Variant report

Variant	nsv830100
Chromosome Location	chr4:143216951-143393305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1436)
CpG islands
(count:489)
Chromatin interactive
region (count:86)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1436 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:143356828-143357244	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr4:143348669-143348921	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr4:143328695-143329751	HCT-116	colon:	n/a	n/a
4	ATF3	chr4:143329015-143329429	A549	lung:	n/a	n/a
5	ATF3	chr4:143329103-143329732	A549	lung:	n/a	n/a
6	BATF	chr4:143337763-143338124	GM12878	blood:	n/a	chr4:143338040-143338049
7	BCL11A	chr4:143348560-143348908	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL11A	chr4:143326567-143326904	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:143348709-143348868	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr4:143326597-143326837	GM12878	blood:	n/a	n/a
11	BCL3	chr4:143329035-143329532	A549	lung:	n/a	chr4:143329213-143329222 chr4:143329212-143329221
12	BCL3	chr4:143328888-143329606	A549	lung:	n/a	chr4:143329213-143329222 chr4:143329212-143329221
13	BCLAF1	chr4:143274272-143274612	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:143326168-143327057	GM12878	blood:	n/a	chr4:143326645-143326654 chr4:143326646-143326655 chr4:143326646-143326655
15	BHLHE40	chr4:143326537-143326694	HepG2	liver:	n/a	chr4:143326645-143326654 chr4:143326646-143326655 chr4:143326646-143326655
16	BHLHE40	chr4:143274328-143274365	K562	blood:	n/a	n/a
17	BHLHE40	chr4:143328472-143328566	GM12878	blood:	n/a	n/a
18	BHLHE40	chr4:143327366-143327784	GM12878	blood:	n/a	n/a
19	BHLHE40	chr4:143326598-143326796	K562	blood:	n/a	chr4:143326645-143326654 chr4:143326646-143326655 chr4:143326646-143326655
20	BHLHE40	chr4:143326298-143326786	A549	lung:	n/a	chr4:143326645-143326654 chr4:143326646-143326655 chr4:143326646-143326655
21	BRCA1	chr4:143274375-143274623	Hela-S3	cervix:	n/a	n/a
22	CBX3	chr4:143318407-143318969	HCT-116	colon:	n/a	n/a
23	CBX3	chr4:143317385-143317719	HCT-116	colon:	n/a	n/a
24	CBX3	chr4:143325211-143325787	HCT-116	colon:	n/a	n/a
25	CBX3	chr4:143317329-143317815	HCT-116	colon:	n/a	n/a
26	CEBPB	chr4:143268418-143268721	K562	blood:	n/a	chr4:143268592-143268603
27	CEBPB	chr4:143369469-143369747	A549	lung:	n/a	chr4:143369629-143369640 chr4:143369629-143369642
28	CEBPB	chr4:143328773-143329684	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:143305214-143305665	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr4:143323335-143323684	IMR90	lung:	n/a	n/a
31	CEBPB	chr4:143274304-143274614	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:143291302-143291561	A549	lung:	n/a	chr4:143291454-143291465 chr4:143291456-143291465 chr4:143291456-143291465 chr4:143291456-143291465 chr4:143291454-143291467 chr4:143291456-143291465 chr4:143291454-143291467 chr4:143291456-143291467
33	CEBPB	chr4:143326021-143327054	IMR90	lung:	n/a	chr4:143326150-143326163
34	CEBPB	chr4:143305173-143305676	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr4:143328577-143329755	HCT-116	colon:	n/a	n/a
36	CEBPB	chr4:143318282-143318632	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:143328829-143329661	A549	lung:	n/a	n/a
38	CEBPB	chr4:143300393-143300779	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:143324175-143324529	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:143369463-143369788	HepG2	liver:	n/a	chr4:143369629-143369640 chr4:143369629-143369642
41	CEBPB	chr4:143323423-143323616	A549	lung:	n/a	n/a
42	CEBPB	chr4:143318335-143318610	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:143268414-143268784	HepG2	liver:	n/a	chr4:143268592-143268603
44	CEBPB	chr4:143268439-143268738	A549	lung:	n/a	chr4:143268592-143268603
45	CEBPB	chr4:143272060-143272410	MCF-7	breast:	n/a	n/a
46	CEBPB	chr4:143268403-143268725	MCF-7	breast:	n/a	chr4:143268592-143268603
47	CEBPB	chr4:143324181-143324641	IMR90	lung:	n/a	n/a
48	CEBPB	chr4:143317325-143317873	HCT-116	colon:	n/a	n/a
49	CEBPB	chr4:143291268-143291599	HepG2	liver:	n/a	chr4:143291454-143291465 chr4:143291456-143291465 chr4:143291456-143291465 chr4:143291456-143291465 chr4:143291454-143291467 chr4:143291456-143291465 chr4:143291454-143291467 chr4:143291456-143291467
50	CEBPB	chr4:143268318-143268885	HCT-116	colon:	n/a	chr4:143268592-143268603

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:143275181-143275231	AG10803	skin:	n/a
2	chr4:143275181-143275231	AG10803	skin:	n/a
3	chr4:143286770-143286820	GM12892	blood:	n/a
4	chr4:143217765-143217815	GM12878	blood:	n/a
5	chr4:143286770-143286820	SK-N-SH	brain:	n/a
6	chr4:143327279-143327329	GM06990	blood:	n/a
7	chr4:143301382-143301432	GM19239	blood:	n/a
8	chr4:143324090-143324140	SAEC	small airway:	n/a
9	chr4:143275181-143275231	HL-60	blood:	n/a
10	chr4:143327279-143327329	IMR90	lung:	fetal
