Variant report

Variant	nsv832611
Chromosome Location	chr13:51766472-51938314
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2206)
CpG islands
(count:2505)
Chromatin interactive
region (count:74)
LncRNA
region (count:10)
Mature miRNA
region (count: 1)
miRNA target
sites (count:3)

(count:2206 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:51860674-51860817	K562	blood:	n/a	n/a
2	ARID3A	chr13:51865482-51865840	HepG2	liver:	n/a	n/a
3	ATF2	chr13:51877088-51877765	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr13:51877049-51877842	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr13:51817855-51818456	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr13:51860522-51860912	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr13:51817889-51818404	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr13:51904714-51905344	GM12878	blood:	n/a	n/a
9	ATF2	chr13:51904834-51905318	GM12878	blood:	n/a	n/a
10	ATF2	chr13:51818742-51819572	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr13:51818597-51819382	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr13:51879031-51879417	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr13:51795887-51796535	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr13:51815905-51815983	K562	blood:	n/a	n/a
15	BACH1	chr13:51817953-51818260	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr13:51796858-51797275	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr13:51912245-51912492	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr13:51920484-51920847	GM12878	blood:	n/a	chr13:51920696-51920707 chr13:51920697-51920707
19	BATF	chr13:51920489-51920846	GM12878	blood:	n/a	chr13:51920696-51920707 chr13:51920697-51920707
20	BATF	chr13:51904904-51905249	GM12878	blood:	n/a	n/a
21	BCL11A	chr13:51904870-51905279	GM12878	blood:	n/a	n/a
22	BCL11A	chr13:51877134-51877341	H1-hESC	embryonic stem cell:	n/a	n/a
23	BCL11A	chr13:51904823-51905357	GM12878	blood:	n/a	n/a
24	BHLHE40	chr13:51796182-51796368	K562	blood:	n/a	n/a
25	BHLHE40	chr13:51796032-51796501	GM12878	blood:	n/a	n/a
26	BHLHE40	chr13:51904773-51905993	GM12878	blood:	n/a	n/a
27	BHLHE40	chr13:51860578-51860784	K562	blood:	n/a	n/a
28	BHLHE40	chr13:51813223-51813229	GM12878	blood:	n/a	n/a
29	BHLHE40	chr13:51904158-51904233	K562	blood:	n/a	chr13:51904180-51904189 chr13:51904180-51904189 chr13:51904181-51904190
30	BRCA1	chr13:51905015-51905190	GM12878	blood:	n/a	n/a
31	BRCA1	chr13:51877242-51877808	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr13:51912376-51912421	GM12878	blood:	n/a	n/a
33	CCNT2	chr13:51937579-51937779	K562	blood:	n/a	n/a
34	CEBPB	chr13:51886212-51886503	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr13:51799841-51800122	H1-hESC	embryonic stem cell:	n/a	chr13:51800018-51800029
36	CEBPB	chr13:51866869-51866955	HepG2	liver:	n/a	n/a
37	CEBPB	chr13:51830778-51831062	A549	lung:	n/a	chr13:51830896-51830907
38	CEBPB	chr13:51927604-51927824	HepG2	liver:	n/a	chr13:51927749-51927766
39	CEBPB	chr13:51836393-51836644	HepG2	liver:	n/a	chr13:51836515-51836526 chr13:51836517-51836528 chr13:51836517-51836526
40	CEBPB	chr13:51815908-51816124	IMR90	lung:	n/a	n/a
41	CEBPB	chr13:51879240-51879530	K562	blood:	n/a	chr13:51879352-51879363
42	CEBPB	chr13:51879190-51879520	IMR90	lung:	n/a	chr13:51879352-51879363
43	CEBPB	chr13:51830745-51831048	IMR90	lung:	n/a	chr13:51830896-51830907
44	CEBPB	chr13:51923871-51923876	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr13:51792421-51792686	HepG2	liver:	n/a	n/a
46	CEBPB	chr13:51792408-51792594	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:51815944-51815990	A549	lung:	n/a	n/a
48	CEBPB	chr13:51799249-51799454	K562	blood:	n/a	n/a
49	CEBPB	chr13:51924798-51924955	HepG2	liver:	n/a	chr13:51924848-51924859
50	CEBPB	chr13:51810482-51810615	HepG2	liver:	n/a	chr13:51810563-51810574

(count:2505 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:51796887-51796937	Jurkat	blood:	n/a
2	chr13:51818035-51818085	ovcar-3	ovarian:	n/a
3	chr13:51872358-51872408	SAEC	small airway:	n/a
4	chr13:51855006-51855056	NT2-D1	testis:	n/a
