Variant report

Variant	nsv826072
Chromosome Location	chr11:104662708-104768357
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:104716018-104716072	HepG2	liver:	n/a	n/a
2	BATF	chr11:104690270-104690487	GM12878	blood:	n/a	n/a
3	BATF	chr11:104753441-104753681	GM12878	blood:	n/a	n/a
4	BCL3	chr11:104761233-104761516	GM12878	blood:	n/a	n/a
5	BCL3	chr11:104761069-104761606	GM12878	blood:	n/a	n/a
6	BHLHE40	chr11:104752556-104752567	GM12878	blood:	n/a	n/a
7	BHLHE40	chr11:104747879-104748167	GM12878	blood:	n/a	n/a
8	CEBPB	chr11:104662767-104663009	A549	lung:	n/a	chr11:104662933-104662944 chr11:104662933-104662946 chr11:104662935-104662946
9	CEBPB	chr11:104712717-104713077	IMR90	lung:	n/a	chr11:104712750-104712758 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
10	CEBPB	chr11:104712719-104713038	A549	lung:	n/a	chr11:104712750-104712758 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
11	CEBPB	chr11:104712797-104713014	Hela-S3	cervix:	n/a	chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
12	CEBPB	chr11:104712754-104712944	H1-hESC	embryonic stem cell:	n/a	chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
13	CEBPB	chr11:104663649-104663908	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr11:104662811-104663019	HepG2	liver:	n/a	chr11:104662933-104662944 chr11:104662933-104662946 chr11:104662935-104662946
15	CEBPB	chr11:104700818-104701119	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:104701685-104701820	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:104712733-104713048	K562	blood:	n/a	chr11:104712750-104712758 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
18	CEBPB	chr11:104712712-104713052	HepG2	liver:	n/a	chr11:104712750-104712758 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712895-104712904 chr11:104712893-104712906 chr11:104712848-104712859 chr11:104712893-104712904 chr11:104712895-104712906 chr11:104712895-104712904 chr11:104712893-104712906
19	CEBPB	chr11:104763488-104764195	IMR90	lung:	n/a	n/a
20	CHD1	chr11:104766544-104766551	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr11:104670088-104670208	GM12878	blood:	n/a	n/a
22	CTCF	chr11:104665340-104665490	Caco-2	colon:	n/a	n/a
23	CTCF	chr11:104665360-104665510	HCM	heart:	n/a	n/a
24	CTCF	chr11:104694501-104694634	GM13977	blood:	n/a	chr11:104694544-104694562 chr11:104694546-104694567
25	CTCF	chr11:104744100-104744250	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr11:104756080-104756230	NHEK	skin:	n/a	n/a
27	CTCF	chr11:104665320-104665470	HPF	lung:	n/a	n/a
28	CTCF	chr11:104750266-104750488	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr11:104665380-104665530	HMF	breast:	n/a	n/a
30	CTCF	chr11:104744125-104744229	GM13977	blood:	n/a	n/a
31	CTCF	chr11:104665340-104665490	NHEK	skin:	n/a	n/a
32	CTCF	chr11:104694558-104694607	HepG2	liver:	n/a	n/a
33	CTCF	chr11:104703023-104703198	K562	blood:	n/a	n/a
34	CTCF	chr11:104694480-104694630	GM06990	blood:	n/a	chr11:104694544-104694562 chr11:104694546-104694567
35	CTCF	chr11:104744180-104744330	HMF	breast:	n/a	n/a
36	CTCF	chr11:104665320-104665470	HMEC	breast:	n/a	n/a
37	CTCF	chr11:104665380-104665530	HUVEC	blood vessel:	n/a	n/a
38	CTCF	chr11:104665400-104665550	AG10803	skin:	n/a	n/a
39	CTCF	chr11:104744101-104744257	GM19238	blood:	n/a	n/a
40	CTCF	chr11:104744120-104744270	GM12865	blood:	n/a	n/a
41	CTCF	chr11:104750352-104750509	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr11:104694500-104694650	NHDF-neo	bronchial:	n/a	chr11:104694544-104694562 chr11:104694546-104694567
43	CTCF	chr11:104756109-104756128	MCF-7	breast:	n/a	n/a
44	CTCF	chr11:104756082-104756179	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr11:104750380-104750530	HepG2	liver:	n/a	n/a
46	CTCF	chr11:104744080-104744230	HEEpiC	esophagus:	n/a	n/a
47	CTCF	chr11:104744160-104744310	HCT-116	colon:	n/a	n/a
48	CTCF	chr11:104750300-104750450	Caco-2	colon:	n/a	n/a
49	CTCF	chr11:104676409-104676473	GM13976	blood:	n/a	n/a
50	CTCF	chr11:104665440-104665590	HFF-Myc	foreskin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104758259-104758309	HRPEpiC	eye:	n/a
2	chr11:104762787-104762837	ovcar-3	ovarian:	n/a
3	chr11:104758259-104758309	GM12891	blood:	n/a
4	chr11:104762787-104762837	GM12892	blood:	n/a
5	chr11:104758259-104758309	AG09319	gingival:	n/a
6	chr11:104758766-104758816	PFSK-1	brain:	n/a
7	chr11:104758766-104758816	AG10803	skin:	n/a
8	chr11:104758259-104758309	HEEpiC	esophagus:	n/a
9	chr11:104758259-104758309	H1-hESC	embryonic stem cell:	embryo
