Variant report

Variant	nsv897844
Chromosome Location	chr11:67772729-67793014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1957)
CpG islands
(count:1832)
Chromatin interactive
region (count:84)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1957 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:67776891-67777356	K562	blood:	n/a	n/a
2	ARID3A	chr11:67784995-67785244	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:67780816-67781200	HepG2	liver:	n/a	n/a
4	ATF1	chr11:67777013-67777242	K562	blood:	n/a	n/a
5	ATF3	chr11:67784181-67785090	A549	lung:	n/a	chr11:67784303-67784316 chr11:67784305-67784316 chr11:67784303-67784316
6	ATF3	chr11:67781471-67782584	A549	lung:	n/a	n/a
7	ATF3	chr11:67777103-67778538	A549	lung:	n/a	n/a
8	ATF3	chr11:67777383-67778323	A549	lung:	n/a	n/a
9	ATF3	chr11:67780514-67781156	A549	lung:	n/a	n/a
10	ATF3	chr11:67781331-67782561	A549	lung:	n/a	n/a
11	ATF3	chr11:67776792-67777250	K562	blood:	n/a	n/a
12	ATF3	chr11:67780581-67781324	A549	lung:	n/a	n/a
13	BACH1	chr11:67788128-67788410	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr11:67783438-67787248	A549	lung:	n/a	chr11:67786129-67786142 chr11:67786729-67786742 chr11:67785759-67785768 chr11:67784722-67784731 chr11:67785985-67785994
15	BCL3	chr11:67776809-67783348	A549	lung:	n/a	chr11:67782268-67782277
16	BCL3	chr11:67777390-67783349	A549	lung:	n/a	chr11:67782268-67782277
17	BCL3	chr11:67783431-67786996	A549	lung:	n/a	chr11:67786129-67786142 chr11:67786729-67786742 chr11:67785759-67785768 chr11:67784722-67784731 chr11:67785985-67785994
18	BCL3	chr11:67787937-67788806	A549	lung:	n/a	n/a
19	BHLHE40	chr11:67775944-67776167	HepG2	liver:	n/a	n/a
20	BHLHE40	chr11:67777215-67777241	GM12878	blood:	n/a	n/a
21	BHLHE40	chr11:67777673-67778077	HepG2	liver:	n/a	n/a
22	BHLHE40	chr11:67784301-67784584	HepG2	liver:	n/a	n/a
23	BHLHE40	chr11:67781713-67782037	A549	lung:	n/a	n/a
24	BHLHE40	chr11:67780711-67781056	HepG2	liver:	n/a	n/a
25	BHLHE40	chr11:67784301-67784650	K562	blood:	n/a	n/a
26	BHLHE40	chr11:67777586-67778103	A549	lung:	n/a	n/a
27	BHLHE40	chr11:67773992-67774128	HepG2	liver:	n/a	n/a
28	BHLHE40	chr11:67784322-67784701	A549	lung:	n/a	n/a
29	BHLHE40	chr11:67776907-67777143	A549	lung:	n/a	n/a
30	BHLHE40	chr11:67776577-67778070	K562	blood:	n/a	n/a
31	BHLHE40	chr11:67784291-67785257	HepG2	liver:	n/a	n/a
32	BRCA1	chr11:67788904-67788905	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr11:67777072-67778731	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr11:67784064-67784752	Hela-S3	cervix:	n/a	n/a
35	BRCA1	chr11:67779769-67780240	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr11:67781683-67782476	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr11:67780672-67781094	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr11:67776487-67777967	K562	blood:	n/a	n/a
39	CBX3	chr11:67781077-67781281	K562	blood:	n/a	n/a
40	CBX3	chr11:67776853-67777215	K562	blood:	n/a	n/a
41	CBX3	chr11:67774974-67775304	K562	blood:	n/a	n/a
42	CCNT2	chr11:67777590-67777790	K562	blood:	n/a	n/a
43	CEBPB	chr11:67777504-67778243	IMR90	lung:	n/a	chr11:67777683-67777694
44	CEBPB	chr11:67784236-67784793	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:67784342-67784764	A549	lung:	n/a	n/a
46	CEBPB	chr11:67777534-67777945	HepG2	liver:	n/a	chr11:67777683-67777694
47	CEBPB	chr11:67781622-67782699	A549	lung:	n/a	n/a
48	CEBPB	chr11:67777399-67778017	MCF-7	breast:	n/a	chr11:67777683-67777694
49	CEBPB	chr11:67784264-67784773	MCF-7	breast:	n/a	n/a
50	CEBPB	chr11:67779700-67780107	Hela-S3	cervix:	n/a	n/a

(count:1832 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67776030-67776080	NH-A	brain:	n/a
2	chr11:67786085-67786135	HRE	kidney:	n/a
3	chr11:67776030-67776080	NH-A	brain:	n/a
4	chr11:67786085-67786135	HRE	kidney:	n/a
5	chr11:67777682-67777732	HIPEpiC	eye:	n/a
6	chr11:67784489-67784539	HPAEpiC	pulmonary alveolar:	n/a
7	chr11:67777618-67777668	MCF10A-Er-Src	breast:	n/a
