Variant report

Variant	esv1800372
Chromosome Location	chr11:94182992-94227993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:830)
CpG islands
(count:1100)
Chromatin interactive
region (count:49)
LncRNA
region (count:2)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:830 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:94226621-94227809	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:94226817-94227053	K562	blood:	n/a	n/a
3	ARID3A	chr11:94190158-94190455	K562	blood:	n/a	n/a
4	ARID3A	chr11:94226313-94226540	K562	blood:	n/a	n/a
5	ATF1	chr11:94202722-94202923	K562	blood:	n/a	n/a
6	ATF1	chr11:94226839-94227255	K562	blood:	n/a	n/a
7	ATF2	chr11:94190859-94191286	GM12878	blood:	n/a	n/a
8	ATF2	chr11:94202590-94203078	GM12878	blood:	n/a	n/a
9	ATF2	chr11:94226375-94227236	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr11:94192680-94193125	GM12878	blood:	n/a	n/a
11	ATF2	chr11:94202437-94203093	GM12878	blood:	n/a	n/a
12	ATF2	chr11:94192705-94193059	GM12878	blood:	n/a	n/a
13	ATF2	chr11:94227299-94227715	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr11:94226566-94227214	GM12878	blood:	n/a	n/a
15	ATF2	chr11:94206409-94207070	GM12878	blood:	n/a	n/a
16	ATF2	chr11:94206315-94207163	GM12878	blood:	n/a	n/a
17	ATF2	chr11:94226652-94227512	GM12878	blood:	n/a	n/a
18	ATF2	chr11:94190887-94191278	GM12878	blood:	n/a	n/a
19	ATF2	chr11:94226438-94227189	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr11:94189034-94189433	HCT-116	colon:	n/a	n/a
21	ATF3	chr11:94190901-94191198	K562	blood:	n/a	n/a
22	BACH1	chr11:94226529-94227423	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr11:94190380-94190664	K562	blood:	n/a	n/a
24	BATF	chr11:94206447-94206972	GM12878	blood:	n/a	n/a
25	BATF	chr11:94192706-94193076	GM12878	blood:	n/a	n/a
26	BATF	chr11:94202619-94202935	GM12878	blood:	n/a	n/a
27	BATF	chr11:94206462-94206951	GM12878	blood:	n/a	n/a
28	BATF	chr11:94202501-94202988	GM12878	blood:	n/a	n/a
29	BATF	chr11:94190861-94191247	GM12878	blood:	n/a	n/a
30	BATF	chr11:94192692-94193101	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:94206571-94206984	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:94202628-94202903	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:94202633-94202934	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:94192717-94193037	GM12878	blood:	n/a	n/a
35	BCL11A	chr11:94206606-94206926	GM12878	blood:	n/a	n/a
36	BCL3	chr11:94182483-94183043	A549	lung:	n/a	n/a
37	BCL3	chr11:94206427-94206992	GM12878	blood:	n/a	n/a
38	BCLAF1	chr11:94206455-94207001	GM12878	blood:	n/a	n/a
39	BCLAF1	chr11:94190851-94191212	GM12878	blood:	n/a	n/a
40	BCLAF1	chr11:94206462-94206978	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:94226647-94227663	K562	blood:	n/a	n/a
42	BHLHE40	chr11:94206435-94206990	GM12878	blood:	n/a	n/a
43	BHLHE40	chr11:94202204-94203137	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:94226945-94227545	GM12878	blood:	n/a	n/a
45	BHLHE40	chr11:94186624-94186760	GM12878	blood:	n/a	n/a
46	BHLHE40	chr11:94192797-94193020	GM12878	blood:	n/a	n/a
47	BRCA1	chr11:94226371-94227630	H1-hESC	embryonic stem cell:	n/a	chr11:94227016-94227025
48	BRCA1	chr11:94226675-94227414	GM12878	blood:	n/a	chr11:94227016-94227025
49	BRCA1	chr11:94226782-94227267	HepG2	liver:	n/a	chr11:94227016-94227025
50	BRCA1	chr11:94226214-94228062	Hela-S3	cervix:	n/a	chr11:94227016-94227025

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:94226991-94227041	BE2_C	brain:	n/a
2	chr11:94227380-94227430	HEEpiC	esophagus:	n/a
3	chr11:94226991-94227041	BE2_C	brain:	n/a
4	chr11:94227380-94227430	HEEpiC	esophagus:	n/a
5	chr11:94226537-94226587	IMR90	lung:	fetal
6	chr11:94227125-94227175	HCT-116	colon:	n/a
7	chr11:94227380-94227430	AG04449	skin:	fetal
8	chr11:94227038-94227088	ovcar-3	ovarian:	n/a
9	chr11:94227583-94227633	K562	blood:	n/a
10	chr11:94227180-94227230	AG09309	skin:	n/a
11	chr11:94224044-94224094	U87	brain:	n/a
12	chr11:94227183-94227233	GM06990	blood:	n/a
13	chr11:94227106-94227156	ECC-1	luminal epithelium:	n/a
14	chr11:94227320-94227370	HIPEpiC	eye:	n/a
15	chr11:94227109-94227159	NB4	blood:	n/a
16	chr11:94226991-94227041	HRPEpiC	eye:	n/a
17	chr11:94227180-94227230	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:94226767-94226817	LNCaP	prostate:	n/a
19	chr11:94226537-94226587	Hepatocyte	liver:	n/a
20	chr11:94227125-94227175	HCF	heart:	n/a
21	chr11:94227183-94227233	SK-N-MC	brain:	n/a
22	chr11:94227109-94227159	ProgFib	skin:	n/a
23	chr11:94227320-94227370	K562	blood:	n/a
24	chr11:94227180-94227230	A549	lung:	n/a
25	chr11:94227125-94227175	LNCaP	prostate:	n/a
26	chr11:94227081-94227131	NB4	blood:	n/a
