Variant report

Variant	nsv553455
Chromosome Location	chr11:9077652-9114999
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:689)
CpG islands
(count:1098)
Chromatin interactive
region (count:43)
LncRNA
region (count:7)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:689 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:9114802-9115029	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:9099950-9100188	K562	blood:	n/a	n/a
3	ATF1	chr11:9095458-9095507	K562	blood:	n/a	n/a
4	ATF2	chr11:9082226-9082802	GM12878	blood:	n/a	n/a
5	ATF2	chr11:9082081-9082804	GM12878	blood:	n/a	n/a
6	BACH1	chr11:9087974-9088007	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr11:9082271-9082786	GM12878	blood:	n/a	chr11:9082572-9082580 chr11:9082463-9082474
8	BATF	chr11:9082154-9082811	GM12878	blood:	n/a	chr11:9082572-9082580 chr11:9082463-9082474
9	BATF	chr11:9110264-9110538	GM12878	blood:	n/a	n/a
10	BATF	chr11:9093262-9093527	GM12878	blood:	n/a	n/a
11	BCL11A	chr11:9082240-9082819	GM12878	blood:	n/a	chr11:9082575-9082584 chr11:9082803-9082816
12	BCL11A	chr11:9082283-9082676	GM12878	blood:	n/a	chr11:9082575-9082584
13	BCL3	chr11:9082229-9082703	GM12878	blood:	n/a	chr11:9082575-9082584
14	BCLAF1	chr11:9082182-9082786	GM12878	blood:	n/a	chr11:9082575-9082584
15	BCLAF1	chr11:9082128-9082821	GM12878	blood:	n/a	chr11:9082575-9082584 chr11:9082803-9082816
16	BHLHE40	chr11:9082262-9082778	GM12878	blood:	n/a	n/a
17	CEBPB	chr11:9092763-9093022	HepG2	liver:	n/a	n/a
18	CEBPB	chr11:9092774-9093033	A549	lung:	n/a	n/a
19	CEBPB	chr11:9107388-9107527	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:9082140-9082893	GM12878	blood:	n/a	n/a
21	CEBPB	chr11:9104352-9104551	K562	blood:	n/a	n/a
22	CEBPB	chr11:9104308-9104498	IMR90	lung:	n/a	n/a
23	CEBPB	chr11:9092718-9093049	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr11:9087187-9087527	Hela-S3	cervix:	n/a	chr11:9087368-9087379
25	CEBPB	chr11:9087128-9087934	A549	lung:	n/a	chr11:9087368-9087379
26	CEBPB	chr11:9087181-9087534	K562	blood:	n/a	chr11:9087368-9087379
27	CEBPB	chr11:9087105-9087540	HepG2	liver:	n/a	chr11:9087368-9087379
28	CEBPB	chr11:9092803-9092992	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr11:9087146-9087794	A549	lung:	n/a	chr11:9087368-9087379
30	CEBPB	chr11:9082257-9082691	GM12878	blood:	n/a	n/a
31	CEBPB	chr11:9087155-9087685	IMR90	lung:	n/a	chr11:9087368-9087379
32	CHD2	chr11:9082228-9082690	GM12878	blood:	n/a	n/a
33	CREB1	chr11:9082116-9082869	GM12878	blood:	n/a	n/a
34	CREB1	chr11:9082141-9082855	GM12878	blood:	n/a	n/a
35	CREB1	chr11:9112790-9113069	A549	lung:	n/a	n/a
36	CTCF	chr11:9114851-9114917	GM10248	blood:	n/a	chr11:9114890-9114903
37	CTCF	chr11:9114761-9115032	K562	blood:	n/a	chr11:9114890-9114903
38	CTCF	chr11:9114738-9115050	IMR90	lung:	n/a	chr11:9114890-9114903
39	CTCF	chr11:9082220-9082370	HVMF	connective:	n/a	chr11:9082314-9082330 chr11:9082313-9082331
40	CTCF	chr11:9082234-9082410	HepG2	liver:	n/a	chr11:9082314-9082330 chr11:9082313-9082331
41	CTCF	chr11:9099920-9100070	GM12864	blood:	n/a	n/a
42	CTCF	chr11:9082200-9082350	GM12878	blood:	n/a	chr11:9082314-9082330 chr11:9082313-9082331
43	CTCF	chr11:9114760-9114910	GM06990	blood:	n/a	chr11:9114890-9114903
44	CTCF	chr11:9082280-9082430	GM12875	blood:	n/a	chr11:9082314-9082330 chr11:9082313-9082331
45	CTCF	chr11:9082200-9082350	MCF-7	breast:	n/a	chr11:9082314-9082330 chr11:9082313-9082331
46	CTCF	chr11:9082220-9082370	MCF-7	breast:	n/a	chr11:9082314-9082330 chr11:9082313-9082331
47	CTCF	chr11:9097240-9097390	NHEK	skin:	n/a	n/a
48	CTCF	chr11:9082120-9082410	GM12864	blood:	n/a	chr11:9082314-9082330 chr11:9082313-9082331
