Variant report

Variant	nsv1007619
Chromosome Location	chr4:120014898-120112460
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:687)
CpG islands
(count:428)
Chromatin interactive
region (count:36)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:687 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:120069300-120069382	K562	blood:	n/a	n/a
2	ARID3A	chr4:120061121-120061568	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:120034563-120034635	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:120020305-120020333	K562	blood:	n/a	n/a
5	ATF1	chr4:120024459-120024838	K562	blood:	n/a	n/a
6	ATF3	chr4:120024333-120024882	A549	lung:	n/a	n/a
7	ATF3	chr4:120034410-120034782	HCT-116	colon:	n/a	n/a
8	ATF3	chr4:120024490-120024806	K562	blood:	n/a	n/a
9	ATF3	chr4:120024332-120025018	HCT-116	colon:	n/a	n/a
10	ATF3	chr4:120024370-120024929	A549	lung:	n/a	n/a
11	ATF3	chr4:120024324-120024955	HCT-116	colon:	n/a	n/a
12	BACH1	chr4:120064017-120064337	K562	blood:	n/a	n/a
13	BACH1	chr4:120023606-120023664	K562	blood:	n/a	n/a
14	BACH1	chr4:120064009-120064372	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr4:120043723-120043785	K562	blood:	n/a	n/a
16	BCL3	chr4:120023637-120024906	A549	lung:	n/a	n/a
17	BHLHE40	chr4:120023932-120024184	HepG2	liver:	n/a	n/a
18	BHLHE40	chr4:120045731-120045795	K562	blood:	n/a	n/a
19	CBX3	chr4:120024314-120025029	HCT-116	colon:	n/a	n/a
20	CBX3	chr4:120034414-120034855	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:120034232-120034884	HCT-116	colon:	n/a	n/a
22	CEBPB	chr4:120024426-120024900	A549	lung:	n/a	n/a
23	CEBPB	chr4:120026757-120027115	IMR90	lung:	n/a	chr4:120026921-120026934 chr4:120026899-120026912 chr4:120026922-120026933 chr4:120026921-120026932
24	CEBPB	chr4:120024542-120024761	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:120023818-120024305	A549	lung:	n/a	n/a
26	CEBPB	chr4:120027464-120027562	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:120034329-120034884	A549	lung:	n/a	chr4:120034597-120034608
28	CEBPB	chr4:120024043-120025008	IMR90	lung:	n/a	n/a
29	CEBPB	chr4:120014237-120014989	A549	lung:	n/a	chr4:120014307-120014318
30	CEBPB	chr4:120034213-120034960	HCT-116	colon:	n/a	chr4:120034597-120034608
31	CEBPB	chr4:120020489-120020985	A549	lung:	n/a	chr4:120020578-120020589 chr4:120020578-120020591 chr4:120020909-120020920 chr4:120020578-120020591 chr4:120020908-120020921
32	CEBPB	chr4:120023726-120025088	A549	lung:	n/a	n/a
33	CEBPB	chr4:120024651-120024806	K562	blood:	n/a	n/a
34	CEBPB	chr4:120060446-120060797	IMR90	lung:	n/a	chr4:120060612-120060625
35	CEBPB	chr4:120020408-120020706	MCF-7	breast:	n/a	chr4:120020578-120020589 chr4:120020578-120020591 chr4:120020578-120020591
36	CEBPB	chr4:120034433-120034773	HepG2	liver:	n/a	chr4:120034597-120034608
37	CEBPB	chr4:120023929-120024255	HepG2	liver:	n/a	n/a
38	CEBPB	chr4:120060537-120060793	A549	lung:	n/a	chr4:120060612-120060625
39	CEBPB	chr4:120024384-120024891	ECC-1	luminal epithelium:	n/a	n/a
40	CEBPB	chr4:120020255-120021096	Hela-S3	cervix:	n/a	chr4:120020578-120020589 chr4:120020578-120020591 chr4:120020909-120020920 chr4:120020578-120020591 chr4:120020908-120020921
41	CEBPB	chr4:120026796-120027093	K562	blood:	n/a	chr4:120026921-120026934 chr4:120026899-120026912 chr4:120026922-120026933 chr4:120026921-120026932
42	CEBPB	chr4:120023849-120025007	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr4:120034354-120034881	Hela-S3	cervix:	n/a	chr4:120034597-120034608
44	CEBPB	chr4:120034507-120034821	A549	lung:	n/a	chr4:120034597-120034608
45	CEBPB	chr4:120034361-120034805	A549	lung:	n/a	chr4:120034597-120034608
46	CEBPB	chr4:120034471-120034710	K562	blood:	n/a	chr4:120034597-120034608
47	CEBPB	chr4:120060450-120060925	Hela-S3	cervix:	n/a	chr4:120060612-120060625
48	CEBPB	chr4:120026910-120026953	H1-hESC	embryonic stem cell:	n/a	chr4:120026921-120026934 chr4:120026922-120026933 chr4:120026921-120026932
49	CEBPB	chr4:120034393-120034832	IMR90	lung:	n/a	chr4:120034597-120034608
50	CEBPB	chr4:120034470-120034729	MCF-7	breast:	n/a	chr4:120034597-120034608

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120057110-120057160	AoSMC	blood vessel:	n/a
2	chr4:120057110-120057160	AoSMC	blood vessel:	n/a
3	chr4:120056829-120056879	BJ	skin:	n/a
4	chr4:120038219-120038269	Hela-S3	cervix:	n/a
5	chr4:120061211-120061261	GM12891	blood:	n/a
6	chr4:120057818-120057868	T-47D	breast:	n/a
7	chr4:120057110-120057160	AG04450	lung:	fetal
8	chr4:120038219-120038269	NHBE	bronchial:	n/a
9	chr4:120057110-120057160	PFSK-1	brain:	n/a
10	chr4:120038219-120038269	HEK293	kidney:	embryo
