Variant report

Variant	esv1809270
Chromosome Location	chr11:15504338-15528140
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:134)
CpG islands
(count:61)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:134 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:15504760-15505122	GM12878	blood:	n/a	n/a
2	BATF	chr11:15504772-15505063	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:15510761-15511046	HepG2	liver:	n/a	n/a
4	CEBPB	chr11:15510776-15511013	MCF-7	breast:	n/a	n/a
5	CEBPB	chr11:15510781-15510981	IMR90	lung:	n/a	n/a
6	CTCF	chr11:15514900-15515050	GM12873	blood:	n/a	chr11:15514904-15514912
7	CTCF	chr11:15522262-15522457	GM12878	blood:	n/a	n/a
8	CTCF	chr11:15514940-15515090	GM12875	blood:	n/a	n/a
9	CTCF	chr11:15522360-15522418	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr11:15514820-15514970	HEK293	kidney:	n/a	chr11:15514904-15514912
11	CTCF	chr11:15514755-15515043	H1-hESC	embryonic stem cell:	n/a	chr11:15514904-15514912
12	CTCF	chr11:15514840-15514990	HCT-116	colon:	n/a	chr11:15514904-15514912
13	CTCF	chr11:15514900-15515050	HAc	cerebellar:	n/a	chr11:15514904-15514912
14	CTCF	chr11:15514900-15515050	GM06990	blood:	n/a	chr11:15514904-15514912
15	CTCF	chr11:15514820-15514970	RPTEC	kidney:	n/a	chr11:15514904-15514912
16	CTCF	chr11:15514920-15515070	GM12871	blood:	n/a	n/a
17	CTCF	chr11:15522361-15522378	K562	blood:	n/a	n/a
18	CTCF	chr11:15514780-15514930	GM12869	blood:	n/a	chr11:15514904-15514912
19	CTCF	chr11:15514780-15514930	NHEK	skin:	n/a	chr11:15514904-15514912
20	CTCF	chr11:15514802-15515060	H1-hESC	embryonic stem cell:	n/a	chr11:15514904-15514912
21	CTCF	chr11:15522345-15522443	GM19238	blood:	n/a	n/a
22	CTCF	chr11:15514840-15514990	RPTEC	kidney:	n/a	chr11:15514904-15514912
23	CTCF	chr11:15522315-15522445	GM12892	blood:	n/a	n/a
24	CUX1	chr11:15504783-15505120	GM12878	blood:	n/a	n/a
25	E2F4	chr11:15514502-15514988	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr11:15515951-15516151	MCF10A-Er-Src	breast:	n/a	n/a
27	EBF1	chr11:15504746-15505409	GM12878	blood:	n/a	chr11:15504953-15504964 chr11:15504955-15504965 chr11:15504955-15504964
28	EBF1	chr11:15504822-15505142	GM12878	blood:	n/a	chr11:15504953-15504964 chr11:15504955-15504965 chr11:15504955-15504964
29	EBF1	chr11:15504810-15505139	GM12878	blood:	n/a	chr11:15504953-15504964 chr11:15504955-15504965 chr11:15504955-15504964
30	EP300	chr11:15515480-15515817	T-47D	breast:	n/a	n/a
31	EP300	chr11:15504816-15505108	GM12878	blood:	n/a	chr11:15504887-15504901 chr11:15504886-15504900 chr11:15504984-15504998
32	EP300	chr11:15504827-15505146	GM12878	blood:	n/a	chr11:15504887-15504901 chr11:15504886-15504900 chr11:15504984-15504998
33	ESR1	chr11:15515538-15515850	T-47D	breast:	n/a	n/a
34	ESR1	chr11:15515392-15516002	T-47D	breast:	n/a	n/a
35	ESR1	chr11:15515420-15516027	T-47D	breast:	n/a	n/a
36	ESR1	chr11:15515463-15515976	T-47D	breast:	n/a	n/a
37	ESR1	chr11:15515452-15515915	T-47D	breast:	n/a	n/a
38	ESR1	chr11:15515467-15515905	T-47D	breast:	n/a	n/a
39	FOS	chr11:15514527-15514989	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr11:15510942-15511157	MCF10A-Er-Src	breast:	n/a	chr11:15511050-15511061
41	FOS	chr11:15510927-15511201	MCF10A-Er-Src	breast:	n/a	chr11:15511050-15511061
42	FOS	chr11:15514554-15514880	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr11:15514532-15514886	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr11:15515805-15516074	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr11:15515525-15516016	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr11:15510976-15511136	MCF10A-Er-Src	breast:	n/a	chr11:15511050-15511061
47	FOS	chr11:15510900-15511233	MCF10A-Er-Src	breast:	n/a	chr11:15511050-15511061
48	FOS	chr11:15514525-15514878	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr11:15515552-15516081	MCF10A-Er-Src	breast:	n/a	n/a
