Variant report

Variant	esv1802058
Chromosome Location	chr12:58028127-58062667
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:225)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:225 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:58052917-58052954	K562	blood:	n/a	n/a
2	ARID3A	chr12:58053876-58054094	K562	blood:	n/a	n/a
3	ARID3A	chr12:58055441-58055657	K562	blood:	n/a	n/a
4	ATF1	chr12:58055347-58055542	K562	blood:	n/a	n/a
5	ATF3	chr12:58053763-58054224	A549	lung:	n/a	n/a
6	ATF3	chr12:58053791-58054171	K562	blood:	n/a	n/a
7	BDP1	chr12:58053797-58054120	K562	blood:	n/a	n/a
8	BHLHE40	chr12:58032593-58032812	K562	blood:	n/a	n/a
9	BHLHE40	chr12:58035918-58036093	K562	blood:	n/a	n/a
10	CBX3	chr12:58039642-58040152	HCT-116	colon:	n/a	n/a
11	CBX3	chr12:58047846-58048154	K562	blood:	n/a	n/a
12	CBX3	chr12:58039697-58039990	K562	blood:	n/a	n/a
13	CBX3	chr12:58039655-58040025	K562	blood:	n/a	n/a
14	CBX3	chr12:58047815-58048146	K562	blood:	n/a	n/a
15	CBX3	chr12:58039719-58039954	HCT-116	colon:	n/a	n/a
16	CEBPB	chr12:58060576-58060620	K562	blood:	n/a	n/a
17	CEBPB	chr12:58033101-58033307	HepG2	liver:	n/a	n/a
18	CEBPB	chr12:58051700-58051935	K562	blood:	n/a	n/a
19	CEBPB	chr12:58034075-58034222	IMR90	lung:	n/a	chr12:58034136-58034147 chr12:58034138-58034149 chr12:58034136-58034149 chr12:58034136-58034149
20	CEBPB	chr12:58033956-58034303	K562	blood:	n/a	chr12:58034136-58034147 chr12:58034138-58034149 chr12:58034136-58034149 chr12:58034136-58034149
21	CEBPB	chr12:58033110-58033268	K562	blood:	n/a	n/a
22	CEBPB	chr12:58051621-58051953	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr12:58062486-58062674	HepG2	liver:	n/a	chr12:58062576-58062587
24	CEBPB	chr12:58062458-58062705	K562	blood:	n/a	chr12:58062576-58062587
25	CEBPB	chr12:58051560-58051922	MCF-7	breast:	n/a	n/a
26	CEBPB	chr12:58033976-58034282	HepG2	liver:	n/a	chr12:58034136-58034147 chr12:58034138-58034149 chr12:58034136-58034149 chr12:58034136-58034149
27	CEBPB	chr12:58062480-58062667	A549	lung:	n/a	chr12:58062576-58062587
28	CEBPZ	chr12:58039734-58040005	HepG2	liver:	n/a	n/a
29	CHD2	chr12:58053921-58054006	K562	blood:	n/a	n/a
30	CTCF	chr12:58031139-58031533	MCF-7	breast:	n/a	n/a
31	CTCF	chr12:58031080-58031230	HFF	foreskin:	n/a	n/a
32	CTCF	chr12:58031400-58031550	RPTEC	kidney:	n/a	n/a
33	CTCF	chr12:58031260-58031410	AG10803	skin:	n/a	n/a
34	CTCF	chr12:58031218-58031312	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr12:58031360-58031510	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr12:58031100-58031250	MCF-7	breast:	n/a	n/a
37	CTCF	chr12:58031240-58031390	RPTEC	kidney:	n/a	n/a
38	CTCF	chr12:58031180-58031330	RPTEC	kidney:	n/a	n/a
39	CTCF	chr12:58031300-58031450	AG04449	skin:	n/a	n/a
40	CTCF	chr12:58031260-58031410	HMEC	breast:	n/a	n/a
41	CTCF	chr12:58031200-58031350	MCF-7	breast:	n/a	n/a
42	CTCF	chr12:58031240-58031390	HCT-116	colon:	n/a	n/a
43	CTCF	chr12:58031300-58031450	HMF	breast:	n/a	n/a
44	CTCF	chr12:58031200-58031350	HepG2	liver:	n/a	n/a
45	CTCF	chr12:58031367-58031376	Spleen_OC	spleen:	n/a	n/a
46	CTCF	chr12:58031280-58031430	HAc	cerebellar:	n/a	n/a
47	CTCF	chr12:58028194-58028325	Hela-S3	cervix:	n/a	n/a
48	CTCF	chr12:58051580-58051730	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr12:58031201-58031329	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:58031380-58031449	Spleen_OC	spleen:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:58030134-58030184	H1-hESC	embryonic stem cell:	embryo
2	chr12:58030134-58030184	Jurkat	blood:	n/a
3	chr12:58030134-58030184	HEEpiC	esophagus:	n/a
4	chr12:58030134-58030184	CMK	blood:	n/a
5	chr12:58030134-58030184	MCF-7	breast:	n/a
6	chr12:58030134-58030184	GM19239	blood:	n/a
7	chr12:58030134-58030184	U87	brain:	n/a
8	chr12:58030134-58030184	HCT-116	colon:	n/a
9	chr12:58030134-58030184	GM12892	blood:	n/a
10	chr12:58030134-58030184	HMEC	breast:	n/a
11	chr12:58030134-58030184	HepG2	liver:	n/a
12	chr12:58030134-58030184	SK-N-SH	brain:	n/a
13	chr12:58030134-58030184	HRPEpiC	eye:	n/a
14	chr12:58030134-58030184	SKMC	muscle:	n/a
15	chr12:58030134-58030184	RPTEC	kidney:	n/a
16	chr12:58030134-58030184	MCF10A-Er-Src	breast:	n/a
