Variant report

Variant	nsv1045933
Chromosome Location	chr11:16023805-16067955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:16023336-16024035	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:16052263-16052509	K562	blood:	n/a	n/a
3	ATF1	chr11:16052274-16052579	K562	blood:	n/a	n/a
4	BACH1	chr11:16033921-16034188	K562	blood:	n/a	n/a
5	BHLHE40	chr11:16023691-16023958	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:16023484-16023920	HepG2	liver:	n/a	n/a
7	BHLHE40	chr11:16033980-16034264	K562	blood:	n/a	n/a
8	CEBPB	chr11:16055623-16056015	IMR90	lung:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
9	CEBPB	chr11:16023407-16023816	ECC-1	luminal epithelium:	n/a	chr11:16023525-16023536
10	CEBPB	chr11:16050008-16050352	IMR90	lung:	n/a	n/a
11	CEBPB	chr11:16037772-16037939	HepG2	liver:	n/a	chr11:16037859-16037872
12	CEBPB	chr11:16023383-16023851	ECC-1	luminal epithelium:	n/a	chr11:16023525-16023536
13	CEBPB	chr11:16055566-16056076	A549	lung:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
14	CEBPB	chr11:16055709-16055917	K562	blood:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
15	CEBPB	chr11:16023309-16023866	A549	lung:	n/a	chr11:16023525-16023536
16	CEBPB	chr11:16030588-16030944	IMR90	lung:	n/a	chr11:16030738-16030749 chr11:16030765-16030776 chr11:16030738-16030747
17	CEBPB	chr11:16023388-16023829	HepG2	liver:	n/a	chr11:16023525-16023536
18	CEBPB	chr11:16055681-16055980	MCF-7	breast:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
19	CEBPB	chr11:16055740-16055905	HepG2	liver:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
20	CEBPB	chr11:16023332-16023887	Hela-S3	cervix:	n/a	chr11:16023525-16023536
21	CEBPB	chr11:16023254-16023866	A549	lung:	n/a	chr11:16023525-16023536
22	CEBPB	chr11:16055582-16056011	K562	blood:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
23	CEBPB	chr11:16055606-16056049	K562	blood:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
24	CEBPB	chr11:16030594-16030954	K562	blood:	n/a	chr11:16030738-16030749 chr11:16030765-16030776 chr11:16030738-16030747
25	CEBPB	chr11:16055627-16055997	ECC-1	luminal epithelium:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
26	CEBPB	chr11:16055630-16056003	H1-hESC	embryonic stem cell:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
27	CEBPB	chr11:16023328-16023820	MCF-7	breast:	n/a	chr11:16023525-16023536
28	CEBPB	chr11:16023305-16023857	HCT-116	colon:	n/a	chr11:16023525-16023536
29	CEBPB	chr11:16023202-16023888	IMR90	lung:	n/a	chr11:16023525-16023536
30	CEBPB	chr11:16055606-16056025	ECC-1	luminal epithelium:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
31	CEBPB	chr11:16055644-16055981	Hela-S3	cervix:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
32	CEBPB	chr11:16023449-16023874	MCF-7	breast:	n/a	chr11:16023525-16023536
33	CEBPB	chr11:16030651-16030861	H1-hESC	embryonic stem cell:	n/a	chr11:16030738-16030749 chr11:16030765-16030776 chr11:16030738-16030747
34	CEBPB	chr11:16055734-16055955	MCF-7	breast:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
35	CEBPB	chr11:16023451-16023848	HCT-116	colon:	n/a	chr11:16023525-16023536
36	CEBPB	chr11:16055699-16055891	HepG2	liver:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
37	CEBPB	chr11:16023345-16023825	A549	lung:	n/a	chr11:16023525-16023536
38	CEBPB	chr11:16030597-16030950	HepG2	liver:	n/a	chr11:16030738-16030749 chr11:16030765-16030776 chr11:16030738-16030747
39	CEBPB	chr11:16055630-16056006	A549	lung:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
40	CEBPB	chr11:16023342-16023879	HepG2	liver:	n/a	chr11:16023525-16023536
41	CEBPB	chr11:16030604-16030899	Hela-S3	cervix:	n/a	chr11:16030738-16030749 chr11:16030765-16030776 chr11:16030738-16030747
42	CEBPB	chr11:16030602-16030928	A549	lung:	n/a	chr11:16030738-16030749 chr11:16030765-16030776 chr11:16030738-16030747
43	CEBPB	chr11:16055593-16055975	A549	lung:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
44	CEBPB	chr11:16055627-16056005	HepG2	liver:	n/a	chr11:16055813-16055822 chr11:16055813-16055822 chr11:16055811-16055822 chr11:16055813-16055822 chr11:16055813-16055822
45	CTCF	chr11:16062760-16062910	RPTEC	kidney:	n/a	n/a
46	CTCF	chr11:16023660-16023810	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr11:16038360-16038510	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr11:16040620-16040770	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr11:16062799-16063002	GM12878	blood:	n/a	n/a
