Variant report

Variant	nsv898365
Chromosome Location	chr11:106944975-107430300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2015)
CpG islands
(count:1223)
Chromatin interactive
region (count:105)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2015 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:107114621-107115003	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:107328280-107328788	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:107073929-107074099	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:107328127-107328887	K562	blood:	n/a	n/a
5	ARID3A	chr11:107028240-107028924	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:107420016-107420307	K562	blood:	n/a	n/a
7	ARID3A	chr11:107067338-107067971	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:107298678-107298818	K562	blood:	n/a	n/a
9	ARID3A	chr11:107372561-107372562	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:107256191-107256678	HepG2	liver:	n/a	n/a
11	ARID3A	chr11:107068416-107069073	HepG2	liver:	n/a	n/a
12	ARID3A	chr11:107279204-107280430	HepG2	liver:	n/a	n/a
13	ARID3A	chr11:107073226-107073508	HepG2	liver:	n/a	n/a
14	ARID3A	chr11:107401280-107401282	K562	blood:	n/a	n/a
15	ARID3A	chr11:107298390-107298697	HepG2	liver:	n/a	n/a
16	ARID3A	chr11:107125887-107126018	K562	blood:	n/a	n/a
17	ATF1	chr11:107240708-107240809	K562	blood:	n/a	n/a
18	ATF1	chr11:107298560-107298761	K562	blood:	n/a	n/a
19	ATF1	chr11:107328463-107328763	K562	blood:	n/a	n/a
20	ATF1	chr11:107359188-107359352	K562	blood:	n/a	n/a
21	ATF1	chr11:107411871-107411961	K562	blood:	n/a	n/a
22	ATF1	chr11:107119900-107120053	K562	blood:	n/a	n/a
23	ATF1	chr11:107118328-107118368	K562	blood:	n/a	n/a
24	ATF2	chr11:107419878-107420193	GM12878	blood:	n/a	n/a
25	ATF2	chr11:107328307-107328946	GM12878	blood:	n/a	n/a
26	ATF2	chr11:107241054-107241483	GM12878	blood:	n/a	n/a
27	ATF3	chr11:107328396-107328669	HepG2	liver:	n/a	n/a
28	ATF3	chr11:107328243-107328841	HepG2	liver:	n/a	n/a
29	ATF3	chr11:107328394-107328774	H1-hESC	embryonic stem cell:	n/a	n/a
30	ATF3	chr11:107328369-107328693	GM12878	blood:	n/a	n/a
31	ATF3	chr11:107328251-107328813	GM12878	blood:	n/a	n/a
32	ATF3	chr11:107328335-107328738	H1-hESC	embryonic stem cell:	n/a	n/a
33	ATF3	chr11:107328375-107328670	K562	blood:	n/a	n/a
34	BACH1	chr11:107267990-107268348	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr11:106987326-106987333	K562	blood:	n/a	n/a
36	BACH1	chr11:107011043-107011106	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr11:107161599-107161648	K562	blood:	n/a	n/a
38	BATF	chr11:107134920-107135143	GM12878	blood:	n/a	chr11:107134970-107134980
39	BATF	chr11:106988737-106989031	GM12878	blood:	n/a	chr11:106988893-106988904
40	BHLHE40	chr11:107123612-107123903	GM12878	blood:	n/a	n/a
41	BHLHE40	chr11:107298617-107298890	K562	blood:	n/a	n/a
42	BHLHE40	chr11:107419983-107420258	GM12878	blood:	n/a	n/a
43	BHLHE40	chr11:107123579-107123932	K562	blood:	n/a	n/a
44	BHLHE40	chr11:107328231-107328803	K562	blood:	n/a	n/a
45	BHLHE40	chr11:107279399-107279754	HepG2	liver:	n/a	n/a
46	BHLHE40	chr11:107130509-107130831	K562	blood:	n/a	n/a
47	BHLHE40	chr11:107120661-107120879	K562	blood:	n/a	n/a
48	BHLHE40	chr11:107125712-107125922	K562	blood:	n/a	n/a
49	BRCA1	chr11:107328002-107328799	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr11:107363833-107364256	HCT-116	colon:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:107328605-107328655	ovcar-3	ovarian:	n/a
2	chr11:107047888-107047938	HRE	kidney:	n/a
3	chr11:107328605-107328655	SK-N-MC	brain:	n/a
4	chr11:107328605-107328655	ovcar-3	ovarian:	n/a
5	chr11:107047888-107047938	HRE	kidney:	n/a
6	chr11:107328605-107328655	SK-N-MC	brain:	n/a
7	chr11:107420502-107420552	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:107232729-107232779	SAEC	small airway:	n/a
9	chr11:107232729-107232779	Hela-S3	cervix:	n/a
10	chr11:107328690-107328740	Hepatocyte	liver:	n/a
11	chr11:107044383-107044433	NH-A	brain:	n/a
12	chr11:107420502-107420552	HUVEC	blood vessel:	n/a
13	chr11:107232729-107232779	SK-N-SH	brain:	n/a
14	chr11:107328690-107328740	BJ	skin:	n/a
15	chr11:107232729-107232779	NT2-D1	testis:	n/a
16	chr11:107243587-107243637	SAEC	small airway:	n/a
17	chr11:107328442-107328492	PFSK-1	brain:	n/a
18	chr11:107328586-107328636	HepG2	liver:	n/a
19	chr11:107324751-107324801	NHBE	bronchial:	n/a
20	chr11:107328442-107328492	HCPEpiC	choroid plexus:	n/a
21	chr11:107328690-107328740	Caco-2	colon:	n/a
22	chr11:107331110-107331160	RPTEC	kidney:	n/a
23	chr11:107328442-107328492	H1-hESC	embryonic stem cell:	embryo
24	chr11:107047888-107047938	HEK293	kidney:	embryo
25	chr11:107048184-107048234	NT2-D1	testis:	n/a
26	chr11:107047494-107047544	HRE	kidney:	n/a
