Variant report

Variant	esv3347258
Chromosome Location	chr12:56267734-56298106
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:149)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:149 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:56292906-56293231	K562	blood:	n/a	n/a
2	ATF1	chr12:56292905-56293173	K562	blood:	n/a	n/a
3	CBX3	chr12:56271594-56272011	K562	blood:	n/a	n/a
4	CBX3	chr12:56292782-56293170	K562	blood:	n/a	n/a
5	CBX3	chr12:56271609-56272019	K562	blood:	n/a	n/a
6	CEBPB	chr12:56292949-56293020	K562	blood:	n/a	n/a
7	CEBPB	chr12:56282392-56282592	HepG2	liver:	n/a	n/a
8	CTCF	chr12:56293080-56293230	NHDF-neo	bronchial:	n/a	n/a
9	CTCF	chr12:56287140-56287290	HEK293	kidney:	n/a	chr12:56287280-56287287
10	CTCF	chr12:56293020-56293170	NHDF-neo	bronchial:	n/a	n/a
11	CTCF	chr12:56293180-56293330	NB4	blood:	n/a	n/a
12	CTCF	chr12:56293080-56293230	AG09319	gingival:	n/a	n/a
13	CTCF	chr12:56287200-56287350	MCF-7	breast:	n/a	chr12:56287280-56287287
14	CTCF	chr12:56287260-56287410	Hela-S3	cervix:	n/a	chr12:56287280-56287287
15	CTCF	chr12:56287260-56287410	NHEK	skin:	n/a	chr12:56287280-56287287
16	CTCF	chr12:56293000-56293150	NB4	blood:	n/a	n/a
17	CTCF	chr12:56293140-56293290	AG09309	skin:	n/a	n/a
18	CTCF	chr12:56270738-56270787	LNCaP	prostate:	n/a	n/a
19	CTCF	chr12:56293109-56293266	Hela-S3	cervix:	n/a	n/a
20	CTCF	chr12:56293060-56293210	HMEC	breast:	n/a	n/a
21	CTCF	chr12:56285217-56285251	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:56293182-56293214	GM10266	blood:	n/a	n/a
23	CTCF	chr12:56293156-56293216	GM10248	blood:	n/a	n/a
24	CTCF	chr12:56287217-56287330	Hela-S3	cervix:	n/a	chr12:56287280-56287287
25	CUX1	chr12:56292864-56293065	K562	blood:	n/a	n/a
26	CUX1	chr12:56274909-56274919	GM12878	blood:	n/a	n/a
27	EBF1	chr12:56274877-56275113	GM12878	blood:	n/a	n/a
28	EGR1	chr12:56292830-56293188	K562	blood:	n/a	n/a
29	EGR1	chr12:56292807-56293266	K562	blood:	n/a	n/a
30	EP300	chr12:56292897-56293098	K562	blood:	n/a	n/a
31	FOS	chr12:56268389-56268630	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr12:56274864-56275168	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr12:56274820-56275137	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr12:56274815-56275195	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr12:56274819-56275205	MCF10A-Er-Src	breast:	n/a	n/a
36	FOSL1	chr12:56292829-56293079	K562	blood:	n/a	chr12:56292981-56292992
37	FOSL1	chr12:56292777-56293176	K562	blood:	n/a	chr12:56292981-56292992
38	FOSL2	chr12:56294143-56294488	HepG2	liver:	n/a	n/a
39	GATA2	chr12:56292844-56293255	K562	blood:	n/a	chr12:56293027-56293034
40	HNF4A	chr12:56282414-56282699	HepG2	liver:	n/a	chr12:56282549-56282564
41	HNF4A	chr12:56282282-56282682	HepG2	liver:	n/a	chr12:56282549-56282564
42	HNF4G	chr12:56282386-56282702	HepG2	liver:	n/a	chr12:56282548-56282563
43	IRF1	chr12:56271562-56271574	K562	blood:	n/a	n/a
44	JUN	chr12:56292745-56293223	K562	blood:	n/a	n/a
45	JUND	chr12:56269241-56269394	H1-hESC	embryonic stem cell:	n/a	n/a
46	JUND	chr12:56292828-56293183	K562	blood:	n/a	n/a
47	JUND	chr12:56274426-56274447	HepG2	liver:	n/a	n/a
48	KAP1	chr12:56271499-56271887	U2OS	brain:	n/a	n/a
49	KAP1	chr12:56271417-56271890	HEK293	kidney:	n/a	n/a
