Variant report

Variant	esv2757492
Chromosome Location	chr12:25233781-25252178
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	ARID3A	chr12:25235795-25235843	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:25249026-25249147	HepG2	liver:	n/a	chr12:25249113-25249124
3	CEBPB	chr12:25248961-25249271	A549	lung:	n/a	chr12:25249113-25249124
4	CTCF	chr12:25237840-25237990	GM12871	blood:	n/a	n/a
5	CTCF	chr12:25237960-25238110	GM06990	blood:	n/a	n/a
6	CTCF	chr12:25237900-25238050	HEK293	kidney:	n/a	n/a
7	CTCF	chr12:25248880-25249030	AG04450	lung:	n/a	n/a
8	CTCF	chr12:25244600-25244750	Caco-2	colon:	n/a	n/a
9	CTCF	chr12:25237880-25238030	SK-N-SH_RA	brain:	n/a	n/a
10	CTCF	chr12:25237900-25238050	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr12:25248920-25249070	HMF	breast:	n/a	n/a
12	CTCF	chr12:25237800-25237950	HepG2	liver:	n/a	n/a
13	CTCF	chr12:25237900-25238050	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr12:25237832-25238028	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr12:25248940-25249090	GM12872	blood:	n/a	n/a
16	CTCF	chr12:25237819-25238069	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr12:25237807-25238116	H1-hESC	embryonic stem cell:	n/a	n/a
18	E2F4	chr12:25242775-25242951	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr12:25242675-25243014	MCF10A-Er-Src	breast:	n/a	chr12:25242840-25242848
20	FOS	chr12:25243476-25243869	MCF10A-Er-Src	breast:	n/a	chr12:25243709-25243716 chr12:25243711-25243720 chr12:25243712-25243719 chr12:25243711-25243719 chr12:25243710-25243720 chr12:25243709-25243721
21	FOS	chr12:25243494-25243888	MCF10A-Er-Src	breast:	n/a	chr12:25243709-25243716 chr12:25243711-25243720 chr12:25243712-25243719 chr12:25243711-25243719 chr12:25243710-25243720 chr12:25243709-25243721
22	FOS	chr12:25242675-25243030	MCF10A-Er-Src	breast:	n/a	chr12:25242840-25242848
23	FOS	chr12:25242679-25243023	MCF10A-Er-Src	breast:	n/a	chr12:25242840-25242848
24	FOS	chr12:25243459-25243849	MCF10A-Er-Src	breast:	n/a	chr12:25243709-25243716 chr12:25243711-25243720 chr12:25243712-25243719 chr12:25243711-25243719 chr12:25243710-25243720 chr12:25243709-25243721
25	FOS	chr12:25243540-25243819	MCF10A-Er-Src	breast:	n/a	chr12:25243709-25243716 chr12:25243711-25243720 chr12:25243712-25243719 chr12:25243711-25243719 chr12:25243710-25243720 chr12:25243709-25243721
26	FOSL2	chr12:25243550-25243950	SK-N-SH	brain:	n/a	chr12:25243709-25243716 chr12:25243711-25243720 chr12:25243712-25243719 chr12:25243711-25243719 chr12:25243710-25243720 chr12:25243709-25243721
27	FOXA1	chr12:25235640-25235877	HepG2	liver:	n/a	chr12:25235832-25235844
28	FOXA1	chr12:25235555-25235961	HepG2	liver:	n/a	chr12:25235832-25235844
29	FOXA1	chr12:25235547-25235940	HepG2	liver:	n/a	chr12:25235832-25235844
30	FOXA2	chr12:25235651-25235867	HepG2	liver:	n/a	chr12:25235832-25235844
31	FOXA2	chr12:25235389-25236210	HepG2	liver:	n/a	chr12:25235832-25235844
32	JUND	chr12:25243639-25243856	HepG2	liver:	n/a	chr12:25243709-25243716 chr12:25243711-25243720 chr12:25243712-25243719 chr12:25243711-25243719 chr12:25243709-25243720 chr12:25243710-25243720 chr12:25243709-25243721
33	JUND	chr12:25243611-25243616	H1-hESC	embryonic stem cell:	n/a	n/a
34	MAFF	chr12:25252019-25252307	K562	blood:	n/a	chr12:25252125-25252143
35	MAFF	chr12:25251973-25252235	HepG2	liver:	n/a	chr12:25252125-25252143
36	MAFK	chr12:25251976-25252308	IMR90	lung:	n/a	chr12:25252127-25252142
37	MAFK	chr12:25242815-25242928	HepG2	liver:	n/a	chr12:25242867-25242881 chr12:25242868-25242879 chr12:25242869-25242880 chr12:25242869-25242880 chr12:25242864-25242880
38	MAFK	chr12:25251978-25252289	HepG2	liver:	n/a	chr12:25252127-25252142
39	MAFK	chr12:25252010-25252286	K562	blood:	n/a	chr12:25252127-25252142
40	MAFK	chr12:25251966-25252314	HepG2	liver:	n/a	chr12:25252127-25252142
41	MYC	chr12:25242759-25242980	MCF10A-Er-Src	breast:	n/a	n/a
42	MYC	chr12:25242719-25242929	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr12:25250709-25251594	GM12878	blood:	n/a	n/a
44	POLR2A	chr12:25235775-25235975	MCF10A-Er-Src	breast:	n/a	n/a
45	POLR2A	chr12:25244842-25244967	K562	blood:	n/a	n/a
46	POLR2A	chr12:25239028-25240217	GM12878	blood:	n/a	n/a
47	POLR2A	chr12:25243006-25243443	GM12878	blood:	n/a	n/a
48	POLR2A	chr12:25238098-25238647	GM12878	blood:	n/a	n/a
49	POLR2A	chr12:25237736-25238262	GM12878	blood:	n/a	n/a
