Variant report

Variant	nsv1039130
Chromosome Location	chr11:67512329-67709792
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2797)
CpG islands
(count:916)
Chromatin interactive
region (count:10)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2797 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:67525774-67525796	K562	blood:	n/a	n/a
2	ATF1	chr11:67572955-67573090	K562	blood:	n/a	n/a
3	ATF1	chr11:67546855-67547018	K562	blood:	n/a	n/a
4	ATF3	chr11:67593917-67594176	K562	blood:	n/a	n/a
5	BATF	chr11:67697714-67698270	GM12878	blood:	n/a	n/a
6	BATF	chr11:67675477-67675829	GM12878	blood:	n/a	n/a
7	BATF	chr11:67615409-67615586	GM12878	blood:	n/a	n/a
8	BATF	chr11:67571990-67572187	GM12878	blood:	n/a	chr11:67572041-67572051
9	BATF	chr11:67646855-67647126	GM12878	blood:	n/a	n/a
10	BATF	chr11:67556628-67556900	GM12878	blood:	n/a	n/a
11	BATF	chr11:67571884-67572418	GM12878	blood:	n/a	chr11:67572041-67572051
12	BATF	chr11:67559731-67559980	GM12878	blood:	n/a	n/a
13	BATF	chr11:67651724-67652105	GM12878	blood:	n/a	n/a
14	BATF	chr11:67555151-67555449	GM12878	blood:	n/a	n/a
15	BATF	chr11:67648065-67648547	GM12878	blood:	n/a	n/a
16	BATF	chr11:67675453-67675797	GM12878	blood:	n/a	n/a
17	BATF	chr11:67652428-67652731	GM12878	blood:	n/a	n/a
18	BATF	chr11:67667021-67667379	GM12878	blood:	n/a	n/a
19	BATF	chr11:67644982-67645399	GM12878	blood:	n/a	chr11:67645088-67645096
20	BATF	chr11:67574662-67574949	GM12878	blood:	n/a	n/a
21	BATF	chr11:67572577-67572827	GM12878	blood:	n/a	n/a
22	BATF	chr11:67644809-67645315	GM12878	blood:	n/a	chr11:67645088-67645096
23	BATF	chr11:67647999-67648547	GM12878	blood:	n/a	n/a
24	BATF	chr11:67627161-67627468	GM12878	blood:	n/a	n/a
25	BATF	chr11:67706536-67706734	GM12878	blood:	n/a	n/a
26	BATF	chr11:67548820-67549170	GM12878	blood:	n/a	chr11:67549020-67549031
27	BATF	chr11:67606914-67607130	GM12878	blood:	n/a	n/a
28	BATF	chr11:67567330-67567611	GM12878	blood:	n/a	n/a
29	BATF	chr11:67648616-67648960	GM12878	blood:	n/a	n/a
30	BATF	chr11:67548940-67549181	GM12878	blood:	n/a	chr11:67549020-67549031
31	BATF	chr11:67646832-67647124	GM12878	blood:	n/a	n/a
32	BATF	chr11:67555087-67555437	GM12878	blood:	n/a	n/a
33	BATF	chr11:67697656-67698323	GM12878	blood:	n/a	n/a
34	BATF	chr11:67627170-67627405	GM12878	blood:	n/a	n/a
35	BATF	chr11:67651682-67652098	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:67557563-67557812	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:67697965-67698299	GM12878	blood:	n/a	n/a
38	BCL11A	chr11:67551659-67551843	GM12878	blood:	n/a	n/a
39	BCL11A	chr11:67559808-67560040	GM12878	blood:	n/a	n/a
40	BCL11A	chr11:67675592-67675748	GM12878	blood:	n/a	chr11:67675704-67675713
41	BCL11A	chr11:67555194-67555488	GM12878	blood:	n/a	chr11:67555323-67555332
42	BCL11A	chr11:67556040-67556201	GM12878	blood:	n/a	n/a
43	BCL11A	chr11:67647974-67648564	GM12878	blood:	n/a	n/a
44	BCL11A	chr11:67648648-67648946	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:67697951-67698286	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:67571942-67572288	GM12878	blood:	n/a	chr11:67572039-67572048
47	BCL11A	chr11:67644956-67645403	GM12878	blood:	n/a	chr11:67645173-67645182
48	BCL11A	chr11:67555126-67555504	GM12878	blood:	n/a	chr11:67555323-67555332
49	BCL11A	chr11:67645219-67645410	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:67601358-67601522	GM12878	blood:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67656390-67656440	SK-N-MC	brain:	n/a
2	chr11:67656390-67656440	SK-N-MC	brain:	n/a
3	chr11:67577512-67577562	HMEC	breast:	n/a
4	chr11:67577512-67577562	IMR90	lung:	fetal
5	chr11:67656357-67656407	AG09309	skin:	n/a
6	chr11:67656357-67656407	NH-A	brain:	n/a
7	chr11:67572729-67572779	HNPCEpiC	eye:	n/a
8	chr11:67572999-67573049	U87	brain:	n/a
9	chr11:67573741-67573791	HPAEpiC	pulmonary alveolar:	n/a
10	chr11:67559939-67559989	BE2_C	brain:	n/a
11	chr11:67572999-67573049	NB4	blood:	n/a
12	chr11:67656390-67656440	T-47D	breast:	n/a
13	chr11:67573103-67573153	A549	lung:	n/a
14	chr11:67656357-67656407	BJ	skin:	n/a
15	chr11:67572714-67572764	HRPEpiC	eye:	n/a
16	chr11:67572999-67573049	NHBE	bronchial:	n/a
17	chr11:67574013-67574063	AoSMC	blood vessel:	n/a
18	chr11:67572716-67572766	HRPEpiC	eye:	n/a
