Variant report

Variant	nsv430403
Chromosome Location	chr11:68297201-68448324
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2058)
CpG islands
(count:1711)
Chromatin interactive
region (count:153)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2058 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:68300214-68300881	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:68347156-68347163	HepG2	liver:	n/a	n/a
3	ATF1	chr11:68426689-68426926	K562	blood:	n/a	n/a
4	ATF1	chr11:68360355-68360555	K562	blood:	n/a	n/a
5	ATF2	chr11:68384285-68384565	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF3	chr11:68444920-68445282	K562	blood:	n/a	n/a
7	ATF3	chr11:68444942-68445257	K562	blood:	n/a	n/a
8	BACH1	chr11:68301337-68301472	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:68352694-68352894	H1-hESC	embryonic stem cell:	n/a	chr11:68352766-68352780
10	BACH1	chr11:68445041-68445223	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr11:68351595-68351636	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL3	chr11:68430980-68431226	GM12878	blood:	n/a	n/a
13	BCL3	chr11:68346859-68347386	GM12878	blood:	n/a	n/a
14	BCL3	chr11:68346967-68347212	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:68351551-68351879	K562	blood:	n/a	n/a
16	BHLHE40	chr11:68300207-68300768	HepG2	liver:	n/a	n/a
17	BHLHE40	chr11:68431056-68431228	K562	blood:	n/a	n/a
18	BHLHE40	chr11:68426591-68426915	HepG2	liver:	n/a	n/a
19	BHLHE40	chr11:68446822-68447146	K562	blood:	n/a	n/a
20	BHLHE40	chr11:68445013-68445213	K562	blood:	n/a	n/a
21	BHLHE40	chr11:68426566-68426930	K562	blood:	n/a	n/a
22	BRCA1	chr11:68445032-68445162	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr11:68351478-68351797	H1-hESC	embryonic stem cell:	n/a	n/a
24	BRCA1	chr11:68323548-68323554	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr11:68414327-68414720	HCT-116	colon:	n/a	n/a
26	CBX3	chr11:68444903-68445204	K562	blood:	n/a	n/a
27	CBX3	chr11:68414349-68414636	K562	blood:	n/a	n/a
28	CBX3	chr11:68414323-68414608	K562	blood:	n/a	n/a
29	CCNT2	chr11:68382845-68382930	K562	blood:	n/a	n/a
30	CCNT2	chr11:68445024-68445215	K562	blood:	n/a	chr11:68445096-68445105
31	CEBPB	chr11:68368842-68369170	HepG2	liver:	n/a	chr11:68368988-68368997 chr11:68368988-68368997 chr11:68368988-68368997 chr11:68368986-68368997 chr11:68368988-68368999 chr11:68368988-68368997 chr11:68368986-68368999
32	CEBPB	chr11:68445076-68445268	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr11:68368885-68369145	IMR90	lung:	n/a	chr11:68368988-68368997 chr11:68368988-68368997 chr11:68368988-68368997 chr11:68368986-68368997 chr11:68368988-68368999 chr11:68368988-68368997 chr11:68368986-68368999
34	CEBPB	chr11:68300205-68300698	HepG2	liver:	n/a	n/a
35	CEBPB	chr11:68320173-68320373	A549	lung:	n/a	chr11:68320248-68320259
36	CEBPB	chr11:68310119-68310492	IMR90	lung:	n/a	n/a
37	CEBPB	chr11:68320168-68320398	K562	blood:	n/a	chr11:68320248-68320259
38	CEBPB	chr11:68426641-68426915	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr11:68300158-68300583	MCF-7	breast:	n/a	n/a
40	CEBPB	chr11:68365478-68365496	IMR90	lung:	n/a	n/a
41	CEBPB	chr11:68350365-68350946	IMR90	lung:	n/a	n/a
42	CEBPB	chr11:68426226-68426965	IMR90	lung:	n/a	n/a
43	CEBPB	chr11:68400333-68400603	K562	blood:	n/a	n/a
44	CEBPB	chr11:68350377-68350722	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr11:68370129-68370157	HepG2	liver:	n/a	n/a
46	CEBPB	chr11:68320084-68320408	Hela-S3	cervix:	n/a	chr11:68320248-68320259
47	CEBPB	chr11:68351502-68351962	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr11:68320068-68320422	A549	lung:	n/a	chr11:68320248-68320259
49	CEBPB	chr11:68368890-68369102	K562	blood:	n/a	chr11:68368988-68368997 chr11:68368988-68368997 chr11:68368988-68368997 chr11:68368986-68368997 chr11:68368988-68368999 chr11:68368988-68368997 chr11:68368986-68368999
50	CEBPB	chr11:68381219-68381290	K562	blood:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:68427020-68427070	HRCEpiC	kidney:	n/a
