Variant report

Variant	nsv1035918
Chromosome Location	chr11:119853069-119879255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:119869183-119869254	H1-hESC	embryonic stem cell:	n/a	chr11:119869201-119869212
2	CEBPB	chr11:119876410-119876514	HepG2	liver:	n/a	n/a
3	CEBPB	chr11:119869053-119869350	HepG2	liver:	n/a	chr11:119869201-119869212
4	CHD1	chr11:119873499-119873589	GM12878	blood:	n/a	n/a
5	CTCF	chr11:119854175-119854311	MCF-7	breast:	n/a	n/a
6	CTCF	chr11:119854184-119854298	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr11:119866580-119866730	GM12873	blood:	n/a	chr11:119866665-119866674
8	CTCF	chr11:119870060-119870210	HMEC	breast:	n/a	n/a
9	CTCF	chr11:119866614-119866716	MCF-7	breast:	n/a	chr11:119866665-119866674
10	CTCF	chr11:119866560-119866710	HEEpiC	esophagus:	n/a	chr11:119866665-119866674
11	CTCF	chr11:119869960-119870110	GM12872	blood:	n/a	n/a
12	CTCF	chr11:119864502-119864709	Pancreas_OC	pancreas:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
13	CTCF	chr11:119870060-119870210	HCM	heart:	n/a	n/a
14	CTCF	chr11:119854172-119854313	GM19240	blood:	n/a	n/a
15	CTCF	chr11:119870060-119870210	GM12864	blood:	n/a	n/a
16	CTCF	chr11:119870083-119870220	MCF-7	breast:	n/a	n/a
17	CTCF	chr11:119854060-119854210	GM12870	blood:	n/a	n/a
18	CTCF	chr11:119870080-119870230	HVMF	connective:	n/a	n/a
19	CTCF	chr11:119870060-119870210	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr11:119870060-119870210	WERI-Rb-1	eye:	n/a	n/a
21	CTCF	chr11:119870100-119870250	HEK293	kidney:	n/a	n/a
22	CTCF	chr11:119870120-119870270	HCT-116	colon:	n/a	n/a
23	CTCF	chr11:119869920-119870070	A549	lung:	n/a	n/a
24	CTCF	chr11:119870080-119870230	GM12875	blood:	n/a	n/a
25	CTCF	chr11:119869995-119870282	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr11:119870085-119870217	GM12891	blood:	n/a	n/a
27	CTCF	chr11:119866620-119866733	MCF-7	breast:	n/a	chr11:119866665-119866674
28	CTCF	chr11:119854080-119854401	K562	blood:	n/a	n/a
29	CTCF	chr11:119866640-119866790	BE2_C	brain:	n/a	chr11:119866665-119866674
30	CTCF	chr11:119854120-119854270	SK-N-SH_RA	brain:	n/a	n/a
31	CTCF	chr11:119870109-119870186	A549	lung:	n/a	n/a
32	CTCF	chr11:119869997-119870307	GM12878	blood:	n/a	n/a
33	CTCF	chr11:119870100-119870250	GM06990	blood:	n/a	n/a
34	CTCF	chr11:119870121-119870194	MCF-7	breast:	n/a	n/a
35	CTCF	chr11:119854020-119854170	BE2_C	brain:	n/a	n/a
36	CTCF	chr11:119866580-119866730	WERI-Rb-1	eye:	n/a	chr11:119866665-119866674
37	CTCF	chr11:119854120-119854270	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr11:119870069-119870251	GM19238	blood:	n/a	n/a
39	CTCF	chr11:119864560-119864710	HEEpiC	esophagus:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
40	CTCF	chr11:119864540-119864690	GM12878	blood:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
41	CTCF	chr11:119870120-119870270	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr11:119870100-119870250	HMF	breast:	n/a	n/a
43	CTCF	chr11:119864620-119864770	HMEC	breast:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
44	CTCF	chr11:119869780-119869930	SAEC	small airway:	n/a	n/a
45	CTCF	chr11:119854160-119854310	GM12875	blood:	n/a	n/a
46	CTCF	chr11:119854120-119854270	GM12874	blood:	n/a	n/a
47	CTCF	chr11:119866614-119866707	H1-hESC	embryonic stem cell:	n/a	chr11:119866665-119866674
48	CTCF	chr11:119869972-119870322	K562	blood:	n/a	n/a
49	CTCF	chr11:119864600-119864750	K562	blood:	n/a	chr11:119864634-119864647 chr11:119864632-119864650
50	CTCF	chr11:119866580-119866730	SK-N-SH_RA	brain:	n/a	chr11:119866665-119866674

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:119862409-119862459	HRPEpiC	eye:	n/a
2	chr11:119872718-119872768	Jurkat	blood:	n/a
3	chr11:119862409-119862459	H1-hESC	embryonic stem cell:	embryo
4	chr11:119862409-119862459	HCPEpiC	choroid plexus:	n/a
5	chr11:119872718-119872768	HRE	kidney:	n/a
6	chr11:119862409-119862459	HRCEpiC	kidney:	n/a
7	chr11:119862409-119862459	AG09319	gingival:	n/a
8	chr11:119872718-119872768	CMK	blood:	n/a
9	chr11:119862409-119862459	NH-A	brain:	n/a
10	chr11:119862409-119862459	MCF10A-Er-Src	breast:	n/a
11	chr11:119862409-119862459	SK-N-MC	brain:	n/a
12	chr11:119862409-119862459	HCF	heart:	n/a
13	chr11:119872718-119872768	GM12891	blood:	n/a
14	chr11:119862409-119862459	NT2-D1	testis:	n/a
15	chr11:119872718-119872768	MCF10A-Er-Src	breast:	n/a
16	chr11:119862409-119862459	NHDF-neo	bronchial:	n/a
17	chr11:119872718-119872768	AG09309	skin:	n/a
18	chr11:119872718-119872768	Caco-2	colon:	n/a
19	chr11:119862409-119862459	PANC-1	pancreas:	n/a
20	chr11:119872718-119872768	IMR90	lung:	fetal
