Variant report

Variant	nsv897210
Chromosome Location	chr11:34349427-34381075
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1762)
CpG islands
(count:1225)
Chromatin interactive
region (count:78)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1762 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:34354251-34354423	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:34380203-34380277	K562	blood:	n/a	n/a
3	ARID3A	chr11:34380766-34381328	K562	blood:	n/a	n/a
4	ARID3A	chr11:34379463-34379663	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:34360799-34361380	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:34380557-34381309	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:34366546-34367248	HepG2	liver:	n/a	n/a
8	ATF1	chr11:34375032-34375150	K562	blood:	n/a	n/a
9	ATF2	chr11:34380747-34381278	GM12878	blood:	n/a	n/a
10	ATF2	chr11:34380729-34381166	GM12878	blood:	n/a	n/a
11	ATF2	chr11:34380823-34381228	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr11:34373344-34374066	GM12878	blood:	n/a	n/a
13	ATF2	chr11:34373268-34374104	GM12878	blood:	n/a	n/a
14	ATF3	chr11:34366361-34367233	A549	lung:	n/a	n/a
15	ATF3	chr11:34380550-34381164	A549	lung:	n/a	n/a
16	ATF3	chr11:34366818-34367077	HepG2	liver:	n/a	n/a
17	ATF3	chr11:34366491-34367207	A549	lung:	n/a	n/a
18	ATF3	chr11:34366700-34367222	HepG2	liver:	n/a	n/a
19	BACH1	chr11:34378619-34378620	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr11:34380513-34380996	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr11:34380612-34381168	K562	blood:	n/a	n/a
22	BATF	chr11:34373605-34373977	GM12878	blood:	n/a	n/a
23	BATF	chr11:34356950-34357188	GM12878	blood:	n/a	n/a
24	BATF	chr11:34373267-34374033	GM12878	blood:	n/a	n/a
25	BCL11A	chr11:34373603-34373976	GM12878	blood:	n/a	n/a
26	BCL11A	chr11:34360766-34361087	GM12878	blood:	n/a	n/a
27	BCL3	chr11:34367949-34368543	A549	lung:	n/a	n/a
28	BCL3	chr11:34360702-34361332	A549	lung:	n/a	n/a
29	BCL3	chr11:34360618-34361152	A549	lung:	n/a	n/a
30	BCL3	chr11:34366342-34367253	A549	lung:	n/a	n/a
31	BCL3	chr11:34367427-34368607	A549	lung:	n/a	chr11:34367492-34367501
32	BCL3	chr11:34366247-34367234	A549	lung:	n/a	n/a
33	BCLAF1	chr11:34373551-34373906	GM12878	blood:	n/a	n/a
34	BCLAF1	chr11:34373297-34374067	GM12878	blood:	n/a	chr11:34373492-34373501
35	BCLAF1	chr11:34379272-34379740	GM12878	blood:	n/a	chr11:34379463-34379472 chr11:34379559-34379572 chr11:34379462-34379475 chr11:34379485-34379494
36	BCLAF1	chr11:34380672-34381238	GM12878	blood:	n/a	n/a
37	BHLHE40	chr11:34380568-34380762	HepG2	liver:	n/a	n/a
38	BHLHE40	chr11:34379566-34379879	K562	blood:	n/a	n/a
39	BHLHE40	chr11:34360785-34361082	GM12878	blood:	n/a	n/a
40	BHLHE40	chr11:34380142-34380246	K562	blood:	n/a	n/a
41	BHLHE40	chr11:34379405-34381141	HepG2	liver:	n/a	n/a
42	BHLHE40	chr11:34380537-34381159	A549	lung:	n/a	n/a
43	BHLHE40	chr11:34380492-34381105	K562	blood:	n/a	n/a
44	BHLHE40	chr11:34379361-34381271	GM12878	blood:	n/a	n/a
45	BHLHE40	chr11:34357063-34357077	GM12878	blood:	n/a	n/a
46	BRCA1	chr11:34379369-34380404	Hela-S3	cervix:	n/a	n/a
47	CBX3	chr11:34380473-34381189	K562	blood:	n/a	n/a
48	CBX3	chr11:34379354-34379684	K562	blood:	n/a	n/a
49	CCNT2	chr11:34378615-34378815	K562	blood:	n/a	n/a
50	CCNT2	chr11:34379435-34379769	K562	blood:	n/a	n/a

