Variant report

Variant	nsv897839
Chromosome Location	chr11:67765056-67793014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2590)
CpG islands
(count:2689)
Chromatin interactive
region (count:95)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2590 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

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	chr11:67780816-67781200	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:67769722-67769736	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:67784995-67785244	HepG2	liver:	n/a	n/a
5	ATF1	chr11:67777013-67777242	K562	blood:	n/a	n/a
6	ATF2	chr11:67771439-67771886	GM12878	blood:	n/a	n/a
7	ATF3	chr11:67784181-67785090	A549	lung:	n/a	chr11:67784303-67784316 chr11:67784305-67784316 chr11:67784303-67784316
8	ATF3	chr11:67781471-67782584	A549	lung:	n/a	n/a
9	ATF3	chr11:67777383-67778323	A549	lung:	n/a	n/a
10	ATF3	chr11:67780514-67781156	A549	lung:	n/a	n/a
11	ATF3	chr11:67781331-67782561	A549	lung:	n/a	n/a
12	ATF3	chr11:67776792-67777250	K562	blood:	n/a	n/a
13	ATF3	chr11:67771495-67771797	K562	blood:	n/a	chr11:67771598-67771607
14	ATF3	chr11:67777103-67778538	A549	lung:	n/a	n/a
15	ATF3	chr11:67780581-67781324	A549	lung:	n/a	n/a
16	ATF3	chr11:67771505-67771926	A549	lung:	n/a	chr11:67771598-67771607
17	BACH1	chr11:67788128-67788410	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr11:67771542-67771872	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr11:67764221-67765106	A549	lung:	n/a	n/a
20	BCL3	chr11:67777390-67783349	A549	lung:	n/a	chr11:67782268-67782277
21	BCL3	chr11:67770938-67771181	GM12878	blood:	n/a	chr11:67770982-67770991 chr11:67770983-67770996 chr11:67771018-67771027 chr11:67771028-67771037
22	BCL3	chr11:67776809-67783348	A549	lung:	n/a	chr11:67782268-67782277
23	BCL3	chr11:67783431-67786996	A549	lung:	n/a	chr11:67786129-67786142 chr11:67786729-67786742 chr11:67785759-67785768 chr11:67784722-67784731 chr11:67785985-67785994
24	BCL3	chr11:67787937-67788806	A549	lung:	n/a	n/a
25	BCL3	chr11:67783438-67787248	A549	lung:	n/a	chr11:67786129-67786142 chr11:67786729-67786742 chr11:67785759-67785768 chr11:67784722-67784731 chr11:67785985-67785994
26	BCLAF1	chr11:67771345-67771879	GM12878	blood:	n/a	chr11:67771597-67771606
27	BCLAF1	chr11:67770818-67771249	GM12878	blood:	n/a	chr11:67770982-67770991 chr11:67770983-67770996 chr11:67771018-67771027 chr11:67771028-67771037
28	BHLHE40	chr11:67769551-67769812	K562	blood:	n/a	n/a
29	BHLHE40	chr11:67776907-67777143	A549	lung:	n/a	n/a
30	BHLHE40	chr11:67769526-67770501	GM12878	blood:	n/a	n/a
31	BHLHE40	chr11:67771468-67771833	HepG2	liver:	n/a	n/a
32	BHLHE40	chr11:67776577-67778070	K562	blood:	n/a	n/a
33	BHLHE40	chr11:67784291-67785257	HepG2	liver:	n/a	n/a
34	BHLHE40	chr11:67771479-67771917	K562	blood:	n/a	n/a
35	BHLHE40	chr11:67780711-67781056	HepG2	liver:	n/a	n/a
36	BHLHE40	chr11:67771448-67771870	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:67775944-67776167	HepG2	liver:	n/a	n/a
38	BHLHE40	chr11:67769596-67769806	HepG2	liver:	n/a	n/a
39	BHLHE40	chr11:67769512-67769893	HepG2	liver:	n/a	n/a
40	BHLHE40	chr11:67777673-67778077	HepG2	liver:	n/a	n/a
41	BHLHE40	chr11:67773992-67774128	HepG2	liver:	n/a	n/a
42	BHLHE40	chr11:67784301-67784584	HepG2	liver:	n/a	n/a
43	BHLHE40	chr11:67777215-67777241	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:67771019-67771237	K562	blood:	n/a	n/a
45	BHLHE40	chr11:67777586-67778103	A549	lung:	n/a	n/a
46	BHLHE40	chr11:67784301-67784650	K562	blood:	n/a	n/a
47	BHLHE40	chr11:67781713-67782037	A549	lung:	n/a	n/a
48	BHLHE40	chr11:67770874-67771243	GM12878	blood:	n/a	chr11:67770996-67771012
49	BHLHE40	chr11:67784322-67784701	A549	lung:	n/a	n/a
50	BRCA1	chr11:67770167-67770264	GM12878	blood:	n/a	n/a

(count:2689 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67775301-67775351	NHBE	bronchial:	n/a
2	chr11:67770404-67770454	AoSMC	blood vessel:	n/a
3	chr11:67775857-67775907	Jurkat	blood:	n/a
4	chr11:67789123-67789173	A549	lung:	n/a
5	chr11:67765141-67765191	GM19239	blood:	n/a
