Variant report

Variant	nsv1014068
Chromosome Location	chr2:52960353-53169617
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	ARID3A	chr2:53161835-53161893	HepG2	liver:	n/a	n/a
2	ATF2	chr2:53161624-53162186	GM12878	blood:	n/a	n/a
3	ATF2	chr2:53161550-53162230	GM12878	blood:	n/a	n/a
4	ATF2	chr2:53124799-53125218	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr2:53161366-53162095	HCT-116	colon:	n/a	n/a
6	BATF	chr2:53166348-53166822	GM12878	blood:	n/a	n/a
7	BATF	chr2:53161603-53162043	GM12878	blood:	n/a	chr2:53161802-53161813 chr2:53161799-53161809 chr2:53161784-53161795
8	BATF	chr2:53161569-53162046	GM12878	blood:	n/a	chr2:53161802-53161813 chr2:53161799-53161809 chr2:53161784-53161795
9	BCL11A	chr2:53166415-53166672	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:53152851-53153076	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:53158346-53158507	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:53161743-53162072	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
13	BCL11A	chr2:53161550-53162089	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
14	BCL3	chr2:53161702-53162170	GM12878	blood:	n/a	chr2:53161787-53161796 chr2:53161788-53161797 chr2:53161801-53161810 chr2:53161802-53161811
15	BCL3	chr2:53108842-53109038	GM12878	blood:	n/a	chr2:53108968-53108977
16	BHLHE40	chr2:53161740-53162175	GM12878	blood:	n/a	n/a
17	BRCA1	chr2:53032201-53032207	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr2:53160924-53162066	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr2:53037501-53037624	H1-hESC	embryonic stem cell:	n/a	n/a
20	CBX3	chr2:53161275-53162160	HCT-116	colon:	n/a	n/a
21	CBX3	chr2:53048683-53049186	HCT-116	colon:	n/a	n/a
22	CBX3	chr2:53161249-53162217	HCT-116	colon:	n/a	chr2:53162199-53162210
23	CBX3	chr2:53108658-53109304	HCT-116	colon:	n/a	n/a
24	CEBPB	chr2:53122149-53122189	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr2:53122154-53122200	Hela-S3	cervix:	n/a	chr2:53122180-53122191
26	CEBPB	chr2:53160427-53162176	HCT-116	colon:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
27	CEBPB	chr2:53002901-53003198	A549	lung:	n/a	n/a
28	CEBPB	chr2:53161266-53162009	A549	lung:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
29	CEBPB	chr2:52989878-52990124	HepG2	liver:	n/a	chr2:52990014-52990025
30	CEBPB	chr2:52990470-52990921	IMR90	lung:	n/a	chr2:52990766-52990777 chr2:52990767-52990778 chr2:52990768-52990777
31	CEBPB	chr2:53108744-53109210	IMR90	lung:	n/a	n/a
32	CEBPB	chr2:53032076-53032260	A549	lung:	n/a	chr2:53032220-53032233 chr2:53032222-53032233 chr2:53032220-53032231
33	CEBPB	chr2:53123954-53124241	IMR90	lung:	n/a	chr2:53124077-53124088 chr2:53124075-53124088 chr2:53124075-53124086
34	CEBPB	chr2:53145768-53146137	Hela-S3	cervix:	n/a	chr2:53145956-53145969
35	CEBPB	chr2:53016681-53016865	HepG2	liver:	n/a	chr2:53016744-53016755
36	CEBPB	chr2:53161386-53161765	ECC-1	luminal epithelium:	n/a	chr2:53161529-53161540 chr2:53161549-53161560
37	CEBPB	chr2:53094201-53094581	IMR90	lung:	n/a	n/a
38	CEBPB	chr2:52972320-52972582	K562	blood:	n/a	chr2:52972476-52972487
39	CEBPB	chr2:53005825-53006043	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr2:53161220-53162079	IMR90	lung:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
41	CEBPB	chr2:53005783-53005972	HepG2	liver:	n/a	n/a
42	CEBPB	chr2:53089862-53090309	A549	lung:	n/a	chr2:53090036-53090044
43	CEBPB	chr2:53002959-53003131	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr2:52976939-52977247	A549	lung:	n/a	n/a
45	CEBPB	chr2:53131724-53132020	MCF-7	breast:	n/a	chr2:53131973-53131984
46	CEBPB	chr2:52972338-52972613	H1-hESC	embryonic stem cell:	n/a	chr2:52972476-52972487
47	CEBPB	chr2:53155376-53155506	A549	lung:	n/a	n/a
48	CEBPB	chr2:53161204-53162173	HCT-116	colon:	n/a	chr2:53161529-53161540 chr2:53161549-53161560 chr2:53161857-53161869
49	CEBPB	chr2:53122020-53122313	A549	lung:	n/a	chr2:53122180-53122191
50	CEBPB	chr2:53122010-53122340	HepG2	liver:	n/a	chr2:53122180-53122191