5	chr13:51796887-51796937	Jurkat	blood:	n/a
6	chr13:51818035-51818085	ovcar-3	ovarian:	n/a
7	chr13:51872358-51872408	SAEC	small airway:	n/a
8	chr13:51855006-51855056	NT2-D1	testis:	n/a
9	chr13:51825774-51825824	HUVEC	blood vessel:	n/a
10	chr13:51818035-51818085	NHDF-neo	bronchial:	n/a
11	chr13:51915047-51915097	MCF10A-Er-Src	breast:	n/a
12	chr13:51796714-51796764	AG09309	skin:	n/a
13	chr13:51819465-51819515	GM12878	blood:	n/a
14	chr13:51858967-51859017	Hepatocyte	liver:	n/a
15	chr13:51796714-51796764	BJ	skin:	n/a
16	chr13:51825918-51825968	SAEC	small airway:	n/a
17	chr13:51797139-51797189	A549	lung:	n/a
18	chr13:51818035-51818085	NH-A	brain:	n/a
19	chr13:51796265-51796315	SK-N-SH_RA	brain:	n/a
20	chr13:51872358-51872408	Jurkat	blood:	n/a
21	chr13:51786758-51786808	LNCaP	prostate:	n/a
22	chr13:51826043-51826093	Hepatocyte	liver:	n/a
23	chr13:51796887-51796937	PANC-1	pancreas:	n/a
24	chr13:51786758-51786808	Hepatocyte	liver:	n/a
25	chr13:51822685-51822735	GM06990	blood:	n/a
26	chr13:51914201-51914251	Jurkat	blood:	n/a
27	chr13:51818035-51818085	HIPEpiC	eye:	n/a
28	chr13:51855413-51855463	HCPEpiC	choroid plexus:	n/a
29	chr13:51796714-51796764	HUVEC	blood vessel:	n/a
30	chr13:51825918-51825968	LNCaP	prostate:	n/a
31	chr13:51914201-51914251	GM19239	blood:	n/a
32	chr13:51825774-51825824	HRCEpiC	kidney:	n/a
33	chr13:51858967-51859017	AG04449	skin:	fetal
34	chr13:51914201-51914251	HCT-116	colon:	n/a
35	chr13:51913736-51913786	PrEC	prostate:	n/a
36	chr13:51825918-51825968	HEK293	kidney:	embryo
37	chr13:51914201-51914251	HepG2	liver:	n/a
38	chr13:51796887-51796937	HAEpiC	amniotic membrane:	n/a
39	chr13:51797139-51797189	HL-60	blood:	n/a
40	chr13:51797139-51797189	NHDF-neo	bronchial:	n/a
41	chr13:51795926-51795976	NHDF-neo	bronchial:	n/a
42	chr13:51796223-51796273	NB4	blood:	n/a
43	chr13:51825057-51825107	Caco-2	colon:	n/a
44	chr13:51825774-51825824	SK-N-SH	brain:	n/a
45	chr13:51819465-51819515	HepG2	liver:	n/a
46	chr13:51795680-51795730	NHDF-neo	bronchial:	n/a
47	chr13:51822685-51822735	HRCEpiC	kidney:	n/a
48	chr13:51795926-51795976	NT2-D1	testis:	n/a
49	chr13:51914201-51914251	LNCaP	prostate:	n/a
50	chr13:51855413-51855463	HCT-116	colon:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr13:51785516..51788256-chr13:51793082..51795168,2	MCF-7	breast:
2	chr13:51820571..51823207-chr13:51824938..51826606,2	MCF-7	breast:
3	chr13:51909461..51913387-chr13:51914393..51916609,4	MCF-7	breast:
4	chr13:51796898..51797532-chr13:51860320..51860855,2	MCF-7	breast:
5	chr13:51889117..51892002-chr13:51899188..51901236,2	K562	blood:
6	chr13:51779357..51781194-chr13:51784004..51785686,2	K562	blood:
7	chr13:51865697..51869236-chr13:52025777..52029444,4	K562	blood:
8	chr13:51828873..51831199-chr13:51831782..51833897,3	K562	blood:
9	chr13:51913987..51916839-chr13:51917071..51920239,3	MCF-7	breast:
10	chr13:51785516..51788256-chr13:51793082..51795168,2	MCF-7	breast:
11	chr13:51846623..51849523-chr13:51854210..51856738,2	K562	blood:
12	chr13:51792474..51795123-chr13:51810834..51812856,2	MCF-7	breast:
13	chr13:51779322..51781536-chr13:51783405..51785158,2	MCF-7	breast:
14	chr13:51883357..51884920-chr13:51891392..51893202,2	K562	blood:
15	chr13:51848648..51850306-chr13:51854222..51856639,2	MCF-7	breast:
16	chr13:51909461..51913387-chr13:51914393..51916609,4	MCF-7	breast:
17	chr13:51699716..51700497-chr13:51860213..51860971,2	MCF-7	breast:
18	chr13:51836812..51837615-chr13:51860099..51861219,3	MCF-7	breast:
19	chr13:51893791..51895785-chr13:51947309..51949061,2	K562	blood:
20	chr13:51796112..51796761-chr13:51836717..51837532,2	MCF-7	breast:
21	chr13:51722837..51724133-chr13:51860193..51861210,11	MCF-7	breast:
22	chr13:51820571..51823207-chr13:51824938..51826606,2	MCF-7	breast:
23	chr13:51881497..51883529-chr13:52026918..52029105,2	MCF-7	breast:
24	chr13:51828873..51831199-chr13:51831782..51833897,3	K562	blood:
25	chr13:51848648..51850306-chr13:51854222..51856639,2	MCF-7	breast:
26	chr13:51918928..51921784-chr13:52026483..52029040,3	K562	blood:
27	chr13:51828567..51831393-chr13:51834161..51836601,2	K562	blood:
