Variant report

Variant	nsv832171
Chromosome Location	chr11:58725930-58878839
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2302)
CpG islands
(count:2750)
Chromatin interactive
region (count:25)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2302 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:58792609-58792905	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:58874268-58874746	HepG2	liver:	n/a	n/a
3	ATF1	chr11:58864804-58864948	K562	blood:	n/a	n/a
4	ATF1	chr11:58779639-58779652	K562	blood:	n/a	n/a
5	ATF2	chr11:58831402-58832419	GM12878	blood:	n/a	n/a
6	ATF2	chr11:58825833-58826405	GM12878	blood:	n/a	n/a
7	ATF2	chr11:58874015-58875031	GM12878	blood:	n/a	n/a
8	ATF2	chr11:58874286-58874870	GM12878	blood:	n/a	n/a
9	ATF2	chr11:58874344-58874770	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr11:58864502-58864964	GM12878	blood:	n/a	n/a
11	ATF2	chr11:58869726-58870352	GM12878	blood:	n/a	n/a
12	ATF2	chr11:58831671-58832143	GM12878	blood:	n/a	n/a
13	ATF2	chr11:58869606-58870352	GM12878	blood:	n/a	n/a
14	ATF2	chr11:58874367-58874899	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chr11:58869743-58869963	K562	blood:	n/a	n/a
16	BACH1	chr11:58825972-58826213	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr11:58869800-58870060	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr11:58873974-58874757	H1-hESC	embryonic stem cell:	n/a	chr11:58874543-58874557
19	BATF	chr11:58826199-58826498	GM12878	blood:	n/a	n/a
20	BATF	chr11:58831471-58831776	GM12878	blood:	n/a	n/a
21	BATF	chr11:58760001-58760259	GM12878	blood:	n/a	chr11:58760105-58760116
22	BATF	chr11:58831786-58832150	GM12878	blood:	n/a	chr11:58831926-58831934
23	BATF	chr11:58831416-58832275	GM12878	blood:	n/a	chr11:58831926-58831934
24	BATF	chr11:58818940-58819193	GM12878	blood:	n/a	n/a
25	BATF	chr11:58875256-58875548	GM12878	blood:	n/a	n/a
26	BATF	chr11:58869559-58870293	GM12878	blood:	n/a	n/a
27	BATF	chr11:58862752-58863071	GM12878	blood:	n/a	n/a
28	BATF	chr11:58874419-58874727	GM12878	blood:	n/a	chr11:58874543-58874553 chr11:58874547-58874557 chr11:58874542-58874553
29	BATF	chr11:58875555-58875818	GM12878	blood:	n/a	chr11:58875662-58875670
30	BCL11A	chr11:58875271-58875606	GM12878	blood:	n/a	n/a
31	BCL11A	chr11:58818899-58819262	GM12878	blood:	n/a	chr11:58819091-58819100
32	BCL11A	chr11:58831483-58831904	GM12878	blood:	n/a	n/a
33	BCL11A	chr11:58862690-58863069	GM12878	blood:	n/a	chr11:58862903-58862912
34	BCL11A	chr11:58862711-58863079	GM12878	blood:	n/a	chr11:58862903-58862912
35	BCL11A	chr11:58869760-58870216	GM12878	blood:	n/a	n/a
36	BCL11A	chr11:58869844-58870260	GM12878	blood:	n/a	n/a
37	BCL11A	chr11:58818878-58819275	GM12878	blood:	n/a	chr11:58819091-58819100
38	BCL11A	chr11:58831528-58832157	GM12878	blood:	n/a	n/a
39	BCL3	chr11:58831794-58832281	GM12878	blood:	n/a	n/a
40	BCL3	chr11:58869751-58870129	GM12878	blood:	n/a	n/a
41	BCLAF1	chr11:58869650-58870315	GM12878	blood:	n/a	n/a
42	BCLAF1	chr11:58873883-58874436	GM12878	blood:	n/a	chr11:58874084-58874097
43	BCLAF1	chr11:58869623-58870275	GM12878	blood:	n/a	n/a
44	BHLHE40	chr11:58792570-58792935	HepG2	liver:	n/a	chr11:58792752-58792765 chr11:58792748-58792769
45	BHLHE40	chr11:58869743-58870232	GM12878	blood:	n/a	n/a
46	BHLHE40	chr11:58825938-58826278	GM12878	blood:	n/a	n/a
47	BHLHE40	chr11:58862780-58863126	GM12878	blood:	n/a	n/a
48	BHLHE40	chr11:58873768-58874942	GM12878	blood:	n/a	chr11:58874078-58874094 chr11:58874166-58874182 chr11:58873986-58874002 chr11:58874149-58874165 chr11:58873949-58873965
49	BHLHE40	chr11:58874616-58874646	K562	blood:	n/a	n/a
50	BHLHE40	chr11:58865311-58865484	GM12878	blood:	n/a	n/a

(count:2750 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:58830355-58830405	RPTEC	kidney:	n/a
2	chr11:58866721-58866771	ovcar-3	ovarian:	n/a
3	chr11:58874608-58874658	HAEpiC	amniotic membrane:	n/a
4	chr11:58873955-58874005	HAEpiC	amniotic membrane:	n/a
5	chr11:58830610-58830660	Hepatocyte	liver:	n/a
6	chr11:58830355-58830405	RPTEC	kidney:	n/a
7	chr11:58866721-58866771	ovcar-3	ovarian:	n/a
8	chr11:58874608-58874658	HAEpiC	amniotic membrane:	n/a
9	chr11:58873955-58874005	HAEpiC	amniotic membrane:	n/a
10	chr11:58830610-58830660	Hepatocyte	liver:	n/a
11	chr11:58728533-58728583	NHBE	bronchial:	n/a
12	chr11:58731505-58731555	ECC-1	luminal epithelium:	n/a
13	chr11:58731357-58731407	HCPEpiC	choroid plexus:	n/a
14	chr11:58736000-58736050	HEK293	kidney:	embryo
15	chr11:58870494-58870544	Hepatocyte	liver:	n/a
16	chr11:58866721-58866771	HCF	heart:	n/a
