Variant report

Variant	esv2513904
Chromosome Location	chr11:71852934-71892793
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71863826-71864078	K562	blood:	n/a	n/a
2	ARID3A	chr11:71855048-71855363	K562	blood:	n/a	n/a
3	ATF1	chr11:71855078-71855400	K562	blood:	n/a	n/a
4	ATF3	chr11:71854980-71855362	K562	blood:	n/a	n/a
5	BACH1	chr11:71855102-71855389	K562	blood:	n/a	chr11:71855183-71855197
6	BACH1	chr11:71855082-71855372	H1-hESC	embryonic stem cell:	n/a	chr11:71855183-71855197
7	BATF	chr11:71855059-71855340	GM12878	blood:	n/a	n/a
8	BCLAF1	chr11:71855051-71855430	GM12878	blood:	n/a	n/a
9	BHLHE40	chr11:71874120-71874221	K562	blood:	n/a	n/a
10	BHLHE40	chr11:71855065-71855353	K562	blood:	n/a	n/a
11	CBX3	chr11:71876288-71876548	K562	blood:	n/a	n/a
12	CBX3	chr11:71876267-71876538	K562	blood:	n/a	n/a
13	CEBPB	chr11:71884923-71885216	IMR90	lung:	n/a	n/a
14	CEBPB	chr11:71871429-71871762	IMR90	lung:	n/a	n/a
15	CEBPB	chr11:71856124-71856610	IMR90	lung:	n/a	n/a
16	CEBPB	chr11:71865867-71866166	K562	blood:	n/a	n/a
17	CEBPB	chr11:71856053-71856684	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr11:71856194-71856488	A549	lung:	n/a	n/a
19	CEBPB	chr11:71885020-71885043	K562	blood:	n/a	n/a
20	CEBPB	chr11:71889113-71889199	K562	blood:	n/a	chr11:71889130-71889143
21	CEBPB	chr11:71871545-71871605	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr11:71885580-71885641	K562	blood:	n/a	chr11:71885590-71885601 chr11:71885589-71885602 chr11:71885589-71885600
23	CEBPB	chr11:71856236-71856591	A549	lung:	n/a	n/a
24	CEBPB	chr11:71884912-71885998	Hela-S3	cervix:	n/a	chr11:71885590-71885601 chr11:71885589-71885602 chr11:71885589-71885600
25	CEBPB	chr11:71885414-71885768	HepG2	liver:	n/a	chr11:71885590-71885601 chr11:71885589-71885602 chr11:71885589-71885600
26	CEBPD	chr11:71863755-71864253	K562	blood:	n/a	n/a
27	CEBPD	chr11:71863720-71864192	K562	blood:	n/a	n/a
28	CHD2	chr11:71856201-71856502	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr11:71885399-71885770	Hela-S3	cervix:	n/a	n/a
30	CREB1	chr11:71855040-71855320	A549	lung:	n/a	n/a
31	CTCF	chr11:71855420-71855570	GM12874	blood:	n/a	n/a
32	CTCF	chr11:71892780-71892978	Kidney_OC	kidney:	n/a	chr11:71892904-71892925 chr11:71892910-71892926
33	CTCF	chr11:71855220-71855370	AG04450	lung:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
34	CTCF	chr11:71854037-71854231	GM12878	blood:	n/a	chr11:71854101-71854122
35	CTCF	chr11:71855097-71855396	Spleen_OC	spleen:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
36	CTCF	chr11:71874207-71874529	K562	blood:	n/a	n/a
37	CTCF	chr11:71855140-71855290	GM12801	blood:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
38	CTCF	chr11:71855091-71855336	GM12891	blood:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
39	CTCF	chr11:71855020-71855170	HAc	cerebellar:	n/a	n/a
40	CTCF	chr11:71892640-71892790	HRE	kidney:	n/a	n/a
41	CTCF	chr11:71855160-71855310	HVMF	connective:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
42	CTCF	chr11:71855140-71855290	HBMEC	blood vessel:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
43	CTCF	chr11:71855115-71855369	Kidney_OC	kidney:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
44	CTCF	chr11:71854023-71854167	GM19238	blood:	n/a	chr11:71854101-71854122
45	CTCF	chr11:71855090-71855421	K562	blood:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
46	CTCF	chr11:71865338-71865382	MCF-7	breast:	n/a	n/a
47	CTCF	chr11:71854030-71854181	MCF-7	breast:	n/a	chr11:71854101-71854122
48	CTCF	chr11:71892780-71892930	AG10803	skin:	n/a	chr11:71892904-71892925 chr11:71892910-71892926
49	CTCF	chr11:71855180-71855330	RPTEC	kidney:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246
50	CTCF	chr11:71855110-71855331	MCF-7	breast:	n/a	chr11:71855223-71855244 chr11:71855229-71855245 chr11:71855233-71855241 chr11:71855228-71855246

