Variant report

Variant	esv2754892
Chromosome Location	chr12:9136351-9179007
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr12:9149189-9149755	GM12878	blood:	n/a	n/a
2	ATF2	chr12:9149130-9149794	GM12878	blood:	n/a	n/a
3	ATF3	chr12:9149339-9149593	K562	blood:	n/a	n/a
4	BATF	chr12:9149209-9149741	GM12878	blood:	n/a	chr12:9149517-9149527
5	BATF	chr12:9149225-9149726	GM12878	blood:	n/a	chr12:9149517-9149527
6	BCL11A	chr12:9149206-9149813	GM12878	blood:	n/a	n/a
7	BCL11A	chr12:9149263-9149694	GM12878	blood:	n/a	n/a
8	BCL3	chr12:9149247-9149637	GM12878	blood:	n/a	n/a
9	BCL3	chr12:9149268-9149693	GM12878	blood:	n/a	n/a
10	BCLAF1	chr12:9149146-9149803	GM12878	blood:	n/a	n/a
11	BCLAF1	chr12:9149203-9149686	GM12878	blood:	n/a	n/a
12	BHLHE40	chr12:9148737-9148745	K562	blood:	n/a	n/a
13	BHLHE40	chr12:9149326-9149685	GM12878	blood:	n/a	n/a
14	BRCA1	chr12:9161478-9161486	GM12878	blood:	n/a	n/a
15	CEBPB	chr12:9161156-9161391	K562	blood:	n/a	chr12:9161363-9161374 chr12:9161292-9161303
16	CEBPB	chr12:9138659-9138821	Hela-S3	cervix:	n/a	chr12:9138759-9138770
17	CEBPB	chr12:9147191-9147442	A549	lung:	n/a	chr12:9147301-9147318 chr12:9147294-9147305 chr12:9147302-9147315 chr12:9147302-9147315 chr12:9147294-9147307 chr12:9147280-9147293 chr12:9147303-9147314
18	CEBPB	chr12:9149153-9149774	GM12878	blood:	n/a	n/a
19	CEBPB	chr12:9138649-9138900	HepG2	liver:	n/a	chr12:9138759-9138770
20	CEBPB	chr12:9161262-9161471	HepG2	liver:	n/a	chr12:9161363-9161374 chr12:9161292-9161303
21	CEBPB	chr12:9144367-9144627	K562	blood:	n/a	n/a
22	CEBPB	chr12:9138641-9138876	IMR90	lung:	n/a	chr12:9138759-9138770
23	CEBPB	chr12:9147164-9147471	HepG2	liver:	n/a	chr12:9147301-9147318 chr12:9147294-9147305 chr12:9147302-9147315 chr12:9147302-9147315 chr12:9147294-9147307 chr12:9147280-9147293 chr12:9147303-9147314
24	CEBPB	chr12:9168156-9168179	HepG2	liver:	n/a	n/a
25	CEBPB	chr12:9147167-9147365	K562	blood:	n/a	chr12:9147301-9147318 chr12:9147294-9147305 chr12:9147302-9147315 chr12:9147302-9147315 chr12:9147294-9147307 chr12:9147280-9147293 chr12:9147303-9147314
26	CHD2	chr12:9149330-9149735	GM12878	blood:	n/a	n/a
27	CTCF	chr12:9149410-9149590	GM12878	blood:	n/a	n/a
28	CTCF	chr12:9142635-9142730	K562	blood:	n/a	n/a
29	CTCF	chr12:9165080-9165230	SAEC	small airway:	n/a	n/a
30	CTCF	chr12:9164640-9164790	GM12867	blood:	n/a	n/a
31	CTCF	chr12:9171538-9171593	LNCaP	prostate:	n/a	n/a
32	CTCF	chr12:9166343-9166378	LNCaP	prostate:	n/a	n/a
33	CUX1	chr12:9149209-9149723	GM12878	blood:	n/a	n/a
34	E2F4	chr12:9141925-9141936	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr12:9149286-9149724	GM12878	blood:	n/a	n/a
36	EBF1	chr12:9137821-9137997	GM12878	blood:	n/a	n/a
37	EBF1	chr12:9149319-9149856	GM12878	blood:	n/a	n/a
38	ELK1	chr12:9149415-9149646	GM12878	blood:	n/a	n/a
39	EP300	chr12:9149224-9149699	GM12878	blood:	n/a	n/a
40	EP300	chr12:9149206-9150021	GM12878	blood:	n/a	n/a
41	EP300	chr12:9149956-9150097	GM12878	blood:	n/a	n/a
42	EP300	chr12:9149247-9149715	GM12878	blood:	n/a	n/a
43	EP300	chr12:9149270-9149970	GM12878	blood:	n/a	n/a
44	FAM48A	chr12:9152150-9152318	GM12878	blood:	n/a	n/a
45	FOS	chr12:9149323-9149987	HUVEC	blood vessel:	n/a	chr12:9149517-9149524 chr12:9149514-9149525 chr12:9149920-9149934
46	FOS	chr12:9149367-9149623	MCF10A-Er-Src	breast:	n/a	chr12:9149517-9149524 chr12:9149514-9149525
47	FOS	chr12:9149424-9149624	MCF10A-Er-Src	breast:	n/a	chr12:9149517-9149524 chr12:9149514-9149525
48	FOS	chr12:9149368-9149585	MCF10A-Er-Src	breast:	n/a	chr12:9149517-9149524 chr12:9149514-9149525
49	FOSL1	chr12:9149388-9149728	K562	blood:	n/a	chr12:9149517-9149524
50	FOSL2	chr12:9149271-9149652	SK-N-SH	brain:	n/a	chr12:9149517-9149524

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:9141740-9141790	HUVEC	blood vessel:	n/a
2	chr12:9162872-9162922	GM12891	blood:	n/a
3	chr12:9162872-9162922	AG04449	skin:	fetal
4	chr12:9162872-9162922	Hepatocyte	liver:	n/a