6	chr11:67775301-67775351	NHBE	bronchial:	n/a
7	chr11:67770404-67770454	AoSMC	blood vessel:	n/a
8	chr11:67775857-67775907	Jurkat	blood:	n/a
9	chr11:67789123-67789173	A549	lung:	n/a
10	chr11:67765141-67765191	GM19239	blood:	n/a
11	chr11:67772273-67772323	Jurkat	blood:	n/a
12	chr11:67776030-67776080	T-47D	breast:	n/a
13	chr11:67765720-67765770	GM12892	blood:	n/a
14	chr11:67770665-67770715	Jurkat	blood:	n/a
15	chr11:67777770-67777820	ECC-1	luminal epithelium:	n/a
16	chr11:67765720-67765770	GM12878	blood:	n/a
17	chr11:67786085-67786135	BJ	skin:	n/a
18	chr11:67792744-67792794	NHBE	bronchial:	n/a
19	chr11:67776030-67776080	HEEpiC	esophagus:	n/a
20	chr11:67780637-67780687	ProgFib	skin:	n/a
21	chr11:67765204-67765254	AG04449	skin:	fetal
22	chr11:67777715-67777765	BJ	skin:	n/a
23	chr11:67774728-67774778	GM06990	blood:	n/a
24	chr11:67775857-67775907	HCT-116	colon:	n/a
25	chr11:67770929-67770979	Hepatocyte	liver:	n/a
26	chr11:67792744-67792794	HRCEpiC	kidney:	n/a
27	chr11:67770665-67770715	ovcar-3	ovarian:	n/a
28	chr11:67768362-67768412	HNPCEpiC	eye:	n/a
29	chr11:67786199-67786249	CMK	blood:	n/a
30	chr11:67768362-67768412	GM19239	blood:	n/a
31	chr11:67774728-67774778	HUVEC	blood vessel:	n/a
32	chr11:67777618-67777668	MCF10A-Er-Src	breast:	n/a
33	chr11:67770665-67770715	NB4	blood:	n/a
34	chr11:67786269-67786319	Hepatocyte	liver:	n/a
35	chr11:67777215-67777265	HEEpiC	esophagus:	n/a
36	chr11:67770929-67770979	HCPEpiC	choroid plexus:	n/a
37	chr11:67776576-67776626	HNPCEpiC	eye:	n/a
38	chr11:67780637-67780687	AG04450	lung:	fetal
39	chr11:67786085-67786135	HRCEpiC	kidney:	n/a
40	chr11:67783257-67783307	PANC-1	pancreas:	n/a
41	chr11:67765204-67765254	SK-N-MC	brain:	n/a
42	chr11:67780637-67780687	RPTEC	kidney:	n/a
43	chr11:67789326-67789376	PrEC	prostate:	n/a
44	chr11:67776030-67776080	Hela-S3	cervix:	n/a
45	chr11:67777664-67777714	MCF10A-Er-Src	breast:	n/a
46	chr11:67765720-67765770	RPTEC	kidney:	n/a
47	chr11:67778641-67778691	AoSMC	blood vessel:	n/a
48	chr11:67786199-67786249	HL-60	blood:	n/a
49	chr11:67778641-67778691	HUVEC	blood vessel:	n/a
50	chr11:67790185-67790235	AG10803	skin:	n/a

(count:95 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:67770966..67773282-chr11:67774269..67777181,2	K562	blood:
2	chr11:67777900..67778811-chr16:15188045..15188733,2	Hela-S3	cervix:
3	chr11:67778253..67781107-chr11:67810420..67812608,2	K562	blood:
4	chr11:67785661..67786548-chr19:18433349..18434217,2	Hela-S3	cervix:
5	chr11:67776633..67779501-chr11:67798153..67800329,2	K562	blood:
6	chr11:67762605..67767485-chr11:67767779..67773135,10	K562	blood:
7	chr11:67777387..67778242-chr15:50716543..50717165,2	Hela-S3	cervix:
8	chr11:67763621..67766711-chr11:67769461..67772575,7	MCF-7	breast:
9	chr11:67791239..67794033-chr11:67979567..67982575,4	MCF-7	breast:
10	chr11:67770338..67773597-chr11:67780108..67784129,5	K562	blood:
11	chr11:67779784..67784526-chr11:67980026..67983056,5	MCF-7	breast:
12	chr11:67776156..67776785-chr11:67788500..67789123,2	MCF-7	breast:
13	chr11:67770463..67774040-chr11:67774088..67778740,6	K562	blood:
14	chr1:11969474..11970311-chr11:67771036..67771591,2	HCT-116	colon:
15	chr11:67785418..67788114-chr11:67980159..67983027,2	MCF-7	breast:
16	chr11:67767693..67769603-chr11:67779964..67781851,2	K562	blood:
17	chr11:67771065..67771769-chr11:67787544..67788124,2	MCF-7	breast:
18	chr1:210547287..210547789-chr11:67782156..67782711,2	Hela-S3	cervix:
19	chr11:67777507..67778379-chr16:57496418..57497191,2	Hela-S3	cervix:
20	chr11:67791829..67792701-chr11:67805432..67806435,3	MCF-7	breast:
21	chr11:67774356..67776475-chr11:67979797..67981596,2	MCF-7	breast:
22	chr11:67776362..67777982-chr11:67979637..67981259,2	K562	blood:
23	chr1:226249482..226250105-chr11:67777477..67778223,2	Hela-S3	cervix:
24	chr11:67762444..67764941-chr11:67774417..67777074,2	K562	blood:
25	chr11:67777934..67778464-chr17:56708221..56708843,2	Hela-S3	cervix:
26	chr11:67777361..67777944-chr6:32935719..32936511,2	Hela-S3	cervix:
27	chr11:67777550..67778251-chr19:18433596..18434198,2	Hela-S3	cervix:
28	chr11:67770966..67773282-chr11:67774269..67777181,2	K562	blood:
29	chr11:67783191..67785391-chr11:67975759..67978285,2	K562	blood:
30	chr11:67787554..67789987-chr11:67792495..67796734,5	K562	blood:
31	chr11:67778033..67778757-chr7:66205095..66205707,2	Hela-S3	cervix:
32	chr11:67777145..67777897-chr5:179050213..179051026,2	Hela-S3	cervix:
33	chr11:67770133..67772267-chr11:67796388..67798189,2	K562	blood:
34	chr11:67778899..67781457-chr11:67928106..67930738,2	K562	blood:
35	chr11:67770112..67773137-chr11:67777240..67779852,3	K562	blood:
36	chr11:67777484..67778360-chr5:271623..272155,2	Hela-S3	cervix:
37	chr11:67792299..67793938-chr11:67945521..67947128,2	MCF-7	breast:
38	chr11:67770129..67772999-chr11:67979313..67982279,4	K562	blood:
39	chr11:67770463..67774040-chr11:67774088..67778740,6	K562	blood:
40	chr11:67770998..67775364-chr11:67887455..67891345,5	MCF-7	breast:
41	chr11:67787958..67790078-chr11:67980039..67982910,2	MCF-7	breast:
42	chr11:67790805..67792830-chr11:68162793..68164803,2	K562	blood:
43	chr11:67783919..67784466-chr7:35734315..35735218,2	Hela-S3	cervix:
44	chr11:67784552..67785411-chr6:30293809..30294405,2	Hela-S3	cervix:
45	chr11:67777277..67778126-chr5:177631110..177631694,2	Hela-S3	cervix:
46	chr11:67770218..67773172-chr11:67805064..67808057,3	K562	blood:
47	chr11:67777219..67778102-chr7:105752408..105753213,2	Hela-S3	cervix:
48	chr11:67770338..67773597-chr11:67780108..67784129,5	K562	blood:
49	chr11:67771335..67773099-chr11:67888319..67890316,2	MCF-7	breast:
50	chr11:67780250..67781973-chr11:67889456..67890963,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ALDH3B1	TF binding region
UNC93B1	TF binding region
ALDH3B1	CpG island
UNC93B1	CpG island
ENSG00000171067	chromatin interactions
ENSG00000257365	chromatin interactions
ENSG00000249915	chromatin interactions
ENSG00000123268	chromatin interactions
ENSG00000255236	chromatin interactions
ENSG00000204257	chromatin interactions
ENSG00000169045	chromatin interactions
ENSG00000173588	chromatin interactions
ENSG00000101439	chromatin interactions
ENSG00000102978	chromatin interactions
ENSG00000188215	chromatin interactions
ENSG00000204569	chromatin interactions
ENSG00000172115	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000110721	chromatin interactions
ENSG00000141401	chromatin interactions
ENSG00000173715	chromatin interactions
ENSG00000122557	chromatin interactions
ENSG00000167799	chromatin interactions
ENSG00000272831	chromatin interactions
ENSG00000110700	chromatin interactions
ENSG00000111665	chromatin interactions
ENSG00000270604	chromatin interactions
ENSG00000231074	chromatin interactions
ENSG00000036054	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000110057	chromatin interactions
ENSG00000248925	chromatin interactions
ENSG00000243335	chromatin interactions
ENSG00000272562	chromatin interactions
ENSG00000271122	chromatin interactions
ENSG00000204599	chromatin interactions
ENSG00000110066	chromatin interactions
ENSG00000110719	chromatin interactions
ENSG00000196678	chromatin interactions
ENSG00000110880	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000105281	chromatin interactions
ENSG00000255306	chromatin interactions
ENSG00000204256	chromatin interactions
ENSG00000201801	chromatin interactions
ENSG00000085721	chromatin interactions
ENSG00000130520	chromatin interactions
ENSG00000110717	chromatin interactions
ENSG00000008282	chromatin interactions
ENSG00000260735	chromatin interactions
ENSG00000102897	chromatin interactions
ENSG00000111602	chromatin interactions
ENSG00000006534	chromatin interactions
ENSG00000123358	chromatin interactions
ENSG00000089280	chromatin interactions
ENSG00000163041	chromatin interactions
ENSG00000138592	chromatin interactions

Extended variants
