Variant report

Variant	nsv520700
Chromosome Location	chr2:111931421-111948809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:282)
CpG islands
(count:122)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:111933981-111934200	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:111936124-111937346	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:111943267-111943396	HepG2	liver:	n/a	n/a
4	BCL3	chr2:111936234-111937002	A549	lung:	n/a	n/a
5	BHLHE40	chr2:111943124-111943418	GM12878	blood:	n/a	n/a
6	BHLHE40	chr2:111943167-111943663	K562	blood:	n/a	n/a
7	BHLHE40	chr2:111943036-111943407	HepG2	liver:	n/a	n/a
8	BRCA1	chr2:111936486-111936726	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:111936180-111936925	HepG2	liver:	n/a	chr2:111936491-111936502
10	CEBPB	chr2:111936314-111936707	IMR90	lung:	n/a	chr2:111936491-111936502
11	CEBPB	chr2:111943753-111944103	HepG2	liver:	n/a	n/a
12	CEBPB	chr2:111936298-111936870	HepG2	liver:	n/a	chr2:111936491-111936502
13	CEBPB	chr2:111942582-111942937	K562	blood:	n/a	chr2:111942768-111942779
14	CEBPB	chr2:111934149-111934945	HepG2	liver:	n/a	chr2:111934594-111934605
15	CEBPB	chr2:111942587-111942909	HepG2	liver:	n/a	chr2:111942768-111942779
16	CEBPB	chr2:111939321-111939627	HepG2	liver:	n/a	n/a
17	CEBPB	chr2:111934415-111934771	IMR90	lung:	n/a	chr2:111934594-111934605
18	CEBPB	chr2:111934404-111934814	K562	blood:	n/a	chr2:111934594-111934605
19	CEBPB	chr2:111934290-111934879	A549	lung:	n/a	chr2:111934594-111934605
20	CEBPB	chr2:111934159-111934986	HepG2	liver:	n/a	chr2:111934594-111934605
21	CEBPB	chr2:111936256-111937059	A549	lung:	n/a	chr2:111936491-111936502
22	CEBPB	chr2:111943805-111944068	A549	lung:	n/a	n/a
23	CEBPB	chr2:111942623-111942928	IMR90	lung:	n/a	chr2:111942768-111942779
24	CEBPB	chr2:111936311-111936786	A549	lung:	n/a	chr2:111936491-111936502
25	CEBPB	chr2:111936347-111936637	HepG2	liver:	n/a	chr2:111936491-111936502
26	CEBPB	chr2:111934443-111934759	K562	blood:	n/a	chr2:111934594-111934605
27	CEBPB	chr2:111936308-111936920	A549	lung:	n/a	chr2:111936491-111936502
28	CEBPB	chr2:111934424-111934762	Hela-S3	cervix:	n/a	chr2:111934594-111934605
29	CEBPB	chr2:111934049-111934785	A549	lung:	n/a	chr2:111934594-111934605
30	CEBPB	chr2:111942606-111942910	A549	lung:	n/a	chr2:111942768-111942779
31	CEBPB	chr2:111936241-111936754	HepG2	liver:	n/a	chr2:111936491-111936502
32	CEBPB	chr2:111934503-111934683	HepG2	liver:	n/a	chr2:111934594-111934605
33	CEBPB	chr2:111934355-111934755	MCF-7	breast:	n/a	chr2:111934594-111934605
34	CEBPB	chr2:111934461-111934735	ECC-1	luminal epithelium:	n/a	chr2:111934594-111934605
35	CEBPD	chr2:111936314-111936801	HepG2	liver:	n/a	n/a
36	CHD2	chr2:111934049-111934344	HepG2	liver:	n/a	n/a
37	CHD2	chr2:111943217-111943292	GM12878	blood:	n/a	n/a
38	CREB1	chr2:111943104-111943449	A549	lung:	n/a	n/a
39	CREB1	chr2:111943233-111943443	A549	lung:	n/a	n/a
40	CREB1	chr2:111936428-111936815	A549	lung:	n/a	n/a
41	CTCF	chr2:111944517-111944857	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr2:111943872-111943915	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr2:111944696-111944746	Medullo	brain:	n/a	n/a
44	CTCF	chr2:111944620-111944770	K562	blood:	n/a	n/a
45	CTCF	chr2:111944600-111944750	HEK293	kidney:	n/a	n/a
46	CTCF	chr2:111944612-111944816	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr2:111944560-111944710	HepG2	liver:	n/a	n/a
48	CTCF	chr2:111944540-111944690	A549	lung:	n/a	n/a
49	CTCF	chr2:111936400-111936550	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr2:111944701-111944752	NHEK	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:111936357-111936407	SAEC	small airway:	n/a
2	chr2:111932156-111932206	HCT-116	colon:	n/a
3	chr2:111936357-111936407	HEK293	kidney:	embryo
4	chr2:111932156-111932206	NHDF-neo	bronchial:	n/a
5	chr2:111932156-111932206	SAEC	small airway:	n/a
6	chr2:111936357-111936407	RPTEC	kidney:	n/a
7	chr2:111932156-111932206	BJ	skin:	n/a
8	chr2:111936357-111936407	AG04450	lung:	fetal
9	chr2:111936357-111936407	ECC-1	luminal epithelium:	n/a
10	chr2:111936357-111936407	HCM	heart:	n/a
11	chr2:111932156-111932206	GM06990	blood:	n/a
12	chr2:111936357-111936407	ProgFib	skin:	n/a
13	chr2:111936357-111936407	GM12878	blood:	n/a
14	chr2:111932156-111932206	NHBE	bronchial:	n/a
15	chr2:111932156-111932206	AG04449	skin:	fetal
16	chr2:111936357-111936407	PANC-1	pancreas:	n/a
17	chr2:111932156-111932206	K562	blood:	n/a
18	chr2:111936357-111936407	HIPEpiC	eye:	n/a
19	chr2:111932156-111932206	NB4	blood:	n/a
20	chr2:111932156-111932206	HCF	heart:	n/a
21	chr2:111932156-111932206	GM12891	blood:	n/a
22	chr2:111936357-111936407	HRE	kidney:	n/a
23	chr2:111932156-111932206	SKMC	muscle:	n/a
24	chr2:111936357-111936407	A549	lung:	n/a
25	chr2:111936357-111936407	AoSMC	blood vessel:	n/a
26	chr2:111932156-111932206	MCF10A-Er-Src	breast:	n/a
27	chr2:111932156-111932206	NH-A	brain:	n/a
28	chr2:111936357-111936407	U87	brain:	n/a
29	chr2:111932156-111932206	BE2_C	brain:	n/a
30	chr2:111932156-111932206	Caco-2	colon:	n/a
31	chr2:111932156-111932206	AG10803	skin:	n/a
32	chr2:111932156-111932206	AG09309	skin:	n/a
33	chr2:111936357-111936407	NT2-D1	testis:	n/a
34	chr2:111932156-111932206	RPTEC	kidney:	n/a
35	chr2:111936357-111936407	ovcar-3	ovarian:	n/a
36	chr2:111932156-111932206	HepG2	liver:	n/a
37	chr2:111936357-111936407	PFSK-1	brain:	n/a
38	chr2:111936357-111936407	HRPEpiC	eye:	n/a
39	chr2:111936357-111936407	PrEC	prostate:	n/a
40	chr2:111936357-111936407	IMR90	lung:	fetal
