Variant report

Variant	nsv1004503
Chromosome Location	chr2:55324276-55343705
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:810)
CpG islands
(count:185)
Chromatin interactive
region (count:31)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:810 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:55327031-55327942	K562	blood:	n/a	chr2:55327796-55327812
2	ARID3A	chr2:55333339-55333652	K562	blood:	n/a	n/a
3	ARID3A	chr2:55336364-55337044	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:55339730-55339919	K562	blood:	n/a	n/a
5	ARID3A	chr2:55343213-55343825	K562	blood:	n/a	n/a
6	ARID3A	chr2:55324829-55325004	K562	blood:	n/a	n/a
7	ARID3A	chr2:55338562-55339162	K562	blood:	n/a	n/a
8	ARID3A	chr2:55338953-55339524	HepG2	liver:	n/a	n/a
9	ATF1	chr2:55327022-55327751	K562	blood:	n/a	n/a
10	ATF1	chr2:55342889-55343581	K562	blood:	n/a	n/a
11	ATF1	chr2:55333344-55333688	K562	blood:	n/a	n/a
12	ATF3	chr2:55336357-55337150	A549	lung:	n/a	n/a
13	ATF3	chr2:55342809-55343566	K562	blood:	n/a	n/a
14	ATF3	chr2:55338847-55339232	K562	blood:	n/a	n/a
15	ATF3	chr2:55326937-55327390	K562	blood:	n/a	n/a
16	ATF3	chr2:55333276-55333643	K562	blood:	n/a	n/a
17	BACH1	chr2:55338776-55339255	K562	blood:	n/a	chr2:55339035-55339049
18	BACH1	chr2:55338803-55339256	H1-hESC	embryonic stem cell:	n/a	chr2:55339035-55339049
19	BCL3	chr2:55336395-55337177	A549	lung:	n/a	n/a
20	BCL3	chr2:55336285-55337161	A549	lung:	n/a	n/a
21	BHLHE40	chr2:55343380-55343848	K562	blood:	n/a	n/a
22	BHLHE40	chr2:55338879-55340432	K562	blood:	n/a	n/a
23	BHLHE40	chr2:55338877-55339405	HepG2	liver:	n/a	n/a
24	BRCA1	chr2:55326986-55327540	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr2:55338810-55339977	K562	blood:	n/a	n/a
26	CBX3	chr2:55342909-55343546	K562	blood:	n/a	n/a
27	CCNT2	chr2:55338955-55340313	K562	blood:	n/a	n/a
28	CCNT2	chr2:55324862-55325282	K562	blood:	n/a	n/a
29	CCNT2	chr2:55343202-55343687	K562	blood:	n/a	n/a
30	CCNT2	chr2:55324567-55324609	K562	blood:	n/a	n/a
31	CCNT2	chr2:55333403-55333632	K562	blood:	n/a	n/a
32	CEBPB	chr2:55338818-55339256	A549	lung:	n/a	n/a
33	CEBPB	chr2:55327013-55328046	K562	blood:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215
34	CEBPB	chr2:55333308-55333695	IMR90	lung:	n/a	chr2:55333495-55333506
35	CEBPB	chr2:55333289-55333667	K562	blood:	n/a	chr2:55333495-55333506
36	CEBPB	chr2:55327042-55327431	ECC-1	luminal epithelium:	n/a	chr2:55327205-55327216 chr2:55327204-55327215
37	CEBPB	chr2:55340664-55340864	HepG2	liver:	n/a	chr2:55340800-55340811
38	CEBPB	chr2:55343117-55343651	K562	blood:	n/a	n/a
39	CEBPB	chr2:55333336-55333671	A549	lung:	n/a	chr2:55333495-55333506
40	CEBPB	chr2:55338856-55339605	IMR90	lung:	n/a	n/a
41	CEBPB	chr2:55342734-55343724	HCT-116	colon:	n/a	n/a
42	CEBPB	chr2:55338886-55339646	HepG2	liver:	n/a	n/a
43	CEBPB	chr2:55338895-55339215	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr2:55338997-55339151	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr2:55333280-55333596	A549	lung:	n/a	chr2:55333495-55333506
46	CEBPB	chr2:55326958-55327386	A549	lung:	n/a	chr2:55327205-55327216 chr2:55327204-55327215
47	CEBPB	chr2:55333332-55333669	Hela-S3	cervix:	n/a	chr2:55333495-55333506
48	CEBPB	chr2:55342698-55343784	HCT-116	colon:	n/a	n/a
49	CEBPB	chr2:55343161-55343580	K562	blood:	n/a	n/a
50	CEBPB	chr2:55327008-55328037	A549	lung:	n/a	chr2:55327566-55327579 chr2:55327205-55327216 chr2:55327204-55327215

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:55339218-55339268	SK-N-SH_RA	brain:	n/a
2	chr2:55339218-55339268	HRE	kidney:	n/a
3	chr2:55339218-55339268	SK-N-SH_RA	brain:	n/a
4	chr2:55339218-55339268	HRE	kidney:	n/a
5	chr2:55339939-55339989	Jurkat	blood:	n/a
6	chr2:55339939-55339989	HL-60	blood:	n/a
7	chr2:55327371-55327421	GM12891	blood:	n/a
8	chr2:55339218-55339268	HCM	heart:	n/a
9	chr2:55339939-55339989	AoSMC	blood vessel:	n/a
10	chr2:55339939-55339989	SK-N-SH_RA	brain:	n/a
11	chr2:55339939-55339989	MCF10A-Er-Src	breast:	n/a
12	chr2:55339939-55339989	GM12891	blood:	n/a
13	chr2:55339218-55339268	PFSK-1	brain:	n/a
14	chr2:55339939-55339989	MCF-7	breast:	n/a
15	chr2:55339939-55339989	CMK	blood:	n/a
