEEpiC	esophagus:	n/a
35	chr1:46216195-46216245	NHBE	bronchial:	n/a
36	chr1:46273758-46273808	RPTEC	kidney:	n/a
37	chr1:46216671-46216721	GM06990	blood:	n/a
38	chr1:46269397-46269447	Jurkat	blood:	n/a
39	chr1:46269305-46269355	A549	lung:	n/a
40	chr1:46216195-46216245	RPTEC	kidney:	n/a
41	chr1:46220388-46220438	SK-N-SH_RA	brain:	n/a
42	chr1:46269788-46269838	HEK293	kidney:	embryo
43	chr1:46196138-46196188	HNPCEpiC	eye:	n/a
44	chr1:46378857-46378907	GM12878	blood:	n/a
45	chr1:46196138-46196188	PFSK-1	brain:	n/a
46	chr1:46216609-46216659	NHBE	bronchial:	n/a
47	chr1:46215879-46215929	MCF10A-Er-Src	breast:	n/a
48	chr1:46269394-46269444	HUVEC	blood vessel:	n/a
49	chr1:46269324-46269374	MCF10A-Er-Src	breast:	n/a
50	chr1:46273758-46273808	HL-60	blood:	n/a

(count:238 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr1:45985980..45988948-chr1:46213742..46217743,4	K562	blood:
2	chr1:46262358..46264763-chr1:46264907..46267822,2	K562	blood:
3	chr1:46232525..46235856-chr1:46237252..46240769,3	K562	blood:
4	chr1:46270679..46272758-chr1:46394759..46396446,2	K562	blood:
5	chr1:46149604..46155141-chr1:46267151..46271003,9	MCF-7	breast:
6	chr1:46346412..46348926-chr1:46358537..46360878,2	K562	blood:
7	chr1:46328886..46331555-chr1:46334023..46336229,2	K562	blood:
8	chr1:46211582..46213293-chr1:46216678..46219405,2	MCF-7	breast:
9	chr1:46272793..46275785-chr1:46276929..46278577,2	MCF-7	breast:
10	chr1:46216081..46216708-chr12:6579747..6580345,2	Hela-S3	cervix:
11	chr1:46329534..46331128-chr1:46362467..46364128,2	K562	blood:
12	chr1:46244095..46246858-chr1:46259918..46262871,2	K562	blood:
13	chr1:46268721..46270472-chr1:46322326..46324669,2	K562	blood:
14	chr1:46370026..46372652-chr1:46374945..46376718,2	K562	blood:
15	chr1:46216566..46218068-chr1:46223422..46225042,2	K562	blood:
16	chr1:46149977..46154848-chr1:46211592..46220262,26	K562	blood:
17	chr1:46049190..46051065-chr1:46268579..46270111,2	K562	blood:
18	chr1:46202156..46204427-chr1:46206183..46208440,2	K562	blood:
19	chr1:46278125..46279001-chr1:46347298..46347802,2	MCF-7	breast:
20	chr1:46152211..46153942-chr1:46345305..46348053,3	K562	blood:
21	chr1:46327585..46329581-chr1:46331185..46333590,2	K562	blood:
22	chr1:46383655..46385679-chr1:46387567..46389104,2	K562	blood:
23	chr1:46269099..46269845-chr11:10829742..10830680,2	Hela-S3	cervix:
24	chr1:46215876..46219394-chr1:46266629..46270801,6	K562	blood:
25	chr1:46334716..46337442-chr1:46355883..46358850,3	K562	blood:
26	chr1:46216128..46216886-chr11:62432686..62433305,2	Hela-S3	cervix:
27	chr1:46330055..46331827-chr1:46334729..46336546,2	K562	blood:
28	chr1:46151374..46154014-chr1:46272958..46275099,2	K562	blood:
29	chr1:46213853..46218009-chr1:46218217..46220727,8	K562	blood:
30	chr1:46205176..46209135-chr1:46209626..46211583,3	K562	blood:
31	chr1:46212304..46214621-chr1:46214734..46217216,4	MCF-7	breast:
32	chr1:46151070..46155000-chr1:46230734..46234846,4	K562	blood:
33	chr1:46270044..46272656-chr1:46278992..46281641,2	K562	blood:
34	chr1:46267822..46271619-chr1:46271668..46274699,5	K562	blood:
35	chr1:46329534..46331128-chr1:46362467..46364128,2	K562	blood:
36	chr1:46201467..46205050-chr1:46211028..46217340,6	K562	blood:
37	chr1:46291760..46294499-chr1:46299751..46301295,2	K562	blood:
38	chr1:46192510..46194017-chr1:46223382..46224964,2	K562	blood:
39	chr1:46328886..46331555-chr1:46334023..46336229,2	K562	blood:
40	chr1:46294880..46298299-chr1:46298592..46300540,3	K562	blood:
41	chr1:46321425..46323613-chr1:46327352..46330305,2	K562	blood:
42	chr1:46360342..46362505-chr1:46373607..46378298,4	K562	blood:
43	chr1:46338140..46340180-chr1:46341007..46342585,2	MCF-7	breast:
44	chr1:46298641..46301041-chr1:46305694..46307488,2	K562	blood:
45	chr1:45972293..45974739-chr1:46350771..46352345,2	K562	blood:
46	chr1:46270679..46272758-chr1:46394759..46396446,2	K562	blood:
47	chr1:46241636..46244183-chr1:46246863..46248467,2	K562	blood:
48	chr1:46152480..46154825-chr1:46237407..46240193,2	K562	blood:
49	chr1:46319707..46321501-chr1:46343782..46345819,2	K562	blood:
50	chr1:46194844..46197684-chr1:46203861..46206233,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAST2-3	chr1:46220237-46220295	NONHSAT002970
2	lnc-MAST2-3	chr1:46216682-46216920	NONHSAT002970
3	lnc-PIK3R3-1	chr1:46396865-46397420	ENSG00000248250
4	lnc-PIK3R3-1	chr1:46398107-46399249	ENSG00000248250

No data

Variant related genes	Relation type
MAST2	TF binding region
ENSG00000236111	TF binding region
TMA16P2	TF binding region
IPP	TF binding region
MAST2	CpG island
ENSG00000236111	CpG island
TMA16P2	CpG island
IPP	CpG island
ENSG00000121067	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000177606	chromatin interactions
ENSG00000081870	chromatin interactions
ENSG00000085433	chromatin interactions
ENSG00000117448	chromatin interactions