50	CTCF	chr11:16062873-16063079	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:16034942-16034992	Caco-2	colon:	n/a
2	chr11:16034942-16034992	HRCEpiC	kidney:	n/a
3	chr11:16034942-16034992	HCPEpiC	choroid plexus:	n/a
4	chr11:16034942-16034992	HCT-116	colon:	n/a
5	chr11:16034942-16034992	NHBE	bronchial:	n/a
6	chr11:16034942-16034992	AoSMC	blood vessel:	n/a
7	chr11:16034942-16034992	HIPEpiC	eye:	n/a
8	chr11:16034942-16034992	AG09319	gingival:	n/a
9	chr11:16034942-16034992	HRPEpiC	eye:	n/a
10	chr11:16034942-16034992	SAEC	small airway:	n/a
11	chr11:16034942-16034992	GM12878	blood:	n/a
12	chr11:16034942-16034992	AG09309	skin:	n/a
13	chr11:16034942-16034992	PrEC	prostate:	n/a
14	chr11:16034942-16034992	ProgFib	skin:	n/a
15	chr11:16034942-16034992	HNPCEpiC	eye:	n/a
16	chr11:16034942-16034992	MCF-7	breast:	n/a
17	chr11:16034942-16034992	LNCaP	prostate:	n/a
18	chr11:16034942-16034992	NH-A	brain:	n/a
19	chr11:16034942-16034992	Hepatocyte	liver:	n/a
20	chr11:16034942-16034992	HCM	heart:	n/a
21	chr11:16034942-16034992	HPAEpiC	pulmonary alveolar:	n/a
22	chr11:16034942-16034992	SKMC	muscle:	n/a
23	chr11:16034942-16034992	AG04449	skin:	fetal
24	chr11:16034942-16034992	PFSK-1	brain:	n/a
25	chr11:16034942-16034992	GM12891	blood:	n/a
26	chr11:16034942-16034992	HCF	heart:	n/a
27	chr11:16034942-16034992	MCF10A-Er-Src	breast:	n/a
28	chr11:16034942-16034992	RPTEC	kidney:	n/a
29	chr11:16034942-16034992	T-47D	breast:	n/a
30	chr11:16034942-16034992	NHDF-neo	bronchial:	n/a
31	chr11:16034942-16034992	HAEpiC	amniotic membrane:	n/a
32	chr11:16034942-16034992	SK-N-MC	brain:	n/a
33	chr11:16034942-16034992	NT2-D1	testis:	n/a
34	chr11:16034942-16034992	HepG2	liver:	n/a
35	chr11:16034942-16034992	HEEpiC	esophagus:	n/a
36	chr11:16034942-16034992	BE2_C	brain:	n/a
37	chr11:16034942-16034992	ovcar-3	ovarian:	n/a
38	chr11:16034942-16034992	U87	brain:	n/a
39	chr11:16034942-16034992	HUVEC	blood vessel:	n/a
40	chr11:16034942-16034992	CMK	blood:	n/a
41	chr11:16034942-16034992	AG04450	lung:	fetal
42	chr11:16034942-16034992	Hela-S3	cervix:	n/a
43	chr11:16034942-16034992	NB4	blood:	n/a
44	chr11:16034942-16034992	A549	lung:	n/a
45	chr11:16034942-16034992	HL-60	blood:	n/a
46	chr11:16034942-16034992	K562	blood:	n/a
47	chr11:16034942-16034992	IMR90	lung:	fetal
48	chr11:16034942-16034992	Jurkat	blood:	n/a
49	chr11:16034942-16034992	GM19239	blood:	n/a
50	chr11:16034942-16034992	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr11:15987618..15990384-chr11:16022034..16024122,2	K562	blood:
2	chr11:16021826..16024394-chr11:16625714..16628105,2	K562	blood:
3	chr11:16022109..16024928-chr11:16030034..16031853,2	K562	blood:
4	chr11:16062557..16063363-chr11:16634999..16635927,3	MCF-7	breast:
5	chr11:16031461..16034142-chr11:16036035..16038140,2	K562	blood:
6	chr11:16051749..16054417-chr11:16055912..16059434,4	K562	blood:
7	chr11:16022109..16024928-chr11:16030034..16031853,2	K562	blood:
8	chr11:16035545..16037231-chr11:16626707..16629465,2	K562	blood:
9	chr11:16049316..16051485-chr11:16053091..16055803,3	K562	blood:
10	chr11:16039156..16041121-chr11:16045276..16047949,2	K562	blood:
11	chr11:16067749..16070410-chr11:16071659..16073364,2	K562	blood:
12	chr11:16034951..16037801-chr11:16040174..16041965,2	K562	blood:
13	chr11:16032786..16036451-chr11:16039084..16041674,3	K562	blood:
14	chr11:16061504..16063486-chr11:16064879..16066876,2	K562	blood:
15	chr11:16044417..16046496-chr11:16053170..16054681,2	MCF-7	breast:
16	chr11:16060678..16062242-chr11:16069879..16072547,3	K562	blood:
17	chr11:16041921..16047548-chr11:16050958..16052889,4	K562	blood:
18	chr11:16034162..16035790-chr11:16047391..16049636,2	K562	blood:
19	chr11:16049316..16051485-chr11:16053091..16055803,3	K562	blood:
20	chr11:16039156..16041121-chr11:16045276..16047949,2	K562	blood:
21	chr11:16061504..16063486-chr11:16064879..16066876,2	K562	blood:
22	chr11:16051749..16054417-chr11:16055912..16059434,4	K562	blood:
23	chr11:16034162..16035790-chr11:16047391..16049636,2	K562	blood:
24	chr11:16031398..16034021-chr11:16626227..16628644,2	K562	blood:
25	chr11:16033382..16036196-chr11:16045412..16048891,3	K562	blood:
26	chr11:16020621..16022625-chr11:16024207..16026994,2	K562	blood:
27	chr11:16031461..16033992-chr11:16035845..16037535,2	K562	blood:
28	chr11:16041768..16046202-chr11:16046544..16050056,4	K562	blood:
29	chr11:16033382..16036196-chr11:16045412..16048891,3	K562	blood:
30	chr11:16032786..16036451-chr11:16039084..16041674,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf58-1	chr11:16052969-16053061	ENSG00000254878.1
2	lnc-C11orf58-1	chr11:16044736-16044839	ENSG00000254878.1
3	lnc-C11orf58-5	chr11:16067794-16067836	NONHSAT018169
4	lnc-C11orf58-5	chr11:16065774-16065800	NONHSAT018169

Variant related genes	Relation type
ENSG00000254878	TF binding region
SOX6	TF binding region
ENSG00000254878	CpG island
SOX6	CpG island
ENSG00000110693	chromatin interactions
ENSG00000254878	chromatin interactions

Extended variants
information (count: 1407 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572633814	chr11:16023843-16023844	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs540038844	chr11:16023888-16023889	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs183659495	chr11:16023889-16023890	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs546549413	chr11:16023916-16023917	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs571860529	chr11:16023938-16023939	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs564976124	chr11:16023991-16023992	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539300360	chr11:16024022-16024023	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550920167	chr11:16024075-16024076	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs145257935	chr11:16024076-16024077	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs188993655	chr11:16024136-16024137	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs201685516	chr11:16024141-16024142	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs555109966	chr11:16024145-16024146	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs573326821	chr11:16024218-16024219	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs180888296	chr11:16024249-16024250	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs558896371	chr11:16024278-16024279	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187387432	chr11:16024315-16024316	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs151051425	chr11:16024316-16024317	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs563379137	chr11:16024329-16024330	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544183614	chr11:16024355-16024356	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs575108786	chr11:16024366-16024367	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs542369366	chr11:16024371-16024372	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs139782807	chr11:16024380-16024381	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs149808513	chr11:16024388-16024389	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs546309755	chr11:16024426-16024427	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs564874562	chr11:16024431-16024432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532738031	chr11:16024446-16024447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs551245794	chr11:16024471-16024472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs569530323	chr11:16024478-16024479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190573950	chr11:16024503-16024504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs548771874	chr11:16024512-16024513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567005684	chr11:16024515-16024516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs61172429	chr11:16024525-16024526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs534278979	chr11:16024538-16024539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576818878	chr11:16024543-16024544	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558729623	chr11:16024550-16024551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs181843449	chr11:16024709-16024710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537812308	chr11:16024718-16024719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556841945	chr11:16024809-16024810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs145706780	chr11:16024835-16024836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373168753	chr11:16024899-16024900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs140538784	chr11:16024941-16024942	