Variant report

Variant	nsv826073
Chromosome Location	chr11:106064382-106122340
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:240)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:240 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:106079677-106079902	HepG2	liver:	n/a	n/a
2	CBX3	chr11:106093413-106093648	K562	blood:	n/a	n/a
3	CEBPB	chr11:106080716-106081014	HepG2	liver:	n/a	chr11:106080871-106080882
4	CEBPB	chr11:106071822-106071996	HepG2	liver:	n/a	chr11:106071944-106071955
5	CEBPB	chr11:106099902-106099946	K562	blood:	n/a	n/a
6	CEBPB	chr11:106090748-106090782	K562	blood:	n/a	chr11:106090756-106090767
7	CEBPB	chr11:106090617-106090888	HepG2	liver:	n/a	chr11:106090756-106090767
8	CTCF	chr11:106095000-106095150	SK-N-SH_RA	brain:	n/a	n/a
9	CTCF	chr11:106102480-106102630	AG09319	gingival:	n/a	n/a
10	CTCF	chr11:106102400-106102550	A549	lung:	n/a	n/a
11	CTCF	chr11:106095100-106095250	HEEpiC	esophagus:	n/a	n/a
12	CTCF	chr11:106102479-106102601	LNCaP	prostate:	n/a	n/a
13	CTCF	chr11:106095800-106095950	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr11:106095040-106095190	HCFaa	heart:	n/a	n/a
15	CTCF	chr11:106095840-106095990	HMF	breast:	n/a	n/a
16	CTCF	chr11:106102480-106102630	NHLF	lung:	n/a	n/a
17	CTCF	chr11:106102420-106102570	HCFaa	heart:	n/a	n/a
18	CTCF	chr11:106095700-106095850	HCT-116	colon:	n/a	n/a
19	CTCF	chr11:106102440-106102590	AG04449	skin:	n/a	n/a
20	CTCF	chr11:106102420-106102570	NHEK	skin:	n/a	n/a
21	CTCF	chr11:106102462-106102575	Medullo	brain:	n/a	n/a
22	CTCF	chr11:106099840-106099990	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr11:106102420-106102570	HEK293	kidney:	n/a	n/a
24	CTCF	chr11:106102380-106102530	HCM	heart:	n/a	n/a
25	CTCF	chr11:106076560-106076710	HL-60	blood:	n/a	n/a
26	CTCF	chr11:106102320-106102470	HAc	cerebellar:	n/a	n/a
27	CTCF	chr11:106099860-106100010	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr11:106102380-106102530	HFF	foreskin:	n/a	n/a
29	CTCF	chr11:106095040-106095190	RPTEC	kidney:	n/a	n/a
30	CTCF	chr11:106094960-106095110	HCPEpiC	choroid plexus:	n/a	n/a
31	CTCF	chr11:106094920-106095070	HPF	lung:	n/a	n/a
32	CTCF	chr11:106095020-106095170	HEK293	kidney:	n/a	n/a
33	CTCF	chr11:106102460-106102610	HCM	heart:	n/a	n/a
34	CTCF	chr11:106102427-106102728	A549	lung:	n/a	n/a
35	CTCF	chr11:106094996-106095219	GM12878	blood:	n/a	n/a
36	CTCF	chr11:106102447-106102610	ProgFib	skin:	n/a	n/a
37	CTCF	chr11:106102440-106102590	AG09319	gingival:	n/a	n/a
38	CTCF	chr11:106094960-106095110	GM12872	blood:	n/a	n/a
39	CTCF	chr11:106102220-106102370	GM06990	blood:	n/a	n/a
40	CTCF	chr11:106102480-106102630	HMF	breast:	n/a	n/a
41	CTCF	chr11:106102440-106102590	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr11:106077597-106077624	GM20000	blood:	n/a	n/a
43	CTCF	chr11:106079680-106079830	Caco-2	colon:	n/a	n/a
44	CTCF	chr11:106094963-106095224	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr11:106102460-106102610	AG10803	skin:	n/a	n/a
46	CTCF	chr11:106102380-106102530	HVMF	connective:	n/a	n/a
47	CTCF	chr11:106102460-106102610	HMF	breast:	n/a	n/a
48	CTCF	chr11:106095820-106095970	NHEK	skin:	n/a	n/a
49	CTCF	chr11:106095040-106095190	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr11:106102460-106102610	BJ	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:106120370-106120420	A549	lung:	n/a
2	chr11:106120370-106120420	ovcar-3	ovarian:	n/a
3	chr11:106120370-106120420	HMEC	breast:	n/a
4	chr11:106120109-106120159	AG10803	skin:	n/a
5	chr11:106120370-106120420	ECC-1	luminal epithelium:	n/a
6	chr11:106120109-106120159	ECC-1	luminal epithelium:	n/a
7	chr11:106120370-106120420	MCF10A-Er-Src	breast:	n/a
8	chr11:106120370-106120420	MCF-7	breast:	n/a
9	chr11:106120370-106120420	NHBE	bronchial:	n/a
10	chr11:106120109-106120159	HMEC	breast:	n/a
11	chr11:106120109-106120159	NT2-D1	testis:	n/a
12	chr11:106120370-106120420	HIPEpiC	eye:	n/a
13	chr11:106120370-106120420	HUVEC	blood vessel:	n/a
14	chr11:106120370-106120420	NH-A	brain:	n/a
15	chr11:106120109-106120159	ProgFib	skin:	n/a
16	chr11:106120109-106120159	GM19239	blood:	n/a
17	chr11:106120370-106120420	LNCaP	prostate:	n/a
18	chr11:106120109-106120159	AG09319	gingival:	n/a
19	chr11:106120370-106120420	Caco-2	colon:	n/a
20	chr11:106120109-106120159	PFSK-1	brain:	n/a
21	chr11:106120370-106120420	NT2-D1	testis:	n/a
22	chr11:106120109-106120159	HUVEC	blood vessel:	n/a
23	chr11:106120370-106120420	HPAEpiC	pulmonary alveolar:	n/a
24	chr11:106120370-106120420	HNPCEpiC	eye:	n/a
25	chr11:106120370-106120420	HRE	kidney:	n/a
26	chr11:106120109-106120159	GM12892	blood:	n/a
27	chr11:106120109-106120159	GM06990	blood:	n/a
28	chr11:106120370-106120420	HEK293	kidney:	embryo
29	chr11:106120370-106120420	AG04450	lung:	fetal
30	chr11:106120109-106120159	IMR90	lung:	fetal
31	chr11:106120370-106120420	GM12892	blood:	n/a
32	chr11:106120109-106120159	AoSMC	blood vessel:	n/a
33	chr11:106120370-106120420	NB4	blood:	n/a
34	chr11:106120109-106120159	MCF10A-Er-Src	breast:	n/a
35	chr11:106120109-106120159	SKMC	muscle:	n/a
36	chr11:106120109-106120159	GM12891	blood:	n/a
37	chr11:106120370-106120420	PrEC	prostate:	n/a
38	chr11:106120370-106120420	IMR90	lung:	fetal
39	chr11:106120109-106120159	HRPEpiC	eye:	n/a
40	chr11:106120370-106120420	GM12891	blood:	n/a
41	chr11:106120370-106120420	SAEC	small airway:	n/a
42	chr11:106120370-106120420	RPTEC	kidney:	n/a
43	chr11:106120109-106120159	HNPCEpiC	eye:	n/a
44	chr11:106120370-106120420	K562	blood:	n/a
45	chr11:106120109-106120159	HCT-116	colon:	n/a
46	chr11:106120109-106120159	HRCEpiC	kidney:	n/a
47	chr11:106120109-106120159	RPTEC	kidney:	n/a
48	chr11:106120370-106120420	GM06990	blood:	n/a
49	chr11:106120109-106120159	U87	brain:	n/a
50	chr11:106120109-106120159	AG04450	lung:	fetal