10	chr11:104762787-104762837	ECC-1	luminal epithelium:	n/a
11	chr11:104758259-104758309	HRE	kidney:	n/a
12	chr11:104758259-104758309	U87	brain:	n/a
13	chr11:104758259-104758309	MCF10A-Er-Src	breast:	n/a
14	chr11:104762787-104762837	HEK293	kidney:	embryo
15	chr11:104758259-104758309	HCM	heart:	n/a
16	chr11:104762787-104762837	HUVEC	blood vessel:	n/a
17	chr11:104758766-104758816	GM19239	blood:	n/a
18	chr11:104758766-104758816	U87	brain:	n/a
19	chr11:104758766-104758816	AoSMC	blood vessel:	n/a
20	chr11:104762787-104762837	NHBE	bronchial:	n/a
21	chr11:104762787-104762837	PFSK-1	brain:	n/a
22	chr11:104762787-104762837	HEEpiC	esophagus:	n/a
23	chr11:104758766-104758816	GM12892	blood:	n/a
24	chr11:104758259-104758309	PANC-1	pancreas:	n/a
25	chr11:104758259-104758309	SK-N-MC	brain:	n/a
26	chr11:104758766-104758816	HUVEC	blood vessel:	n/a
27	chr11:104758766-104758816	AG09309	skin:	n/a
28	chr11:104758766-104758816	HRPEpiC	eye:	n/a
29	chr11:104762787-104762837	PrEC	prostate:	n/a
30	chr11:104758766-104758816	HCPEpiC	choroid plexus:	n/a
31	chr11:104758259-104758309	GM19239	blood:	n/a
32	chr11:104758259-104758309	HUVEC	blood vessel:	n/a
33	chr11:104758766-104758816	RPTEC	kidney:	n/a
34	chr11:104758259-104758309	HIPEpiC	eye:	n/a
35	chr11:104762787-104762837	HRPEpiC	eye:	n/a
36	chr11:104758766-104758816	AG04449	skin:	fetal
37	chr11:104762787-104762837	NT2-D1	testis:	n/a
38	chr11:104758259-104758309	RPTEC	kidney:	n/a
39	chr11:104758259-104758309	Caco-2	colon:	n/a
40	chr11:104758766-104758816	MCF10A-Er-Src	breast:	n/a
41	chr11:104762787-104762837	BJ	skin:	n/a
42	chr11:104758766-104758816	HMEC	breast:	n/a
43	chr11:104758766-104758816	T-47D	breast:	n/a
44	chr11:104758766-104758816	ECC-1	luminal epithelium:	n/a
45	chr11:104758766-104758816	NHBE	bronchial:	n/a
46	chr11:104758259-104758309	A549	lung:	n/a
47	chr11:104762787-104762837	SK-N-MC	brain:	n/a
48	chr11:104762787-104762837	HCPEpiC	choroid plexus:	n/a
49	chr11:104762787-104762837	Jurkat	blood:	n/a
50	chr11:104762787-104762837	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:104715402..104717976-chr11:104720645..104722717,2	K562	blood:
2	chr11:104702644..104703296-chr17:57832337..57832880,2	MCF-7	breast:
3	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:
4	chr11:104715402..104717976-chr11:104720645..104722717,2	K562	blood:
5	chr11:104747404..104750313-chr11:104761050..104763216,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-2	chr11:104767944-104768195	NR_034071
2	lnc-CASP12-2	chr11:104757418-104757539	NR_034063
3	lnc-CASP12-2	chr11:104763058-104763230	NR_034067
4	lnc-CASP12-2	chr11:104767944-104768195	NR_034067
5	lnc-CASP12-2	chr11:104763058-104763230	NR_034068
6	lnc-CASP12-2	chr11:104757923-104758028	NR_034066
7	lnc-CASP12-2	chr11:104757418-104757539	NR_034065
8	lnc-CASP12-2	chr11:104763058-104763230	NR_034071
9	lnc-CASP12-2	chr11:104757418-104757539	NR_034066
10	lnc-CASP12-2	chr11:104757418-104757539	NR_034067
11	lnc-CASP12-2	chr11:104757923-104758028	NR_034065
12	lnc-CASP12-2	chr11:104761097-104761250	NR_034065
13	lnc-CASP12-2	chr11:104767944-104768195	NR_034061
14	lnc-CASP12-2	chr11:104763624-104763718	NR_034071
15	lnc-CASP12-2	chr11:104757418-104757539	NR_034064
16	lnc-CASP12-2	chr11:104761897-104762131	NR_034070
17	lnc-CASP12-2	chr11:104757418-104757539	NR_034070
18	lnc-CASP12-2	chr11:104761101-104761250	NR_034064
19	lnc-CASP12-2	chr11:104761897-104762131	NR_034063
20	lnc-CASP12-2	chr11:104761097-104761250	NR_034071
21	lnc-CASP12-2	chr11:104757923-104758028	NR_034070
22	lnc-CASP12-2	chr11:104761097-104761250	NR_034061
23	lnc-CASP12-2	chr11:104761101-104761250	NR_034068
24	lnc-CASP12-2	chr11:104757418-104757539	NR_034061
25	lnc-CASP12-2	chr11:104767944-104768195	NR_034064
26	lnc-CASP12-2	chr11:104763058-104763230	NR_034061
27	lnc-CASP12-2	chr11:104757923-104758028	NR_034061
28	lnc-CASP12-2	chr11:104761925-104762131	NR_034064
29	lnc-CASP12-2	chr11:104761097-104761250	NR_034070
30	lnc-CASP12-2	chr11:104761101-104761250	NR_034063
31	lnc-CASP12-2	chr11:104757923-104758028	NR_034071
32	lnc-CASP12-2	chr11:104763058-104763230	NR_034065
33	lnc-CASP12-2	chr11:104761101-104761250	NR_034067
34	lnc-CASP12-2	chr11:104763058-104763230	NR_034070
35	lnc-CASP12-2	chr11:104767944-104768195	NR_034070
36	lnc-CASP12-2	chr11:104757418-104757539	NR_034068
37	lnc-CASP12-2	chr11:104767944-104768195	NR_034063
38	lnc-CASP12-2	chr11:104757418-104757539	NR_034071
