Variant report

Variant	esv2762892
Chromosome Location	chr11:4541825-4619236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:581)
CpG islands
(count:1100)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:581 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:4560933-4561036	K562	blood:	n/a	n/a
2	ARID3A	chr11:4568278-4568297	HepG2	liver:	n/a	n/a
3	ATF1	chr11:4601664-4601807	K562	blood:	n/a	n/a
4	BACH1	chr11:4580944-4580984	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr11:4544032-4544147	K562	blood:	n/a	n/a
6	CEBPB	chr11:4569325-4569525	A549	lung:	n/a	chr11:4569397-4569410
7	CEBPB	chr11:4551821-4552021	A549	lung:	n/a	n/a
8	CEBPB	chr11:4568337-4568455	HepG2	liver:	n/a	n/a
9	CEBPB	chr11:4578528-4578549	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD1	chr11:4591087-4591112	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr11:4560848-4561180	HepG2	liver:	n/a	n/a
12	CTCF	chr11:4560960-4561110	GM12864	blood:	n/a	n/a
13	CTCF	chr11:4560980-4561130	HRPEpiC	eye:	n/a	n/a
14	CTCF	chr11:4560831-4561204	A549	lung:	n/a	n/a
15	CTCF	chr11:4560928-4561166	GM10266	blood:	n/a	n/a
16	CTCF	chr11:4572900-4573050	GM12866	blood:	n/a	n/a
17	CTCF	chr11:4561320-4561470	HMF	breast:	n/a	n/a
18	CTCF	chr11:4572920-4573070	HMF	breast:	n/a	n/a
19	CTCF	chr11:4560960-4561110	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr11:4572960-4573110	A549	lung:	n/a	n/a
21	CTCF	chr11:4572960-4573110	HAc	cerebellar:	n/a	n/a
22	CTCF	chr11:4572947-4573082	GM10266	blood:	n/a	n/a
23	CTCF	chr11:4572940-4573090	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr11:4560920-4561070	HMEC	breast:	n/a	n/a
25	CTCF	chr11:4573040-4573190	HCM	heart:	n/a	n/a
26	CTCF	chr11:4560960-4561110	GM12867	blood:	n/a	n/a
27	CTCF	chr11:4560919-4561159	GM19240	blood:	n/a	n/a
28	CTCF	chr11:4560945-4561161	HepG2	liver:	n/a	n/a
29	CTCF	chr11:4560960-4561110	HMF	breast:	n/a	n/a
30	CTCF	chr11:4572940-4573090	GM12869	blood:	n/a	n/a
31	CTCF	chr11:4560932-4561139	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr11:4553060-4553210	HEK293	kidney:	n/a	n/a
33	CTCF	chr11:4601880-4602030	A549	lung:	n/a	n/a
34	CTCF	chr11:4572920-4573070	GM12872	blood:	n/a	n/a
35	CTCF	chr11:4560880-4561030	HAc	cerebellar:	n/a	n/a
36	CTCF	chr11:4560980-4561130	GM12878	blood:	n/a	n/a
37	CTCF	chr11:4572920-4573070	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr11:4560980-4561130	K562	blood:	n/a	n/a
39	CTCF	chr11:4572999-4573093	GM10248	blood:	n/a	n/a
40	CTCF	chr11:4573285-4573354	GM12878	blood:	n/a	n/a
41	CTCF	chr11:4572980-4573130	WI-38	lung:	n/a	n/a
42	CTCF	chr11:4573000-4573150	GM12869	blood:	n/a	n/a
43	CTCF	chr11:4560835-4561243	IMR90	lung:	n/a	n/a
44	CTCF	chr11:4560949-4561130	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:4560938-4561150	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr11:4560883-4561322	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:4572803-4573243	MCF-7	breast:	n/a	n/a
48	CTCF	chr11:4561304-4561367	Medullo	brain:	n/a	n/a
49	CTCF	chr11:4560824-4561220	A549	lung:	n/a	n/a
50	CTCF	chr11:4572920-4573070	Hela-S3	cervix:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:4566853-4566903	HMEC	breast:	n/a
2	chr11:4566380-4566430	SK-N-MC	brain:	n/a
3	chr11:4566853-4566903	HMEC	breast:	n/a
4	chr11:4566380-4566430	SK-N-MC	brain:	n/a
5	chr11:4565489-4565539	SK-N-MC	brain:	n/a
6	chr11:4597246-4597296	MCF-7	breast:	n/a
7	chr11:4606632-4606682	AG10803	skin:	n/a
8	chr11:4615540-4615590	HNPCEpiC	eye:	n/a
9	chr11:4566169-4566219	BE2_C	brain:	n/a
10	chr11:4599997-4600047	ECC-1	luminal epithelium:	n/a
11	chr11:4597246-4597296	ECC-1	luminal epithelium:	n/a
12	chr11:4615540-4615590	HEK293	kidney:	embryo
13	chr11:4600034-4600084	SKMC	muscle:	n/a
14	chr11:4606701-4606751	SKMC	muscle:	n/a
15	chr11:4566853-4566903	Hela-S3	cervix:	n/a
16	chr11:4590491-4590541	SK-N-SH_RA	brain:	n/a
17	chr11:4599997-4600047	HCT-116	colon:	n/a
18	chr11:4615540-4615590	MCF10A-Er-Src	breast:	n/a
19	chr11:4566853-4566903	PFSK-1	brain:	n/a
