Variant report

Variant	nsv946144
Chromosome Location	chr1:113428625-113446146
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:114)
CpG islands
(count:0)
Chromatin interactive
region (count:26)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:114 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr1:113432160-113432197	K562	blood:	n/a	n/a
2	ATF1	chr1:113431369-113431645	K562	blood:	n/a	n/a
3	BACH1	chr1:113430716-113430722	K562	blood:	n/a	n/a
4	BHLHE40	chr1:113431202-113431700	K562	blood:	n/a	n/a
5	CBX3	chr1:113436046-113436428	K562	blood:	n/a	n/a
6	CBX3	chr1:113436070-113436699	K562	blood:	n/a	n/a
7	CBX3	chr1:113431039-113431607	K562	blood:	n/a	n/a
8	CCNT2	chr1:113436504-113436740	K562	blood:	n/a	n/a
9	CCNT2	chr1:113431343-113431678	K562	blood:	n/a	n/a
10	CEBPD	chr1:113436308-113436895	K562	blood:	n/a	n/a
11	CEBPD	chr1:113436380-113436825	K562	blood:	n/a	n/a
12	CUX1	chr1:113431379-113431612	K562	blood:	n/a	n/a
13	EP300	chr1:113436383-113436881	K562	blood:	n/a	n/a
14	EP300	chr1:113444068-113444295	K562	blood:	n/a	n/a
15	EP300	chr1:113436612-113436687	K562	blood:	n/a	n/a
16	EP300	chr1:113431329-113431692	K562	blood:	n/a	n/a
17	FOS	chr1:113430688-113430829	MCF10A-Er-Src	breast:	n/a	n/a
18	FOSL2	chr1:113430423-113430819	SK-N-SH	brain:	n/a	n/a
19	FOXA1	chr1:113442233-113442494	HepG2	liver:	n/a	n/a
20	FOXA2	chr1:113442158-113442477	HepG2	liver:	n/a	n/a
21	FOXA2	chr1:113440125-113440466	A549	lung:	n/a	n/a
22	GATA1	chr1:113435885-113437214	K562	blood:	n/a	chr1:113436055-113436076 chr1:113436062-113436069 chr1:113436062-113436069 chr1:113436062-113436069
23	GATA1	chr1:113435939-113436865	PBDE	blood:	n/a	chr1:113436055-113436076 chr1:113436062-113436069 chr1:113436062-113436069 chr1:113436062-113436069
24	GATA2	chr1:113436378-113436766	K562	blood:	n/a	n/a
25	GATA2	chr1:113436366-113436840	K562	blood:	n/a	n/a
26	GATA2	chr1:113436486-113436779	K562	blood:	n/a	n/a
27	HMGN3	chr1:113437512-113437571	K562	blood:	n/a	n/a
28	JUN	chr1:113446114-113449570	K562	blood:	n/a	chr1:113448078-113448086 chr1:113447824-113447833
29	JUND	chr1:113430494-113430870	K562	blood:	n/a	n/a
30	JUND	chr1:113431289-113431606	K562	blood:	n/a	n/a
31	JUND	chr1:113436152-113436764	K562	blood:	n/a	n/a
32	KAP1	chr1:113436116-113436468	K562	blood:	n/a	n/a
33	KAP1	chr1:113439426-113439792	U2OS	brain:	n/a	n/a
34	KAP1	chr1:113439419-113439806	HEK293	kidney:	n/a	n/a
35	MAFF	chr1:113430524-113430886	HepG2	liver:	n/a	chr1:113430710-113430728
36	MAFF	chr1:113431430-113431630	K562	blood:	n/a	n/a
37	MAFF	chr1:113430527-113430894	K562	blood:	n/a	chr1:113430710-113430728
38	MAFK	chr1:113430470-113430901	IMR90	lung:	n/a	chr1:113430712-113430727
39	MAFK	chr1:113430534-113430901	HepG2	liver:	n/a	chr1:113430712-113430727
40	MAFK	chr1:113430527-113430886	K562	blood:	n/a	chr1:113430712-113430727
41	MAFK	chr1:113430660-113430781	Hela-S3	cervix:	n/a	chr1:113430712-113430727
42	MAFK	chr1:113431417-113431600	K562	blood:	n/a	n/a
43	MAFK	chr1:113430525-113430880	HepG2	liver:	n/a	chr1:113430712-113430727
44	MAX	chr1:113431321-113431545	K562	blood:	n/a	n/a
45	MAZ	chr1:113431365-113431694	K562	blood:	n/a	n/a
46	MAZ	chr1:113436409-113436728	K562	blood:	n/a	n/a
47	MYC	chr1:113440221-113440350	K562	blood:	n/a	n/a
48	MYC	chr1:113438957-113439008	GM12878	blood:	n/a	n/a
49	NFYA	chr1:113438153-113438353	K562	blood:	n/a	chr1:113438171-113438189 chr1:113438196-113438214
50	NFYB	chr1:113437664-113438397	K562	blood:	n/a	chr1:113438193-113438208 chr1:113438168-113438183

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:113441028..113443640-chr1:113445198..113447610,3	MCF-7	breast:
2	chr1:113424770..113426373-chr1:113429791..113432690,2	MCF-7	breast:
3	chr1:113445118..113448523-chr1:113453652..113455842,3	MCF-7	breast:
4	chr1:113442871..113445131-chr1:113497859..113500702,2	K562	blood:
5	chr1:113444785..113447653-chr1:113457108..113462049,4	K562	blood:
6	chr1:113445067..113447939-chr1:113458429..113462240,3	K562	blood:
7	chr1:113342047..113343911-chr1:113444698..113447399,2	K562	blood:
8	chr1:113446024..113448381-chr1:113497759..113499583,2	K562	blood:
9	chr1:113432563..113435506-chr1:113438129..113441050,2	K562	blood:
10	chr1:113445368..113447569-chr1:113467662..113470258,2	K562	blood:
11	chr1:113429664..113431749-chr1:113436515..113438078,2	K562	blood:
12	chr1:113428651..113431158-chr1:113614317..113616709,2	K562	blood:
13	chr1:113429664..113431749-chr1:113436515..113438078,2	K562	blood:
14	chr1:113441801..113445545-chr1:113447072..113449494,3	K562	blood:
15	chr1:113445849..113448733-chr1:113470984..113473265,2	K562	blood:
16	chr1:113424350..113426244-chr1:113426854..113428692,2	MCF-7	breast:
17	chr1:113446003..113448854-chr1:113463781..113465733,2	MCF-7	breast:
18	chr1:113422181..113424521-chr1:113435432..113438293,2	K562	blood:
19	chr1:113442578..113444928-chr1:113615994..113617542,2	K562	blood:
20	chr1:113441028..113443640-chr1:113445198..113447610,3	MCF-7	breast:
21	chr1:113439726..113442354-chr1:113496714..113499544,2	K562	blood:
22	chr1:113425134..113427690-chr1:113436011..113438422,2	K562	blood:
23	chr1:113424435..113426998-chr1:113430244..113432680,3	K562	blood:
24	chr1:113445363..113447698-chr1:113464880..113466505,2	K562	blood:
25	chr1:113430436..113432167-chr1:113476191..113478962,2	K562	blood:
26	chr1:113428151..113431386-chr1:113432346..113435654,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000228040	TF binding region
ENSG00000226419	chromatin interactions
ENSG00000228040	chromatin interactions
ENSG00000229020	chromatin interactions
ENSG00000238198	chromatin interactions
ENSG00000198799	chromatin interactions
ENSG00000155380	chromatin interactions

Extended variants
information (count: 708 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:708 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143363132	chr1:113428627-113428628	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs76958220	chr1:113428632-113428633	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs552698175	chr1:113428735-113428736	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs368072854	chr1:113428787-113428788	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs6670866	chr1:113428827-113428828	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs541623563	chr1:113428850-113428851	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs139382038	chr1:113428882-113428883	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs183678683	chr1:113428946-113428947	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs578215188	chr1:113428984-113428985	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs186102520	chr1:113428985-113428986	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs563659916	chr1:113429009-113429010	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs529350571	chr1:113429027-113429028	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs549449815	chr1:113429074-113429075	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs559893267	chr1:113429083-113429084	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs142813544	chr1:113429112-113429113	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs61819997	chr1:113429172-113429173	Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs576025042	chr1:113429187-113429188	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs61819998	chr1:113429215-113429216	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs113921918	chr1:113429225-113429226	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs537334962	chr1:113429263-113429264	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs190679616	chr1:113429309-113429310	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs140933443	chr1:113429316-113429317	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs183337997	chr1:113429338-113429339	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs186961584	chr1:113429355-113429356	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs572619931	chr1:113429459-113429460	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs564872638	chr1:113429502-113429503	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs534880996	chr1:113429609-113429610	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs111933827	chr1:113429612-113429613	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs558312714	chr1:113429628-113429629	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs532310781	chr1:113429649-113429650	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs578136079	chr1:113429663-113429664	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs149809024	chr1:113429666-113429667	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs192223188	chr1:113429713-113429714	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs570856798	chr1:113429740-113429741	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs538271126	chr1:113429743-113429744	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs543056160	chr1:113429792-113429793	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs182867606	chr1:113429813-113429814	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs550285082	chr1:113429820-113429821	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs568587896	chr1:113429834-113429835	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs528564006	chr1:113429883-113429884	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs60788883	chr1:113429926-113429927	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs398074280	chr1:113429936-113429937	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs397739823	chr1:113429937-113429938	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs147899149	chr1:113430072-113430073	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs565080441	chr1:113430079-113430080	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs187905066	chr1:113430088-113430089	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs550415392	chr1:113430115-113430116	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs75926411	chr1:113430166-113430167	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs57549167	chr1:113430200-113430201	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs546213809	chr1:113430205-113430206	Weak transcription Genic enhancers Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	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
