Variant report

Variant	nsv830015
Chromosome Location	chr1:63261143-63455296
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1571)
CpG islands
(count:244)
Chromatin interactive
region (count:56)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1571 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:63307245-63307618	K562	blood:	n/a	n/a
2	ARID3A	chr1:63420898-63421182	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:63307285-63307622	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:63334925-63335542	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:63357843-63358193	HepG2	liver:	n/a	n/a
6	ATF1	chr1:63335228-63335247	K562	blood:	n/a	n/a
7	ATF2	chr1:63276169-63276824	GM12878	blood:	n/a	n/a
8	ATF2	chr1:63266283-63266851	GM12878	blood:	n/a	n/a
9	ATF2	chr1:63428776-63429288	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr1:63276064-63276973	GM12878	blood:	n/a	n/a
11	ATF2	chr1:63266351-63266823	GM12878	blood:	n/a	n/a
12	BACH1	chr1:63428271-63428287	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr1:63440161-63440368	H1-hESC	embryonic stem cell:	n/a	chr1:63440282-63440296
14	BACH1	chr1:63377735-63377948	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr1:63428891-63429167	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr1:63276635-63276842	GM12878	blood:	n/a	n/a
17	BATF	chr1:63429884-63430168	GM12878	blood:	n/a	n/a
18	BATF	chr1:63276612-63276857	GM12878	blood:	n/a	n/a
19	BCL11A	chr1:63276571-63276846	GM12878	blood:	n/a	chr1:63276738-63276747
20	BCL11A	chr1:63429876-63430152	GM12878	blood:	n/a	n/a
21	BCL11A	chr1:63266380-63266777	GM12878	blood:	n/a	n/a
22	BCL11A	chr1:63276629-63276837	GM12878	blood:	n/a	chr1:63276738-63276747
23	BCLAF1	chr1:63266357-63266936	GM12878	blood:	n/a	n/a
24	BCLAF1	chr1:63266280-63266988	GM12878	blood:	n/a	n/a
25	BHLHE40	chr1:63359854-63359870	K562	blood:	n/a	n/a
26	BHLHE40	chr1:63429717-63429989	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:63429013-63429213	GM12878	blood:	n/a	n/a
28	BHLHE40	chr1:63266382-63267009	GM12878	blood:	n/a	n/a
29	BHLHE40	chr1:63384873-63384991	K562	blood:	n/a	n/a
30	BHLHE40	chr1:63275563-63275800	GM12878	blood:	n/a	n/a
31	BHLHE40	chr1:63379699-63379702	K562	blood:	n/a	n/a
32	CEBPB	chr1:63309743-63310089	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr1:63341239-63341508	HepG2	liver:	n/a	chr1:63341361-63341372
34	CEBPB	chr1:63333993-63334313	K562	blood:	n/a	chr1:63334151-63334162
35	CEBPB	chr1:63335923-63336136	K562	blood:	n/a	n/a
36	CEBPB	chr1:63301728-63301987	K562	blood:	n/a	n/a
37	CEBPB	chr1:63335946-63336085	HepG2	liver:	n/a	n/a
38	CEBPB	chr1:63357830-63358256	MCF-7	breast:	n/a	n/a
39	CEBPB	chr1:63429489-63429689	HepG2	liver:	n/a	chr1:63429658-63429669 chr1:63429658-63429669 chr1:63429658-63429671
40	CEBPB	chr1:63335857-63336196	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:63335755-63336215	IMR90	lung:	n/a	n/a
42	CEBPB	chr1:63416935-63417227	IMR90	lung:	n/a	chr1:63417084-63417095
43	CEBPB	chr1:63453813-63454144	IMR90	lung:	n/a	chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453961-63453970 chr1:63453959-63453970 chr1:63453961-63453972 chr1:63453961-63453970 chr1:63453961-63453972 chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453959-63453972
44	CEBPB	chr1:63453863-63454097	MCF-7	breast:	n/a	chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453961-63453970 chr1:63453959-63453970 chr1:63453961-63453972 chr1:63453961-63453970 chr1:63453961-63453972 chr1:63453959-63453972 chr1:63453961-63453970 chr1:63453959-63453972
45	CEBPB	chr1:63434219-63434419	IMR90	lung:	n/a	chr1:63434326-63434337
46	CEBPB	chr1:63416957-63417272	HepG2	liver:	n/a	chr1:63417084-63417095
47	CEBPB	chr1:63357820-63358204	HepG2	liver:	n/a	n/a
48	CEBPB	chr1:63304682-63304943	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr1:63357819-63358182	HepG2	liver:	n/a	n/a
