Variant report

Variant	nsv518962
Chromosome Location	chr12:124561803-124583446
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:116)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:116 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr12:124582998-124583224	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr12:124573916-124574248	GM12878	blood:	n/a	n/a
3	BHLHE40	chr12:124573203-124573420	K562	blood:	n/a	chr12:124573254-124573267
4	CEBPB	chr12:124581463-124581692	HepG2	liver:	n/a	n/a
5	CEBPB	chr12:124573834-124574111	HepG2	liver:	n/a	n/a
6	CTCF	chr12:124580830-124580970	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr12:124580820-124580970	WERI-Rb-1	eye:	n/a	n/a
8	CTCF	chr12:124580860-124581010	BE2_C	brain:	n/a	n/a
9	CTCF	chr12:124578191-124578199	GM19239	blood:	n/a	n/a
10	CTCF	chr12:124577110-124578190	GM19239	blood:	n/a	n/a
11	CTCF	chr12:124574720-124574870	GM12869	blood:	n/a	chr12:124574779-124574792
12	CTCF	chr12:124580879-124580915	MCF-7	breast:	n/a	n/a
13	CTCF	chr12:124570020-124570170	GM12864	blood:	n/a	n/a
14	CTCF	chr12:124575060-124575210	BE2_C	brain:	n/a	n/a
15	CTCF	chr12:124574900-124575050	GM12870	blood:	n/a	n/a
16	ELF1	chr12:124573807-124573989	HepG2	liver:	n/a	n/a
17	ELF1	chr12:124573759-124574007	HepG2	liver:	n/a	n/a
18	EP300	chr12:124571613-124573408	SK-N-SH	brain:	n/a	chr12:124573290-124573297
19	EP300	chr12:124572295-124572591	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr12:124573771-124574015	HepG2	liver:	n/a	n/a
21	EP300	chr12:124572323-124572606	SK-N-SH_RA	brain:	n/a	n/a
22	ESR1	chr12:124573810-124574361	T-47D	breast:	n/a	n/a
23	ESR1	chr12:124573766-124574449	T-47D	breast:	n/a	n/a
24	FOSL2	chr12:124573737-124574347	HepG2	liver:	n/a	n/a
25	FOSL2	chr12:124573823-124574355	HepG2	liver:	n/a	n/a
26	FOXA1	chr12:124582965-124583147	T-47D	breast:	n/a	n/a
27	FOXA1	chr12:124574168-124574360	T-47D	breast:	n/a	n/a
28	FOXA1	chr12:124573727-124574384	HepG2	liver:	n/a	n/a
29	FOXA1	chr12:124574191-124574340	T-47D	breast:	n/a	n/a
30	FOXA1	chr12:124572395-124572649	T-47D	breast:	n/a	n/a
31	FOXA1	chr12:124573761-124574012	T-47D	breast:	n/a	n/a
32	FOXA1	chr12:124572411-124572651	T-47D	breast:	n/a	n/a
33	FOXA1	chr12:124573752-124573988	T-47D	breast:	n/a	n/a
34	FOXA2	chr12:124573857-124574461	A549	lung:	n/a	n/a
35	FOXA2	chr12:124573805-124573986	HepG2	liver:	n/a	n/a
36	FOXA2	chr12:124573749-124574361	A549	lung:	n/a	n/a
37	GABPA	chr12:124573923-124574304	Hela-S3	cervix:	n/a	n/a
38	GATA2	chr12:124571806-124573001	SH-SY5Y	brain:	n/a	chr12:124572243-124572252 chr12:124572244-124572261
39	GATA2	chr12:124577428-124578095	K562	blood:	n/a	n/a
40	GATA2	chr12:124566632-124566951	SH-SY5Y	brain:	n/a	n/a
41	GATA2	chr12:124573864-124574305	K562	blood:	n/a	n/a
42	GATA3	chr12:124573744-124574004	T-47D	breast:	n/a	n/a
43	GATA3	chr12:124572243-124572678	SH-SY5Y	brain:	n/a	chr12:124572243-124572252 chr12:124572244-124572261
44	GATA3	chr12:124573745-124574009	T-47D	breast:	n/a	n/a
45	GATA3	chr12:124574173-124574390	T-47D	breast:	n/a	n/a
46	GATA3	chr12:124574169-124574428	T-47D	breast:	n/a	n/a
47	GATA3	chr12:124572357-124572684	T-47D	breast:	n/a	n/a
48	GTF2F1	chr12:124568241-124568368	H1-hESC	embryonic stem cell:	n/a	n/a
49	IRF4	chr12:124573850-124574355	GM12878	blood:	n/a	n/a
50	IRF4	chr12:124573864-124574328	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:124582865-124582915	GM12891	blood:	n/a
