Variant report

Variant	nsv832149
Chromosome Location	chr11:50142116-50316451
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:285)
CpG islands
(count:2200)
Chromatin interactive
region (count:3)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:285 , 50 per page) page: 1 2 3 4 5 6

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	ATF3	chr11:50257564-50257818	K562	blood:	n/a	chr11:50257726-50257746 chr11:50257724-50257737 chr11:50257584-50257592 chr11:50257723-50257738 chr11:50257725-50257736
3	BATF	chr11:50251866-50252053	GM12878	blood:	n/a	n/a
4	BHLHE40	chr11:50257408-50257634	K562	blood:	n/a	chr11:50257599-50257615
5	CCNT2	chr11:50257299-50257888	K562	blood:	n/a	n/a
6	CEBPB	chr11:50185114-50185392	HepG2	liver:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
7	CEBPB	chr11:50182673-50182737	HepG2	liver:	n/a	chr11:50182687-50182698
8	CEBPB	chr11:50180269-50180536	MCF-7	breast:	n/a	n/a
9	CEBPB	chr11:50256005-50256238	K562	blood:	n/a	chr11:50256104-50256115
10	CEBPB	chr11:50202142-50202359	HepG2	liver:	n/a	chr11:50202284-50202295
11	CEBPB	chr11:50145990-50146140	HepG2	liver:	n/a	chr11:50146064-50146075
12	CEBPB	chr11:50230060-50230405	MCF-7	breast:	n/a	n/a
13	CEBPB	chr11:50256020-50256220	HepG2	liver:	n/a	chr11:50256104-50256115
14	CEBPB	chr11:50233638-50233794	HepG2	liver:	n/a	n/a
15	CEBPB	chr11:50185206-50185319	A549	lung:	n/a	chr11:50185257-50185274 chr11:50185258-50185271 chr11:50185259-50185270 chr11:50185258-50185269
16	CEBPB	chr11:50202172-50202422	IMR90	lung:	n/a	chr11:50202284-50202295
17	CREB1	chr11:50257549-50258023	K562	blood:	n/a	chr11:50257724-50257737
18	CREB1	chr11:50257411-50258094	K562	blood:	n/a	chr11:50257724-50257737
19	CTCF	chr11:50246753-50246827	Kidney_OC	kidney:	n/a	n/a
20	CTCF	chr11:50262617-50262644	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr11:50305210-50305247	GM20000	blood:	n/a	n/a
22	CTCF	chr11:50305777-50305808	Lung_OC	lung:	n/a	n/a
23	CTCF	chr11:50284186-50284275	GM20000	blood:	n/a	n/a
24	CTCF	chr11:50227575-50227627	LNCaP	prostate:	n/a	n/a
25	CTCF	chr11:50252669-50252790	Fibrobl	skin:	n/a	n/a
26	CTCF	chr11:50203704-50203730	Fibrobl	skin:	n/a	n/a
27	CTCF	chr11:50251547-50251577	MCF-7	breast:	n/a	n/a
28	CTCF	chr11:50257340-50257490	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
29	CTCF	chr11:50294779-50294808	GM20000	blood:	n/a	n/a
30	CTCF	chr11:50252435-50252463	GM13977	blood:	n/a	n/a
31	CTCF	chr11:50304509-50304621	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr11:50220602-50220640	MCF-7	breast:	n/a	n/a
33	CTCF	chr11:50257360-50257510	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
34	CTCF	chr11:50165390-50165477	LNCaP	prostate:	n/a	n/a
35	CTCF	chr11:50165100-50165250	GM12866	blood:	n/a	n/a
36	CTCF	chr11:50293200-50293350	SAEC	small airway:	n/a	n/a
37	CTCF	chr11:50251518-50251615	Gliobla	brain:	n/a	n/a
38	CTCF	chr11:50257370-50257473	SK-N-SH_RA	brain:	n/a	chr11:50257436-50257449
39	CTCF	chr11:50170484-50170584	LNCaP	prostate:	n/a	chr11:50170540-50170547
40	CTCF	chr11:50189348-50189444	GM13976	blood:	n/a	n/a
41	CTCF	chr11:50161852-50161908	GM20000	blood:	n/a	n/a
42	CTCF	chr11:50160554-50160643	GM20000	blood:	n/a	n/a
43	CTCF	chr11:50162853-50162864	GM20000	blood:	n/a	n/a
44	CTCF	chr11:50207190-50207225	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr11:50251549-50251566	GM12878	blood:	n/a	n/a
46	CTCF	chr11:50143702-50143807	Gliobla	brain:	n/a	n/a
47	CTCF	chr11:50316423-50316519	GM10266	blood:	n/a	n/a
48	CTCF	chr11:50264695-50264726	GM10266	blood:	n/a	n/a
49	CTCF	chr11:50214639-50214695	LNCaP	prostate:	n/a	n/a
50	CTCF	chr11:50300095-50300112	GM10248	blood:	n/a	n/a