28	chr13:51845376..51847763-chr13:51852812..51854700,2	MCF-7	breast:
29	chr13:51836812..51837615-chr13:51860099..51861219,3	MCF-7	breast:
30	chr13:51772912..51774432-chr13:51786710..51788758,2	K562	blood:
31	chr13:51804724..51807237-chr13:51815591..51817634,2	MCF-7	breast:
32	chr13:51825741..51827924-chr13:51832786..51834447,2	MCF-7	breast:
33	chr13:51885872..51888143-chr13:51888698..51890403,2	MCF-7	breast:
34	chr13:51796898..51797532-chr13:51860320..51860855,2	MCF-7	breast:
35	chr13:51928537..51930997-chr13:51935943..51937476,2	MCF-7	breast:
36	chr13:51722852..51723780-chr13:51858091..51858924,2	MCF-7	breast:
37	chr13:51699608..51700542-chr13:51860268..51861161,4	K562	blood:
38	chr13:51889117..51892002-chr13:51899188..51901236,2	K562	blood:
39	chr13:51772912..51774432-chr13:51786710..51788758,2	K562	blood:
40	chr13:51818423..51819959-chr13:51823241..51825450,2	MCF-7	breast:
41	chr13:51831560..51833601-chr13:52377914..52379439,2	K562	blood:
42	chr13:51779322..51781536-chr13:51783405..51785158,2	MCF-7	breast:
43	chr13:51722919..51723811-chr13:51860090..51861195,8	MCF-7	breast:
44	chr13:51812537..51814566-chr13:51816955..51818623,2	K562	blood:
45	chr13:51919543..51922334-chr13:51931291..51934011,2	K562	blood:
46	chr13:51928398..51929906-chr13:51933549..51935466,2	MCF-7	breast:
47	chr13:51860286..51861138-chr17:4948410..4949066,2	MCF-7	breast:
48	chr13:51793406..51795432-chr13:51797315..51800295,2	K562	blood:
49	chr13:51779357..51781194-chr13:51784004..51785686,2	K562	blood:
50	chr13:51845376..51847763-chr13:51852812..51854700,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SERPINE3-4	chr13:51801383-51801565	NONHSAT033893
2	lnc-DHRS12-8	chr13:51935701-51936371	ENSG00000269965.1
3	lnc-FAM124A-1	chr13:51770017-51770217	NONHSAT033891
4	lnc-INTS6-1	chr13:51898734-51899105	XLOC_010617
5	lnc-INTS6-1	chr13:51894020-51894187	XLOC_010617
6	lnc-SERPINE3-4	chr13:51795151-51798286	ncRnaDb_ncrna_FR376720_3
7	lnc-SERPINE3-4	chr13:51799257-51799492	NONHSAT033893
8	lnc-SERPINE3-2	chr13:51835089-51836507	NONHSAT033894
9	lnc-SERPINE3-4	chr13:51796513-51796705	NONHSAT033893
10	lnc-DHRS12-7	chr13:51936795-51937579	ENSG00000270101.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5693	chr13:51922712-51922733	MIMAT0022486

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	INTS6	hsa-miR-1	chr13:51935739-51935760
2	INTS6	hsa-miR-30a-5p	chr13:51938306-51938327
3	INTS6	hsa-miR-155-5p	chr13:51936283-51936305

Variant related genes	Relation type
MIR5693	TF binding region
FAM124A	TF binding region
SERPINE3	TF binding region
ENSG00000269965	TF binding region
SLMO2P2	TF binding region
ENSG00000270101	TF binding region
MIR5693	CpG island
FAM124A	CpG island
SERPINE3	CpG island
ENSG00000269965	CpG island
SLMO2P2	CpG island
ENSG00000270101	CpG island
ENSG00000102786	chromatin interactions
ENSG00000150510	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000224892	chromatin interactions
ENSG00000269965	chromatin interactions
ENSG00000102796	chromatin interactions
ENSG00000231856	chromatin interactions
ENSG00000253309	chromatin interactions
NUP98	miRNA target sites
NUP50	miRNA target sites

Extended variants
information (count: 5748 )
Associated
traits (count: 123 )

Variant overlapped rSNPs/rCNVs (count:5748 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533197327	chr13:51766502-51766503	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs540328833	chr13:51766506-51766507	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs147967827	chr13:51766514-51766515	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs369553203	chr13:51766519-51766520	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs560411768	chr13:51766523-51766524	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs561051051	chr13:51766605-51766606	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs149941847	chr13:51766637-51766638	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs145239754	chr13:51766674-51766675	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs149172631	chr13:51766678-51766679	