20	chr11:4566380-4566430	HPAEpiC	pulmonary alveolar:	n/a
21	chr11:4599637-4599687	K562	blood:	n/a
22	chr11:4590491-4590541	BJ	skin:	n/a
23	chr11:4565489-4565539	GM12892	blood:	n/a
24	chr11:4608359-4608409	Caco-2	colon:	n/a
25	chr11:4608359-4608409	GM19239	blood:	n/a
26	chr11:4615540-4615590	SAEC	small airway:	n/a
27	chr11:4590491-4590541	HNPCEpiC	eye:	n/a
28	chr11:4566380-4566430	ovcar-3	ovarian:	n/a
29	chr11:4615540-4615590	A549	lung:	n/a
30	chr11:4599997-4600047	Jurkat	blood:	n/a
31	chr11:4566380-4566430	NT2-D1	testis:	n/a
32	chr11:4600034-4600084	HRE	kidney:	n/a
33	chr11:4608359-4608409	H1-hESC	embryonic stem cell:	embryo
34	chr11:4615063-4615113	HMEC	breast:	n/a
35	chr11:4566380-4566430	HepG2	liver:	n/a
36	chr11:4590536-4590586	AG04450	lung:	fetal
37	chr11:4606701-4606751	LNCaP	prostate:	n/a
38	chr11:4615063-4615113	HAEpiC	amniotic membrane:	n/a
39	chr11:4566853-4566903	IMR90	lung:	fetal
40	chr11:4599637-4599687	HRCEpiC	kidney:	n/a
41	chr11:4606632-4606682	BJ	skin:	n/a
42	chr11:4566169-4566219	H1-hESC	embryonic stem cell:	embryo
43	chr11:4615063-4615113	GM06990	blood:	n/a
44	chr11:4599033-4599083	AG04449	skin:	fetal
45	chr11:4565489-4565539	MCF-7	breast:	n/a
46	chr11:4615540-4615590	HepG2	liver:	n/a
47	chr11:4615540-4615590	BE2_C	brain:	n/a
48	chr11:4566380-4566430	T-47D	breast:	n/a
49	chr11:4566853-4566903	SK-N-SH_RA	brain:	n/a
50	chr11:4615540-4615590	HEEpiC	esophagus:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:4595698..4599305-chr11:4600956..4604069,3	K562	blood:
2	chr11:4614691..4617476-chr11:4618507..4620828,3	K562	blood:
3	chr11:4563397..4564933-chr11:4566554..4568624,2	K562	blood:
4	chr11:4558523..4560457-chr11:4563023..4565124,2	K562	blood:
5	chr1:45195876..45196736-chr11:4594433..4595433,5	Hela-S3	cervix:
6	chr11:4208297..4209495-chr11:4560565..4561805,6	K562	blood:
7	chr11:4208647..4209327-chr11:4572350..4573087,2	MCF-7	breast:
8	chr11:4598261..4600650-chr11:4609395..4611487,2	K562	blood:
9	chr11:4563433..4564999-chr11:4565844..4568054,2	K562	blood:
10	chr11:4208191..4209065-chr11:4560550..4561852,3	MCF-7	breast:
11	chr11:4535006..4537782-chr11:4538961..4542552,3	K562	blood:
12	chr11:4604767..4606458-chr11:4610235..4612075,2	K562	blood:
13	chr11:4604767..4606458-chr11:4610235..4612075,2	K562	blood:
14	chr11:4558523..4560457-chr11:4563023..4565124,2	K562	blood:
15	chr11:4618307..4620413-chr11:4621041..4623976,4	K562	blood:
16	chr11:4575133..4577035-chr11:4578318..4580954,2	K562	blood:
17	chr11:4202964..4204119-chr11:4560777..4561880,3	MCF-7	breast:
18	chr11:4563397..4564933-chr11:4566554..4568624,2	K562	blood:
19	chr11:4575133..4577035-chr11:4578318..4580954,2	K562	blood:
20	chr11:4208891..4209471-chr11:4572771..4573597,3	MCF-7	breast:
21	chr11:4544362..4546597-chr11:4548286..4550810,3	K562	blood:
22	chr11:4208014..4209388-chr11:4560615..4561905,12	MCF-7	breast:
23	chr11:4544362..4546597-chr11:4548286..4550810,3	K562	blood:

No data

Variant related genes	Relation type
OR52M1	TF binding region
OR52M2P	TF binding region
OR52I2	TF binding region
OR52I1	TF binding region
C11orf40	TF binding region
OR52M1	CpG island
OR52M2P	CpG island
OR52I2	CpG island
OR52I1	CpG island
C11orf40	CpG island
ENSG00000232268	chromatin interactions
ENSG00000254480	chromatin interactions
ENSG00000171987	chromatin interactions
ENSG00000197790	chromatin interactions
ENSG00000167333	chromatin interactions
ENSG00000226616	chromatin interactions

Extended variants
