Variant report

Variant	nsv826522
Chromosome Location	chr12:117316379-117317264
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:244)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr12:117316311-117316987	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr12:117316753-117316877	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD2	chr12:117316388-117316908	Hela-S3	cervix:	n/a	chr12:117316815-117316825
4	CTBP2	chr12:117316706-117317573	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr12:117316800-117316950	WERI-Rb-1	eye:	n/a	n/a
6	E2F4	chr12:117316443-117316582	MCF10A-Er-Src	breast:	n/a	n/a
7	ELK1	chr12:117316910-117317108	Hela-S3	cervix:	n/a	n/a
8	ELK1	chr12:117316399-117316599	Hela-S3	cervix:	n/a	n/a
9	GTF2F1	chr12:117316422-117317155	Hela-S3	cervix:	n/a	n/a
10	HA-E2F1	chr12:117316210-117316815	MCF-7	breast:	n/a	n/a
11	HA-E2F1	chr12:117317058-117317944	MCF-7	breast:	n/a	n/a
12	HDAC2	chr12:117316283-117317121	MCF-7	breast:	n/a	chr12:117317061-117317075
13	MAFK	chr12:117316390-117316488	Hela-S3	cervix:	n/a	n/a
14	MAX	chr12:117316376-117317060	Hela-S3	cervix:	n/a	chr12:117316655-117316665
15	MAZ	chr12:117316310-117317076	Hela-S3	cervix:	n/a	chr12:117316655-117316665
16	MXI1	chr12:117316397-117317020	Hela-S3	cervix:	n/a	n/a
17	MYC	chr12:117316495-117316498	MCF-7	breast:	n/a	n/a
18	MYC	chr12:117316472-117316479	MCF10A-Er-Src	breast:	n/a	n/a
19	NR2F2	chr12:117316196-117316834	MCF-7	breast:	n/a	n/a
20	POLR2A	chr12:117316414-117316636	MCF-7	breast:	n/a	n/a
21	POLR2A	chr12:117316234-117317093	HCT-116	colon:	n/a	n/a
22	POLR2A	chr12:117316331-117317010	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr12:117316325-117317095	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr12:117316664-117317547	H1-neurons	neurons:	n/a	n/a
25	POLR2A	chr12:117316645-117316973	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr12:117316686-117317062	Hela-S3	cervix:	n/a	n/a
27	POLR2A	chr12:117316446-117317053	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr12:117316313-117317030	HCT-116	colon:	n/a	n/a
29	RAD21	chr12:117316347-117316623	Hela-S3	cervix:	n/a	chr12:117316512-117316526
30	RCOR1	chr12:117316288-117317050	Hela-S3	cervix:	n/a	n/a
31	RFX5	chr12:117316340-117317081	Hela-S3	cervix:	n/a	n/a
32	SMARCB1	chr12:117316356-117318213	Hela-S3	cervix:	n/a	n/a
33	SMC3	chr12:117316329-117316845	Hela-S3	cervix:	n/a	n/a
34	STAT3	chr12:117316205-117316706	MCF10A-Er-Src	breast:	n/a	chr12:117316657-117316669 chr12:117316473-117316484
35	STAT3	chr12:117317192-117317227	MCF10A-Er-Src	breast:	n/a	n/a
36	STAT3	chr12:117316298-117316661	MCF10A-Er-Src	breast:	n/a	chr12:117316473-117316484
37	STAT3	chr12:117316385-117316585	MCF10A-Er-Src	breast:	n/a	chr12:117316473-117316484
38	STAT3	chr12:117316366-117316640	MCF10A-Er-Src	breast:	n/a	chr12:117316473-117316484
39	STAT3	chr12:117316405-117316584	Hela-S3	cervix:	n/a	chr12:117316473-117316484
40	SUZ12	chr12:117316189-117319614	NT2-D1	testis:	n/a	n/a
41	TBP	chr12:117316392-117316928	Hela-S3	cervix:	n/a	n/a
42	TBP	chr12:117316711-117316951	H1-hESC	embryonic stem cell:	n/a	n/a
43	TFAP2A	chr12:117316254-117317069	Hela-S3	cervix:	n/a	chr12:117316448-117316463
44	TFAP2C	chr12:117316201-117317098	Hela-S3	cervix:	n/a	n/a
45	UBTF	chr12:117316787-117316814	K562	blood:	n/a	n/a
46	USF2	chr12:117316482-117316665	Hela-S3	cervix:	n/a	n/a
47	YY1	chr12:117316370-117316844	HCT-116	colon:	n/a	chr12:117316817-117316831 chr12:117316740-117316754 chr12:117316820-117316834 chr12:117316739-117316748
48	ZKSCAN1	chr12:117316547-117317086	Hela-S3	cervix:	n/a	n/a
49	ZNF143	chr12:117316405-117316808	Hela-S3	cervix:	n/a	n/a
50	ZNF263	chr12:117316348-117317103	HEK293-T-REx	kidney:	n/a	chr12:117316779-117316788