21	chr11:119872718-119872768	Hepatocyte	liver:	n/a
22	chr11:119862409-119862459	RPTEC	kidney:	n/a
23	chr11:119872718-119872768	ECC-1	luminal epithelium:	n/a
24	chr11:119872718-119872768	HRPEpiC	eye:	n/a
25	chr11:119862409-119862459	Hepatocyte	liver:	n/a
26	chr11:119872718-119872768	HRCEpiC	kidney:	n/a
27	chr11:119862409-119862459	U87	brain:	n/a
28	chr11:119862409-119862459	HCM	heart:	n/a
29	chr11:119872718-119872768	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:119872718-119872768	GM06990	blood:	n/a
31	chr11:119862409-119862459	HNPCEpiC	eye:	n/a
32	chr11:119862409-119862459	GM12891	blood:	n/a
33	chr11:119862409-119862459	HRE	kidney:	n/a
34	chr11:119872718-119872768	GM12892	blood:	n/a
35	chr11:119872718-119872768	NT2-D1	testis:	n/a
36	chr11:119862409-119862459	Jurkat	blood:	n/a
37	chr11:119862409-119862459	HMEC	breast:	n/a
38	chr11:119862409-119862459	PFSK-1	brain:	n/a
39	chr11:119872718-119872768	A549	lung:	n/a
40	chr11:119862409-119862459	ECC-1	luminal epithelium:	n/a
41	chr11:119862409-119862459	T-47D	breast:	n/a
42	chr11:119862409-119862459	NB4	blood:	n/a
43	chr11:119862409-119862459	ProgFib	skin:	n/a
44	chr11:119872718-119872768	AG04450	lung:	fetal
45	chr11:119872718-119872768	HCPEpiC	choroid plexus:	n/a
46	chr11:119872718-119872768	T-47D	breast:	n/a
47	chr11:119872718-119872768	NH-A	brain:	n/a
48	chr11:119862409-119862459	HEEpiC	esophagus:	n/a
49	chr11:119862409-119862459	GM12878	blood:	n/a
50	chr11:119872718-119872768	HUVEC	blood vessel:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:119599184..119600753-chr11:119861551..119864175,2	MCF-7	breast:
2	chr11:119853779..119856334-chr11:119866020..119869388,3	K562	blood:
3	chr11:119853779..119856334-chr11:119866020..119869388,3	K562	blood:
4	chr11:119855228..119858162-chr11:119871012..119872668,2	K562	blood:
5	chr11:119865550..119868461-chr11:119874925..119876802,2	K562	blood:
6	chr11:119855228..119858162-chr11:119871012..119872668,2	K562	blood:
7	chr11:119847784..119851574-chr11:119854250..119856305,4	K562	blood:
8	chr11:119867354..119869206-chr11:119872754..119874804,2	K562	blood:
9	chr11:119848644..119851574-chr11:119854250..119856097,2	K562	blood:
10	chr11:119875923..119878520-chr11:119878673..119880916,2	K562	blood:
11	chr11:119867354..119869206-chr11:119872754..119874804,2	K562	blood:
12	chr11:119875923..119878520-chr11:119878673..119880916,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-831A10.1.1-1	chr11:119859300-119859589	NONHSAT024697
2	lnc-RP11-831A10.1.1-1	chr11:119865303-119865413	NONHSAT024698
3	lnc-RP11-831A10.1.1-1	chr11:119859300-119859513	NONHSAT024700
4	lnc-RP11-831A10.1.1-1	chr11:119859300-119859589	NONHSAT024698
5	lnc-RP11-831A10.1.1-1	chr11:119858675-119858936	NONHSAT024700
6	lnc-RP11-831A10.1.1-1	chr11:119859990-119860175	NONHSAT024699
7	lnc-RP11-831A10.1.1-1	chr11:119859297-119859589	XLOC_009578
8	lnc-RP11-831A10.1.1-1	chr11:119863386-119863425	XLOC_009578
9	lnc-RP11-831A10.1.1-1	chr11:119865303-119865411	XLOC_009578
10	lnc-RP11-831A10.1.1-1	chr11:119858517-119859513	XLOC_009578
11	lnc-RP11-831A10.1.1-1	chr11:119859300-119859513	NONHSAT024699
12	lnc-RP11-831A10.1.1-1	chr11:119861913-119862015	NONHSAT024697
13	lnc-RP11-831A10.1.1-1	chr11:119859300-119859543	ENSG00000254863
14	lnc-RP11-831A10.1.1-1	chr11:119858663-119858936	ENSG00000254863
15	lnc-RP11-831A10.1.1-1	chr11:119865303-119865413	NONHSAT024700
16	lnc-RP11-831A10.1.1-1	chr11:119858675-119858936	NONHSAT024698
17	lnc-RP11-831A10.1.1-1	chr11:119865597-119865746	ENSG00000254863
18	lnc-RP11-831A10.1.1-1	chr11:119859990-119860165	ENSG00000254863
19	lnc-RP11-831A10.1.1-1	chr11:119859889-119860165	XLOC_009578
20	lnc-RP11-831A10.1.1-1	chr11:119858675-119858936	NONHSAT024699
21	lnc-RP11-831A10.1.1-1	chr11:119865303-119865418	ENSG00000254863
22	lnc-RP11-831A10.1.1-1	chr11:119865303-119865400	XLOC_009578
23	lnc-RP11-831A10.1.1-1	chr11:119858675-119858936	NONHSAT024697
24	lnc-RP11-831A10.1.1-1	chr11:119859473-119859610	ENSG00000254863
25	lnc-RP11-831A10.1.1-1	chr11:119859374-119859513	ENSG00000254863
26	lnc-RP11-831A10.1.1-1	chr11:119859990-119860134	NONHSAT024697
27	lnc-RP11-831A10.1.1-1	chr11:119860166-119860388	ENSG00000254863

No data

Variant related genes	Relation type
ENSG00000254863	TF binding region
ENSG00000254863	CpG island
ENSG00000254863	chromatin interactions
ENSG00000254854	chromatin interactions
ENSG00000110400	chromatin interactions
MITF	miRNA target sites

Extended variants