2	chr11:68417376-68417426	SK-N-SH_RA	brain:	n/a
3	chr11:68433833-68433883	NT2-D1	testis:	n/a
4	chr11:68427020-68427070	HRCEpiC	kidney:	n/a
5	chr11:68417376-68417426	SK-N-SH_RA	brain:	n/a
6	chr11:68433833-68433883	NT2-D1	testis:	n/a
7	chr11:68417633-68417683	HNPCEpiC	eye:	n/a
8	chr11:68436821-68436871	BE2_C	brain:	n/a
9	chr11:68436786-68436836	Jurkat	blood:	n/a
10	chr11:68417787-68417837	NH-A	brain:	n/a
11	chr11:68417633-68417683	HRE	kidney:	n/a
12	chr11:68350410-68350460	HRE	kidney:	n/a
13	chr11:68433177-68433227	ECC-1	luminal epithelium:	n/a
14	chr11:68436821-68436871	HIPEpiC	eye:	n/a
15	chr11:68433177-68433227	HMEC	breast:	n/a
16	chr11:68377237-68377287	HCT-116	colon:	n/a
17	chr11:68381554-68381604	IMR90	lung:	fetal
18	chr11:68436750-68436800	A549	lung:	n/a
19	chr11:68437843-68437893	IMR90	lung:	fetal
20	chr11:68427020-68427070	GM06990	blood:	n/a
21	chr11:68381554-68381604	T-47D	breast:	n/a
22	chr11:68437927-68437977	HAEpiC	amniotic membrane:	n/a
23	chr11:68433177-68433227	A549	lung:	n/a
24	chr11:68436821-68436871	Hela-S3	cervix:	n/a
25	chr11:68438384-68438434	HPAEpiC	pulmonary alveolar:	n/a
26	chr11:68437843-68437893	HCT-116	colon:	n/a
27	chr11:68442135-68442185	GM12892	blood:	n/a
28	chr11:68381554-68381604	HCF	heart:	n/a
29	chr11:68437736-68437786	HIPEpiC	eye:	n/a
30	chr11:68436750-68436800	RPTEC	kidney:	n/a
31	chr11:68436750-68436800	NHDF-neo	bronchial:	n/a
32	chr11:68377237-68377287	T-47D	breast:	n/a
33	chr11:68442135-68442185	HCM	heart:	n/a
34	chr11:68438384-68438434	GM06990	blood:	n/a
35	chr11:68436821-68436871	NHBE	bronchial:	n/a
36	chr11:68433177-68433227	K562	blood:	n/a
37	chr11:68444995-68445045	A549	lung:	n/a
38	chr11:68384193-68384243	MCF10A-Er-Src	breast:	n/a
39	chr11:68417787-68417837	Jurkat	blood:	n/a
40	chr11:68437736-68437786	HL-60	blood:	n/a
41	chr11:68381554-68381604	SK-N-SH_RA	brain:	n/a
42	chr11:68433177-68433227	U87	brain:	n/a
43	chr11:68382427-68382477	Hepatocyte	liver:	n/a
44	chr11:68350410-68350460	GM12891	blood:	n/a
45	chr11:68433833-68433883	MCF10A-Er-Src	breast:	n/a
46	chr11:68310695-68310745	MCF-7	breast:	n/a
47	chr11:68438384-68438434	NB4	blood:	n/a
48	chr11:68417633-68417683	SAEC	small airway:	n/a
49	chr11:68427020-68427070	GM12892	blood:	n/a
50	chr11:68381554-68381604	Jurkat	blood:	n/a

(count:153 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr11:68368469..68370336-chr11:68372617..68375106,2	K562	blood:
2	chr11:68306937..68308679-chr11:68348704..68351247,2	K562	blood:
3	chr11:68227855..68229553-chr11:68312062..68313959,2	MCF-7	breast:
4	chr11:68337484..68339031-chr11:68341269..68342985,2	MCF-7	breast:
5	chr11:68311501..68313206-chr11:68322676..68324188,2	MCF-7	breast:
6	chr11:68315876..68319088-chr11:68319892..68321906,3	K562	blood:
7	chr11:68435908..68438326-chr11:68443679..68445760,3	MCF-7	breast:
8	chr11:68324963..68327580-chr11:68329924..68332655,2	K562	blood:
9	chr11:68226828..68228925-chr11:68351073..68354033,2	MCF-7	breast:
10	chr11:68418144..68420030-chr11:68444884..68447498,2	MCF-7	breast:
11	chr11:68409405..68411019-chr11:68416021..68418622,2	K562	blood:
12	chr11:68419680..68421498-chr11:68423594..68425610,2	MCF-7	breast:
13	chr11:68236521..68239221-chr11:68297356..68298866,2	K562	blood:
14	chr11:68296455..68299790-chr11:68302079..68305805,5	MCF-7	breast:
15	chr11:68321048..68322861-chr11:68335454..68337526,2	K562	blood:
16	chr11:68354109..68357094-chr11:68364432..68366868,2	K562	blood:
17	chr11:68419429..68422148-chr11:68428160..68429865,2	MCF-7	breast:
18	chr11:68321048..68322861-chr11:68335454..68337526,2	K562	blood:
19	chr11:68423670..68425970-chr11:68426279..68428599,2	K562	blood:
20	chr11:68341428..68343456-chr11:68357720..68359630,3	K562	blood:
21	chr11:68371917..68374314-chr11:68378485..68380168,2	K562	blood:
22	chr11:68350011..68354393-chr11:68355875..68359494,4	K562	blood:
23	chr11:68315876..68319088-chr11:68319892..68321906,3	K562	blood:
24	chr11:68430375..68432724-chr11:68436949..68439714,2	K562	blood:
25	chr11:68305109..68307127-chr11:69485059..69487954,2	MCF-7	breast:
26	chr11:68311700..68314036-chr11:68318661..68320225,2	MCF-7	breast:
27	chr11:68342166..68344146-chr11:68345413..68347616,3	K562	blood:
28	chr11:68294325..68295955-chr11:68298713..68301491,2	MCF-7	breast:
29	chr11:68341428..68343456-chr11:68357720..68359630,3	K562	blood:
30	chr11:68298372..68300264-chr11:68312543..68314090,2	MCF-7	breast:
31	chr11:68301595..68304272-chr11:68304634..68307122,2	K562	blood:
32	chr11:68424737..68427356-chr11:68575061..68577127,2	K562	blood:
33	chr11:68417241..68420173-chr11:68448190..68450545,3	MCF-7	breast:
34	chr11:68335758..68338909-chr11:68341383..68344239,4	K562	blood:
35	chr11:68295992..68298851-chr14:22471442..22473971,2	MCF-7	breast:
36	chr11:68300115..68300648-chr2:99979539..99980039,2	NB4	blood:
37	chr11:68371303..68373283-chr11:68380791..68382427,2	K562	blood:
38	chr11:68310824..68313673-chr11:68317930..68320124,2	MCF-7	breast:
39	chr11:68430986..68432628-chr11:68605537..68607627,2	K562	blood:
40	chr11:68445096..68447782-chr11:68640876..68643520,2	K562	blood:
41	chr11:68282250..68282768-chr11:68411139..68411711,2	MCF-7	breast:
42	chr11:68343924..68346416-chr11:68347081..68348862,2	MCF-7	breast:
43	chr11:68442099..68444777-chr11:68444837..68447598,2	K562	blood:
44	chr11:68436257..68438284-chr11:68444133..68447068,2	MCF-7	breast:
45	chr11:68443139..68444777-chr11:68444837..68446823,2	K562	blood:
46	chr11:68387155..68388983-chr11:68408036..68409715,2	MCF-7	breast:
47	chr11:68410774..68412696-chr11:68425006..68427802,2	K562	blood:
48	chr11:68377961..68378895-chr11:68856305..68856827,2	MCF-7	breast:
49	chr11:68306937..68308679-chr11:68348704..68351247,2	K562	blood:
50	chr11:68330297..68331992-chr11:68334158..68336760,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTL5-1	chr11:68383260-68383487	ENSG00000260808.1
2	lnc-MTL5-1	chr11:68383213-68383487	ENSG00000260808.1
3	lnc-MTL5-1	chr11:68383657-68383915	ENSG00000260808.1
4	lnc-MTL5-1	chr11:68383657-68383754	ENSG00000260808.1
5	lnc-MTL5-1	chr11:68383350-68383487	ENSG00000260808.1
6	lnc-MTL5-1	chr11:68383943-68384179	ENSG00000260808.1
7	lnc-MTL5-1	chr11:68380367-68380689	ENSG00000260808.1
8	lnc-MTL5-1	chr11:68383657-68383698	ENSG00000260808.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	SAPS3	hsa-miR-20a-5p	chr11:68381848-68381870
2	SAPS3	hsa-miR-130b-3p	chr11:68381846-68381868
3	SAPS3	hsa-miR-130b-3p	chr11:68380755-68380776
4	PPP6R3	hsa-miR-20a-5p	chr11:68381863-68381869

Variant related genes	Relation type
PPP6R3	TF binding region
ENSG00000260808	TF binding region
ENSG00000266854	TF binding region
GAL	TF binding region
PPP6R3	CpG island
ENSG00000260808	CpG island
ENSG00000266854	CpG island
GAL	CpG island
ENSG00000069482	chromatin interactions
ENSG00000149716	chromatin interactions
ENSG00000110075	chromatin interactions
ENSG00000110090	chromatin interactions
ENSG00000132749	chromatin interactions
ENSG00000260808	chromatin interactions

Extended variants
information (count: 6436 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:6436 , 50 per page) page: 1 2 3 4 5 6 7 ... 129

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17149156	chr11:68297201-68297202	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543043843	chr11:68297246-68297247	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs578014829	chr11:68297272-68297273	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs545275803	chr11:68297319-68297320	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs573361850	chr11:68297391-68297392	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs540761086	chr11:68297426-68297427	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs560492741	chr11:68297432-68297433	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559256759	chr11:68297584-68297585	