(count:1225 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34379053-34379103	HCF	heart:	n/a
2	chr11:34363786-34363836	PFSK-1	brain:	n/a
3	chr11:34380546-34380596	Caco-2	colon:	n/a
4	chr11:34378293-34378343	HEEpiC	esophagus:	n/a
5	chr11:34375707-34375757	BE2_C	brain:	n/a
6	chr11:34379053-34379103	HCF	heart:	n/a
7	chr11:34363786-34363836	PFSK-1	brain:	n/a
8	chr11:34380546-34380596	Caco-2	colon:	n/a
9	chr11:34378293-34378343	HEEpiC	esophagus:	n/a
10	chr11:34375707-34375757	BE2_C	brain:	n/a
11	chr11:34377921-34377971	HNPCEpiC	eye:	n/a
12	chr11:34380546-34380596	IMR90	lung:	fetal
13	chr11:34380839-34380889	H1-hESC	embryonic stem cell:	embryo
14	chr11:34377921-34377971	ProgFib	skin:	n/a
15	chr11:34363786-34363836	ECC-1	luminal epithelium:	n/a
16	chr11:34378884-34378934	HRCEpiC	kidney:	n/a
17	chr11:34378921-34378971	HMEC	breast:	n/a
18	chr11:34378975-34379025	PANC-1	pancreas:	n/a
19	chr11:34378975-34379025	HUVEC	blood vessel:	n/a
20	chr11:34378797-34378847	LNCaP	prostate:	n/a
21	chr11:34378975-34379025	SAEC	small airway:	n/a
22	chr11:34379731-34379781	GM12891	blood:	n/a
23	chr11:34378805-34378855	MCF-7	breast:	n/a
24	chr11:34350440-34350490	AG09309	skin:	n/a
25	chr11:34380695-34380745	GM19239	blood:	n/a
26	chr11:34378797-34378847	SK-N-SH	brain:	n/a
27	chr11:34378956-34379006	SKMC	muscle:	n/a
28	chr11:34375707-34375757	CMK	blood:	n/a
29	chr11:34378956-34379006	RPTEC	kidney:	n/a
30	chr11:34363786-34363836	K562	blood:	n/a
31	chr11:34350440-34350490	PFSK-1	brain:	n/a
32	chr11:34350440-34350490	SAEC	small airway:	n/a
33	chr11:34380598-34380648	NT2-D1	testis:	n/a
34	chr11:34378797-34378847	HepG2	liver:	n/a
35	chr11:34380546-34380596	HIPEpiC	eye:	n/a
36	chr11:34377921-34377971	HUVEC	blood vessel:	n/a
37	chr11:34380695-34380745	SKMC	muscle:	n/a
38	chr11:34378805-34378855	HAEpiC	amniotic membrane:	n/a
39	chr11:34379731-34379781	BE2_C	brain:	n/a
40	chr11:34379731-34379781	ProgFib	skin:	n/a
41	chr11:34380598-34380648	HepG2	liver:	n/a
42	chr11:34380839-34380889	AG04449	skin:	fetal
43	chr11:34375707-34375757	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:34377618-34377668	LNCaP	prostate:	n/a
45	chr11:34380695-34380745	K562	blood:	n/a
46	chr11:34380546-34380596	HNPCEpiC	eye:	n/a
47	chr11:34379053-34379103	NH-A	brain:	n/a
48	chr11:34379565-34379615	HNPCEpiC	eye:	n/a
49	chr11:34378975-34379025	NHBE	bronchial:	n/a
50	chr11:34379731-34379781	GM06990	blood:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:34295466..34297998-chr11:34348756..34350438,2	MCF-7	breast:
2	chr11:34368701..34370901-chr11:34379752..34381357,2	K562	blood:
3	chr11:34195614..34196183-chr11:34380130..34380656,2	MCF-7	breast:
4	chr11:34378671..34379417-chr17:56708715..56709403,2	Hela-S3	cervix:
5	chr11:34065587..34067431-chr11:34358883..34361873,2	K562	blood:
6	chr11:34126304..34129768-chr11:34376546..34381116,4	MCF-7	breast:
7	chr11:34365763..34368722-chr11:34368922..34370946,2	MCF-7	breast:
8	chr11:34360672..34363341-chr11:34364599..34366363,2	MCF-7	breast:
9	chr11:34073205..34075094-chr11:34377742..34380453,3	MCF-7	breast:
10	chr11:34368537..34371450-chr11:34371767..34375088,3	K562	blood:
11	chr11:34359062..34360575-chr11:34363505..34365400,2	K562	blood:
12	chr11:34380138..34380872-chr6:26284638..26285343,2	Hela-S3	cervix:
13	chr11:34295048..34297358-chr11:34352691..34354542,2	MCF-7	breast:
14	chr11:34351980..34355833-chr11:34364485..34369065,5	MCF-7	breast:
15	chr11:34366426..34367988-chr11:34371579..34373367,2	MCF-7	breast:
16	chr11:34380524..34381238-chr11:34489841..34490388,3	K562	blood:
17	chr11:34357216..34358836-chr11:34360327..34362099,2	K562	blood:
18	chr11:34342106..34344369-chr11:34352747..34354682,2	MCF-7	breast:
19	chr11:34380514..34381443-chr11:34513937..34515065,4	K562	blood:
20	chr11:34380939..34381848-chr11:34514131..34515008,2	MCF-7	breast:
21	chr11:34127120..34127834-chr11:34380752..34381319,3	MCF-7	breast:
22	chr11:34352862..34355628-chr11:34375081..34377214,3	MCF-7	breast:
23	chr11:34368701..34370901-chr11:34379752..34381357,2	K562	blood:
24	chr11:34379701..34380202-chr13:76805632..76806132,2	NB4	blood:
25	chr11:34368537..34371450-chr11:34371767..34375088,3	K562	blood:
26	chr11:34170082..34170878-chr11:34380526..34381351,2	K562	blood:
27	chr11:34380153..34381078-chr20:60718993..60719935,2	Hela-S3	cervix:
28	chr11:34378273..34378978-chr5:138941341..138941940,2	Hela-S3	cervix:
29	chr11:34243758..34246398-chr11:34366962..34369270,2	MCF-7	breast:
30	chr11:34182869..34184565-chr11:34366720..34369400,2	K562	blood:
31	chr11:34363297..34366211-chr11:34370921..34372477,2	K562	blood:
32	chr11:34295678..34297424-chr11:34350802..34352838,2	MCF-7	breast:
33	chr11:34186780..34187813-chr11:34380499..34381345,5	MCF-7	breast:
34	chr11:34366426..34367988-chr11:34371579..34373367,2	MCF-7	breast:
35	chr11:34351980..34355833-chr11:34364485..34369065,5	MCF-7	breast:
36	chr11:34353541..34355614-chr11:34357152..34360138,2	MCF-7	breast:
37	chr11:34187084..34188044-chr11:34380825..34381630,2	MCF-7	breast:
38	chr11:34346331..34348538-chr11:34354788..34356481,2	MCF-7	breast:
39	chr11:34380108..34380740-chr17:43662186..43662724,2	Hela-S3	cervix:
40	chr11:34018304..34019124-chr11:34380429..34381489,5	MCF-7	breast:
41	chr11:34194734..34196633-chr11:34370779..34372924,2	MCF-7	breast:
42	chr11:34195400..34196504-chr11:34379832..34381736,16	MCF-7	breast:
43	chr11:34345030..34348316-chr11:34348388..34351447,3	K562	blood:
44	chr11:34363297..34366211-chr11:34370921..34372477,2	K562	blood:
45	chr11:34186902..34187899-chr11:34380166..34381049,3	K562	blood:
46	chr11:34283475..34285529-chr11:34358260..34360841,2	MCF-7	breast:
47	chr11:34009660..34010197-chr11:34380190..34381055,2	MCF-7	breast:
48	chr11:33879158..33879864-chr11:34380802..34381795,2	MCF-7	breast:
49	chr11:34071981..34076766-chr11:34377622..34383038,7	MCF-7	breast:
50	chr11:34197728..34198296-chr11:34380470..34381106,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ELF5-4	chr11:34356665-34357550	NONHSAT018749

