Variant report

Variant	nsv898175
Chromosome Location	chr11:92623349-92668826
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:121)
CpG islands
(count:550)
Chromatin interactive
region (count:3)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:121 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:92655599-92655826	A549	lung:	n/a	chr11:92655725-92655736 chr11:92655723-92655734
2	CEBPB	chr11:92662336-92662687	IMR90	lung:	n/a	chr11:92662509-92662518 chr11:92662509-92662518 chr11:92662509-92662518 chr11:92662507-92662518 chr11:92662509-92662518
3	CEBPB	chr11:92661406-92661723	HepG2	liver:	n/a	chr11:92661540-92661551 chr11:92661542-92661551 chr11:92661542-92661551 chr11:92661542-92661551 chr11:92661540-92661553 chr11:92661542-92661551
4	CEBPB	chr11:92655588-92655866	IMR90	lung:	n/a	chr11:92655725-92655736 chr11:92655723-92655734
5	CEBPB	chr11:92628424-92628576	A549	lung:	n/a	n/a
6	CEBPB	chr11:92662359-92662677	A549	lung:	n/a	chr11:92662509-92662518 chr11:92662509-92662518 chr11:92662509-92662518 chr11:92662507-92662518 chr11:92662509-92662518
7	CEBPB	chr11:92655574-92655889	HepG2	liver:	n/a	chr11:92655725-92655736 chr11:92655723-92655734
8	CTCF	chr11:92653820-92653970	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr11:92654395-92654545	GM12878	blood:	n/a	n/a
10	CTCF	chr11:92657557-92657594	LNCaP	prostate:	n/a	n/a
11	CTCF	chr11:92654400-92654550	BE2_C	brain:	n/a	n/a
12	CTCF	chr11:92634200-92634350	HepG2	liver:	n/a	n/a
13	CTCF	chr11:92653740-92653890	SK-N-SH_RA	brain:	n/a	n/a
14	CTCF	chr11:92630500-92630536	Lung_OC	lung:	n/a	n/a
15	CTCF	chr11:92667880-92668030	GM12871	blood:	n/a	n/a
16	CTCF	chr11:92634180-92634330	GM12869	blood:	n/a	n/a
17	CTCF	chr11:92654460-92654610	BE2_C	brain:	n/a	n/a
18	E2F4	chr11:92629977-92630112	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr11:92662386-92662756	MCF10A-Er-Src	breast:	n/a	n/a
20	EBF1	chr11:92654348-92654527	GM12878	blood:	n/a	n/a
21	EP300	chr11:92626562-92626764	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr11:92653034-92654737	SK-N-SH	brain:	n/a	n/a
23	EP300	chr11:92635625-92635920	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr11:92653372-92653937	SK-N-SH_RA	brain:	n/a	n/a
25	EP300	chr11:92653319-92653932	SK-N-SH_RA	brain:	n/a	n/a
26	EP300	chr11:92626501-92626829	SK-N-SH_RA	brain:	n/a	n/a
27	FOS	chr11:92665180-92665492	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr11:92662279-92662679	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr11:92662344-92662669	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr11:92662289-92662682	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr11:92665225-92665493	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr11:92662905-92663139	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr11:92662920-92663120	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr11:92662939-92663078	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr11:92665196-92665479	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr11:92662295-92662717	MCF10A-Er-Src	breast:	n/a	n/a
37	FOSL2	chr11:92665178-92665545	A549	lung:	n/a	n/a
38	FOXA1	chr11:92652201-92652532	T-47D	breast:	n/a	n/a
39	FOXA1	chr11:92625918-92626251	T-47D	breast:	n/a	chr11:92626140-92626155
40	FOXA1	chr11:92625948-92626228	T-47D	breast:	n/a	chr11:92626140-92626155
41	FOXA1	chr11:92652749-92652951	T-47D	breast:	n/a	n/a
42	GABPA	chr11:92647209-92647300	HepG2	liver:	n/a	n/a
43	GATA2	chr11:92653168-92654515	SH-SY5Y	brain:	n/a	chr11:92653771-92653783 chr11:92653923-92653933 chr11:92653773-92653781
44	GATA2	chr11:92635429-92636144	SH-SY5Y	brain:	n/a	chr11:92635606-92635622 chr11:92635604-92635625
45	GATA3	chr11:92624879-92625035	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr11:92654200-92654337	SH-SY5Y	brain:	n/a	n/a
47	GATA3	chr11:92625917-92626228	T-47D	breast:	n/a	n/a
48	GATA3	chr11:92635620-92635954	SK-N-SH	brain:	n/a	n/a
49	GATA3	chr11:92653460-92654064	SK-N-SH	brain:	n/a	chr11:92653771-92653783 chr11:92653923-92653933 chr11:92653773-92653781
50	GATA3	chr11:92653424-92653928	SH-SY5Y	brain:	n/a	chr11:92653771-92653783 chr11:92653773-92653781