27	chr11:94226925-94226975	HCM	heart:	n/a
28	chr11:94226537-94226587	HRPEpiC	eye:	n/a
29	chr11:94226991-94227041	LNCaP	prostate:	n/a
30	chr11:94226767-94226817	Jurkat	blood:	n/a
31	chr11:94226991-94227041	ovcar-3	ovarian:	n/a
32	chr11:94226925-94226975	AG09319	gingival:	n/a
33	chr11:94226991-94227041	SK-N-MC	brain:	n/a
34	chr11:94226991-94227041	HCM	heart:	n/a
35	chr11:94227081-94227131	GM19239	blood:	n/a
36	chr11:94226767-94226817	BE2_C	brain:	n/a
37	chr11:94227109-94227159	SKMC	muscle:	n/a
38	chr11:94227380-94227430	HCT-116	colon:	n/a
39	chr11:94227320-94227370	NB4	blood:	n/a
40	chr11:94226925-94226975	SK-N-MC	brain:	n/a
41	chr11:94227180-94227230	RPTEC	kidney:	n/a
42	chr11:94227180-94227230	ECC-1	luminal epithelium:	n/a
43	chr11:94227183-94227233	HEK293	kidney:	embryo
44	chr11:94227109-94227159	HEK293	kidney:	embryo
45	chr11:94227125-94227175	NHDF-neo	bronchial:	n/a
46	chr11:94207287-94207337	HIPEpiC	eye:	n/a
47	chr11:94227380-94227430	ProgFib	skin:	n/a
48	chr11:94227106-94227156	IMR90	lung:	fetal
49	chr11:94226537-94226587	HAEpiC	amniotic membrane:	n/a
50	chr11:94227006-94227056	BJ	skin:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:93473689..93475609-chr11:94224502..94227416,2	K562	blood:
2	chr11:94223520..94226395-chr11:94275795..94278274,2	K562	blood:
3	chr11:94217659..94221782-chr11:94225032..94227665,4	K562	blood:
4	chr11:94213824..94217124-chr11:94225921..94227775,3	MCF-7	breast:
5	chr11:94183974..94185530-chr11:94194298..94197151,2	K562	blood:
6	chr11:94222232..94224873-chr11:94225304..94228914,3	K562	blood:
7	chr11:94213539..94215601-chr11:94228089..94230235,2	K562	blood:
8	chr11:94209182..94211578-chr11:94214221..94216536,2	K562	blood:
9	chr11:94183974..94185530-chr11:94194298..94197151,2	K562	blood:
10	chr11:94210078..94211620-chr11:94214056..94215721,2	K562	blood:
11	chr11:94226771..94229140-chr11:94275887..94279295,4	K562	blood:
12	chr11:94208946..94211928-chr11:94232056..94233967,2	MCF-7	breast:
13	chr11:94185882..94188334-chr11:94225104..94227120,2	K562	blood:
14	chr11:94213347..94215361-chr11:94222222..94224695,2	K562	blood:
15	chr11:94219618..94222085-chr11:94222930..94224543,2	K562	blood:
16	chr11:94200661..94202892-chr11:94224214..94225865,2	K562	blood:
17	chr11:94190407..94192299-chr11:94225577..94228062,2	K562	blood:
18	chr11:94202207..94203763-chr11:94208218..94210423,2	K562	blood:
19	chr11:94208132..94210778-chr19:13263700..13265621,2	K562	blood:
20	chr11:94205860..94208809-chr11:94208935..94211441,2	K562	blood:
21	chr11:94217826..94221118-chr11:94222264..94225071,4	K562	blood:
22	chr11:94202180..94204828-chr11:94212256..94213888,2	K562	blood:
23	chr11:93860234..93863458-chr11:94225545..94228425,3	K562	blood:
24	chr11:94187673..94189503-chr11:94190154..94193053,2	K562	blood:
25	chr11:94219714..94224180-chr11:94224527..94226991,4	MCF-7	breast:
26	chr11:94226700..94227357-chr19:7293430..7294141,2	Hela-S3	cervix:
27	chr11:94200661..94202892-chr11:94224214..94225865,2	K562	blood:
28	chr11:94225979..94229384-chr11:94230397..94235421,9	K562	blood:
29	chr11:94181248..94183636-chr11:94224875..94226934,2	MCF-7	breast:
30	chr11:94198479..94200826-chr11:94200987..94202578,2	K562	blood:
31	chr11:94210098..94212202-chr11:94216700..94218600,2	K562	blood:
32	chr11:94217826..94221118-chr11:94222264..94225071,4	K562	blood:
33	chr11:94226544..94227246-chr17:33904994..33905713,2	Hela-S3	cervix:
34	chr11:94210098..94212202-chr11:94216700..94218600,2	K562	blood:
35	chr11:94225466..94228271-chr11:94275709..94278301,3	K562	blood:
36	chr11:94226137..94228706-chr11:94300541..94302920,2	K562	blood:
37	chr11:94213347..94215361-chr11:94222222..94224695,2	K562	blood:
38	chr11:94213449..94216550-chr11:94217098..94220299,3	K562	blood:
39	chr11:94209182..94211578-chr11:94214221..94216536,2	K562	blood:
40	chr11:94202180..94204828-chr11:94212256..94213888,2	K562	blood:
41	chr11:94226287..94227152-chr12:49524847..49525416,2	Hela-S3	cervix:
42	chr11:94213449..94216550-chr11:94217098..94220299,3	K562	blood:
43	chr11:94219618..94222085-chr11:94222930..94224543,2	K562	blood:
44	chr11:94180184..94182302-chr11:94227182..94229296,2	K562	blood:
45	chr11:93914625..93916953-chr11:94227203..94228744,2	MCF-7	breast:
46	chr11:93472910..93474648-chr11:94197238..94199366,2	MCF-7	breast:
47	chr11:94210078..94211620-chr11:94214056..94215721,2	K562	blood:
48	chr11:94187673..94189503-chr11:94190154..94193053,2	K562	blood:
49	chr11:94202207..94203763-chr11:94208218..94210423,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR83-1	chr11:94206074-94206627	ENSG00000255893.1
