Variant report

Variant	nsv470302
Chromosome Location	chr12:74505531-74592708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:425)
CpG islands
(count:427)
Chromatin interactive
region (count:54)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:425 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:74562651-74562972	K562	blood:	n/a	n/a
2	ATF1	chr12:74562685-74562943	K562	blood:	n/a	n/a
3	ATF1	chr12:74565359-74565694	K562	blood:	n/a	n/a
4	ATF1	chr12:74505524-74505833	K562	blood:	n/a	n/a
5	BHLHE40	chr12:74564438-74565831	K562	blood:	n/a	n/a
6	CBX3	chr12:74505433-74505896	HCT-116	colon:	n/a	n/a
7	CBX3	chr12:74564451-74565685	K562	blood:	n/a	n/a
8	CBX3	chr12:74568726-74569098	K562	blood:	n/a	n/a
9	CBX3	chr12:74568678-74569478	K562	blood:	n/a	n/a
10	CCNT2	chr12:74564372-74564872	K562	blood:	n/a	n/a
11	CCNT2	chr12:74565335-74565669	K562	blood:	n/a	n/a
12	CEBPB	chr12:74523593-74523771	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr12:74579197-74579397	K562	blood:	n/a	n/a
14	CEBPB	chr12:74579176-74579416	HepG2	liver:	n/a	n/a
15	CEBPB	chr12:74523898-74524098	HepG2	liver:	n/a	chr12:74524027-74524038
16	CEBPB	chr12:74523983-74524169	A549	lung:	n/a	chr12:74524027-74524038
17	CEBPB	chr12:74582394-74582629	K562	blood:	n/a	n/a
18	CEBPB	chr12:74505523-74505779	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr12:74538300-74538814	K562	blood:	n/a	n/a
20	CEBPB	chr12:74579207-74579455	IMR90	lung:	n/a	n/a
21	CEBPB	chr12:74543240-74543419	HepG2	liver:	n/a	chr12:74543280-74543291
22	CHD2	chr12:74564446-74565068	K562	blood:	n/a	chr12:74564765-74564775
23	CHD2	chr12:74505628-74505708	GM12878	blood:	n/a	n/a
24	CTCF	chr12:74505388-74505912	MCF-7	breast:	n/a	n/a
25	CTCF	chr12:74505680-74505830	GM12864	blood:	n/a	n/a
26	CTCF	chr12:74591580-74591730	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr12:74505582-74505737	A549	lung:	n/a	n/a
28	CTCF	chr12:74505640-74505790	GM12871	blood:	n/a	n/a
29	CTCF	chr12:74505541-74505772	ECC-1	luminal epithelium:	n/a	n/a
30	CTCF	chr12:74505515-74505796	ECC-1	luminal epithelium:	n/a	n/a
31	CTCF	chr12:74505356-74506008	SK-N-SH	brain:	n/a	n/a
32	CTCF	chr12:74505940-74506090	SAEC	small airway:	n/a	n/a
33	CTCF	chr12:74505640-74505790	A549	lung:	n/a	n/a
34	CTCF	chr12:74505580-74505730	AG09319	gingival:	n/a	n/a
35	CTCF	chr12:74505560-74505754	A549	lung:	n/a	n/a
36	CTCF	chr12:74505580-74505730	NB4	blood:	n/a	n/a
37	CTCF	chr12:74505620-74505770	RPTEC	kidney:	n/a	n/a
38	CTCF	chr12:74505580-74505730	HA-sp	spinal cord:	n/a	n/a
39	CTCF	chr12:74505560-74505808	LNCaP	prostate:	n/a	n/a
40	CTCF	chr12:74505600-74505750	GM12868	blood:	n/a	n/a
41	CTCF	chr12:74505640-74505790	SAEC	small airway:	n/a	n/a
42	CTCF	chr12:74505620-74505770	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr12:74505580-74505730	GM12867	blood:	n/a	n/a
44	CTCF	chr12:74505680-74505830	NHEK	skin:	n/a	n/a
45	CTCF	chr12:74505620-74505770	GM12874	blood:	n/a	n/a
46	CTCF	chr12:74505640-74505790	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr12:74505620-74505770	HepG2	liver:	n/a	n/a
48	CTCF	chr12:74505591-74505787	A549	lung:	n/a	n/a
49	CTCF	chr12:74505580-74505730	HCFaa	heart:	n/a	n/a
50	CTCF	chr12:74505600-74505750	HMF	breast:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74564932-74564982	SK-N-SH	brain:	n/a
2	chr12:74561645-74561695	ECC-1	luminal epithelium:	n/a
3	chr12:74564932-74564982	ProgFib	skin:	n/a
4	chr12:74564856-74564906	HNPCEpiC	eye:	n/a
5	chr12:74565116-74565166	NT2-D1	testis:	n/a
6	chr12:74564932-74564982	HCF	heart:	n/a
7	chr12:74564932-74564982	HL-60	blood:	n/a
8	chr12:74564932-74564982	PrEC	prostate:	n/a
9	chr12:74565563-74565613	GM12878	blood:	n/a
10	chr12:74564932-74564982	AoSMC	blood vessel:	n/a
11	chr12:74564523-74564573	SAEC	small airway:	n/a
12	chr12:74561645-74561695	HCF	heart:	n/a
13	chr12:74564847-74564897	SK-N-MC	brain:	n/a
14	chr12:74564856-74564906	HCT-116	colon:	n/a
15	chr12:74565563-74565613	HCPEpiC	choroid plexus:	n/a
16	chr12:74564856-74564906	NB4	blood:	n/a
17	chr12:74561645-74561695	HIPEpiC	eye:	n/a
18	chr12:74564856-74564906	GM12891	blood:	n/a
19	chr12:74565563-74565613	NHDF-neo	bronchial:	n/a
20	chr12:74565563-74565613	HRE	kidney:	n/a
21	chr12:74564523-74564573	Hepatocyte	liver:	n/a
22	chr12:74565116-74565166	MCF10A-Er-Src	breast:	n/a
23	chr12:74564523-74564573	NT2-D1	testis:	n/a