17	chr12:58030134-58030184	AG09309	skin:	n/a
18	chr12:58030134-58030184	NHBE	bronchial:	n/a
19	chr12:58030134-58030184	HCF	heart:	n/a
20	chr12:58030134-58030184	HAEpiC	amniotic membrane:	n/a
21	chr12:58030134-58030184	HCPEpiC	choroid plexus:	n/a
22	chr12:58030134-58030184	ECC-1	luminal epithelium:	n/a
23	chr12:58030134-58030184	PFSK-1	brain:	n/a
24	chr12:58030134-58030184	ovcar-3	ovarian:	n/a
25	chr12:58030134-58030184	A549	lung:	n/a
26	chr12:58030134-58030184	NT2-D1	testis:	n/a
27	chr12:58030134-58030184	BJ	skin:	n/a
28	chr12:58030134-58030184	Caco-2	colon:	n/a
29	chr12:58030134-58030184	NB4	blood:	n/a
30	chr12:58030134-58030184	IMR90	lung:	fetal
31	chr12:58030134-58030184	HNPCEpiC	eye:	n/a
32	chr12:58030134-58030184	SAEC	small airway:	n/a
33	chr12:58030134-58030184	HUVEC	blood vessel:	n/a
34	chr12:58030134-58030184	AG09319	gingival:	n/a
35	chr12:58030134-58030184	PrEC	prostate:	n/a
36	chr12:58030134-58030184	HEK293	kidney:	embryo
37	chr12:58030134-58030184	HCM	heart:	n/a
38	chr12:58030134-58030184	GM12878	blood:	n/a
39	chr12:58030134-58030184	HL-60	blood:	n/a
40	chr12:58030134-58030184	ProgFib	skin:	n/a
41	chr12:58030134-58030184	SK-N-MC	brain:	n/a
42	chr12:58030134-58030184	AG04450	lung:	fetal
43	chr12:58030134-58030184	NHDF-neo	bronchial:	n/a
44	chr12:58030134-58030184	AG10803	skin:	n/a
45	chr12:58030134-58030184	K562	blood:	n/a
46	chr12:58030134-58030184	GM12891	blood:	n/a
47	chr12:58030134-58030184	AoSMC	blood vessel:	n/a
48	chr12:58030134-58030184	Hepatocyte	liver:	n/a
49	chr12:58030134-58030184	NH-A	brain:	n/a
50	chr12:58030134-58030184	HRCEpiC	kidney:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:58033421..58035422-chr12:58138952..58140845,2	K562	blood:
2	chr12:58030492..58032233-chr12:58033542..58035528,2	K562	blood:
3	chr12:58062107..58064323-chr12:58086416..58089211,2	K562	blood:
4	chr12:58026019..58028946-chr12:58148453..58151531,3	K562	blood:
5	chr12:57935626..57940631-chr12:58026197..58030320,5	K562	blood:
6	chr12:58031339..58033541-chr12:58068001..58070861,2	K562	blood:
7	chr12:58026571..58028240-chr12:58118727..58121626,2	MCF-7	breast:
8	chr12:57974514..57977193-chr12:58031041..58032907,2	K562	blood:
9	chr12:58055005..58057718-chr12:58138111..58140068,2	K562	blood:
10	chr12:57997114..58001112-chr12:58025485..58030490,5	MCF-7	breast:
11	chr12:57909076..57912703-chr12:58030683..58034118,3	K562	blood:
12	chr12:57908910..57916122-chr12:58022622..58031573,17	K562	blood:
13	chr12:58026791..58028467-chr12:58032868..58035456,2	K562	blood:
14	chr12:57983391..57985108-chr12:58026747..58028430,2	MCF-7	breast:
15	chr12:57983573..57987941-chr12:58024849..58028209,5	MCF-7	breast:
16	chr12:58046923..58049149-chr12:58061909..58063818,2	K562	blood:
17	chr12:57908910..57916403-chr12:58022622..58028885,15	K562	blood:
18	chr12:58030492..58032233-chr12:58033542..58035528,2	K562	blood:
19	chr12:58024113..58026472-chr12:58028228..58030289,2	K562	blood:

No data

Variant related genes	Relation type
B4GALNT1	TF binding region
B4GALNT1	CpG island
ENSG00000208028	chromatin interactions
ENSG00000135452	chromatin interactions
ENSG00000135446	chromatin interactions
ENSG00000175197	chromatin interactions
ENSG00000166987	chromatin interactions
ENSG00000166986	chromatin interactions
ENSG00000155980	chromatin interactions
ENSG00000139266	chromatin interactions
ENSG00000135454	chromatin interactions
ENSG00000135506	chromatin interactions
ENSG00000242990	chromatin interactions
ENSG00000257499	chromatin interactions
ENSG00000255737	chromatin interactions
ENSG00000238436	chromatin interactions
ENSG00000178498	chromatin interactions
ENSG00000175203	chromatin interactions
ENSG00000166908	chromatin interactions

Extended variants
information (count: 1124 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575572182	chr12:58028142-58028143	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs531654401	chr12:58028234-58028235	Weak transcription	TF binding region Chromatin interactive region	13 gene(s)	Overlapped CNVs	n/a
3	rs544560489	chr12:58028268-58028269	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs571279964	chr12:58028283-58028284	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