11	chr4:120056829-120056879	AoSMC	blood vessel:	n/a
12	chr4:120057818-120057868	HCT-116	colon:	n/a
13	chr4:120061211-120061261	HEEpiC	esophagus:	n/a
14	chr4:120015469-120015519	HMEC	breast:	n/a
15	chr4:120038219-120038269	Caco-2	colon:	n/a
16	chr4:120057818-120057868	GM06990	blood:	n/a
17	chr4:120038219-120038269	NB4	blood:	n/a
18	chr4:120057818-120057868	SAEC	small airway:	n/a
19	chr4:120055608-120055658	NHBE	bronchial:	n/a
20	chr4:120038219-120038269	GM12892	blood:	n/a
21	chr4:120061211-120061261	HRPEpiC	eye:	n/a
22	chr4:120038219-120038269	NH-A	brain:	n/a
23	chr4:120038219-120038269	HRE	kidney:	n/a
24	chr4:120038219-120038269	AoSMC	blood vessel:	n/a
25	chr4:120015469-120015519	SAEC	small airway:	n/a
26	chr4:120057818-120057868	IMR90	lung:	fetal
27	chr4:120056829-120056879	IMR90	lung:	fetal
28	chr4:120061211-120061261	MCF10A-Er-Src	breast:	n/a
29	chr4:120055608-120055658	HRE	kidney:	n/a
30	chr4:120038219-120038269	ECC-1	luminal epithelium:	n/a
31	chr4:120015469-120015519	T-47D	breast:	n/a
32	chr4:120057110-120057160	Jurkat	blood:	n/a
33	chr4:120015469-120015519	NHDF-neo	bronchial:	n/a
34	chr4:120055608-120055658	A549	lung:	n/a
35	chr4:120057110-120057160	U87	brain:	n/a
36	chr4:120038219-120038269	MCF-7	breast:	n/a
37	chr4:120038219-120038269	K562	blood:	n/a
38	chr4:120055608-120055658	HCM	heart:	n/a
39	chr4:120061211-120061261	HUVEC	blood vessel:	n/a
40	chr4:120057110-120057160	HEK293	kidney:	embryo
41	chr4:120056829-120056879	ovcar-3	ovarian:	n/a
42	chr4:120056829-120056879	LNCaP	prostate:	n/a
43	chr4:120061211-120061261	AG04450	lung:	fetal
44	chr4:120061211-120061261	BJ	skin:	n/a
45	chr4:120015469-120015519	NH-A	brain:	n/a
46	chr4:120015469-120015519	A549	lung:	n/a
47	chr4:120015469-120015519	PFSK-1	brain:	n/a
48	chr4:120038219-120038269	ovcar-3	ovarian:	n/a
49	chr4:120038219-120038269	HIPEpiC	eye:	n/a
50	chr4:120038219-120038269	ProgFib	skin:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120072229..120075010-chr4:120089681..120092174,2	K562	blood:
2	chr4:120096520..120098803-chr4:120098872..120101479,2	K562	blood:
3	chr4:120015958..120018191-chr4:120019171..120021900,2	MCF-7	breast:
4	chr4:119967207..119969277-chr4:120017510..120021674,3	MCF-7	breast:
5	chr4:120026582..120029647-chr4:120131891..120134886,3	MCF-7	breast:
6	chr4:120015958..120018191-chr4:120019171..120021900,2	MCF-7	breast:
7	chr4:119964664..119967824-chr4:120028894..120031199,3	MCF-7	breast:
8	chr4:120018111..120021033-chr4:120132660..120135354,3	MCF-7	breast:
9	chr4:120059391..120062207-chr4:120131058..120133617,2	MCF-7	breast:
10	chr4:120035133..120037765-chr4:120132862..120135100,2	MCF-7	breast:
11	chr4:120060909..120063531-chr4:120066181..120067927,2	MCF-7	breast:
12	chr4:119989699..119991632-chr4:120032879..120034725,2	MCF-7	breast:
13	chr4:120110664..120112250-chr4:120132207..120134016,2	K562	blood:
14	chr4:120001166..120004043-chr4:120014693..120016511,3	MCF-7	breast:
15	chr4:120021974..120023552-chr4:120133050..120134987,2	MCF-7	breast:
16	chr4:120033457..120035928-chr4:120042450..120044760,2	MCF-7	breast:
17	chr4:120060171..120063563-chr4:120128883..120130877,3	MCF-7	breast:
18	chr4:120107053..120109251-chr4:120131734..120133629,2	MCF-7	breast:
19	chr4:120082797..120084965-chr4:120133823..120135965,2	MCF-7	breast:
20	chr4:120033922..120036234-chr4:120037431..120039972,2	K562	blood:
21	chr4:120100153..120102490-chr4:120128940..120130617,2	MCF-7	breast:
22	chr4:120072229..120075010-chr4:120089681..120092174,2	K562	blood:
23	chr4:120014220..120018464-chr4:120020403..120024000,3	MCF-7	breast:
24	chr4:120021896..120024544-chr4:120027887..120030777,2	MCF-7	breast:
25	chr4:120060909..120063531-chr4:120066181..120067927,2	MCF-7	breast:
26	chr4:120109943..120112104-chr4:120116524..120118250,2	MCF-7	breast:
27	chr4:120033922..120036234-chr4:120037431..120039972,2	K562	blood:
28	chr4:120033457..120035928-chr4:120042450..120044760,2	MCF-7	breast:
29	chr4:120014220..120018464-chr4:120020403..120024000,3	MCF-7	breast:
30	chr4:120013479..120014990-chr4:120129629..120131701,2	MCF-7	breast:
31	chr4:120105848..120109387-chr4:120131964..120134946,3	MCF-7	breast:
32	chr4:120033091..120034925-chr4:120132885..120135454,2	MCF-7	breast:
33	chr4:120026501..120028052-chr4:120132868..120134580,2	MCF-7	breast:
34	chr4:120032730..120035461-chr4:120133316..120136122,2	MCF-7	breast:
35	chr4:120021896..120024544-chr4:120027887..120030777,2	MCF-7	breast:
36	chr4:120096520..120098803-chr4:120098872..120101479,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-455G16.1.1-1	chr4:120038634-120039855	XLOC_004054