No data

Variant related genes	Relation type
ENSG00000254708	TF binding region
ABTB2	TF binding region
ENSG00000254708	CpG island
ABTB2	CpG island
ENSG00000135372	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000136527	chromatin interactions
ENSG00000259802	chromatin interactions
ENSG00000145495	chromatin interactions
ENSG00000201867	chromatin interactions
ENSG00000131508	chromatin interactions
ENSG00000166016	chromatin interactions
ENSG00000254708	chromatin interactions
ENSG00000135387	chromatin interactions

Extended variants
information (count: 1174 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1174 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377256514	chr11:34349427-34349428	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs554965368	chr11:34349432-34349433	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543014110	chr11:34349434-34349435	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs574891867	chr11:34349449-34349450	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs537517580	chr11:34349453-34349454	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs144582122	chr11:34349481-34349482	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs539605387	chr11:34349489-34349490	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148489396	chr11:34349508-34349509	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs372730030	chr11:34349577-34349578	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs2755171	chr11:34349623-34349624	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs190018106	chr11:34349699-34349700	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs375955922	chr11:34349702-34349703	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs540936217	chr11:34349737-34349738	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs144615870	chr11:34349753-34349754	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs529661384	chr11:34349843-34349844	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs182426368	chr11:34349897-34349898	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs78647166	chr11:34349898-34349899	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576663515	chr11:34349956-34349957	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs1268732	chr11:34349976-34349977	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs375389226	chr11:34350014-34350015	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs552777854	chr11:34350025-34350026	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs185521861	chr11:34350070-34350071	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs528751280	chr11:34350087-34350088	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs548923261	chr11:34350189-34350190	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs568431920	chr11:34350190-34350191	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555461894	chr11:34350203-34350204	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs189546864	chr11:34350210-34350211	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs1269119	chr11:34350353-34350354	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs147888069	chr11:34350378-34350379	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs538444129	chr11:34350440-34350441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs541460964	chr11:34350445-34350446	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs559843766	chr11:34350557-34350558	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs139883438	chr11:34350585-34350586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs572150246	chr11:34350601-34350602	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs182875696	chr11:34350691-34350692	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs554457910	chr11:34350710-34350711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs554592937	chr11:34350711-34350712	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145402103	chr11:34350719-34350720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs574073756	chr11:34350835-34350836	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs151069732	chr11:34350882-34350883	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543820812	chr11:34350885-34350886	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141026906	chr11:34350891-34350892	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs150253432	chr11:34350916-34350917	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs545586013	chr11:34350927-34350928	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs559871645	chr11:34350946-34350947	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs528714154	chr11:34351064-34351065	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs577969160	chr11:34351094-34351095	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs145853172	chr11:34351122-34351123	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs188772948	chr11:34351123-34351124	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548886868	chr11:34351136-34351137	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD

Chromatin state (count:1500 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34336200-34358200	Weak transcription	Thymus	Thymus
2	chr11:34339000-34357400	Weak transcription	Fetal Thymus	thymus
3	chr11:34340000-34353200	Weak transcription	Small Intestine	intestine
4	chr11:34340800-34352200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr11:34341000-34352400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:34341200-34352200	Weak transcription	HSMM	muscle
7	chr11:34343600-34350800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr11:34346600-34351000	Weak transcription	Aorta	Aorta
9	chr11:34346600-34353800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:34347000-34349600	Weak transcription	Lung	lung
11	chr11:34347000-34349600	Weak transcription	A549	lung
12	chr11:34347000-34350800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:34347000-34355600	Weak transcription	GM12878-XiMat	blood
14	chr11:34347800-34354400	Enhancers	Fetal Stomach	stomach
15	chr11:34348000-34353200	Enhancers	Fetal Muscle Leg	muscle
16	chr11:34348400-34350000	Enhancers	Fetal Muscle Trunk	muscle
17	chr11:34348400-34350200	Enhancers	Left Ventricle	heart
18	chr11:34348400-34350200	Enhancers	Ovary	ovary
19	chr11:34348400-34351200	Enhancers	Fetal Lung	lung
20	chr11:34348400-34351600	Enhancers	Right Ventricle	heart
21	chr11:34348400-34354400	Enhancers	Psoas Muscle	Psoas
22	chr11:34348600-34352800	Enhancers	Fetal Heart	heart
23	chr11:34348600-34353600	Enhancers	Colon Smooth Muscle	Colon
24	chr11:34348600-34353800	Enhancers	Rectal Smooth Muscle	rectum
25	chr11:34348800-34349800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:34348800-34350000	Enhancers	Brain Angular Gyrus	brain
27	chr11:34348800-34350200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr11:34348800-34350200	Enhancers	Brain Substantia Nigra	brain
29	chr11:34348800-34350400	Enhancers	Liver	Liver
30	chr11:34348800-34350600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr11:34348800-34351200	Enhancers	Brain Germinal Matrix	brain
32	chr11:34348800-34351800	Enhancers	HepG2	liver
33	chr11:34348800-34352000	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr11:34349000-34349600	Enhancers	Pancreas	Pancrea
35	chr11:34349000-34349800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr11:34349000-34349800	Enhancers	Right Atrium	heart
37	chr11:34349000-34349800	Flanking Active TSS	Stomach Smooth Muscle	stomach
38	chr11:34349000-34349800	Enhancers	NHLF	lung
39	chr11:34349000-34350000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr11:34349000-34350200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:34349000-34350200	Enhancers	Placenta	Placenta
42	chr11:34349000-34350800	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr11:34349000-34350800	Enhancers	Fetal Brain Male	brain
44	chr11:34349000-34351000	Enhancers	Brain Anterior Caudate	brain
45	chr11:34349000-34351600	Enhancers	Adipose Nuclei	Adipose
46	chr11:34349000-34352000	Enhancers	Skeletal Muscle Female	skeletal muscle
47	chr11:34349200-34351000	Enhancers	Duodenum Smooth Muscle	Duodenum
48	chr11:34349400-34349800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr11:34349400-34349800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr11:34349400-34349800	Flanking Active TSS	Brain Cingulate Gyrus	brain

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