16	chr2:55339218-55339268	Hela-S3	cervix:	n/a
17	chr2:55327371-55327421	AG09309	skin:	n/a
18	chr2:55327371-55327421	PFSK-1	brain:	n/a
19	chr2:55327371-55327421	Hela-S3	cervix:	n/a
20	chr2:55339939-55339989	BE2_C	brain:	n/a
21	chr2:55327371-55327421	H1-hESC	embryonic stem cell:	embryo
22	chr2:55339218-55339268	LNCaP	prostate:	n/a
23	chr2:55327371-55327421	HAEpiC	amniotic membrane:	n/a
24	chr2:55339939-55339989	NH-A	brain:	n/a
25	chr2:55327371-55327421	HRPEpiC	eye:	n/a
26	chr2:55339939-55339989	HPAEpiC	pulmonary alveolar:	n/a
27	chr2:55327371-55327421	HMEC	breast:	n/a
28	chr2:55339218-55339268	PrEC	prostate:	n/a
29	chr2:55339218-55339268	GM12892	blood:	n/a
30	chr2:55339218-55339268	NB4	blood:	n/a
31	chr2:55339939-55339989	GM12878	blood:	n/a
32	chr2:55339939-55339989	HCPEpiC	choroid plexus:	n/a
33	chr2:55339218-55339268	HNPCEpiC	eye:	n/a
34	chr2:55339218-55339268	AG04449	skin:	fetal
35	chr2:55339218-55339268	HCPEpiC	choroid plexus:	n/a
36	chr2:55327371-55327421	ECC-1	luminal epithelium:	n/a
37	chr2:55327371-55327421	SKMC	muscle:	n/a
38	chr2:55339218-55339268	T-47D	breast:	n/a
39	chr2:55327371-55327421	CMK	blood:	n/a
40	chr2:55327371-55327421	MCF10A-Er-Src	breast:	n/a
41	chr2:55327371-55327421	ovcar-3	ovarian:	n/a
42	chr2:55327371-55327421	A549	lung:	n/a
43	chr2:55327371-55327421	RPTEC	kidney:	n/a
44	chr2:55327371-55327421	NT2-D1	testis:	n/a
45	chr2:55339218-55339268	HUVEC	blood vessel:	n/a
46	chr2:55339939-55339989	ECC-1	luminal epithelium:	n/a
47	chr2:55327371-55327421	HL-60	blood:	n/a
48	chr2:55327371-55327421	GM12892	blood:	n/a
49	chr2:55327371-55327421	NH-A	brain:	n/a
50	chr2:55339939-55339989	HEEpiC	esophagus:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:55273237..55279836-chr2:55336432..55344363,17	K562	blood:
2	chr2:55331372..55335609-chr2:55337059..55340698,6	K562	blood:
3	chr2:55323307..55326609-chr2:55326695..55329491,3	K562	blood:
4	chr2:55276735..55279463-chr2:55327258..55330571,3	K562	blood:
5	chr2:55343511..55346556-chr2:55364762..55366710,3	K562	blood:
6	chr2:55323307..55326609-chr2:55326695..55329491,3	K562	blood:
7	chr2:55287997..55290069-chr2:55324008..55326423,2	K562	blood:
8	chr2:55274277..55278619-chr2:55322679..55324935,4	K562	blood:
9	chr2:55312676..55314647-chr2:55325733..55328474,2	K562	blood:
10	chr2:55339781..55342552-chr2:55346442..55349594,4	K562	blood:
11	chr2:55317970..55321435-chr2:55328777..55332297,3	K562	blood:
12	chr2:54341515..54343973-chr2:55337394..55340042,2	MCF-7	breast:
13	chr2:55332689..55335529-chr2:55338275..55340328,2	MCF-7	breast:
14	chr2:55275064..55278271-chr2:55336145..55339086,3	MCF-7	breast:
15	chr2:55275100..55278867-chr2:55332257..55335062,4	K562	blood:
16	chr2:55326463..55328844-chr2:55338475..55342420,4	K562	blood:
17	chr2:55323589..55325752-chr2:55333096..55335881,2	MCF-7	breast:
18	chr2:55278333..55279964-chr2:55343174..55345064,2	MCF-7	breast:
19	chr2:55327279..55331330-chr2:55337574..55341174,5	K562	blood:
20	chr2:55322057..55324846-chr2:55364507..55366032,2	K562	blood:
21	chr2:55274277..55275806-chr2:55323435..55326407,2	K562	blood:
22	chr2:55322759..55325369-chr2:55329915..55332847,3	MCF-7	breast:
23	chr2:55323175..55325737-chr2:55325839..55328414,2	MCF-7	breast:
24	chr2:55273237..55280299-chr2:55335301..55344768,18	K562	blood:
25	chr2:55278300..55281080-chr2:55325086..55327233,3	K562	blood:
26	chr2:55322759..55325369-chr2:55329915..55332847,3	MCF-7	breast:
27	chr2:55323175..55325737-chr2:55325839..55328414,2	MCF-7	breast:
28	chr2:55326388..55330538-chr2:55335061..55337994,3	K562	blood:
29	chr2:55341952..55344762-chr2:55357897..55359885,2	K562	blood:
30	chr2:55325626..55328074-chr2:55345685..55348277,2	K562	blood:
31	chr2:55276927..55278545-chr2:55322721..55325631,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C2orf63-2	chr2:55339656-55339703	NONHSAT070760

No data

Variant related genes	Relation type
RTN4	TF binding region
ENSG00000266376	TF binding region
RTN4	CpG island
ENSG00000266376	CpG island
ENSG00000115310	chromatin interactions
ENSG00000170634	chromatin interactions
ENSG00000266376	chromatin interactions

Extended variants
