Variant report

Variant	nsv428041
Chromosome Location	chr2:63027947-63206574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1112)
CpG islands
(count:122)
Chromatin interactive
region (count:39)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1112 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:63147182-63147609	K562	blood:	n/a	n/a
2	ARID3A	chr2:63098672-63098993	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:63193989-63194437	K562	blood:	n/a	n/a
4	ATF1	chr2:63085452-63085932	K562	blood:	n/a	n/a
5	ATF1	chr2:63029057-63029178	K562	blood:	n/a	n/a
6	ATF1	chr2:63147293-63147470	K562	blood:	n/a	n/a
7	ATF3	chr2:63147194-63147545	K562	blood:	n/a	n/a
8	BACH1	chr2:63196006-63196075	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:63124572-63124603	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:63180920-63180935	K562	blood:	n/a	n/a
11	BACH1	chr2:63147261-63147506	K562	blood:	n/a	n/a
12	BATF	chr2:63058894-63059246	GM12878	blood:	n/a	chr2:63059088-63059099 chr2:63059022-63059033
13	BATF	chr2:63058916-63059191	GM12878	blood:	n/a	chr2:63059088-63059099 chr2:63059022-63059033
14	BATF	chr2:63027869-63028186	GM12878	blood:	n/a	n/a
15	BCL11A	chr2:63058818-63059229	GM12878	blood:	n/a	n/a
16	BCL11A	chr2:63155159-63155435	GM12878	blood:	n/a	n/a
17	BHLHE40	chr2:63042597-63042611	GM12878	blood:	n/a	n/a
18	BHLHE40	chr2:63194100-63194450	K562	blood:	n/a	n/a
19	BHLHE40	chr2:63155122-63155516	GM12878	blood:	n/a	n/a
20	BHLHE40	chr2:63155306-63155393	K562	blood:	n/a	n/a
21	BHLHE40	chr2:63028047-63028071	A549	lung:	n/a	n/a
22	BRCA1	chr2:63040277-63040301	GM12878	blood:	n/a	n/a
23	BRCA1	chr2:63192117-63192192	Hela-S3	cervix:	n/a	n/a
24	CBX3	chr2:63146934-63147651	K562	blood:	n/a	n/a
25	CBX3	chr2:63155169-63155513	K562	blood:	n/a	n/a
26	CBX3	chr2:63098671-63099100	HCT-116	colon:	n/a	n/a
27	CBX3	chr2:63098576-63099076	HCT-116	colon:	n/a	n/a
28	CCNT2	chr2:63147382-63147511	K562	blood:	n/a	n/a
29	CCNT2	chr2:63174632-63174975	K562	blood:	n/a	n/a
30	CCNT2	chr2:63194089-63194445	K562	blood:	n/a	chr2:63194280-63194300
31	CCNT2	chr2:63085538-63085958	K562	blood:	n/a	n/a
32	CEBPB	chr2:63112155-63112236	HepG2	liver:	n/a	n/a
33	CEBPB	chr2:63029241-63029577	A549	lung:	n/a	n/a
34	CEBPB	chr2:63176488-63176738	IMR90	lung:	n/a	chr2:63176630-63176641 chr2:63176632-63176641 chr2:63176631-63176642
35	CEBPB	chr2:63176501-63176696	A549	lung:	n/a	chr2:63176630-63176641 chr2:63176632-63176641 chr2:63176631-63176642
36	CEBPB	chr2:63093255-63093335	K562	blood:	n/a	chr2:63093283-63093294
37	CEBPB	chr2:63119178-63119372	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr2:63188991-63189181	A549	lung:	n/a	chr2:63189113-63189124
39	CEBPB	chr2:63189097-63189130	H1-hESC	embryonic stem cell:	n/a	chr2:63189113-63189124
40	CEBPB	chr2:63122780-63122984	Hela-S3	cervix:	n/a	chr2:63122876-63122887
41	CEBPB	chr2:63194125-63194490	K562	blood:	n/a	n/a
42	CEBPB	chr2:63176491-63176778	K562	blood:	n/a	chr2:63176630-63176641 chr2:63176632-63176641 chr2:63176631-63176642
43	CEBPB	chr2:63033411-63033707	K562	blood:	n/a	chr2:63033561-63033572
44	CEBPB	chr2:63093201-63093421	H1-hESC	embryonic stem cell:	n/a	chr2:63093283-63093294
45	CEBPB	chr2:63098558-63098994	A549	lung:	n/a	chr2:63098808-63098819
46	CEBPB	chr2:63122687-63123116	IMR90	lung:	n/a	chr2:63122876-63122887
47	CEBPB	chr2:63194127-63194419	K562	blood:	n/a	n/a
48	CEBPB	chr2:63033410-63033720	H1-hESC	embryonic stem cell:	n/a	chr2:63033561-63033572
49	CEBPB	chr2:63033307-63033883	HCT-116	colon:	n/a	chr2:63033561-63033572
50	CEBPB	chr2:63160555-63160909	A549	lung:	n/a	chr2:63160738-63160749

