Variant report

Variant	esv3379698
Chromosome Location	chr4:150998652-151001000
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:314)
CpG islands
(count:733)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:150999880-151000018	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:150999232-150999272	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr4:151000262-151000541	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr4:151000571-151000648	GM12878	blood:	n/a	n/a
5	CEBPB	chr4:151000898-151001193	A549	lung:	n/a	chr4:151001044-151001055
6	CEBPB	chr4:150999039-150999353	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr4:151000880-151001192	IMR90	lung:	n/a	chr4:151001044-151001055
8	CEBPB	chr4:151000454-151000685	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr4:150999159-151000788	Hela-S3	cervix:	n/a	chr4:150999727-150999737 chr4:150999722-150999732 chr4:150999363-150999373
10	CREB1	chr4:150999094-150999572	A549	lung:	n/a	n/a
11	CREB1	chr4:150999068-150999492	H1-hESC	embryonic stem cell:	n/a	n/a
12	CREB1	chr4:150999115-150999474	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTBP2	chr4:150999878-151000831	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr4:151000520-151000670	Caco-2	colon:	n/a	chr4:151000638-151000651
15	CTCF	chr4:151000520-151000670	HEK293	kidney:	n/a	chr4:151000638-151000651
16	CTCF	chr4:151000490-151000750	MCF-7	breast:	n/a	chr4:151000638-151000651
17	CTCF	chr4:151000360-151000510	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr4:151000520-151000670	SK-N-SH_RA	brain:	n/a	chr4:151000638-151000651
19	CTCF	chr4:151000560-151000710	GM12875	blood:	n/a	chr4:151000638-151000651
20	CTCF	chr4:151000420-151000570	BJ	skin:	n/a	n/a
21	CTCF	chr4:151000580-151000730	AoAF	blood vessel:	n/a	chr4:151000638-151000651
22	CTCF	chr4:150999440-150999590	SK-N-SH_RA	brain:	n/a	n/a
23	CTCF	chr4:150999460-150999610	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr4:151000380-151000530	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr4:151000580-151000728	GM19238	blood:	n/a	chr4:151000638-151000651
26	CTCF	chr4:151000480-151000630	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr4:151000520-151000670	HRE	kidney:	n/a	chr4:151000638-151000651
28	CTCF	chr4:151000580-151000730	GM12864	blood:	n/a	chr4:151000638-151000651
29	CTCF	chr4:151000480-151000630	NHDF-neo	bronchial:	n/a	n/a
30	CTCF	chr4:151000546-151000734	MCF-7	breast:	n/a	chr4:151000638-151000651
31	CTCF	chr4:151000400-151000550	HPF	lung:	n/a	n/a
32	CTCF	chr4:151000680-151000830	RPTEC	kidney:	n/a	n/a
33	CTCF	chr4:151000520-151000670	NHDF-neo	bronchial:	n/a	chr4:151000638-151000651
34	CTCF	chr4:151000520-151000670	MCF-7	breast:	n/a	chr4:151000638-151000651
35	CTCF	chr4:151000576-151000676	MCF-7	breast:	n/a	chr4:151000638-151000651
36	CTCF	chr4:151000560-151000710	WERI-Rb-1	eye:	n/a	chr4:151000638-151000651
37	CTCF	chr4:151000580-151000730	HRPEpiC	eye:	n/a	chr4:151000638-151000651
38	CTCF	chr4:151000527-151000730	MCF-7	breast:	n/a	chr4:151000638-151000651
39	CTCF	chr4:151000400-151000550	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:151000340-151000490	GM12865	blood:	n/a	n/a
41	CTCF	chr4:150999480-150999630	HCPEpiC	choroid plexus:	n/a	n/a
42	CTCF	chr4:151000300-151000450	HVMF	connective:	n/a	n/a
43	CTCF	chr4:151000520-151000670	AG04450	lung:	n/a	chr4:151000638-151000651
44	CTCF	chr4:151000400-151000550	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr4:151000460-151000610	HRPEpiC	eye:	n/a	n/a
46	CTCF	chr4:151000580-151000730	SK-N-SH_RA	brain:	n/a	chr4:151000638-151000651
47	CTCF	chr4:150999360-150999510	AG09319	gingival:	n/a	n/a
48	CTCF	chr4:151000500-151000650	GM12866	blood:	n/a	n/a
49	CTCF	chr4:151000460-151000610	Caco-2	colon:	n/a	n/a
50	CTCF	chr4:151000510-151000709	Hela-S3	cervix:	n/a	chr4:151000638-151000651