39	lnc-CASP12-2	chr11:104761897-104762131	NR_034061
40	lnc-CASP12-2	chr11:104767944-104768195	NR_034065
41	lnc-CASP12-2	chr11:104763058-104763230	NR_034064
42	lnc-CASP12-2	chr11:104763058-104763230	NR_034063
43	lnc-CASP12-2	chr11:104761097-104761250	NR_034066
44	lnc-CASP12-2	chr11:104763058-104763230	NR_034066
45	lnc-CASP12-2	chr11:104763624-104763718	NR_034070

Variant related genes	Relation type
ENSG00000254569	TF binding region
ENSG00000254569	CpG island

Extended variants
information (count: 3280 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:3280 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75242048	chr11:104662729-104662730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs185992972	chr11:104662781-104662782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532406229	chr11:104662796-104662797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs113466270	chr11:104662797-104662798	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs374612425	chr11:104662801-104662802	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs568669517	chr11:104662802-104662803	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1200639	chr11:104662896-104662897	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs547928533	chr11:104662939-104662940	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568138930	chr11:104662950-104662951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189668219	chr11:104663052-104663053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs572742754	chr11:104663057-104663058	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553708688	chr11:104663066-104663067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181990205	chr11:104663067-104663068	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs186320999	chr11:104663068-104663069	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368172431	chr11:104663235-104663236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs60759097	chr11:104663250-104663251	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370259175	chr11:104663259-104663260	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201952419	chr11:104663267-104663268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573481549	chr11:104663281-104663282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541049486	chr11:104663295-104663296	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200022132	chr11:104663330-104663331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190965443	chr11:104663345-104663346	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575864137	chr11:104663397-104663398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs183554905	chr11:104663409-104663410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs561399525	chr11:104663410-104663411	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34090818	chr11:104663411-104663412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs574852470	chr11:104663420-104663421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs1212492	chr11:104663428-104663429	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540288585	chr11:104663480-104663481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs370013580	chr11:104663500-104663501	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148988216	chr11:104663528-104663529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1200640	chr11:104663580-104663581	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs35226234	chr11:104663609-104663610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562439626	chr11:104663614-104663615	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74509320	chr11:104663633-104663634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376608021	chr11:104663676-104663677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547967737	chr11:104663683-104663684	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs145778963	chr11:104663684-104663685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs527354345	chr11:104663692-104663693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs547094603	chr11:104663708-104663709	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs188645482	chr11:104663764-104663765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539346613	chr11:104663765-104663766	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551405111	chr11:104663772-104663773	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191335947	