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:63054079-63054129	T-47D	breast:	n/a
2	chr2:63054079-63054129	HEK293	kidney:	embryo
3	chr2:63198779-63198829	GM12878	blood:	n/a
4	chr2:63198779-63198829	K562	blood:	n/a
5	chr2:63054079-63054129	PFSK-1	brain:	n/a
6	chr2:63054079-63054129	GM06990	blood:	n/a
7	chr2:63198779-63198829	NH-A	brain:	n/a
8	chr2:63054079-63054129	BJ	skin:	n/a
9	chr2:63054079-63054129	U87	brain:	n/a
10	chr2:63054079-63054129	HRPEpiC	eye:	n/a
11	chr2:63054079-63054129	NH-A	brain:	n/a
12	chr2:63198779-63198829	LNCaP	prostate:	n/a
13	chr2:63198779-63198829	HCF	heart:	n/a
14	chr2:63198779-63198829	IMR90	lung:	fetal
15	chr2:63198779-63198829	AG09309	skin:	n/a
16	chr2:63198779-63198829	A549	lung:	n/a
17	chr2:63198779-63198829	HCT-116	colon:	n/a
18	chr2:63198779-63198829	HMEC	breast:	n/a
19	chr2:63198779-63198829	HUVEC	blood vessel:	n/a
20	chr2:63198779-63198829	U87	brain:	n/a
21	chr2:63198779-63198829	SK-N-MC	brain:	n/a
22	chr2:63054079-63054129	HCPEpiC	choroid plexus:	n/a
23	chr2:63198779-63198829	NT2-D1	testis:	n/a
24	chr2:63054079-63054129	HEEpiC	esophagus:	n/a
25	chr2:63054079-63054129	HMEC	breast:	n/a
26	chr2:63054079-63054129	SK-N-MC	brain:	n/a
27	chr2:63054079-63054129	H1-hESC	embryonic stem cell:	embryo
28	chr2:63198779-63198829	ECC-1	luminal epithelium:	n/a
29	chr2:63198779-63198829	AoSMC	blood vessel:	n/a
30	chr2:63054079-63054129	Caco-2	colon:	n/a
31	chr2:63054079-63054129	BE2_C	brain:	n/a
32	chr2:63198779-63198829	NB4	blood:	n/a
33	chr2:63054079-63054129	GM12878	blood:	n/a
34	chr2:63054079-63054129	Hepatocyte	liver:	n/a
35	chr2:63054079-63054129	MCF10A-Er-Src	breast:	n/a
36	chr2:63054079-63054129	IMR90	lung:	fetal
37	chr2:63054079-63054129	A549	lung:	n/a
38	chr2:63198779-63198829	HEEpiC	esophagus:	n/a
39	chr2:63198779-63198829	GM12892	blood:	n/a
40	chr2:63054079-63054129	PANC-1	pancreas:	n/a
41	chr2:63198779-63198829	Hepatocyte	liver:	n/a
42	chr2:63054079-63054129	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:63054079-63054129	AG10803	skin:	n/a
44	chr2:63198779-63198829	SAEC	small airway:	n/a
45	chr2:63198779-63198829	HPAEpiC	pulmonary alveolar:	n/a
46	chr2:63054079-63054129	HCM	heart:	n/a
47	chr2:63198779-63198829	AG04449	skin:	fetal
48	chr2:63054079-63054129	HIPEpiC	eye:	n/a
49	chr2:63054079-63054129	HRCEpiC	kidney:	n/a
50	chr2:63054079-63054129	ovcar-3	ovarian:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:63133462..63135677-chr2:63137317..63139030,2	K562	blood:
2	chr2:63117694..63119578-chr2:63120956..63124175,3	K562	blood:
3	chr2:63048902..63052950-chr2:63053080..63055706,3	MCF-7	breast:
4	chr2:63075968..63078397-chr2:63103396..63106295,2	K562	blood:
5	chr2:63022334..63025310-chr2:63029781..63031632,2	K562	blood:
6	chr2:63191776..63193498-chr2:63200792..63203464,2	K562	blood:
7	chr2:63124782..63127343-chr2:63145602..63147733,2	K562	blood:
8	chr2:63183438..63186080-chr2:63202635..63205180,2	MCF-7	breast:
9	chr2:63075968..63078397-chr2:63103396..63106295,2	K562	blood:
10	chr2:63164960..63167848-chr2:63174412..63177357,2	K562	blood:
11	chr2:63117694..63119578-chr2:63120956..63124175,3	K562	blood:
12	chr2:63117183..63119296-chr2:63120402..63122456,2	K562	blood:
13	chr2:63164960..63167848-chr2:63174412..63177357,2	K562	blood:
14	chr2:62931425..62934210-chr2:63054270..63056290,2	K562	blood:
15	chr2:63137511..63140178-chr2:63144215..63146349,2	K562	blood:
16	chr2:63048902..63052950-chr2:63053080..63055706,3	MCF-7	breast:
17	chr2:63100581..63102591-chr2:63109262..63110838,2	K562	blood:
18	chr2:63073137..63075941-chr2:63076155..63077726,2	K562	blood:
19	chr2:63162041..63163676-chr2:63176897..63178564,2	K562	blood:
20	chr2:63162041..63163676-chr2:63176897..63178564,2	K562	blood:
21	chr2:63153391..63155926-chr2:63157542..63159626,2	MCF-7	breast:
22	chr2:63100581..63102591-chr2:63109262..63110838,2	K562	blood:
23	chr2:63117183..63119296-chr2:63120402..63122456,2	K562	blood:
24	chr2:63117999..63119855-chr2:63122529..63125407,3	K562	blood:
25	chr2:63183438..63186080-chr2:63202635..63205180,2	MCF-7	breast:
26	chr2:63133462..63135677-chr2:63137317..63139030,2	K562	blood:
27	chr2:63191784..63193400-chr2:63196726..63198557,2	K562	blood:
28	chr2:63153752..63155559-chr2:63158267..63160556,2	K562	blood:
29	chr2:63153391..63155926-chr2:63157542..63159626,2	MCF-7	breast:
30	chr2:62683948..62684543-chr2:63029469..63030266,2	K562	blood:
31	chr2:63113535..63116069-chr2:63274358..63277343,2	K562	blood:
32	chr2:63122000..63124046-chr2:63128331..63130829,2	MCF-7	breast:
33	chr2:63117999..63119855-chr2:63122529..63125407,3	K562	blood:
34	chr2:63073137..63075941-chr2:63076155..63077726,2	K562	blood:
35	chr2:62931568..62934164-chr2:63117410..63120199,2	K562	blood:
36	chr2:63137511..63140178-chr2:63144215..63146349,2	K562	blood:
37	chr2:63153752..63155559-chr2:63158267..63160556,2	K562	blood:
38	chr2:63122000..63124046-chr2:63128331..63130829,2	MCF-7	breast:
39	chr2:63124782..63127343-chr2:63145602..63147733,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDPCP-2	chr2:63085508-63085573	ENSG00000226605.1
2	lnc-WDPCP-2	chr2:63053199-63053383	ENSG00000226605.1
3	lnc-OTX1-6	chr2:63047595-63047839	uc_64_+
4	lnc-WDPCP-7	chr2:63126676-63126780	refGeneNc_632_NR_027069
5	lnc-WDPCP-7	chr2:63124611-63126082	refGeneNc_632_NR_027069
6	lnc-WDPCP-7	chr2:63127121-63127286	refGeneNc_632_NR_027069
7	lnc-WDPCP-7	chr2:63128075-63128350	refGeneNc_632_NR_027069
8	lnc-WDPCP-8	chr2:63047595-63047839	uc_64_-
9	lnc-OTX1-4	chr2:63167051-63167417	NONHSAT071040

