Variant report

Variant	esv3398984
Chromosome Location	chr15:51574559-51577866
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:86)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:86 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr15:51575390-51575568	GM10266	blood:	n/a	n/a
2	CTCF	chr15:51575415-51575525	HUVEC	blood vessel:	n/a	n/a
3	CTCF	chr15:51575360-51575510	GM12867	blood:	n/a	n/a
4	CTCF	chr15:51575340-51575490	GM12866	blood:	n/a	n/a
5	CTCF	chr15:51575400-51575550	GM12873	blood:	n/a	n/a
6	CTCF	chr15:51575280-51575430	GM12868	blood:	n/a	n/a
7	CTCF	chr15:51575394-51575526	MCF-7	breast:	n/a	n/a
8	CTCF	chr15:51575380-51575530	GM12865	blood:	n/a	n/a
9	CTCF	chr15:51575380-51575530	GM12872	blood:	n/a	n/a
10	CTCF	chr15:51575400-51575550	GM12864	blood:	n/a	n/a
11	CTCF	chr15:51575340-51575490	GM12874	blood:	n/a	n/a
12	CTCF	chr15:51575674-51575729	GM13976	blood:	n/a	n/a
13	CTCF	chr15:51575400-51575550	AG04449	skin:	n/a	n/a
14	CTCF	chr15:51575380-51575530	HMF	breast:	n/a	n/a
15	CTCF	chr15:51575380-51575530	HAc	cerebellar:	n/a	n/a
16	CTCF	chr15:51575360-51575510	GM12865	blood:	n/a	n/a
17	CTCF	chr15:51575410-51575515	GM19239	blood:	n/a	n/a
18	CTCF	chr15:51575440-51575590	GM12871	blood:	n/a	n/a
19	CTCF	chr15:51575464-51575485	LNCaP	prostate:	n/a	n/a
20	CTCF	chr15:51575357-51575581	T-47D	breast:	n/a	n/a
21	CTCF	chr15:51575454-51575461	LNCaP	prostate:	n/a	n/a
22	CTCF	chr15:51575380-51575530	GM12867	blood:	n/a	n/a
23	CTCF	chr15:51575540-51575690	GM12867	blood:	n/a	n/a
24	CTCF	chr15:51575440-51575590	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr15:51575840-51575990	GM12871	blood:	n/a	n/a
26	CTCF	chr15:51575360-51575510	GM12872	blood:	n/a	n/a
27	CTCF	chr15:51575315-51575555	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr15:51575380-51575530	GM12864	blood:	n/a	n/a
29	CTCF	chr15:51575403-51575533	K562	blood:	n/a	n/a
30	CTCF	chr15:51575380-51575530	HL-60	blood:	n/a	n/a
31	CTCF	chr15:51575280-51575430	GM12865	blood:	n/a	n/a
32	CTCF	chr15:51575380-51575530	GM12870	blood:	n/a	n/a
33	CTCF	chr15:51575400-51575550	GM06990	blood:	n/a	n/a
34	CTCF	chr15:51575380-51575530	GM06990	blood:	n/a	n/a
35	CTCF	chr15:51575468-51575533	LNCaP	prostate:	n/a	n/a
36	CTCF	chr15:51574780-51574930	GM06990	blood:	n/a	n/a
37	CTCF	chr15:51575260-51575410	GM12866	blood:	n/a	n/a
38	CTCF	chr15:51575356-51575554	GM12878	blood:	n/a	n/a
39	CTCF	chr15:51575180-51575330	GM12864	blood:	n/a	n/a
40	CTCF	chr15:51575380-51575530	GM12875	blood:	n/a	n/a
41	CTCF	chr15:51575400-51575550	GM12869	blood:	n/a	n/a
42	CTCF	chr15:51575380-51575530	GM12878	blood:	n/a	n/a
43	CTCF	chr15:51575280-51575430	HMEC	breast:	n/a	n/a
44	CTCF	chr15:51575360-51575510	GM12873	blood:	n/a	n/a
45	CTCF	chr15:51575299-51575617	GM12878	blood:	n/a	n/a
46	CTCF	chr15:51575380-51575529	GM13976	blood:	n/a	n/a
47	CTCF	chr15:51575332-51575585	K562	blood:	n/a	n/a
48	CTCF	chr15:51575368-51575560	GM10248	blood:	n/a	n/a
49	CTCF	chr15:51575380-51575530	HVMF	connective:	n/a	n/a
50	CTCF	chr15:51575424-51575491	MCF-7	breast:	n/a	n/a

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:51574618..51575812-chr15:51673135..51674386,4	MCF-7	breast:
2	chr15:51573015..51575119-chr15:51672522..51674124,19	MCF-7	breast:
3	chr15:51568163..51571047-chr15:51573352..51576170,3	MCF-7	breast:
4	chr15:51576151..51578472-chr15:51666319..51669259,2	MCF-7	breast:
5	chr15:51573458..51575048-chr15:51673491..51675129,2	MCF-7	breast:
6	chr15:51577515..51580026-chr15:51665371..51667352,2	MCF-7	breast:
7	chr15:51572199..51575130-chr15:51658067..51661201,3	MCF-7	breast:
8	chr15:51573553..51574678-chr15:51674522..51675665,6	MCF-7	breast:
9	chr15:51577066..51580410-chr15:51672799..51675704,3	MCF-7	breast:
10	chr15:51425211..51425789-chr15:51573674..51574562,2	MCF-7	breast:
11	chr15:51577243..51581816-chr15:51658096..51661289,5	MCF-7	breast:
12	chr15:51570765..51572650-chr15:51575389..51576979,2	MCF-7	breast:

No data

Variant related genes	Relation type
CYP19A1	TF binding region
ENSG00000259701	TF binding region
ENSG00000137869	chromatin interactions
ENSG00000259194	chromatin interactions
ENSG00000259701	chromatin interactions

Extended variants
information (count: 156 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:156 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143901510	chr15:51574599-51574600	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs148575419	chr15:51574647-51574648	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs536512312	chr15:51574712-51574713	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs538878872	chr15:51574746-51574747	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs553693459	chr15:51574747-51574748	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs572170437	chr15:51574751-51574752	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs57457557	chr15:51574766-51574767	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs561821606	chr15:51574772-51574773	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs573728853	chr15:51574773-51574774	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs146599147	chr15:51574776-51574777	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs57838664	chr15:51574786-51574787	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs374888412	chr15:51574791-51574792	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs554924522	chr15:51574794-51574795	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs59247362	chr15:51574797-51574798	Weak transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs556534193	chr15:51574806-51574807	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs368327716	chr15:51574807-51574808	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs12101420	chr15:51574853-51574854	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs560539691	chr15:51574858-51574859	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs12101421	chr15:51574901-51574902	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs549127804	chr15:51574902-51574903	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs57553306	chr15:51574908-51574909	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs567355045	chr15:51574921-51574922	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs182812715	chr15:51574931-51574932	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs143837499	chr15:51574932-51574933	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs571181487	chr15:51574952-51574953	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538572774	chr15:51574955-51574956	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs188245277	chr15:51574998-51574999	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs58724502	chr15:51575009-51575010	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs191698661	chr15:51575016-51575017	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs1902579	chr15:51575092-51575093	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs147834386	chr15:51575097-51575098	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs370655521	chr15:51575098-51575099	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs11853261	chr15:51575145-51575146	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs115511441	chr15:51575204-51575205	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs562750195	chr15:51575216-51575217	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs34503596	chr15:51575228-51575229	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs140518975	chr15:51575232-51575233	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs183597017	chr15:51575251-51575252	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs368565242	chr15:51575312-51575313	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs527922878	chr15:51575328-51575329	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs549590651	chr15:51575345-51575346	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs59236653	chr15:51575348-51575349	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs150972916	chr15:51575356-51575357	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs57654996	chr15:51575358-51575359	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs116712458	chr15:51575395-51575396	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs35384027	chr15:51575406-51575407	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs138147793	chr15:51575475-51575476	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs1902580	chr15:51575501-51575502	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs115768009	chr15:51575502-51575503	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs547407018	chr15:51575520-51575521	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51572600-51575200	Genic enhancers	Placenta	Placenta
2	chr15:51573000-51574800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr15:51573200-51575000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr15:51573400-51574600	Enhancers	Fetal Stomach	stomach
5	chr15:51573400-51574800	Enhancers	Adipose Nuclei	Adipose
6	chr15:51573400-51575000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr15:51573400-51575000	Enhancers	Fetal Muscle Leg	muscle
8	chr15:51573400-51575200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr15:51573400-51575400	Enhancers	Brain Hippocampus Middle	brain
10	chr15:51573600-51574800	Weak transcription	Brain Substantia Nigra	brain
11	chr15:51573600-51575000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr15:51573600-51575000	Enhancers	GM12878-XiMat	blood
13	chr15:51573800-51574600	Enhancers	HSMMtube	muscle
14	chr15:51573800-51574800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr15:51573800-51574800	Enhancers	Skeletal Muscle Female	skeletal muscle
16	chr15:51573800-51575000	Enhancers	NHDF-Ad	bronchial
17	chr15:51574000-51575000	Enhancers	HepG2	liver
18	chr15:51574000-51575200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr15:51574000-51575200	Enhancers	Stomach Mucosa	stomach
20	chr15:51574400-51574800	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr15:51574400-51575000	Enhancers	Duodenum Mucosa	Duodenum
22	chr15:51574400-51575000	Enhancers	Spleen	Spleen
23	chr15:51574400-51575400	Enhancers	Brain Angular Gyrus	brain
24	chr15:51574400-51576200	Enhancers	Primary B cells from peripheral blood	blood
25	chr15:51574600-51575000	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr15:51574600-51575000	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr15:51574600-51576600	Enhancers	Primary monocytes fromperipheralblood	blood
28	chr15:51574800-51575000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr15:51574800-51575000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
30	chr15:51574800-51575000	Flanking Active TSS	Brain Anterior Caudate	brain
31	chr15:51574800-51575000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
32	chr15:51574800-51575000	Enhancers	Esophagus	oesophagus
33	chr15:51574800-51575000	Enhancers	Left Ventricle	heart
34	chr15:51574800-51575000	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr15:51574800-51575000	Enhancers	Right Atrium	heart
36	chr15:51574800-51575000	Enhancers	Monocytes-CD14+_RO01746	blood
37	chr15:51574800-51575400	Enhancers	Brain Substantia Nigra	brain
38	chr15:51574800-51575600	Weak transcription	Adipose Nuclei	Adipose
39	chr15:51574800-51576000	Enhancers	Primary B cells from cord blood	blood
40	chr15:51575000-51575200	Flanking Active TSS	Duodenum Mucosa	Duodenum
41	chr15:51575000-51575600	Flanking Active TSS	GM12878-XiMat	blood
42	chr15:51575000-51575800	Active TSS	Brain Inferior Temporal Lobe	brain
43	chr15:51575000-51575800	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr15:51575000-51575800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
45	chr15:51575000-51576000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:51575000-51576000	Active TSS	Brain Anterior Caudate	brain
47	chr15:51575000-51577800	Weak transcription	Fetal Muscle Leg	muscle
48	chr15:51575000-51578600	Weak transcription	HepG2	liver
49	chr15:51575000-51580400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr15:51575000-51580400	Weak transcription	Rectal Mucosa Donor 31	rectum

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