Variant report

Variant	esv32668
Chromosome Location	chr11:64743070-64758087
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	chr11:64757727-64757927	K562	blood:	n/a	n/a
2	ARID3A	chr11:64745294-64745426	K562	blood:	n/a	n/a
3	BACH1	chr11:64757614-64758241	K562	blood:	n/a	n/a
4	BCL11A	chr11:64745231-64745379	H1-hESC	embryonic stem cell:	n/a	chr11:64745316-64745325
5	CBX3	chr11:64745137-64745511	K562	blood:	n/a	n/a
6	CBX3	chr11:64757550-64758060	K562	blood:	n/a	n/a
7	CEBPB	chr11:64755333-64755540	HepG2	liver:	n/a	chr11:64755419-64755430
8	CEBPB	chr11:64755380-64755557	A549	lung:	n/a	chr11:64755419-64755430
9	CHD2	chr11:64746093-64746356	K562	blood:	n/a	n/a
10	CTCF	chr11:64756000-64756150	GM12875	blood:	n/a	n/a
11	CUX1	chr11:64757710-64758075	K562	blood:	n/a	n/a
12	CUX1	chr11:64747124-64747143	GM12878	blood:	n/a	n/a
13	E2F6	chr11:64757691-64757897	K562	blood:	n/a	n/a
14	EGR1	chr11:64744765-64745080	K562	blood:	n/a	chr11:64744963-64744976 chr11:64744963-64744976 chr11:64744962-64744977 chr11:64744963-64744976
15	EGR1	chr11:64744826-64745111	K562	blood:	n/a	chr11:64744963-64744976 chr11:64744963-64744976 chr11:64744962-64744977 chr11:64744963-64744976
16	ELF1	chr11:64757514-64758086	K562	blood:	n/a	chr11:64757792-64757805 chr11:64757794-64757805
17	ELF1	chr11:64757648-64757955	K562	blood:	n/a	chr11:64757792-64757805 chr11:64757794-64757805
18	EP300	chr11:64757681-64757873	K562	blood:	n/a	chr11:64757794-64757803
19	GABPA	chr11:64757621-64757980	K562	blood:	n/a	n/a
20	GABPA	chr11:64757571-64757982	K562	blood:	n/a	n/a
21	HCFC1	chr11:64757793-64757811	K562	blood:	n/a	n/a
22	HEY1	chr11:64757611-64757958	K562	blood:	n/a	n/a
23	HNF4A	chr11:64755593-64756271	HepG2	liver:	n/a	chr11:64756092-64756107
24	HNF4A	chr11:64755926-64756191	HepG2	liver:	n/a	chr11:64756092-64756107
25	HNF4A	chr11:64755521-64755827	HepG2	liver:	n/a	n/a
26	HNF4A	chr11:64754331-64754539	HepG2	liver:	n/a	chr11:64754413-64754428
27	HNF4A	chr11:64755978-64756163	HepG2	liver:	n/a	chr11:64756092-64756107
28	HNF4A	chr11:64755463-64755866	HepG2	liver:	n/a	n/a
29	HNF4G	chr11:64754273-64754569	HepG2	liver:	n/a	chr11:64754414-64754429
30	JUND	chr11:64757685-64758024	K562	blood:	n/a	chr11:64757983-64757990
31	MAFF	chr11:64757880-64758169	HepG2	liver:	n/a	chr11:64758007-64758025 chr11:64758006-64758020
32	MAFF	chr11:64757792-64758200	K562	blood:	n/a	chr11:64758007-64758025 chr11:64758006-64758020
33	MAFF	chr11:64755826-64755990	HepG2	liver:	n/a	n/a
34	MAFK	chr11:64754396-64754493	HepG2	liver:	n/a	n/a
35	MAFK	chr11:64745348-64745349	K562	blood:	n/a	n/a
36	MAFK	chr11:64757879-64758116	HepG2	liver:	n/a	chr11:64758012-64758023 chr11:64758006-64758020 chr11:64758013-64758024 chr11:64758010-64758019 chr11:64758005-64758021 chr11:64758008-64758023 chr11:64758013-64758024 chr11:64758003-64758023 chr11:64758011-64758025 chr11:64758009-64758019
37	MAFK	chr11:64757849-64758191	IMR90	lung:	n/a	chr11:64758012-64758023 chr11:64758006-64758020 chr11:64758013-64758024 chr11:64758010-64758019 chr11:64758005-64758021 chr11:64758008-64758023 chr11:64758013-64758024 chr11:64758003-64758023 chr11:64758011-64758025 chr11:64758009-64758019
38	MAFK	chr11:64755730-64756072	HepG2	liver:	n/a	n/a
39	MAFK	chr11:64755769-64756087	HepG2	liver:	n/a	n/a
40	MAFK	chr11:64754325-64754506	HepG2	liver:	n/a	n/a
41	MAFK	chr11:64757838-64758184	HepG2	liver:	n/a	chr11:64758012-64758023 chr11:64758006-64758020 chr11:64758013-64758024 chr11:64758010-64758019 chr11:64758005-64758021 chr11:64758008-64758023 chr11:64758013-64758024 chr11:64758003-64758023 chr11:64758011-64758025 chr11:64758009-64758019
42	MAFK	chr11:64757712-64758203	K562	blood:	n/a	chr11:64758012-64758023 chr11:64758006-64758020 chr11:64758013-64758024 chr11:64758010-64758019 chr11:64758005-64758021 chr11:64758008-64758023 chr11:64758013-64758024 chr11:64758003-64758023 chr11:64758011-64758025 chr11:64758009-64758019
43	MAX	chr11:64745203-64745405	NB4	blood:	n/a	n/a
44	MAX	chr11:64745291-64745313	K562	blood:	n/a	n/a
45	MAX	chr11:64757654-64757976	K562	blood:	n/a	chr11:64757862-64757871
46	MAX	chr11:64757479-64758021	K562	blood:	n/a	chr11:64757862-64757871