5	chr12:9141740-9141790	ECC-1	luminal epithelium:	n/a
6	chr12:9141775-9141825	NB4	blood:	n/a
7	chr12:9142341-9142391	HL-60	blood:	n/a
8	chr12:9141775-9141825	AoSMC	blood vessel:	n/a
9	chr12:9162872-9162922	SK-N-SH	brain:	n/a
10	chr12:9142341-9142391	BJ	skin:	n/a
11	chr12:9142341-9142391	SK-N-SH	brain:	n/a
12	chr12:9162872-9162922	RPTEC	kidney:	n/a
13	chr12:9142341-9142391	BE2_C	brain:	n/a
14	chr12:9162872-9162922	HCF	heart:	n/a
15	chr12:9141775-9141825	A549	lung:	n/a
16	chr12:9142341-9142391	HMEC	breast:	n/a
17	chr12:9141775-9141825	LNCaP	prostate:	n/a
18	chr12:9141740-9141790	HCF	heart:	n/a
19	chr12:9141740-9141790	AG09309	skin:	n/a
20	chr12:9141775-9141825	U87	brain:	n/a
21	chr12:9141775-9141825	SKMC	muscle:	n/a
22	chr12:9141775-9141825	GM12891	blood:	n/a
23	chr12:9141775-9141825	HMEC	breast:	n/a
24	chr12:9142341-9142391	AoSMC	blood vessel:	n/a
25	chr12:9142341-9142391	NT2-D1	testis:	n/a
26	chr12:9162872-9162922	NHBE	bronchial:	n/a
27	chr12:9141740-9141790	HIPEpiC	eye:	n/a
28	chr12:9162872-9162922	HRE	kidney:	n/a
29	chr12:9141740-9141790	PFSK-1	brain:	n/a
30	chr12:9141740-9141790	BJ	skin:	n/a
31	chr12:9142341-9142391	Hepatocyte	liver:	n/a
32	chr12:9141740-9141790	AG04450	lung:	fetal
33	chr12:9162872-9162922	HNPCEpiC	eye:	n/a
34	chr12:9141775-9141825	HCPEpiC	choroid plexus:	n/a
35	chr12:9141775-9141825	Hela-S3	cervix:	n/a
36	chr12:9162872-9162922	Jurkat	blood:	n/a
37	chr12:9141740-9141790	GM06990	blood:	n/a
38	chr12:9142341-9142391	AG10803	skin:	n/a
39	chr12:9141740-9141790	Caco-2	colon:	n/a
40	chr12:9141740-9141790	CMK	blood:	n/a
41	chr12:9141775-9141825	HEK293	kidney:	embryo
42	chr12:9142341-9142391	RPTEC	kidney:	n/a
43	chr12:9141740-9141790	HPAEpiC	pulmonary alveolar:	n/a
44	chr12:9141740-9141790	NHBE	bronchial:	n/a
45	chr12:9141775-9141825	HAEpiC	amniotic membrane:	n/a
46	chr12:9141775-9141825	NH-A	brain:	n/a
47	chr12:9141775-9141825	HCT-116	colon:	n/a
48	chr12:9142341-9142391	AG04449	skin:	fetal
49	chr12:9142341-9142391	NB4	blood:	n/a
50	chr12:9141740-9141790	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:9157659..9159439-chr12:9161450..9164436,2	K562	blood:
2	chr12:9100812..9102729-chr12:9160116..9162568,2	MCF-7	breast:
3	chr12:9157659..9159439-chr12:9161450..9164436,2	K562	blood:
4	chr12:9101626..9103314-chr12:9176948..9179841,2	MCF-7	breast:
5	chr12:9101350..9103616-chr12:9157581..9159140,2	K562	blood:
6	chr12:9064573..9067189-chr12:9176082..9178403,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-M6PR-1	chr12:9140908-9141026	ENSG00000257105.1
2	lnc-M6PR-1	chr12:9139771-9140077	ENSG00000257105.1
3	lnc-PHC1-3	chr12:9162022-9162659	NONHSAT026377
4	lnc-PHC1-3	chr12:9144802-9144906	NONHSAT026376
5	lnc-PHC1-3	chr12:9161571-9161671	NONHSAT026377
6	lnc-PHC1-3	chr12:9142808-9142941	NONHSAT026378
7	lnc-M6PR-1	chr12:9149093-9149162	ENSG00000257105.1
8	lnc-PHC1-3	chr12:9162022-9162112	NONHSAT026376
9	lnc-PHC1-3	chr12:9161571-9161671	NONHSAT026376
10	lnc-PHC1-3	chr12:9144802-9144888	NONHSAT026378

Variant related genes	Relation type
ENSG00000257105	TF binding region
KLRG1	TF binding region
ENSG00000257105	CpG island
KLRG1	CpG island
ENSG00000003056	chromatin interactions
ENSG00000111752	chromatin interactions
ENSG00000139187	chromatin interactions

Extended variants
information (count: 910 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:910 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2110192	chr12:9136351-9136352	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143879136	chr12:9136411-9136412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367849246	chr12:9136425-9136426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35246321	chr12:9136483-9136484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1121401	chr12:9136622-9136623	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs184937813	chr12:9136645-9136646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368178786	