Variant report

Variant	nsv897214
Chromosome Location	chr11:34764251-34821948
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	chr11:34812906-34812934	K562	blood:	n/a	n/a
2	ARID3A	chr11:34812201-34812444	K562	blood:	n/a	n/a
3	ARID3A	chr11:34804939-34806559	HepG2	liver:	n/a	chr11:34806400-34806416
4	ARID3A	chr11:34804472-34804673	HepG2	liver:	n/a	n/a
5	ATF1	chr11:34779809-34780240	K562	blood:	n/a	n/a
6	ATF1	chr11:34805606-34805830	K562	blood:	n/a	n/a
7	BACH1	chr11:34816262-34816669	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr11:34817624-34817766	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr11:34816276-34816610	K562	blood:	n/a	n/a
10	BATF	chr11:34813278-34813568	GM12878	blood:	n/a	n/a
11	BATF	chr11:34813285-34813593	GM12878	blood:	n/a	n/a
12	BHLHE40	chr11:34779851-34780219	K562	blood:	n/a	n/a
13	CBX3	chr11:34819087-34819402	K562	blood:	n/a	n/a
14	CBX3	chr11:34811209-34811581	K562	blood:	n/a	n/a
15	CBX3	chr11:34819036-34819509	K562	blood:	n/a	n/a
16	CCNT2	chr11:34779935-34780226	K562	blood:	n/a	n/a
17	CEBPB	chr11:34771864-34772195	A549	lung:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
18	CEBPB	chr11:34805336-34806039	HepG2	liver:	n/a	n/a
19	CEBPB	chr11:34771854-34772228	Hela-S3	cervix:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
20	CEBPB	chr11:34805484-34805566	K562	blood:	n/a	n/a
21	CEBPB	chr11:34771852-34772206	ECC-1	luminal epithelium:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
22	CEBPB	chr11:34806101-34806377	HepG2	liver:	n/a	n/a
23	CEBPB	chr11:34796996-34797313	HepG2	liver:	n/a	chr11:34797157-34797168
24	CEBPB	chr11:34771885-34772200	HepG2	liver:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
25	CEBPB	chr11:34778485-34779012	A549	lung:	n/a	n/a
26	CEBPB	chr11:34771764-34772224	MCF-7	breast:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
27	CEBPB	chr11:34780028-34780030	K562	blood:	n/a	n/a
28	CEBPB	chr11:34771773-34772263	MCF-7	breast:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
29	CEBPB	chr11:34805447-34805639	HepG2	liver:	n/a	n/a
30	CEBPB	chr11:34771848-34772232	IMR90	lung:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
31	CEBPB	chr11:34778438-34778980	MCF-7	breast:	n/a	n/a
32	CEBPB	chr11:34806084-34806399	HepG2	liver:	n/a	n/a
33	CEBPB	chr11:34778660-34778757	HepG2	liver:	n/a	n/a
34	CEBPB	chr11:34778541-34778849	A549	lung:	n/a	n/a
35	CEBPB	chr11:34771995-34772115	H1-hESC	embryonic stem cell:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
36	CEBPB	chr11:34771785-34772251	A549	lung:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
37	CEBPB	chr11:34805905-34806033	A549	lung:	n/a	n/a
38	CEBPB	chr11:34775926-34776263	IMR90	lung:	n/a	n/a
39	CEBPB	chr11:34776079-34776182	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr11:34771864-34772225	A549	lung:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
41	CEBPB	chr11:34771899-34772181	K562	blood:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
42	CEBPB	chr11:34775968-34776236	HepG2	liver:	n/a	n/a
43	CEBPB	chr11:34771864-34772249	ECC-1	luminal epithelium:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
44	CEBPB	chr11:34805386-34805909	HepG2	liver:	n/a	n/a
45	CEBPB	chr11:34797104-34797211	A549	lung:	n/a	chr11:34797157-34797168
46	CEBPB	chr11:34797026-34797266	K562	blood:	n/a	chr11:34797157-34797168
47	CEBPB	chr11:34805350-34806477	HepG2	liver:	n/a	n/a
48	CEBPB	chr11:34771955-34772074	HepG2	liver:	n/a	chr11:34772038-34772049 chr11:34772037-34772050 chr11:34772037-34772048 chr11:34772039-34772048
49	CEBPD	chr11:34805401-34805863	HepG2	liver:	n/a	n/a
50	CEBPD	chr11:34806111-34806387	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:34814081-34814131	HEEpiC	esophagus:	n/a
2	chr11:34779084-34779134	Jurkat	blood:	n/a
3	chr11:34771918-34771968	HRCEpiC	kidney:	n/a
4	chr11:34779084-34779134	HEEpiC	esophagus:	n/a
5	chr11:34814081-34814131	CMK	blood:	n/a
6	chr11:34779084-34779134	HL-60	blood:	n/a
7	chr11:34814081-34814131	AG04449	skin:	fetal
8	chr11:34814081-34814131	MCF-7	breast:	n/a
9	chr11:34771918-34771968	PFSK-1	brain:	n/a
10	chr11:34771918-34771968	HEK293	kidney:	embryo
11	chr11:34779084-34779134	NH-A	brain:	n/a
12	chr11:34771918-34771968	PrEC	prostate:	n/a
13	chr11:34814081-34814131	PrEC	prostate:	n/a
14	chr11:34814081-34814131	HCF	heart:	n/a
15	chr11:34771918-34771968	HCT-116	colon:	n/a
16	chr11:34779084-34779134	SKMC	muscle:	n/a
17	chr11:34814081-34814131	IMR90	lung:	fetal
18	chr11:34814081-34814131	HCPEpiC	choroid plexus:	n/a
19	chr11:34771918-34771968	ovcar-3	ovarian:	n/a
20	chr11:34771918-34771968	SAEC	small airway:	n/a
21	chr11:34814081-34814131	GM12891	blood:	n/a
22	chr11:34771918-34771968	HRE	kidney:	n/a
23	chr11:34779084-34779134	AG09319	gingival:	n/a
24	chr11:34779084-34779134	HEK293	kidney:	embryo
25	chr11:34771918-34771968	GM19239	blood:	n/a
26	chr11:34814081-34814131	NH-A	brain:	n/a
27	chr11:34814081-34814131	AG09319	gingival:	n/a
28	chr11:34779084-34779134	BJ	skin:	n/a
29	chr11:34779084-34779134	HAEpiC	amniotic membrane:	n/a
30	chr11:34771918-34771968	Hela-S3	cervix:	n/a
31	chr11:34779084-34779134	SAEC	small airway:	n/a
32	chr11:34814081-34814131	BE2_C	brain:	n/a
