Variant report

Variant	nsv880244
Chromosome Location	chr4:148764252-148920089
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1636)
CpG islands
(count:672)
Chromatin interactive
region (count:72)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1636 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:148787969-148788298	K562	blood:	n/a	chr4:148788038-148788054
2	ATF2	chr4:148905146-148905549	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:148864088-148864910	GM12878	blood:	n/a	chr4:148864728-148864735
4	ATF2	chr4:148767365-148767976	GM12878	blood:	n/a	n/a
5	ATF2	chr4:148902175-148902940	GM12878	blood:	n/a	n/a
6	ATF2	chr4:148787816-148788380	GM12878	blood:	n/a	n/a
7	ATF2	chr4:148767312-148767995	GM12878	blood:	n/a	n/a
8	ATF2	chr4:148864139-148864803	GM12878	blood:	n/a	chr4:148864728-148864735
9	ATF2	chr4:148902227-148902856	GM12878	blood:	n/a	n/a
10	ATF3	chr4:148764435-148764607	K562	blood:	n/a	n/a
11	BACH1	chr4:148872002-148872363	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:148871841-148872264	K562	blood:	n/a	n/a
13	BATF	chr4:148767566-148767838	GM12878	blood:	n/a	n/a
14	BATF	chr4:148864272-148864651	GM12878	blood:	n/a	n/a
15	BATF	chr4:148864246-148864664	GM12878	blood:	n/a	n/a
16	BATF	chr4:148902422-148902835	GM12878	blood:	n/a	n/a
17	BATF	chr4:148902392-148902837	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:148864303-148864562	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:148864208-148864680	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:148902479-148902777	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:148767557-148767865	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:148767443-148767836	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:148902394-148902862	GM12878	blood:	n/a	n/a
24	BCL3	chr4:148767436-148767940	GM12878	blood:	n/a	n/a
25	BCLAF1	chr4:148864138-148864663	GM12878	blood:	n/a	n/a
26	BCLAF1	chr4:148767506-148767907	GM12878	blood:	n/a	n/a
27	BCLAF1	chr4:148787843-148788348	GM12878	blood:	n/a	chr4:148787972-148787981
28	BCLAF1	chr4:148902292-148902869	GM12878	blood:	n/a	n/a
29	BCLAF1	chr4:148767473-148767952	GM12878	blood:	n/a	n/a
30	BHLHE40	chr4:148767322-148768199	GM12878	blood:	n/a	chr4:148767725-148767738
31	BHLHE40	chr4:148787881-148788290	GM12878	blood:	n/a	n/a
32	BHLHE40	chr4:148878653-148878950	GM12878	blood:	n/a	n/a
33	BHLHE40	chr4:148902448-148902796	GM12878	blood:	n/a	n/a
34	BHLHE40	chr4:148864181-148864947	GM12878	blood:	n/a	n/a
35	BHLHE40	chr4:148865713-148865743	GM12878	blood:	n/a	n/a
36	CCNT2	chr4:148843357-148843586	K562	blood:	n/a	chr4:148843482-148843502
37	CEBPB	chr4:148885736-148886004	IMR90	lung:	n/a	n/a
38	CEBPB	chr4:148820689-148821008	IMR90	lung:	n/a	chr4:148820843-148820854
39	CEBPB	chr4:148862724-148862920	A549	lung:	n/a	n/a
40	CEBPB	chr4:148889828-148890161	K562	blood:	n/a	chr4:148889959-148889972 chr4:148889959-148889970 chr4:148889959-148889972
41	CEBPB	chr4:148841496-148841564	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr4:148785706-148786039	IMR90	lung:	n/a	chr4:148785861-148785872
43	CEBPB	chr4:148896510-148896793	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:148785752-148786005	A549	lung:	n/a	chr4:148785861-148785872