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs182314141	chr13:51766682-51766683	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552140138	chr13:51766703-51766704	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs115642853	chr13:51766738-51766739	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs116213219	chr13:51766741-51766742	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs187650583	chr13:51766743-51766744	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs9568541	chr13:51766756-51766757	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs192860028	chr13:51766763-51766764	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs554156474	chr13:51766886-51766887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555225458	chr13:51766911-51766912	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs142363594	chr13:51766914-51766915	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs538345158	chr13:51766964-51766965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567558059	chr13:51766980-51766981	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs536510922	chr13:51766997-51766998	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs548762591	chr13:51766999-51767000	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs370811008	chr13:51767018-51767019	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs369836655	chr13:51767021-51767022	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs375956723	chr13:51767117-51767118	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs537739193	chr13:51767123-51767124	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs557679961	chr13:51767131-51767132	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs577595187	chr13:51767135-51767136	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs540304886	chr13:51767136-51767137	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs560552163	chr13:51767153-51767154	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs556415872	chr13:51767210-51767211	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs147868012	chr13:51767233-51767234	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs141557779	chr13:51767347-51767348	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs562929581	chr13:51767357-51767358	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs544809681	chr13:51767366-51767367	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs531987032	chr13:51767386-51767387	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs552080908	chr13:51767429-51767430	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs9316529	chr13:51767441-51767442	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs373645224	chr13:51767489-51767490	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs184785658	chr13:51767519-51767520	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs546250058	chr13:51767546-51767547	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs566467386	chr13:51767571-51767572	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs377017001	chr13:51767581-51767582	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs377508181	chr13:51767593-51767594	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs147102713	chr13:51767622-51767623	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs188618900	chr13:51767637-51767638	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs192993229	chr13:51767650-51767651	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs559038194	chr13:51767678-51767679	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs11843433	chr13:51767682-51767683	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:123)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Retinoblastoma	21504564	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Mental retardation	17502991	CNVD
Retinoblastoma	17502991	CNVD
Bipolar disorder	18458673	CNVD
Liposarcoma	21253554	CNVD
T-cell lymphomas	19863542	CNVD
Cervical cancer	21062161	CNVD
microdeletion syndrome	19284877	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	19435819	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Myelofibrosis	22110671	CNVD
