Variant report

Variant	esv3322785
Chromosome Location	chr15:52028185-52031033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:434)
CpG islands
(count:672)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:434 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:52030198-52030789	K562	blood:	n/a	n/a
2	ATF2	chr15:52028196-52028741	GM12878	blood:	n/a	n/a
3	BACH1	chr15:52029717-52029835	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr15:52028233-52028654	GM12878	blood:	n/a	chr15:52028448-52028459
5	BATF	chr15:52028341-52028612	GM12878	blood:	n/a	chr15:52028448-52028459
6	BCL11A	chr15:52028309-52028583	GM12878	blood:	n/a	n/a
7	BCL11A	chr15:52028263-52028604	GM12878	blood:	n/a	n/a
8	BCL3	chr15:52028271-52028680	GM12878	blood:	n/a	n/a
9	BCLAF1	chr15:52028889-52029353	GM12878	blood:	n/a	chr15:52029025-52029034
10	BHLHE40	chr15:52029000-52029713	K562	blood:	n/a	chr15:52029489-52029505 chr15:52029365-52029381
11	BHLHE40	chr15:52029161-52029337	A549	lung:	n/a	n/a
12	BHLHE40	chr15:52028370-52029413	GM12878	blood:	n/a	chr15:52029365-52029381
13	BHLHE40	chr15:52029786-52030120	GM12878	blood:	n/a	chr15:52030058-52030074 chr15:52030064-52030080
14	BRCA1	chr15:52030225-52030482	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr15:52028945-52029266	Hela-S3	cervix:	n/a	n/a
16	CBX3	chr15:52029005-52029373	K562	blood:	n/a	n/a
17	CCNT2	chr15:52029073-52030235	K562	blood:	n/a	n/a
18	CEBPB	chr15:52030326-52030401	K562	blood:	n/a	n/a
19	CEBPB	chr15:52028281-52028521	K562	blood:	n/a	n/a
20	CEBPB	chr15:52028249-52028567	IMR90	lung:	n/a	n/a
21	CEBPB	chr15:52029067-52029071	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr15:52028941-52029323	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr15:52030188-52030365	Hela-S3	cervix:	n/a	n/a
24	CHD1	chr15:52029671-52029855	GM12878	blood:	n/a	n/a
25	CHD2	chr15:52029224-52029252	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr15:52030287-52030288	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr15:52029090-52029534	K562	blood:	n/a	n/a
28	CHD2	chr15:52028927-52030475	GM12878	blood:	n/a	n/a
29	CHD2	chr15:52029998-52030373	K562	blood:	n/a	n/a
30	CHD2	chr15:52029017-52030497	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr15:52029405-52029825	H1-hESC	embryonic stem cell:	n/a	n/a
32	CREB1	chr15:52030201-52030593	H1-hESC	embryonic stem cell:	n/a	chr15:52030359-52030372
33	CREB1	chr15:52029466-52030521	A549	lung:	n/a	chr15:52030359-52030372
34	CREB1	chr15:52029993-52030703	K562	blood:	n/a	chr15:52030359-52030372
35	CREB1	chr15:52029763-52030681	GM12878	blood:	n/a	chr15:52030359-52030372
36	CREB1	chr15:52029772-52030643	GM12878	blood:	n/a	chr15:52030359-52030372
37	CREB1	chr15:52030160-52030458	A549	lung:	n/a	chr15:52030359-52030372
38	CTBP2	chr15:52029244-52030405	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr15:52029200-52029350	AG04449	skin:	n/a	n/a
40	CTCF	chr15:52029522-52029596	GM19239	blood:	n/a	n/a
41	CTCF	chr15:52029220-52029370	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr15:52027309-52028223	SK-N-SH	brain:	n/a	n/a
43	CTCF	chr15:52029200-52029350	GM12872	blood:	n/a	n/a
44	CTCF	chr15:52029220-52029370	HMEC	breast:	n/a	n/a
45	CTCF	chr15:52029200-52029350	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr15:52029320-52029470	GM12867	blood:	n/a	chr15:52029364-52029377
47	CTCF	chr15:52029538-52029579	MCF-7	breast:	n/a	n/a
48	CTCF	chr15:52029041-52029174	GM12878	blood:	n/a	n/a
49	CTCF	chr15:52030040-52030190	SK-N-SH_RA	brain:	n/a	chr15:52030173-52030182
50	CTCF	chr15:52029120-52029270	GM12872	blood:	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	chr15:52030164-52030214	GM12892	blood:	n/a
2	chr15:52030164-52030214	GM12892	blood:	n/a
3	chr15:52029231-52029281	HCM	heart:	n/a
4	chr15:52030641-52030691	HEEpiC	esophagus:	n/a
5	chr15:52030746-52030796	BJ	skin:	n/a
6	chr15:52030128-52030178	AG09309	skin:	n/a
7	chr15:52030199-52030249	CMK	blood:	n/a