47	MAX	chr11:64757759-64757936	K562	blood:	n/a	chr11:64757862-64757871
48	MAZ	chr11:64745200-64745342	GM12878	blood:	n/a	n/a
49	MAZ	chr11:64745270-64745391	K562	blood:	n/a	n/a
50	MAZ	chr11:64744963-64745517	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64756382-64756432	HEK293	kidney:	embryo
2	chr11:64756382-64756432	SK-N-SH_RA	brain:	n/a
3	chr11:64756382-64756432	HIPEpiC	eye:	n/a
4	chr11:64756382-64756432	BJ	skin:	n/a
5	chr11:64756382-64756432	GM19239	blood:	n/a
6	chr11:64756382-64756432	HCF	heart:	n/a
7	chr11:64756382-64756432	AG10803	skin:	n/a
8	chr11:64756382-64756432	HCM	heart:	n/a
9	chr11:64756382-64756432	AoSMC	blood vessel:	n/a
10	chr11:64756382-64756432	NT2-D1	testis:	n/a
11	chr11:64756382-64756432	Caco-2	colon:	n/a
12	chr11:64756382-64756432	HRCEpiC	kidney:	n/a
13	chr11:64756382-64756432	PANC-1	pancreas:	n/a
14	chr11:64756382-64756432	SK-N-MC	brain:	n/a
15	chr11:64756382-64756432	NHBE	bronchial:	n/a
16	chr11:64756382-64756432	MCF-7	breast:	n/a
17	chr11:64756382-64756432	HAEpiC	amniotic membrane:	n/a
18	chr11:64756382-64756432	K562	blood:	n/a
19	chr11:64756382-64756432	AG04450	lung:	fetal
20	chr11:64756382-64756432	HCPEpiC	choroid plexus:	n/a
21	chr11:64756382-64756432	GM12892	blood:	n/a
22	chr11:64756382-64756432	AG09309	skin:	n/a
23	chr11:64756382-64756432	HMEC	breast:	n/a
24	chr11:64756382-64756432	HCT-116	colon:	n/a
25	chr11:64756382-64756432	CMK	blood:	n/a
26	chr11:64756382-64756432	SAEC	small airway:	n/a
27	chr11:64756382-64756432	NB4	blood:	n/a
28	chr11:64756382-64756432	HUVEC	blood vessel:	n/a
29	chr11:64756382-64756432	SK-N-SH	brain:	n/a
30	chr11:64756382-64756432	Jurkat	blood:	n/a
31	chr11:64756382-64756432	NHDF-neo	bronchial:	n/a
32	chr11:64756382-64756432	ECC-1	luminal epithelium:	n/a
33	chr11:64756382-64756432	PFSK-1	brain:	n/a
34	chr11:64756382-64756432	IMR90	lung:	fetal
35	chr11:64756382-64756432	Hela-S3	cervix:	n/a
36	chr11:64756382-64756432	LNCaP	prostate:	n/a
37	chr11:64756382-64756432	U87	brain:	n/a
38	chr11:64756382-64756432	NH-A	brain:	n/a
39	chr11:64756382-64756432	HL-60	blood:	n/a
40	chr11:64756382-64756432	A549	lung:	n/a
41	chr11:64756382-64756432	Hepatocyte	liver:	n/a
42	chr11:64756382-64756432	ovcar-3	ovarian:	n/a
43	chr11:64756382-64756432	GM12878	blood:	n/a
44	chr11:64756382-64756432	HEEpiC	esophagus:	n/a
45	chr11:64756382-64756432	AG04449	skin:	fetal
46	chr11:64756382-64756432	H1-hESC	embryonic stem cell:	embryo
47	chr11:64756382-64756432	BE2_C	brain:	n/a
48	chr11:64756382-64756432	GM06990	blood:	n/a
49	chr11:64756382-64756432	HRPEpiC	eye:	n/a
50	chr11:64756382-64756432	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64641742..64644629-chr11:64755120..64758066,2	MCF-7	breast:
2	chr11:64693891..64698050-chr11:64753803..64757942,3	K562	blood:
3	chr11:64739428..64743212-chr11:64780553..64782608,3	K562	blood:
4	chr11:64750017..64751752-chr11:64754322..64756444,2	K562	blood:
5	chr11:64681631..64685240-chr11:64749836..64753249,3	K562	blood:
6	chr11:64737496..64741049-chr11:64742327..64745214,4	K562	blood:
7	chr11:64739549..64741143-chr11:64741750..64744421,2	K562	blood:
8	chr11:64646103..64648605-chr11:64754086..64755797,2	MCF-7	breast:
9	chr11:64750017..64751752-chr11:64754322..64756444,2	K562	blood:
10	chr11:64754069..64755968-chr11:64760951..64763260,2	MCF-7	breast:
11	chr11:64743732..64745431-chr11:64877675..64879183,2	K562	blood:
12	chr11:64743929..64746814-chr11:64767297..64768810,2	K562	blood:
13	chr11:64681631..64684611-chr11:64749836..64752402,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf85-1	chr11:64755418-64757986	NONHSAT022046

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	BATF2	hsa-miR-122-5p	chr11:64755476-64755498

Variant related genes	Relation type
C11orf85	TF binding region
BATF2	TF binding region
C11orf85	CpG island
BATF2	CpG island
ENSG00000068971	chromatin interactions
ENSG00000254501	chromatin interactions
ENSG00000149823	chromatin interactions
ENSG00000273003	chromatin interactions
ENSG00000110046	chromatin interactions
ENSG00000168070	chromatin interactions
ENSG00000110047	chromatin interactions
