Variant report

Variant	esv1821495
Chromosome Location	chr12:74517828-74647299
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:323)
CpG islands
(count:428)
Chromatin interactive
region (count:59)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:323 , 50 per page) page: 1 2 3 4 5 6 7

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	chr12:74565359-74565694	K562	blood:	n/a	n/a
3	ATF1	chr12:74562685-74562943	K562	blood:	n/a	n/a
4	BHLHE40	chr12:74564438-74565831	K562	blood:	n/a	n/a
5	CBX3	chr12:74568726-74569098	K562	blood:	n/a	n/a
6	CBX3	chr12:74568678-74569478	K562	blood:	n/a	n/a
7	CBX3	chr12:74564451-74565685	K562	blood:	n/a	n/a
8	CCNT2	chr12:74564372-74564872	K562	blood:	n/a	n/a
9	CCNT2	chr12:74565335-74565669	K562	blood:	n/a	n/a
10	CEBPB	chr12:74523898-74524098	HepG2	liver:	n/a	chr12:74524027-74524038
11	CEBPB	chr12:74633585-74633954	HepG2	liver:	n/a	n/a
12	CEBPB	chr12:74629122-74629482	K562	blood:	n/a	n/a
13	CEBPB	chr12:74621716-74622011	IMR90	lung:	n/a	n/a
14	CEBPB	chr12:74579207-74579455	IMR90	lung:	n/a	n/a
15	CEBPB	chr12:74523593-74523771	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr12:74629133-74629483	K562	blood:	n/a	n/a
17	CEBPB	chr12:74538300-74538814	K562	blood:	n/a	n/a
18	CEBPB	chr12:74582394-74582629	K562	blood:	n/a	n/a
19	CEBPB	chr12:74579197-74579397	K562	blood:	n/a	n/a
20	CEBPB	chr12:74637033-74637227	K562	blood:	n/a	chr12:74637153-74637164
21	CEBPB	chr12:74621712-74622235	A549	lung:	n/a	n/a
22	CEBPB	chr12:74637031-74637293	HepG2	liver:	n/a	chr12:74637153-74637164
23	CEBPB	chr12:74523983-74524169	A549	lung:	n/a	chr12:74524027-74524038
24	CEBPB	chr12:74579176-74579416	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:74637060-74637260	H1-hESC	embryonic stem cell:	n/a	chr12:74637153-74637164
26	CEBPB	chr12:74543240-74543419	HepG2	liver:	n/a	chr12:74543280-74543291
27	CEBPD	chr12:74629056-74629545	K562	blood:	n/a	n/a
28	CEBPD	chr12:74629170-74629552	K562	blood:	n/a	n/a
29	CHD1	chr12:74630885-74630911	GM12878	blood:	n/a	n/a
30	CHD2	chr12:74564446-74565068	K562	blood:	n/a	chr12:74564765-74564775
31	CHD2	chr12:74621238-74621247	HepG2	liver:	n/a	n/a
32	CTCF	chr12:74638658-74638731	LNCaP	prostate:	n/a	n/a
33	CTCF	chr12:74570529-74570633	LNCaP	prostate:	n/a	n/a
34	CTCF	chr12:74590177-74590185	K562	blood:	n/a	n/a
35	CTCF	chr12:74564355-74564551	K562	blood:	n/a	n/a
36	CTCF	chr12:74563702-74563822	K562	blood:	n/a	n/a
37	CTCF	chr12:74586897-74586906	MCF-7	breast:	n/a	n/a
38	CTCF	chr12:74618310-74618394	GM20000	blood:	n/a	n/a
39	CTCF	chr12:74562945-74562949	K562	blood:	n/a	n/a
40	CTCF	chr12:74591580-74591730	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr12:74521464-74521516	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr12:74637202-74637245	GM10248	blood:	n/a	n/a
43	CTCF	chr12:74612432-74612489	GM20000	blood:	n/a	n/a
44	CTCF	chr12:74549787-74549819	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr12:74610900-74611050	Caco-2	colon:	n/a	n/a
46	CUX1	chr12:74563633-74563959	K562	blood:	n/a	n/a
47	CUX1	chr12:74562758-74563017	K562	blood:	n/a	n/a
48	CUX1	chr12:74566631-74566816	K562	blood:	n/a	n/a
49	E2F4	chr12:74621694-74622246	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr12:74567269-74567324	MCF10A-Er-Src	breast:	n/a	n/a

(count:428 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:74561645-74561695	NT2-D1	testis:	n/a
2	chr12:74561645-74561695	NT2-D1	testis:	n/a
3	chr12:74564932-74564982	GM12892	blood:	n/a
4	chr12:74561645-74561695	HRPEpiC	eye:	n/a
5	chr12:74564847-74564897	HCT-116	colon:	n/a
6	chr12:74564847-74564897	NB4	blood:	n/a
7	chr12:74565116-74565166	AG04450	lung:	fetal
8	chr12:74564847-74564897	RPTEC	kidney:	n/a
9	chr12:74564523-74564573	HAEpiC	amniotic membrane:	n/a
10	chr12:74564856-74564906	SKMC	muscle:	n/a
11	chr12:74564847-74564897	NH-A	brain:	n/a
12	chr12:74565563-74565613	HEK293	kidney:	embryo
13	chr12:74565116-74565166	AoSMC	blood vessel:	n/a
14	chr12:74564523-74564573	MCF-7	breast:	n/a
15	chr12:74564847-74564897	HNPCEpiC	eye:	n/a
16	chr12:74565563-74565613	A549	lung:	n/a
17	chr12:74564847-74564897	Hepatocyte	liver:	n/a
18	chr12:74565116-74565166	AG09319	gingival:	n/a
19	chr12:74565116-74565166	H1-hESC	embryonic stem cell:	embryo
20	chr12:74564856-74564906	HEK293	kidney:	embryo
21	chr12:74561645-74561695	NB4	blood:	n/a