information (count: 3360 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3360 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113874710	chr11:4541839-4541840	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577152498	chr11:4541841-4541842	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs2566202	chr11:4541853-4541854	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs551884369	chr11:4541871-4541872	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs181588477	chr11:4541878-4541879	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs575221206	chr11:4541900-4541901	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs139127156	chr11:4541901-4541902	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148700317	chr11:4541915-4541916	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs117625147	chr11:4541971-4541972	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs73439815	chr11:4541983-4541984	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs147416706	chr11:4541986-4541987	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs545869611	chr11:4542034-4542035	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs73439816	chr11:4542119-4542120	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs191055494	chr11:4542132-4542133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs117421267	chr11:4542138-4542139	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369369775	chr11:4542169-4542170	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs145319271	chr11:4542212-4542213	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548915462	chr11:4542242-4542243	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs144439685	chr11:4542255-4542256	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs558457586	chr11:4542256-4542257	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs183062578	chr11:4542295-4542296	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs578197000	chr11:4542298-4542299	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs550333440	chr11:4542304-4542305	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567906181	chr11:4542340-4542341	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575947649	chr11:4542375-4542376	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs2709131	chr11:4542381-4542382	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs552617823	chr11:4542457-4542458	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556171117	chr11:4542470-4542471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs570898664	chr11:4542495-4542496	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559880853	chr11:4542518-4542519	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534977061	chr11:4542548-4542549	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538377853	chr11:4542803-4542804	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7131138	chr11:4542813-4542814	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs190374124	chr11:4542832-4542833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs571929181	chr11:4542834-4542835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs80296763	chr11:4542836-4542837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs529118325	chr11:4542848-4542849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs10500605	chr11:4542852-4542853	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs557003755	chr11:4542854-4542855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147218618	chr11:4542954-4542955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs16907464	chr11:4543008-4543009	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs11032597	chr11:4543032-4543033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs56186485	chr11:4543045-4543046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs546984932	chr11:4543046-4543047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs182841143	chr11:4543079-4543080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs11032598	chr11:4543123-4543124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs557632018	chr11:4543126-4543127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569488444	chr11:4543131-4543132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs199945040	chr11:4543173-4543174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs386750014	chr11:4543175-4543176	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Breast cancer	19432969	CNVD
