Variant report

Variant	esv3474074
Chromosome Location	chr11:46740876-46745174
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:115)
CpG islands
(count:244)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:115 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:46739747-46740958	HepG2	liver:	n/a	n/a
2	BRCA1	chr11:46741180-46741221	HepG2	liver:	n/a	n/a
3	CBX3	chr11:46744326-46744574	K562	blood:	n/a	n/a
4	CBX3	chr11:46744282-46744716	K562	blood:	n/a	n/a
5	CEBPB	chr11:46740455-46740974	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:46740524-46740932	HepG2	liver:	n/a	n/a
7	CEBPB	chr11:46744828-46744995	HepG2	liver:	n/a	chr11:46744909-46744920
8	CEBPB	chr11:46740522-46740956	HepG2	liver:	n/a	n/a
9	CEBPD	chr11:46740489-46741094	HepG2	liver:	n/a	n/a
10	CHD2	chr11:46740517-46740886	HepG2	liver:	n/a	n/a
11	CTCF	chr11:46744460-46744610	HepG2	liver:	n/a	n/a
12	CTCF	chr11:46740860-46741010	HepG2	liver:	n/a	n/a
13	EP300	chr11:46740427-46740979	HepG2	liver:	n/a	chr11:46740866-46740879
14	EP300	chr11:46740335-46740969	HepG2	liver:	n/a	chr11:46740866-46740879
15	FOSL2	chr11:46740506-46740988	HepG2	liver:	n/a	n/a
16	FOXA1	chr11:46740525-46741005	HepG2	liver:	n/a	n/a
17	FOXA1	chr11:46740425-46740947	HepG2	liver:	n/a	n/a
18	FOXA1	chr11:46740529-46740964	HepG2	liver:	n/a	n/a
19	FOXA1	chr11:46740450-46741314	HepG2	liver:	n/a	n/a
20	FOXA2	chr11:46742046-46742477	A549	lung:	n/a	n/a
21	FOXA2	chr11:46740501-46740898	HepG2	liver:	n/a	n/a
22	HDAC2	chr11:46739578-46740945	HepG2	liver:	n/a	n/a
23	HDAC2	chr11:46739669-46740957	HepG2	liver:	n/a	n/a
24	HEY1	chr11:46742019-46742402	HepG2	liver:	n/a	n/a
25	HEY1	chr11:46740465-46742012	HepG2	liver:	n/a	n/a
26	HEY1	chr11:46742829-46743493	HepG2	liver:	n/a	n/a
27	HEY1	chr11:46743536-46745241	HepG2	liver:	n/a	n/a
28	HEY1	chr11:46739579-46742651	HepG2	liver:	n/a	n/a
29	HNF4A	chr11:46740449-46740884	HepG2	liver:	n/a	chr11:46740679-46740694
30	HNF4A	chr11:46739639-46740980	HepG2	liver:	n/a	chr11:46739787-46739802 chr11:46739837-46739855 chr11:46740679-46740694 chr11:46739838-46739853 chr11:46739789-46739801
31	HNF4G	chr11:46740473-46740937	HepG2	liver:	n/a	chr11:46740679-46740694
32	JUND	chr11:46740561-46740885	HepG2	liver:	n/a	n/a
33	JUND	chr11:46740480-46740943	HepG2	liver:	n/a	n/a
34	MAFK	chr11:46740583-46740906	HepG2	liver:	n/a	n/a
35	MAFK	chr11:46741181-46741183	HepG2	liver:	n/a	n/a
36	MAX	chr11:46741637-46741641	HepG2	liver:	n/a	n/a
37	MAX	chr11:46740534-46740945	HepG2	liver:	n/a	n/a
38	MAX	chr11:46739543-46741963	HepG2	liver:	n/a	chr11:46741848-46741858
39	MAX	chr11:46739461-46741099	A549	lung:	n/a	n/a
40	MAZ	chr11:46739693-46740911	HepG2	liver:	n/a	n/a
41	MAZ	chr11:46741656-46741748	HepG2	liver:	n/a	n/a
42	MBD4	chr11:46739585-46741341	HepG2	liver:	n/a	n/a
43	MBD4	chr11:46739639-46741057	HepG2	liver:	n/a	n/a
44	MEF2A	chr11:46742857-46743172	K562	blood:	n/a	n/a
45	MXI1	chr11:46741451-46741725	HepG2	liver:	n/a	n/a
46	MXI1	chr11:46739656-46740994	HepG2	liver:	n/a	n/a
47	MYBL2	chr11:46741405-46742145	HepG2	liver:	n/a	n/a