22	chr12:74565563-74565613	SK-N-MC	brain:	n/a
23	chr12:74565116-74565166	GM19239	blood:	n/a
24	chr12:74561645-74561695	AG09319	gingival:	n/a
25	chr12:74565116-74565166	NHBE	bronchial:	n/a
26	chr12:74565116-74565166	AG10803	skin:	n/a
27	chr12:74564523-74564573	HRPEpiC	eye:	n/a
28	chr12:74561645-74561695	T-47D	breast:	n/a
29	chr12:74565563-74565613	HCF	heart:	n/a
30	chr12:74564932-74564982	HCT-116	colon:	n/a
31	chr12:74564932-74564982	AG04449	skin:	fetal
32	chr12:74564856-74564906	HCT-116	colon:	n/a
33	chr12:74564847-74564897	HRPEpiC	eye:	n/a
34	chr12:74564856-74564906	MCF-7	breast:	n/a
35	chr12:74564932-74564982	HAEpiC	amniotic membrane:	n/a
36	chr12:74564932-74564982	HNPCEpiC	eye:	n/a
37	chr12:74565116-74565166	HRCEpiC	kidney:	n/a
38	chr12:74564856-74564906	ECC-1	luminal epithelium:	n/a
39	chr12:74564847-74564897	NHDF-neo	bronchial:	n/a
40	chr12:74564847-74564897	U87	brain:	n/a
41	chr12:74565563-74565613	NB4	blood:	n/a
42	chr12:74565563-74565613	HAEpiC	amniotic membrane:	n/a
43	chr12:74564856-74564906	A549	lung:	n/a
44	chr12:74564856-74564906	AG10803	skin:	n/a
45	chr12:74565563-74565613	NHBE	bronchial:	n/a
46	chr12:74561645-74561695	LNCaP	prostate:	n/a
47	chr12:74564523-74564573	Hepatocyte	liver:	n/a
48	chr12:74561645-74561695	SKMC	muscle:	n/a
49	chr12:74565116-74565166	SK-N-SH	brain:	n/a
50	chr12:74564523-74564573	AG09309	skin:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr12:74522697..74525336-chr12:74527749..74530439,2	K562	blood:
2	chr12:74531548..74535089-chr12:74542302..74547555,5	K562	blood:
3	chr12:74642568..74645294-chr12:74647466..74649300,2	K562	blood:
4	chr12:74564280..74566761-chr12:74606459..74609033,2	K562	blood:
5	chr12:74644729..74646901-chr12:74673133..74675574,2	K562	blood:
6	chr12:74573561..74575455-chr12:74654364..74657073,2	K562	blood:
7	chr12:74535843..74538591-chr12:74539511..74542141,2	K562	blood:
8	chr12:74630058..74632714-chr12:74633651..74635328,2	MCF-7	breast:
9	chr12:74563522..74565469-chr12:74584135..74585819,3	K562	blood:
10	chr12:74576003..74577686-chr12:74589371..74591140,2	K562	blood:
11	chr12:74564480..74567461-chr12:74575954..74578864,3	K562	blood:
12	chr12:74528403..74529928-chr12:74531825..74534781,2	K562	blood:
13	chr12:74596988..74600008-chr12:74601826..74604825,3	K562	blood:
14	chr12:74545641..74548957-chr12:74555890..74557729,3	K562	blood:
15	chr12:74565564..74567447-chr12:74573536..74575120,2	K562	blood:
16	chr12:74584693..74586459-chr12:74588249..74590521,2	K562	blood:
17	chr12:74576003..74577686-chr12:74589371..74591140,2	K562	blood:
18	chr12:74596988..74600008-chr12:74601826..74604825,3	K562	blood:
19	chr12:74389722..74391980-chr12:74584509..74586133,2	K562	blood:
20	chr12:74620606..74623587-chr12:74624395..74628549,4	K562	blood:
21	chr12:74620606..74623587-chr12:74624395..74628549,4	K562	blood:
22	chr12:74536886..74539098-chr12:74541490..74544013,2	MCF-7	breast:
23	chr12:74522697..74525336-chr12:74527749..74530439,2	K562	blood:
24	chr12:74576549..74579038-chr12:74580124..74581922,2	MCF-7	breast:
25	chr12:74528403..74529928-chr12:74531825..74534781,2	K562	blood:
26	chr12:74527061..74530059-chr12:74931122..74933872,2	MCF-7	breast:
27	chr12:74609981..74612603-chr12:74615480..74618314,2	K562	blood:
28	chr12:74531548..74535089-chr12:74542302..74547555,5	K562	blood:
29	chr12:74526468..74528133-chr12:74535792..74537959,2	MCF-7	breast:
30	chr12:74576549..74579038-chr12:74580124..74581922,2	MCF-7	breast:
31	chr12:74545641..74548768-chr12:74554696..74557729,3	K562	blood:
32	chr12:74545641..74548768-chr12:74554696..74557729,3	K562	blood:
33	chr12:74584693..74586459-chr12:74588249..74590521,2	K562	blood:
34	chr12:74552737..74556720-chr12:74559479..74564261,5	K562	blood:
35	chr12:74536886..74539098-chr12:74541490..74544013,2	MCF-7	breast:
36	chr12:74535843..74538591-chr12:74539511..74542141,2	K562	blood:
37	chr12:74584848..74587275-chr12:74588348..74590290,2	MCF-7	breast:
38	chr12:74636496..74638215-chr12:74687391..74689120,2	K562	blood:
39	chr12:74547425..74549185-chr12:74551970..74554441,2	MCF-7	breast:
40	chr12:74609981..74612603-chr12:74615480..74618314,2	K562	blood:
41	chr12:74526468..74528133-chr12:74535792..74537959,2	MCF-7	breast:
42	chr12:74545641..74548957-chr12:74555890..74557729,3	K562	blood:
43	chr12:74564280..74566761-chr12:74606459..74609033,2	K562	blood:
44	chr12:74539088..74540893-chr12:74543258..74546036,3	K562	blood:
45	chr12:74539088..74540893-chr12:74543258..74546036,3	K562	blood:
46	chr12:74564480..74567461-chr12:74575954..74578864,3	K562	blood:
47	chr12:74540805..74543327-chr12:74544789..74546497,2	K562	blood:
48	chr12:74630058..74632714-chr12:74633651..74635328,2	MCF-7	breast:
49	chr12:74560053..74562479-chr12:74564625..74566537,2	K562	blood:
50	chr12:74584848..74587275-chr12:74588348..74590290,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNC2-3	chr12:74644265-74644361	ENSG00000257183.1
2	lnc-KCNC2-3	chr12:74642417-74642627	ENSG00000257183.1

No data

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

Extended variants
information (count: 3350 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3350 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568153609	chr12:74520028-74520029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs34043703	chr12:74520034-74520035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs397791125	chr12:74520040-74520041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs568631029	chr12:74520048-74520049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542550363	chr12:74520051-74520052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183750569	chr12:74520058-74520059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537914072	chr12:74520064-74520065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527876584	chr12:74520085-74520086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548007187	chr12:74520108-74520109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs538179212	chr12:74520131-74520132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559974527	chr12:74520141-74520142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532103738	chr12:74520170-74520171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551727273	chr12:74520183-74520184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568526857	chr12:74520196-74520197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537705900	chr12:74520220-74520221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs548185112	chr12:74520221-74520222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs568385610	chr12:74520223-74520224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs188481591	chr12:74520245-74520246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531841023	chr12:74520263-74520264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs11179931	chr12:74520270-74520271	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs577386569	chr12:74520289-74520290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs539957467	chr12:74520292-74520293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs556558963	chr12:74520293-74520294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs576510132	chr12:74520307-74520308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542253310	chr12:74520315-74520316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555774177	chr12:74520324-74520325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs572729440	chr12:74520356-74520357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541242262	chr12:74520362-74520363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564723140	chr12:74520364-74520365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532044745	chr12:74520391-74520392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs375729220	chr12:74520398-74520399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368344207	chr12:74520401-74520402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371942001	chr12:74520405-74520406	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs71458170	chr12:74520440-74520441	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs182814025	chr12:74520445-74520446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147987059	chr12:74520446-74520447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs527607582	chr12:74520460-74520461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547244158	chr12:74520462-74520463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570671791	chr12:74520465-74520466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61657486	chr12:74520468-74520469	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs556689530	