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:117316716-117316766	SK-N-MC	brain:	n/a
2	chr12:117316665-117316715	BE2_C	brain:	n/a
3	chr12:117316882-117316932	HL-60	blood:	n/a
4	chr12:117316665-117316715	HRE	kidney:	n/a
5	chr12:117316490-117316540	HIPEpiC	eye:	n/a
6	chr12:117316665-117316715	SK-N-SH_RA	brain:	n/a
7	chr12:117316490-117316540	GM12891	blood:	n/a
8	chr12:117316882-117316932	NH-A	brain:	n/a
9	chr12:117316882-117316932	GM19239	blood:	n/a
10	chr12:117316882-117316932	NB4	blood:	n/a
11	chr12:117316490-117316540	NHDF-neo	bronchial:	n/a
12	chr12:117316490-117316540	PFSK-1	brain:	n/a
13	chr12:117316716-117316766	GM06990	blood:	n/a
14	chr12:117316716-117316766	AG04449	skin:	fetal
15	chr12:117316716-117316766	NHBE	bronchial:	n/a
16	chr12:117316490-117316540	RPTEC	kidney:	n/a
17	chr12:117316665-117316715	MCF-7	breast:	n/a
18	chr12:117316716-117316766	HMEC	breast:	n/a
19	chr12:117316490-117316540	ovcar-3	ovarian:	n/a
20	chr12:117316716-117316766	HIPEpiC	eye:	n/a
21	chr12:117316665-117316715	NHBE	bronchial:	n/a
22	chr12:117316665-117316715	U87	brain:	n/a
23	chr12:117316882-117316932	ovcar-3	ovarian:	n/a
24	chr12:117316716-117316766	NHDF-neo	bronchial:	n/a
25	chr12:117316716-117316766	NB4	blood:	n/a
26	chr12:117316490-117316540	MCF-7	breast:	n/a
27	chr12:117316490-117316540	LNCaP	prostate:	n/a
28	chr12:117316882-117316932	SK-N-SH_RA	brain:	n/a
29	chr12:117316490-117316540	U87	brain:	n/a
30	chr12:117316716-117316766	Jurkat	blood:	n/a
31	chr12:117316665-117316715	PFSK-1	brain:	n/a
32	chr12:117316882-117316932	NHDF-neo	bronchial:	n/a
33	chr12:117316882-117316932	AG04449	skin:	fetal
34	chr12:117316716-117316766	IMR90	lung:	fetal
35	chr12:117316716-117316766	HAEpiC	amniotic membrane:	n/a
36	chr12:117316716-117316766	Caco-2	colon:	n/a
37	chr12:117316716-117316766	HCT-116	colon:	n/a
38	chr12:117316665-117316715	AG09309	skin:	n/a
39	chr12:117316882-117316932	AG04450	lung:	fetal
40	chr12:117316490-117316540	HCT-116	colon:	n/a
41	chr12:117316716-117316766	HPAEpiC	pulmonary alveolar:	n/a
42	chr12:117316716-117316766	HCF	heart:	n/a
43	chr12:117316490-117316540	HCPEpiC	choroid plexus:	n/a
44	chr12:117316490-117316540	AoSMC	blood vessel:	n/a
45	chr12:117316716-117316766	NH-A	brain:	n/a
46	chr12:117316716-117316766	Hepatocyte	liver:	n/a
47	chr12:117316882-117316932	HRCEpiC	kidney:	n/a
48	chr12:117316882-117316932	HCM	heart:	n/a
49	chr12:117316716-117316766	AG09319	gingival:	n/a
50	chr12:117316882-117316932	SAEC	small airway:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr12:117314859..117317028-chr12:117347500..117350151,4	MCF-7	breast:
2	chr12:117317029..117319301-chr12:117346996..117349580,2	MCF-7	breast:
3	chr12:117174783..117176988-chr12:117316113..117318785,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HRK-1	chr12:117316878-117317422	NONHSAT030971

No data

Variant related genes	Relation type
HRK	TF binding region
HRK	CpG island
ENSG00000111412	chromatin interactions
ENSG00000174989	chromatin interactions
ENSG00000135119	chromatin interactions