information (count: 1221 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs308328	chr11:67765056-67765057	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547619552	chr11:67765061-67765062	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs566022186	chr11:67765101-67765102	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs374851269	chr11:67765106-67765107	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs191380954	chr11:67765107-67765108	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs183686953	chr11:67765128-67765129	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs576000334	chr11:67765136-67765137	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs367793190	chr11:67765137-67765138	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs199971783	chr11:67765161-67765162	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs112921257	chr11:67765163-67765164	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs11428176	chr11:67765164-67765165	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs537052532	chr11:67765174-67765175	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs3179926	chr11:67765189-67765190	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs372258608	chr11:67765194-67765195	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs376833917	chr11:67765245-67765246	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs369589225	chr11:67765266-67765267	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs373991204	chr11:67765285-67765286	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs377098262	chr11:67765287-67765288	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs113443942	chr11:67765307-67765308	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs375664874	chr11:67765364-67765365	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs541260587	chr11:67765366-67765367	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs559924530	chr11:67765373-67765374	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs376117357	chr11:67765374-67765375	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs572030312	chr11:67765397-67765398	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs545846894	chr11:67765403-67765404	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs564046143	chr11:67765433-67765434	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs550466296	chr11:67765435-67765436	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs142793584	chr11:67765498-67765499	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs308327	chr11:67765507-67765508	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs74882787	chr11:67765546-67765547	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs3751086	chr11:67765642-67765643	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs547262516	chr11:67765696-67765697	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs565837193	chr11:67765712-67765713	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs539277800	chr11:67765713-67765714	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs539072978	chr11:67765720-67765721	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs569826127	chr11:67765721-67765722	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs7481955	chr11:67765791-67765792	Weak transcription Genic enhancers Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs373895695	chr11:67765806-67765807	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs188005475	chr11:67765807-67765808	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs376118889	chr11:67765810-67765811	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs202000198	chr11:67765817-67765818	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs370543151	chr11:67765888-67765889	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs527745192	chr11:67765913-67765914	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs555387083	chr11:67765963-67765964	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs369543173	chr11:67765975-67765976	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs535362708	chr11:67765997-67765998	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs557414575	chr11:67765999-67766000	Weak transcription Genic enhancers Enhancers Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs553406249	chr11:67766013-67766014	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs368094076	chr11:67766022-67766023	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs578100990	chr11:67766027-67766028	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	4 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:1655 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67759000-67766000	Weak transcription	Liver	Liver