ENSG00000232467	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000163516	chromatin interactions
ENSG00000159596	chromatin interactions
ENSG00000114331	chromatin interactions
ENSG00000230896	chromatin interactions
ENSG00000086015	chromatin interactions
ENSG00000214756	chromatin interactions
ENSG00000160113	chromatin interactions
ENSG00000132780	chromatin interactions
ENSG00000122557	chromatin interactions
ENSG00000122566	chromatin interactions
ENSG00000117450	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000122565	chromatin interactions
ENSG00000085999	chromatin interactions
ENSG00000271122	chromatin interactions
ENSG00000053372	chromatin interactions
ENSG00000137449	chromatin interactions
ENSG00000090060	chromatin interactions
ENSG00000260806	chromatin interactions
ENSG00000159592	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000197429	chromatin interactions
ENSG00000255874	chromatin interactions
ENSG00000139190	chromatin interactions
ENSG00000247624	chromatin interactions
ENSG00000081791	chromatin interactions
ENSG00000127463	chromatin interactions
ENSG00000206597	chromatin interactions
ENSG00000110321	chromatin interactions
ENSG00000236111	chromatin interactions

Extended variants
information (count: 7790 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:7790 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138284697	chr1:46189266-46189267	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs370638818	chr1:46189348-46189349	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs114528358	chr1:46189366-46189367	Weak transcription Strong transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs554045807	chr1:46189405-46189406	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189473193	chr1:46189489-46189490	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs181377003	chr1:46189501-46189502	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs541760344	chr1:46189515-46189516	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs28617418	chr1:46189526-46189527	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs185969893	chr1:46189533-46189534	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs190731124	chr1:46189536-46189537	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs28378621	chr1:46189554-46189555	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs574323583	chr1:46189572-46189573	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs541321639	chr1:46189620-46189621	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs28508523	chr1:46189625-46189626	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs541496490	chr1:46189639-46189640	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs375762726	chr1:46189640-46189641	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs142876656	chr1:46189654-46189655	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs552163881	chr1:46189672-46189673	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs563771025	chr1:46189674-46189675	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs531282682	chr1:46189675-46189676	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs28594599	chr1:46189685-46189686	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs371812448	chr1:46189707-46189708	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs567876218	chr1:46189731-46189732	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs535274858	chr1:46189734-46189735	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs28538325	chr1:46189782-46189783	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
26	rs565980596	chr1:46189785-46189786	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs539386503	chr1:46189806-46189807	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs181778852	chr1:46189852-46189853	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
29	rs576553641	chr1:46189866-46189867	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs187228323	chr1:46189875-46189876	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376080591	chr1:46189885-46189886	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs549313435	chr1:46189899-46189900	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs373142724	chr1:46189924-46189925	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs565747561	chr1:46189977-46189978	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs370292616	chr1:46190064-46190065	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs578184521	chr1:46190110-46190111	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs543165933	chr1:46190124-46190125	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs545404173	chr1:46190211-46190212	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs568760272	chr1:46190224-46190225	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs556360544	chr1:46190259-46190260	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184182741	chr1:46190270-46190271	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs563734198	chr1:46190337-46190338	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs28575494	chr1:46190429-46190430	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