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:150999899-150999949	HIPEpiC	eye:	n/a
2	chr4:150999899-150999949	HIPEpiC	eye:	n/a
3	chr4:151000014-151000064	SK-N-MC	brain:	n/a
4	chr4:150999949-150999999	HRCEpiC	kidney:	n/a
5	chr4:151000014-151000064	AoSMC	blood vessel:	n/a
6	chr4:150999042-150999092	GM12878	blood:	n/a
7	chr4:150999899-150999949	MCF10A-Er-Src	breast:	n/a
8	chr4:150999923-150999973	GM06990	blood:	n/a
9	chr4:150999899-150999949	U87	brain:	n/a
10	chr4:150999911-150999961	ECC-1	luminal epithelium:	n/a
11	chr4:151000014-151000064	SK-N-SH_RA	brain:	n/a
12	chr4:150999251-150999301	AG04449	skin:	fetal
13	chr4:151000084-151000134	AG09319	gingival:	n/a
14	chr4:151000684-151000734	HCM	heart:	n/a
15	chr4:150999911-150999961	NB4	blood:	n/a
16	chr4:150999547-150999597	A549	lung:	n/a
17	chr4:150999042-150999092	SK-N-MC	brain:	n/a
18	chr4:151000014-151000064	HL-60	blood:	n/a
19	chr4:150999923-150999973	A549	lung:	n/a
20	chr4:150999899-150999949	HCM	heart:	n/a
21	chr4:150999905-150999955	HCM	heart:	n/a
22	chr4:150999905-150999955	ProgFib	skin:	n/a
23	chr4:151000684-151000734	ovcar-3	ovarian:	n/a
24	chr4:150999547-150999597	HUVEC	blood vessel:	n/a
25	chr4:150999547-150999597	AG04450	lung:	fetal
26	chr4:151000014-151000064	NB4	blood:	n/a
27	chr4:150999251-150999301	SK-N-MC	brain:	n/a
28	chr4:150999899-150999949	ProgFib	skin:	n/a
29	chr4:150999911-150999961	MCF10A-Er-Src	breast:	n/a
30	chr4:150999911-150999961	Caco-2	colon:	n/a
31	chr4:150999949-150999999	AG10803	skin:	n/a
32	chr4:150999251-150999301	NHDF-neo	bronchial:	n/a
33	chr4:150999923-150999973	Hepatocyte	liver:	n/a
34	chr4:150999547-150999597	BE2_C	brain:	n/a
35	chr4:150999251-150999301	ECC-1	luminal epithelium:	n/a
36	chr4:150999949-150999999	MCF10A-Er-Src	breast:	n/a
37	chr4:150999547-150999597	HEEpiC	esophagus:	n/a
38	chr4:150999949-150999999	GM06990	blood:	n/a
39	chr4:150999042-150999092	AoSMC	blood vessel:	n/a
40	chr4:150999911-150999961	PANC-1	pancreas:	n/a
41	chr4:150999042-150999092	RPTEC	kidney:	n/a
42	chr4:150999923-150999973	AG04449	skin:	fetal
43	chr4:151000084-151000134	HMEC	breast:	n/a
44	chr4:150999923-150999973	HRE	kidney:	n/a
45	chr4:151000235-151000285	NT2-D1	testis:	n/a
46	chr4:150999905-150999955	PrEC	prostate:	n/a
47	chr4:150999547-150999597	HL-60	blood:	n/a
48	chr4:150999905-150999955	Hepatocyte	liver:	n/a
49	chr4:151000084-151000134	NT2-D1	testis:	n/a
50	chr4:150999251-150999301	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:42758633..42759495-chr4:150999375..150999897,2	Hela-S3	cervix:
2	chr4:151000698..151001437-chr4:151130301..151131200,2	MCF-7	breast:

No data

Variant related genes	Relation type
DCLK2	TF binding region
DCLK2	CpG island
ENSG00000238721	chromatin interactions
ENSG00000268643	chromatin interactions
ENSG00000105722	chromatin interactions