chr12:9136657-9136658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188971491	chr12:9136706-9136707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534339425	chr12:9136804-9136805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs207472647	chr12:9136825-9136826	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs148600240	chr12:9136892-9136893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs554264707	chr12:9136974-9136975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141872480	chr12:9137034-9137035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs12820395	chr12:9137096-9137097	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs181651951	chr12:9137143-9137144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146261727	chr12:9137244-9137245	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12423765	chr12:9137278-9137279	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs7132930	chr12:9137288-9137289	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs372064519	chr12:9137296-9137297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs185644291	chr12:9137322-9137323	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs191301310	chr12:9137383-9137384	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568723746	chr12:9137456-9137457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139392389	chr12:9137619-9137620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs80244042	chr12:9137768-9137769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs398076406	chr12:9137778-9137779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35689537	chr12:9137779-9137780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs199954060	chr12:9137780-9137781	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs74902858	chr12:9137852-9137853	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs398076407	chr12:9137860-9137861	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs397851218	chr12:9137861-9137862	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs144111387	chr12:9137876-9137877	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs35366093	chr12:9138106-9138107	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2080116	chr12:9138183-9138184	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs55939602	chr12:9138239-9138240	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs180888384	chr12:9138314-9138315	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2080117	chr12:9138341-9138342	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs150982797	chr12:9138371-9138372	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532146808	chr12:9138393-9138394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs377237996	chr12:9138467-9138468	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs28769384	chr12:9138523-9138524	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs12426857	chr12:9138530-9138531	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs185787628	chr12:9138552-9138553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs191035712	chr12:9138599-9138600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs149787681	chr12:9138675-9138676	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs145720907	chr12:9138696-9138697	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs563092775	chr12:9138744-9138745	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs201891696	chr12:9138774-9138775	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs114643277	chr12:9138893-9138894	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs10842660	chr12:9138897-9138898	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs548502285	chr12:9138921-9138922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Epilepsy	21858020	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