2	lnc-GPR83-1	chr11:94206710-94206736	ENSG00000255893.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548l	chr11:94199711-94199732	MIMAT0005889

No data

Variant related genes	Relation type
ENSG00000255893	TF binding region
ANKRD49	TF binding region
MRE11A	TF binding region
MIR548L	TF binding region
ENSG00000255893	CpG island
ANKRD49	CpG island
MRE11A	CpG island
MIR548L	CpG island
ENSG00000196371	chromatin interactions
ENSG00000110218	chromatin interactions
ENSG00000166012	chromatin interactions
ENSG00000020922	chromatin interactions
ENSG00000168876	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000221230	chromatin interactions
ENSG00000171105	chromatin interactions
ENSG00000182919	chromatin interactions
ENSG00000108733	chromatin interactions
ENSG00000258017	chromatin interactions
ENSG00000134627	chromatin interactions
ENSG00000255893	chromatin interactions
ENSG00000267598	chromatin interactions
ENSG00000123416	chromatin interactions

Extended variants
information (count: 1770 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1770 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs499952	chr11:94182992-94182993	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs553287267	chr11:94183000-94183001	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs560420754	chr11:94183023-94183024	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs147414791	chr11:94183080-94183081	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs538869251	chr11:94183102-94183103	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs522596	chr11:94183148-94183149	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs575552103	chr11:94183175-94183176	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76411833	chr11:94183195-94183196	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs569426310	chr11:94183199-94183200	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs145158453	chr11:94183203-94183204	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs369416822	chr11:94183242-94183243	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs187503741	chr11:94183317-94183318	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs551888953	chr11:94183345-94183346	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs191282786	chr11:94183373-94183374	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs77891285	chr11:94183399-94183400	Weak transcription Strong transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs533105843	chr11:94183451-94183452	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs544899325	chr11:94183466-94183467	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143963226	chr11:94183475-94183476	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs111628013	chr11:94183476-94183477	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs548978624	chr11:94183505-94183506	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs370769414	chr11:94183629-94183630	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs560913783	chr11:94183649-94183650	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs369381695	chr11:94183705-94183706	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs528164283	chr11:94183723-94183724	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs546632935	chr11:94183782-94183783	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs7119572	chr11:94183807-94183808	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs374342832	chr11:94183828-94183829	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs562162291	chr11:94183834-94183835	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs201642494	chr11:94183864-94183865	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs148628602	chr11:94183877-94183878	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs372731403	chr11:94183885-94183886	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs142066128	chr11:94183908-94183909	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs113220421	chr11:94183920-94183921	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs2509942	chr11:94183940-94183941	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs184543472	chr11:94184026-94184027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs554893797	chr11:94184032-94184033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141475747	chr11:94184070-94184071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs554535714	chr11:94184073-94184074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs143890311	chr11:94184088-94184089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533947304	chr11:94184139-94184140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs558984729	chr11:94184144-94184145	