Papillary thyroid carcinoma	21436994	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
Breast cancer	17603634	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
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
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
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Medulloblastoma	21979893	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ovarian cancer	21720365	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Asthma	20841430	CNVD
Aetanephric adenomas	20802469	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	21956041	CNVD
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	16573809	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Breast cancer	17899364	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Melanoma	19671679	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:157 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:113421400-113435200	Weak transcription	Fetal Heart	heart
2	chr1:113425000-113430200	Weak transcription	Fetal Intestine Large	intestine
3	chr1:113425200-113430400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:113425600-113429600	Weak transcription	Colonic Mucosa	Colon
5	chr1:113425600-113430000	Weak transcription	Fetal Intestine Small	intestine
6	chr1:113425600-113430200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:113425600-113430400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr1:113425600-113430400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:113425600-113430400	Weak transcription	Right Atrium	heart
10	chr1:113425800-113430200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr1:113425800-113430200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr1:113425800-113430200	Weak transcription	HSMM	muscle
13	chr1:113425800-113430400	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr1:113425800-113430400	Weak transcription	HSMMtube	muscle
15	chr1:113425800-113435200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr1:113426200-113429400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr1:113426600-113430200	Weak transcription	K562	blood
18	chr1:113427800-113429000	Enhancers	Stomach Mucosa	stomach
19	chr1:113428400-113429600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr1:113428600-113429600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr1:113429000-113429400	Weak transcription	Stomach Mucosa	stomach
22	chr1:113429400-113430800	Enhancers	Stomach Mucosa	stomach
23	chr1:113429600-113430000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:113429600-113430000	Enhancers	Duodenum Mucosa	Duodenum
25	chr1:113429600-113430600	Enhancers	Colonic Mucosa	Colon
26	chr1:113429800-113430000	Enhancers	Small Intestine	intestine
27	chr1:113430000-113430600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:113430000-113430600	Flanking Active TSS	Duodenum Mucosa	Duodenum
29	chr1:113430000-113431200	Enhancers	Fetal Intestine Small	intestine
30	chr1:113430000-113431400	Enhancers	Gastric	stomach
31	chr1:113430200-113430600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:113430200-113430600	Enhancers	Fetal Intestine Large	intestine
33	chr1:113430200-113430800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr1:113430200-113430800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:113430200-113430800	Enhancers	HSMM	muscle
36	chr1:113430200-113432400	Enhancers	K562	blood
37	chr1:113430400-113430600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr1:113430400-113430600	Enhancers	Right Atrium	heart
39	chr1:113430400-113430600	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr1:113430400-113430600	Enhancers	NHLF	lung
41	chr1:113430400-113430800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr1:113430400-113430800	Enhancers	HSMMtube	muscle
43	chr1:113430400-113431400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr1:113430600-113430800	Weak transcription	Right Atrium	heart
45	chr1:113430600-113431000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:113430600-113431200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr1:113430600-113431400	Enhancers	Duodenum Mucosa	Duodenum
48	chr1:113430800-113431400	Weak transcription	Stomach Mucosa	stomach
49	chr1:113431000-113431400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:113431200-113431400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links