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs199806617	chr11:68297594-68297595	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs7941318	chr11:68297632-68297633	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs6591340	chr11:68297636-68297637	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs143404075	chr11:68297692-68297693	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs530762223	chr11:68297705-68297706	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs572248375	chr11:68297730-68297731	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs146806949	chr11:68297756-68297757	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371856401	chr11:68297778-68297779	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs542987326	chr11:68297798-68297799	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs185708595	chr11:68297806-68297807	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs11826997	chr11:68297884-68297885	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs546696298	chr11:68297892-68297893	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs571713131	chr11:68297937-68297938	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs539229982	chr11:68298012-68298013	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs191436419	chr11:68298017-68298018	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs561261268	chr11:68298062-68298063	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112837133	chr11:68298091-68298092	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531798663	chr11:68298101-68298102	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs141417481	chr11:68298126-68298127	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs117121003	chr11:68298134-68298135	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs571463425	chr11:68298205-68298206	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs145637684	chr11:68298206-68298207	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138365148	chr11:68298280-68298281	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547727966	chr11:68298323-68298324	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs115648218	chr11:68298367-68298368	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs142840109	chr11:68298406-68298407	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566357093	chr11:68298420-68298421	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs146251466	chr11:68298477-68298478	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs17149158	chr11:68298483-68298484	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs563377088	chr11:68298511-68298512	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7106259	chr11:68298512-68298513	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs542540829	chr11:68298513-68298514	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs75805066	chr11:68298514-68298515	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs528089830	chr11:68298517-68298518	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs181187576	chr11:68298597-68298598	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs200415366	chr11:68298608-68298609	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs7124078	chr11:68298633-68298634	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs532151947	chr11:68298636-68298637	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs143892274	chr11:68298775-68298776	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs371258451	chr11:68298776-68298777	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs113364687	chr11:68298779-68298780	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs67798708	chr11:68298819-68298820	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD
small cell lung cancer	17426248	CNVD
Gastric cancer	18160780	CNVD
Lung cancer	21569311	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Bladder cancer	21909424	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20459607	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Breast cancer	17850661	CNVD