No.	Distal block	Cell Line	Cell type
1	chr11:71823336..71825069-chr11:71869762..71871942,2	K562	blood:
2	chr11:71855220..71857768-chr11:71870927..71873588,3	K562	blood:
3	chr11:71882037..71883991-chr11:71899030..71901488,2	K562	blood:
4	chr11:71736115..71737039-chr11:71854770..71856004,4	MCF-7	breast:
5	chr11:71853125..71854944-chr11:71891324..71892926,2	MCF-7	breast:
6	chr11:71736299..71737011-chr11:71854769..71855288,2	K562	blood:
7	chr11:71814518..71815081-chr11:71892378..71893328,2	MCF-7	breast:
8	chr11:71848622..71850667-chr11:71854281..71856804,2	MCF-7	breast:
9	chr11:71853234..71854961-chr11:71893001..71894509,2	MCF-7	breast:
10	chr11:71814495..71816095-chr11:71889921..71892170,2	MCF-7	breast:
11	chr11:71849346..71852118-chr11:71862000..71864280,2	K562	blood:
12	chr11:71851522..71853498-chr11:71890827..71892489,2	K562	blood:
13	chr11:71853125..71854944-chr11:71891324..71892926,2	MCF-7	breast:
14	chr11:71851522..71853498-chr11:71890827..71892489,2	K562	blood:
15	chr11:71822765..71825342-chr11:71891494..71894881,3	MCF-7	breast:
16	chr11:71891814..71894783-chr11:71939408..71941980,2	MCF-7	breast:
17	chr11:71802059..71803123-chr11:71892536..71893396,4	MCF-7	breast:
18	chr11:71876184..71878568-chr11:71933790..71935887,2	K562	blood:
19	chr11:71821644..71823933-chr11:71854873..71856774,3	MCF-7	breast:
20	chr11:71850218..71852679-chr11:71853502..71855781,2	MCF-7	breast:
21	chr11:71726841..71727497-chr11:71854902..71855407,2	MCF-7	breast:
22	chr11:71817497..71819718-chr11:71852568..71855106,2	MCF-7	breast:
23	chr11:71870250..71872525-chr11:71873469..71876026,2	K562	blood:
24	chr11:71808840..71811674-chr11:71882236..71884134,2	MCF-7	breast:
25	chr11:71887728..71891423-chr11:71933064..71936414,3	MCF-7	breast:
26	chr11:71820348..71823346-chr11:71883678..71885281,2	MCF-7	breast:
27	chr11:71822348..71825348-chr11:71852319..71854832,3	MCF-7	breast:
28	chr11:71822984..71825234-chr11:71889608..71891986,2	K562	blood:
29	chr11:71855220..71857768-chr11:71870927..71873588,3	K562	blood:
30	chr11:71821717..71826052-chr11:71851780..71856774,7	MCF-7	breast:
31	chr11:71814410..71815140-chr11:71854813..71855316,2	MCF-7	breast:
32	chr11:71812901..71816436-chr11:71891648..71895235,3	MCF-7	breast:
33	chr11:71870250..71872525-chr11:71873469..71876026,2	K562	blood:
34	chr11:71892089..71899767-chr11:71932198..71938426,12	MCF-7	breast:
35	chr11:71868137..71870587-chr11:71874511..71876205,2	K562	blood:
36	chr11:71688550..71689500-chr11:71854791..71855728,4	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHOX2A-1	chr11:71874366-71874423	ENSG00000204971.3

Variant related genes	Relation type
ENSG00000255860	TF binding region
ENSG00000256518	TF binding region
ENSG00000165458	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000110203	chromatin interactions
ENSG00000238768	chromatin interactions
ENSG00000110195	chromatin interactions
ENSG00000110200	chromatin interactions
ENSG00000256518	chromatin interactions