50	CEBPB	chr1:63357792-63358234	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:63384921-63384971	HL-60	blood:	n/a
2	chr1:63429038-63429088	SK-N-SH	brain:	n/a
3	chr1:63372303-63372353	LNCaP	prostate:	n/a
4	chr1:63419352-63419402	NH-A	brain:	n/a
5	chr1:63429038-63429088	AG04449	skin:	fetal
6	chr1:63384921-63384971	K562	blood:	n/a
7	chr1:63429038-63429088	HPAEpiC	pulmonary alveolar:	n/a
8	chr1:63429038-63429088	LNCaP	prostate:	n/a
9	chr1:63419352-63419402	IMR90	lung:	fetal
10	chr1:63429038-63429088	K562	blood:	n/a
11	chr1:63372303-63372353	MCF10A-Er-Src	breast:	n/a
12	chr1:63372303-63372353	GM12891	blood:	n/a
13	chr1:63419352-63419402	NT2-D1	testis:	n/a
14	chr1:63419352-63419402	NHBE	bronchial:	n/a
15	chr1:63429038-63429088	U87	brain:	n/a
16	chr1:63419352-63419402	HCM	heart:	n/a
17	chr1:63372303-63372353	PANC-1	pancreas:	n/a
18	chr1:63419352-63419402	HRE	kidney:	n/a
19	chr1:63384921-63384971	HCPEpiC	choroid plexus:	n/a
20	chr1:63384921-63384971	NB4	blood:	n/a
21	chr1:63429038-63429088	HCT-116	colon:	n/a
22	chr1:63384921-63384971	SKMC	muscle:	n/a
23	chr1:63372303-63372353	AG10803	skin:	n/a
24	chr1:63419352-63419402	HRPEpiC	eye:	n/a
25	chr1:63429038-63429088	GM12891	blood:	n/a
26	chr1:63384921-63384971	AG09309	skin:	n/a
27	chr1:63429038-63429088	NT2-D1	testis:	n/a
28	chr1:63372303-63372353	Hela-S3	cervix:	n/a
29	chr1:63429038-63429088	SKMC	muscle:	n/a
30	chr1:63384921-63384971	MCF10A-Er-Src	breast:	n/a
31	chr1:63372303-63372353	ECC-1	luminal epithelium:	n/a
32	chr1:63372303-63372353	HNPCEpiC	eye:	n/a
33	chr1:63384921-63384971	NT2-D1	testis:	n/a
34	chr1:63429038-63429088	Hepatocyte	liver:	n/a
35	chr1:63384921-63384971	HAEpiC	amniotic membrane:	n/a
36	chr1:63372303-63372353	U87	brain:	n/a
37	chr1:63419352-63419402	HIPEpiC	eye:	n/a
38	chr1:63372303-63372353	BE2_C	brain:	n/a
39	chr1:63429038-63429088	HNPCEpiC	eye:	n/a
40	chr1:63429038-63429088	GM06990	blood:	n/a
41	chr1:63372303-63372353	ovcar-3	ovarian:	n/a
42	chr1:63372303-63372353	CMK	blood:	n/a
43	chr1:63419352-63419402	T-47D	breast:	n/a
44	chr1:63372303-63372353	SK-N-MC	brain:	n/a
45	chr1:63419352-63419402	HCPEpiC	choroid plexus:	n/a
46	chr1:63372303-63372353	T-47D	breast:	n/a
47	chr1:63419352-63419402	SK-N-SH	brain:	n/a
48	chr1:63372303-63372353	HRPEpiC	eye:	n/a
49	chr1:63429038-63429088	GM12892	blood:	n/a
50	chr1:63429038-63429088	HMEC	breast:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:63275626..63278892-chr1:63281499..63283482,3	K562	blood:
2	chr1:63449158..63452125-chr1:63453992..63456042,2	K562	blood:
3	chr1:63394564..63396637-chr1:63401280..63403618,2	K562	blood:
4	chr1:63356759..63358990-chr1:63365285..63367618,2	K562	blood:
5	chr1:63379512..63381178-chr1:63389230..63392288,3	K562	blood:
6	chr1:63307631..63310506-chr1:63317147..63319485,2	K562	blood:
7	chr1:63267101..63268725-chr1:63271819..63273320,2	K562	blood:
8	chr1:63368475..63370307-chr1:63372752..63375346,2	K562	blood:
9	chr1:63367185..63369129-chr1:63369906..63371778,2	K562	blood:
10	chr1:63261407..63263722-chr1:63269152..63270721,2	K562	blood:
11	chr1:63259687..63262004-chr1:63264703..63267099,2	K562	blood:
12	chr1:63425794..63427328-chr1:63429160..63430808,2	K562	blood:
13	chr1:63306962..63307948-chr1:63455117..63455729,2	MCF-7	breast:
14	chr1:63249971..63252339-chr1:63270685..63272940,3	K562	blood:
15	chr1:63363718..63366869-chr1:63368181..63370923,3	K562	blood:
16	chr1:63403166..63403785-chr10:20783474..20784387,2	MCF-7	breast:
17	chr1:63449158..63452125-chr1:63453992..63456042,2	K562	blood:
18	chr1:63267101..63268725-chr1:63271819..63273320,2	K562	blood:
19	chr1:63271102..63273649-chr1:63283773..63286559,2	K562	blood:
20	chr1:63299113..63301230-chr1:63303804..63305805,2	K562	blood:
21	chr1:63271308..63273102-chr1:63273879..63275805,2	K562	blood:
22	chr1:63379512..63381021-chr1:63389977..63392288,2	K562	blood:
23	chr1:63379512..63381178-chr1:63389230..63392288,3	K562	blood:
24	chr1:63271102..63272988-chr1:63282387..63285273,2	K562	blood:
25	chr1:63266221..63268725-chr1:63270799..63273320,2	K562	blood:
26	chr1:63301720..63303514-chr1:63307887..63310417,3	K562	blood:
27	chr1:63271308..63273102-chr1:63273879..63275805,2	K562	blood:
28	chr1:63307067..63307832-chr1:63371765..63372683,2	K562	blood:
29	chr1:63379512..63381021-chr1:63389977..63392288,2	K562	blood:
30	chr1:63410664..63413172-chr1:63421317..63423276,2	K562	blood:
31	chr1:63280803..63282516-chr1:63283760..63285416,2	K562	blood:
32	chr1:63280803..63282516-chr1:63283760..63285416,2	K562	blood:
33	chr1:63307631..63310506-chr1:63317147..63319485,2	K562	blood:
34	chr1:63248479..63250985-chr1:63262589..63265231,2	K562	blood:
35	chr1:62876198..62878432-chr1:63376499..63378400,2	K562	blood:
36	chr1:63271102..63273649-chr1:63283773..63286559,2	K562	blood:
37	chr1:63295049..63297767-chr1:63299902..63301435,2	K562	blood:
38	chr1:63368475..63370307-chr1:63372752..63375346,2	K562	blood:
39	chr1:63299113..63301230-chr1:63303804..63305805,2	K562	blood:
40	chr1:63261407..63263722-chr1:63269152..63270721,2	K562	blood:
41	chr1:63386826..63389497-chr1:63390101..63393681,3	K562	blood:
42	chr1:63295049..63297767-chr1:63299902..63301435,2	K562	blood:
43	chr1:63425794..63427328-chr1:63429160..63430808,2	K562	blood:
44	chr1:63356759..63358990-chr1:63365285..63367618,2	K562	blood:
45	chr1:63394564..63396637-chr1:63401280..63403618,2	K562	blood:
46	chr1:63307067..63307832-chr1:63371765..63372683,2	K562	blood:
47	chr1:63386826..63389497-chr1:63390101..63393681,3	K562	blood:
48	chr1:63266221..63268725-chr1:63270799..63273320,2	K562	blood:
49	chr1:63306962..63307948-chr1:63455117..63455729,2	MCF-7	breast:
50	chr1:63252409..63254988-chr1:63270726..63273127,2	K562	blood:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DOCK7-3	chr1:63397343-63397529	ucscGeneNc_uc001dav_2
2	lnc-ANGPTL3-5	chr1:63263663-63263917	NONHSAT003643
3	lnc-DOCK7-5	chr1:63436975-63437279	ucscGeneNc_uc001daw_1
4	lnc-DOCK7-3	chr1:63402503-63402614	ucscGeneNc_uc001dav_2
5	lnc-ATG4C-4	chr1:63370851-63371153	NONHSAT003646
6	lnc-DOCK7-3	chr1:63398420-63398521	ucscGeneNc_uc001dav_2
7	lnc-ANGPTL3-5	chr1:63262466-63262569	NONHSAT003643
8	lnc-ATG4C-5	chr1:63401006-63401412	NONHSAT003647
9	lnc-DOCK7-3	chr1:63399663-63399824	ucscGeneNc_uc001dav_2
10	lnc-ATG4C-1	chr1:63366965-63367310	XLOC_000229
11	lnc-ATG4C-5	chr1:63397295-63397462	NONHSAT003647
12	lnc-DOCK7-5	chr1:63428699-63428783	ucscGeneNc_uc001daw_1
13	lnc-ATG4C-1	chr1:63361680-63361780	XLOC_000229
14	lnc-ATG4C-5	chr1:63377509-63377756	NONHSAT003647
15	lnc-DOCK7-3	chr1:63400806-63400941	ucscGeneNc_uc001dav_2
16	lnc-DOCK7-5	chr1:63408411-63408683	ucscGeneNc_uc001daw_1

No data

Variant related genes	Relation type
ENSG00000237163	TF binding region
ATG4C	TF binding region
ENSG00000234318	TF binding region
ENSG00000237163	CpG island
ATG4C	CpG island
ENSG00000234318	CpG island
ENSG00000125703	chromatin interactions
ENSG00000237163	chromatin interactions

Extended variants
information (count: 5387 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:5387 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566318568	chr1:63261271-63261272	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs10159254	chr1:63261286-63261287	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs71643650	chr1:63261350-63261351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs12129919	chr1:63261356-63261357	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs573939556	chr1:63261390-63261391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs71643651	chr1:63261437-63261438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544402893	chr1:63261439-63261440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs556295664	chr1:63261474-63261475	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34988880	chr1:63261478-63261479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145604000	