50	POLR2A	chr12:25238184-25238605	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:25246439-25246489	HRPEpiC	eye:	n/a
2	chr12:25246439-25246489	A549	lung:	n/a
3	chr12:25246439-25246489	RPTEC	kidney:	n/a
4	chr12:25246439-25246489	NHDF-neo	bronchial:	n/a
5	chr12:25246439-25246489	HL-60	blood:	n/a
6	chr12:25246439-25246489	PANC-1	pancreas:	n/a
7	chr12:25246439-25246489	HAEpiC	amniotic membrane:	n/a
8	chr12:25246439-25246489	ProgFib	skin:	n/a
9	chr12:25246439-25246489	H1-hESC	embryonic stem cell:	embryo
10	chr12:25246439-25246489	NB4	blood:	n/a
11	chr12:25246439-25246489	SKMC	muscle:	n/a
12	chr12:25246439-25246489	AG10803	skin:	n/a
13	chr12:25246439-25246489	K562	blood:	n/a
14	chr12:25246439-25246489	ECC-1	luminal epithelium:	n/a
15	chr12:25246439-25246489	U87	brain:	n/a
16	chr12:25246439-25246489	CMK	blood:	n/a
17	chr12:25246439-25246489	HCF	heart:	n/a
18	chr12:25246439-25246489	Caco-2	colon:	n/a
19	chr12:25246439-25246489	SAEC	small airway:	n/a
20	chr12:25246439-25246489	HRCEpiC	kidney:	n/a
21	chr12:25246439-25246489	T-47D	breast:	n/a
22	chr12:25246439-25246489	NH-A	brain:	n/a
23	chr12:25246439-25246489	ovcar-3	ovarian:	n/a
24	chr12:25246439-25246489	AG09319	gingival:	n/a
25	chr12:25246439-25246489	HIPEpiC	eye:	n/a
26	chr12:25246439-25246489	NT2-D1	testis:	n/a
27	chr12:25246439-25246489	HCPEpiC	choroid plexus:	n/a
28	chr12:25246439-25246489	PrEC	prostate:	n/a
29	chr12:25246439-25246489	Hepatocyte	liver:	n/a
30	chr12:25246439-25246489	IMR90	lung:	fetal
31	chr12:25246439-25246489	NHBE	bronchial:	n/a
32	chr12:25246439-25246489	GM12892	blood:	n/a
33	chr12:25246439-25246489	HUVEC	blood vessel:	n/a
34	chr12:25246439-25246489	BJ	skin:	n/a
35	chr12:25246439-25246489	PFSK-1	brain:	n/a
36	chr12:25246439-25246489	HNPCEpiC	eye:	n/a
37	chr12:25246439-25246489	HEK293	kidney:	embryo
38	chr12:25246439-25246489	HCT-116	colon:	n/a
39	chr12:25246439-25246489	AG04450	lung:	fetal
40	chr12:25246439-25246489	AoSMC	blood vessel:	n/a
41	chr12:25246439-25246489	HepG2	liver:	n/a
42	chr12:25246439-25246489	SK-N-SH_RA	brain:	n/a
43	chr12:25246439-25246489	GM12878	blood:	n/a
44	chr12:25246439-25246489	AG04449	skin:	fetal
45	chr12:25246439-25246489	GM12891	blood:	n/a
46	chr12:25246439-25246489	HCM	heart:	n/a
47	chr12:25246439-25246489	Jurkat	blood:	n/a
48	chr12:25246439-25246489	GM06990	blood:	n/a
49	chr12:25246439-25246489	GM19239	blood:	n/a
50	chr12:25246439-25246489	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:25232452..25234531-chr12:25239537..25241668,2	MCF-7	breast:
2	chr12:25232452..25234531-chr12:25239537..25241668,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASC1-2	chr12:25245649-25246834	NONHSAT027340

Variant related genes	Relation type
LRMP	TF binding region
ENSG00000258546	TF binding region
LRMP	CpG island
ENSG00000258546	CpG island

Extended variants
information (count: 730 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:730 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7976028	chr12:25233781-25233782	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184960316	chr12:25233782-25233783	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188201880	chr12:25233800-25233801	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs73284742	chr12:25233810-25233811	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs541322467	chr12:25233814-25233815	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144198242	chr12:25233829-25233830	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs7976264	chr12:25233857-25233858	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs192274617	chr12:25233872-25233873	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs151075671	chr12:25233893-25233894	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184429669	chr12:25233914-25233915	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552699145	chr12:25233928-25233929	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76634422	chr12:25233950-25233951	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534862965	chr12:25233959-25233960	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547288001	chr12:25233960-25233961	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568631595	chr12:25233980-25233981	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs6487452	chr12:25233987-25233988	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs371583476	chr12:25233991-25233992	