49	CTCF	chr11:9082136-9082394	K562	blood:	n/a	chr11:9082314-9082330 chr11:9082313-9082331
50	CTCF	chr11:9088020-9088170	GM12873	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:9112471-9112521	Hepatocyte	liver:	n/a
2	chr11:9113167-9113217	PFSK-1	brain:	n/a
3	chr11:9113458-9113508	Hela-S3	cervix:	n/a
4	chr11:9087524-9087574	NH-A	brain:	n/a
5	chr11:9113179-9113229	T-47D	breast:	n/a
6	chr11:9113194-9113244	HRCEpiC	kidney:	n/a
7	chr11:9113167-9113217	RPTEC	kidney:	n/a
8	chr11:9113190-9113240	HCT-116	colon:	n/a
9	chr11:9112715-9112765	HNPCEpiC	eye:	n/a
10	chr11:9113370-9113420	HEEpiC	esophagus:	n/a
11	chr11:9112715-9112765	GM19239	blood:	n/a
12	chr11:9113184-9113234	HRE	kidney:	n/a
13	chr11:9113152-9113202	HRCEpiC	kidney:	n/a
14	chr11:9113458-9113508	Caco-2	colon:	n/a
15	chr11:9114431-9114481	A549	lung:	n/a
16	chr11:9099393-9099443	SK-N-SH	brain:	n/a
17	chr11:9113458-9113508	HepG2	liver:	n/a
18	chr11:9113184-9113234	HCPEpiC	choroid plexus:	n/a
19	chr11:9113179-9113229	A549	lung:	n/a
20	chr11:9112471-9112521	HIPEpiC	eye:	n/a
21	chr11:9113167-9113217	HNPCEpiC	eye:	n/a
22	chr11:9112214-9112264	MCF-7	breast:	n/a
23	chr11:9087524-9087574	SK-N-SH_RA	brain:	n/a
24	chr11:9113152-9113202	NT2-D1	testis:	n/a
25	chr11:9114431-9114481	HRPEpiC	eye:	n/a
26	chr11:9087524-9087574	PrEC	prostate:	n/a
27	chr11:9099393-9099443	ovcar-3	ovarian:	n/a
28	chr11:9113370-9113420	A549	lung:	n/a
29	chr11:9112989-9113039	PrEC	prostate:	n/a
30	chr11:9112471-9112521	Hela-S3	cervix:	n/a
31	chr11:9113152-9113202	Hela-S3	cervix:	n/a
32	chr11:9112715-9112765	SK-N-SH	brain:	n/a
33	chr11:9112715-9112765	SK-N-MC	brain:	n/a
34	chr11:9112471-9112521	NB4	blood:	n/a
35	chr11:9113146-9113196	AG10803	skin:	n/a
36	chr11:9113146-9113196	HCF	heart:	n/a
37	chr11:9113194-9113244	HRE	kidney:	n/a
38	chr11:9113179-9113229	Caco-2	colon:	n/a
39	chr11:9113146-9113196	HUVEC	blood vessel:	n/a
40	chr11:9113458-9113508	HCT-116	colon:	n/a
41	chr11:9112471-9112521	AG09309	skin:	n/a
42	chr11:9087524-9087574	AoSMC	blood vessel:	n/a
43	chr11:9112214-9112264	NH-A	brain:	n/a
44	chr11:9108982-9109032	MCF10A-Er-Src	breast:	n/a
45	chr11:9113194-9113244	GM12892	blood:	n/a
46	chr11:9113167-9113217	HCF	heart:	n/a
47	chr11:9108982-9109032	IMR90	lung:	fetal
48	chr11:9108982-9109032	HAEpiC	amniotic membrane:	n/a
49	chr11:9099393-9099443	U87	brain:	n/a
50	chr11:9112989-9113039	NT2-D1	testis:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:9088310..9090421-chr11:9092696..9094493,2	K562	blood:
2	chr11:9093993..9096683-chr11:9129654..9132296,2	MCF-7	breast:
3	chr11:9104308..9107322-chr11:9124502..9128223,3	MCF-7	breast:
4	chr11:9075149..9076918-chr11:9084166..9086058,2	K562	blood:
5	chr11:9075127..9077709-chr11:9146787..9148861,2	MCF-7	breast:
6	chr11:9109700..9116224-chr11:9155740..9163743,14	MCF-7	breast:
7	chr11:9114158..9114977-chr11:9142176..9142774,2	MCF-7	breast:
8	chr11:9110779..9112949-chr14:50359771..50361759,2	MCF-7	breast:
9	chr11:9098428..9102271-chr11:9102420..9106613,4	MCF-7	breast:
10	chr11:9081414..9083188-chr11:9094934..9097421,2	MCF-7	breast:
11	chr11:9112943..9114701-chr11:9593377..9596594,3	MCF-7	breast:
12	chr11:9097322..9098871-chr11:9128931..9130944,2	MCF-7	breast:
13	chr11:9114626..9115314-chr11:9154013..9154891,3	MCF-7	breast:
14	chr11:8383029..8385250-chr11:9080797..9083272,2	K562	blood:
15	chr11:9108004..9116385-chr11:9156452..9162678,21	MCF-7	breast:
16	chr11:9079042..9082011-chr11:9084095..9086895,2	MCF-7	breast:
17	chr11:9092833..9094684-chr11:9112419..9114154,2	MCF-7	breast:
18	chr11:9088310..9090421-chr11:9092696..9094493,2	K562	blood:
19	chr11:9104308..9106078-chr11:9156890..9159293,2	MCF-7	breast:
20	chr11:9113356..9115182-chr11:9141033..9143763,3	MCF-7	breast:
21	chr11:9109432..9111291-chr11:9117498..9119505,2	K562	blood:
22	chr11:9108929..9110845-chr11:9168410..9170250,2	MCF-7	breast:
23	chr11:9094776..9100228-chr11:9109116..9115745,9	MCF-7	breast:
24	chr11:9079563..9082027-chr11:9110788..9112419,2	K562	blood:
25	chr11:9097322..9099854-chr11:9158017..9160893,2	MCF-7	breast:
26	chr11:9090840..9093994-chr11:9109730..9112612,4	MCF-7	breast:
27	chr11:9098428..9102271-chr11:9102420..9106613,4	MCF-7	breast:
28	chr11:9096772..9098814-chr11:9159653..9161311,2	MCF-7	breast:
29	chr11:9114649..9115533-chr11:9142208..9142895,3	MCF-7	breast:
30	chr11:9104158..9106515-chr11:9110510..9112401,2	K562	blood:
31	chr11:9088886..9093572-chr11:9094471..9099536,5	MCF-7	breast:
32	chr11:9099831..9100572-chr11:9159061..9159678,2	MCF-7	breast:
33	chr11:9078089..9081038-chr11:9097785..9099533,2	K562	blood:
34	chr11:9078071..9079689-chr9:92219545..92221105,2	MCF-7	breast:
35	chr11:9088886..9093572-chr11:9094471..9099536,5	MCF-7	breast:
36	chr11:9085105..9088993-chr11:9089153..9093371,4	K562	blood:
37	chr11:9114505..9115469-chr11:9158990..9159883,2	MCF-7	breast:
38	chr11:9079042..9082011-chr11:9084095..9086895,2	MCF-7	breast:
39	chr11:9070098..9074605-chr11:9077166..9080417,4	K562	blood:
40	chr11:9081414..9083188-chr11:9094934..9097421,2	MCF-7	breast:
41	chr11:9109535..9113708-chr11:9115640..9120311,8	MCF-7	breast:
42	chr11:9096453..9100009-chr11:9109171..9113548,7	MCF-7	breast:
43	chr11:9099703..9100633-chr11:9159006..9159677,3	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKIP1-2	chr11:9086079-9088694	NONHSAT017906
2	lnc-AKIP1-2	chr11:9081155-9081286	ENSG00000253973.2
3	lnc-AKIP1-2	chr11:9080767-9081286	NONHSAT017906
4	lnc-AKIP1-2	chr11:9078798-9079002	ENSG00000253973.2
5	lnc-AKIP1-7	chr11:9078045-9078561	NONHSAT017903
6	lnc-AKIP1-2	chr11:9078786-9078831	ENSG00000253973.2
7	lnc-AKIP1-2	chr11:9086079-9086701	ENSG00000253973.2

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5691	chr11:9111897-9111918	MIMAT0022483

No data

Variant related genes	Relation type
ENSG00000253973	TF binding region
MIR5691	TF binding region
KRT8P41	TF binding region
SCUBE2	TF binding region
ENSG00000253973	CpG island
MIR5691	CpG island
KRT8P41	CpG island
SCUBE2	CpG island
ENSG00000175356	chromatin interactions
ENSG00000264984	chromatin interactions
ENSG00000213538	chromatin interactions
ENSG00000166483	chromatin interactions
ENSG00000130222	chromatin interactions
ENSG00000165527	chromatin interactions
ENSG00000253973	chromatin interactions

Extended variants
information (count: 1473 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:1473 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7396115	chr11:9077652-9077653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs144044619	chr11:9077695-9077696	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs548628319	chr11:9077724-9077725	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568658905	chr11:9077767-9077768	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs146348373	chr11:9077787-9077788	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139649988	chr11:9077796-9077797	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs571168885	chr11:9077869-9077870	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs141886683	chr11:9077883-9077884	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs554506184	chr11:9077890-9077891	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs117872228	chr11:9077896-9077897	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs574242371	chr11:9077898-9077899	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150623738	chr11:9077929-9077930	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556695476	chr11:9077940-9077941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs139679680	chr11:9077964-9077965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs545061521	chr11:9078089-9078090	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs553902594	chr11:9078101-9078102	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