27	chr11:107328690-107328740	HMEC	breast:	n/a
28	chr11:107328657-107328707	U87	brain:	n/a
29	chr11:107232729-107232779	H1-hESC	embryonic stem cell:	embryo
30	chr11:107328525-107328575	SKMC	muscle:	n/a
31	chr11:107328690-107328740	HEEpiC	esophagus:	n/a
32	chr11:107328690-107328740	PANC-1	pancreas:	n/a
33	chr11:107328636-107328686	U87	brain:	n/a
34	chr11:107328657-107328707	LNCaP	prostate:	n/a
35	chr11:107328636-107328686	SKMC	muscle:	n/a
36	chr11:107328586-107328636	NHBE	bronchial:	n/a
37	chr11:107232729-107232779	A549	lung:	n/a
38	chr11:107328559-107328609	AG09309	skin:	n/a
39	chr11:107326471-107326521	HCF	heart:	n/a
40	chr11:107328559-107328609	U87	brain:	n/a
41	chr11:107047494-107047544	HRPEpiC	eye:	n/a
42	chr11:107243587-107243637	AG04449	skin:	fetal
43	chr11:107328914-107328964	HPAEpiC	pulmonary alveolar:	n/a
44	chr11:107328559-107328609	T-47D	breast:	n/a
45	chr11:107331110-107331160	HMEC	breast:	n/a
46	chr11:107328525-107328575	Jurkat	blood:	n/a
47	chr11:107328690-107328740	NHBE	bronchial:	n/a
48	chr11:107048184-107048234	K562	blood:	n/a
49	chr11:107047494-107047544	SK-N-SH	brain:	n/a
50	chr11:107328586-107328636	ECC-1	luminal epithelium:	n/a

(count:105 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr11:107297886..107300140-chr11:107301084..107303948,2	K562	blood:
2	chr11:107258832..107260455-chr11:107266741..107268577,2	K562	blood:
3	chr11:107173736..107175485-chr11:107175928..107178317,2	K562	blood:
4	chr11:107216471..107218529-chr11:107219942..107221612,2	K562	blood:
5	chr11:107241951..107244732-chr11:107327122..107328857,2	K562	blood:
6	chr11:107328376..107329012-chr20:10654520..10655433,2	HCT-116	colon:
7	chr11:107284097..107287065-chr11:107292500..107294611,2	MCF-7	breast:
8	chr11:107215828..107218529-chr11:107218963..107221832,3	K562	blood:
9	chr11:107265232..107267832-chr11:107267875..107270757,2	K562	blood:
10	chr11:107294275..107298559-chr11:107301689..107304153,3	K562	blood:
11	chr11:107096224..107098662-chr11:107099428..107101008,2	K562	blood:
12	chr11:107297886..107300140-chr11:107301084..107303948,2	K562	blood:
13	chr11:106989221..106991888-chr11:106999463..107001388,2	K562	blood:
14	chr11:107321712..107323606-chr11:107324966..107327081,2	K562	blood:
15	chr11:107237489..107239255-chr11:107241546..107243344,2	K562	blood:
16	chr11:107146912..107148719-chr11:107151854..107154613,2	MCF-7	breast:
17	chr11:107069683..107071743-chr11:107086703..107088900,2	K562	blood:
18	chr11:107405244..107407798-chr11:107410887..107412865,2	K562	blood:
19	chr11:107342962..107345043-chr11:107346726..107348566,2	K562	blood:
20	chr11:107311896..107313858-chr11:107327138..107329604,2	K562	blood:
21	chr11:106999107..107000959-chr11:107001303..107003964,3	K562	blood:
22	chr11:107402166..107405031-chr11:107412950..107414876,2	K562	blood:
23	chr11:107282183..107285508-chr11:107287409..107291356,4	K562	blood:
24	chr11:107096224..107098662-chr11:107099428..107101008,2	K562	blood:
25	chr11:107321712..107323606-chr11:107324966..107327081,2	K562	blood:
26	chr11:107173736..107175485-chr11:107175928..107178317,2	K562	blood:
27	chr11:107420177..107420684-chr11:107560050..107560867,2	MCF-7	breast:
28	chr11:107419756..107420397-chr11:107769086..107769608,2	K562	blood:
29	chr11:107308119..107310078-chr11:107327101..107329844,2	K562	blood:
30	chr11:107321719..107323399-chr11:107326158..107328000,2	MCF-7	breast:
31	chr11:107374400..107376459-chr11:107377850..107380613,2	K562	blood:
32	chr11:106989221..106991888-chr11:106999463..107001388,2	K562	blood:
33	chr11:107321712..107324920-chr11:107324966..107329578,5	K562	blood:
34	chr11:107123368..107125286-chr11:107129770..107131910,2	K562	blood:
35	chr11:107121227..107123059-chr11:107129085..107131752,2	K562	blood:
36	chr11:107423484..107425068-chr11:107427739..107430641,2	K562	blood:
37	chr11:107424774..107426508-chr11:107431508..107433789,2	K562	blood:
38	chr11:107290994..107293212-chr11:107294451..107296538,3	K562	blood:
39	chr11:107213050..107215630-chr11:107219007..107221031,2	K562	blood:
40	chr11:107411230..107412987-chr11:107414940..107417572,2	K562	blood:
41	chr1:28908024..28908798-chr11:107328064..107328889,2	HCT-116	colon:
42	chr11:107146912..107148719-chr11:107151854..107154613,2	MCF-7	breast:
43	chr11:107399887..107402432-chr11:107404521..107406655,2	K562	blood:
44	chr11:107237489..107239255-chr11:107241546..107243344,2	K562	blood:
45	chr11:107374400..107376459-chr11:107377850..107380613,2	K562	blood:
46	chr11:107316142..107319127-chr11:107320782..107322583,2	K562	blood:
47	chr11:107285740..107288014-chr11:107318312..107321068,2	K562	blood:
48	chr11:107069683..107071743-chr11:107086703..107088900,2	K562	blood:
49	chr11:107290994..107293212-chr11:107294451..107296538,3	K562	blood:
50	chr11:107292984..107295950-chr11:107297622..107299672,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CWF19L2-1	chr11:107184094-107184136	NONHSAT023993
2	lnc-CWF19L2-1	chr11:107181806-107181958	XLOC_009544
3	lnc-CWF19L2-1	chr11:107182858-107186997	ENSG00000261098.1
4	lnc-CWF19L2-1	chr11:107182073-107186290	XLOC_009544
5	lnc-CWF19L2-2	chr11:107384618-107385205	predAs_engstrom06_BG031574_1
6	lnc-CWF19L2-1	chr11:107184592-107184806	NONHSAT023993
7	lnc-CWF19L2-1	chr11:107183057-107184045	NONHSAT023993

No data

Variant related genes	Relation type
ENSG00000261098	TF binding region
SMARCE1P1	TF binding region
ENSG00000255353	TF binding region
CWF19L2	TF binding region
ENSG00000261098	CpG island
SMARCE1P1	CpG island
ENSG00000255353	CpG island
CWF19L2	CpG island
ENSG00000137760	chromatin interactions
ENSG00000197989	chromatin interactions
ENSG00000152404	chromatin interactions
ENSG00000101384	chromatin interactions

Extended variants
information (count: 13682 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:13682 , 50 per page) page: 1 2 3 4 5 6 7 ... 274

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376215109	chr11:106962406-106962407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75121761	chr11:106962471-106962472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs373707398	chr11:106962482-106962483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182105862	chr11:106962484-106962485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs554022818	chr11:106962496-106962497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs541801706	chr11:106962514-106962515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs73000321	chr11:106962523-106962524	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs186660610	chr11:106962528-106962529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554592919	chr11:106962544-106962545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74716022	chr11:106962559-106962560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576438223	chr11:106962585-106962586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377446042	chr11:106973438-106973439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573285118	chr11:106973439-106973440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567818434	chr11:106973520-106973521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs56259394	chr11:106973604-106973605	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs549730844	chr11:106973622-106973623	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs571330956	chr11:106973656-106973657	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs538676035	chr11:106973668-106973669	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs553960124	chr11:106973674-106973675	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs572547733	chr11:106973683-106973684	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs533701343	chr11:106973687-106973688	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs11212032	chr11:106973692-106973693	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs183750222	chr11:106973706-106973707	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs544538223	chr11:106973728-106973729	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs79238197	chr11:106973730-106973731	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs1840568	chr11:106973788-106973789	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs186887325	chr11:106973789-106973790	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs559990756	chr11:106973794-106973795	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs191784950	chr11:106973819-106973820	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs549271988	chr11:106973820-106973821	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs561163569	chr11:106973862-106973863	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs139026530	chr11:106973875-106973876	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs34657554	chr11:106973879-106973880	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs184995221	chr11:106973883-106973884	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs571642837	chr11:106973899-106973900	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs538644070	chr11:106973900-106973901	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs373055210	chr11:106973934-106973935	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs574011987	chr11:106973950-106973951	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs565999180	chr11:106973951-106973952	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs2462397	