41	chr2:111936357-111936407	CMK	blood:	n/a
42	chr2:111936357-111936407	AG04449	skin:	fetal
43	chr2:111936357-111936407	Hepatocyte	liver:	n/a
44	chr2:111932156-111932206	Jurkat	blood:	n/a
45	chr2:111936357-111936407	AG09319	gingival:	n/a
46	chr2:111932156-111932206	HNPCEpiC	eye:	n/a
47	chr2:111932156-111932206	AG04450	lung:	fetal
48	chr2:111936357-111936407	GM06990	blood:	n/a
49	chr2:111936357-111936407	HAEpiC	amniotic membrane:	n/a
50	chr2:111936357-111936407	NHDF-neo	bronchial:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:111933860..111937323-chr2:111941659..111944364,3	MCF-7	breast:
2	chr2:111932435..111934094-chr2:111935075..111937395,2	K562	blood:
3	chr2:111923929..111929033-chr2:111931509..111935010,6	K562	blood:
4	chr2:111940752..111942733-chr2:111943898..111945698,2	K562	blood:
5	chr2:111928406..111930864-chr2:111931206..111933246,3	MCF-7	breast:
6	chr2:111877906..111880347-chr2:111931458..111933494,2	K562	blood:
7	chr2:111927830..111930159-chr2:111935150..111938142,2	MCF-7	breast:
8	chr2:111877706..111880445-chr2:111936498..111939733,3	K562	blood:
9	chr2:111943401..111945501-chr2:111991303..111993728,2	K562	blood:
10	chr2:111926311..111928837-chr2:111932498..111934410,2	MCF-7	breast:
11	chr2:111946509..111948789-chr2:111950661..111953491,2	MCF-7	breast:
12	chr2:111932337..111934178-chr2:111951308..111954213,2	K562	blood:
13	chr2:111938737..111942201-chr2:111942427..111945208,3	K562	blood:
14	chr2:111939569..111942503-chr2:111952728..111955469,2	MCF-7	breast:
15	chr2:111919430..111921560-chr2:111931169..111932920,2	K562	blood:
16	chr2:111940752..111942733-chr2:111943898..111945698,2	K562	blood:
17	chr2:111941236..111945109-chr2:111946384..111948560,3	K562	blood:
18	chr2:111932435..111934094-chr2:111935075..111937395,2	K562	blood:
19	chr2:111941236..111945109-chr2:111946384..111948560,3	K562	blood:
20	chr2:111933860..111937323-chr2:111941659..111944364,3	MCF-7	breast:
21	chr2:111941236..111945109-chr2:111946384..111948613,3	K562	blood:
22	chr2:111938737..111942201-chr2:111942427..111945208,3	K562	blood:
23	chr2:111941236..111945109-chr2:111946384..111948613,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000230499	TF binding region
ENSG00000230499	CpG island
ENSG00000230499	chromatin interactions
ENSG00000153094	chromatin interactions

Extended variants
information (count: 673 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs726430	chr2:111931421-111931422	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs112216162	chr2:111931424-111931425	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181470260	chr2:111931436-111931437	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs534141463	chr2:111931451-111931452	Bivalent Enhancer Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs553933053	chr2:111931521-111931522	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs566260165	chr2:111931569-111931570	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368811564	chr2:111931588-111931589	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs535176520	chr2:111931589-111931590	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs73954987	chr2:111931644-111931645	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs111543556	chr2:111931654-111931655	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369097514	chr2:111931662-111931663	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs544144658	chr2:111931760-111931761	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs569706551	chr2:111931766-111931767	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs138519808	chr2:111931810-111931811	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540466357	chr2:111931856-111931857	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs185765972	chr2:111931938-111931939	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs149240442	chr2:111931968-111931969	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs144462360	chr2:111931985-111931986	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112436120	chr2:111932008-111932009	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs542744938	chr2:111932020-111932021	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs372574658	chr2:111932032-111932033	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs138537222	chr2:111932035-111932036	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs557636309	chr2:111932054-111932055	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs531631975	chr2:111932103-111932104	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs551719329	chr2:111932110-111932111	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs6726007	chr2:111932122-111932123	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs190139218	chr2:111932253-111932254	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12621071	chr2:111932267-111932268	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs114673801	chr2:111932275-111932276	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs144051681	chr2:111932331-111932332	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536405294	chr2:111932346-111932347	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs548804426	chr2:111932358-111932359	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs568905228	chr2:111932359-111932360	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs115606867	chr2:111932371-111932372	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs76363161	chr2:111932401-111932402	