Variant report

Variant	nsv1047502
Chromosome Location	chr11:50121285-50651567
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:867)
CpG islands
(count:2382)
Chromatin interactive
region (count:3)
LncRNA
region (count:47)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:867 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr11:50257555-50257921	K562	blood:	n/a	n/a
2	ATF1	chr11:50409411-50409611	K562	blood:	n/a	n/a
3	ATF1	chr11:50381201-50381204	K562	blood:	n/a	n/a
4	ATF3	chr11:50257564-50257818	K562	blood:	n/a	chr11:50257726-50257746 chr11:50257724-50257737 chr11:50257584-50257592 chr11:50257723-50257738 chr11:50257725-50257736
5	BATF	chr11:50251866-50252053	GM12878	blood:	n/a	n/a
6	BATF	chr11:50649412-50649706	GM12878	blood:	n/a	n/a
7	BCL11A	chr11:50648090-50648219	GM12878	blood:	n/a	n/a
8	BHLHE40	chr11:50649351-50649715	HepG2	liver:	n/a	n/a
9	BHLHE40	chr11:50609960-50609990	GM12878	blood:	n/a	n/a
10	BHLHE40	chr11:50257408-50257634	K562	blood:	n/a	chr11:50257599-50257615
11	BRCA1	chr11:50609964-50609989	GM12878	blood:	n/a	n/a
12	BRCA1	chr11:50651254-50651872	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr11:50646199-50646219	GM12878	blood:	n/a	n/a
14	CCNT2	chr11:50134957-50135155	K562	blood:	n/a	n/a
15	CCNT2	chr11:50257299-50257888	K562	blood:	n/a	n/a
16	CEBPB	chr11:50132343-50132599	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:50202142-50202359	HepG2	liver:	n/a	chr11:50202284-50202295
18	CEBPB	chr11:50256020-50256220	HepG2	liver:	n/a	chr11:50256104-50256115
19	CEBPB	chr11:50134957-50135324	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr11:50132313-50132582	IMR90	lung:	n/a	n/a
21	CEBPB	chr11:50409463-50409610	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:50180269-50180536	MCF-7	breast:	n/a	n/a
24	CEBPB	chr11:50202172-50202422	IMR90	lung:	n/a	chr11:50202284-50202295
25	CEBPB	chr11:50185114-50185392	HepG2	liver:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
26	CEBPB	chr11:50182673-50182737	HepG2	liver:	n/a	chr11:50182687-50182698
27	CEBPB	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
28	CEBPB	chr11:50185206-50185319	A549	lung:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
29	CEBPB	chr11:50145990-50146140	HepG2	liver:	n/a	chr11:50146064-50146075
30	CEBPB	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
31	CHD1	chr11:50134958-50135158	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr11:50382847-50382977	GM12878	blood:	n/a	n/a
33	CHD1	chr11:50409410-50409777	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chr11:50609964-50609986	GM12878	blood:	n/a	n/a
35	CHD2	chr11:50609872-50609989	GM12878	blood:	n/a	n/a
36	CHD2	chr11:50491957-50491986	Hela-S3	cervix:	n/a	n/a
37	CHD2	chr11:50614701-50614706	HepG2	liver:	n/a	n/a
38	CHD2	chr11:50522282-50522663	Hela-S3	cervix:	n/a	n/a
39	CHD2	chr11:50651424-50651872	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr11:50257411-50258094	K562	blood:	n/a	chr11:50257724-50257737
41	CREB1	chr11:50257549-50258023	K562	blood:	n/a	chr11:50257724-50257737
42	CTCF	chr11:50133540-50133690	Hela-S3	cervix:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
43	CTCF	chr11:50382446-50382672	IMR90	lung:	n/a	n/a
44	CTCF	chr11:50133600-50133750	HPAF	blood vessel:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
45	CTCF	chr11:50252665-50252796	Gliobla	brain:	n/a	n/a
46	CTCF	chr11:50304509-50304621	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr11:50251547-50251577	MCF-7	breast:	n/a	n/a
48	CTCF	chr11:50133600-50133750	AoAF	blood vessel:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687
49	CTCF	chr11:50207190-50207225	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr11:50133660-50133810	HMF	breast:	n/a	chr11:50133670-50133686 chr11:50133672-50133681 chr11:50133669-50133687