Human papillomavirus	17975027	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Cancer	17160897	CNVD
Esophageal squamous carcinoma	18405350	CNVD

Chromatin state (count:3660 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:68265200-68302600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:68268600-68303800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:68276000-68305600	Weak transcription	Fetal Brain Male	brain
4	chr11:68276600-68304000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr11:68277600-68336000	Strong transcription	Dnd41	blood
6	chr11:68283000-68358200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:68284200-68297600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr11:68286200-68300200	Strong transcription	Hela-S3	cervix
9	chr11:68286400-68303200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr11:68286800-68297400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
11	chr11:68287000-68297400	Strong transcription	Osteobl	bone
12	chr11:68287000-68299200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr11:68287200-68298200	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr11:68287200-68301200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr11:68288600-68309000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr11:68291000-68297800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
17	chr11:68292400-68297600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr11:68292600-68301400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr11:68292600-68308200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:68293200-68297600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr11:68293200-68302200	Weak transcription	Brain Substantia Nigra	brain
22	chr11:68293400-68298200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr11:68293600-68297400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr11:68293600-68299800	Strong transcription	NHEK	skin
25	chr11:68293600-68300000	Strong transcription	A549	lung
26	chr11:68294800-68297400	Enhancers	Right Ventricle	heart
27	chr11:68294800-68297600	Enhancers	Psoas Muscle	Psoas
28	chr11:68295000-68297600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr11:68295000-68301400	Weak transcription	Brain Cingulate Gyrus	brain
30	chr11:68295400-68298000	Weak transcription	Gastric	stomach
31	chr11:68295400-68300600	Weak transcription	Colonic Mucosa	Colon
32	chr11:68295400-68300600	Weak transcription	Rectal Smooth Muscle	rectum
33	chr11:68295400-68301400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr11:68295400-68305200	Weak transcription	HMEC	breast
35	chr11:68295400-68306600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr11:68295600-68298400	Weak transcription	Stomach Smooth Muscle	stomach
37	chr11:68295600-68299000	Weak transcription	Ovary	ovary
38	chr11:68295600-68299000	Weak transcription	HepG2	liver
39	chr11:68295600-68300200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr11:68295600-68302600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr11:68295600-68305600	Weak transcription	Fetal Brain Female	brain
42	chr11:68295800-68306200	Weak transcription	HSMMtube	muscle
43	chr11:68296200-68298000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr11:68296200-68302600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr11:68296400-68297400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
46	chr11:68296400-68297400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr11:68296400-68299000	Weak transcription	HUES6 Cell Line	embryonic stem cell
48	chr11:68296400-68299000	Weak transcription	Stomach Mucosa	stomach
49	chr11:68296400-68299200	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr11:68296400-68300000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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