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs578019477	chr2:111932427-111932428	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs534077535	chr2:111932457-111932458	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs182415514	chr2:111932466-111932467	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs59884235	chr2:111932484-111932485	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542779179	chr2:111932493-111932494	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs562859169	chr2:111932501-111932502	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs374507952	chr2:111932508-111932509	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs576466873	chr2:111932545-111932546	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs185914116	chr2:111932551-111932552	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564936383	chr2:111932566-111932567	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs372330314	chr2:111932604-111932605	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs528021666	chr2:111932613-111932614	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs7596789	chr2:111932616-111932617	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs368173951	chr2:111932629-111932630	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs140886157	chr2:111932667-111932668	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Astrocytoma	22246337	CNVD
Myelofibrosis	22110671	CNVD
Ocular motor apraxia	21572526	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Idiopathic chronic pancreatitis	21549014	CNVD
Mental retardation	21549014	CNVD
Maculopathy	20981449	CNVD
Nephronophthisis	22470819	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	23813976	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:228 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:111920800-111943000	Weak transcription	Right Ventricle	heart
2	chr2:111921200-111939400	Weak transcription	Right Atrium	heart
3	chr2:111921400-111932200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:111924000-111931600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr2:111924400-111931600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr2:111925000-111932200	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr2:111925000-111934000	Weak transcription	Fetal Intestine Large	intestine
8	chr2:111925600-111931600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:111925800-111931600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr2:111926200-111933400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr2:111926200-111934400	Weak transcription	Adipose Nuclei	Adipose
12	chr2:111927000-111931800	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr2:111927000-111933600	Weak transcription	Left Ventricle	heart
14	chr2:111929200-111932200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr2:111929400-111932400	Weak transcription	Pancreas	Pancrea
16	chr2:111929400-111933800	Weak transcription	Gastric	stomach
17	chr2:111929400-111934000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:111929400-111942200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr2:111929600-111931600	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr2:111929600-111933800	Weak transcription	HMEC	breast
21	chr2:111929800-111933800	Weak transcription	A549	lung
22	chr2:111930600-111934200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:111931200-111932400	Weak transcription	Esophagus	oesophagus
24	chr2:111931400-111931800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
25	chr2:111931400-111932000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
26	chr2:111931400-111932200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:111931400-111932400	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr2:111931400-111932600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr2:111931600-111932400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
30	chr2:111931600-111932400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr2:111931600-111932400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr2:111931600-111932600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr2:111931600-111932600	Enhancers	iPS-15b Cell Line	embryonic stem cell
34	chr2:111931600-111933000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr2:111931600-111933400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr2:111931800-111932200	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr2:111931800-111932400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr2:111931800-111933800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr2:111932200-111932600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr2:111932200-111932600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr2:111932200-111932600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr2:111932200-111932600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr2:111932200-111939200	Weak transcription	Cortex derived primary cultured neurospheres	brain
44	chr2:111932400-111932600	Enhancers	Esophagus	oesophagus
45	chr2:111932400-111932600	Enhancers	Pancreas	Pancrea
46	chr2:111932600-111933000	Weak transcription	Esophagus	oesophagus
47	chr2:111932600-111933000	Weak transcription	Pancreas	Pancrea
48	chr2:111932600-111934200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:111932800-111937600	Enhancers	Liver	Liver
50	chr2:111933000-111934800	Enhancers	Esophagus	oesophagus

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