Variant report

Variant	esv1801614
Chromosome Location	chr1:47211670-47220059
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	BACH1	chr1:47219844-47220138	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr1:47213518-47213675	K562	blood:	n/a	n/a
3	CEBPB	chr1:47215503-47215846	A549	lung:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
4	CEBPB	chr1:47215344-47215906	MCF-7	breast:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
5	CEBPB	chr1:47215455-47215845	ECC-1	luminal epithelium:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
6	CEBPB	chr1:47215480-47215843	HepG2	liver:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
7	CEBPB	chr1:47215508-47215825	H1-hESC	embryonic stem cell:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
8	CEBPB	chr1:47215468-47215839	MCF-7	breast:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
9	CEBPB	chr1:47215481-47215838	K562	blood:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
10	CEBPB	chr1:47215490-47215852	Hela-S3	cervix:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
11	CEBPB	chr1:47215478-47215819	IMR90	lung:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
12	CEBPB	chr1:47215442-47215851	ECC-1	luminal epithelium:	n/a	chr1:47215660-47215669 chr1:47215659-47215670 chr1:47215660-47215669 chr1:47215660-47215669
13	CHD2	chr1:47213435-47213663	Hela-S3	cervix:	n/a	chr1:47213485-47213495
14	CTCF	chr1:47213420-47213570	GM12873	blood:	n/a	chr1:47213550-47213568
15	CTCF	chr1:47213460-47213610	GM12871	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
16	CTCF	chr1:47213460-47213610	GM12872	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
17	CTCF	chr1:47213480-47213630	HVMF	connective:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
18	CTCF	chr1:47213311-47213712	K562	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
19	CTCF	chr1:47213760-47213910	AG09309	skin:	n/a	n/a
20	CTCF	chr1:47213460-47213610	BE2_C	brain:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
21	CTCF	chr1:47213520-47213670	HepG2	liver:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
22	CTCF	chr1:47213440-47213590	GM12878	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
23	CTCF	chr1:47213500-47213650	AG10803	skin:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
24	CTCF	chr1:47213341-47213733	HCT-116	colon:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
25	CTCF	chr1:47213426-47213663	MCF-7	breast:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
26	CTCF	chr1:47213087-47213164	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr1:47213920-47214070	HMEC	breast:	n/a	n/a
28	CTCF	chr1:47213323-47213751	HepG2	liver:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
29	CTCF	chr1:47213440-47213652	A549	lung:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
30	CTCF	chr1:47213177-47213206	Kidney_OC	kidney:	n/a	n/a
31	CTCF	chr1:47213520-47213670	GM12864	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
32	CTCF	chr1:47213413-47213689	MCF-7	breast:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
33	CTCF	chr1:47213500-47213650	HBMEC	blood vessel:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
34	CTCF	chr1:47213280-47213430	GM12866	blood:	n/a	n/a
35	CTCF	chr1:47213500-47213650	HMF	breast:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
36	CTCF	chr1:47213480-47213630	GM12873	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
37	CTCF	chr1:47213461-47213616	GM10266	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
38	CTCF	chr1:47213500-47213650	AG09319	gingival:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
39	CTCF	chr1:47213401-47213698	LNCaP	prostate:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
40	CTCF	chr1:47213379-47213737	GM12878	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
41	CTCF	chr1:47213440-47213590	K562	blood:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
42	CTCF	chr1:47212980-47213130	HVMF	connective:	n/a	n/a
43	CTCF	chr1:47212980-47213130	K562	blood:	n/a	n/a
44	CTCF	chr1:47213480-47213630	AG04450	lung:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
45	CTCF	chr1:47213820-47213970	HEK293	kidney:	n/a	n/a
46	CTCF	chr1:47213314-47214000	A549	lung:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
47	CTCF	chr1:47213480-47213630	NHLF	lung:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
48	CTCF	chr1:47213520-47213670	WI-38	lung:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
49	CTCF	chr1:47213451-47213694	HepG2	liver:	n/a	chr1:47213550-47213568 chr1:47213552-47213573
50	CTCF	chr1:47213540-47213690	HCT-116	colon:	n/a	chr1:47213550-47213568 chr1:47213552-47213573

No.	Distal block	Cell Line	Cell type
1	chr1:47214409..47216295-chr1:47223394..47224946,2	MCF-7	breast:
2	chr1:47169118..47170712-chr1:47210648..47212362,2	K562	blood:
3	chr1:47175505..47177633-chr1:47210573..47212769,2	K562	blood:
4	chr1:47212538..47216219-chr1:47220374..47223664,7	MCF-7	breast:
5	chr1:47213914..47217812-chr1:47218184..47221016,4	MCF-7	breast:
6	chr1:47216575..47218085-chr1:47218744..47221209,2	MCF-7	breast:
7	chr1:47209911..47212671-chr1:47214457..47216011,2	MCF-7	breast:
8	chr1:46908079..46908925-chr1:47213075..47213991,2	K562	blood:
9	chr1:47209911..47212671-chr1:47214457..47216011,2	MCF-7	breast:
10	chr1:47216575..47218085-chr1:47218744..47221209,2	MCF-7	breast:
11	chr1:47213914..47217812-chr1:47218184..47221016,4	MCF-7	breast:

Variant related genes	Relation type
CYP4B1	TF binding region
ENSG00000142973	chromatin interactions