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577282477	chr11:94184146-94184147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs59302226	chr11:94184201-94184202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs66655623	chr11:94184202-94184203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs372804708	chr11:94184230-94184231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545172649	chr11:94184253-94184254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563503922	chr11:94184254-94184255	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375809790	chr11:94184276-94184277	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537260901	chr11:94184278-94184279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557465074	chr11:94184287-94184288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Mantle cell lymphoma	19029149	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1642 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:94152200-94206200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr11:94154400-94183600	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr11:94157400-94194200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr11:94157400-94216600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr11:94157400-94226200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:94157600-94226400	Weak transcription	Esophagus	oesophagus
7	chr11:94161000-94183000	Strong transcription	Dnd41	blood
8	chr11:94162800-94216400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:94162800-94225800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr11:94163000-94186000	Weak transcription	Fetal Brain Male	brain
11	chr11:94163000-94192800	Weak transcription	HSMMtube	muscle
12	chr11:94163000-94199200	Weak transcription	Brain Cingulate Gyrus	brain
13	chr11:94163000-94206000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr11:94163000-94207200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr11:94163400-94221000	Weak transcription	Psoas Muscle	Psoas
16	chr11:94166600-94216400	Weak transcription	Gastric	stomach
17	chr11:94166800-94202200	Weak transcription	Stomach Mucosa	stomach
18	chr11:94167200-94206000	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr11:94167400-94226400	Weak transcription	Small Intestine	intestine
20	chr11:94167600-94206000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr11:94168800-94191000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr11:94169800-94199000	Weak transcription	Rectal Smooth Muscle	rectum
23	chr11:94169800-94215400	Weak transcription	Brain Angular Gyrus	brain
24	chr11:94170000-94192600	Weak transcription	Aorta	Aorta
25	chr11:94170000-94192800	Weak transcription	Right Ventricle	heart
26	chr11:94170000-94192800	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr11:94170000-94194200	Weak transcription	Spleen	Spleen
28	chr11:94170200-94192400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr11:94170400-94192200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr11:94171200-94183000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:94172200-94190200	Weak transcription	K562	blood
32	chr11:94172400-94183200	Strong transcription	Primary T cells from cord blood	blood
33	chr11:94172800-94183000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr11:94172800-94183200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr11:94175600-94183000	Strong transcription	Duodenum Mucosa	Duodenum
36	chr11:94175600-94183200	Strong transcription	Primary monocytes fromperipheralblood	blood
37	chr11:94175800-94183000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr11:94177800-94192600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr11:94178400-94192800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr11:94178400-94221600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr11:94178600-94189200	Weak transcription	Stomach Smooth Muscle	stomach
42	chr11:94178600-94192400	Weak transcription	HUVEC	blood vessel
43	chr11:94179000-94192600	Weak transcription	Brain Hippocampus Middle	brain
44	chr11:94179000-94192600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr11:94179000-94226000	Weak transcription	Colonic Mucosa	Colon
46	chr11:94179200-94186400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr11:94179200-94186400	Weak transcription	Fetal Kidney	kidney
48	chr11:94179200-94189800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr11:94179200-94199000	Weak transcription	Fetal Brain Female	brain
50	chr11:94179200-94200000	Weak transcription	Skeletal Muscle Female	skeletal muscle

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