19	chr11:67577512-67577562	GM06990	blood:	n/a
20	chr11:67559939-67559989	PFSK-1	brain:	n/a
21	chr11:67656357-67656407	SKMC	muscle:	n/a
22	chr11:67572988-67573038	PANC-1	pancreas:	n/a
23	chr11:67573103-67573153	AoSMC	blood vessel:	n/a
24	chr11:67572988-67573038	HCPEpiC	choroid plexus:	n/a
25	chr11:67574013-67574063	SK-N-SH_RA	brain:	n/a
26	chr11:67656357-67656407	HL-60	blood:	n/a
27	chr11:67574013-67574063	NHBE	bronchial:	n/a
28	chr11:67571294-67571344	HNPCEpiC	eye:	n/a
29	chr11:67571294-67571344	PFSK-1	brain:	n/a
30	chr11:67573103-67573153	SKMC	muscle:	n/a
31	chr11:67573741-67573791	PANC-1	pancreas:	n/a
32	chr11:67572716-67572766	BJ	skin:	n/a
33	chr11:67573103-67573153	AG09309	skin:	n/a
34	chr11:67572729-67572779	NB4	blood:	n/a
35	chr11:67571294-67571344	U87	brain:	n/a
36	chr11:67559939-67559989	K562	blood:	n/a
37	chr11:67572999-67573049	MCF10A-Er-Src	breast:	n/a
38	chr11:67572729-67572779	MCF-7	breast:	n/a
39	chr11:67653560-67653610	H1-hESC	embryonic stem cell:	embryo
40	chr11:67574013-67574063	HepG2	liver:	n/a
41	chr11:67572729-67572779	Hepatocyte	liver:	n/a
42	chr11:67574013-67574063	CMK	blood:	n/a
43	chr11:67577512-67577562	Caco-2	colon:	n/a
44	chr11:67571294-67571344	Caco-2	colon:	n/a
45	chr11:67572988-67573038	GM12878	blood:	n/a
46	chr11:67568593-67568643	RPTEC	kidney:	n/a
47	chr11:67572714-67572764	HCT-116	colon:	n/a
48	chr11:67574013-67574063	HRCEpiC	kidney:	n/a
49	chr11:67656357-67656407	Hepatocyte	liver:	n/a
50	chr11:67656357-67656407	PrEC	prostate:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67571227..67572733-chr3:125634522..125636253,2	MCF-7	breast:
2	chr11:67395020..67397974-chr11:67571574..67573157,2	MCF-7	breast:
3	chr11:67572608..67573347-chr4:3956745..3957344,2	Hela-S3	cervix:
4	chr11:67407400..67409857-chr11:67556404..67559360,2	MCF-7	breast:
5	chr11:67396168..67397948-chr11:67571471..67573438,2	K562	blood:
6	chr1:8938391..8938936-chr11:67572724..67573509,2	Hela-S3	cervix:
7	chr11:67349032..67351635-chr11:67571367..67573562,2	K562	blood:
8	chr11:67615533..67616044-chr11:67722872..67723766,2	K562	blood:
9	chr1:150551803..150552520-chr11:67572791..67573460,2	Hela-S3	cervix:
10	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDUFS8-2	chr11:67655624-67655795	ENSG00000251637
2	lnc-NDUFS8-2	chr11:67654932-67654973	XLOC_009181
3	lnc-UNC93B1-3	chr11:67702034-67702179	ENSG00000254610
4	lnc-NDUFS8-2	chr11:67645965-67646246	l_505_chr11:67645566-67653308_testes
5	lnc-NDUFS8-6	chr11:67703029-67703397	NONHSAT022485
6	lnc-NDUFS8-2	chr11:67653124-67653308	l_505_chr11:67645566-67653308_testes
7	lnc-NDUFS8-2	chr11:67653484-67654125	l_505_chr11:67645566-67653308_testes
8	lnc-UNC93B1-3	chr11:67704246-67704462	ENSG00000254610
9	lnc-NDUFS8-2	chr11:67655621-67655795	XLOC_009181
10	lnc-NDUFS8-2	chr11:67673481-67673821	ENSG00000251637
11	lnc-NDUFS8-2	chr11:67654222-67654559	l_505_chr11:67645566-67653308_testes
12	lnc-NDUFS8-2	chr11:67653917-67654160	XLOC_009181
13	lnc-NDUFS8-2	chr11:67661350-67661552	XLOC_009181
14	lnc-NDUFS8-2	chr11:67654061-67654160	ENSG00000251637
15	lnc-NDUFS8-2	chr11:67645567-67645953	l_505_chr11:67645566-67653308_testes
16	lnc-NDUFV1-2	chr11:67547802-67550430	ENSG00000248509
17	lnc-UNC93B1-8	chr11:67679200-67679534	expReg_chr11_6588_-
18	lnc-UNC93B1-3	chr11:67707154-67707245	ENSG00000254610
19	lnc-NDUFV1-2	chr11:67544666-67545111	ENSG00000248509

No data

Variant related genes	Relation type
ENSG00000221553	TF binding region
RNU6-46P	TF binding region
RPS3AP40	TF binding region
FAM86C2P	TF binding region
ENSG00000254792	TF binding region
ENSG00000251637	TF binding region
ENSG00000254610	TF binding region
ENSG00000255147	TF binding region
ALG1L8P	TF binding region
ENSG00000254850	TF binding region
ENSG00000221553	CpG island
RNU6-46P	CpG island
RPS3AP40	CpG island
FAM86C2P	CpG island
ENSG00000254792	CpG island
ENSG00000251637	CpG island
ENSG00000254610	CpG island
ENSG00000255147	CpG island
ALG1L8P	CpG island
ENSG00000254850	CpG island
ENSG00000167799	chromatin interactions
ENSG00000251669	chromatin interactions
ENSG00000143384	chromatin interactions
ENSG00000074800	chromatin interactions
ENSG00000171084	chromatin interactions
ENSG00000253917	chromatin interactions