33	chr11:34779084-34779134	NT2-D1	testis:	n/a
34	chr11:34771918-34771968	Caco-2	colon:	n/a
35	chr11:34779084-34779134	T-47D	breast:	n/a
36	chr11:34814081-34814131	Hepatocyte	liver:	n/a
37	chr11:34779084-34779134	HCF	heart:	n/a
38	chr11:34814081-34814131	NT2-D1	testis:	n/a
39	chr11:34814081-34814131	NB4	blood:	n/a
40	chr11:34771918-34771968	HepG2	liver:	n/a
41	chr11:34814081-34814131	SK-N-SH_RA	brain:	n/a
42	chr11:34814081-34814131	HMEC	breast:	n/a
43	chr11:34779084-34779134	U87	brain:	n/a
44	chr11:34779084-34779134	ovcar-3	ovarian:	n/a
45	chr11:34779084-34779134	MCF10A-Er-Src	breast:	n/a
46	chr11:34779084-34779134	BE2_C	brain:	n/a
47	chr11:34771918-34771968	AoSMC	blood vessel:	n/a
48	chr11:34771918-34771968	HL-60	blood:	n/a
49	chr11:34771918-34771968	BE2_C	brain:	n/a
50	chr11:34771918-34771968	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr11:34802267..34806129-chr11:34812467..34815224,3	K562	blood:
2	chr11:34775760..34778139-chr11:34861633..34864027,2	K562	blood:
3	chr11:34807272..34809273-chr11:34809643..34812382,3	K562	blood:
4	chr11:34621214..34622751-chr11:34769844..34772782,2	MCF-7	breast:
5	chr11:34660366..34662512-chr11:34808028..34810446,2	MCF-7	breast:
6	chr11:34819205..34826551-chr11:34829823..34835499,8	K562	blood:
7	chr11:34804567..34805318-chr11:34844825..34845441,2	MCF-7	breast:
8	chr11:34807272..34809273-chr11:34809643..34812382,3	K562	blood:
9	chr11:34805559..34807304-chr11:34808633..34811203,2	K562	blood:
10	chr11:34768738..34771170-chr11:34853652..34856105,2	K562	blood:
11	chr11:34802267..34806129-chr11:34812467..34815224,3	K562	blood:
12	chr11:34820151..34822976-chr11:34824163..34828080,3	K562	blood:
13	chr11:34809055..34812032-chr11:34846075..34848426,2	K562	blood:
14	chr11:34814107..34816684-chr11:34826234..34828652,3	K562	blood:
15	chr11:34777504..34779332-chr11:34816777..34819047,2	MCF-7	breast:
16	chr11:34777504..34779332-chr11:34816777..34819047,2	MCF-7	breast:
17	chr11:34805559..34807304-chr11:34808633..34811203,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EHF-5	chr11:34764453-34764746	NONHSAT018763

Variant related genes	Relation type
ENSG00000270491	TF binding region
ENSG00000270491	CpG island

Extended variants
information (count: 2166 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2166 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11604069	chr11:34764251-34764252	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371078767	chr11:34764261-34764262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs575537130	chr11:34764270-34764271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143315598	chr11:34764282-34764283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557964168	chr11:34764339-34764340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558268443	chr11:34764352-34764353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11601923	chr11:34764354-34764355	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs375485512	chr11:34764376-34764377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545687916	chr11:34764456-34764457	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs2859927	chr11:34764459-34764460	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
11	rs1355223	chr11:34764479-34764480	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
12	rs528391627	chr11:34764504-34764505	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
13	rs113768293	chr11:34764509-34764510	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs372545564	chr11:34764529-34764530	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs114319596	chr11:34764540-34764541	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs530403146	chr11:34764541-34764542	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs116313441	chr11:34764574-34764575	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs570463474	chr11:34764658-34764659	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs532998568	chr11:34764663-34764664	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs547238505	chr11:34764706-34764707	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs567038309	chr11:34764716-34764717	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs188517264	chr11:34764745-34764746	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs556077589	chr11:34764774-34764775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs371515191	chr11:34764775-34764776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs537838945	chr11:34764790-34764791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558089916	chr11:34764800-34764801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs191920285	chr11:34764801-34764802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555493418	chr11:34764814-34764815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552764775	chr11:34764845-34764846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77731323	chr11:34764894-34764895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4756168	chr11:34764919-34764920	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs368814011	chr11:34764996-34764997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184467409	