2	lnc-RP11-455G16.1.1-1	chr4:120038634-120039855	XLOC_004054
3	lnc-RP11-455G16.1.1-1	chr4:120040688-120040908	XLOC_004054
4	lnc-RP11-455G16.1.1-1	chr4:120049353-120049505	XLOC_004054
5	lnc-RP11-455G16.1.1-1	chr4:120038634-120039855	XLOC_004054
6	lnc-RP11-455G16.1.1-1	chr4:120038634-120039855	XLOC_004054
7	lnc-RP11-455G16.1.1-1	chr4:120049353-120049505	XLOC_004054
8	lnc-RP11-455G16.1.1-1	chr4:120040688-120040847	XLOC_004054
9	lnc-RP11-455G16.1.1-1	chr4:120040678-120040984	XLOC_004054
10	lnc-RP11-455G16.1.1-1	chr4:120040688-120040847	XLOC_004054
11	lnc-RP11-455G16.1.1-1	chr4:120043362-120043513	XLOC_004054
12	lnc-RP11-455G16.1.1-1	chr4:120042792-120043419	XLOC_004054
13	lnc-RP11-455G16.1.1-1	chr4:120040688-120040990	XLOC_004054

No data

Variant related genes	Relation type
MYOZ2	TF binding region
MYOZ2	CpG island
ENSG00000178636	chromatin interactions
ENSG00000249356	chromatin interactions
ENSG00000145390	chromatin interactions
BCL2L11	miRNA target sites

Extended variants
information (count: 3646 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3646 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17050077	chr4:120014898-120014899	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs186980711	chr4:120014949-120014950	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs530422063	chr4:120014959-120014960	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs550160183	chr4:120014962-120014963	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs564165066	chr4:120015014-120015015	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs532898533	chr4:120015032-120015033	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs547141858	chr4:120015049-120015050	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs371002716	chr4:120015088-120015089	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs145806569	chr4:120015109-120015110	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs200351949	chr4:120015131-120015132	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs147073179	chr4:120015133-120015134	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs35018022	chr4:120015134-120015135	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs3052107	chr4:120015143-120015144	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs397724356	chr4:120015144-120015145	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs549691024	chr4:120015153-120015154	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs77320171	chr4:120015180-120015181	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs538195499	chr4:120015211-120015212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147766759	chr4:120015229-120015230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141256987	chr4:120015233-120015234	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs190826723	chr4:120015254-120015255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs534013389	chr4:120015258-120015259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs59979212	chr4:120015277-120015278	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572942404	chr4:120015314-120015315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs183004779	chr4:120015319-120015320	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188035889	chr4:120015325-120015326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575182723	chr4:120015341-120015342	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377765417	chr4:120015357-120015358	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs543769324	chr4:120015388-120015389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4632642	chr4:120015440-120015441	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs114751674	chr4:120015448-120015449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539939263	chr4:120015465-120015466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560236885	chr4:120015493-120015494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192456335	chr4:120015527-120015528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115320472	chr4:120015556-120015557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11943226	chr4:120015562-120015563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs569532331	chr4:120015653-120015654	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11939080	chr4:120015693-120015694	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs551773539	chr4:120015694-120015695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs146949853	chr4:120015709-120015710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182947615	