24	chr12:74564856-74564906	HUVEC	blood vessel:	n/a
25	chr12:74561645-74561695	ProgFib	skin:	n/a
26	chr12:74565563-74565613	AG09309	skin:	n/a
27	chr12:74561645-74561695	HNPCEpiC	eye:	n/a
28	chr12:74564847-74564897	HCF	heart:	n/a
29	chr12:74561645-74561695	MCF-7	breast:	n/a
30	chr12:74561645-74561695	HRPEpiC	eye:	n/a
31	chr12:74564847-74564897	GM19239	blood:	n/a
32	chr12:74564856-74564906	PrEC	prostate:	n/a
33	chr12:74564932-74564982	HAEpiC	amniotic membrane:	n/a
34	chr12:74564523-74564573	SK-N-SH_RA	brain:	n/a
35	chr12:74564856-74564906	AG04450	lung:	fetal
36	chr12:74564932-74564982	AG09309	skin:	n/a
37	chr12:74561645-74561695	HCT-116	colon:	n/a
38	chr12:74564932-74564982	NB4	blood:	n/a
39	chr12:74561645-74561695	AoSMC	blood vessel:	n/a
40	chr12:74565116-74565166	NH-A	brain:	n/a
41	chr12:74565116-74565166	Hepatocyte	liver:	n/a
42	chr12:74564847-74564897	HCT-116	colon:	n/a
43	chr12:74565116-74565166	GM12892	blood:	n/a
44	chr12:74564847-74564897	Jurkat	blood:	n/a
45	chr12:74565116-74565166	GM19239	blood:	n/a
46	chr12:74565116-74565166	T-47D	breast:	n/a
47	chr12:74561645-74561695	GM12892	blood:	n/a
48	chr12:74564932-74564982	T-47D	breast:	n/a
49	chr12:74561645-74561695	PANC-1	pancreas:	n/a
50	chr12:74564847-74564897	ECC-1	luminal epithelium:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:74522697..74525336-chr12:74527749..74530439,2	K562	blood:
2	chr12:74584693..74586459-chr12:74588249..74590521,2	K562	blood:
3	chr12:74560053..74562479-chr12:74564625..74566537,2	K562	blood:
4	chr12:74531548..74535089-chr12:74542302..74547555,5	K562	blood:
5	chr12:74576003..74577686-chr12:74589371..74591140,2	K562	blood:
6	chr12:74535843..74538591-chr12:74539511..74542141,2	K562	blood:
7	chr12:74505591..74506172-chr12:74759484..74759999,2	MCF-7	breast:
8	chr12:74531548..74535089-chr12:74542302..74547555,5	K562	blood:
9	chr12:74508582..74510560-chr12:74931489..74932997,2	MCF-7	breast:
10	chr12:74552737..74556720-chr12:74559479..74564261,5	K562	blood:
11	chr12:74565564..74567447-chr12:74573536..74575120,2	K562	blood:
12	chr12:74576003..74577686-chr12:74589371..74591140,2	K562	blood:
13	chr12:74576549..74579038-chr12:74580124..74581922,2	MCF-7	breast:
14	chr12:74564480..74567461-chr12:74575954..74578864,3	K562	blood:
15	chr12:74539088..74540893-chr12:74543258..74546036,3	K562	blood:
16	chr12:74584848..74587275-chr12:74588348..74590290,2	MCF-7	breast:
17	chr12:74535843..74538591-chr12:74539511..74542141,2	K562	blood:
18	chr12:74578180..74580078-chr12:74586581..74588937,2	K562	blood:
19	chr12:74527061..74530059-chr12:74931122..74933872,2	MCF-7	breast:
20	chr12:74560053..74562479-chr12:74564625..74566537,2	K562	blood:
21	chr12:74564480..74567461-chr12:74575954..74578864,3	K562	blood:
22	chr12:74563522..74565469-chr12:74584135..74585819,3	K562	blood:
23	chr12:74540805..74543327-chr12:74544789..74546497,2	K562	blood:
24	chr12:74545641..74548957-chr12:74555890..74557729,3	K562	blood:
25	chr12:74536886..74539098-chr12:74541490..74544013,2	MCF-7	breast:
26	chr12:74547425..74549185-chr12:74551970..74554441,2	MCF-7	breast:
27	chr12:74505546..74506081-chr12:74710850..74711455,2	MCF-7	breast:
28	chr12:74536886..74539098-chr12:74541490..74544013,2	MCF-7	breast:
29	chr12:74545641..74548957-chr12:74555890..74557729,3	K562	blood:
30	chr12:74573561..74575455-chr12:74654364..74657073,2	K562	blood:
31	chr12:74505191..74505755-chr12:74710574..74711440,3	MCF-7	breast:
32	chr12:74517100..74519637-chr12:74522625..74525226,2	K562	blood:
33	chr12:74505591..74506415-chr18:8130965..8131756,2	MCF-7	breast:
34	chr12:74526468..74528133-chr12:74535792..74537959,2	MCF-7	breast:
35	chr12:74505239..74506034-chr12:74759124..74759988,3	MCF-7	breast:
36	chr12:74564280..74566761-chr12:74606459..74609033,2	K562	blood:
37	chr12:74389722..74391980-chr12:74584509..74586133,2	K562	blood:
38	chr12:74584693..74586459-chr12:74588249..74590521,2	K562	blood:
39	chr12:74528403..74529928-chr12:74531825..74534781,2	K562	blood:
40	chr12:74517100..74519637-chr12:74522625..74525226,2	K562	blood:
41	chr12:74564462..74568132-chr12:74683426..74687604,5	K562	blood:
42	chr12:74505235..74505774-chr12:74710528..74711393,3	K562	blood:
43	chr12:74545641..74548768-chr12:74554696..74557729,3	K562	blood:
44	chr12:74565564..74567447-chr12:74573536..74575120,2	K562	blood:
45	chr12:74526468..74528133-chr12:74535792..74537959,2	MCF-7	breast:
46	chr12:74584848..74587275-chr12:74588348..74590290,2	MCF-7	breast:
47	chr12:74578180..74580078-chr12:74586581..74588937,2	K562	blood:
48	chr12:74545641..74548768-chr12:74554696..74557729,3	K562	blood:
49	chr12:74540805..74543327-chr12:74544789..74546497,2	K562	blood:
50	chr12:74522697..74525336-chr12:74527749..74530439,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000258320	TF binding region
ENSG00000258320	CpG island
ENSG00000253719	chromatin interactions
ENSG00000251138	chromatin interactions
ENSG00000257386	chromatin interactions
ENSG00000258320	chromatin interactions
ENSG00000257364	chromatin interactions

Extended variants
information (count: 1934 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1934 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11179922	chr12:74505531-74505532	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150947899	chr12:74505538-74505539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11503769	chr12:74505568-74505569	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs190812480	chr12:74505571-74505572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11519906	chr12:74505585-74505586	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs536785769	chr12:74505600-74505601	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs140883051	chr12:74505609-74505610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563979124	chr12:74505614-74505615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs552926770	chr12:74505631-74505632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145848530	chr12:74505672-74505673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34471503	chr12:74505713-74505714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538910550	chr12:74505731-74505732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs558831143	chr12:74505737-74505738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs575744027	chr12:74505756-74505757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs146604991	chr12:74505759-74505760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80018966	chr12:74505768-74505769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573634912	chr12:74505779-74505780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs76744538	chr12:74505790-74505791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs150258996	chr12:74505791-74505792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34412369	chr12:74505797-74505798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371336755	chr12:74505811-74505812	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs369170770	chr12:74505826-74505827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs564656125	chr12:74505828-74505829	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545750120	chr12:74505829-74505830	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11519908	chr12:74505853-74505854	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs376265282	chr12:74505872-74505873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs546611614	chr12:74505884-74505885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11503770	chr12:74505901-74505902	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs565031352	chr12:74505933-74505934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530874802	chr12:74505934-74505935	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138733784	chr12:74505944-74505945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567480685	chr12:74505948-74505949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112362364	chr12:74505954-74505955	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs546703050	chr12:74505956-74505957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566485950	chr12:74506028-74506029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538648167	chr12:74506087-74506088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs566822111	chr12:74506091-74506092	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75750905	chr12:74506092-74506093	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs368796287	chr12:74506099-74506100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538560401	chr12:74506117-74506118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535729037	chr12:74506125-74506126	