(count:2382 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50220426-50220476	HIPEpiC	eye:	n/a
2	chr11:50258750-50258800	HEK293	kidney:	embryo
3	chr11:50220426-50220476	SK-N-SH_RA	brain:	n/a
4	chr11:50220426-50220476	HIPEpiC	eye:	n/a
5	chr11:50258750-50258800	HEK293	kidney:	embryo
6	chr11:50220426-50220476	SK-N-SH_RA	brain:	n/a
7	chr11:50257256-50257306	NH-A	brain:	n/a
8	chr11:50257771-50257821	Hepatocyte	liver:	n/a
9	chr11:50220107-50220157	PrEC	prostate:	n/a
10	chr11:50254503-50254553	AG04449	skin:	fetal
11	chr11:50206561-50206611	PrEC	prostate:	n/a
12	chr11:50227476-50227526	BE2_C	brain:	n/a
13	chr11:50257625-50257675	GM19239	blood:	n/a
14	chr11:50220343-50220393	AG10803	skin:	n/a
15	chr11:50236153-50236203	Hepatocyte	liver:	n/a
16	chr11:50220107-50220157	SKMC	muscle:	n/a
17	chr11:50257625-50257675	HIPEpiC	eye:	n/a
18	chr11:50257979-50258029	ovcar-3	ovarian:	n/a
19	chr11:50257256-50257306	Hela-S3	cervix:	n/a
20	chr11:50220107-50220157	BJ	skin:	n/a
21	chr11:50227079-50227129	HepG2	liver:	n/a
22	chr11:50227476-50227526	HEEpiC	esophagus:	n/a
23	chr11:50258273-50258323	K562	blood:	n/a
24	chr11:50238214-50238264	NHDF-neo	bronchial:	n/a
25	chr11:50231261-50231311	ovcar-3	ovarian:	n/a
26	chr11:50220343-50220393	SKMC	muscle:	n/a
27	chr11:50257633-50257683	MCF10A-Er-Src	breast:	n/a
28	chr11:50206530-50206580	NT2-D1	testis:	n/a
29	chr11:50206606-50206656	HMEC	breast:	n/a
30	chr11:50256574-50256624	LNCaP	prostate:	n/a
31	chr11:50227476-50227526	A549	lung:	n/a
32	chr11:50257625-50257675	Caco-2	colon:	n/a
33	chr11:50368251-50368301	HIPEpiC	eye:	n/a
34	chr11:50206606-50206656	GM12878	blood:	n/a
35	chr11:50257979-50258029	NB4	blood:	n/a
36	chr11:50241016-50241066	NH-A	brain:	n/a
37	chr11:50227265-50227315	HPAEpiC	pulmonary alveolar:	n/a
38	chr11:50236153-50236203	NT2-D1	testis:	n/a
39	chr11:50258273-50258323	GM12892	blood:	n/a
40	chr11:50227102-50227152	SK-N-SH_RA	brain:	n/a
41	chr11:50220426-50220476	HAEpiC	amniotic membrane:	n/a
42	chr11:50206606-50206656	NH-A	brain:	n/a
43	chr11:50226789-50226839	HepG2	liver:	n/a
44	chr11:50256574-50256624	ovcar-3	ovarian:	n/a
45	chr11:50371681-50371731	HNPCEpiC	eye:	n/a
46	chr11:50227476-50227526	MCF10A-Er-Src	breast:	n/a
47	chr11:50258750-50258800	PFSK-1	brain:	n/a
48	chr11:50257496-50257546	AG09309	skin:	n/a
49	chr11:50226789-50226839	GM12891	blood:	n/a
50	chr11:50236153-50236203	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:
2	chr11:50256839..50259422-chr11:50261676..50263683,2	K562	blood:
3	chr11:50172306..50174473-chr11:50176469..50178865,2	K562	blood:

(count:47 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-9	chr11:50379775-50379803	NONHSAT021345
2	lnc-OR4C13-7	chr11:50266792-50266965	NONHSAT021338
3	lnc-OR4C13-9	chr11:50379313-50379548	NR_024504
4	lnc-OR4C13-9	chr11:50368739-50368821	NONHSAT021344
5	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
6	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
7	lnc-OR4C12-1	chr11:50232840-50233106	XLOC_009440
8	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
9	lnc-OR4C13-9	chr11:50378065-50378165	NR_024504
10	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021345
11	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
12	lnc-OR4C13-1	chr11:50261115-50261299	NONHSAT021336
13	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021344
14	lnc-OR4C13-9	chr11:50368318-50368359	NONHSAT021344
15	lnc-OR4C13-9	chr11:50375274-50375391	NR_024504
16	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
17	lnc-OR4C13-9	chr11:50378065-50378165	NONHSAT021345
18	lnc-OR4C13-1	chr11:50263752-50263827	ENSG00000254518
19	lnc-OR4C13-9	chr11:50368739-50368821	NR_024504
20	lnc-OR4C13-9	chr11:50368318-50368359	NR_024504
21	lnc-OR4C13-7	chr11:50320143-50320239	NONHSAT021340
22	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340
23	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
24	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
25	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021345
26	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
27	lnc-OR4C13-7	chr11:50266792-50266898	NONHSAT021339
28	lnc-OR4C13-9	chr11:50375235-50375391	NONHSAT021344
29	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336
30	lnc-OR4C13-9	chr11:50379313-50379802	NONHSAT021344
31	lnc-OR4C13-9	chr11:50379313-50379548	NONHSAT021345
32	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
33	lnc-OR4C13-7	chr11:50320710-50320877	NONHSAT021340
34	lnc-OR4C13-1	chr11:50263752-50263827	NONHSAT021336
35	lnc-OR4C13-7	chr11:50266852-50266898	NONHSAT021340
36	lnc-OR4C13-9	chr11:50379775-50379802	NR_024504
37	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
38	lnc-OR4C13-9	chr11:50376439-50376850	NONHSAT021344
39	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
40	lnc-OR4C13-1	chr11:50262310-50262433	ENSG00000254518
41	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
42	lnc-OR4C13-1	chr11:50261115-50261299	ENSG00000254518
43	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343
44	lnc-OR4C12-1	chr11:50231598-50231759	XLOC_009440
45	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
46	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
47	lnc-OR4C13-1	chr11:50262310-50262433	NONHSAT021336

No data

Variant related genes	Relation type
ENSG00000255500	TF binding region
ENSG00000254840	TF binding region
ENSG00000255001	TF binding region
ENSG00000236919	TF binding region
ENSG00000255442	TF binding region
ENSG00000254518	TF binding region
ENSG00000255042	TF binding region
ENSG00000214883	TF binding region
ENSG00000255500	CpG island
ENSG00000254840	CpG island
ENSG00000255001	CpG island
ENSG00000236919	CpG island
ENSG00000255442	CpG island
ENSG00000254518	CpG island
ENSG00000255042	CpG island
ENSG00000214883	CpG island
ENSG00000254518	chromatin interactions

Extended variants
information (count: 20748 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:20748 , 50 per page) page: 1 2 3 4 5 6 7 ... 415