50	FOXA1	chr11:15515431-15515889	T-47D	breast:	n/a	chr11:15515668-15515683

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:15522727-15522777	HCT-116	colon:	n/a
2	chr11:15522727-15522777	HMEC	breast:	n/a
3	chr11:15522727-15522777	IMR90	lung:	fetal
4	chr11:15522727-15522777	HPAEpiC	pulmonary alveolar:	n/a
5	chr11:15522727-15522777	HRE	kidney:	n/a
6	chr11:15522727-15522777	ECC-1	luminal epithelium:	n/a
7	chr11:15522727-15522777	Hela-S3	cervix:	n/a
8	chr11:15522727-15522777	PrEC	prostate:	n/a
9	chr11:15522727-15522777	MCF10A-Er-Src	breast:	n/a
10	chr11:15522727-15522777	PFSK-1	brain:	n/a
11	chr11:15522727-15522777	NHDF-neo	bronchial:	n/a
12	chr11:15522727-15522777	HCM	heart:	n/a
13	chr11:15522727-15522777	BJ	skin:	n/a
14	chr11:15522727-15522777	LNCaP	prostate:	n/a
15	chr11:15522727-15522777	GM19239	blood:	n/a
16	chr11:15522727-15522777	H1-hESC	embryonic stem cell:	embryo
17	chr11:15522727-15522777	U87	brain:	n/a
18	chr11:15522727-15522777	Caco-2	colon:	n/a
19	chr11:15522727-15522777	HCF	heart:	n/a
20	chr11:15522727-15522777	NHBE	bronchial:	n/a
21	chr11:15522727-15522777	SAEC	small airway:	n/a
22	chr11:15522727-15522777	ovcar-3	ovarian:	n/a
23	chr11:15522727-15522777	HCPEpiC	choroid plexus:	n/a
24	chr11:15522727-15522777	HepG2	liver:	n/a
25	chr11:15522727-15522777	HRPEpiC	eye:	n/a
26	chr11:15522727-15522777	GM12878	blood:	n/a
27	chr11:15522727-15522777	HEK293	kidney:	embryo
28	chr11:15522727-15522777	BE2_C	brain:	n/a
29	chr11:15522727-15522777	AG04449	skin:	fetal
30	chr11:15522727-15522777	AG04450	lung:	fetal
31	chr11:15522727-15522777	Jurkat	blood:	n/a
32	chr11:15522727-15522777	NB4	blood:	n/a
33	chr11:15522727-15522777	AG09319	gingival:	n/a
34	chr11:15522727-15522777	NT2-D1	testis:	n/a
35	chr11:15522727-15522777	SK-N-MC	brain:	n/a
36	chr11:15522727-15522777	T-47D	breast:	n/a
37	chr11:15522727-15522777	NH-A	brain:	n/a
38	chr11:15522727-15522777	SK-N-SH	brain:	n/a
39	chr11:15522727-15522777	K562	blood:	n/a
40	chr11:15522727-15522777	A549	lung:	n/a
41	chr11:15522727-15522777	AG10803	skin:	n/a
42	chr11:15522727-15522777	MCF-7	breast:	n/a
43	chr11:15522727-15522777	CMK	blood:	n/a
44	chr11:15522727-15522777	HUVEC	blood vessel:	n/a
45	chr11:15522727-15522777	ProgFib	skin:	n/a
46	chr11:15522727-15522777	GM12891	blood:	n/a
47	chr11:15522727-15522777	HNPCEpiC	eye:	n/a
48	chr11:15522727-15522777	Hepatocyte	liver:	n/a
49	chr11:15522727-15522777	GM06990	blood:	n/a
50	chr11:15522727-15522777	SKMC	muscle:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:15505909..15508417-chr11:15510028..15514073,3	K562	blood:
2	chr11:15505909..15508417-chr11:15510028..15514073,3	K562	blood:
3	chr11:15452166..15452849-chr11:15515237..15515829,2	MCF-7	breast:
4	chr11:15512584..15515913-chr11:15518069..15521001,3	MCF-7	breast:
5	chr11:15262063..15264369-chr11:15524628..15526995,2	K562	blood:
6	chr11:15505528..15508330-chr11:15511468..15514048,2	MCF-7	breast:
7	chr11:15512584..15515913-chr11:15518069..15521001,3	MCF-7	breast:
8	chr11:15519281..15521349-chr11:15523623..15525618,2	MCF-7	breast:
9	chr11:15519281..15521349-chr11:15523623..15525618,2	MCF-7	breast:
10	chr11:15515373..15516180-chr11:15636691..15637607,7	MCF-7	breast:
11	chr11:15515373..15516180-chr11:15636691..15637625,4	MCF-7	breast:
12	chr11:15527389..15529322-chr11:15534222..15536632,2	MCF-7	breast:
13	chr11:15505528..15508330-chr11:15511468..15514048,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000253072	TF binding region
ENSG00000253072	CpG island

Extended variants