ENSG00000084207	chromatin interactions
ENSG00000230679	chromatin interactions
ENSG00000158483	chromatin interactions
KIF21B	miRNA target sites
TMC7	miRNA target sites
ADAM9	miRNA target sites
TP53	miRNA target sites
ABTB1	miRNA target sites
VOPP1	miRNA target sites

Extended variants
information (count: 9255 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:9255 , 50 per page) page: 1 2 3 4 5 6 7 ... 186

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183408381	chr11:67512333-67512334	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372380001	chr11:67512334-67512335	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs527545315	chr11:67512337-67512338	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375713287	chr11:67512340-67512341	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538438368	chr11:67512342-67512343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs12799214	chr11:67512353-67512354	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs187747950	chr11:67512363-67512364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs578184680	chr11:67512378-67512379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs144771122	chr11:67512382-67512383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550018117	chr11:67512423-67512424	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs7947609	chr11:67512463-67512464	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs373668625	chr11:67512491-67512492	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs34436372	chr11:67512518-67512519	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs566411583	chr11:67512534-67512535	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs4930509	chr11:67512540-67512541	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs558569536	chr11:67512542-67512543	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs201721818	chr11:67512550-67512551	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs373251179	chr11:67512551-67512552	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs576752946	chr11:67512552-67512553	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs537806952	chr11:67512555-67512556	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs193175440	chr11:67512585-67512586	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs574164361	chr11:67512586-67512587	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs541635504	chr11:67512613-67512614	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs4930510	chr11:67512625-67512626	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs561402230	chr11:67512631-67512632	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs529004462	chr11:67512637-67512638	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs545772225	chr11:67512646-67512647	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs564367445	chr11:67512648-67512649	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs531614563	chr11:67512655-67512656	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs373880002	chr11:67512657-67512658	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs207471989	chr11:67512663-67512664	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs550354282	chr11:67512675-67512676	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs550123421	chr11:67512676-67512677	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs111211056	chr11:67512679-67512680	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs562181063	chr11:67512686-67512687	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
36	rs376436363	chr11:67512692-67512693	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs11821203	chr11:67512695-67512696	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs371875618	chr11:67512699-67512700	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