information (count: 1098 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7129717	chr11:119853069-119853070	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573871621	chr11:119853074-119853075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541186243	chr11:119853083-119853084	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143378996	chr11:119853096-119853097	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs17123519	chr11:119853138-119853139	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs545421332	chr11:119853139-119853140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs111444487	chr11:119853252-119853253	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs116626600	chr11:119853256-119853257	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs549258908	chr11:119853291-119853292	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs576274475	chr11:119853306-119853307	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs567580684	chr11:119853352-119853353	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs114305804	chr11:119853398-119853399	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs546759703	chr11:119853408-119853409	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs595167	chr11:119853430-119853431	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs148194050	chr11:119853444-119853445	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs557762042	chr11:119853445-119853446	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569546144	chr11:119853456-119853457	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs537392002	chr11:119853480-119853481	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374654055	chr11:119853505-119853506	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs117563194	chr11:119853517-119853518	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573955927	chr11:119853518-119853519	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541243661	chr11:119853527-119853528	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529802670	chr11:119853566-119853567	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs553189638	chr11:119853575-119853576	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs189005438	chr11:119853582-119853583	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545170109	chr11:119853592-119853593	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563744854	chr11:119853595-119853596	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs191307612	chr11:119853600-119853601	Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs376270906	chr11:119853612-119853613	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs75964569	chr11:119853613-119853614	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528723423	chr11:119853633-119853634	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs576958322	chr11:119853637-119853638	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182045294	chr11:119853671-119853672	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565312788	chr11:119853689-119853690	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533094434	chr11:119853696-119853697	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187084554	chr11:119853733-119853734	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373147226	chr11:119853757-119853758	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs141172913	chr11:119853795-119853796	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191833417	chr11:119853820-119853821	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184811071	chr11:119853841-119853842	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs190185133	chr11:119853852-119853853	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553252840	chr11:119853874-119853875	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193108832	chr11:119853888-119853889	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150718340	chr11:119853933-119853934	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185591634	chr11:119853945-119853946	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575662891	chr11:119853958-119853959	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542625261	chr11:119853974-119853975	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560929312	chr11:119853987-119853988	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74984550	chr11:119854036-119854037	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs189284645	chr11:119854044-119854045	Enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Developmental delay	21147756	CNVD
Emanuel syndrome	21549014	CNVD
Emanuel syndrome	18184694	CNVD
Non-syndromic sensorineural hearing loss	18184694	CNVD
Acute lymphoblastic leukemia	22581003	CNVD