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572876613	chr11:16024942-16024943	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369282839	chr11:16024974-16024975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145883375	chr11:16024987-16024988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79325715	chr11:16024988-16024989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185980273	chr11:16025001-16025002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543814268	chr11:16025012-16025013	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs190304843	chr11:16025037-16025038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563197506	chr11:16025040-16025041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146639730	chr11:16025087-16025088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myelofibrosis	22110671	CNVD
Cancer	24489367	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Neuroblastoma	19435921	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16004800-16024600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:16011000-16033800	Weak transcription	Left Ventricle	heart
3	chr11:16021200-16024000	Enhancers	NHEK	skin
4	chr11:16021200-16025400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:16021400-16024200	Enhancers	NH-A	brain
6	chr11:16022600-16024800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:16022800-16024400	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr11:16022800-16024400	Enhancers	Fetal Intestine Large	intestine
9	chr11:16022800-16024400	Enhancers	Fetal Intestine Small	intestine
10	chr11:16022800-16024800	Enhancers	HepG2	liver
11	chr11:16022800-16025000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:16023000-16024000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr11:16023000-16024000	Enhancers	HSMM	muscle
14	chr11:16023000-16024200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:16023000-16024200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
16	chr11:16023000-16024200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:16023000-16024400	Enhancers	Fetal Stomach	stomach
18	chr11:16023000-16024400	Enhancers	Ovary	ovary
19	chr11:16023000-16025000	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr11:16023200-16024400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:16023200-16024400	Enhancers	Liver	Liver
22	chr11:16023200-16025000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr11:16023400-16024000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:16023400-16024000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr11:16023400-16024000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr11:16023400-16024000	Flanking Active TSS	Osteobl	bone
27	chr11:16023400-16024200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr11:16023400-16035400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:16023600-16024000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr11:16023600-16024000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr11:16023600-16024000	Flanking Active TSS	Hela-S3	cervix
32	chr11:16023600-16024200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:16023600-16024200	Active TSS	Pancreatic Islets	Pancreatic Islet
34	chr11:16023600-16024400	Enhancers	Brain Germinal Matrix	brain
35	chr11:16023600-16025200	Enhancers	Fetal Heart	heart
36	chr11:16023600-16025200	Enhancers	Skeletal Muscle Female	skeletal muscle
37	chr11:16023800-16024000	Flanking Active TSS	A549	lung
38	chr11:16023800-16024000	Enhancers	HUVEC	blood vessel
39	chr11:16023800-16024000	Flanking Active TSS	NHLF	lung
40	chr11:16023800-16024400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr11:16023800-16024400	Enhancers	HMEC	breast
42	chr11:16023800-16024400	Enhancers	NHDF-Ad	bronchial
43	chr11:16023800-16024600	Weak transcription	Psoas Muscle	Psoas
44	chr11:16023800-16025000	Enhancers	Fetal Lung	lung
45	chr11:16023800-16027600	Weak transcription	K562	blood
46	chr11:16023800-16027800	Weak transcription	Duodenum Mucosa	Duodenum
47	chr11:16023800-16029200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr11:16023800-16033200	Weak transcription	Fetal Muscle Leg	muscle
49	chr11:16023800-16033800	Weak transcription	Small Intestine	intestine
50	chr11:16023800-16035000	Weak transcription	Brain Substantia Nigra	brain

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