45	CEBPB	chr4:148889840-148890110	H1-hESC	embryonic stem cell:	n/a	chr4:148889959-148889972 chr4:148889959-148889970 chr4:148889959-148889972
46	CEBPB	chr4:148889864-148890057	Hela-S3	cervix:	n/a	chr4:148889959-148889972 chr4:148889959-148889970 chr4:148889959-148889972
47	CEBPB	chr4:148902207-148902934	GM12878	blood:	n/a	n/a
48	CEBPB	chr4:148889810-148890112	HepG2	liver:	n/a	chr4:148889959-148889972 chr4:148889959-148889970 chr4:148889959-148889972
49	CEBPB	chr4:148785675-148786045	HepG2	liver:	n/a	chr4:148785861-148785872
50	CEBPB	chr4:148793790-148793797	A549	lung:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148885518-148885568	SAEC	small airway:	n/a
2	chr4:148885518-148885568	SAEC	small airway:	n/a
3	chr4:148878178-148878228	PFSK-1	brain:	n/a
4	chr4:148787393-148787443	AG04449	skin:	fetal
5	chr4:148767763-148767813	CMK	blood:	n/a
6	chr4:148878178-148878228	HMEC	breast:	n/a
7	chr4:148896994-148897044	GM19239	blood:	n/a
8	chr4:148863880-148863930	PANC-1	pancreas:	n/a
9	chr4:148885518-148885568	Hepatocyte	liver:	n/a
10	chr4:148848918-148848968	AG09309	skin:	n/a
11	chr4:148861409-148861459	ovcar-3	ovarian:	n/a
12	chr4:148767763-148767813	AG10803	skin:	n/a
13	chr4:148878178-148878228	AG10803	skin:	n/a
14	chr4:148863880-148863930	NHDF-neo	bronchial:	n/a
15	chr4:148785459-148785509	AG09309	skin:	n/a
16	chr4:148767763-148767813	SK-N-SH	brain:	n/a
17	chr4:148863880-148863930	HRCEpiC	kidney:	n/a
18	chr4:148785459-148785509	PANC-1	pancreas:	n/a
19	chr4:148878178-148878228	HepG2	liver:	n/a
20	chr4:148861409-148861459	GM12892	blood:	n/a
21	chr4:148785459-148785509	GM12878	blood:	n/a
22	chr4:148787393-148787443	SAEC	small airway:	n/a
23	chr4:148863880-148863930	K562	blood:	n/a
24	chr4:148863880-148863930	ProgFib	skin:	n/a
25	chr4:148787393-148787443	SK-N-MC	brain:	n/a
26	chr4:148785459-148785509	HL-60	blood:	n/a
27	chr4:148885518-148885568	HCF	heart:	n/a
28	chr4:148863880-148863930	RPTEC	kidney:	n/a
29	chr4:148767763-148767813	Hela-S3	cervix:	n/a
30	chr4:148890890-148890940	SAEC	small airway:	n/a
31	chr4:148787393-148787443	SKMC	muscle:	n/a
32	chr4:148787393-148787443	HMEC	breast:	n/a
33	chr4:148785459-148785509	AG04449	skin:	fetal
34	chr4:148861409-148861459	Jurkat	blood:	n/a
35	chr4:148896994-148897044	K562	blood:	n/a
36	chr4:148915072-148915122	AG04449	skin:	fetal
37	chr4:148896994-148897044	SK-N-SH	brain:	n/a
38	chr4:148767763-148767813	GM19239	blood:	n/a
39	chr4:148863880-148863930	U87	brain:	n/a
40	chr4:148885518-148885568	PFSK-1	brain:	n/a
41	chr4:148915072-148915122	LNCaP	prostate:	n/a
42	chr4:148785459-148785509	GM19239	blood:	n/a
43	chr4:148787393-148787443	HL-60	blood:	n/a
44	chr4:148787393-148787443	AG10803	skin:	n/a
45	chr4:148890890-148890940	PrEC	prostate:	n/a
46	chr4:148767763-148767813	Jurkat	blood:	n/a
47	chr4:148861409-148861459	HEEpiC	esophagus:	n/a
48	chr4:148890890-148890940	SK-N-SH	brain:	n/a
49	chr4:148915072-148915122	MCF10A-Er-Src	breast:	n/a
50	chr4:148861409-148861459	HNPCEpiC	eye:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:148768907..148770611-chr4:148774533..148777296,2	MCF-7	breast:
2	chr18:74943168..74943668-chr4:148794019..148794668,2	MCF-7	breast:
3	chr4:148764386..148764894-chr4:148787805..148788335,2	MCF-7	breast:
4	chr4:148629250..148629859-chr4:148787588..148788271,2	K562	blood:
5	chr4:148805327..148807342-chr4:148810157..148812638,2	MCF-7	breast:
6	chr4:148653910..148654658-chr4:148787711..148788598,2	MCF-7	breast:
7	chr4:148805327..148807342-chr4:148810157..148812638,2	MCF-7	breast:
8	chr4:148517290..148518095-chr4:148787896..148788545,2	MCF-7	breast:
9	chr20:58508769..58509347-chr4:148787638..148788516,2	MCF-7	breast:
10	chr4:148517547..148518065-chr4:148788601..148789204,2	MCF-7	breast:
11	chr4:148447258..148447941-chr4:148845761..148846516,2	MCF-7	breast:
12	chr4:148787670..148788596-chr4:148796263..148797180,2	MCF-7	breast:
13	chr4:148912653..148914620-chr4:148915114..148916621,2	MCF-7	breast:
14	chr4:148904893..148905747-chr4:149073698..149074268,3	MCF-7	breast:
15	chr4:148439722..148440301-chr4:148788057..148788672,2	MCF-7	breast:
16	chr4:148846022..148846608-chr4:149073964..149074698,2	MCF-7	breast:
17	chr4:148881694..148883564-chr4:148895633..148897317,2	MCF-7	breast:
18	chr4:148766756..148768552-chr4:148771059..148773482,2	K562	blood:
19	chr4:148764386..148764894-chr4:148787805..148788335,2	MCF-7	breast:
20	chr4:148870240..148873199-chr4:148874453..148876510,2	MCF-7	breast:
21	chr4:148844312..148847259-chr4:149048458..149051451,2	MCF-7	breast:
22	chr4:148793093..148794809-chr4:148796760..148798646,2	MCF-7	breast:
23	chr4:148851806..148854793-chr4:148858894..148861508,2	MCF-7	breast:
24	chr11:65028482..65030482-chr4:148764578..148767409,2	MCF-7	breast:
25	chr4:148884380..148886490-chr4:148890987..148892658,2	MCF-7	breast:
26	chr4:148439677..148440826-chr4:148787272..148788626,10	K562	blood:
27	chr4:148509882..148511690-chr4:148787031..148789794,2	MCF-7	breast:
28	chr4:148793093..148794809-chr4:148796760..148798646,2	MCF-7	breast:
29	chr4:148602747..148604694-chr4:148786468..148788057,2	MCF-7	breast:
30	chr15:60771041..60771603-chr4:148849105..148849605,2	Hela-S3	cervix:
31	chr4:148787670..148788596-chr4:148796263..148797180,2	MCF-7	breast:
32	chr4:148812422..148814436-chr4:148818946..148820969,2	MCF-7	breast:
33	chr4:148796743..148799400-chr4:148805764..148808570,2	K562	blood:
34	chr4:148912653..148914620-chr4:148915114..148916621,2	MCF-7	breast:
35	chr4:148603821..148605355-chr4:148862724..148865467,2	MCF-7	breast:
36	chr4:148881694..148883564-chr4:148895633..148897317,2	MCF-7	breast:
37	chr4:148628378..148630020-chr4:148787161..148788732,34	MCF-7	breast:
38	chr4:148758665..148761189-chr4:148775794..148779059,3	MCF-7	breast:
39	chr4:148904914..148905846-chr4:148975159..148976054,4	MCF-7	breast:
40	chr4:148905210..148905806-chr4:148931427..148932338,2	MCF-7	breast:
41	chr4:148603830..148606131-chr4:148782942..148784655,2	MCF-7	breast:
42	chr4:148812422..148814436-chr4:148818946..148820969,2	MCF-7	breast:
43	chr4:148851806..148854793-chr4:148858894..148861508,2	MCF-7	breast:
44	chr4:148803698..148806694-chr4:148808526..148810051,2	K562	blood:
45	chr4:148803698..148806694-chr4:148808526..148810051,2	K562	blood:
46	chr4:148796743..148799400-chr4:148805764..148808570,2	K562	blood:
47	chr4:148628975..148629992-chr4:148787437..148788720,7	MCF-7	breast:
48	chr4:148757037..148759184-chr4:148779427..148781406,2	MCF-7	breast:
49	chr4:148757333..148759139-chr4:148766122..148768312,2	MCF-7	breast:
50	chr4:148520581..148521262-chr4:148787695..148788489,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NR3C2-5	chr4:148837680-148838537	NONHSAT098692