information (count: 882 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs377021665	chr11:15504349-15504350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs147377907	chr11:15504386-15504387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs139513424	chr11:15504400-15504401	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs530233617	chr11:15504437-15504438	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs115640750	chr11:15504453-15504454	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs559334856	chr11:15504460-15504461	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs190399834	chr11:15504461-15504462	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs577695307	chr11:15504493-15504494	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560254216	chr11:15504494-15504495	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs527656727	chr11:15504520-15504521	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs116206449	chr11:15504542-15504543	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs570774196	chr11:15504559-15504560	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs201446252	chr11:15504603-15504604	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs532397887	chr11:15504606-15504607	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs550606496	chr11:15504608-15504609	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs111420774	chr11:15504609-15504610	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs536494748	chr11:15504647-15504648	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs181750926	chr11:15504666-15504667	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs144003736	chr11:15504678-15504679	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs114895825	chr11:15504691-15504692	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs7479720	chr11:15504748-15504749	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs76353792	chr11:15504793-15504794	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs576771246	chr11:15504869-15504870	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs544842103	chr11:15504872-15504873	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs5789895	chr11:15504886-15504887	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs398097381	chr11:15504894-15504895	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs201493730	chr11:15504895-15504896	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs573475618	chr11:15504906-15504907	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs556630695	chr11:15504938-15504939	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs574682872	chr11:15504949-15504950	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs542047107	chr11:15504951-15504952	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs560336927	chr11:15504985-15504986	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs527746911	chr11:15505012-15505013	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs7480915	chr11:15505028-15505029	Enhancers Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs186304296	chr11:15505040-15505041	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs531658092	chr11:15505067-15505068	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs374765027	chr11:15505121-15505122	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs190186195	chr11:15505191-15505192	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs572746681	chr11:15505234-15505235	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs529890198	chr11:15505241-15505242	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs180716056	chr11:15505286-15505287	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs112950144	chr11:15505324-15505325	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs10766256	chr11:15505342-15505343	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs185199266	chr11:15505353-15505354	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs558371588	chr11:15505433-15505434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570424003	chr11:15505439-15505440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190797257	chr11:15505516-15505517	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537483608	chr11:15505538-15505539	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148696986	chr11:15505547-15505548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs564866079	chr11:15505562-15505563	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