8	chr11:67790185-67790235	Caco-2	colon:	n/a
9	chr11:67777682-67777732	HCF	heart:	n/a
10	chr11:67777664-67777714	A549	lung:	n/a
11	chr11:67789326-67789376	AG10803	skin:	n/a
12	chr11:67777215-67777265	BJ	skin:	n/a
13	chr11:67777215-67777265	MCF10A-Er-Src	breast:	n/a
14	chr11:67790185-67790235	AG09319	gingival:	n/a
15	chr11:67777715-67777765	RPTEC	kidney:	n/a
16	chr11:67786199-67786249	HIPEpiC	eye:	n/a
17	chr11:67778641-67778691	HRCEpiC	kidney:	n/a
18	chr11:67777715-67777765	HEEpiC	esophagus:	n/a
19	chr11:67792744-67792794	BJ	skin:	n/a
20	chr11:67774728-67774778	HL-60	blood:	n/a
21	chr11:67789326-67789376	HRPEpiC	eye:	n/a
22	chr11:67784489-67784539	PANC-1	pancreas:	n/a
23	chr11:67790185-67790235	K562	blood:	n/a
24	chr11:67777952-67778002	AG09319	gingival:	n/a
25	chr11:67777770-67777820	U87	brain:	n/a
26	chr11:67786199-67786249	AG09309	skin:	n/a
27	chr11:67789123-67789173	ProgFib	skin:	n/a
28	chr11:67786269-67786319	ProgFib	skin:	n/a
29	chr11:67776030-67776080	HUVEC	blood vessel:	n/a
30	chr11:67790185-67790235	HNPCEpiC	eye:	n/a
31	chr11:67786269-67786319	PANC-1	pancreas:	n/a
32	chr11:67789045-67789095	CMK	blood:	n/a
33	chr11:67777664-67777714	NH-A	brain:	n/a
34	chr11:67774728-67774778	SAEC	small airway:	n/a
35	chr11:67777770-67777820	SK-N-MC	brain:	n/a
36	chr11:67775972-67776022	BE2_C	brain:	n/a
37	chr11:67777682-67777732	IMR90	lung:	fetal
38	chr11:67775763-67775813	HRE	kidney:	n/a
39	chr11:67788125-67788175	SK-N-SH	brain:	n/a
40	chr11:67786085-67786135	BE2_C	brain:	n/a
41	chr11:67775857-67775907	Caco-2	colon:	n/a
42	chr11:67777215-67777265	HNPCEpiC	eye:	n/a
43	chr11:67775972-67776022	K562	blood:	n/a
44	chr11:67789045-67789095	HCM	heart:	n/a
45	chr11:67775763-67775813	AG10803	skin:	n/a
46	chr11:67776123-67776173	PFSK-1	brain:	n/a
47	chr11:67786269-67786319	HAEpiC	amniotic membrane:	n/a
48	chr11:67776123-67776173	AoSMC	blood vessel:	n/a
49	chr11:67775972-67776022	GM19239	blood:	n/a
50	chr11:67790185-67790235	NB4	blood:	n/a

(count:84 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:210547287..210547789-chr11:67782156..67782711,2	Hela-S3	cervix:
2	chr11:67784552..67785411-chr6:30293809..30294405,2	Hela-S3	cervix:
3	chr11:67777523..67778410-chr6:36562073..36562583,2	Hela-S3	cervix:
4	chr11:67770218..67773172-chr11:67805064..67808057,3	K562	blood:
5	chr11:67770463..67774040-chr11:67774088..67778740,6	K562	blood:
6	chr11:67777900..67778811-chr16:15188045..15188733,2	Hela-S3	cervix:
7	chr11:67777631..67778251-chr12:109124964..109125585,2	Hela-S3	cervix:
8	chr11:67770112..67773137-chr11:67777240..67779852,3	K562	blood:
9	chr11:67778899..67781457-chr11:67928106..67930738,2	K562	blood:
10	chr11:67777733..67778469-chr7:25164455..25165345,2	Hela-S3	cervix:
11	chr11:67782340..67787471-chr11:67792467..67797834,9	K562	blood:
12	chr11:67792188..67795052-chr3:168699147..168701968,2	MCF-7	breast:
13	chr11:67770803..67771657-chr11:67784324..67785201,2	Hela-S3	cervix:
14	chr11:67771335..67773099-chr11:67888319..67890316,2	MCF-7	breast:
15	chr11:67776362..67777982-chr11:67979637..67981259,2	K562	blood:
16	chr11:67762444..67764941-chr11:67774417..67777074,2	K562	blood:
17	chr11:67783919..67784466-chr7:35734315..35735218,2	Hela-S3	cervix:
18	chr11:67790100..67792204-chr11:67793798..67795840,2	K562	blood:
19	chr11:67779784..67784526-chr11:67980026..67983056,5	MCF-7	breast:
20	chr11:67774356..67776475-chr11:67979797..67981596,2	MCF-7	breast:
21	chr11:67776156..67776785-chr11:67788500..67789123,2	MCF-7	breast:
22	chr11:67777483..67778251-chr12:52444740..52445403,2	Hela-S3	cervix:
23	chr11:67780000..67780893-chr20:23617975..23618833,2	Hela-S3	cervix:
24	chr11:67772162..67773973-chr11:67887199..67889790,2	K562	blood:
25	chr11:67777341..67778230-chr6:30584211..30585027,2	Hela-S3	cervix:
26	chr11:67785418..67788114-chr11:67980159..67983027,2	MCF-7	breast:
27	chr11:67770966..67773282-chr11:67774269..67777181,2	K562	blood:
28	chr11:67777277..67778126-chr5:177631110..177631694,2	Hela-S3	cervix:
29	chr11:67770463..67774040-chr11:67774088..67778740,6	K562	blood:
30	chr11:67770129..67772999-chr11:67979313..67982279,4	K562	blood:
31	chr1:226249482..226250105-chr11:67777477..67778223,2	Hela-S3	cervix:
32	chr11:67762605..67767485-chr11:67767779..67773135,10	K562	blood:
33	chr11:67777444..67778431-chr14:65453288..65454088,2	Hela-S3	cervix:
34	chr11:66511759..66512273-chr11:67777321..67778059,2	Hela-S3	cervix:
35	chr11:65270883..65271821-chr11:67776699..67777645,2	Hela-S3	cervix:
36	chr11:67777407..67777988-chr12:94853154..94854035,2	Hela-S3	cervix:
37	chr11:67770998..67775364-chr11:67887455..67891345,5	MCF-7	breast:
38	chr11:67770338..67773597-chr11:67780108..67784129,5	K562	blood:
39	chr11:67777146..67778108-chr3:99979311..99980252,2	Hela-S3	cervix:
40	chr11:67777507..67778379-chr16:57496418..57497191,2	Hela-S3	cervix:
41	chr11:67783063..67785124-chr11:67886491..67888333,2	K562	blood:
42	chr11:67778033..67778757-chr7:66205095..66205707,2	Hela-S3	cervix:
43	chr11:67777550..67778251-chr19:18433596..18434198,2	Hela-S3	cervix:
44	chr11:67780250..67781973-chr11:67889456..67890963,2	MCF-7	breast:
45	chr11:67785661..67786548-chr19:18433349..18434217,2	Hela-S3	cervix:
46	chr11:67777600..67778189-chr16:20911130..20911849,2	Hela-S3	cervix:
47	chr11:67787554..67789987-chr11:67792495..67796734,5	K562	blood:
48	chr11:67776892..67777625-chr11:67788855..67789447,2	MCF-7	breast:
49	chr11:67776787..67779464-chr11:67789576..67791598,2	K562	blood:
50	chr11:67777145..67777897-chr5:179050213..179051026,2	Hela-S3	cervix:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93B1-2	chr11:67792277-67792529	ENSG00000255306.1
2	lnc-UNC93B1-1	chr11:67776909-67782033	NONHSAT022487
3	lnc-UNC93B1-1	chr11:67784328-67784501	NONHSAT022487
4	lnc-UNC93B1-2	chr11:67792655-67792800	ENSG00000255306.1

No data

Variant related genes	Relation type
ALDH3B1	TF binding region
UNC93B1	TF binding region
ALDH3B1	CpG island
UNC93B1	CpG island
ENSG00000110066	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000204599	chromatin interactions
ENSG00000036054	chromatin interactions
ENSG00000006534	chromatin interactions
ENSG00000085721	chromatin interactions
ENSG00000172115	chromatin interactions
ENSG00000249915	chromatin interactions
ENSG00000272831	chromatin interactions
ENSG00000231074	chromatin interactions
ENSG00000138592	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000255236	chromatin interactions
ENSG00000130520	chromatin interactions
ENSG00000111602	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000243335	chromatin interactions
ENSG00000110717	chromatin interactions
ENSG00000270604	chromatin interactions
ENSG00000163041	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000102978	chromatin interactions
ENSG00000111665	chromatin interactions
ENSG00000272562	chromatin interactions
ENSG00000102897	chromatin interactions
ENSG00000248925	chromatin interactions
ENSG00000110057	chromatin interactions
ENSG00000188215	chromatin interactions
ENSG00000122557	chromatin interactions
ENSG00000173715	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000260735	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000110880	chromatin interactions
ENSG00000271122	chromatin interactions
ENSG00000257365	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000101439	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000173588	chromatin interactions
ENSG00000110719	chromatin interactions
ENSG00000141401	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000196678	chromatin interactions
ENSG00000008282	chromatin interactions

Extended variants