Ovarian neoplasms	16753589	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Retinoblastoma	22278416	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-syndromic sensorineural hearing loss	16829213	CNVD
Non-syndromic sensorineural hearing loss	16760666	CNVD
Squamous cell cancer	20885788	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Neurocytoma	17123091	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Central neurocytomas	17123091	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Hepatocellular carcinoma	16750200	CNVD
Multiple myeloma	17550852	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Acute myeloid leukemia	19651601	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	20409316	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Heart disease	20551144	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Cancer	17440070	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119846800-119853200	Weak transcription	Fetal Brain Female	brain
2	chr11:119846800-119858600	Weak transcription	Fetal Heart	heart
3	chr11:119847800-119853400	Weak transcription	Brain Anterior Caudate	brain
4	chr11:119848400-119853200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr11:119848400-119854200	Weak transcription	Brain Angular Gyrus	brain
6	chr11:119849200-119853200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr11:119849200-119853400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:119850600-119853200	Weak transcription	Brain Hippocampus Middle	brain
9	chr11:119851400-119855400	Enhancers	Brain Germinal Matrix	brain
10	chr11:119851800-119853400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr11:119853000-119856200	Enhancers	Brain Substantia Nigra	brain
12	chr11:119853200-119853400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr11:119853200-119853800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:119853200-119853800	Enhancers	Fetal Lung	lung
15	chr11:119853200-119854600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr11:119853200-119855200	Enhancers	Fetal Brain Female	brain
17	chr11:119853200-119855600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr11:119853200-119856600	Enhancers	Brain Cingulate Gyrus	brain
19	chr11:119853200-119856800	Enhancers	Brain Hippocampus Middle	brain
20	chr11:119853400-119853600	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr11:119853400-119853600	Bivalent Enhancer	Fetal Muscle Leg	muscle
22	chr11:119853400-119854200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr11:119853400-119854200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
24	chr11:119853400-119854200	Enhancers	Fetal Thymus	thymus
25	chr11:119853400-119854400	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr11:119853400-119854400	Enhancers	Esophagus	oesophagus
27	chr11:119853400-119854400	Enhancers	Fetal Brain Male	brain
28	chr11:119853400-119854600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr11:119853400-119854600	Enhancers	Adipose Nuclei	Adipose
30	chr11:119853400-119854600	Enhancers	Brain Anterior Caudate	brain
31	chr11:119853600-119853800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:119853600-119854400	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:119853600-119854400	Enhancers	Fetal Muscle Leg	muscle
34	chr11:119853600-119854600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr11:119853600-119854600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr11:119853800-119854000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr11:119853800-119854000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
38	chr11:119853800-119854200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr11:119853800-119854400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:119854000-119854200	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr11:119854000-119854200	Enhancers	Left Ventricle	heart
42	chr11:119854000-119854400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr11:119854200-119854600	Enhancers	Brain Angular Gyrus	brain
44	chr11:119854200-119862200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
45	chr11:119854400-119859200	Weak transcription	Fetal Brain Male	brain
46	chr11:119854400-119859200	Weak transcription	Left Ventricle	heart
47	chr11:119854400-119860800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr11:119854600-119855600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr11:119854600-119855800	Weak transcription	Brain Angular Gyrus	brain
50	chr11:119854600-119859000	Weak transcription	Brain Anterior Caudate	brain

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