chr12:74520472-74520473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201965053	chr12:74520482-74520483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs369280938	chr12:74520496-74520497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535463044	chr12:74520508-74520509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555757536	chr12:74520509-74520510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565264666	chr12:74520526-74520527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541726726	chr12:74520528-74520529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371806858	chr12:74520529-74520530	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs557888432	chr12:74520587-74520588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374657982	chr12:74520605-74520606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Breast cancer	20409316	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:74520000-74528200	Weak transcription	K562	blood
2	chr12:74523600-74524000	Enhancers	Brain Cingulate Gyrus	brain
3	chr12:74523600-74524000	Active TSS	Ovary	ovary
4	chr12:74531200-74531600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr12:74544000-74544400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr12:74545400-74545600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr12:74545600-74546600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:74545600-74547400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr12:74546000-74546400	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr12:74546000-74546800	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr12:74546000-74546800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr12:74546200-74546800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
13	chr12:74546200-74547000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr12:74546400-74546800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr12:74546400-74546800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
16	chr12:74546600-74547200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr12:74548800-74563400	Weak transcription	K562	blood
18	chr12:74561200-74561600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr12:74563400-74565200	Active TSS	K562	blood
20	chr12:74564600-74565400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:74565200-74565400	Transcr. at gene 5' and 3'	K562	blood
22	chr12:74565400-74566600	Active TSS	K562	blood
23	chr12:74566600-74566800	Flanking Active TSS	K562	blood
24	chr12:74566800-74567000	Active TSS	K562	blood
25	chr12:74567000-74567200	Flanking Active TSS	K562	blood
26	chr12:74567200-74567400	Enhancers	K562	blood
27	chr12:74576000-74578600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr12:74578200-74578800	ZNF genes & repeats	Pancreas	Pancrea
29	chr12:74578400-74579000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr12:74578600-74578800	Enhancers	Gastric	stomach
31	chr12:74578600-74579000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr12:74578600-74579200	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr12:74579200-74581000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr12:74586600-74587600	Enhancers	Brain Germinal Matrix	brain
35	chr12:74587600-74589200	Weak transcription	Brain Germinal Matrix	brain
36	chr12:74589200-74590200	Enhancers	Brain Germinal Matrix	brain
37	chr12:74597800-74598200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr12:74597800-74598200	Enhancers	HMEC	breast
39	chr12:74597800-74598400	Enhancers	H1 Cell Line	embryonic stem cell
40	chr12:74598000-74629200	Weak transcription	K562	blood
41	chr12:74611200-74611600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr12:74629200-74630200	Enhancers	K562	blood
43	chr12:74630200-74634800	Weak transcription	K562	blood
44	chr12:74634800-74635200	Strong transcription	K562	blood
45	chr12:74635200-74636200	Weak transcription	K562	blood
46	chr12:74636000-74636400	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr12:74636000-74636800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr12:74636200-74636600	Strong transcription	K562	blood
49	chr12:74636600-74678000	Weak transcription	K562	blood
50	chr12:74640200-74640600	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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