ENSG00000213465	chromatin interactions

Extended variants
information (count: 606 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548574503	chr11:64743111-64743112	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs74712974	chr11:64743144-64743145	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs151298562	chr11:64743178-64743179	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs547721420	chr11:64743179-64743180	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs187855390	chr11:64743192-64743193	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs189726893	chr11:64743223-64743224	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183097155	chr11:64743242-64743243	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs569816612	chr11:64743297-64743298	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs537981925	chr11:64743332-64743333	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187822325	chr11:64743338-64743339	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs111922018	chr11:64743356-64743357	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs562107833	chr11:64743421-64743422	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140577588	chr11:64743434-64743435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs527686553	chr11:64743452-64743453	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs571347408	chr11:64743500-64743501	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs150477154	chr11:64743502-64743503	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs191979144	chr11:64743510-64743511	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs574223369	chr11:64743524-64743525	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs543221748	chr11:64743552-64743553	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs547742133	chr11:64743571-64743572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556516795	chr11:64743596-64743597	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs1152642	chr11:64743621-64743622	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs61893588	chr11:64743711-64743712	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs149129479	chr11:64743730-64743731	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564965710	chr11:64743808-64743809	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs533169948	chr11:64743820-64743821	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs527283053	chr11:64743846-64743847	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs540996203	chr11:64743875-64743876	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs185204605	chr11:64743922-64743923	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs188522585	chr11:64744003-64744004	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs564982523	chr11:64744033-64744034	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs17146543	chr11:64744059-64744060	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs550025788	chr11:64744126-64744127	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs192900336	chr11:64744138-64744139	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs532324644	chr11:64744180-64744181	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs551469416	chr11:64744243-64744244	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs114190142	chr11:64744267-64744268	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs569741033	chr11:64744306-64744307	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs184949981	chr11:64744320-64744321	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs533953592	chr11:64744340-64744341	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs535236671	chr11:64744366-64744367	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs553716701	chr11:64744398-64744399	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs74409604	chr11:64744428-64744429	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs199793617	chr11:64744438-64744439	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs567636590	chr11:64744465-64744466	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs536574319	chr11:64744471-64744472	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs555041842	chr11:64744496-64744497	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs565364324	chr11:64744557-64744558	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs534301313	chr11:64744566-64744567	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs554057138	chr11:64744624-64744625	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:232 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64740000-64743200	Enhancers	Primary B cells from cord blood	blood