39	rs548038886	chr11:67512723-67512724	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs566274638	chr11:67512735-67512736	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs533720722	chr11:67512741-67512742	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs11821167	chr11:67512752-67512753	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs570282951	chr11:67512753-67512754	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs374410289	chr11:67512773-67512774	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs555703484	chr11:67512781-67512782	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs567847962	chr11:67512795-67512796	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs535153137	chr11:67512797-67512798	ZNF genes & repeats Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs553595190	chr11:67512807-67512808	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs368751655	chr11:67512808-67512809	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs370204937	chr11:67512809-67512810	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21373257	CNVD
speech delay	21373257	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1175 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67499800-67512800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr11:67499800-67515200	Weak transcription	Right Atrium	heart
3	chr11:67500000-67521400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr11:67506000-67512600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:67511000-67513000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr11:67511200-67513000	Enhancers	Fetal Heart	heart
7	chr11:67511600-67512400	Enhancers	Placenta	Placenta
8	chr11:67512000-67512600	Weak transcription	Gastric	stomach
9	chr11:67512400-67512600	Active TSS	Fetal Lung	lung
10	chr11:67512400-67521000	Weak transcription	Placenta	Placenta
11	chr11:67512600-67512800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:67512600-67512800	Enhancers	Left Ventricle	heart
13	chr11:67512600-67513000	Flanking Active TSS	Fetal Lung	lung
14	chr11:67512600-67513000	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
15	chr11:67512600-67513200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:67512600-67513200	Enhancers	Esophagus	oesophagus
17	chr11:67512600-67513200	ZNF genes & repeats	Fetal Kidney	kidney
18	chr11:67512600-67513200	ZNF genes & repeats	Gastric	stomach
19	chr11:67512600-67513200	Active TSS	Pancreas	Pancrea
20	chr11:67512600-67513200	Enhancers	Spleen	Spleen
21	chr11:67512800-67513000	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr11:67512800-67513200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:67512800-67513200	Genic enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:67512800-67513200	Bivalent/Poised TSS	NHDF-Ad	bronchial
25	chr11:67513000-67513200	Active TSS	Fetal Lung	lung
26	chr11:67513000-67515600	Weak transcription	Fetal Heart	heart
27	chr11:67513000-67519000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr11:67513200-67514000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr11:67513200-67521400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:67513200-67525400	Weak transcription	Fetal Kidney	kidney
31	chr11:67514400-67515400	Enhancers	Primary B cells from peripheral blood	blood
32	chr11:67514600-67515000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr11:67514800-67515200	Enhancers	Fetal Stomach	stomach
34	chr11:67515200-67515400	Weak transcription	Fetal Stomach	stomach
35	chr11:67515400-67515800	Enhancers	Fetal Stomach	stomach
36	chr11:67515600-67516200	Enhancers	Fetal Heart	heart
37	chr11:67515600-67516600	Enhancers	Colon Smooth Muscle	Colon
38	chr11:67515800-67521200	Weak transcription	Fetal Stomach	stomach
39	chr11:67516200-67521200	Weak transcription	Fetal Heart	heart
40	chr11:67517600-67524400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr11:67521000-67521200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:67521000-67521200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr11:67521000-67521600	Enhancers	Fetal Muscle Leg	muscle
44	chr11:67521000-67521600	Enhancers	Ovary	ovary
45	chr11:67521000-67521600	Enhancers	Rectal Smooth Muscle	rectum
46	chr11:67521000-67522200	Enhancers	Placenta	Placenta
47	chr11:67521200-67521600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr11:67521200-67521600	Enhancers	Fetal Heart	heart
49	chr11:67521200-67521800	Enhancers	Fetal Stomach	stomach
50	chr11:67521200-67524200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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