Variant report

Variant	nsv899289
Chromosome Location	chr12:74528830-74609860
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:427)
Chromatin interactive
region (count:46)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 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	chr12:74562651-74562972	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	BHLHE40	chr12:74564438-74565831	K562	blood:	n/a	n/a
5	CBX3	chr12:74568726-74569098	K562	blood:	n/a	n/a
6	CBX3	chr12:74564451-74565685	K562	blood:	n/a	n/a
7	CBX3	chr12:74568678-74569478	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	chr12:74579176-74579416	HepG2	liver:	n/a	n/a
11	CEBPB	chr12:74579197-74579397	K562	blood:	n/a	n/a
12	CEBPB	chr12:74538300-74538814	K562	blood:	n/a	n/a
13	CEBPB	chr12:74582394-74582629	K562	blood:	n/a	n/a
14	CEBPB	chr12:74543240-74543419	HepG2	liver:	n/a	chr12:74543280-74543291
15	CEBPB	chr12:74579207-74579455	IMR90	lung:	n/a	n/a
16	CHD2	chr12:74564446-74565068	K562	blood:	n/a	chr12:74564765-74564775
17	CTCF	chr12:74549787-74549819	Pancreas_OC	pancreas:	n/a	n/a
18	CTCF	chr12:74590177-74590185	K562	blood:	n/a	n/a
19	CTCF	chr12:74563702-74563822	K562	blood:	n/a	n/a
20	CTCF	chr12:74562945-74562949	K562	blood:	n/a	n/a
21	CTCF	chr12:74564355-74564551	K562	blood:	n/a	n/a
22	CTCF	chr12:74570529-74570633	LNCaP	prostate:	n/a	n/a
23	CTCF	chr12:74586897-74586906	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:74591580-74591730	Hela-S3	cervix:	n/a	n/a
25	CUX1	chr12:74562758-74563017	K562	blood:	n/a	n/a
26	CUX1	chr12:74566631-74566816	K562	blood:	n/a	n/a
27	CUX1	chr12:74563633-74563959	K562	blood:	n/a	n/a
28	E2F4	chr12:74575135-74575536	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr12:74567269-74567324	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F6	chr12:74564552-74565641	K562	blood:	n/a	chr12:74564766-74564778
31	E2F6	chr12:74565392-74565633	K562	blood:	n/a	n/a
32	E2F6	chr12:74564551-74565208	K562	blood:	n/a	chr12:74564766-74564778
33	ELF1	chr12:74564549-74565654	K562	blood:	n/a	chr12:74565563-74565572
34	ELF1	chr12:74564413-74565706	K562	blood:	n/a	chr12:74565563-74565572
35	EP300	chr12:74606206-74606242	GM12878	blood:	n/a	n/a
36	EP300	chr12:74565485-74565662	GM12878	blood:	n/a	n/a
37	EP300	chr12:74564514-74564551	K562	blood:	n/a	n/a
38	EP300	chr12:74566453-74566797	K562	blood:	n/a	n/a
39	EP300	chr12:74565359-74565742	K562	blood:	n/a	chr12:74565669-74565683 chr12:74565670-74565684 chr12:74565668-74565682
40	FAM48A	chr12:74544125-74544596	GM12878	blood:	n/a	n/a
41	FOS	chr12:74567249-74567301	MCF10A-Er-Src	breast:	n/a	n/a
42	GABPA	chr12:74565407-74565656	K562	blood:	n/a	n/a
43	GABPA	chr12:74565219-74565642	K562	blood:	n/a	n/a
44	GABPA	chr12:74564563-74565062	K562	blood:	n/a	chr12:74564756-74564765 chr12:74564844-74564851
45	GATA3	chr12:74562659-74562896	T-47D	breast:	n/a	n/a
46	GATA3	chr12:74590058-74590204	SH-SY5Y	brain:	n/a	n/a
47	GTF2B	chr12:74565276-74565668	K562	blood:	n/a	n/a
48	GTF2B	chr12:74564507-74564759	K562	blood:	n/a	n/a
49	GTF2F1	chr12:74564502-74564777	K562	blood:	n/a	n/a
50	GTF2F1	chr12:74565270-74565697	K562	blood:	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	chr12:74565563-74565613	AG09309	skin:	n/a
2	chr12:74565116-74565166	GM12892	blood:	n/a
3	chr12:74561645-74561695	IMR90	lung:	fetal
4	chr12:74561645-74561695	HRCEpiC	kidney:	n/a
5	chr12:74561645-74561695	HUVEC	blood vessel:	n/a
6	chr12:74564847-74564897	HRE	kidney:	n/a
7	chr12:74565563-74565613	GM12892	blood:	n/a
8	chr12:74564847-74564897	A549	lung:	n/a
9	chr12:74565116-74565166	AG04450	lung:	fetal
10	chr12:74564932-74564982	SK-N-SH	brain:	n/a
11	chr12:74564523-74564573	CMK	blood:	n/a
12	chr12:74564847-74564897	PFSK-1	brain:	n/a
13	chr12:74564932-74564982	BJ	skin:	n/a
14	chr12:74564847-74564897	AG04450	lung:	fetal
15	chr12:74565563-74565613	NHDF-neo	bronchial:	n/a
16	chr12:74565563-74565613	ECC-1	luminal epithelium:	n/a
17	chr12:74565563-74565613	Jurkat	blood:	n/a
18	chr12:74564523-74564573	AG09319	gingival:	n/a
19	chr12:74561645-74561695	NH-A	brain:	n/a
20	chr12:74564523-74564573	Hepatocyte	liver:	n/a
21	chr12:74561645-74561695	SK-N-SH_RA	brain:	n/a
22	chr12:74564523-74564573	GM12891	blood:	n/a
23	chr12:74561645-74561695	NHBE	bronchial:	n/a
24	chr12:74564523-74564573	HCF	heart:	n/a
25	chr12:74565116-74565166	HMEC	breast:	n/a
26	chr12:74564932-74564982	ECC-1	luminal epithelium:	n/a
27	chr12:74564932-74564982	PrEC	prostate:	n/a
28	chr12:74564523-74564573	AG10803	skin:	n/a
29	chr12:74565116-74565166	ovcar-3	ovarian:	n/a
30	chr12:74564856-74564906	HRE	kidney:	n/a
31	chr12:74564932-74564982	SKMC	muscle:	n/a
32	chr12:74564523-74564573	HNPCEpiC	eye:	n/a
33	chr12:74565116-74565166	A549	lung:	n/a
34	chr12:74561645-74561695	Caco-2	colon:	n/a
35	chr12:74564856-74564906	GM19239	blood:	n/a
36	chr12:74564856-74564906	GM06990	blood:	n/a
37	chr12:74564523-74564573	Caco-2	colon:	n/a
38	chr12:74564932-74564982	NHBE	bronchial:	n/a
39	chr12:74564523-74564573	NHBE	bronchial:	n/a
40	chr12:74561645-74561695	HepG2	liver:	n/a
41	chr12:74564856-74564906	K562	blood:	n/a
42	chr12:74565116-74565166	PFSK-1	brain:	n/a
43	chr12:74564847-74564897	U87	brain:	n/a
44	chr12:74564523-74564573	HRE	kidney:	n/a
45	chr12:74564847-74564897	GM06990	blood:	n/a
46	chr12:74565563-74565613	HNPCEpiC	eye:	n/a
47	chr12:74561645-74561695	MCF10A-Er-Src	breast:	n/a
48	chr12:74564847-74564897	NH-A	brain:	n/a
49	chr12:74561645-74561695	SK-N-SH	brain:	n/a
50	chr12:74564847-74564897	SAEC	small airway:	n/a