5	rs372349757	chr12:58028304-58028305	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
6	rs202216644	chr12:58028342-58028343	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
7	rs34271193	chr12:58028361-58028362	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs200259419	chr12:58028363-58028364	Weak transcription	TF binding region Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
9	rs189218233	chr12:58028380-58028381	Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
10	rs536448766	chr12:58028452-58028453	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs555159115	chr12:58028463-58028464	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs192575585	chr12:58028466-58028467	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs537113899	chr12:58028487-58028488	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs147522030	chr12:58028494-58028495	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs369422168	chr12:58028513-58028514	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs576796581	chr12:58028535-58028536	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs140083336	chr12:58028556-58028557	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs372285811	chr12:58028592-58028593	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs184828989	chr12:58028596-58028597	Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs188074810	chr12:58028743-58028744	Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs12578587	chr12:58028746-58028747	Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs181073477	chr12:58028770-58028771	Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs563109625	chr12:58028825-58028826	Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs531714155	chr12:58028852-58028853	Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs6581147	chr12:58028863-58028864	Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs528430725	chr12:58028867-58028868	Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
27	rs114637968	chr12:58028914-58028915	Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
28	rs532447160	chr12:58028948-58028949	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs547720602	chr12:58029058-58029059	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs566252797	chr12:58029065-58029066	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs201752146	chr12:58029104-58029105	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs12298852	chr12:58029243-58029244	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs12312189	chr12:58029250-58029251	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs7958927	chr12:58029261-58029262	Weak transcription	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs377404253	chr12:58029277-58029278	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs548819596	chr12:58029283-58029284	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs570287592	chr12:58029329-58029330	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs545455732	chr12:58029342-58029343	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs151005661	chr12:58029357-58029358	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs552913986	chr12:58029376-58029377	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs576870480	chr12:58029382-58029383	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs369657330	chr12:58029443-58029444	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs61935730	chr12:58029458-58029459	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs552895749	chr12:58029479-58029480	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs201447338	chr12:58029485-58029486	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs28807177	chr12:58029486-58029487	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs116567422	chr12:58029487-58029488	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs71084774	chr12:58029489-58029490	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs199549439	chr12:58029490-58029491	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs574659554	chr12:58029497-58029498	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