Extended variants
information (count: 104 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:104 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563509011	chr4:150998671-150998672	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs111996967	chr4:150998674-150998675	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs533336487	chr4:150998733-150998734	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs79788742	chr4:150998760-150998761	Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs372157848	chr4:150998870-150998871	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs552820907	chr4:150998878-150998879	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs150719061	chr4:150998898-150998899	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs528485065	chr4:150998910-150998911	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs72730319	chr4:150998937-150998938	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs568577431	chr4:150999029-150999030	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs199544269	chr4:150999035-150999036	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs550817125	chr4:150999047-150999048	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs76774998	chr4:150999062-150999063	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs539390704	chr4:150999066-150999067	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs374492582	chr4:150999100-150999101	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs10005992	chr4:150999112-150999113	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs573006374	chr4:150999145-150999146	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs10028598	chr4:150999167-150999168	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs535438558	chr4:150999187-150999188	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs112573840	chr4:150999217-150999218	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs376837887	chr4:150999218-150999219	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs575015426	chr4:150999258-150999259	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs543880212	chr4:150999264-150999265	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
24	rs563576595	chr4:150999285-150999286	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
25	rs376325776	chr4:150999298-150999299	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
26	rs577360641	chr4:150999340-150999341	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200676797	chr4:150999368-150999369	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs546227887	chr4:150999381-150999382	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs36215766	chr4:150999384-150999385	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs560001259	chr4:150999407-150999408	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs143228216	chr4:150999411-150999412	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs145903637	chr4:150999412-150999413	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs142444871	chr4:150999484-150999485	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs548619524	chr4:150999487-150999488	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs562035515	chr4:150999494-150999495	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs531056603	chr4:150999503-150999504	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs551084816	chr4:150999539-150999540	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs570602241	chr4:150999551-150999552	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs533154100	chr4:150999643-150999644	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs546434375	chr4:150999646-150999647	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs566772089	chr4:150999654-150999655	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs535357646	chr4:150999689-150999690	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs145979500	chr4:150999791-150999792	Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs530550002	chr4:150999823-150999824	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568500006	chr4:150999851-150999852	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs537592416	chr4:150999880-150999881	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs190436258	chr4:150999908-150999909	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs577622463	chr4:150999952-150999953	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs13144463	chr4:150999968-150999969	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs28501392	chr4:150999971-150999972	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

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
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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150994000-150999000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:150994400-150998800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:150994600-150998800	Weak transcription	HSMM	muscle
4	chr4:150994800-150998800	Weak transcription	Adipose Nuclei	Adipose
5	chr4:150994800-150998800	Weak transcription	Colon Smooth Muscle	Colon
6	chr4:150995000-150998800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr4:150995000-150998800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:150995000-150998800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:150995000-150998800	Weak transcription	HSMMtube	muscle
10	chr4:150995000-150998800	Weak transcription	NH-A	brain
11	chr4:150995000-150998800	Weak transcription	NHDF-Ad	bronchial
12	chr4:150995000-150998800	Weak transcription	NHLF	lung
13	chr4:150995200-150998800	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr4:150995400-150998800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr4:150995400-150998800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr4:150995400-150998800	Weak transcription	Osteobl	bone
17	chr4:150998200-150998800	Enhancers	Fetal Heart	heart
18	chr4:150998400-150998800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
19	chr4:150998400-150998800	Enhancers	Brain Substantia Nigra	brain
20	chr4:150998400-150998800	Enhancers	Left Ventricle	heart
21	chr4:150998400-150998800	Enhancers	Ovary	ovary
22	chr4:150998400-150998800	Enhancers	Rectal Smooth Muscle	rectum
23	chr4:150998400-150999000	Flanking Active TSS	Brain Cingulate Gyrus	brain
24	chr4:150998400-150999000	Flanking Active TSS	Brain Germinal Matrix	brain
25	chr4:150998400-150999200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr4:150998400-150999400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:150998400-151000400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:150998400-151001800	Active TSS	Fetal Kidney	kidney
29	chr4:150998400-151002400	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr4:150998600-150998800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:150998600-150998800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr4:150998600-150998800	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr4:150998600-150998800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:150998600-150998800	Flanking Active TSS	Brain Angular Gyrus	brain
35	chr4:150998600-150998800	Flanking Active TSS	Brain Anterior Caudate	brain
36	chr4:150998600-150998800	Enhancers	HUVEC	blood vessel
37	chr4:150998600-150999000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr4:150998600-150999000	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr4:150998600-150999000	Flanking Active TSS	Fetal Brain Female	brain
40	chr4:150998600-150999000	Flanking Active TSS	A549	lung
41	chr4:150998600-150999200	Flanking Active TSS	Fetal Brain Male	brain
42	chr4:150998600-150999200	Flanking Active TSS	Stomach Smooth Muscle	stomach
43	chr4:150998600-151000400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
44	chr4:150998600-151002600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr4:150998800-150999000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
46	chr4:150998800-150999000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr4:150998800-150999000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
48	chr4:150998800-150999000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:150998800-150999000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr4:150998800-150999000	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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