8	chr15:52030641-52030691	HCPEpiC	choroid plexus:	n/a
9	chr15:52030685-52030735	MCF10A-Er-Src	breast:	n/a
10	chr15:52029533-52029583	U87	brain:	n/a
11	chr15:52029533-52029583	HAEpiC	amniotic membrane:	n/a
12	chr15:52030164-52030214	GM12891	blood:	n/a
13	chr15:52030746-52030796	MCF-7	breast:	n/a
14	chr15:52029533-52029583	PrEC	prostate:	n/a
15	chr15:52029231-52029281	HUVEC	blood vessel:	n/a
16	chr15:52030519-52030569	Caco-2	colon:	n/a
17	chr15:52030685-52030735	HCT-116	colon:	n/a
18	chr15:52030001-52030051	PrEC	prostate:	n/a
19	chr15:52030199-52030249	ProgFib	skin:	n/a
20	chr15:52029231-52029281	ProgFib	skin:	n/a
21	chr15:52030199-52030249	SK-N-SH	brain:	n/a
22	chr15:52030641-52030691	Hepatocyte	liver:	n/a
23	chr15:52030746-52030796	HRCEpiC	kidney:	n/a
24	chr15:52029231-52029281	HCPEpiC	choroid plexus:	n/a
25	chr15:52030164-52030214	SK-N-SH	brain:	n/a
26	chr15:52030164-52030214	SK-N-MC	brain:	n/a
27	chr15:52030641-52030691	AG04450	lung:	fetal
28	chr15:52029231-52029281	BE2_C	brain:	n/a
29	chr15:52030164-52030214	AG04450	lung:	fetal
30	chr15:52030746-52030796	Hela-S3	cervix:	n/a
31	chr15:52030001-52030051	GM12891	blood:	n/a
32	chr15:52030641-52030691	RPTEC	kidney:	n/a
33	chr15:52030001-52030051	NHBE	bronchial:	n/a
34	chr15:52030199-52030249	ECC-1	luminal epithelium:	n/a
35	chr15:52029533-52029583	HEK293	kidney:	embryo
36	chr15:52030128-52030178	GM19239	blood:	n/a
37	chr15:52030685-52030735	GM12878	blood:	n/a
38	chr15:52030641-52030691	K562	blood:	n/a
39	chr15:52030164-52030214	BE2_C	brain:	n/a
40	chr15:52029152-52029202	SK-N-SH	brain:	n/a
41	chr15:52030641-52030691	SK-N-SH_RA	brain:	n/a
42	chr15:52030199-52030249	SK-N-SH_RA	brain:	n/a
43	chr15:52030199-52030249	U87	brain:	n/a
44	chr15:52029533-52029583	AG10803	skin:	n/a
45	chr15:52030128-52030178	HCF	heart:	n/a
46	chr15:52029231-52029281	HNPCEpiC	eye:	n/a
47	chr15:52029152-52029202	GM12891	blood:	n/a
48	chr15:52030199-52030249	MCF-7	breast:	n/a
49	chr15:52030519-52030569	NB4	blood:	n/a
50	chr15:52030746-52030796	ovcar-3	ovarian:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:52029378..52032499-chr15:52121077..52123299,3	MCF-7	breast:
2	chr15:52027363..52032665-chr15:52041435..52046045,23	MCF-7	breast:
3	chr15:52030420..52032691-chr15:52120807..52123246,2	MCF-7	breast:
4	chr15:52029591..52032408-chr15:52042418..52044684,3	K562	blood:
5	chr15:52028180..52031136-chr15:52040562..52045385,6	MCF-7	breast:
6	chr15:52028355..52032748-chr15:52040539..52046492,10	K562	blood:
7	chr15:51911576..51916583-chr15:52027382..52031699,5	MCF-7	breast:
8	chr15:51762002..51764362-chr15:52028309..52030001,2	MCF-7	breast:
9	chr15:51950953..51953753-chr15:52026333..52028408,2	MCF-7	breast:
10	chr15:52030561..52031125-chr15:52068898..52069830,2	K562	blood:
11	chr15:51914058..51915723-chr15:52028393..52030272,2	MCF-7	breast:
12	chr15:52029435..52031649-chr15:52311154..52313570,2	K562	blood:
13	chr15:52005662..52007756-chr15:52028876..52031424,2	MCF-7	breast:
14	chr15:52026672..52029372-chr15:52056834..52058990,2	MCF-7	breast:
15	chr12:64614231..64616104-chr15:52029344..52031052,2	MCF-7	breast:
16	chr15:51941822..51942724-chr15:52027267..52028353,3	MCF-7	breast:
17	chr15:52026416..52029376-chr15:52033345..52036135,2	K562	blood:

No data

Variant related genes	Relation type
LYSMD2	TF binding region
LYSMD2	CpG island
ENSG00000259296	chromatin interactions
ENSG00000174206	chromatin interactions
ENSG00000138594	chromatin interactions
ENSG00000128872	chromatin interactions
ENSG00000069956	chromatin interactions
ENSG00000259438	chromatin interactions
ENSG00000140280	chromatin interactions
ENSG00000104093	chromatin interactions
ENSG00000259377	chromatin interactions

Extended variants