Disease	PMID	Source
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
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Glioblastoma multiforme	17387387	CNVD
liposarcomas	17372913	CNVD
Non-small cell lung cancer	24170126	CNVD
Cancer	16751803	CNVD
Bladder cancer	21909424	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	17661082	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Hodgkin''s lymphoma	18179710	CNVD
Autism	20531469	CNVD
Rhabdomyosarcoma	16790082	CNVD
Renal cell carcinoma	18765545	CNVD
Urothelial cell carcinoma	18451213	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21138945	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Myelofibrosis	22110671	CNVD
Phyllodes tumor	17334353	CNVD
Glaucoma	21310917	CNVD
Breast cancer	16272173	CNVD
Mental retardation	19951919	CNVD
Glaucoma	21447600	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Developmental delay	21267005	CNVD
12q14 microdeletion syndrome	21267005	CNVD
Developmental delay	19277063	CNVD
Dwarfism	19277063	CNVD
Fibroblasts	20926602	CNVD
Follicular lymphoma	18703704	CNVD
Acute myeloid leukemia	21251322	CNVD
Glycogen storage disease	18421352	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Glioblastoma multiforme	20080666	CNVD
Medulloblastoma	19270706	CNVD
Breast cancer	17133270	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Breast cancer	21364760	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:58027200-58033600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr12:58027600-58028200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr12:58027600-58034000	Weak transcription	K562	blood
4	chr12:58027800-58030600	Weak transcription	A549	lung
5	chr12:58028000-58028200	Bivalent Enhancer	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr12:58031200-58031400	Enhancers	A549	lung
7	chr12:58031800-58032200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
8	chr12:58032200-58032600	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr12:58032600-58032800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr12:58032600-58033000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr12:58032600-58033400	Enhancers	H9 Cell Line	embryonic stem cell
12	chr12:58032600-58036000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr12:58033200-58033400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr12:58033400-58033600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
15	chr12:58033800-58034400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr12:58034000-58034400	Enhancers	Adipose Nuclei	Adipose
17	chr12:58034000-58034400	Enhancers	K562	blood
18	chr12:58034200-58034400	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr12:58034400-58034800	Flanking Active TSS	K562	blood
20	chr12:58034800-58036600	Enhancers	K562	blood
21	chr12:58035000-58035800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr12:58035200-58036000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr12:58036600-58039800	Weak transcription	K562	blood
24	chr12:58039800-58040200	Active TSS	K562	blood
25	chr12:58048600-58049400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:58049400-58049800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr12:58049400-58050200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr12:58049800-58050000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr12:58051000-58051400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr12:58051000-58051800	Enhancers	Brain Substantia Nigra	brain
31	chr12:58051200-58051600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr12:58051200-58052200	Enhancers	Liver	Liver
33	chr12:58051400-58051800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr12:58051800-58052800	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr12:58052200-58054200	Enhancers	K562	blood
36	chr12:58054200-58055200	Weak transcription	K562	blood
37	chr12:58055200-58055600	Enhancers	K562	blood
38	chr12:58055600-58060400	Weak transcription	K562	blood
39	chr12:58060400-58061200	Enhancers	K562	blood

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