(count:2200 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:50239550-50239600	HCPEpiC	choroid plexus:	n/a
2	chr11:50257256-50257306	AG04450	lung:	fetal
3	chr11:50227079-50227129	Caco-2	colon:	n/a
4	chr11:50260762-50260812	AG04449	skin:	fetal
5	chr11:50239550-50239600	HCPEpiC	choroid plexus:	n/a
6	chr11:50257256-50257306	AG04450	lung:	fetal
7	chr11:50227079-50227129	Caco-2	colon:	n/a
8	chr11:50260762-50260812	AG04449	skin:	fetal
9	chr11:50206530-50206580	AoSMC	blood vessel:	n/a
10	chr11:50219952-50220002	NHDF-neo	bronchial:	n/a
11	chr11:50238009-50238059	AG09319	gingival:	n/a
12	chr11:50241016-50241066	AG09309	skin:	n/a
13	chr11:50258750-50258800	SAEC	small airway:	n/a
14	chr11:50254503-50254553	LNCaP	prostate:	n/a
15	chr11:50234973-50235023	A549	lung:	n/a
16	chr11:50206561-50206611	T-47D	breast:	n/a
17	chr11:50238009-50238059	MCF-7	breast:	n/a
18	chr11:50227265-50227315	SK-N-SH_RA	brain:	n/a
19	chr11:50206561-50206611	H1-hESC	embryonic stem cell:	embryo
20	chr11:50241016-50241066	LNCaP	prostate:	n/a
21	chr11:50257979-50258029	NH-A	brain:	n/a
22	chr11:50257830-50257880	MCF10A-Er-Src	breast:	n/a
23	chr11:50257625-50257675	HCPEpiC	choroid plexus:	n/a
24	chr11:50236153-50236203	HIPEpiC	eye:	n/a
25	chr11:50260762-50260812	HRE	kidney:	n/a
26	chr11:50257496-50257546	AG04450	lung:	fetal
27	chr11:50227079-50227129	HIPEpiC	eye:	n/a
28	chr11:50220343-50220393	HMEC	breast:	n/a
29	chr11:50241016-50241066	AG10803	skin:	n/a
30	chr11:50257633-50257683	K562	blood:	n/a
31	chr11:50257256-50257306	SAEC	small airway:	n/a
32	chr11:50238107-50238157	GM19239	blood:	n/a
33	chr11:50220107-50220157	HCPEpiC	choroid plexus:	n/a
34	chr11:50257771-50257821	LNCaP	prostate:	n/a
35	chr11:50220107-50220157	GM06990	blood:	n/a
36	chr11:50227476-50227526	HAEpiC	amniotic membrane:	n/a
37	chr11:50206530-50206580	GM06990	blood:	n/a
38	chr11:50220389-50220439	HEEpiC	esophagus:	n/a
39	chr11:50220107-50220157	AG04450	lung:	fetal
40	chr11:50227199-50227249	AG09309	skin:	n/a
41	chr11:50257625-50257675	H1-hESC	embryonic stem cell:	embryo