Hereditary prostate cancer	22028916	CNVD
Glioblastoma multiforme	22286061	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Prostate cancer	17217626	CNVD
Ovarian cancer	21781307	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21990379	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:3180 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51750200-51767000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr13:51754600-51770000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr13:51759000-51767800	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr13:51766000-51767200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr13:51766200-51767000	Enhancers	HUVEC	blood vessel
6	chr13:51770000-51770200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr13:51774000-51774400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr13:51774400-51785800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr13:51776200-51777800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr13:51776200-51777800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr13:51776200-51778000	Enhancers	HUVEC	blood vessel
12	chr13:51776600-51776800	Enhancers	NHDF-Ad	bronchial
13	chr13:51776600-51777200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr13:51777000-51777200	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
15	chr13:51777400-51777600	Enhancers	NHDF-Ad	bronchial
16	chr13:51777600-51777800	Bivalent Enhancer	NHDF-Ad	bronchial
17	chr13:51780200-51780400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
18	chr13:51782800-51783600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr13:51782800-51783600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr13:51783000-51783200	Enhancers	H9 Cell Line	embryonic stem cell
21	chr13:51783000-51783600	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr13:51783000-51783800	Enhancers	H1 Cell Line	embryonic stem cell
23	chr13:51783000-51784200	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr13:51783200-51783600	Enhancers	iPS-20b Cell Line	embryonic stem cell
25	chr13:51783400-51785400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr13:51783600-51786000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr13:51783600-51786000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr13:51783600-51786200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr13:51783800-51786000	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr13:51784200-51786000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr13:51785400-51787000	Enhancers	H9 Cell Line	embryonic stem cell
32	chr13:51785400-51787400	Enhancers	Fetal Stomach	stomach
33	chr13:51785800-51786400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr13:51785800-51786800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr13:51786000-51786200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr13:51786000-51786200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr13:51786000-51786200	Enhancers	Colon Smooth Muscle	Colon
38	chr13:51786000-51786800	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr13:51786000-51787000	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr13:51786000-51787000	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr13:51786000-51787800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr13:51786200-51786800	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr13:51786200-51787000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr13:51786200-51787200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr13:51786200-51790600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr13:51786400-51795600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr13:51786800-51787000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
48	chr13:51786800-51787400	Enhancers	Fetal Brain Male	brain
49	chr13:51786800-51793800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr13:51787000-51787200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell

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