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:53004359-53004409	HepG2	liver:	n/a
2	chr2:53004359-53004409	AG04449	skin:	fetal
3	chr2:53160678-53160728	AG09309	skin:	n/a
4	chr2:53094222-53094272	HRE	kidney:	n/a
5	chr2:53160678-53160728	HL-60	blood:	n/a
6	chr2:53105695-53105745	HMEC	breast:	n/a
7	chr2:53160678-53160728	NH-A	brain:	n/a
8	chr2:53105695-53105745	SK-N-MC	brain:	n/a
9	chr2:53105695-53105745	HNPCEpiC	eye:	n/a
10	chr2:53107842-53107892	GM06990	blood:	n/a
11	chr2:53107842-53107892	Caco-2	colon:	n/a
12	chr2:53105695-53105745	AG09309	skin:	n/a
13	chr2:53160678-53160728	K562	blood:	n/a
14	chr2:53160678-53160728	ProgFib	skin:	n/a
15	chr2:53105695-53105745	CMK	blood:	n/a
16	chr2:53160678-53160728	HEEpiC	esophagus:	n/a
17	chr2:53004359-53004409	ProgFib	skin:	n/a
18	chr2:53107842-53107892	MCF-7	breast:	n/a
19	chr2:53160678-53160728	NB4	blood:	n/a
20	chr2:53160678-53160728	HEK293	kidney:	embryo
21	chr2:53105695-53105745	HUVEC	blood vessel:	n/a
22	chr2:53105695-53105745	HEEpiC	esophagus:	n/a
23	chr2:53107842-53107892	HPAEpiC	pulmonary alveolar:	n/a
24	chr2:53160678-53160728	A549	lung:	n/a
25	chr2:53107842-53107892	BJ	skin:	n/a
26	chr2:53105695-53105745	AoSMC	blood vessel:	n/a
27	chr2:53004359-53004409	HCF	heart:	n/a
28	chr2:53004359-53004409	NHBE	bronchial:	n/a
29	chr2:53094222-53094272	A549	lung:	n/a
30	chr2:53004359-53004409	NH-A	brain:	n/a
31	chr2:53107842-53107892	NHBE	bronchial:	n/a
32	chr2:53160678-53160728	AG04450	lung:	fetal
33	chr2:53105695-53105745	U87	brain:	n/a
34	chr2:53105695-53105745	HCT-116	colon:	n/a
35	chr2:53004359-53004409	LNCaP	prostate:	n/a
36	chr2:53160678-53160728	HRPEpiC	eye:	n/a
37	chr2:53160678-53160728	HCF	heart:	n/a
38	chr2:53004359-53004409	Hepatocyte	liver:	n/a
39	chr2:53160678-53160728	PFSK-1	brain:	n/a
40	chr2:53004359-53004409	HCT-116	colon:	n/a
41	chr2:53105695-53105745	T-47D	breast:	n/a
42	chr2:53094222-53094272	HCF	heart:	n/a
43	chr2:53160678-53160728	GM06990	blood:	n/a
44	chr2:53160678-53160728	Hepatocyte	liver:	n/a
45	chr2:53094222-53094272	NT2-D1	testis:	n/a
46	chr2:53105695-53105745	NHBE	bronchial:	n/a
47	chr2:53107842-53107892	NB4	blood:	n/a
48	chr2:53105695-53105745	PANC-1	pancreas:	n/a
49	chr2:53160678-53160728	PrEC	prostate:	n/a
50	chr2:53094222-53094272	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:53048846..53049807-chr2:53183875..53184416,2	MCF-7	breast:
2	chr2:53103066..53106486-chr2:53106611..53109718,3	MCF-7	breast:
3	chr2:53103066..53106486-chr2:53106611..53109718,3	MCF-7	breast:
4	chr2:53037286..53038157-chr2:53203093..53203814,3	MCF-7	breast:
5	chr2:53115077..53117448-chr2:53686034..53688851,2	MCF-7	breast:
6	chr2:53048584..53050700-chr2:53053856..53055982,2	K562	blood:
7	chr2:53132852..53133808-chr20:52198265..52198765,2	MCF-7	breast:
8	chr2:53037360..53037874-chr2:53428995..53429598,2	MCF-7	breast:
9	chr2:53048584..53050700-chr2:53053856..53055982,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-1	chr2:53124381-53124442	ENSG00000228033
2	lnc-CHAC2-6	chr2:53110381-53110593	NONHSAT070683
3	lnc-CHAC2-1	chr2:53091373-53091454	XLOC_001470
4	lnc-ASB3-1	chr2:53137102-53137158	ENSG00000228033
5	lnc-CHAC2-1	chr2:53093519-53093769	XLOC_001470
6	lnc-ASB3-1	chr2:53124381-53124442	ENSG00000228033
7	lnc-ASB3-1	chr2:53137102-53137158	ENSG00000228033