Extended variants
information (count: 1610 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:1610 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557278312	chr11:71852941-71852942	Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs577101860	chr11:71852945-71852946	Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs189813263	chr11:71852967-71852968	Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs111649414	chr11:71852971-71852972	Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs520360	chr11:71852973-71852974	Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs112210984	chr11:71852976-71852977	Enhancers Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs633850	chr11:71853004-71853005	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs182184890	chr11:71853011-71853012	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs150475708	chr11:71853018-71853019	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs563669305	chr11:71853026-71853027	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs633879	chr11:71853027-71853028	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374382165	chr11:71853047-71853048	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs149602080	chr11:71853054-71853055	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs566754500	chr11:71853071-71853072	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs533820358	chr11:71853081-71853082	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs187161936	chr11:71853091-71853092	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs376888903	chr11:71853097-71853098	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs11235451	chr11:71853099-71853100	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs374227552	chr11:71853124-71853125	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs522381	chr11:71853240-71853241	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs635100	chr11:71853275-71853276	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs542795129	chr11:71853295-71853296	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs554870777	chr11:71853314-71853315	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573196485	chr11:71853329-71853330	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs470642	chr11:71853376-71853377	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs635556	chr11:71853397-71853398	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs565139163	chr11:71853416-71853417	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs201890135	chr11:71853425-71853426	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577142271	chr11:71853461-71853462	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs184524814	chr11:71853468-71853469	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs201027143	chr11:71853517-71853518	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs2852395	chr11:71853518-71853519	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
33	rs372042322	chr11:71853595-71853596	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs142024885	chr11:71853674-71853675	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs28490487	chr11:71853686-71853687	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs565626024	chr11:71853725-71853726	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs116188028	chr11:71853727-71853728	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs148500075	chr11:71853729-71853730	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs552399426	chr11:71853737-71853738	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs570373837	chr11:71853776-71853777	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs28464315	chr11:71853805-71853806	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs4081422	chr11:71853877-71853878	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs7129441	chr11:71853878-71853879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs4081423	chr11:71853888-71853889	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs2846212	chr11:71854003-71854004	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs386754861	chr11:71854008-71854009	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs648612	chr11:71854009-71854010	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs554733669	chr11:71854029-71854030	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs113790500	chr11:71854046-71854047	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs144283701	chr11:71854073-71854074	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71846800-71853400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:71848400-71854600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr11:71849800-71853600	Genic enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:71850600-71853400	Enhancers	NHDF-Ad	bronchial
5	chr11:71850800-71853000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:71850800-71853200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr11:71850800-71853400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr11:71850800-71853400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr11:71850800-71853600	Enhancers	Hela-S3	cervix
10	chr11:71850800-71856200	Enhancers	HMEC	breast
11	chr11:71851000-71853200	Enhancers	Placenta	Placenta
12	chr11:71851000-71853400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr11:71851200-71856200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr11:71851400-71853400	Genic enhancers	Primary neutrophils fromperipheralblood	blood
15	chr11:71851600-71853200	Genic enhancers	Monocytes-CD14+_RO01746	blood
16	chr11:71851800-71853200	Enhancers	Placenta Amnion	Placenta Amnion
17	chr11:71851800-71853200	Enhancers	NHLF	lung
18	chr11:71852000-71853200	Enhancers	HSMMtube	muscle
19	chr11:71852200-71854800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:71852400-71853000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
21	chr11:71852400-71853000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
22	chr11:71852600-71853000	Weak transcription	Primary B cells from cord blood	blood
23	chr11:71852600-71853000	Flanking Active TSS	NHEK	skin
24	chr11:71852600-71853400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr11:71852600-71853400	Enhancers	NH-A	brain
26	chr11:71852600-71853800	Enhancers	Fetal Thymus	thymus
27	chr11:71852600-71854400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr11:71852800-71853000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr11:71852800-71853400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr11:71852800-71853400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr11:71852800-71853400	Enhancers	Osteobl	bone
32	chr11:71852800-71853600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr11:71852800-71853600	Enhancers	Skeletal Muscle Female	skeletal muscle
34	chr11:71852800-71853600	Enhancers	HSMM	muscle
35	chr11:71852800-71855000	Weak transcription	A549	lung
36	chr11:71853000-71853400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:71853000-71853600	Enhancers	Muscle Satellite Cultured Cells	--
38	chr11:71853000-71854400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:71853000-71854400	Enhancers	NHEK	skin
40	chr11:71853000-71856200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr11:71853200-71853400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr11:71853200-71854200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr11:71853200-71854400	Weak transcription	Placenta	Placenta
44	chr11:71853200-71854800	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr11:71853200-71855400	Weak transcription	NHLF	lung
46	chr11:71853400-71853600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr11:71853400-71853800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr11:71853400-71854400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
49	chr11:71853400-71854400	Weak transcription	Osteobl	bone
50	chr11:71853400-71854800	Enhancers	Primary neutrophils fromperipheralblood	blood

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