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:106065586..106067829-chr11:106070773..106072940,2	K562	blood:
2	chr11:106086341..106089092-chr11:106089266..106092353,3	K562	blood:
3	chr11:106086341..106089092-chr11:106089266..106092353,3	K562	blood:
4	chr11:106111158..106112968-chr11:106121606..106123242,2	K562	blood:
5	chr11:106065586..106067829-chr11:106070773..106072940,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AASDHPPT-1	chr11:106122188-106122264	NONHSAT023981
2	lnc-AASDHPPT-1	chr11:106120963-106120994	XLOC_009269
3	lnc-AASDHPPT-1	chr11:106120691-106121317	NONHSAT023977
4	lnc-AASDHPPT-1	chr11:106120746-106120994	NONHSAT023978
5	lnc-AASDHPPT-1	chr11:106122134-106122238	NONHSAT023980
6	lnc-AASDHPPT-2	chr11:106105687-106105763	NONHSAT023976
7	lnc-AASDHPPT-1	chr11:106122188-106122264	NONHSAT023982
8	lnc-AASDHPPT-1	chr11:106120746-106120994	XLOC_009269

No data

Variant related genes	Relation type
ENSG00000254811	TF binding region
ENSG00000254811	CpG island
ENSG00000254811	chromatin interactions
MIB1	miRNA target sites

Extended variants
information (count: 1610 )
Associated
traits (count: 101 )