chr11:34764997-34764998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs541289303	chr11:34765008-34765009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376658503	chr11:34765010-34765011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs79813216	chr11:34765012-34765013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs546388181	chr11:34765014-34765015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189292453	chr11:34765016-34765017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182327982	chr11:34765018-34765019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112905068	chr11:34765033-34765034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544642971	chr11:34765034-34765035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113185125	chr11:34765035-34765036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs4756169	chr11:34765044-34765045	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs76359854	chr11:34765053-34765054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs79672967	chr11:34765056-34765057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201716029	chr11:34765092-34765093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376578198	chr11:34765093-34765094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560156970	chr11:34765098-34765099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs144102400	chr11:34765103-34765104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185431579	chr11:34765106-34765107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	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
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34752800-34770800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:34759800-34780000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:34760200-34774400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:34760200-34776200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr11:34760200-34776800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr11:34760400-34787000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr11:34762200-34776000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr11:34764200-34764400	Enhancers	Psoas Muscle	Psoas
9	chr11:34764600-34766800	Weak transcription	Psoas Muscle	Psoas
10	chr11:34764800-34776200	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr11:34765000-34777000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:34765200-34787000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr11:34765400-34765600	Enhancers	Fetal Intestine Large	intestine
14	chr11:34766200-34767000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr11:34766200-34767400	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr11:34766200-34767400	Enhancers	HepG2	liver
17	chr11:34766800-34767000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr11:34766800-34767000	Enhancers	Brain Cingulate Gyrus	brain
19	chr11:34766800-34767000	Enhancers	Pancreas	Pancrea
20	chr11:34766800-34767000	Enhancers	Psoas Muscle	Psoas
21	chr11:34766800-34767200	Enhancers	Brain Anterior Caudate	brain
22	chr11:34766800-34767200	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr11:34766800-34767400	Enhancers	Duodenum Mucosa	Duodenum
24	chr11:34766800-34767400	Enhancers	Gastric	stomach
25	chr11:34767000-34769600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr11:34767000-34770000	Weak transcription	Psoas Muscle	Psoas
27	chr11:34767000-34770800	Weak transcription	Pancreas	Pancrea
28	chr11:34767400-34768400	Weak transcription	Duodenum Mucosa	Duodenum
29	chr11:34767400-34769600	Weak transcription	Placenta	Placenta
30	chr11:34767400-34769800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr11:34767400-34770200	Weak transcription	Gastric	stomach
32	chr11:34768600-34768800	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr11:34768600-34769000	Enhancers	Fetal Intestine Small	intestine
34	chr11:34768600-34769200	Enhancers	Sigmoid Colon	Sigmoid Colon
35	chr11:34768800-34769000	Enhancers	Duodenum Mucosa	Duodenum
36	chr11:34768800-34769000	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr11:34768800-34778200	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr11:34769000-34771000	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr11:34769400-34779800	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr11:34769600-34769800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr11:34769600-34770200	Strong transcription	Placenta	Placenta
42	chr11:34769600-34770200	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr11:34769600-34771600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr11:34769800-34771200	Enhancers	Esophagus	oesophagus
45	chr11:34769800-34773400	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr11:34769800-34773600	Enhancers	Breast Myoepithelial Primary Cells	Breast
47	chr11:34770000-34770200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr11:34770000-34770200	Enhancers	Adipose Nuclei	Adipose
49	chr11:34770000-34771000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr11:34770000-34773000	Enhancers	Skeletal Muscle Male	skeletal muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links