44	rs543068612	chr1:46190432-46190433	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs561468092	chr1:46190449-46190450	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs80050446	chr1:46190465-46190466	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs200440275	chr1:46190548-46190549	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529045751	chr1:46190585-46190586	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs547557003	chr1:46190717-46190718	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565767355	chr1:46190734-46190735	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	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
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	17875760	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:4104 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:46154600-46206600	Weak transcription	Brain Substantia Nigra	brain
2	chr1:46154800-46192600	Weak transcription	Pancreas	Pancrea
3	chr1:46155000-46215800	Weak transcription	Small Intestine	intestine
4	chr1:46155600-46204600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr1:46155800-46215600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr1:46156800-46203800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:46157400-46209800	Weak transcription	Brain Cingulate Gyrus	brain
8	chr1:46159800-46194800	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr1:46160800-46215400	Weak transcription	Brain Hippocampus Middle	brain
10	chr1:46161000-46196200	Weak transcription	NHEK	skin
11	chr1:46161200-46192800	Weak transcription	Spleen	Spleen
12	chr1:46161200-46196000	Weak transcription	GM12878-XiMat	blood
13	chr1:46161200-46206600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr1:46161400-46192000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr1:46162200-46192600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr1:46162600-46191400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr1:46163600-46196200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr1:46163600-46197400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr1:46163600-46215600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr1:46165600-46207000	Weak transcription	Colon Smooth Muscle	Colon
21	chr1:46174600-46192600	Weak transcription	Thymus	Thymus
22	chr1:46174600-46192800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr1:46174600-46206400	Weak transcription	Brain Germinal Matrix	brain
24	chr1:46174600-46215600	Weak transcription	Brain Angular Gyrus	brain
25	chr1:46174600-46215600	Weak transcription	Esophagus	oesophagus
26	chr1:46175000-46196400	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr1:46177800-46192800	Weak transcription	Rectal Smooth Muscle	rectum
28	chr1:46177800-46215600	Weak transcription	Gastric	stomach
29	chr1:46178000-46192600	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr1:46178000-46195800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:46178000-46195800	Weak transcription	Fetal Kidney	kidney
32	chr1:46178000-46209200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr1:46178000-46209800	Weak transcription	Fetal Brain Male	brain
34	chr1:46178000-46209800	Weak transcription	Lung	lung
35	chr1:46178000-46215600	Weak transcription	Aorta	Aorta
36	chr1:46178400-46192000	Weak transcription	Duodenum Mucosa	Duodenum
37	chr1:46179600-46206400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:46179600-46209000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr1:46180200-46192000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr1:46180400-46192600	Weak transcription	Fetal Thymus	thymus
41	chr1:46180400-46215600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
42	chr1:46180800-46193400	Weak transcription	Dnd41	blood
43	chr1:46181200-46191800	Weak transcription	Fetal Stomach	stomach
44	chr1:46181600-46192800	Weak transcription	Placenta	Placenta
45	chr1:46181800-46215600	Weak transcription	Fetal Brain Female	brain
46	chr1:46182000-46192400	Weak transcription	Fetal Muscle Trunk	muscle
47	chr1:46182000-46192800	Weak transcription	Duodenum Smooth Muscle	Duodenum
48	chr1:46182000-46193200	Weak transcription	Stomach Smooth Muscle	stomach
49	chr1:46182000-46203200	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr1:46182000-46206600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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