11	chr4:143269319-143269369	NHDF-neo	bronchial:	n/a
12	chr4:143326541-143326591	MCF-7	breast:	n/a
13	chr4:143269319-143269369	K562	blood:	n/a
14	chr4:143269319-143269369	H1-hESC	embryonic stem cell:	embryo
15	chr4:143269319-143269369	HRCEpiC	kidney:	n/a
16	chr4:143269319-143269369	AG04449	skin:	fetal
17	chr4:143275181-143275231	T-47D	breast:	n/a
18	chr4:143269319-143269369	Caco-2	colon:	n/a
19	chr4:143324090-143324140	MCF-7	breast:	n/a
20	chr4:143286770-143286820	Jurkat	blood:	n/a
21	chr4:143301382-143301432	MCF-7	breast:	n/a
22	chr4:143327279-143327329	AG10803	skin:	n/a
23	chr4:143326541-143326591	HL-60	blood:	n/a
24	chr4:143286770-143286820	HCT-116	colon:	n/a
25	chr4:143269319-143269369	BE2_C	brain:	n/a
26	chr4:143326541-143326591	HCPEpiC	choroid plexus:	n/a
27	chr4:143217765-143217815	AG04450	lung:	fetal
28	chr4:143324090-143324140	H1-hESC	embryonic stem cell:	embryo
29	chr4:143327279-143327329	AG09319	gingival:	n/a
30	chr4:143275181-143275231	HCM	heart:	n/a
31	chr4:143326541-143326591	SAEC	small airway:	n/a
32	chr4:143286770-143286820	MCF10A-Er-Src	breast:	n/a
33	chr4:143217765-143217815	SK-N-SH_RA	brain:	n/a
34	chr4:143275181-143275231	K562	blood:	n/a
35	chr4:143324090-143324140	SKMC	muscle:	n/a
36	chr4:143326541-143326591	AG09309	skin:	n/a
37	chr4:143301382-143301432	AG09319	gingival:	n/a
38	chr4:143275181-143275231	HNPCEpiC	eye:	n/a
39	chr4:143326541-143326591	HCF	heart:	n/a
40	chr4:143327279-143327329	AG04449	skin:	fetal
41	chr4:143324090-143324140	AG09309	skin:	n/a
42	chr4:143327279-143327329	HCF	heart:	n/a
43	chr4:143217765-143217815	HEEpiC	esophagus:	n/a
44	chr4:143269319-143269369	MCF-7	breast:	n/a
45	chr4:143326541-143326591	HEEpiC	esophagus:	n/a
46	chr4:143327279-143327329	Hepatocyte	liver:	n/a
47	chr4:143326541-143326591	MCF10A-Er-Src	breast:	n/a
48	chr4:143324090-143324140	HIPEpiC	eye:	n/a
49	chr4:143324090-143324140	HCM	heart:	n/a
50	chr4:143326541-143326591	RPTEC	kidney:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:143248197..143251091-chr4:143251124..143253025,2	MCF-7	breast:
2	chr4:143389462..143399452-chr4:143428707..143442488,28	MCF-7	breast:
3	chr4:143277710..143279872-chr4:143280001..143282986,2	K562	blood:
4	chr4:143272607..143274373-chr4:143277065..143279303,2	MCF-7	breast:
5	chr4:143311891..143313419-chr4:143319289..143320920,2	MCF-7	breast:
6	chr4:143281985..143283743-chr4:143392131..143394850,2	MCF-7	breast:
7	chr4:143370028..143372952-chr4:143766841..143769136,2	MCF-7	breast:
8	chr4:143277710..143279872-chr4:143280001..143282986,2	K562	blood:
9	chr4:143345499..143347923-chr4:143391680..143394549,2	MCF-7	breast:
10	chr4:143360196..143364725-chr4:143377583..143382490,5	MCF-7	breast:
11	chr4:143347061..143349810-chr4:143351941..143353442,2	MCF-7	breast:
12	chr4:143377586..143379612-chr4:143380437..143382675,2	MCF-7	breast:
13	chr4:143368553..143371081-chr4:143381328..143384317,2	MCF-7	breast:
14	chr4:143391122..143393717-chr4:143678959..143680972,2	MCF-7	breast:
15	chr4:143274011..143274935-chr4:143946210..143946920,2	MCF-7	breast:
16	chr4:143325204..143328052-chr4:143329369..143331375,2	K562	blood:
17	chr4:143333597..143335971-chr4:143337267..143338808,2	MCF-7	breast:
18	chr4:143374144..143376062-chr4:143381954..143384712,2	MCF-7	breast:
19	chr4:143327600..143329351-chr4:143391019..143392587,2	MCF-7	breast:
20	chr4:143363779..143366801-chr4:143367868..143370229,3	K562	blood:
21	chr4:143391421..143397876-chr4:143484529..143495051,12	MCF-7	breast:
22	chr4:143248197..143251091-chr4:143251124..143253025,2	MCF-7	breast:
23	chr4:143372548..143374141-chr4:143377111..143379331,2	MCF-7	breast:
24	chr4:143371682..143373996-chr4:143377086..143381453,3	MCF-7	breast:
25	chr4:143362260..143364644-chr4:143393395..143395678,2	MCF-7	breast:
26	chr4:143334587..143337797-chr4:143392954..143395413,3	MCF-7	breast:
27	chr4:143272607..143274373-chr4:143277065..143279303,2	MCF-7	breast:
28	chr4:143360196..143364725-chr4:143377583..143382490,5	MCF-7	breast:
29	chr4:143351692..143359150-chr4:143392769..143399702,12	MCF-7	breast:
30	chr4:143377636..143380466-chr4:143419571..143421151,2	MCF-7	breast:
31	chr4:143326852..143329330-chr4:143520781..143523143,2	MCF-7	breast:
32	chr4:143385183..143386744-chr4:143537618..143539562,2	MCF-7	breast:
33	chr4:143246175..143247898-chr4:143247988..143249905,2	MCF-7	breast:
34	chr4:143311891..143313419-chr4:143319289..143320920,2	MCF-7	breast:
35	chr4:143322243..143323903-chr4:143325098..143328296,3	MCF-7	breast:
36	chr4:143254956..143256541-chr4:143392223..143394166,2	MCF-7	breast:
37	chr4:143377913..143379697-chr4:143381987..143384286,3	MCF-7	breast:
38	chr4:143377586..143379612-chr4:143380437..143382675,2	MCF-7	breast:
39	chr4:143371682..143373996-chr4:143377086..143381453,3	MCF-7	breast:
40	chr4:143323626..143325827-chr4:143327783..143329444,2	MCF-7	breast:
41	chr4:143246175..143247898-chr4:143247988..143249905,2	MCF-7	breast:
42	chr4:143378836..143380380-chr4:143385450..143387701,2	MCF-7	breast:
43	chr4:143367680..143375723-chr4:143391908..143397720,10	MCF-7	breast:
44	chr4:143276856..143278860-chr4:143299385..143301357,2	MCF-7	breast:
45	chr4:143371522..143373447-chr4:143534155..143537026,2	MCF-7	breast:
46	chr4:143327592..143330271-chr4:143378912..143381553,2	MCF-7	breast:
47	chr4:143345499..143347923-chr4:143391680..143394549,2	MCF-7	breast:
48	chr4:143356129..143358446-chr4:143393710..143395467,2	MCF-7	breast:
49	chr4:143326731..143329100-chr4:143388048..143390704,2	MCF-7	breast:
50	chr4:143389165..143391591-chr4:143488298..143490460,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IL15-1	chr4:143238391-143238699	NONHSAT098533

No data

Variant related genes	Relation type
INPP4B	TF binding region
LSM3P4	TF binding region
INPP4B	CpG island
LSM3P4	CpG island
ENSG00000266411	chromatin interactions
ENSG00000251248	chromatin interactions
ENSG00000109452	chromatin interactions
ENSG00000263931	chromatin interactions
ENSG00000249806	chromatin interactions

Extended variants
information (count: 6527 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:6527 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72722463	chr4:143216975-143216976	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs534956169	chr4:143216989-143216990	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs146060928	chr4:143217028-143217029	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs544947690	chr4:143217039-143217040	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs140209306	chr4:143217046-143217047	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs549602387	chr4:143217076-143217077	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs191856055	chr4:143217136-143217137	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs35089223	chr4:143217218-143217219	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs578240763	chr4:143217221-143217222	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs76613805	chr4:143217230-143217231	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs77555272	chr4:143217234-143217235	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs571058132	chr4:143217286-143217287	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs531961125	chr4:143217303-143217304	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs547023160	chr4:143217313-143217314	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs2130685	chr4:143217318-143217319	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs557395173	chr4:143217321-143217322	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs575370335	chr4:143217344-143217345	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs3775683	chr4:143217386-143217387	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs2172023	chr4:143217391-143217392	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2172024	chr4:143217404-143217405	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs140587777	chr4:143217441-143217442	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183670262	chr4:143217450-143217451	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs140010091	chr4:143217513-143217514	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs188323043	chr4:143217536-143217537	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192360264	chr4:143217620-143217621	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185111850	chr4:143217676-143217677	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs114546188	chr4:143217686-143217687	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567695936	chr4:143217697-143217698	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs115099929	chr4:143217734-143217735	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs376655938	chr4:143217774-143217775	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2636651	chr4:143217837-143217838	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs578251349	chr4:143217871-143217872	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538926450	chr4:143217918-143217919	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs578162521	chr4:143217925-143217926	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554388786	chr4:143217998-143217999	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2627810	chr4:143218017-143218018	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs190214463	chr4:143218026-143218027	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560805785	chr4:143218079-143218080	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs370774066	chr4:143218089-143218090	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2636652	chr4:143218113-143218114	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs35339401	chr4:143218137-143218138	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs79872701	chr4:143218150-143218151	