50	KAP1	chr12:56271441-56272144	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:56295588-56295638	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:56295588-56295638	MCF10A-Er-Src	breast:	n/a
3	chr12:56269767-56269817	HCT-116	colon:	n/a
4	chr12:56295588-56295638	Hela-S3	cervix:	n/a
5	chr12:56295588-56295638	GM12891	blood:	n/a
6	chr12:56269767-56269817	SKMC	muscle:	n/a
7	chr12:56269767-56269817	PrEC	prostate:	n/a
8	chr12:56269767-56269817	CMK	blood:	n/a
9	chr12:56269767-56269817	PANC-1	pancreas:	n/a
10	chr12:56295588-56295638	SK-N-SH_RA	brain:	n/a
11	chr12:56269767-56269817	NB4	blood:	n/a
12	chr12:56295588-56295638	Caco-2	colon:	n/a
13	chr12:56269767-56269817	Hela-S3	cervix:	n/a
14	chr12:56269767-56269817	HIPEpiC	eye:	n/a
15	chr12:56269767-56269817	AG04450	lung:	fetal
16	chr12:56295588-56295638	AG04450	lung:	fetal
17	chr12:56295588-56295638	HEEpiC	esophagus:	n/a
18	chr12:56269767-56269817	BJ	skin:	n/a
19	chr12:56295588-56295638	GM19239	blood:	n/a
20	chr12:56295588-56295638	GM12892	blood:	n/a
21	chr12:56269767-56269817	MCF10A-Er-Src	breast:	n/a
22	chr12:56295588-56295638	HRCEpiC	kidney:	n/a
23	chr12:56295588-56295638	NT2-D1	testis:	n/a
24	chr12:56295588-56295638	NHDF-neo	bronchial:	n/a
25	chr12:56269767-56269817	U87	brain:	n/a
26	chr12:56295588-56295638	HMEC	breast:	n/a
27	chr12:56269767-56269817	AG10803	skin:	n/a
28	chr12:56295588-56295638	HRPEpiC	eye:	n/a
29	chr12:56269767-56269817	ProgFib	skin:	n/a
30	chr12:56295588-56295638	SK-N-MC	brain:	n/a
31	chr12:56269767-56269817	Jurkat	blood:	n/a
32	chr12:56295588-56295638	A549	lung:	n/a
33	chr12:56269767-56269817	HL-60	blood:	n/a
34	chr12:56269767-56269817	MCF-7	breast:	n/a
35	chr12:56269767-56269817	AG04449	skin:	fetal
36	chr12:56269767-56269817	HRE	kidney:	n/a
37	chr12:56295588-56295638	HEK293	kidney:	embryo
38	chr12:56269767-56269817	GM12891	blood:	n/a
39	chr12:56269767-56269817	SK-N-SH_RA	brain:	n/a
40	chr12:56269767-56269817	HAEpiC	amniotic membrane:	n/a
41	chr12:56269767-56269817	GM12892	blood:	n/a
42	chr12:56295588-56295638	U87	brain:	n/a
43	chr12:56269767-56269817	HCF	heart:	n/a
44	chr12:56295588-56295638	IMR90	lung:	fetal
45	chr12:56269767-56269817	HMEC	breast:	n/a
46	chr12:56269767-56269817	SAEC	small airway:	n/a
47	chr12:56295588-56295638	LNCaP	prostate:	n/a
48	chr12:56269767-56269817	ECC-1	luminal epithelium:	n/a
49	chr12:56295588-56295638	HepG2	liver:	n/a
50	chr12:56295588-56295638	NHBE	bronchial:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:56220693..56225301-chr12:56284725..56289550,5	MCF-7	breast:
2	chr12:56224247..56225882-chr12:56295667..56297229,2	MCF-7	breast:
3	chr12:56251018..56252886-chr12:56269364..56271809,2	MCF-7	breast:
4	chr12:56279349..56281773-chr12:56292727..56294743,2	MCF-7	breast:
5	chr12:56222854..56224376-chr12:56275059..56277720,2	MCF-7	breast:
6	chr12:56221810..56225034-chr12:56267373..56269273,5	MCF-7	breast:
7	chr12:56265141..56267648-chr12:56273330..56275768,2	K562	blood:
8	chr12:56276249..56278200-chr12:56283079..56285139,3	K562	blood:
9	chr12:56210407..56211916-chr12:56266892..56269258,2	MCF-7	breast:
10	chr12:56276249..56278200-chr12:56283079..56285139,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DGKA-2	chr12:56275021-56275253	NONHSAT028711