2	chr11:67759200-67770400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr11:67759200-67770400	Weak transcription	Right Atrium	heart
4	chr11:67760200-67767600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr11:67761400-67769800	Genic enhancers	Primary B cells from peripheral blood	blood
6	chr11:67761600-67765600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr11:67761800-67765200	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr11:67761800-67765200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr11:67761800-67765400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr11:67761800-67765600	Strong transcription	Primary neutrophils fromperipheralblood	blood
11	chr11:67761800-67765600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr11:67762000-67770400	Weak transcription	NHLF	lung
13	chr11:67762400-67765200	Weak transcription	Thymus	Thymus
14	chr11:67762400-67765600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr11:67762600-67765400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr11:67762800-67767000	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr11:67762800-67767200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr11:67763400-67765200	Enhancers	Fetal Intestine Large	intestine
19	chr11:67763400-67767000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:67763600-67766000	Genic enhancers	A549	lung
21	chr11:67763600-67766200	Enhancers	Rectal Mucosa Donor 29	rectum
22	chr11:67763600-67769800	Genic enhancers	Primary monocytes fromperipheralblood	blood
23	chr11:67763800-67766200	Genic enhancers	Primary B cells from cord blood	blood
24	chr11:67763800-67770400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr11:67764000-67765400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr11:67764000-67765600	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr11:67764000-67767400	Enhancers	Primary T cells fromperipheralblood	blood
28	chr11:67764000-67768400	Genic enhancers	GM12878-XiMat	blood
29	chr11:67764200-67765200	Enhancers	Lung	lung
30	chr11:67764200-67765200	Enhancers	Pancreas	Pancrea
31	chr11:67764200-67765400	Enhancers	Colonic Mucosa	Colon
32	chr11:67764200-67765400	Genic enhancers	Gastric	stomach
33	chr11:67764200-67766400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr11:67764200-67767000	Genic enhancers	Spleen	Spleen
35	chr11:67764200-67770000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
36	chr11:67764400-67770600	Weak transcription	Small Intestine	intestine
37	chr11:67764600-67765200	Enhancers	Placenta	Placenta
38	chr11:67764600-67767000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr11:67764600-67767800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr11:67764600-67769400	Weak transcription	Fetal Lung	lung
41	chr11:67764600-67769600	Weak transcription	Brain Substantia Nigra	brain
42	chr11:67764600-67770000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr11:67764600-67770000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:67764600-67770000	Weak transcription	Fetal Muscle Leg	muscle
45	chr11:67764600-67770600	Weak transcription	Right Ventricle	heart
46	chr11:67764800-67765200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr11:67764800-67765200	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr11:67764800-67765200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr11:67764800-67765200	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr11:67764800-67765400	Enhancers	H1 Cell Line	embryonic stem cell

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