chr4:120015719-120015720	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11939118	chr4:120015799-120015800	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs187493993	chr4:120015806-120015807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs148144014	chr4:120015819-120015820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs192937548	chr4:120015831-120015832	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs114600158	chr4:120015835-120015836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141923105	chr4:120015866-120015867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs558067901	chr4:120015869-120015870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11935300	chr4:120015886-120015887	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs184571866	chr4:120015887-120015888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs78380139	chr4:120015922-120015923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	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
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1013 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120009000-120017600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr4:120009200-120019000	Weak transcription	Fetal Intestine Large	intestine
3	chr4:120013000-120015400	Enhancers	Stomach Mucosa	stomach
4	chr4:120013200-120015200	Enhancers	HepG2	liver
5	chr4:120014000-120015000	Enhancers	Pancreas	Pancrea
6	chr4:120014200-120015000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:120014200-120016000	Enhancers	HUVEC	blood vessel
8	chr4:120014400-120015000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:120014400-120015000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr4:120014400-120015000	Enhancers	Muscle Satellite Cultured Cells	--
11	chr4:120014400-120015000	Enhancers	Colonic Mucosa	Colon
12	chr4:120014400-120015000	Enhancers	Sigmoid Colon	Sigmoid Colon
13	chr4:120014400-120015000	Enhancers	HSMM	muscle
14	chr4:120014400-120015000	Enhancers	NH-A	brain
15	chr4:120014400-120015000	Enhancers	Osteobl	bone
16	chr4:120014400-120015200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:120014400-120015200	Flanking Active TSS	A549	lung
18	chr4:120014400-120015600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
19	chr4:120014600-120015000	Enhancers	Right Atrium	heart
20	chr4:120014600-120015400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:120014600-120015600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr4:120014600-120015600	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr4:120014600-120015800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr4:120014800-120015000	Enhancers	Left Ventricle	heart
25	chr4:120014800-120015000	Enhancers	Skeletal Muscle Female	skeletal muscle
26	chr4:120014800-120019000	Enhancers	Rectal Mucosa Donor 31	rectum
27	chr4:120014800-120022800	Weak transcription	NHEK	skin
28	chr4:120014800-120045000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr4:120015000-120016600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:120015000-120016600	Weak transcription	Left Ventricle	heart
31	chr4:120015000-120019000	Weak transcription	Skeletal Muscle Female	skeletal muscle
32	chr4:120015000-120019600	Weak transcription	Osteobl	bone
33	chr4:120015000-120020000	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr4:120015000-120020200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:120015000-120020200	Weak transcription	HSMM	muscle
36	chr4:120015000-120020200	Weak transcription	NH-A	brain
37	chr4:120015000-120021800	Weak transcription	Sigmoid Colon	Sigmoid Colon
38	chr4:120015000-120027800	Weak transcription	Right Atrium	heart
39	chr4:120015200-120017000	Enhancers	A549	lung
40	chr4:120015600-120016600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr4:120015600-120017800	Weak transcription	Rectal Mucosa Donor 29	rectum
42	chr4:120015600-120020200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr4:120015800-120020200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:120016600-120016800	Enhancers	NHDF-Ad	bronchial
45	chr4:120016600-120017000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr4:120016600-120017000	Enhancers	Left Ventricle	heart
47	chr4:120016600-120017400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr4:120016800-120017000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:120016800-120017600	Weak transcription	NHDF-Ad	bronchial
50	chr4:120017000-120017200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood

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