chr1:63261500-63261501	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112840341	chr1:63261506-63261507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545143195	chr1:63261587-63261588	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542594604	chr1:63261594-63261595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112428626	chr1:63261604-63261605	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs12122434	chr1:63261652-63261653	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs111950634	chr1:63261669-63261670	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs111262930	chr1:63261677-63261678	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs561960577	chr1:63261717-63261718	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs531663903	chr1:63261723-63261724	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs142511960	chr1:63261775-63261776	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs566806455	chr1:63261792-63261793	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs566391318	chr1:63261829-63261830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550122599	chr1:63261858-63261859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144802263	chr1:63261859-63261860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs61765899	chr1:63261876-63261877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74734742	chr1:63261879-63261880	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs74261205	chr1:63261894-63261895	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs60552573	chr1:63261897-63261898	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200588924	chr1:63261963-63261964	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144565967	chr1:63261965-63261966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs183432640	chr1:63261990-63261991	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551169317	chr1:63262083-63262084	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs17123841	chr1:63262099-63262100	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs74076998	chr1:63262113-63262114	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs548520307	chr1:63262121-63262122	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567625565	chr1:63262162-63262163	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs188239226	chr1:63262165-63262166	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs141223287	chr1:63262177-63262178	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs540465242	chr1:63262218-63262219	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs150712642	chr1:63262264-63262265	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs116331233	chr1:63262291-63262292	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532697282	chr1:63262364-63262365	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs192785179	chr1:63262409-63262410	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs561682620	chr1:63262436-63262437	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs386631785	chr1:63262531-63262532	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs188391012	chr1:63262532-63262533	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs149427637	chr1:63262546-63262547	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs191507494	chr1:63262547-63262548	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs548115268	chr1:63262607-63262608	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs566362567	chr1:63262692-63262693	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
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
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	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
Papillary thyroid carcinoma	21436994	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