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	rs180878261	chr11:106064384-106064385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs4755140	chr11:106064416-106064417	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs34257468	chr11:106064423-106064424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538872240	chr11:106064486-106064487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs386757177	chr11:106064488-106064489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs12421469	chr11:106064490-106064491	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs555224513	chr11:106064514-106064515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370019727	chr11:106064515-106064516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540352842	chr11:106064539-106064540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561525122	chr11:106064551-106064552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201190772	chr11:106064598-106064599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185085629	chr11:106064666-106064667	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373859279	chr11:106064685-106064686	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573622952	chr11:106064721-106064722	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs377485371	chr11:106064732-106064733	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs544478930	chr11:106064868-106064869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562792892	chr11:106064869-106064870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs113314269	chr11:106064897-106064898	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34893486	chr11:106064898-106064899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1893173	chr11:106064899-106064900	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs551585221	chr11:106064900-106064901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs374400098	chr11:106064927-106064928	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560322614	chr11:106064956-106064957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs527778762	chr11:106064961-106064962	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs549494982	chr11:106064989-106064990	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567505908	chr11:106065132-106065133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537850211	chr11:106065154-106065155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs550037062	chr11:106065169-106065170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571624677	chr11:106065172-106065173	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190680571	chr11:106065241-106065242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs554052199	chr11:106065282-106065283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs116772555	chr11:106065309-106065310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533642651	chr11:106065323-106065324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569888384	chr11:106065353-106065354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs541286065	chr11:106065393-106065394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7110907	chr11:106065426-106065427	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs149039975	chr11:106065434-106065435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs562501905	chr11:106065437-106065438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577671708	chr11:106065492-106065493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534549777	chr11:106065495-106065496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs142051909	chr11:106065508-106065509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545366399	chr11:106065516-106065517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181933056	chr11:106065517-106065518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs187056131	chr11:106065529-106065530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549159321	chr11:106065555-106065556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191449645	chr11:106065600-106065601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs531566297	chr11:106065630-106065631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs142152763	chr11:106065648-106065649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376008834	chr11:106065649-106065650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76931788	chr11:106065676-106065677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	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
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
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
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD
Melanoma	17363583	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:106057400-106071800	Weak transcription	Pancreas	Pancrea
2	chr11:106063000-106065000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr11:106063600-106064400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:106063800-106065200	Enhancers	Fetal Brain Male	brain
5	chr11:106064800-106065000	Enhancers	Fetal Intestine Large	intestine
6	chr11:106070200-106071000	Enhancers	Small Intestine	intestine
7	chr11:106070800-106073000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr11:106071800-106072000	Enhancers	Pancreas	Pancrea
9	chr11:106072000-106078800	Weak transcription	Pancreas	Pancrea
10	chr11:106072800-106074000	Enhancers	Fetal Intestine Small	intestine
11	chr11:106073000-106073200	Enhancers	Small Intestine	intestine
12	chr11:106073000-106073800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr11:106073000-106074000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr11:106073200-106073800	Weak transcription	Small Intestine	intestine
15	chr11:106073800-106074000	Enhancers	Small Intestine	intestine
16	chr11:106074000-106074200	Enhancers	Fetal Intestine Large	intestine
17	chr11:106074000-106075400	Enhancers	Ovary	ovary
18	chr11:106074000-106075600	Weak transcription	Fetal Intestine Small	intestine
19	chr11:106074000-106079800	Weak transcription	Small Intestine	intestine
20	chr11:106074200-106075400	Weak transcription	Fetal Intestine Large	intestine
21	chr11:106075400-106075600	Enhancers	Fetal Intestine Large	intestine
22	chr11:106075400-106076400	Weak transcription	Ovary	ovary
23	chr11:106075600-106076000	Weak transcription	Fetal Intestine Large	intestine
24	chr11:106075600-106077400	Enhancers	Fetal Intestine Small	intestine
25	chr11:106076000-106077000	Enhancers	Fetal Intestine Large	intestine
26	chr11:106076400-106076800	Enhancers	Ovary	ovary
27	chr11:106076600-106077000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr11:106077000-106078400	Weak transcription	Fetal Intestine Large	intestine
29	chr11:106077400-106078400	Weak transcription	Fetal Intestine Small	intestine
30	chr11:106078400-106084600	Enhancers	Fetal Intestine Small	intestine
31	chr11:106078400-106084800	Enhancers	Fetal Intestine Large	intestine
32	chr11:106078800-106079800	Enhancers	Pancreas	Pancrea
33	chr11:106079000-106080200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr11:106079000-106080600	Enhancers	Duodenum Mucosa	Duodenum
35	chr11:106079200-106080400	Enhancers	Fetal Kidney	kidney
36	chr11:106079200-106080400	Enhancers	HepG2	liver
37	chr11:106079400-106079800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr11:106079600-106080200	Enhancers	Gastric	stomach
39	chr11:106079800-106080400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:106079800-106080400	Enhancers	Small Intestine	intestine
41	chr11:106079800-106084200	Weak transcription	Pancreas	Pancrea
42	chr11:106080600-106082400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr11:106082400-106083200	Enhancers	Duodenum Mucosa	Duodenum
44	chr11:106082400-106083600	Enhancers	Fetal Kidney	kidney
45	chr11:106084200-106084400	ZNF genes & repeats	Pancreas	Pancrea
46	chr11:106084600-106086600	Weak transcription	Fetal Intestine Small	intestine
47	chr11:106084800-106086600	Weak transcription	Fetal Intestine Large	intestine
48	chr11:106086600-106087600	Enhancers	Fetal Intestine Small	intestine
49	chr11:106086600-106089400	Enhancers	Fetal Intestine Large	intestine
50	chr11:106087600-106088000	Weak transcription	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links