craniofacial dysmorphism	21918468	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Alzheimer''s disease	17160897	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:571 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:9133200-9139800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr12:9133600-9138200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr12:9133600-9140600	Weak transcription	Spleen	Spleen
4	chr12:9133800-9139000	Weak transcription	Primary T cells from cord blood	blood
5	chr12:9133800-9164600	Weak transcription	Psoas Muscle	Psoas
6	chr12:9133800-9170200	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr12:9135000-9138400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr12:9135800-9141800	Weak transcription	Primary B cells from cord blood	blood
9	chr12:9136200-9136400	Enhancers	Primary T killer memory cells from peripheral blood	blood
10	chr12:9136400-9137600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr12:9136800-9137400	Enhancers	Primary T cells fromperipheralblood	blood
12	chr12:9136800-9137400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr12:9137400-9137800	Weak transcription	Primary T cells fromperipheralblood	blood
14	chr12:9137400-9137800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr12:9137600-9139800	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chr12:9137600-9139800	Enhancers	Primary T killer memory cells from peripheral blood	blood
17	chr12:9137600-9142000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr12:9137800-9141800	Enhancers	Primary T cells fromperipheralblood	blood
19	chr12:9137800-9141800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr12:9137800-9142200	Enhancers	Primary hematopoietic stem cells short term culture	blood
21	chr12:9138000-9140200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr12:9138000-9142200	Enhancers	Primary T helper cells fromperipheralblood	blood
23	chr12:9138000-9143000	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr12:9138200-9138400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr12:9138400-9138600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr12:9138400-9138600	Enhancers	Lung	lung
27	chr12:9138400-9139800	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr12:9138400-9140200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
29	chr12:9138400-9140200	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr12:9138400-9142200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr12:9138600-9142200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr12:9139000-9142200	Enhancers	Primary T cells from cord blood	blood
33	chr12:9139200-9139600	Enhancers	Fetal Thymus	thymus
34	chr12:9139200-9140000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr12:9139200-9142200	Enhancers	Primary hematopoietic stem cells	blood
36	chr12:9139200-9142200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr12:9139200-9144400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
38	chr12:9139600-9140000	Enhancers	Duodenum Mucosa	Duodenum
39	chr12:9139600-9144600	Weak transcription	Fetal Thymus	thymus
40	chr12:9139800-9140000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr12:9139800-9140600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
42	chr12:9139800-9140800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr12:9139800-9141000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
44	chr12:9139800-9142200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr12:9139800-9142200	Enhancers	Adipose Nuclei	Adipose
46	chr12:9139800-9142200	Enhancers	HUVEC	blood vessel
47	chr12:9139800-9143200	Enhancers	GM12878-XiMat	blood
48	chr12:9140000-9140200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chr12:9140000-9140400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr12:9140000-9140400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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