2	chr12:124582865-124582915	HCF	heart:	n/a
3	chr12:124582865-124582915	GM06990	blood:	n/a
4	chr12:124582865-124582915	HEK293	kidney:	embryo
5	chr12:124582865-124582915	Hela-S3	cervix:	n/a
6	chr12:124582865-124582915	SK-N-MC	brain:	n/a
7	chr12:124582865-124582915	PrEC	prostate:	n/a
8	chr12:124582865-124582915	Jurkat	blood:	n/a
9	chr12:124582865-124582915	HCPEpiC	choroid plexus:	n/a
10	chr12:124582865-124582915	RPTEC	kidney:	n/a
11	chr12:124582865-124582915	SK-N-SH	brain:	n/a
12	chr12:124582865-124582915	T-47D	breast:	n/a
13	chr12:124582865-124582915	HPAEpiC	pulmonary alveolar:	n/a
14	chr12:124582865-124582915	HEEpiC	esophagus:	n/a
15	chr12:124582865-124582915	NB4	blood:	n/a
16	chr12:124582865-124582915	AG10803	skin:	n/a
17	chr12:124582865-124582915	MCF-7	breast:	n/a
18	chr12:124582865-124582915	AG04449	skin:	fetal
19	chr12:124582865-124582915	HUVEC	blood vessel:	n/a
20	chr12:124582865-124582915	HepG2	liver:	n/a
21	chr12:124582865-124582915	NT2-D1	testis:	n/a
22	chr12:124582865-124582915	MCF10A-Er-Src	breast:	n/a
23	chr12:124582865-124582915	HRE	kidney:	n/a
24	chr12:124582865-124582915	Hepatocyte	liver:	n/a
25	chr12:124582865-124582915	ECC-1	luminal epithelium:	n/a
26	chr12:124582865-124582915	Caco-2	colon:	n/a
27	chr12:124582865-124582915	AG04450	lung:	fetal
28	chr12:124582865-124582915	AG09309	skin:	n/a
29	chr12:124582865-124582915	GM12878	blood:	n/a
30	chr12:124582865-124582915	HRPEpiC	eye:	n/a
31	chr12:124582865-124582915	HMEC	breast:	n/a
32	chr12:124582865-124582915	NHBE	bronchial:	n/a
33	chr12:124582865-124582915	SAEC	small airway:	n/a
34	chr12:124582865-124582915	A549	lung:	n/a
35	chr12:124582865-124582915	AoSMC	blood vessel:	n/a
36	chr12:124582865-124582915	BE2_C	brain:	n/a
37	chr12:124582865-124582915	IMR90	lung:	fetal
38	chr12:124582865-124582915	AG09319	gingival:	n/a
39	chr12:124582865-124582915	HCM	heart:	n/a
40	chr12:124582865-124582915	H1-hESC	embryonic stem cell:	embryo
41	chr12:124582865-124582915	LNCaP	prostate:	n/a
42	chr12:124582865-124582915	HCT-116	colon:	n/a
43	chr12:124582865-124582915	ovcar-3	ovarian:	n/a
44	chr12:124582865-124582915	HAEpiC	amniotic membrane:	n/a
45	chr12:124582865-124582915	SKMC	muscle:	n/a
46	chr12:124582865-124582915	NHDF-neo	bronchial:	n/a
47	chr12:124582865-124582915	ProgFib	skin:	n/a
48	chr12:124582865-124582915	SK-N-SH_RA	brain:	n/a
49	chr12:124582865-124582915	K562	blood:	n/a
50	chr12:124582865-124582915	NH-A	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:124581557..124584588-chr12:124587697..124590714,3	K562	blood:
2	chr12:124563279..124565745-chr12:124567751..124569613,2	K562	blood:
3	chr12:124563279..124565745-chr12:124567751..124569613,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF664-2	chr12:124574282-124574327	XLOC_009926
2	lnc-ZNF664-2	chr12:124572821-124573024	XLOC_009926
3	lnc-ZNF664-2	chr12:124575119-124575483	XLOC_009926
4	lnc-ZNF664-2	chr12:124574591-124574717	XLOC_009926
5	lnc-ZNF664-2	chr12:124575119-124575483	XLOC_009926
6	lnc-ZNF664-2	chr12:124574282-124574327	XLOC_009926
7	lnc-ZNF664-2	chr12:124575119-124575483	XLOC_009926
8	lnc-ZNF664-2	chr12:124575119-124576008	XLOC_009926
9	lnc-ZNF664-2	chr12:124574594-124574626	XLOC_009926
10	lnc-ZNF664-2	chr12:124570308-124573142	ENSG00000269923.1
11	lnc-ZNF664-2	chr12:124574282-124574327	XLOC_009926