17	rs565250779	chr11:9078117-9078118	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs572372491	chr11:9078132-9078133	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs565999452	chr11:9078140-9078141	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs535020669	chr11:9078142-9078143	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs557840079	chr11:9078144-9078145	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs540091171	chr11:9078147-9078148	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs371004914	chr11:9078177-9078178	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs7106265	chr11:9078224-9078225	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
25	rs182438170	chr11:9078281-9078282	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs78092554	chr11:9078285-9078286	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs149764021	chr11:9078332-9078333	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs531401072	chr11:9078351-9078352	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs187806617	chr11:9078361-9078362	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs200941108	chr11:9078369-9078370	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs574055089	chr11:9078409-9078410	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs536990463	chr11:9078428-9078429	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs61876347	chr11:9078490-9078491	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs74350783	chr11:9078589-9078590	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs75282852	chr11:9078598-9078599	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs556832667	chr11:9078638-9078639	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs34191466	chr11:9078676-9078677	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs539095974	chr11:9078706-9078707	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs558786878	chr11:9078742-9078743	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs139721679	chr11:9078753-9078754	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs541067331	chr11:9078857-9078858	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs559993871	chr11:9078899-9078900	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs552860197	chr11:9078942-9078943	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs145240335	chr11:9078947-9078948	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
45	rs115161826	chr11:9078987-9078988	Weak transcription Enhancers	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs562673772	chr11:9079042-9079043	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531407670	chr11:9079044-9079045	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs76600754	chr11:9079081-9079082	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs76346115	chr11:9079084-9079085	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs68168878	chr11:9079092-9079093	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:64)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
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
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Dysmorphic features	22052655	CNVD