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs554301930	chr12:25234011-25234012	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs6487453	chr12:25234020-25234021	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs112550529	chr12:25234046-25234047	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558184947	chr12:25234062-25234063	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10629974	chr12:25234085-25234086	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545865771	chr12:25234086-25234087	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs72363605	chr12:25234087-25234088	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542271669	chr12:25234089-25234090	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs397713152	chr12:25234099-25234100	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs370023741	chr12:25234100-25234101	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373129847	chr12:25234101-25234102	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7315058	chr12:25234122-25234123	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12230333	chr12:25234123-25234124	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs540837634	chr12:25234193-25234194	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs559624483	chr12:25234199-25234200	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574673699	chr12:25234215-25234216	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs368405348	chr12:25234234-25234235	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542092972	chr12:25234264-25234265	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563717452	chr12:25234267-25234268	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs528490332	chr12:25234276-25234277	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150208372	chr12:25234290-25234291	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12314451	chr12:25234330-25234331	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs564535214	chr12:25234354-25234355	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553246872	chr12:25234392-25234393	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112460904	chr12:25234393-25234394	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568622681	chr12:25234471-25234472	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs368601106	chr12:25234493-25234494	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147121382	chr12:25234513-25234514	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372133743	chr12:25234559-25234560	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550859703	chr12:25234593-25234594	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs569313795	chr12:25234625-25234626	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs577810649	chr12:25234627-25234628	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs12321656	chr12:25234646-25234647	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Malignant germ cell tumour	17285132	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Myxofibrosarcoma	16751306	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Acute myeloid leukemia	16864856	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	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
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17133270	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	16397240	CNVD
Neurodevelopmental disorder	22521361	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	21509527	CNVD
Autism	22102821	CNVD
Follicular lymphoma	18703704	CNVD
Lung cancer	18438408	CNVD
Lung cancer	21911935	CNVD
Breast cancer	22048815	CNVD
Malignant peripheral nerve sheath tumor	19844265	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Heart disease	21282601	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Gastric cancer	24379144	CNVD
Gastric cancer	19545448	CNVD
Lung cancer	20031968	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung adenocarcinoma	19826477	CNVD
Lung cancer	19525976	CNVD
Lung cancer	19826477	CNVD
Non-small cell lung cancer	19451690	CNVD
Non-small cell lung cancer	17504988	CNVD
Bipolar disorder	19114987	CNVD
Lung cancer	19671679	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
Lung cancer	21569311	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung adenocarcinoma	17982442	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17699850	CNVD