No data

Variant related genes	Relation type
OLA1P3	TF binding region
GSTP1P1	TF binding region
RNU1-69P	TF binding region
OLA1P3	CpG island
GSTP1P1	CpG island
RNU1-69P	CpG island
ENSG00000257569	chromatin interactions
ENSG00000182796	chromatin interactions
ENSG00000257390	chromatin interactions
ENSG00000205323	chromatin interactions
ENSG00000123353	chromatin interactions
ENSG00000135392	chromatin interactions
ENSG00000257966	chromatin interactions

Extended variants
information (count: 1090 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552915231	chr12:56267749-56267750	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs139083136	chr12:56267833-56267834	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs535208345	chr12:56267839-56267840	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs546425653	chr12:56267954-56267955	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs149880314	chr12:56267996-56267997	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs557085646	chr12:56268069-56268070	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs145380582	chr12:56268119-56268120	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs560084797	chr12:56268184-56268185	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs545795564	chr12:56268243-56268244	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs117711057	chr12:56268262-56268263	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs371020410	chr12:56268297-56268298	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs35611383	chr12:56268359-56268360	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs540892251	chr12:56268389-56268390	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs558344148	chr12:56268392-56268393	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs529446804	chr12:56268398-56268399	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs369495004	chr12:56268422-56268423	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs149223535	chr12:56268425-56268426	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs562639468	chr12:56268427-56268428	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs533181911	chr12:56268462-56268463	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs142384176	chr12:56268540-56268541	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs560511600	chr12:56268552-56268553	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs541006912	chr12:56268591-56268592	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs528379319	chr12:56268602-56268603	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs571118819	chr12:56268678-56268679	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs553508934	chr12:56268685-56268686	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs374030073	chr12:56268694-56268695	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs184913329	chr12:56268720-56268721	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs151297005	chr12:56268742-56268743	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs535644161	chr12:56268746-56268747	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs550725812	chr12:56268785-56268786	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs578165267	chr12:56268803-56268804	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs374312031	chr12:56268840-56268841	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs189191495	chr12:56268922-56268923	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs529706769	chr12:56268970-56268971	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs557806169	chr12:56269032-56269033	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs549569793	chr12:56269081-56269082	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs141784638	chr12:56269108-56269109	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs534231510	chr12:56269129-56269130	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs556013481	chr12:56269157-56269158	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs544068533	chr12:56269187-56269188	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs574198079	chr12:56269276-56269277	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs181548595	chr12:56269298-56269299	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs371156709	chr12:56269315-56269316	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs147061948	chr12:56269322-56269323	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs34141262	chr12:56269347-56269348	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs562676303	chr12:56269364-56269365	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs373706352	chr12:56269421-56269422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116714123	chr12:56269459-56269460	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185038224	chr12:56269488-56269489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375826102	chr12:56269519-56269520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	18194544	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
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	20505157	CNVD
Hepatocellular carcinoma	16750200	CNVD
Melanoma	18172304	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	20531469	CNVD
Multiple myeloma	16616336	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21569311	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Glioblastoma multiforme	19115005	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Breast cancer	21509527	CNVD
Lung adenocarcinoma	17982442	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Leukemia	18628472	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Breast cancer	21804112	CNVD

Chromatin state (count:491 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:56267400-56268000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr12:56267400-56269000	Weak transcription	Fetal Thymus	thymus
3	chr12:56267800-56268000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr12:56267800-56268200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr12:56267800-56268400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr12:56267800-56268400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr12:56267800-56268600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr12:56267800-56268600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr12:56267800-56268600	Enhancers	Brain Cingulate Gyrus	brain
10	chr12:56267800-56268800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr12:56268000-56268200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr12:56268000-56268600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr12:56268000-56268600	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr12:56268000-56270200	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr12:56268000-56270200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr12:56268200-56268400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:56268200-56269200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr12:56268200-56269200	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr12:56268200-56269800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:56268200-56270200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr12:56268400-56269600	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr12:56268400-56272200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr12:56268600-56269000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr12:56268600-56269000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr12:56268600-56269800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr12:56268600-56271000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:56268800-56269200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr12:56269000-56269800	Enhancers	Fetal Thymus	thymus
29	chr12:56269000-56270000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:56269000-56270000	Enhancers	iPS-15b Cell Line	embryonic stem cell
31	chr12:56269200-56269400	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr12:56269200-56269800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr12:56269200-56269800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr12:56269200-56269800	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr12:56269200-56270200	Enhancers	H1 Cell Line	embryonic stem cell
36	chr12:56269400-56271400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr12:56269600-56270200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr12:56269800-56270000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr12:56269800-56270200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr12:56269800-56270200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr12:56269800-56270400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr12:56269800-56274600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr12:56270000-56270600	Enhancers	HSMMtube	muscle
44	chr12:56270200-56273600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr12:56270600-56292600	Weak transcription	HSMMtube	muscle
46	chr12:56271000-56271800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr12:56271400-56271800	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
48	chr12:56271800-56275200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr12:56272200-56272400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr12:56272400-56274600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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