chr11:106973966-106973967	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs11824598	chr11:106973982-106973983	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs555241712	chr11:106973985-106973986	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs2465776	chr11:106974038-106974039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538069667	chr11:106974069-106974070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs556485582	chr11:106974172-106974173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs578034523	chr11:106974183-106974184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1598456	chr11:106974257-106974258	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs190278675	chr11:106974277-106974278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs181880613	chr11:106974291-106974292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372699759	chr11:106974356-106974357	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Obesity	19966786	CNVD
Renal cell carcinoma	21668985	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	21811512	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164920	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:4632 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106962400-106962600	Weak transcription	Pancreas	Pancrea
2	chr11:106973400-106973600	Enhancers	HepG2	liver
3	chr11:106973400-106973800	Enhancers	Spleen	Spleen
4	chr11:106973400-106974200	Enhancers	Fetal Muscle Leg	muscle
5	chr11:106973600-106974000	Enhancers	Fetal Brain Female	brain
6	chr11:106973600-106974000	Flanking Active TSS	HepG2	liver
7	chr11:106973600-106974600	Enhancers	Fetal Heart	heart
8	chr11:106973600-106975000	Enhancers	Fetal Muscle Trunk	muscle
9	chr11:106974000-106974200	Enhancers	HepG2	liver
10	chr11:106986800-106987600	Enhancers	Placenta Amnion	Placenta Amnion
11	chr11:106987200-106987600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:106987400-106988800	Enhancers	Fetal Intestine Small	intestine
13	chr11:106987800-106988200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:106988200-106991400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr11:106988800-106992600	Weak transcription	Fetal Intestine Small	intestine
16	chr11:106991400-106991800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:106991400-106992200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr11:106992200-106993800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr11:107001800-107003600	Enhancers	Fetal Intestine Large	intestine
20	chr11:107002200-107003200	Enhancers	Fetal Intestine Small	intestine
21	chr11:107010000-107010200	Enhancers	Brain Germinal Matrix	brain
22	chr11:107010000-107010200	Enhancers	Fetal Brain Female	brain
23	chr11:107010200-107010400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr11:107010200-107010400	Enhancers	Fetal Brain Male	brain
25	chr11:107010200-107010800	Weak transcription	Brain Germinal Matrix	brain
26	chr11:107010800-107011600	Enhancers	Brain Germinal Matrix	brain
27	chr11:107011200-107012800	Enhancers	Fetal Muscle Leg	muscle
28	chr11:107011600-107011800	Enhancers	Fetal Brain Male	brain
29	chr11:107012000-107012400	Enhancers	Fetal Brain Female	brain
30	chr11:107012600-107012800	Enhancers	Fetal Brain Male	brain
31	chr11:107019200-107019600	Enhancers	Liver	Liver
32	chr11:107019600-107021400	Weak transcription	Liver	Liver
33	chr11:107021400-107023000	Enhancers	Liver	Liver
34	chr11:107023000-107027800	Weak transcription	Liver	Liver
35	chr11:107027400-107028400	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr11:107027400-107028800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr11:107027400-107029000	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr11:107027400-107029600	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr11:107027800-107028400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr11:107027800-107028600	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr11:107027800-107028800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
42	chr11:107027800-107029200	Enhancers	HepG2	liver
43	chr11:107027800-107030200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr11:107027800-107030200	Enhancers	Liver	Liver
45	chr11:107028000-107028400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr11:107028000-107032200	Enhancers	Adipose Nuclei	Adipose
47	chr11:107028400-107029000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:107028600-107030000	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr11:107029000-107029600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:107029600-107030400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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