17	chr11:58874733-58874783	AoSMC	blood vessel:	n/a
18	chr11:58874641-58874691	HCF	heart:	n/a
19	chr11:58869855-58869905	GM12891	blood:	n/a
20	chr11:58874207-58874257	GM12891	blood:	n/a
21	chr11:58731634-58731684	HAEpiC	amniotic membrane:	n/a
22	chr11:58731433-58731483	RPTEC	kidney:	n/a
23	chr11:58866721-58866771	HRPEpiC	eye:	n/a
24	chr11:58869823-58869873	HAEpiC	amniotic membrane:	n/a
25	chr11:58874733-58874783	NHDF-neo	bronchial:	n/a
26	chr11:58870494-58870544	BJ	skin:	n/a
27	chr11:58873955-58874005	HPAEpiC	pulmonary alveolar:	n/a
28	chr11:58830191-58830241	IMR90	lung:	fetal
29	chr11:58870494-58870544	NHDF-neo	bronchial:	n/a
30	chr11:58826414-58826464	BE2_C	brain:	n/a
31	chr11:58826414-58826464	AG09309	skin:	n/a
32	chr11:58830857-58830907	HIPEpiC	eye:	n/a
33	chr11:58731505-58731555	K562	blood:	n/a
34	chr11:58874733-58874783	HepG2	liver:	n/a
35	chr11:58874641-58874691	H1-hESC	embryonic stem cell:	embryo
36	chr11:58731104-58731154	HNPCEpiC	eye:	n/a
37	chr11:58736081-58736131	AoSMC	blood vessel:	n/a
38	chr11:58874723-58874773	Hela-S3	cervix:	n/a
39	chr11:58810187-58810237	AG04449	skin:	fetal
40	chr11:58874723-58874773	BE2_C	brain:	n/a
41	chr11:58736081-58736131	HIPEpiC	eye:	n/a
42	chr11:58731505-58731555	RPTEC	kidney:	n/a
43	chr11:58736000-58736050	AG10803	skin:	n/a
44	chr11:58870494-58870544	SKMC	muscle:	n/a
45	chr11:58830355-58830405	SKMC	muscle:	n/a
46	chr11:58810187-58810237	Hepatocyte	liver:	n/a
47	chr11:58874733-58874783	NH-A	brain:	n/a
48	chr11:58866721-58866771	HEEpiC	esophagus:	n/a
49	chr11:58825870-58825920	GM12892	blood:	n/a
50	chr11:58869979-58870029	NT2-D1	testis:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:58873861..58874546-chr5:111496427..111496981,2	Hela-S3	cervix:
2	chr11:58869192..58871421-chr11:58911598..58913836,2	MCF-7	breast:
3	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
4	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
5	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
6	chr11:58873805..58876804-chr17:41466274..41467888,2	K562	blood:
7	chr11:58729566..58731391-chr11:58732930..58735906,2	K562	blood:
8	chr11:58864668..58865554-chr11:58903471..58904061,2	MCF-7	breast:
9	chr11:58875510..58878300-chr11:58880309..58883300,3	MCF-7	breast:
10	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
11	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
12	chr11:58873708..58874686-chr11:63448916..63449711,2	Hela-S3	cervix:
13	chr11:58869989..58871867-chr11:58872289..58874332,2	MCF-7	breast:
14	chr11:58869769..58871706-chr11:58872515..58874019,2	MCF-7	breast:
15	chr11:58863409..58866220-chr11:58910202..58912249,2	K562	blood:
16	chr11:58875233..58875940-chr12:49657802..49658323,2	Hela-S3	cervix:
17	chr11:58762969..58764487-chr11:58768997..58771127,2	K562	blood:
18	chr11:58869975..58872858-chr11:58877240..58880132,2	MCF-7	breast:
19	chr11:58721468..58724070-chr11:58726713..58729457,3	K562	blood:
20	chr11:58873805..58875305-chr17:41466179..41467880,2	MCF-7	breast:
21	chr11:58399679..58402149-chr11:58838160..58840024,2	K562	blood:
22	chr11:58874735..58876453-chr11:58878007..58880480,2	MCF-7	breast:
23	chr11:58726086..58726653-chr11:58902781..58903961,3	K562	blood:
24	chr11:58872425..58874544-chr11:58888169..58890358,2	MCF-7	breast:
25	chr11:58830364..58831268-chr11:58873992..58874927,2	HCT-116	colon:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM111A-1	chr11:58874709-58874769	NONHSAT021500
2	lnc-GLYATL2-2	chr11:58736415-58736546	ENSG00000255240.1
3	lnc-GLYATL2-2	chr11:58761476-58761524	NR_033853
4	lnc-GLYATL2-2	chr11:58825845-58826132	ENSG00000255240.1
5	lnc-GLYATL2-2	chr11:58725690-58726293	ENSG00000255240.1
6	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
7	lnc-GLYATL2-2	chr11:58761476-58761524	ENSG00000255240.1
8	lnc-GLYATL2-2	chr11:58746601-58746758	ENSG00000255240.1
9	lnc-GLYATL2-4	chr11:58735069-58735764	NONHSAT021495
10	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
11	lnc-GLYATL2-2	chr11:58818733-58818781	ENSG00000255240.1
12	lnc-GLYATL2-2	chr11:58825845-58825925	NR_033853
13	lnc-FAM111A-1	chr11:58877013-58877480	NONHSAT021500
14	lnc-GLYATL2-2	chr11:58736426-58736546	ENSG00000255240.1
15	lnc-GLYATL2-2	chr11:58818733-58818781	NR_033853
16	lnc-GLYATL2-2	chr11:58825845-58825923	ENSG00000255240.1
17	lnc-GLYATL2-2	chr11:58822768-58822919	ENSG00000255240.1
18	lnc-FAM111A-1	chr11:58876141-58876185	NONHSAT021500
19	lnc-GLYATL2-2	chr11:58820930-58821099	NR_033853
20	lnc-GLYATL2-2	chr11:58820930-58821099	ENSG00000255240.1