2	chr11:64742800-64746200	Weak transcription	GM12878-XiMat	blood
3	chr11:64742800-64751400	Weak transcription	Primary B cells from peripheral blood	blood
4	chr11:64743200-64746200	Weak transcription	Primary B cells from cord blood	blood
5	chr11:64745000-64745400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr11:64746200-64746600	Enhancers	GM12878-XiMat	blood
7	chr11:64746400-64746600	Enhancers	Primary B cells from cord blood	blood
8	chr11:64747800-64748000	Enhancers	Lung	lung
9	chr11:64748000-64756400	Weak transcription	Lung	lung
10	chr11:64748200-64750200	Enhancers	Fetal Brain Male	brain
11	chr11:64748400-64749000	Enhancers	Brain Substantia Nigra	brain
12	chr11:64749800-64750000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr11:64750000-64750200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
14	chr11:64750000-64750200	Enhancers	Colonic Mucosa	Colon
15	chr11:64750200-64756600	Weak transcription	Colonic Mucosa	Colon
16	chr11:64750200-64757000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr11:64751200-64752600	Enhancers	Primary B cells from cord blood	blood
18	chr11:64751400-64753200	Enhancers	Primary B cells from peripheral blood	blood
19	chr11:64751600-64752600	Enhancers	Primary monocytes fromperipheralblood	blood
20	chr11:64751800-64752600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr11:64752000-64756400	Weak transcription	Right Atrium	heart
22	chr11:64752200-64752400	Enhancers	Sigmoid Colon	Sigmoid Colon
23	chr11:64752200-64752600	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr11:64752400-64752600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:64752400-64752600	Enhancers	Placenta	Placenta
26	chr11:64752400-64752600	Enhancers	GM12878-XiMat	blood
27	chr11:64752400-64756200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr11:64752400-64764200	Weak transcription	Aorta	Aorta
29	chr11:64752600-64755000	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr11:64752600-64755000	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr11:64752600-64755000	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr11:64752600-64755200	Weak transcription	Primary B cells from cord blood	blood
33	chr11:64752600-64755400	Weak transcription	GM12878-XiMat	blood
34	chr11:64752600-64756800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr11:64752800-64755600	Weak transcription	Placenta	Placenta
36	chr11:64753200-64755200	Weak transcription	Primary B cells from peripheral blood	blood
37	chr11:64753400-64753600	Weak transcription	Fetal Intestine Small	intestine
38	chr11:64753800-64755400	Enhancers	HepG2	liver
39	chr11:64754000-64754200	Enhancers	Gastric	stomach
40	chr11:64754000-64754600	ZNF genes & repeats	Fetal Intestine Small	intestine
41	chr11:64754000-64757200	Weak transcription	K562	blood
42	chr11:64754200-64754600	Enhancers	Fetal Intestine Large	intestine
43	chr11:64754200-64756400	Weak transcription	Gastric	stomach
44	chr11:64754600-64755000	Weak transcription	Fetal Intestine Large	intestine
45	chr11:64754600-64755200	Weak transcription	Fetal Intestine Small	intestine
46	chr11:64754600-64756000	Weak transcription	Left Ventricle	heart
47	chr11:64754600-64757200	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr11:64755000-64755200	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr11:64755000-64755400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr11:64755000-64756600	Weak transcription	Duodenum Mucosa	Duodenum

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