information (count: 823 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:823 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143693871	chr2:55324276-55324277	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs535133885	chr2:55324277-55324278	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs555364816	chr2:55324315-55324316	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs377417592	chr2:55324326-55324327	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs13023249	chr2:55324358-55324359	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs537739290	chr2:55324402-55324403	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs147252313	chr2:55324436-55324437	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs138975758	chr2:55324437-55324438	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs111622479	chr2:55324438-55324439	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs5831338	chr2:55324455-55324456	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs76491997	chr2:55324500-55324501	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs557803324	chr2:55324501-55324502	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs577545554	chr2:55324506-55324507	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs10206023	chr2:55324557-55324558	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs80351228	chr2:55324604-55324605	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs577960904	chr2:55324698-55324699	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs184017346	chr2:55324706-55324707	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs560102084	chr2:55324732-55324733	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs114044844	chr2:55324765-55324766	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs529206581	chr2:55324766-55324767	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541821943	chr2:55324781-55324782	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs79993697	chr2:55324785-55324786	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs542610483	chr2:55324844-55324845	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs530861884	chr2:55324849-55324850	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs140984927	chr2:55324865-55324866	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs149826639	chr2:55324893-55324894	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563061497	chr2:55324894-55324895	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs546868142	chr2:55324904-55324905	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs4671238	chr2:55324905-55324906	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs536163227	chr2:55324911-55324912	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs76263502	chr2:55324913-55324914	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs531536469	chr2:55324953-55324954	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs568840485	chr2:55324954-55324955	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs4672016	chr2:55324960-55324961	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs557928588	chr2:55324961-55324962	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs79800828	chr2:55325001-55325002	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs533944670	chr2:55325044-55325045	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs145839248	chr2:55325121-55325122	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs573811512	chr2:55325133-55325134	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs542909818	chr2:55325189-55325190	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs372691457	chr2:55325245-55325246	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs148558013	chr2:55325257-55325258	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs575275574	chr2:55325297-55325298	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs544284786	chr2:55325338-55325339	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs564268709	chr2:55325339-55325340	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs528006452	chr2:55325362-55325363	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs4671239	chr2:55325372-55325373	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs2920875	chr2:55325385-55325386	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs567390574	chr2:55325414-55325415	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs536260552	chr2:55325520-55325521	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Mental retardation	19951919	CNVD