information (count: 106 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:106 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28418531	chr15:52028235-52028236	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs74015725	chr15:52028240-52028241	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs561812280	chr15:52028258-52028259	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs535013451	chr15:52028329-52028330	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs572328378	chr15:52028402-52028403	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs558098249	chr15:52028434-52028435	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs192338594	chr15:52028463-52028464	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs537450940	chr15:52028488-52028489	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs576198197	chr15:52028515-52028516	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs543168596	chr15:52028518-52028519	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs558330387	chr15:52028550-52028551	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs576765518	chr15:52028552-52028553	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs540909553	chr15:52028564-52028565	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs559325449	chr15:52028593-52028594	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs529627980	chr15:52028612-52028613	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs541923120	chr15:52028630-52028631	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs184507846	chr15:52028631-52028632	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs28673300	chr15:52028664-52028665	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs531944318	chr15:52028681-52028682	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs577976224	chr15:52028688-52028689	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs374553999	chr15:52028697-52028698	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs79846015	chr15:52028708-52028709	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs150332493	chr15:52028712-52028713	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs189514077	chr15:52028720-52028721	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs566082527	chr15:52028721-52028722	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs137871916	chr15:52028794-52028795	Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs181777405	chr15:52028819-52028820	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs11636142	chr15:52028827-52028828	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs570100516	chr15:52028830-52028831	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs537141311	chr15:52028841-52028842	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs200169999	chr15:52028850-52028851	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs186050137	chr15:52028875-52028876	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs7165585	chr15:52028914-52028915	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs189584302	chr15:52028918-52028919	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs111379149	chr15:52028952-52028953	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs201435177	chr15:52028954-52028955	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs77507636	chr15:52028956-52028957	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs77716319	chr15:52028982-52028983	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs549795817	chr15:52028997-52028998	Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs541413618	chr15:52029085-52029086	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs180776812	chr15:52029087-52029088	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs530657533	chr15:52029107-52029108	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs186737569	chr15:52029143-52029144	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs565501750	chr15:52029152-52029153	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs72730964	chr15:52029203-52029204	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs537754534	chr15:52029205-52029206	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs537479959	chr15:52029237-52029238	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs566196884	chr15:52029250-52029251	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs530421348	chr15:52029268-52029269	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs548336715	chr15:52029269-52029270	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52013600-52028200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr15:52013600-52028400	Weak transcription	Fetal Brain Female	brain