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs11179923	chr12:74506126-74506127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143647250	chr12:74506158-74506159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553107829	chr12:74506170-74506171	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs182496412	chr12:74506176-74506177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138418061	chr12:74506202-74506203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs564929292	chr12:74506223-74506224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs530692938	chr12:74506254-74506255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544515508	chr12:74506256-74506257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548937234	chr12:74506262-74506263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Autism	22495311	CNVD
Neurodevelopmental disorder	22521361	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
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Burkitt''s lymphoma	20823134	CNVD
abnormal development	18461090	CNVD
Prostate cancer	18632612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
craniofacial dysmorphism	21918468	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	22032731	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
Hodgkin''s lymphoma	18641027	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74504600-74505800	Enhancers	HMEC	breast
2	chr12:74504600-74506200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:74504800-74505600	Enhancers	NHEK	skin
4	chr12:74505800-74513600	Weak transcription	HMEC	breast
5	chr12:74513600-74513800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr12:74513600-74514200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr12:74513600-74514200	Enhancers	HMEC	breast
8	chr12:74514400-74514600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr12:74520000-74528200	Weak transcription	K562	blood
10	chr12:74523600-74524000	Enhancers	Brain Cingulate Gyrus	brain
11	chr12:74523600-74524000	Active TSS	Ovary	ovary
12	chr12:74531200-74531600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr12:74544000-74544400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr12:74545400-74545600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr12:74545600-74546600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr12:74545600-74547400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr12:74546000-74546400	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr12:74546000-74546800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr12:74546000-74546800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr12:74546200-74546800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
21	chr12:74546200-74547000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr12:74546400-74546800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr12:74546400-74546800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
24	chr12:74546600-74547200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr12:74548800-74563400	Weak transcription	K562	blood
26	chr12:74561200-74561600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr12:74563400-74565200	Active TSS	K562	blood
28	chr12:74564600-74565400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr12:74565200-74565400	Transcr. at gene 5' and 3'	K562	blood
30	chr12:74565400-74566600	Active TSS	K562	blood
31	chr12:74566600-74566800	Flanking Active TSS	K562	blood
32	chr12:74566800-74567000	Active TSS	K562	blood
33	chr12:74567000-74567200	Flanking Active TSS	K562	blood
34	chr12:74567200-74567400	Enhancers	K562	blood
35	chr12:74576000-74578600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr12:74578200-74578800	ZNF genes & repeats	Pancreas	Pancrea
37	chr12:74578400-74579000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr12:74578600-74578800	Enhancers	Gastric	stomach
39	chr12:74578600-74579000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr12:74578600-74579200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr12:74579200-74581000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr12:74586600-74587600	Enhancers	Brain Germinal Matrix	brain
43	chr12:74587600-74589200	Weak transcription	Brain Germinal Matrix	brain
44	chr12:74589200-74590200	Enhancers	Brain Germinal Matrix	brain

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