Alzheimer''s disease	17576883	CNVD
Long-qt syndrome	17576883	CNVD
Emphysema	19352772	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chordoma	18071362	CNVD
Breast cancer	16608533	CNVD
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	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
Gastric cancer	17908304	CNVD
Barrett''s syndrome	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Neuroblastoma	21124317	CNVD
Lung adenocarcinoma	17086460	CNVD
Lung cancer	17086460	CNVD
Schizophrenia	21399695	CNVD
Gastric cancer	16891809	CNVD
Cancer	17160897	CNVD
Multiple myeloma	16616336	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Pancreatic cancer	23613489	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:4542800-4544200	Enhancers	Primary T cells from cord blood	blood
2	chr11:4544600-4545600	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr11:4544800-4545400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr11:4548200-4548600	Enhancers	Esophagus	oesophagus
5	chr11:4552800-4553000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr11:4552800-4553200	Enhancers	Placenta	Placenta
7	chr11:4552800-4553200	Active TSS	Stomach Smooth Muscle	stomach
8	chr11:4552800-4553400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr11:4552800-4553400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
10	chr11:4552800-4553400	Enhancers	Esophagus	oesophagus
11	chr11:4564600-4565200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr11:4564600-4565200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr11:4564600-4565400	Enhancers	HUVEC	blood vessel
14	chr11:4564600-4565400	Enhancers	NHEK	skin
15	chr11:4564800-4565200	Enhancers	A549	lung
16	chr11:4564800-4565400	Enhancers	HMEC	breast
17	chr11:4566600-4569800	Enhancers	Liver	Liver
18	chr11:4567200-4568800	Enhancers	Sigmoid Colon	Sigmoid Colon
19	chr11:4567600-4569400	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr11:4567800-4569200	Enhancers	Fetal Intestine Small	intestine
21	chr11:4567800-4569400	Enhancers	Fetal Intestine Large	intestine
22	chr11:4568000-4568400	Enhancers	Stomach Mucosa	stomach
23	chr11:4568000-4569400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr11:4568400-4568600	Enhancers	Gastric	stomach
25	chr11:4568600-4569200	Enhancers	Small Intestine	intestine
26	chr11:4568600-4580600	Weak transcription	Gastric	stomach
27	chr11:4572000-4572400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:4572400-4572600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr11:4572600-4572800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr11:4575200-4575600	Enhancers	K562	blood
31	chr11:4580400-4581600	Enhancers	Pancreas	Pancrea
32	chr11:4580400-4582600	Enhancers	Placenta	Placenta
33	chr11:4580600-4581200	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr11:4580600-4581400	Enhancers	Esophagus	oesophagus
35	chr11:4580600-4581600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr11:4580600-4581600	Enhancers	Gastric	stomach
37	chr11:4580800-4581600	Enhancers	Fetal Lung	lung
38	chr11:4580800-4581800	Enhancers	Fetal Intestine Large	intestine
39	chr11:4580800-4581800	Enhancers	Fetal Intestine Small	intestine
40	chr11:4580800-4582000	Enhancers	Placenta Amnion	Placenta Amnion
41	chr11:4581000-4581200	Flanking Active TSS	Colonic Mucosa	Colon
42	chr11:4581000-4581400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr11:4581000-4581400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr11:4581000-4581400	Enhancers	Breast Myoepithelial Primary Cells	Breast
45	chr11:4581000-4581800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr11:4581000-4582000	Enhancers	Duodenum Mucosa	Duodenum
47	chr11:4581200-4581400	Active TSS	Colonic Mucosa	Colon
48	chr11:4581200-4582000	Enhancers	Stomach Mucosa	stomach
49	chr11:4586400-4588400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr11:4586600-4588600	Enhancers	Adipose Nuclei	Adipose

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