No data

Variant related genes	Relation type
ARHGAP10	TF binding region
ENSG00000270387	TF binding region
ARHGAP10	CpG island
ENSG00000270387	CpG island
ENSG00000128915	chromatin interactions
ENSG00000071205	chromatin interactions
ENSG00000196227	chromatin interactions
ENSG00000164169	chromatin interactions
ENSG00000245534	chromatin interactions
ENSG00000014138	chromatin interactions

Extended variants
information (count: 6021 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:6021 , 50 per page) page: 1 2 3 4 5 6 7 ... 121

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs893024	chr4:148764252-148764253	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189085285	chr4:148764259-148764260	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs567444859	chr4:148764263-148764264	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs536482488	chr4:148764279-148764280	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs556409733	chr4:148764333-148764334	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs576228250	chr4:148764352-148764353	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548989999	chr4:148764356-148764357	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs557825802	chr4:148764358-148764359	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs578001992	chr4:148764431-148764432	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs540326957	chr4:148764488-148764489	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs560241571	chr4:148764506-148764507	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573881348	chr4:148764543-148764544	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs542780771	chr4:148764572-148764573	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182377185	chr4:148764580-148764581	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs151163533	chr4:148764599-148764600	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs186984827	chr4:148764602-148764603	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs77076922	chr4:148764608-148764609	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs17023988	chr4:148764613-148764614	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs527307147	chr4:148764628-148764629	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs139064406	chr4:148764637-148764638	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs147858413	chr4:148764669-148764670	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs368930713	chr4:148764690-148764691	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs567332514	chr4:148764750-148764751	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs149874981	chr4:148764753-148764754	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs549955290	chr4:148764755-148764756	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs569841114	chr4:148764789-148764790	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs377219337	chr4:148764802-148764803	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567577102	chr4:148764829-148764830	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538546357	chr4:148764901-148764902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs28662484	chr4:148764954-148764955	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs372441825	chr4:148764956-148764957	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571529976	chr4:148764961-148764962	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533965552	chr4:148764965-148764966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553765533	chr4:148764971-148764972	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs145869649	chr4:148764976-148764977	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs75559966	chr4:148764986-148764987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs377290627	chr4:148765023-148765024	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs576619096	chr4:148765033-148765034	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369640966	chr4:148765052-148765053	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545352626	chr4:148765086-148765087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs141805733	chr4:148765089-148765090	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs528003175	chr4:148765133-148765134	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs145576086	chr4:148765150-148765151	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs190706461	chr4:148765224-148765225	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs529772738	chr4:148765249-148765250	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs549887534	chr4:148765262-148765263	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs569749427	chr4:148765284-148765285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs180767419	chr4:148765373-148765374	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs185433533	chr4:148765460-148765461	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs190186682	chr4:148765461-148765462	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	21865298	CNVD
Cancer	20164919	CNVD

Chromatin state (count:3054 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148737800-148782200	Weak transcription	Thymus	Thymus
2	chr4:148743200-148782200	Weak transcription	Fetal Intestine Large	intestine
3	chr4:148746400-148768000	Weak transcription	Fetal Intestine Small	intestine
4	chr4:148751400-148776000	Weak transcription	Fetal Stomach	stomach
5	chr4:148753200-148765800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr4:148753200-148767800	Weak transcription	Small Intestine	intestine
7	chr4:148753400-148765800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:148753400-148782000	Weak transcription	Gastric	stomach
9	chr4:148754000-148766200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr4:148754400-148769000	Weak transcription	NHLF	lung
11	chr4:148755600-148773200	Weak transcription	Esophagus	oesophagus
12	chr4:148756400-148766000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr4:148756400-148768000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr4:148756800-148766200	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr4:148756800-148777800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:148757400-148767400	Weak transcription	HUES64 Cell Line	embryonic stem cell
17	chr4:148757400-148767600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:148757600-148766200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr4:148760800-148764600	Enhancers	Colon Smooth Muscle	Colon
20	chr4:148761000-148764600	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr4:148761000-148764600	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr4:148761200-148764400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:148761200-148764800	Enhancers	Fetal Muscle Leg	muscle
24	chr4:148761400-148767800	Weak transcription	Fetal Kidney	kidney
25	chr4:148761800-148764600	Enhancers	Psoas Muscle	Psoas
26	chr4:148761800-148765200	Enhancers	Right Atrium	heart
27	chr4:148762200-148767400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr4:148762400-148767000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr4:148762400-148770000	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr4:148762400-148771000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr4:148762600-148767600	Weak transcription	Fetal Lung	lung
32	chr4:148762800-148775400	Weak transcription	Pancreatic Islets	Pancreatic Islet
33	chr4:148763000-148764600	Enhancers	Rectal Smooth Muscle	rectum
34	chr4:148763000-148765000	Enhancers	Fetal Muscle Trunk	muscle
35	chr4:148763000-148765200	Enhancers	Left Ventricle	heart
36	chr4:148763000-148765200	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr4:148763200-148764400	Weak transcription	GM12878-XiMat	blood
38	chr4:148763200-148764600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:148763200-148768000	Weak transcription	HUVEC	blood vessel
40	chr4:148763200-148771000	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr4:148763200-148796200	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr4:148763600-148764400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr4:148763600-148764400	Enhancers	NH-A	brain
44	chr4:148763600-148764600	Genic enhancers	Aorta	Aorta
45	chr4:148763600-148764600	Enhancers	HMEC	breast
46	chr4:148763600-148764600	Genic enhancers	HSMM	muscle
47	chr4:148763600-148764600	Enhancers	Osteobl	bone
48	chr4:148763600-148764800	Enhancers	K562	blood
49	chr4:148763800-148764600	Enhancers	Brain Angular Gyrus	brain
50	chr4:148763800-148764600	Enhancers	Lung	lung

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