Ovarian cancer	17699850	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164920	CNVD
Gastric cancer	22315472	CNVD
Adenocarcinoma	19001599	CNVD
Non-small cell lung cancer	19001599	CNVD
Pancreatic cancer	20981101	CNVD
Squamous cell cancer	19001599	CNVD
Acute lymphoblastic leukemia	21680795	CNVD
Lung adenocarcinoma	18379350	CNVD
Lung cancer	18379350	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic cancer	21811562	CNVD

Chromatin state (count:236 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:25209400-25264400	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr12:25210000-25262800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr12:25212000-25250800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr12:25214400-25245600	Weak transcription	Ovary	ovary
5	chr12:25214400-25251800	Weak transcription	Fetal Intestine Large	intestine
6	chr12:25215000-25265000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr12:25218600-25239200	Weak transcription	Fetal Intestine Small	intestine
8	chr12:25221600-25235800	Weak transcription	Liver	Liver
9	chr12:25222400-25236000	Weak transcription	Adipose Nuclei	Adipose
10	chr12:25223000-25238000	Weak transcription	Spleen	Spleen
11	chr12:25223400-25235400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr12:25224600-25241600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr12:25225400-25237800	Weak transcription	Lung	lung
14	chr12:25227400-25251000	Weak transcription	Pancreas	Pancrea
15	chr12:25228400-25241200	Weak transcription	Stomach Mucosa	stomach
16	chr12:25228800-25236200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr12:25229000-25237800	Weak transcription	Esophagus	oesophagus
18	chr12:25229000-25253000	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr12:25229200-25241400	Strong transcription	Primary B cells from peripheral blood	blood
20	chr12:25230000-25264600	Strong transcription	Fetal Thymus	thymus
21	chr12:25230600-25235200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:25230600-25240600	Strong transcription	Primary hematopoietic stem cells	blood
23	chr12:25230600-25240600	Strong transcription	GM12878-XiMat	blood
24	chr12:25231600-25237800	Weak transcription	Brain Substantia Nigra	brain
25	chr12:25231600-25240400	Strong transcription	Thymus	Thymus
26	chr12:25231800-25246000	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr12:25232000-25234200	Strong transcription	Primary T helper naive cells from peripheral blood	blood
28	chr12:25232000-25240600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr12:25232000-25241200	Strong transcription	Primary T helper cells PMA-I stimulated	--
30	chr12:25232000-25241400	Strong transcription	Primary T helper cells fromperipheralblood	blood
31	chr12:25232000-25241600	Strong transcription	Dnd41	blood
32	chr12:25232000-25247600	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr12:25232200-25233800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr12:25232200-25234000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr12:25232200-25235000	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr12:25232200-25235200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr12:25232200-25241000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr12:25232200-25263600	Strong transcription	Primary neutrophils fromperipheralblood	blood
39	chr12:25232600-25235400	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr12:25232800-25234000	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
41	chr12:25233200-25233800	Weak transcription	Primary B cells from cord blood	blood
42	chr12:25233200-25242200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
43	chr12:25233400-25234800	Weak transcription	Primary T cells from cord blood	blood
44	chr12:25233800-25238400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr12:25233800-25242200	Strong transcription	Primary B cells from cord blood	blood
46	chr12:25234000-25236200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr12:25234000-25246800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr12:25234200-25236200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
49	chr12:25234800-25247000	Strong transcription	Primary T cells from cord blood	blood
50	chr12:25235000-25242000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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