Myelofibrosis	22110671	CNVD
Microcephaly	20799320	CNVD
camptodactyly	20799320	CNVD
cognitive delay	20799320	CNVD
prenatal and postnatal growth deficiency	20799320	CNVD
ptosis of eyelids	20799320	CNVD
Maculopathy	20981449	CNVD
2p16.1 microdeletion syndrome	22283845	CNVD
Autism	22579565	CNVD
Autism	16963482	CNVD
Autism	21750575	CNVD
idiopathic intellectual disability	16963482	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Multiple myeloma	16616336	CNVD
Follicular lymphoma	17699855	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:55316800-55327200	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr2:55318400-55329600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:55319800-55324600	Weak transcription	Fetal Intestine Small	intestine
4	chr2:55320000-55327200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr2:55321000-55324600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:55321000-55326600	Weak transcription	HMEC	breast
7	chr2:55321400-55326400	Weak transcription	Primary B cells from cord blood	blood
8	chr2:55321600-55325000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr2:55321600-55327400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:55321600-55339400	Weak transcription	Thymus	Thymus
11	chr2:55321800-55324600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr2:55321800-55324600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:55321800-55336400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr2:55322000-55324600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr2:55322000-55324800	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr2:55322000-55326600	Weak transcription	Primary hematopoietic stem cells	blood
17	chr2:55322000-55326600	Weak transcription	NHEK	skin
18	chr2:55322200-55325200	Enhancers	Ovary	ovary
19	chr2:55322600-55327200	Enhancers	HUVEC	blood vessel
20	chr2:55322600-55327800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr2:55322800-55327200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr2:55322800-55327200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr2:55322800-55327200	Enhancers	Adipose Nuclei	Adipose
24	chr2:55323000-55325200	Enhancers	Pancreas	Pancrea
25	chr2:55323400-55324600	Enhancers	Right Ventricle	heart
26	chr2:55323600-55325200	Enhancers	Fetal Brain Male	brain
27	chr2:55323600-55325200	Enhancers	Fetal Heart	heart
28	chr2:55323600-55325200	Enhancers	Rectal Smooth Muscle	rectum
29	chr2:55323600-55325400	Enhancers	Colon Smooth Muscle	Colon
30	chr2:55323600-55325400	Enhancers	Right Atrium	heart
31	chr2:55323600-55325400	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr2:55323600-55325400	Enhancers	Hela-S3	cervix
33	chr2:55323600-55326600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr2:55323600-55326600	Enhancers	HSMMtube	muscle
35	chr2:55323600-55326600	Enhancers	NHLF	lung
36	chr2:55323600-55326800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr2:55323600-55327200	Enhancers	Osteobl	bone
38	chr2:55323600-55328200	Enhancers	K562	blood
39	chr2:55323600-55330000	Enhancers	HSMM	muscle
40	chr2:55323800-55324400	Enhancers	Rectal Mucosa Donor 31	rectum
41	chr2:55323800-55324600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr2:55323800-55324800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr2:55323800-55324800	Enhancers	Brain Angular Gyrus	brain
44	chr2:55323800-55324800	Enhancers	Fetal Brain Female	brain
45	chr2:55323800-55324800	Enhancers	Fetal Lung	lung
46	chr2:55323800-55324800	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr2:55323800-55325000	Enhancers	Fetal Stomach	stomach
48	chr2:55323800-55325000	Enhancers	A549	lung
49	chr2:55323800-55325200	Enhancers	Brain Anterior Caudate	brain
50	chr2:55323800-55325200	Enhancers	Brain Cingulate Gyrus	brain

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