Extended variants
information (count: 31 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:31 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73393797	chr12:117316412-117316413	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs3748262	chr12:117316433-117316434	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs534781840	chr12:117316465-117316466	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs553963135	chr12:117316497-117316498	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs573740715	chr12:117316499-117316500	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs542950853	chr12:117316508-117316509	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs184964520	chr12:117316560-117316561	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs542362458	chr12:117316630-117316631	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs562025424	chr12:117316665-117316666	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs576354897	chr12:117316709-117316710	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs545028940	chr12:117316746-117316747	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs371629002	chr12:117316808-117316809	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs76044829	chr12:117316813-117316814	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs369033217	chr12:117316825-117316826	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs527692317	chr12:117316827-117316828	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs527403009	chr12:117316851-117316852	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs540745934	chr12:117316858-117316859	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs561562118	chr12:117316869-117316870	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs188205576	chr12:117316916-117316917	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
20	rs372986818	chr12:117316930-117316931	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
21	rs372204607	chr12:117316955-117316956	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
22	rs570024379	chr12:117316958-117316959	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
23	rs12227855	chr12:117316970-117316971	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs552175956	chr12:117317046-117317047	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
25	rs11068221	chr12:117317092-117317093	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs535155406	chr12:117317156-117317157	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
27	rs554759298	chr12:117317163-117317164	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
28	rs4767467	chr12:117317168-117317169	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
29	rs535375817	chr12:117317181-117317182	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
30	rs74931914	chr12:117317204-117317205	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
31	rs560391646	chr12:117317224-117317225	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

Disease	PMID	Source
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
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
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	21390271	CNVD
Cancer	20164919	CNVD
Cancer	16751803	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
Wilms tumour	21544195	CNVD
Ovarian cancer	21720365	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Sudden cardiac death	19188705	CNVD
Breast cancer	17133270	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Cryptorchidism	21048976	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Neuroblastoma	20406844	CNVD
Medulloblastoma	16783165	CNVD
mental retardation	16760730	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Lung adenocarcinoma	21045234	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21806811	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117312800-117316400	Weak transcription	Right Atrium	heart
2	chr12:117314000-117316400	Weak transcription	Gastric	stomach
3	chr12:117314800-117316400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr12:117315000-117316400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr12:117315600-117316400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr12:117316000-117316400	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr12:117316000-117316400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr12:117316000-117316400	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr12:117316000-117316400	Bivalent Enhancer	Fetal Muscle Leg	muscle
10	chr12:117316000-117316400	Bivalent Enhancer	Placenta	Placenta
11	chr12:117316000-117316400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
12	chr12:117316000-117316400	Flanking Active TSS	Hela-S3	cervix
13	chr12:117316000-117316600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr12:117316000-117316600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr12:117316000-117316600	Bivalent Enhancer	Esophagus	oesophagus
16	chr12:117316000-117316800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr12:117316000-117317400	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
18	chr12:117316000-117317800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
19	chr12:117316000-117320200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
20	chr12:117316200-117316400	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
21	chr12:117316200-117316400	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
22	chr12:117316200-117316400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr12:117316200-117316400	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:117316200-117316400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
25	chr12:117316200-117316400	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:117316200-117316400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
27	chr12:117316200-117316400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
28	chr12:117316200-117316400	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
29	chr12:117316200-117316400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr12:117316200-117316400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr12:117316200-117316400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr12:117316200-117316400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr12:117316200-117316400	Bivalent/Poised TSS	Brain Angular Gyrus	brain
34	chr12:117316200-117316400	Bivalent Enhancer	Brain Germinal Matrix	brain
35	chr12:117316200-117316400	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
36	chr12:117316200-117316400	Bivalent Enhancer	Colonic Mucosa	Colon
37	chr12:117316200-117316400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
38	chr12:117316200-117316400	Flanking Bivalent TSS/Enh	Fetal Heart	heart
39	chr12:117316200-117316400	Bivalent Enhancer	Fetal Intestine Large	intestine
40	chr12:117316200-117316400	Bivalent Enhancer	Left Ventricle	heart
41	chr12:117316200-117316400	Enhancers	Placenta Amnion	Placenta Amnion
42	chr12:117316200-117316400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
43	chr12:117316200-117316400	Bivalent Enhancer	HSMM	muscle
44	chr12:117316200-117316600	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr12:117316200-117316600	Flanking Bivalent TSS/Enh	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr12:117316200-117316600	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
47	chr12:117316200-117316600	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
48	chr12:117316200-117316600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
49	chr12:117316200-117316600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr12:117316200-117316600	Bivalent Enhancer	NH-A	brain

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