42	chr11:50234973-50235023	AG04450	lung:	fetal
43	chr11:50254503-50254553	GM06990	blood:	n/a
44	chr11:50220107-50220157	H1-hESC	embryonic stem cell:	embryo
45	chr11:50227265-50227315	PFSK-1	brain:	n/a
46	chr11:50226789-50226839	ProgFib	skin:	n/a
47	chr11:50257633-50257683	Hepatocyte	liver:	n/a
48	chr11:50220343-50220393	HEK293	kidney:	embryo
49	chr11:50257625-50257675	K562	blood:	n/a
50	chr11:50257771-50257821	A549	lung:	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:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021340
2	lnc-OR4C13-1	chr11:50257750-50258088	ENSG00000254518
3	lnc-OR4C13-7	chr11:50302810-50303035	NONHSAT021343
4	lnc-OR4C13-1	chr11:50263752-50263827	NONHSAT021336
5	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021340
6	lnc-OR4C12-1	chr11:50232840-50233106	XLOC_009440
7	lnc-OR4C13-1	chr11:50262310-50262433	ENSG00000254518
8	lnc-OR4C13-1	chr11:50261115-50261299	NONHSAT021336
9	lnc-OR4C13-7	chr11:50279538-50279677	NONHSAT021339
10	lnc-OR4C13-1	chr11:50263752-50263827	ENSG00000254518
11	lnc-OR4C13-1	chr11:50257750-50258210	NONHSAT021336
12	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021339
13	lnc-OR4C13-7	chr11:50266852-50266898	NONHSAT021340
14	lnc-OR4C12-1	chr11:50231598-50231759	XLOC_009440
15	lnc-OR4C13-7	chr11:50280085-50280169	NONHSAT021340
16	lnc-OR4C13-7	chr11:50274586-50274767	NONHSAT021339
17	lnc-OR4C13-7	chr11:50266792-50266898	NONHSAT021339
18	lnc-OR4C13-7	chr11:50279839-50280169	NONHSAT021342
19	lnc-OR4C13-1	chr11:50257789-50258088	ENSG00000254518
20	lnc-OR4C13-7	chr11:50302810-50302996	NONHSAT021339
21	lnc-OR4C13-7	chr11:50301870-50302020	NONHSAT021343
22	lnc-OR4C13-7	chr11:50313156-50313246	NONHSAT021340
23	lnc-OR4C13-1	chr11:50261115-50261299	ENSG00000254518
24	lnc-OR4C13-7	chr11:50302810-50303098	NONHSAT021342
25	lnc-OR4C13-7	chr11:50274586-50274778	NONHSAT021338
26	lnc-OR4C13-7	chr11:50266792-50266965	NONHSAT021338
27	lnc-OR4C13-1	chr11:50262310-50262433	NONHSAT021336
28	lnc-OR4C13-7	chr11:50301079-50301142	NONHSAT021343

