Variant report

Variant	nsv1043956
Chromosome Location	chr11:58818144-58882570
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1881)
CpG islands
(count:1954)
Chromatin interactive
region (count:21)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1881 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58874268-58874746	HepG2	liver:	n/a	n/a
2	ATF1	chr11:58864804-58864948	K562	blood:	n/a	n/a
3	ATF2	chr11:58869606-58870352	GM12878	blood:	n/a	n/a
4	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
5	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
6	ATF2	chr11:58874286-58874870	GM12878	blood:	n/a	n/a
7	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
8	ATF2	chr11:58869726-58870352	GM12878	blood:	n/a	n/a
9	ATF2	chr11:58874344-58874770	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
11	ATF2	chr11:58874367-58874899	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr11:58874015-58875031	GM12878	blood:	n/a	n/a
13	ATF3	chr11:58869743-58869963	K562	blood:	n/a	n/a
14	BACH1	chr11:58873974-58874757	H1-hESC	embryonic stem cell:	n/a	chr11:58874543-58874557
15	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr11:58869800-58870060	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr11:58874419-58874727	GM12878	blood:	n/a	chr11:58874543-58874553 chr11:58874547-58874557 chr11:58874542-58874553
18	BATF	chr11:58875256-58875548	GM12878	blood:	n/a	n/a
19	BATF	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
20	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
21	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
22	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
23	BATF	chr11:58869559-58870293	GM12878	blood:	n/a	n/a
24	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
25	BATF	chr11:58875555-58875818	GM12878	blood:	n/a	chr11:58875662-58875670
26	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
27	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
28	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
29	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
30	BCL11A	chr11:58875271-58875606	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:58869760-58870216	GM12878	blood:	n/a	n/a
32	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
33	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
34	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
35	BCL11A	chr11:58869844-58870260	GM12878	blood:	n/a	n/a
36	BCL3	chr11:58869751-58870129	GM12878	blood:	n/a	n/a
37	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
38	BCLAF1	chr11:58869623-58870275	GM12878	blood:	n/a	n/a
39	BCLAF1	chr11:58869650-58870315	GM12878	blood:	n/a	n/a
40	BCLAF1	chr11:58873883-58874436	GM12878	blood:	n/a	chr11:58874084-58874097
41	BHLHE40	chr11:58865311-58865484	GM12878	blood:	n/a	n/a
42	BHLHE40	chr11:58874518-58874815	A549	lung:	n/a	n/a
43	BHLHE40	chr11:58869743-58870232	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:58826040-58826162	K562	blood:	n/a	n/a
45	BHLHE40	chr11:58869799-58869950	K562	blood:	n/a	n/a
46	BHLHE40	chr11:58820953-58821000	K562	blood:	n/a	n/a
47	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
48	BHLHE40	chr11:58862780-58863126	GM12878	blood:	n/a	n/a
49	BHLHE40	chr11:58873768-58874942	GM12878	blood:	n/a	chr11:58874078-58874094 chr11:58874166-58874182 chr11:58873986-58874002 chr11:58874149-58874165 chr11:58873949-58873965
50	BHLHE40	chr11:58874616-58874646	K562	blood:	n/a	n/a