21	lnc-GLYATL2-2	chr11:58746601-58746798	ENSG00000255240.1
22	lnc-GLYATL2-2	chr11:58746601-58746798	NR_033853

No data

Variant related genes	Relation type
GLYATL1P1	TF binding region
ENSG00000255240	TF binding region
GLYATL1P3	TF binding region
GLYATL1P4	TF binding region
ENSG00000254877	TF binding region
ENSG00000254786	TF binding region
FAM111B	TF binding region
GLYATL1P1	CpG island
ENSG00000255240	CpG island
GLYATL1P3	CpG island
GLYATL1P4	CpG island
ENSG00000254877	CpG island
ENSG00000254786	CpG island
FAM111B	CpG island
ENSG00000188825	chromatin interactions
ENSG00000245571	chromatin interactions
ENSG00000133318	chromatin interactions
ENSG00000224032	chromatin interactions
ENSG00000189057	chromatin interactions
ENSG00000254877	chromatin interactions
ENSG00000166801	chromatin interactions
CNOT6	miRNA target sites
GSPT1	miRNA target sites
KIF2A	miRNA target sites

Extended variants
information (count: 6141 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:6141 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554351550	chr11:58725968-58725969	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
2	rs190771834	chr11:58726048-58726049	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs549748261	chr11:58726066-58726067	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs565097815	chr11:58726083-58726084	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs148270610	chr11:58726125-58726126	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs180737025	chr11:58726158-58726159	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs565523711	chr11:58726164-58726165	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs141380455	chr11:58726183-58726184	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs548303977	chr11:58726190-58726191	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs150766192	chr11:58726225-58726226	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs185160933	chr11:58726226-58726227	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs368946653	chr11:58726235-58726236	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs373461037	chr11:58726264-58726265	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs569809007	chr11:58726279-58726280	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs537154893	chr11:58726327-58726328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556436911	chr11:58726393-58726394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs368099704	chr11:58726409-58726410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs578142475	chr11:58726450-58726451	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189917664	chr11:58726457-58726458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs117042065	chr11:58726465-58726466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs554480761	chr11:58726478-58726479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs376490111	chr11:58726486-58726487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs139159587	chr11:58726499-58726500	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs35976703	chr11:58726523-58726524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs138820936	chr11:58726539-58726540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs542657824	chr11:58726565-58726566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs145416280	chr11:58726572-58726573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369026803	chr11:58726583-58726584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561036083	chr11:58726615-58726616	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181227374	chr11:58726624-58726625	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs573225446	chr11:58726635-58726636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185623369	chr11:58726647-58726648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs543900704	chr11:58726697-58726698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564902426	chr11:58726701-58726702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530911044	chr11:58726708-58726709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58888492	chr11:58726722-58726723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs58774221	chr11:58726724-58726725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78644501	chr11:58726792-58726793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558948005	chr11:58726803-58726804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs78573300	