No data

Variant related genes	Relation type
EHBP1	TF binding region
ENSG00000226605	TF binding region
ENSG00000237162	TF binding region
EHBP1	CpG island
ENSG00000226605	CpG island
ENSG00000237162	CpG island
ENSG00000237162	chromatin interactions
ENSG00000115504	chromatin interactions
ENSG00000115507	chromatin interactions
ENSG00000231609	chromatin interactions

Extended variants
information (count: 5687 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:5687 , 50 per page) page: 1 2 3 4 5 6 7 ... 114

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568155189	chr2:63027960-63027961	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182969945	chr2:63027963-63027964	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs536399297	chr2:63027965-63027966	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs145971985	chr2:63027980-63027981	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs566817334	chr2:63028038-63028039	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534258499	chr2:63028181-63028182	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs558892509	chr2:63028194-63028195	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs577141512	chr2:63028212-63028213	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187641978	chr2:63028272-63028273	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs138355621	chr2:63028318-63028319	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574991406	chr2:63028346-63028347	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs192693050	chr2:63028355-63028356	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs542035800	chr2:63028377-63028378	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs560423114	chr2:63028397-63028398	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575137296	chr2:63028401-63028402	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs545751438	chr2:63028414-63028415	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs144460435	chr2:63028421-63028422	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs531165154	chr2:63028423-63028424	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs112956613	chr2:63028424-63028425	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs148580327	chr2:63028429-63028430	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567811219	chr2:63028483-63028484	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528998153	chr2:63028536-63028537	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548361477	chr2:63028548-63028549	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566754318	chr2:63028550-63028551	Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534425935	chr2:63028601-63028602	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552560299	chr2:63028679-63028680	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571133660	chr2:63028739-63028740	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs537805897	chr2:63028765-63028766	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs556560139	chr2:63028772-63028773	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs574969129	chr2:63028791-63028792	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535980872	chr2:63028845-63028846	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144120808	chr2:63028846-63028847	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs5831647	chr2:63028941-63028942	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184685787	chr2:63028945-63028946	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs563892936	chr2:63029050-63029051	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577891247	chr2:63029071-63029072	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147290247	chr2:63029072-63029073	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188027635	chr2:63029083-63029084	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75314299	chr2:63029111-63029112	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561383800	chr2:63029179-63029180	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs528936206	chr2:63029250-63029251	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs540124982	chr2:63029294-63029295	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs547065272	chr2:63029368-63029369	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs562427022	chr2:63029377-63029378	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs374767837	chr2:63029378-63029379	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559038049	chr2:63029406-63029407	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs527841204	chr2:63029439-63029440	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs552742846	chr2:63029441-63029442	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs571055623	chr2:63029561-63029562	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs111731944	chr2:63029570-63029571	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

Disease	PMID	Source
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:2886 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:62982200-63033400	Weak transcription	Fetal Intestine Large	intestine
2	chr2:63010800-63032800	Weak transcription	Primary hematopoietic stem cells	blood
3	chr2:63017000-63029000	Weak transcription	Ovary	ovary
4	chr2:63017000-63032600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr2:63017000-63033400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:63017000-63037400	Weak transcription	NHLF	lung
7	chr2:63017400-63032800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr2:63017400-63049400	Weak transcription	Fetal Heart	heart
9	chr2:63018200-63033400	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr2:63019600-63043400	Weak transcription	Brain Angular Gyrus	brain
11	chr2:63020600-63082000	Weak transcription	Pancreas	Pancrea
12	chr2:63020800-63040200	Weak transcription	Left Ventricle	heart
13	chr2:63022200-63029000	Weak transcription	Osteobl	bone
14	chr2:63022400-63040400	Weak transcription	NHEK	skin
15	chr2:63022400-63041000	Weak transcription	HSMM	muscle
16	chr2:63022600-63029200	Weak transcription	Small Intestine	intestine
17	chr2:63022600-63031800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:63022600-63032800	Weak transcription	Fetal Intestine Small	intestine
19	chr2:63022800-63028200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr2:63022800-63029000	Weak transcription	HMEC	breast
21	chr2:63022800-63032000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr2:63022800-63032800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr2:63022800-63032800	Weak transcription	Fetal Lung	lung
24	chr2:63022800-63033000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:63022800-63034400	Weak transcription	Primary B cells from cord blood	blood
26	chr2:63022800-63035800	Weak transcription	Fetal Kidney	kidney
27	chr2:63023400-63029200	Weak transcription	Adipose Nuclei	Adipose
28	chr2:63023800-63049000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr2:63024000-63032800	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr2:63025000-63028000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr2:63025000-63028400	Weak transcription	NHDF-Ad	bronchial
32	chr2:63025200-63029200	Weak transcription	Stomach Mucosa	stomach
33	chr2:63026200-63029000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr2:63026200-63034200	Strong transcription	HepG2	liver
35	chr2:63027000-63028400	Genic enhancers	A549	lung
36	chr2:63027000-63028600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
37	chr2:63027200-63028000	Enhancers	Primary T helper cells fromperipheralblood	blood
38	chr2:63027200-63028600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr2:63027200-63029600	Enhancers	Liver	Liver
40	chr2:63027400-63028000	Enhancers	Colon Smooth Muscle	Colon
41	chr2:63027400-63029000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr2:63027400-63029200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr2:63027400-63030000	Enhancers	GM12878-XiMat	blood
44	chr2:63027400-63032800	Weak transcription	Primary T cells from cord blood	blood
45	chr2:63027800-63028800	Enhancers	Primary T killer memory cells from peripheral blood	blood
46	chr2:63027800-63029600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
47	chr2:63027800-63029600	Enhancers	Primary T helper cells PMA-I stimulated	--
48	chr2:63027800-63030400	Flanking Active TSS	Dnd41	blood
49	chr2:63028000-63028600	Enhancers	Brain Substantia Nigra	brain
50	chr2:63028000-63028600	Enhancers	Pancreatic Islets	Pancreatic Islet

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