No data

Variant related genes	Relation type
ENSG00000269923	TF binding region
ENSG00000269923	CpG island
NUFIP2	miRNA target sites
GMNN	miRNA target sites
NUDT12	miRNA target sites
CD46	miRNA target sites
RELA	miRNA target sites
CNOT6	miRNA target sites

Extended variants
information (count: 882 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:882 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs825461	chr12:124561803-124561804	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs60339834	chr12:124561847-124561848	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs566875762	chr12:124561866-124561867	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139904119	chr12:124561884-124561885	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs149418024	chr12:124561892-124561893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183086845	chr12:124561902-124561903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs113122866	chr12:124561939-124561940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539246738	chr12:124561980-124561981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557267786	chr12:124561983-124561984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs144843611	chr12:124562000-124562001	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs536700787	chr12:124562100-124562101	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555028081	chr12:124562111-124562112	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571125397	chr12:124562141-124562142	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs139807197	chr12:124562158-124562159	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143212328	chr12:124562169-124562170	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs866639	chr12:124562171-124562172	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs146687865	chr12:124562221-124562222	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs565234456	chr12:124562321-124562322	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs55835646	chr12:124562331-124562332	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs139238964	chr12:124562347-124562348	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563299564	chr12:124562352-124562353	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs530524079	chr12:124562446-124562447	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs542287251	chr12:124562448-124562449	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs547120408	chr12:124562474-124562475	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs77424499	chr12:124562490-124562491	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188075898	chr12:124562511-124562512	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs56242563	chr12:124562523-124562524	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs530445321	chr12:124562527-124562528	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373425604	chr12:124562550-124562551	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs551160981	chr12:124562551-124562552	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs12311118	chr12:124562624-124562625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs184446932	chr12:124562625-124562626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs565525723	chr12:124562667-124562668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs2130383	chr12:124562681-124562682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536287838	chr12:124562691-124562692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566950566	chr12:124562749-124562750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555784595	chr12:124562806-124562807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547199519	chr12:124562832-124562833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116527180	chr12:124562915-124562916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs11057441	chr12:124562949-124562950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558672464	chr12:124562971-124562972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550071142	chr12:124563066-124563067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs375539013	chr12:124563071-124563072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs577879463	chr12:124563225-124563226	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140833057	chr12:124563282-124563283	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557141635	chr12:124563321-124563322	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs575060996	chr12:124563338-124563339	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs542397602	chr12:124563352-124563353	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560677128	chr12:124563434-124563435	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs574224949	chr12:124563494-124563495	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17133270	CNVD
Breast cancer	17603634	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Developmental delay	21457577	CNVD
dysmorphic	21457577	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chordoma	18071362	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19490664	CNVD

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:124553800-124563200	Weak transcription	Stomach Mucosa	stomach
2	chr12:124557600-124562200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:124558800-124562000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr12:124558800-124562400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr12:124558800-124565200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr12:124559600-124571000	Weak transcription	Fetal Intestine Small	intestine
7	chr12:124560400-124562600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:124560800-124562000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr12:124561800-124562600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr12:124562000-124562200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr12:124562000-124562400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr12:124562000-124562600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:124562200-124562400	Flanking Active TSS	H9 Cell Line	embryonic stem cell
14	chr12:124562200-124562600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr12:124562400-124562600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr12:124562400-124567200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr12:124562400-124577400	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr12:124562600-124563000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr12:124562600-124563600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr12:124563000-124563200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr12:124563200-124563400	Enhancers	Stomach Mucosa	stomach
22	chr12:124563200-124563600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr12:124563400-124567200	Weak transcription	Stomach Mucosa	stomach
24	chr12:124563600-124563800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr12:124563800-124565400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr12:124565200-124565600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr12:124565400-124565600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr12:124565400-124565800	Enhancers	H1 Cell Line	embryonic stem cell
29	chr12:124565400-124565800	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr12:124565400-124565800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:124565600-124565800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr12:124565800-124570000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:124565800-124572200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr12:124567200-124567600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr12:124567400-124567600	Enhancers	Stomach Mucosa	stomach
36	chr12:124567400-124567800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr12:124567600-124570400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr12:124567800-124570000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr12:124568600-124592000	Weak transcription	Right Atrium	heart
40	chr12:124569400-124570400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr12:124569600-124570000	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr12:124569600-124570200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr12:124569600-124570200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:124569800-124570000	Enhancers	Brain Germinal Matrix	brain
45	chr12:124570000-124570200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr12:124570000-124570600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr12:124570000-124570800	Enhancers	Fetal Brain Female	brain
48	chr12:124570000-124571000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr12:124570000-124573800	Enhancers	Fetal Stomach	stomach
50	chr12:124570000-124577000	Weak transcription	Pancreas	Pancrea

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