48	MYBL2	chr11:46744059-46744647	HepG2	liver:	n/a	n/a
49	MYBL2	chr11:46739593-46741377	HepG2	liver:	n/a	n/a
50	MYBL2	chr11:46744248-46744715	HepG2	liver:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:46744754-46744804	HCPEpiC	choroid plexus:	n/a
2	chr11:46744754-46744804	GM12892	blood:	n/a
3	chr11:46741405-46741455	HEK293	kidney:	embryo
4	chr11:46741299-46741349	Hepatocyte	liver:	n/a
5	chr11:46744754-46744804	AG04449	skin:	fetal
6	chr11:46741299-46741349	SKMC	muscle:	n/a
7	chr11:46741299-46741349	NB4	blood:	n/a
8	chr11:46741299-46741349	HCT-116	colon:	n/a
9	chr11:46741373-46741423	GM06990	blood:	n/a
10	chr11:46744754-46744804	IMR90	lung:	fetal
11	chr11:46741299-46741349	GM19239	blood:	n/a
12	chr11:46741405-46741455	HRPEpiC	eye:	n/a
13	chr11:46741299-46741349	HRE	kidney:	n/a
14	chr11:46741373-46741423	HL-60	blood:	n/a
15	chr11:46741405-46741455	NB4	blood:	n/a
16	chr11:46741405-46741455	ECC-1	luminal epithelium:	n/a
17	chr11:46744754-46744804	HMEC	breast:	n/a
18	chr11:46744754-46744804	Hepatocyte	liver:	n/a
19	chr11:46744754-46744804	HL-60	blood:	n/a
20	chr11:46741299-46741349	AG04450	lung:	fetal
21	chr11:46741299-46741349	HIPEpiC	eye:	n/a
22	chr11:46741373-46741423	HMEC	breast:	n/a
23	chr11:46741405-46741455	CMK	blood:	n/a
24	chr11:46741373-46741423	AG04449	skin:	fetal
25	chr11:46744754-46744804	SAEC	small airway:	n/a
26	chr11:46741405-46741455	NHBE	bronchial:	n/a
27	chr11:46744754-46744804	Hela-S3	cervix:	n/a
28	chr11:46741299-46741349	BE2_C	brain:	n/a
29	chr11:46744754-46744804	HRPEpiC	eye:	n/a
30	chr11:46744754-46744804	SK-N-SH	brain:	n/a
31	chr11:46741373-46741423	PrEC	prostate:	n/a
32	chr11:46741299-46741349	AG09319	gingival:	n/a
33	chr11:46741299-46741349	ECC-1	luminal epithelium:	n/a
34	chr11:46744754-46744804	AG10803	skin:	n/a
35	chr11:46741299-46741349	RPTEC	kidney:	n/a
36	chr11:46744754-46744804	AG04450	lung:	fetal
37	chr11:46744754-46744804	RPTEC	kidney:	n/a
38	chr11:46741373-46741423	CMK	blood:	n/a
39	chr11:46744754-46744804	Caco-2	colon:	n/a
40	chr11:46741373-46741423	T-47D	breast:	n/a
41	chr11:46741299-46741349	LNCaP	prostate:	n/a
42	chr11:46741373-46741423	HEK293	kidney:	embryo
43	chr11:46741405-46741455	MCF10A-Er-Src	breast:	n/a
44	chr11:46741299-46741349	HRCEpiC	kidney:	n/a
45	chr11:46741299-46741349	GM12892	blood:	n/a
46	chr11:46741373-46741423	AG04450	lung:	fetal
47	chr11:46741405-46741455	GM19239	blood:	n/a
48	chr11:46741405-46741455	K562	blood:	n/a
49	chr11:46741299-46741349	H1-hESC	embryonic stem cell:	embryo
50	chr11:46741299-46741349	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:46742083..46744335-chr11:46763243..46766196,2	K562	blood:
2	chr11:46722213..46727380-chr11:46743173..46747634,5	MCF-7	breast:
3	chr11:46721125..46723767-chr11:46740816..46743369,3	K562	blood:
4	chr11:46738555..46741511-chr11:46744742..46747329,2	K562	blood:
5	chr11:46402912..46405362-chr11:46740261..46742073,2	K562	blood:
6	chr11:46741871..46743470-chr11:46744640..46747616,2	K562	blood:

No data

Variant related genes	Relation type
F2	TF binding region
F2	CpG island
ENSG00000175213	chromatin interactions
ENSG00000110492	chromatin interactions
ENSG00000175220	chromatin interactions
ENSG00000180210	chromatin interactions

Extended variants
information (count: 184 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:184 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145969693	chr11:46740907-46740908	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs113202549	chr11:46741020-46741021	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs142903294	chr11:46741059-46741060	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs370693897	chr11:46741069-46741070	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs566234614	chr11:46741091-46741092	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs374097100	chr11:46741160-46741161	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs35150107	chr11:46741178-46741179	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs533887406	chr11:46741187-46741188	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs371479474	chr11:46741221-46741222	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs547147827	chr11:46741232-46741233	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs570442167	chr11:46741234-46741235	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs376845267	chr11:46741238-46741239	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs144785536	chr11:46741275-46741276	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs148596790	chr11:46741280-46741281	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs368162633	chr11:46741345-46741346	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs374353447	chr11:46741352-46741353	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs142001812	chr11:46741363-46741364	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs147253030	chr11:46741364-46741365	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs371680056	chr11:46741385-46741386	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs200934494	chr11:46741405-46741406	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs151121282	chr11:46741406-46741407	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs377331494	chr11:46741440-46741441	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs556066325	chr11:46741453-46741454	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs2070850	chr11:46741495-46741496	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs141112085	chr11:46741518-46741519	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs149847109	chr11:46741616-46741617	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs571204237	chr11:46741708-46741709	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs572119629	chr11:46741709-46741710	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs541533099	chr11:46741720-46741721	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs564411153	chr11:46741760-46741761	Weak transcription Enhancers Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs577993900	chr11:46741855-46741856	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs543451812	chr11:46741868-46741869	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs564010842	chr11:46741869-46741870	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs3136433	chr11:46741908-46741909	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs549648152	chr11:46741923-46741924	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs147886868	chr11:46741924-46741925	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs528643288	chr11:46741936-46741937	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs547503708	chr11:46741972-46741973	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs112619944	chr11:46741981-46741982	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs375933055	chr11:46741982-46741983	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs532990120	chr11:46742034-46742035	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs376262187	chr11:46742038-46742039	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs369279444	chr11:46742042-46742043	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs367692335	chr11:46742043-46742044	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs147062971	chr11:46742047-46742048	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs201962988	chr11:46742049-46742050	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs569264167	chr11:46742078-46742079	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs144736001	chr11:46742091-46742092	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs201347110	chr11:46742093-46742094	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs200777670	chr11:46742106-46742107	Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Parathyroid adenoma	22454399	CNVD
Medulloblastoma	21979893	CNVD
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
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Chordoma	18071362	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
small cell lung cancer	20016488	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Myelofibrosis	22110671	CNVD
Melanoma	18172304	CNVD
Intracranial ependymoma	16609018	CNVD
Myxofibrosarcoma	16751306	CNVD
Potocki-Shaffer syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Breast cancer	16608533	CNVD
Hirschsprung''s Disease	21712996	CNVD
Follicular lymphoma	20505157	CNVD
Colorectal cancer	21128281	CNVD
Breast cancer	20409316	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19029149	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:46728800-46745600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:46728800-46745600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr11:46739400-46741000	Enhancers	Fetal Intestine Large	intestine
4	chr11:46739400-46741000	Enhancers	Fetal Intestine Small	intestine
5	chr11:46739400-46741000	Enhancers	Stomach Mucosa	stomach
6	chr11:46739600-46741000	Enhancers	Pancreas	Pancrea
7	chr11:46739600-46741800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:46739800-46741000	Flanking Active TSS	A549	lung
9	chr11:46739800-46741400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:46739800-46742000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr11:46739800-46745600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr11:46740000-46741400	Enhancers	Gastric	stomach
13	chr11:46740000-46742400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr11:46740200-46744400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr11:46740200-46745600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr11:46740200-46745600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr11:46740400-46745600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:46740600-46741000	Enhancers	Right Ventricle	heart
19	chr11:46740600-46741200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr11:46740600-46742800	Active TSS	Liver	Liver
21	chr11:46740800-46741400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr11:46740800-46741800	Bivalent/Poised TSS	HepG2	liver
23	chr11:46741000-46742000	Enhancers	A549	lung
24	chr11:46741000-46742400	Weak transcription	Stomach Mucosa	stomach
25	chr11:46741400-46741600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr11:46741400-46744600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr11:46741800-46742400	Flanking Bivalent TSS/Enh	HepG2	liver
28	chr11:46741800-46746800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr11:46742000-46745600	Weak transcription	A549	lung
30	chr11:46742400-46742600	Enhancers	Stomach Mucosa	stomach
31	chr11:46742400-46742800	Flanking Active TSS	HepG2	liver
32	chr11:46742800-46743000	Flanking Active TSS	Liver	Liver
33	chr11:46742800-46743200	Transcr. at gene 5' and 3'	HepG2	liver
34	chr11:46743000-46744400	Transcr. at gene 5' and 3'	Liver	Liver
35	chr11:46743200-46744200	Genic enhancers	HepG2	liver
36	chr11:46744000-46745400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr11:46744200-46745000	Transcr. at gene 5' and 3'	HepG2	liver
38	chr11:46744400-46744800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr11:46744400-46752000	Genic enhancers	Liver	Liver
40	chr11:46744600-46745000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr11:46744800-46745400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr11:46745000-46745400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr11:46745000-46751200	Genic enhancers	HepG2	liver

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