Intellectual disability	22052655	CNVD
Obesity	22052655	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21785460	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:779 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9058400-9099800	Weak transcription	Aorta	Aorta
2	chr11:9066000-9081800	Weak transcription	Small Intestine	intestine
3	chr11:9069000-9080400	Weak transcription	Fetal Intestine Large	intestine
4	chr11:9069000-9092400	Weak transcription	Fetal Intestine Small	intestine
5	chr11:9069200-9083800	Weak transcription	Sigmoid Colon	Sigmoid Colon
6	chr11:9070200-9078600	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr11:9070200-9087400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:9070200-9097200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr11:9070400-9078000	Weak transcription	Gastric	stomach
10	chr11:9070400-9098400	Weak transcription	Colonic Mucosa	Colon
11	chr11:9070600-9087800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr11:9070600-9091600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:9071200-9077800	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:9071200-9087200	Weak transcription	Fetal Brain Male	brain
15	chr11:9074800-9080600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:9075000-9081200	Weak transcription	Duodenum Mucosa	Duodenum
17	chr11:9075000-9088000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr11:9075000-9092600	Weak transcription	Rectal Mucosa Donor 29	rectum
19	chr11:9075200-9087200	Weak transcription	Pancreas	Pancrea
20	chr11:9075600-9078200	Weak transcription	NHDF-Ad	bronchial
21	chr11:9075800-9078200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr11:9076000-9085800	Weak transcription	Placenta	Placenta
23	chr11:9076200-9078400	Weak transcription	HSMMtube	muscle
24	chr11:9076200-9085800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:9076200-9087000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr11:9076200-9087200	Weak transcription	HSMM	muscle
27	chr11:9077000-9079800	Enhancers	Fetal Muscle Leg	muscle
28	chr11:9077400-9077800	Weak transcription	Fetal Muscle Trunk	muscle
29	chr11:9077400-9078000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr11:9077400-9078600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr11:9077400-9079000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:9077400-9079000	Weak transcription	Fetal Stomach	stomach
33	chr11:9077400-9080600	Weak transcription	Stomach Smooth Muscle	stomach
34	chr11:9077600-9078000	Weak transcription	Fetal Lung	lung
35	chr11:9077600-9078800	Enhancers	Adipose Nuclei	Adipose
36	chr11:9077800-9078200	Enhancers	Colon Smooth Muscle	Colon
37	chr11:9077800-9078400	Enhancers	Fetal Muscle Trunk	muscle
38	chr11:9078000-9078400	Enhancers	Gastric	stomach
39	chr11:9078000-9078600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr11:9078000-9079000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:9078000-9079000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr11:9078000-9079000	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr11:9078000-9079000	Enhancers	Fetal Lung	lung
44	chr11:9078200-9078400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr11:9078200-9078400	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr11:9078200-9078600	Enhancers	NHDF-Ad	bronchial
47	chr11:9078400-9078600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr11:9078400-9078800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr11:9078400-9079000	Enhancers	Stomach Mucosa	stomach
50	chr11:9078400-9079200	Weak transcription	Fetal Muscle Trunk	muscle

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