(count:46 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:74564462..74568132-chr12:74683426..74687604,5	K562	blood:
2	chr12:74545641..74548768-chr12:74554696..74557729,3	K562	blood:
3	chr12:74584848..74587275-chr12:74588348..74590290,2	MCF-7	breast:
4	chr12:74531548..74535089-chr12:74542302..74547555,5	K562	blood:
5	chr12:74576549..74579038-chr12:74580124..74581922,2	MCF-7	breast:
6	chr12:74560053..74562479-chr12:74564625..74566537,2	K562	blood:
7	chr12:74564280..74566761-chr12:74606459..74609033,2	K562	blood:
8	chr12:74527061..74530059-chr12:74931122..74933872,2	MCF-7	breast:
9	chr12:74576003..74577686-chr12:74589371..74591140,2	K562	blood:
10	chr12:74535843..74538591-chr12:74539511..74542141,2	K562	blood:
11	chr12:74564280..74566761-chr12:74606459..74609033,2	K562	blood:
12	chr12:74539088..74540893-chr12:74543258..74546036,3	K562	blood:
13	chr12:74539088..74540893-chr12:74543258..74546036,3	K562	blood:
14	chr12:74522697..74525336-chr12:74527749..74530439,2	K562	blood:
15	chr12:74547425..74549185-chr12:74551970..74554441,2	MCF-7	breast:
16	chr12:74578180..74580078-chr12:74586581..74588937,2	K562	blood:
17	chr12:74526468..74528133-chr12:74535792..74537959,2	MCF-7	breast:
18	chr12:74565564..74567447-chr12:74573536..74575120,2	K562	blood:
19	chr12:74584848..74587275-chr12:74588348..74590290,2	MCF-7	breast:
20	chr12:74573561..74575455-chr12:74654364..74657073,2	K562	blood:
21	chr12:74578180..74580078-chr12:74586581..74588937,2	K562	blood:
22	chr12:74528403..74529928-chr12:74531825..74534781,2	K562	blood:
23	chr12:74545641..74548768-chr12:74554696..74557729,3	K562	blood:
24	chr12:74596988..74600008-chr12:74601826..74604825,3	K562	blood:
25	chr12:74596988..74600008-chr12:74601826..74604825,3	K562	blood:
26	chr12:74535843..74538591-chr12:74539511..74542141,2	K562	blood:
27	chr12:74564480..74567461-chr12:74575954..74578864,3	K562	blood:
28	chr12:74584693..74586459-chr12:74588249..74590521,2	K562	blood:
29	chr12:74564480..74567461-chr12:74575954..74578864,3	K562	blood:
30	chr12:74563522..74565469-chr12:74584135..74585819,3	K562	blood:
31	chr12:74576003..74577686-chr12:74589371..74591140,2	K562	blood:
32	chr12:74540805..74543327-chr12:74544789..74546497,2	K562	blood:
33	chr12:74552737..74556720-chr12:74559479..74564261,5	K562	blood:
34	chr12:74545641..74548957-chr12:74555890..74557729,3	K562	blood:
35	chr12:74547425..74549185-chr12:74551970..74554441,2	MCF-7	breast:
36	chr12:74560053..74562479-chr12:74564625..74566537,2	K562	blood:
37	chr12:74584693..74586459-chr12:74588249..74590521,2	K562	blood:
38	chr12:74576549..74579038-chr12:74580124..74581922,2	MCF-7	breast:
39	chr12:74565564..74567447-chr12:74573536..74575120,2	K562	blood:
40	chr12:74389722..74391980-chr12:74584509..74586133,2	K562	blood:
41	chr12:74536886..74539098-chr12:74541490..74544013,2	MCF-7	breast:
42	chr12:74545641..74548957-chr12:74555890..74557729,3	K562	blood:
43	chr12:74531548..74535089-chr12:74542302..74547555,5	K562	blood:
44	chr12:74536886..74539098-chr12:74541490..74544013,2	MCF-7	breast:
45	chr12:74528403..74529928-chr12:74531825..74534781,2	K562	blood:
46	chr12:74540805..74543327-chr12:74544789..74546497,2	K562	blood:

No data

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

Extended variants
information (count: 1674 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1674 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11179933	chr12:74528830-74528831	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs537630906	chr12:74528834-74528835	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs368004901	chr12:74528845-74528846	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs539917841	chr12:74528893-74528894	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs557296328	chr12:74528924-74528925	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569700771	chr12:74528971-74528972	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs535208806	chr12:74528973-74528974	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs11179934	chr12:74528989-74528990	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs191358707	chr12:74529005-74529006	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs11179935	chr12:74529057-74529058	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs183168630	chr12:74529183-74529184	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs11179936	chr12:74529223-74529224	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs186064178	chr12:74529241-74529242	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs200605298	chr12:74529251-74529252	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144894287	chr12:74529252-74529253	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs142630053	chr12:74529278-74529279	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs111801609	chr12:74529286-74529287	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs542715249	chr12:74529290-74529291	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559461607	chr12:74529297-74529298	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs150982464	chr12:74529302-74529303	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs561582306	chr12:74529314-74529315	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs190786474	chr12:74529316-74529317	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs530538309	chr12:74529325-74529326	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183087781	chr12:74529353-74529354	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs376668966	chr12:74529364-74529365	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs551111739	chr12:74529392-74529393	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs11179937	chr12:74529393-74529394	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570787855	chr12:74529398-74529399	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs372348619	chr12:74529414-74529415	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs78981345	chr12:74529421-74529422	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs555496065	chr12:74529423-74529424	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187806814	chr12:74529680-74529681	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs140904130	chr12:74529688-74529689	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs564107749	chr12:74529690-74529691	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs546880799	chr12:74529706-74529707	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs557810142	chr12:74529727-74529728	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs532819554	chr12:74529728-74529729	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs577834913	chr12:74529754-74529755	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs11179938	chr12:74529763-74529764	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs147777838	chr12:74529814-74529815	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs11179939	chr12:74529816-74529817	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs542447032	chr12:74529872-74529873	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs559398349	chr12:74529886-74529887	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs573021527	chr12:74529935-74529936	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs544965710	chr12:74529941-74529942	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs141090361	chr12:74529945-74529946	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs535247702	chr12:74529992-74529993	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs531185595	chr12:74530017-74530018	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs144598301	chr12:74530025-74530026	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs191985352	chr12:74530042-74530043	Inactive region	Chromatin interactive region	2 gene(s)	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:37 , 50 per page) page: 1

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

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