(count:1954 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58826475-58826525	LNCaP	prostate:	n/a
2	chr11:58869823-58869873	HCM	heart:	n/a
3	chr11:58826475-58826525	LNCaP	prostate:	n/a
4	chr11:58869823-58869873	HCM	heart:	n/a
5	chr11:58869663-58869713	GM12891	blood:	n/a
6	chr11:58866721-58866771	HCPEpiC	choroid plexus:	n/a
7	chr11:58826414-58826464	HepG2	liver:	n/a
8	chr11:58874641-58874691	AoSMC	blood vessel:	n/a
9	chr11:58826475-58826525	AG09319	gingival:	n/a
10	chr11:58873955-58874005	NT2-D1	testis:	n/a
11	chr11:58874637-58874687	HIPEpiC	eye:	n/a
12	chr11:58830610-58830660	HIPEpiC	eye:	n/a
13	chr11:58874645-58874695	NHBE	bronchial:	n/a
14	chr11:58874637-58874687	PANC-1	pancreas:	n/a
15	chr11:58830424-58830474	ECC-1	luminal epithelium:	n/a
16	chr11:58828174-58828224	AG04450	lung:	fetal
17	chr11:58830191-58830241	MCF10A-Er-Src	breast:	n/a
18	chr11:58874608-58874658	IMR90	lung:	fetal
19	chr11:58874207-58874257	BJ	skin:	n/a
20	chr11:58869823-58869873	LNCaP	prostate:	n/a
21	chr11:58826475-58826525	HRCEpiC	kidney:	n/a
22	chr11:58874645-58874695	ProgFib	skin:	n/a
23	chr11:58874723-58874773	AG04450	lung:	fetal
24	chr11:58825714-58825764	AoSMC	blood vessel:	n/a
25	chr11:58874645-58874695	RPTEC	kidney:	n/a
26	chr11:58870494-58870544	H1-hESC	embryonic stem cell:	embryo
27	chr11:58866721-58866771	AoSMC	blood vessel:	n/a
28	chr11:58825870-58825920	AG09319	gingival:	n/a
29	chr11:58830355-58830405	NHBE	bronchial:	n/a
30	chr11:58866721-58866771	HRCEpiC	kidney:	n/a
31	chr11:58874641-58874691	NHBE	bronchial:	n/a
32	chr11:58874641-58874691	Caco-2	colon:	n/a
33	chr11:58877370-58877420	HRE	kidney:	n/a
34	chr11:58830191-58830241	H1-hESC	embryonic stem cell:	embryo
35	chr11:58874207-58874257	PrEC	prostate:	n/a
36	chr11:58869663-58869713	AG04449	skin:	fetal
37	chr11:58869979-58870029	HEEpiC	esophagus:	n/a
38	chr11:58825870-58825920	CMK	blood:	n/a
39	chr11:58826475-58826525	SAEC	small airway:	n/a
40	chr11:58826475-58826525	NT2-D1	testis:	n/a
41	chr11:58874645-58874695	MCF-7	breast:	n/a
42	chr11:58869663-58869713	Hela-S3	cervix:	n/a
43	chr11:58869979-58870029	CMK	blood:	n/a
44	chr11:58873955-58874005	IMR90	lung:	fetal
45	chr11:58877370-58877420	HCPEpiC	choroid plexus:	n/a
46	chr11:58874645-58874695	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:58870075-58870125	T-47D	breast:	n/a
48	chr11:58874723-58874773	SAEC	small airway:	n/a
49	chr11:58830355-58830405	Hepatocyte	liver:	n/a
50	chr11:58826414-58826464	BJ	skin:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58873805..58875305-chr17:41466179..41467880,2	MCF-7	breast:
2	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
3	chr11:58875233..58875940-chr12:49657802..49658323,2	Hela-S3	cervix:
4	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
5	chr11:58863409..58866220-chr11:58910202..58912249,2	K562	blood:
6	chr11:58873708..58874686-chr11:63448916..63449711,2	Hela-S3	cervix:
7	chr11:58869192..58871421-chr11:58911598..58913836,2	MCF-7	breast:
8	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
9	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
10	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
11	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
12	chr11:58873861..58874546-chr5:111496427..111496981,2	Hela-S3	cervix:
13	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
14	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
15	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
16	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
17	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:
18	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
19	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
20	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
21	chr11:58873805..58876804-chr17:41466274..41467888,2	K562	blood:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
2	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
3	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
4	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
5	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
6	lnc-FAM111A-1	chr11:58874709-58874769	NONHSAT021500
7	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
8	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
9	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
10	lnc-FAM111A-1	chr11:58876141-58876185	NONHSAT021500
11	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
12	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
13	lnc-FAM111A-1	chr11:58877013-58877480	NONHSAT021500

No data

Variant related genes	Relation type
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
FAM111B	TF binding region
ENSG00000255240	CpG island
GLYATL1P3	CpG island
FAM111B	CpG island
ENSG00000133318	chromatin interactions
ENSG00000189057	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000245571	chromatin interactions
ENSG00000166801	chromatin interactions
ENSG00000224032	chromatin interactions
CNOT6	miRNA target sites
KIF2A	miRNA target sites
GSPT1	miRNA target sites