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:92648684-92648734	AG09309	skin:	n/a
2	chr11:92648684-92648734	AG09309	skin:	n/a
3	chr11:92651425-92651475	AG04450	lung:	fetal
4	chr11:92640593-92640643	BE2_C	brain:	n/a
5	chr11:92648898-92648948	AG09319	gingival:	n/a
6	chr11:92651425-92651475	GM06990	blood:	n/a
7	chr11:92648684-92648734	HEK293	kidney:	embryo
8	chr11:92644726-92644776	Jurkat	blood:	n/a
9	chr11:92648684-92648734	HNPCEpiC	eye:	n/a
10	chr11:92648898-92648948	HepG2	liver:	n/a
11	chr11:92624742-92624792	AG09319	gingival:	n/a
12	chr11:92648898-92648948	T-47D	breast:	n/a
13	chr11:92624742-92624792	SK-N-MC	brain:	n/a
14	chr11:92648753-92648803	HL-60	blood:	n/a
15	chr11:92647563-92647613	SKMC	muscle:	n/a
16	chr11:92644726-92644776	PANC-1	pancreas:	n/a
17	chr11:92648898-92648948	HEEpiC	esophagus:	n/a
18	chr11:92644726-92644776	GM12878	blood:	n/a
19	chr11:92644726-92644776	ovcar-3	ovarian:	n/a
20	chr11:92648753-92648803	HRPEpiC	eye:	n/a
21	chr11:92648684-92648734	T-47D	breast:	n/a
22	chr11:92644726-92644776	HCF	heart:	n/a
23	chr11:92624742-92624792	NB4	blood:	n/a
24	chr11:92640593-92640643	GM12891	blood:	n/a
25	chr11:92624742-92624792	Caco-2	colon:	n/a
26	chr11:92647563-92647613	AG10803	skin:	n/a
27	chr11:92624742-92624792	ECC-1	luminal epithelium:	n/a
28	chr11:92648753-92648803	HCPEpiC	choroid plexus:	n/a
29	chr11:92647563-92647613	HIPEpiC	eye:	n/a
30	chr11:92644726-92644776	LNCaP	prostate:	n/a
31	chr11:92649211-92649261	CMK	blood:	n/a
32	chr11:92640593-92640643	Caco-2	colon:	n/a
33	chr11:92640593-92640643	GM12878	blood:	n/a
34	chr11:92649211-92649261	NHDF-neo	bronchial:	n/a
35	chr11:92644726-92644776	GM19239	blood:	n/a
36	chr11:92647563-92647613	NHDF-neo	bronchial:	n/a
37	chr11:92649211-92649261	BE2_C	brain:	n/a
38	chr11:92648684-92648734	HIPEpiC	eye:	n/a
39	chr11:92648684-92648734	HEEpiC	esophagus:	n/a
40	chr11:92647563-92647613	Hepatocyte	liver:	n/a
41	chr11:92651425-92651475	U87	brain:	n/a
42	chr11:92624742-92624792	HL-60	blood:	n/a
43	chr11:92648898-92648948	PrEC	prostate:	n/a
44	chr11:92640593-92640643	MCF-7	breast:	n/a
45	chr11:92648898-92648948	NB4	blood:	n/a
46	chr11:92624742-92624792	HUVEC	blood vessel:	n/a
47	chr11:92648753-92648803	HCF	heart:	n/a
48	chr11:92648753-92648803	HAEpiC	amniotic membrane:	n/a
49	chr11:92624742-92624792	HAEpiC	amniotic membrane:	n/a
50	chr11:92648753-92648803	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:92653456..92655388-chr11:92655569..92657141,2	K562	blood:
2	chr11:92653456..92655388-chr11:92655569..92657141,2	K562	blood:
3	chr11:28063287..28063865-chr11:92666095..92666970,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC36A4-5	chr11:92647376-92647641	NONHSAT023627
2	lnc-SLC36A4-5	chr11:92648189-92648763	NONHSAT023627
3	lnc-FAT3-1	chr11:92664215-92664425	NONHSAT023629
4	lnc-SLC36A4-5	chr11:92647376-92647641	NONHSAT023626
5	lnc-SLC36A4-5	chr11:92648368-92648767	NONHSAT023628
6	lnc-SLC36A4-5	chr11:92648189-92648287	NONHSAT023628
7	lnc-FAT3-1	chr11:92649005-92649130	NONHSAT023629
8	lnc-SLC36A4-5	chr11:92648149-92648763	NONHSAT023626
9	lnc-SLC36A4-5	chr11:92647509-92647641	NONHSAT023628

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FAT3	hsa-miR-19b-3p	chr11:92626134-92626154
2	FAT3	hsa-miR-16-5p	chr11:92627387-92627409
3	FAT3	hsa-miR-130b-3p	chr11:92626134-92626155
4	FAT3	hsa-miR-16-5p	chr11:92626566-92626588
5	FAT3	hsa-miR-130b-3p	chr11:92626148-92626155
6	FAT3	hsa-miR-19b-3p	chr11:92626147-92626153

Variant related genes	Relation type
SNRPGP16	TF binding region
ENSG00000255127	TF binding region
SNRPGP16	CpG island
ENSG00000255127	CpG island