No data

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

Extended variants
information (count: 2341 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:2341 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193118741	chr11:50142133-50142134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72905325	chr11:50142141-50142142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs551255775	chr11:50142155-50142156	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183384116	chr11:50142160-50142161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs575604769	chr11:50142181-50142182	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536960116	chr11:50142193-50142194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142088098	chr11:50142219-50142220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187702105	chr11:50142249-50142250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566891559	chr11:50142273-50142274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539099557	chr11:50142275-50142276	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs368419363	chr11:50142309-50142310	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs1826835	chr11:50142310-50142311	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs191436264	chr11:50142322-50142323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs11245909	chr11:50142366-50142367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs540012954	chr11:50142369-50142370	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554634844	chr11:50142397-50142398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183610033	chr11:50142442-50142443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113869579	chr11:50142452-50142453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs192845408	chr11:50142456-50142457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138386105	chr11:50142457-50142458	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs374112421	chr11:50142464-50142465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368044628	chr11:50142471-50142472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs564668364	chr11:50142472-50142473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs371261599	chr11:50142478-50142479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs542972211	chr11:50142479-50142480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs185258460	chr11:50142484-50142485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs190360286	chr11:50142496-50142497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532066941	chr11:50142501-50142502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368444212	chr11:50142502-50142503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs566855046	chr11:50142508-50142509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539062125	chr11:50142522-50142523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559089220	chr11:50142523-50142524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569333829	chr11:50142524-50142525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs538341799	chr11:50142545-50142546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs181685019	chr11:50142556-50142557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs149255184	chr11:50142557-50142558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186569197	chr11:50142569-50142570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372881139	chr11:50142578-50142579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377030890	chr11:50142582-50142583	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs576428911	chr11:50142592-50142593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs545436047	chr11:50142593-50142594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs562151991	chr11:50142601-50142602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531259245	chr11:50142604-50142605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs541927294	chr11:50142606-50142607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115722371	chr11:50142611-50142612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530351569	chr11:50142628-50142629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs546955342	chr11:50142657-50142658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189462634	chr11:50142673-50142674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369738589	chr11:50142693-50142694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552559230	chr11:50142735-50142736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

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

Chromatin state (count:65 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:50134400-50146200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr11:50140400-50142200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:50140400-50142600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr11:50142000-50142200	Enhancers	Adipose Nuclei	Adipose
5	chr11:50142200-50144600	Weak transcription	Adipose Nuclei	Adipose
6	chr11:50142200-50145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr11:50142600-50147000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr11:50144600-50147200	Enhancers	Adipose Nuclei	Adipose
9	chr11:50145600-50146000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr11:50145800-50147400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr11:50146000-50147000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr11:50146200-50147400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:50147000-50147400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr11:50147000-50147600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:50151800-50152200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr11:50155000-50155200	Active TSS	HMEC	breast
17	chr11:50155000-50155200	Enhancers	HSMMtube	muscle
18	chr11:50155000-50155200	Enhancers	NH-A	brain
19	chr11:50188200-50189000	Enhancers	Adipose Nuclei	Adipose
20	chr11:50191600-50191800	ZNF genes & repeats	Right Atrium	heart
21	chr11:50191800-50194400	Weak transcription	Right Atrium	heart
22	chr11:50192600-50195800	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
23	chr11:50193600-50193800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr11:50202200-50204200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr11:50206200-50207200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr11:50217000-50218200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
27	chr11:50220000-50220800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr11:50220600-50221200	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
29	chr11:50238000-50238400	ZNF genes & repeats	Esophagus	oesophagus
30	chr11:50242200-50242400	ZNF genes & repeats	Placenta	Placenta
31	chr11:50242400-50246200	Weak transcription	Placenta	Placenta
32	chr11:50246400-50256200	Weak transcription	Placenta	Placenta
33	chr11:50250800-50256200	Weak transcription	K562	blood
34	chr11:50256200-50256400	Enhancers	Placenta	Placenta
35	chr11:50256200-50258600	Active TSS	K562	blood
36	chr11:50256400-50256800	Flanking Active TSS	Placenta	Placenta
37	chr11:50256800-50257200	Active TSS	Placenta	Placenta
38	chr11:50257000-50258200	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
39	chr11:50257200-50257400	Flanking Active TSS	Placenta	Placenta
40	chr11:50257200-50257600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr11:50257200-50257600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr11:50257200-50257600	Active TSS	Primary T cells fromperipheralblood	blood
43	chr11:50257200-50257600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
44	chr11:50257200-50257600	Active TSS	Brain Cingulate Gyrus	brain
45	chr11:50257200-50257600	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr11:50257200-50257600	ZNF genes & repeats	Fetal Stomach	stomach
47	chr11:50257200-50257600	Active TSS	Ovary	ovary
48	chr11:50257200-50257600	Active TSS	Psoas Muscle	Psoas
49	chr11:50257200-50257600	Active TSS	Right Atrium	heart
50	chr11:50257200-50257600	Active TSS	Right Ventricle	heart

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