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374403775	chr11:50124781-50124782	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs567323457	chr11:50124790-50124791	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536453141	chr11:50124796-50124797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs368514516	chr11:50124797-50124798	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs116327800	chr11:50124810-50124811	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs143694102	chr11:50124857-50124858	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs189956986	chr11:50124869-50124870	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs114926767	chr11:50129008-50129009	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs529494050	chr11:50129012-50129013	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs11245894	chr11:50129033-50129034	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs559412557	chr11:50129040-50129041	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs186011377	chr11:50129060-50129061	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs145508901	chr11:50129093-50129094	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs568551621	chr11:50129112-50129113	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs534007787	chr11:50129130-50129131	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs113682456	chr11:50129175-50129176	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs537265728	chr11:50129188-50129189	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs550584042	chr11:50129203-50129204	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs145257215	chr11:50129217-50129218	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs373378117	chr11:50129241-50129242	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs567591849	chr11:50129257-50129258	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs536248113	chr11:50129260-50129261	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs1995041	chr11:50129261-50129262	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs138031910	chr11:50129277-50129278	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs538711537	chr11:50129324-50129325	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs16926834	chr11:50129325-50129326	ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs189574434	chr11:50129388-50129389	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs544023501	chr11:50129408-50129409	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs563825954	chr11:50129413-50129414	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs180808185	chr11:50129454-50129455	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs542923637	chr11:50129456-50129457	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs577343319	chr11:50129483-50129484	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs559275696	chr11:50129500-50129501	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs570499675	chr11:50129510-50129511	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs150562363	chr11:50129513-50129514	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs546207068	chr11:50129522-50129523	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs372348367	chr11:50129543-50129544	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs186728827	chr11:50129553-50129554	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs530595719	chr11:50129561-50129562	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs7104653	chr11:50129598-50129599	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs567555810	chr11:50129633-50129634	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs58677382	chr11:50129655-50129656	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs546940267	chr11:50129664-50129665	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs566444260	chr11:50129673-50129674	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs538664134	chr11:50129689-50129690	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs58447209	chr11:50129708-50129709	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs149267806	chr11:50129718-50129719	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs368235824	chr11:50129723-50129724	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs557093030	chr11:50129746-50129747	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs573899800	chr11:50129751-50129752	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Mortal	21835882	CNVD
Autism	22495309	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	17142309	CNVD
Bipolar disorder	19214233	CNVD
Medulloblastoma	21163964	CNVD
early-passage human iPS cells	21368824	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50129000-50130400	ZNF genes & repeats	Placenta	Placenta
2	chr11:50129400-50129800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:50130400-50131000	Active TSS	Placenta	Placenta
4	chr11:50133000-50133200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr11:50133000-50133800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr11:50133200-50133600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr11:50133200-50134200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr11:50133200-50134400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr11:50133200-50134400	Enhancers	Adipose Nuclei	Adipose
10	chr11:50133600-50133800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr11:50133800-50134000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr11:50133800-50134000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr11:50134000-50134400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr11:50134000-50135000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:50134200-50134400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr11:50134400-50140400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr11:50134400-50146200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:50136600-50136800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
19	chr11:50140400-50142200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr11:50140400-50142600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr11:50141800-50142000	Weak transcription	Adipose Nuclei	Adipose
22	chr11:50142000-50142200	Enhancers	Adipose Nuclei	Adipose
23	chr11:50142200-50144600	Weak transcription	Adipose Nuclei	Adipose
24	chr11:50142200-50145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr11:50142600-50147000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr11:50144600-50147200	Enhancers	Adipose Nuclei	Adipose
27	chr11:50145600-50146000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr11:50145800-50147400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr11:50146000-50147000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr11:50146200-50147400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr11:50147000-50147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr11:50147000-50147600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:50151800-50152200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr11:50155000-50155200	Active TSS	HMEC	breast
35	chr11:50155000-50155200	Enhancers	HSMMtube	muscle
36	chr11:50155000-50155200	Enhancers	NH-A	brain
37	chr11:50188200-50189000	Enhancers	Adipose Nuclei	Adipose
38	chr11:50191600-50191800	ZNF genes & repeats	Right Atrium	heart
39	chr11:50191800-50194400	Weak transcription	Right Atrium	heart
40	chr11:50192600-50195800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
41	chr11:50193600-50193800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:50202200-50204200	Weak transcription	Pancreatic Islets	Pancreatic Islet
43	chr11:50206200-50207200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr11:50217000-50218200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
45	chr11:50220000-50220800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr11:50220600-50221200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
47	chr11:50238000-50238400	ZNF genes & repeats	Esophagus	oesophagus
48	chr11:50242200-50242400	ZNF genes & repeats	Placenta	Placenta
49	chr11:50242400-50246200	Weak transcription	Placenta	Placenta
50	chr11:50246400-50256200	Weak transcription	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links