Extended variants
information (count: 1536 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7118248	chr11:92623349-92623350	Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114765937	chr11:92623401-92623402	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs148992918	chr11:92623404-92623405	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547523440	chr11:92623412-92623413	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs566057926	chr11:92623419-92623420	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs372311173	chr11:92623424-92623425	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7101609	chr11:92623493-92623494	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs570629083	chr11:92623496-92623497	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143757956	chr11:92623497-92623498	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7101614	chr11:92623515-92623516	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs556104448	chr11:92623527-92623528	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567814714	chr11:92623534-92623535	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs575693421	chr11:92623578-92623579	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553526682	chr11:92623587-92623588	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7118363	chr11:92623608-92623609	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs201389078	chr11:92623648-92623649	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376809001	chr11:92623696-92623697	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs371131255	chr11:92623697-92623698	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147702453	chr11:92623703-92623704	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs375962719	chr11:92623718-92623719	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs370311816	chr11:92623737-92623738	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs373759014	chr11:92623746-92623747	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs188175143	chr11:92623748-92623749	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543168460	chr11:92623767-92623768	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs372361857	chr11:92623768-92623769	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs375456244	chr11:92623773-92623774	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs142403035	chr11:92623798-92623799	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372403199	chr11:92623802-92623803	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200639726	chr11:92623824-92623825	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541304164	chr11:92623866-92623867	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559517172	chr11:92623868-92623869	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs12277422	chr11:92623877-92623878	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs371883255	chr11:92623915-92623916	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs114541747	chr11:92623932-92623933	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs570123938	chr11:92623940-92623941	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs200705741	chr11:92623951-92623952	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373527143	chr11:92623958-92623959	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs146396927	chr11:92623960-92623961	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552795179	chr11:92623986-92623987	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369740689	chr11:92624002-92624003	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs373143549	chr11:92624012-92624013	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs34488011	chr11:92624032-92624033	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs376130419	chr11:92624033-92624034	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs370497984	chr11:92624036-92624037	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs138992782	chr11:92624044-92624045	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs547247803	chr11:92624080-92624081	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs565558854	chr11:92624091-92624092	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs577242427	chr11:92624097-92624098	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs373934891	chr11:92624109-92624110	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs539009430	chr11:92624128-92624129	Weak transcription Enhancers Genic enhancers Strong transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Prostate cancer	18632612	CNVD
Breast cancer	17157792	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
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21958427	CNVD
Breast cancer	17133270	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Autism	19546859	CNVD
Fragile x	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Cancer	21499728	CNVD
Breast cancer	19181860	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:142 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:92601800-92623800	Weak transcription	Brain Anterior Caudate	brain
2	chr11:92610800-92626600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr11:92612800-92624000	Weak transcription	Brain Hippocampus Middle	brain
4	chr11:92613400-92626600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr11:92614000-92629400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr11:92616600-92624000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:92616800-92630600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr11:92617200-92625800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:92619400-92624400	Weak transcription	Stomach Smooth Muscle	stomach
10	chr11:92619400-92625200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr11:92619600-92625600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:92619600-92626000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr11:92619600-92626600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr11:92620000-92629200	Weak transcription	Fetal Brain Male	brain
15	chr11:92620200-92628200	Weak transcription	Brain Germinal Matrix	brain
16	chr11:92620400-92625400	Strong transcription	Cortex derived primary cultured neurospheres	brain
17	chr11:92622200-92630800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr11:92622400-92631000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr11:92622800-92624600	Strong transcription	Fetal Brain Female	brain
20	chr11:92623000-92624400	Genic enhancers	Fetal Lung	lung
21	chr11:92623200-92623400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr11:92623200-92624400	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr11:92623200-92624400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr11:92623200-92624400	Strong transcription	Aorta	Aorta
25	chr11:92623200-92624400	Strong transcription	Fetal Stomach	stomach
26	chr11:92623200-92624800	Strong transcription	H9 Cell Line	embryonic stem cell
27	chr11:92623400-92624000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr11:92623800-92624000	Enhancers	Brain Angular Gyrus	brain
29	chr11:92623800-92624000	Enhancers	Brain Substantia Nigra	brain
30	chr11:92623800-92624600	Enhancers	Brain Anterior Caudate	brain
31	chr11:92624000-92624200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr11:92624000-92624400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr11:92624000-92624400	Enhancers	Brain Cingulate Gyrus	brain
34	chr11:92624000-92624400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr11:92624000-92624400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
36	chr11:92624000-92624400	Active TSS	Brain Substantia Nigra	brain
37	chr11:92624000-92624600	Enhancers	Brain Hippocampus Middle	brain
38	chr11:92624200-92625200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr11:92624400-92624600	Enhancers	Brain Substantia Nigra	brain
40	chr11:92624400-92624600	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr11:92624400-92626000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr11:92624400-92626000	Weak transcription	Aorta	Aorta
43	chr11:92624400-92626200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr11:92624400-92627000	Enhancers	Fetal Lung	lung
45	chr11:92624400-92627000	Weak transcription	Fetal Stomach	stomach
46	chr11:92624600-92626200	Weak transcription	Fetal Brain Female	brain
47	chr11:92624800-92626000	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr11:92624800-92629600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr11:92625200-92625400	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr11:92625400-92630800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain

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