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs75538498	chr4:143218151-143218152	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs28537621	chr4:143218154-143218155	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs146354244	chr4:143218159-143218160	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs17015835	chr4:143218208-143218209	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs34251526	chr4:143218236-143218237	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181864750	chr4:143218265-143218266	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554232161	chr4:143218334-143218335	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs532313587	chr4:143218376-143218377	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Mental retardation	17901693	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Obesity	20622171	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Breast cancer	22048815	CNVD
Autism	22241247	CNVD
Glioblastoma multiforme	22286061	CNVD
Renal cell carcinoma	20952505	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3574 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:143187400-143218600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr4:143192000-143219400	Weak transcription	Dnd41	blood
3	chr4:143196000-143225200	Weak transcription	NHDF-Ad	bronchial
4	chr4:143199400-143230800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:143200000-143240000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr4:143204000-143230600	Weak transcription	Left Ventricle	heart
7	chr4:143204200-143229000	Weak transcription	NHEK	skin
8	chr4:143204600-143233600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr4:143206000-143233400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
10	chr4:143207000-143223200	Weak transcription	Aorta	Aorta
11	chr4:143208800-143220400	Weak transcription	Primary hematopoietic stem cells	blood
12	chr4:143209200-143226400	Weak transcription	Fetal Heart	heart
13	chr4:143209800-143229000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr4:143210800-143235400	Weak transcription	Right Ventricle	heart
15	chr4:143211000-143220000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr4:143211600-143224600	Weak transcription	Fetal Muscle Leg	muscle
17	chr4:143212800-143218000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:143214000-143217000	Weak transcription	HSMM	muscle
19	chr4:143214200-143220000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr4:143214200-143230600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr4:143214600-143219000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
22	chr4:143214800-143218200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:143215200-143217200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr4:143215200-143235200	Weak transcription	Osteobl	bone
25	chr4:143215400-143217000	Strong transcription	Primary T cells from cord blood	blood
26	chr4:143215400-143217000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr4:143215400-143217400	Enhancers	Primary T helper cells fromperipheralblood	blood
28	chr4:143215600-143225000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:143215800-143235200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
30	chr4:143216000-143220000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr4:143216200-143217200	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chr4:143216200-143217400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr4:143216200-143234600	Weak transcription	Thymus	Thymus
34	chr4:143216400-143217000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr4:143216600-143217800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:143216600-143219200	Weak transcription	HMEC	breast
37	chr4:143216600-143233600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr4:143216800-143217000	Enhancers	Primary T cells fromperipheralblood	blood
39	chr4:143216800-143217000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr4:143216800-143217600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:143216800-143220000	Weak transcription	HSMMtube	muscle
42	chr4:143216800-143224800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
43	chr4:143217000-143217400	Genic enhancers	Primary T helper 17 cells PMA-I stimulated	--
44	chr4:143217000-143217400	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr4:143217000-143217800	Weak transcription	Primary T cells from cord blood	blood
46	chr4:143217000-143218800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr4:143217000-143220600	Strong transcription	HSMM	muscle
48	chr4:143217000-143222600	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr4:143217200-143218000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr4:143217200-143218000	Weak transcription	Primary T helper cells PMA-I stimulated	--

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