Extended variants
information (count: 2552 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2552 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538337370	chr11:58818161-58818162	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558358308	chr11:58818164-58818165	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573328987	chr11:58818189-58818190	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534510894	chr11:58818245-58818246	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs386753969	chr11:58818267-58818268	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556055130	chr11:58818268-58818269	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574384488	chr11:58818290-58818291	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs150222006	chr11:58818292-58818293	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs562724051	chr11:58818296-58818297	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374436539	chr11:58818304-58818305	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545145691	chr11:58818313-58818314	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs560314435	chr11:58818322-58818323	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113050032	chr11:58818327-58818328	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs527445397	chr11:58818371-58818372	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs186981753	chr11:58818407-58818408	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190274159	chr11:58818411-58818412	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs61740127	chr11:58818416-58818417	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115442742	chr11:58818420-58818421	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs549779379	chr11:58818433-58818434	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs61753959	chr11:58818441-58818442	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546062844	chr11:58818456-58818457	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547143256	chr11:58818465-58818466	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs483371	chr11:58818548-58818549	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs484054	chr11:58818582-58818583	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs182811562	chr11:58818623-58818624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs71486438	chr11:58818633-58818634	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188643550	chr11:58818641-58818642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567993879	chr11:58818645-58818646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs538517498	chr11:58818659-58818660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs556545748	chr11:58818662-58818663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs4939253	chr11:58818757-58818758	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	mRNA abundance
32	rs545495464	chr11:58818763-58818764	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
33	rs553931439	chr11:58818764-58818765	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
34	rs112974544	chr11:58818780-58818781	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
35	rs485984	chr11:58818793-58818794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192956378	chr11:58818800-58818801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542452842	chr11:58818838-58818839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs3824945	chr11:58818869-58818870	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs531526581	chr11:58818877-58818878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs543323276	chr11:58818900-58818901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564911034	chr11:58818904-58818905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185625081	chr11:58818913-58818914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544702090	chr11:58818924-58818925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs369373331	chr11:58818932-58818933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565822068	chr11:58818967-58818968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188836058	chr11:58818975-58818976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs191100964	chr11:58818995-58818996	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571818743	chr11:58819025-58819026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs12226012	chr11:58819035-58819036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10896906	chr11:58819040-58819041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Autism	22495309	CNVD
Autism	20808228	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1358 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58805000-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr11:58805200-58825400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr11:58811400-58818200	Weak transcription	Primary B cells from cord blood	blood
4	chr11:58813600-58825200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr11:58815400-58824400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr11:58816200-58818200	Strong transcription	Primary B cells from peripheral blood	blood
7	chr11:58817000-58818200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr11:58817200-58821800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:58817200-58825200	Weak transcription	Liver	Liver
10	chr11:58817200-58825400	Weak transcription	Fetal Intestine Large	intestine
11	chr11:58817400-58819400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr11:58817400-58822000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr11:58818200-58818600	Genic enhancers	Primary B cells from peripheral blood	blood
14	chr11:58818200-58819400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr11:58818200-58820200	Enhancers	Primary B cells from cord blood	blood
16	chr11:58818600-58825200	Enhancers	Primary B cells from peripheral blood	blood
17	chr11:58818800-58819400	Enhancers	GM12878-XiMat	blood
18	chr11:58819200-58819400	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr11:58819400-58820600	Weak transcription	GM12878-XiMat	blood
20	chr11:58819400-58821200	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr11:58819400-58822000	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr11:58819400-58822600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr11:58820200-58820800	Weak transcription	Primary B cells from cord blood	blood
24	chr11:58820600-58821200	Enhancers	GM12878-XiMat	blood
25	chr11:58820800-58822200	Enhancers	Primary B cells from cord blood	blood
26	chr11:58821200-58821400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr11:58821200-58821600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr11:58821200-58825400	Weak transcription	GM12878-XiMat	blood
29	chr11:58821400-58822200	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr11:58821600-58822400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr11:58821800-58822600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr11:58821800-58822800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr11:58822000-58822600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr11:58822000-58822800	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr11:58822200-58823200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr11:58822200-58824400	Weak transcription	Primary B cells from cord blood	blood
37	chr11:58822400-58823200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr11:58822600-58823200	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr11:58822600-58825200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr11:58822800-58825200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr11:58822800-58825200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
42	chr11:58823200-58825200	Weak transcription	HUES48 Cell Line	embryonic stem cell
43	chr11:58823200-58825200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr11:58823200-58825600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr11:58824400-58824600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:58824400-58825200	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr11:58824400-58825200	Enhancers	Primary B cells from cord blood	blood
48	chr11:58824800-58825600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:58825200-58825400	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr11:58825200-58825400	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell

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