Variant related genes	Relation type
ENSG00000228033	TF binding region
ENSG00000232668	TF binding region
ENSG00000232604	TF binding region
ENSG00000228033	CpG island
ENSG00000232668	CpG island
ENSG00000232604	CpG island

Extended variants
information (count: 6670 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:6670 , 50 per page) page: 1 2 3 4 5 6 7 ... 134

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529371699	chr2:52960367-52960368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113532836	chr2:52960472-52960473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs549048454	chr2:52960482-52960483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145710994	chr2:52960484-52960485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183284938	chr2:52960519-52960520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373143962	chr2:52960571-52960572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs148941476	chr2:52960574-52960575	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs545519237	chr2:52960619-52960620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs7592833	chr2:52960639-52960640	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs552714821	chr2:52960641-52960642	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs566440316	chr2:52960703-52960704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs2626390	chr2:52960727-52960728	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs187456703	chr2:52960745-52960746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs191336800	chr2:52960748-52960749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544067448	chr2:52960766-52960767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375728655	chr2:52960794-52960795	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs547449539	chr2:52960885-52960886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs561787203	chr2:52960887-52960888	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs557896772	chr2:52960950-52960951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs73931435	chr2:52960964-52960965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs540493998	chr2:52960993-52960994	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560131726	chr2:52961013-52961014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs143814450	chr2:52961030-52961031	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184592262	chr2:52961117-52961118	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562629529	chr2:52961118-52961119	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs531650522	chr2:52961145-52961146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs189230722	chr2:52961170-52961171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs571782927	chr2:52961198-52961199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs527991247	chr2:52961202-52961203	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs548055537	chr2:52961221-52961222	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566504014	chr2:52961252-52961253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138496375	chr2:52961258-52961259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs555542627	chr2:52961262-52961263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs530855854	chr2:52961277-52961278	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192633182	chr2:52961282-52961283	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537902974	chr2:52961290-52961291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544040920	chr2:52961298-52961299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs76865820	chr2:52961305-52961306	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs77282924	chr2:52961312-52961313	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs533869690	chr2:52961371-52961372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78822428	chr2:52961389-52961390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs553645179	chr2:52961394-52961395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1840321	chr2:52961407-52961408	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs542619047	chr2:52961443-52961444	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs562495026	chr2:52961489-52961490	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576482437	chr2:52961497-52961498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs545448968	chr2:52961557-52961558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565371958	chr2:52961577-52961578	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs527864680	chr2:52961594-52961595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs13419330	chr2:52961597-52961598	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:63)

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
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Lung cancer	17086460	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
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:237 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52959800-52960600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr2:52959800-52961200	Enhancers	Stomach Mucosa	stomach
3	chr2:52960000-52960400	Enhancers	H1 Cell Line	embryonic stem cell
4	chr2:52960000-52960400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:52960000-52960400	Enhancers	Spleen	Spleen
6	chr2:52960000-52960600	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:52960000-52960600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr2:52960200-52960600	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr2:52960200-52960600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr2:52960600-52961600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr2:52961200-52961600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:52961600-52961800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr2:52968200-52968800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:52972800-52973400	Active TSS	Fetal Heart	heart
15	chr2:53003600-53004200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr2:53003800-53004200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:53004200-53006400	Enhancers	Fetal Intestine Large	intestine
18	chr2:53021800-53022200	Enhancers	Adipose Nuclei	Adipose
19	chr2:53024200-53025200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr2:53025200-53029200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:53027800-53049000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:53029200-53029400	ZNF genes & repeats	ES-WA7 Cell Line	embryonic stem cell
23	chr2:53029200-53029800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr2:53029800-53033200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:53031200-53031800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr2:53031400-53031800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
27	chr2:53033200-53034400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr2:53037600-53037800	Weak transcription	Left Ventricle	heart
29	chr2:53037800-53038000	Enhancers	Left Ventricle	heart
30	chr2:53037800-53038200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:53037800-53038200	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr2:53037800-53038200	Enhancers	Pancreas	Pancrea
33	chr2:53038200-53044600	Weak transcription	Pancreas	Pancrea
34	chr2:53046400-53046800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr2:53046800-53050600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr2:53050600-53051400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr2:53051400-53058200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr2:53057000-53057400	Enhancers	Pancreas	Pancrea
39	chr2:53057400-53059600	Weak transcription	Pancreas	Pancrea
40	chr2:53058200-53059600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr2:53059600-53059800	Enhancers	Pancreas	Pancrea
42	chr2:53059600-53060400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr2:53060400-53062200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr2:53060800-53061400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr2:53062200-53063000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr2:53063000-53063200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr2:53063200-53066000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr2:53071400-53072000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr2:53071400-53072000	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr2:53071800-53072400	Enhancers	iPS-20b Cell Line	embryonic stem cell

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