information (count: 919 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3808969	chr11:67772729-67772730	Enhancers Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553316034	chr11:67772780-67772781	Enhancers Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs151320172	chr11:67772784-67772785	Enhancers Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs545878761	chr11:67772788-67772789	Enhancers Weak transcription Genic enhancers Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs140470274	chr11:67772833-67772834	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs308326	chr11:67772869-67772870	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs75085985	chr11:67772904-67772905	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs115847989	chr11:67772926-67772927	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs529203278	chr11:67772936-67772937	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs546023653	chr11:67772975-67772976	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs554755280	chr11:67772994-67772995	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs12421182	chr11:67773003-67773004	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs559088877	chr11:67773019-67773020	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs532985583	chr11:67773064-67773065	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs150400118	chr11:67773065-67773066	Weak transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs148625130	chr11:67773155-67773156	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs371879944	chr11:67773156-67773157	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs549155057	chr11:67773270-67773271	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs567924058	chr11:67773285-67773286	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs535040910	chr11:67773315-67773316	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs553643449	chr11:67773357-67773358	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs571841208	chr11:67773361-67773362	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs374090202	chr11:67773363-67773364	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs386754526	chr11:67773364-67773365	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs529765821	chr11:67773365-67773366	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs368804490	chr11:67773366-67773367	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs11364118	chr11:67773367-67773368	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs35445091	chr11:67773388-67773389	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs565093082	chr11:67773403-67773404	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs376873168	chr11:67773505-67773506	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs145252679	chr11:67773520-67773521	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs541306979	chr11:67773543-67773544	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs555104764	chr11:67773568-67773569	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs573599241	chr11:67773596-67773597	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs559656926	chr11:67773630-67773631	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs80330533	chr11:67773631-67773632	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs61887537	chr11:67773643-67773644	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs376142790	chr11:67773681-67773682	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs12421254	chr11:67773686-67773687	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs549012150	chr11:67773731-67773732	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs180803476	chr11:67773746-67773747	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs117025069	chr11:67773753-67773754	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs530935059	chr11:67773764-67773765	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs531397027	chr11:67773773-67773774	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs35272803	chr11:67773820-67773821	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs549341648	chr11:67773822-67773823	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs561091526	chr11:67773839-67773840	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs7952122	chr11:67773897-67773898	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs546930874	chr11:67773929-67773930	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs571979455	chr11:67773945-67773946	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1046 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67771600-67772800	Enhancers	Spleen	Spleen