chr11:104663794-104663795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1200641	chr11:104663819-104663820	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs538467108	chr11:104663822-104663823	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116233855	chr11:104663827-104663828	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs373473171	chr11:104663874-104663875	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540680793	chr11:104663894-104663895	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146707627	chr11:104663895-104663896	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:536 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104655800-104668600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr11:104662600-104663200	Enhancers	Fetal Intestine Small	intestine
3	chr11:104662600-104664400	Enhancers	Fetal Heart	heart
4	chr11:104662800-104663600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr11:104662800-104663800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:104663200-104664200	Weak transcription	Fetal Intestine Small	intestine
7	chr11:104663400-104664000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:104663400-104664000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:104663400-104664000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr11:104663400-104664200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr11:104663400-104664200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:104663800-104664200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:104663800-104664400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:104663800-104664400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr11:104664200-104664400	Enhancers	Duodenum Smooth Muscle	Duodenum
16	chr11:104664200-104664400	Enhancers	Fetal Intestine Small	intestine
17	chr11:104664400-104664600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr11:104666800-104667600	Enhancers	Fetal Brain Male	brain
19	chr11:104667000-104667200	Enhancers	Spleen	Spleen
20	chr11:104668600-104668800	Enhancers	Adipose Nuclei	Adipose
21	chr11:104668600-104669200	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr11:104668600-104669400	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr11:104668600-104669400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr11:104668800-104669200	Enhancers	Primary B cells from cord blood	blood
25	chr11:104668800-104669200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr11:104668800-104669200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr11:104668800-104669200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr11:104668800-104669200	Enhancers	Dnd41	blood
29	chr11:104668800-104669200	Enhancers	Monocytes-CD14+_RO01746	blood
30	chr11:104668800-104669400	Enhancers	Primary B cells from peripheral blood	blood
31	chr11:104668800-104669400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:104668800-104669400	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr11:104668800-104669400	Weak transcription	Adipose Nuclei	Adipose
34	chr11:104668800-104670200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr11:104669000-104669200	Enhancers	Primary T cells from cord blood	blood
36	chr11:104669000-104669200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr11:104669000-104669400	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr11:104669200-104669400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
39	chr11:104669200-104669400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr11:104669200-104669400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
41	chr11:104669200-104669600	Flanking Active TSS	Primary T cells from cord blood	blood
42	chr11:104669200-104669600	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
43	chr11:104669200-104669600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
44	chr11:104669200-104669600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
45	chr11:104669200-104669600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr11:104669200-104670000	Flanking Active TSS	Dnd41	blood
47	chr11:104669200-104670400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
48	chr11:104669200-104670600	Flanking Active TSS	Primary B cells from cord blood	blood
49	chr11:104669200-104670600	Active TSS	Duodenum Mucosa	Duodenum
50	chr11:104669200-104670600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood

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