Extended variants
information (count: 266 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:266 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140060406	chr1:47212559-47212560	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs529721088	chr1:47212574-47212575	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35367832	chr1:47212584-47212585	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs78962033	chr1:47212599-47212600	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs566740210	chr1:47212607-47212608	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs78104811	chr1:47212641-47212642	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs552356202	chr1:47212670-47212671	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7549264	chr1:47212673-47212674	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs607945	chr1:47212694-47212695	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs556650041	chr1:47212789-47212790	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs72900763	chr1:47212807-47212808	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs548915602	chr1:47212814-47212815	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs78987039	chr1:47212815-47212816	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs72681921	chr1:47212830-47212831	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs557647807	chr1:47212837-47212838	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs111649819	chr1:47212851-47212852	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs12119120	chr1:47212853-47212854	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs557926278	chr1:47212864-47212865	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs185042540	chr1:47212892-47212893	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs190268531	chr1:47212919-47212920	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543951588	chr1:47212951-47212952	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs137925160	chr1:47212981-47212982	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs142505623	chr1:47213046-47213047	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541769880	chr1:47213104-47213105	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560195059	chr1:47213106-47213107	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs527583264	chr1:47213132-47213133	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs5022931	chr1:47213133-47213134	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs74073074	chr1:47213164-47213165	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs181724382	chr1:47213165-47213166	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144767410	chr1:47213201-47213202	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs72900764	chr1:47213202-47213203	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs72900765	chr1:47213237-47213238	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs138565238	chr1:47213377-47213378	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs594387	chr1:47213386-47213387	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs542641084	chr1:47213411-47213412	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs539734466	chr1:47213415-47213416	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs149298245	chr1:47213464-47213465	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs144585566	chr1:47213485-47213486	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148485381	chr1:47213528-47213529	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376024272	chr1:47213562-47213563	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs555692538	chr1:47213582-47213583	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs574429725	chr1:47213587-47213588	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs541608034	chr1:47213593-47213594	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs560183395	chr1:47213601-47213602	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs58201914	chr1:47213629-47213630	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs12073003	chr1:47213634-47213635	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs564341785	chr1:47213706-47213707	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs538531187	chr1:47213743-47213744	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs141405125	chr1:47213772-47213773	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549905874	chr1:47213798-47213799	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Neuroblastoma	21899760	CNVD
Uveal melanoma	20484589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Glioblastoma	20031968	CNVD
Leukemia	18688285	CNVD
Rett syndrome	21593744	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:92 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47213600-47215600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr1:47213600-47215600	Enhancers	Adipose Nuclei	Adipose
3	chr1:47213800-47214000	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
4	chr1:47213800-47214400	Weak transcription	Right Atrium	heart
5	chr1:47213800-47215200	Enhancers	Esophagus	oesophagus
6	chr1:47213800-47216600	Enhancers	Placenta Amnion	Placenta Amnion
7	chr1:47214000-47215200	Enhancers	Lung	lung
8	chr1:47214400-47215000	Enhancers	Right Atrium	heart
9	chr1:47214400-47215400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr1:47214600-47215600	Enhancers	Hela-S3	cervix
11	chr1:47214600-47215600	Enhancers	NHEK	skin
12	chr1:47214600-47216600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:47214600-47216600	Enhancers	HMEC	breast
14	chr1:47214600-47216800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:47214800-47215200	Enhancers	Left Ventricle	heart
16	chr1:47214800-47215200	Enhancers	Psoas Muscle	Psoas
17	chr1:47214800-47215800	Enhancers	Placenta	Placenta
18	chr1:47214800-47216200	Enhancers	Fetal Intestine Small	intestine
19	chr1:47215000-47216000	Enhancers	Fetal Intestine Large	intestine
20	chr1:47215000-47218200	Weak transcription	Right Atrium	heart
21	chr1:47215200-47215600	Weak transcription	Psoas Muscle	Psoas
22	chr1:47215200-47217400	Weak transcription	Esophagus	oesophagus
23	chr1:47215200-47226000	Weak transcription	Lung	lung
24	chr1:47215400-47215600	Weak transcription	Left Ventricle	heart
25	chr1:47215400-47215600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
26	chr1:47215400-47216000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr1:47215400-47216200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr1:47215600-47216000	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr1:47215600-47216000	Flanking Active TSS	Hela-S3	cervix
30	chr1:47215600-47216000	Flanking Active TSS	NHEK	skin
31	chr1:47215600-47216200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:47215600-47216800	Enhancers	Psoas Muscle	Psoas
33	chr1:47215800-47216400	Enhancers	Duodenum Mucosa	Duodenum
34	chr1:47215800-47217400	Weak transcription	Placenta	Placenta
35	chr1:47216000-47216600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr1:47216000-47216600	Enhancers	NHEK	skin
37	chr1:47216000-47218800	Enhancers	Adipose Nuclei	Adipose
38	chr1:47216000-47219400	Weak transcription	Fetal Intestine Large	intestine
39	chr1:47216200-47218600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr1:47216200-47219400	Weak transcription	Fetal Intestine Small	intestine
41	chr1:47216400-47216600	Enhancers	Left Ventricle	heart
42	chr1:47216400-47219600	Weak transcription	Duodenum Mucosa	Duodenum
43	chr1:47216600-47218200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:47216600-47218200	Weak transcription	HMEC	breast
45	chr1:47216600-47218200	Weak transcription	NHEK	skin
46	chr1:47216600-47218400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr1:47216600-47221600	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr1:47216800-47218200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr1:47217400-47217600	Enhancers	Esophagus	oesophagus
50	chr1:47217400-47217600	Enhancers	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links