2	chr11:67771600-67777200	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr11:67771600-67797600	Weak transcription	Small Intestine	intestine
4	chr11:67772000-67772800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr11:67772000-67772800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:67772000-67772800	Enhancers	Lung	lung
7	chr11:67772000-67773000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr11:67772000-67773000	Enhancers	A549	lung
9	chr11:67772000-67775600	Weak transcription	Fetal Heart	heart
10	chr11:67772000-67775800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr11:67772000-67775800	Weak transcription	Liver	Liver
12	chr11:67772000-67775800	Weak transcription	Esophagus	oesophagus
13	chr11:67772000-67776000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr11:67772000-67776400	Weak transcription	Brain Angular Gyrus	brain
15	chr11:67772000-67776400	Weak transcription	Ovary	ovary
16	chr11:67772000-67776600	Weak transcription	Right Atrium	heart
17	chr11:67772000-67776600	Weak transcription	NH-A	brain
18	chr11:67772000-67776600	Weak transcription	NHDF-Ad	bronchial
19	chr11:67772000-67776800	Weak transcription	Osteobl	bone
20	chr11:67772000-67777000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:67772000-67777200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr11:67772200-67772800	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr11:67772200-67772800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr11:67772200-67772800	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr11:67772200-67772800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr11:67772200-67772800	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr11:67772200-67772800	Enhancers	GM12878-XiMat	blood
28	chr11:67772200-67772800	Enhancers	Hela-S3	cervix
29	chr11:67772200-67773000	Enhancers	Primary B cells from cord blood	blood
30	chr11:67772200-67773000	Enhancers	Primary hematopoietic stem cells short term culture	blood
31	chr11:67772200-67773600	Weak transcription	Primary neutrophils fromperipheralblood	blood
32	chr11:67772200-67773800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr11:67772200-67774200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr11:67772200-67775200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr11:67772200-67775200	Weak transcription	Pancreas	Pancrea
36	chr11:67772200-67775200	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr11:67772200-67775400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr11:67772200-67775400	Weak transcription	Adipose Nuclei	Adipose
39	chr11:67772200-67775400	Weak transcription	Colonic Mucosa	Colon
40	chr11:67772200-67775400	Weak transcription	Fetal Intestine Large	intestine
41	chr11:67772200-67775600	Weak transcription	Gastric	stomach
42	chr11:67772200-67775600	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr11:67772200-67775800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr11:67772200-67775800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chr11:67772200-67775800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr11:67772200-67775800	Weak transcription	HMEC	breast
47	chr11:67772200-67775800	Weak transcription	HSMM	muscle
48	chr11:67772200-67775800	Weak transcription	HSMMtube	muscle
49	chr11:67772200-67776000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr11:67772200-67776000	Weak transcription	NHEK	skin

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