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
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Myelofibrosis	22110671	CNVD
Cancer	24489367	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Neuroblastoma	19435921	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:15500200-15506000	Weak transcription	Fetal Intestine Large	intestine
2	chr11:15502200-15505200	Enhancers	Liver	Liver
3	chr11:15504000-15506000	Weak transcription	Fetal Intestine Small	intestine
4	chr11:15504000-15506400	Enhancers	GM12878-XiMat	blood
5	chr11:15505200-15507400	Weak transcription	Liver	Liver
6	chr11:15506000-15506400	Enhancers	Fetal Intestine Small	intestine
7	chr11:15506000-15506600	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr11:15506000-15506600	Enhancers	Fetal Intestine Large	intestine
9	chr11:15506600-15510600	Weak transcription	Fetal Intestine Large	intestine
10	chr11:15507400-15507600	Enhancers	Liver	Liver
11	chr11:15507600-15508800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr11:15507600-15514800	Weak transcription	Liver	Liver
13	chr11:15508600-15510000	Enhancers	Fetal Brain Male	brain
14	chr11:15510600-15511400	Enhancers	Fetal Intestine Large	intestine
15	chr11:15511400-15513200	Weak transcription	Fetal Intestine Large	intestine
16	chr11:15512200-15520400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr11:15513200-15513600	Enhancers	Fetal Intestine Large	intestine
18	chr11:15513400-15513600	Enhancers	Fetal Intestine Small	intestine
19	chr11:15513600-15514600	Weak transcription	Fetal Intestine Large	intestine
20	chr11:15513600-15514800	Weak transcription	Fetal Intestine Small	intestine
21	chr11:15514600-15523200	Enhancers	Fetal Intestine Large	intestine
22	chr11:15514800-15516200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr11:15514800-15516600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr11:15514800-15520200	Enhancers	Liver	Liver
25	chr11:15514800-15522400	Enhancers	Fetal Intestine Small	intestine
26	chr11:15515200-15515800	Enhancers	Placenta	Placenta
27	chr11:15515200-15516200	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr11:15515400-15515800	Enhancers	Psoas Muscle	Psoas
29	chr11:15515400-15516000	Enhancers	Fetal Muscle Leg	muscle
30	chr11:15515400-15516000	Enhancers	Stomach Mucosa	stomach
31	chr11:15515400-15516000	Enhancers	HSMM	muscle
32	chr11:15515400-15516200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr11:15515400-15516600	Enhancers	Pancreas	Pancrea
34	chr11:15515600-15515800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr11:15515600-15516000	Enhancers	Fetal Kidney	kidney
36	chr11:15515600-15516000	Enhancers	Fetal Lung	lung
37	chr11:15515800-15516200	Weak transcription	Psoas Muscle	Psoas
38	chr11:15515800-15522000	Weak transcription	Placenta	Placenta
39	chr11:15516000-15517400	Weak transcription	Fetal Muscle Leg	muscle
40	chr11:15516000-15518600	Weak transcription	Fetal Lung	lung
41	chr11:15516000-15518800	Weak transcription	Stomach Mucosa	stomach
42	chr11:15516200-15516400	Enhancers	Psoas Muscle	Psoas
43	chr11:15516200-15517600	Weak transcription	Rectal Mucosa Donor 31	rectum
44	chr11:15516400-15516600	Enhancers	Esophagus	oesophagus
45	chr11:15516400-15519000	Weak transcription	Psoas Muscle	Psoas
46	chr11:15516600-15518600	Weak transcription	Pancreas	Pancrea
47	chr11:15516600-15519000	Weak transcription	Esophagus	oesophagus
48	chr11:15517200-15517600	Enhancers	Duodenum Mucosa	Duodenum
49	chr11:15517400-15517800	Enhancers	Fetal Muscle Leg	muscle
50	chr11:15517600-15517800	Enhancers	Rectal Mucosa Donor 31	rectum

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