chr11:58726827-58726828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529705282	chr11:58726842-58726843	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115725045	chr11:58726843-58726844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4271397	chr11:58726844-58726845	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs530496352	chr11:58726921-58726922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147275635	chr11:58726935-58726936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116456816	chr11:58726943-58726944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539246549	chr11:58726956-58726957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs77844906	chr11:58726966-58726967	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191555887	chr11:58727041-58727042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536556664	chr11:58727045-58727046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1734 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:58723000-58726800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr11:58723400-58731000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:58723400-58731000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:58725000-58726000	Enhancers	Liver	Liver
5	chr11:58725000-58728400	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr11:58725400-58726000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:58726000-58726200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr11:58726000-58730600	Weak transcription	Liver	Liver
9	chr11:58726200-58726600	Enhancers	Primary B cells from peripheral blood	blood
10	chr11:58726200-58730800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr11:58726600-58740000	Weak transcription	Primary B cells from peripheral blood	blood
12	chr11:58726800-58727000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr11:58727000-58727400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr11:58727400-58727800	Enhancers	H1 Cell Line	embryonic stem cell
15	chr11:58728400-58730000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr11:58730000-58730200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr11:58730000-58730600	Enhancers	Breast Myoepithelial Primary Cells	Breast
18	chr11:58730200-58730600	Weak transcription	NHEK	skin
19	chr11:58730200-58739400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr11:58730400-58730600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr11:58730400-58730600	Active TSS	Fetal Intestine Small	intestine
22	chr11:58730400-58730800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
23	chr11:58730600-58730800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr11:58730600-58730800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr11:58730600-58730800	Enhancers	Liver	Liver
26	chr11:58730600-58730800	Enhancers	NHEK	skin
27	chr11:58730600-58730800	Enhancers	Osteobl	bone
28	chr11:58730600-58731000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr11:58730600-58731000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:58730600-58731000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
31	chr11:58730600-58731000	Flanking Active TSS	Fetal Intestine Small	intestine
32	chr11:58730600-58731200	Bivalent Enhancer	Fetal Muscle Leg	muscle
33	chr11:58730600-58731800	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr11:58730800-58731000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr11:58730800-58731000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr11:58730800-58731000	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr11:58730800-58731000	Enhancers	Fetal Muscle Trunk	muscle
38	chr11:58730800-58731000	Enhancers	Pancreas	Pancrea
39	chr11:58730800-58731000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
40	chr11:58730800-58731000	Active TSS	Stomach Mucosa	stomach
41	chr11:58730800-58731000	Flanking Active TSS	HSMMtube	muscle
42	chr11:58730800-58731200	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr11:58730800-58731200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr11:58730800-58731200	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr11:58730800-58731200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr11:58730800-58731200	Flanking Active TSS	Liver	Liver
47	chr11:58730800-58731200	Enhancers	Esophagus	oesophagus
48	chr11:58730800-58731200	Active TSS	K562	blood
49	chr11:58730800-58731200	Bivalent/Poised TSS	NHLF	lung
50	chr11:58730800-58731200	Flanking Active TSS	Osteobl	bone

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