Breast cancer	17603634	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
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	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
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:896 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:63250600-63262400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:63250600-63266600	Weak transcription	Gastric	stomach
3	chr1:63250800-63319000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr1:63251000-63266600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr1:63251000-63269600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:63251000-63272600	Weak transcription	Fetal Muscle Leg	muscle
7	chr1:63251000-63274800	Weak transcription	Fetal Intestine Small	intestine
8	chr1:63251000-63296000	Weak transcription	Fetal Thymus	thymus
9	chr1:63251000-63317800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
10	chr1:63251000-63327400	Weak transcription	Fetal Stomach	stomach
11	chr1:63251200-63327400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr1:63251400-63261200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr1:63251400-63264800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr1:63251400-63275600	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr1:63251800-63273000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr1:63252000-63266600	Weak transcription	Colon Smooth Muscle	Colon
17	chr1:63252000-63269600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr1:63252000-63284400	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr1:63252800-63272400	Weak transcription	Primary T cells from cord blood	blood
20	chr1:63257400-63293400	Weak transcription	Brain Anterior Caudate	brain
21	chr1:63258400-63261400	Weak transcription	Monocytes-CD14+_RO01746	blood
22	chr1:63259000-63263200	Enhancers	Primary B cells from peripheral blood	blood
23	chr1:63259000-63263400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr1:63259000-63263600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:63259400-63262800	Enhancers	Brain Substantia Nigra	brain
26	chr1:63259600-63261400	Enhancers	Brain Cingulate Gyrus	brain
27	chr1:63259600-63262000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr1:63259800-63261200	Enhancers	Brain Hippocampus Middle	brain
29	chr1:63259800-63263000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr1:63260200-63261600	Enhancers	Primary B cells from cord blood	blood
31	chr1:63260200-63262200	Weak transcription	GM12878-XiMat	blood
32	chr1:63260200-63273000	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr1:63260800-63261400	Enhancers	Fetal Lung	lung
34	chr1:63260800-63262800	Enhancers	Primary hematopoietic stem cells	blood
35	chr1:63261000-63269400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr1:63261200-63261400	Enhancers	Rectal Smooth Muscle	rectum
37	chr1:63261200-63262800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr1:63261200-63265600	Weak transcription	Brain Hippocampus Middle	brain
39	chr1:63261400-63261600	Enhancers	Placenta	Placenta
40	chr1:63261400-63262000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr1:63261400-63262600	Weak transcription	Brain Cingulate Gyrus	brain
42	chr1:63261400-63266600	Weak transcription	Fetal Lung	lung
43	chr1:63261600-63261800	Flanking Active TSS	Primary B cells from cord blood	blood
44	chr1:63261600-63326400	Weak transcription	Placenta	Placenta
45	chr1:63261800-63262200	Enhancers	Primary B cells from cord blood	blood
46	chr1:63261800-63265000	Weak transcription	Rectal Smooth Muscle	rectum
47	chr1:63262000-63262400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr1:63262000-63262400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
49	chr1:63262200-63262600	Flanking Active TSS	Primary B cells from cord blood	blood
50	chr1:63262200-63262600	Enhancers	GM12878-XiMat	blood

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