3	chr15:52013600-52028800	Weak transcription	Fetal Muscle Trunk	muscle
4	chr15:52019000-52028200	Weak transcription	Brain Substantia Nigra	brain
5	chr15:52020000-52028800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr15:52020200-52029000	Weak transcription	NH-A	brain
7	chr15:52023600-52028200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr15:52024200-52028400	Flanking Active TSS	GM12878-XiMat	blood
9	chr15:52024400-52028400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr15:52024400-52028400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr15:52024400-52028400	Enhancers	Fetal Thymus	thymus
12	chr15:52024400-52028400	Enhancers	Thymus	Thymus
13	chr15:52024400-52028800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr15:52024400-52028800	Weak transcription	Right Ventricle	heart
15	chr15:52024600-52028200	Enhancers	Primary T cells fromperipheralblood	blood
16	chr15:52024600-52028200	Weak transcription	NHDF-Ad	bronchial
17	chr15:52024600-52028200	Weak transcription	NHLF	lung
18	chr15:52024600-52028400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr15:52024600-52028400	Weak transcription	Aorta	Aorta
20	chr15:52024600-52028400	Weak transcription	Fetal Muscle Leg	muscle
21	chr15:52024600-52028400	Weak transcription	Gastric	stomach
22	chr15:52024600-52028400	Weak transcription	NHEK	skin
23	chr15:52024600-52028600	Weak transcription	Fetal Stomach	stomach
24	chr15:52024600-52028800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr15:52024600-52028800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr15:52024600-52028800	Weak transcription	Osteobl	bone
27	chr15:52024600-52029000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr15:52024800-52028200	Weak transcription	Adipose Nuclei	Adipose
29	chr15:52024800-52028400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr15:52024800-52028400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr15:52024800-52028400	Weak transcription	Fetal Intestine Large	intestine
32	chr15:52024800-52028400	Weak transcription	Placenta	Placenta
33	chr15:52024800-52028400	Weak transcription	Stomach Mucosa	stomach
34	chr15:52025000-52028200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr15:52025000-52028200	Weak transcription	Brain Angular Gyrus	brain
36	chr15:52025000-52028400	Weak transcription	Colonic Mucosa	Colon
37	chr15:52025000-52028400	Weak transcription	Pancreas	Pancrea
38	chr15:52025000-52028400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr15:52025000-52028400	Weak transcription	Stomach Smooth Muscle	stomach
40	chr15:52025000-52028600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr15:52025000-52028800	Weak transcription	Left Ventricle	heart
42	chr15:52025200-52028400	Weak transcription	Right Atrium	heart
43	chr15:52025200-52028800	Weak transcription	HSMMtube	muscle
44	chr15:52025400-52029000	Weak transcription	Esophagus	oesophagus
45	chr15:52026400-52028200	Enhancers	Brain Cingulate Gyrus	brain
46	chr15:52026400-52029400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr15:52026600-52028600	Enhancers	K562	blood
48	chr15:52026800-52028400	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr15:52026800-52028800	Weak transcription	Psoas Muscle	Psoas
50	chr15:52026800-52029000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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