Variant report

Variant	esv2758939
Chromosome Location	chr1:72742396-72886813
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	chr1:72750376-72750736	GM12878	blood:	n/a	n/a
2	ATF2	chr1:72750319-72750713	GM12878	blood:	n/a	n/a
3	BACH1	chr1:72748894-72749768	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr1:72748062-72748227	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr1:72750317-72750778	GM12878	blood:	n/a	n/a
6	BATF	chr1:72750337-72750724	GM12878	blood:	n/a	n/a
7	BRCA1	chr1:72748195-72748394	H1-hESC	embryonic stem cell:	n/a	n/a
8	BRCA1	chr1:72750323-72751066	Hela-S3	cervix:	n/a	n/a
9	CCNT2	chr1:72880174-72880370	K562	blood:	n/a	n/a
10	CEBPB	chr1:72878992-72879316	HepG2	liver:	n/a	chr1:72879141-72879154 chr1:72879142-72879153 chr1:72879143-72879152
11	CEBPB	chr1:72863402-72863885	ECC-1	luminal epithelium:	n/a	chr1:72863747-72863760 chr1:72863625-72863634 chr1:72863624-72863635
12	CEBPB	chr1:72818201-72818500	HepG2	liver:	n/a	chr1:72818339-72818350
13	CEBPB	chr1:72832136-72832518	HepG2	liver:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
14	CEBPB	chr1:72832175-72832440	HepG2	liver:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
15	CEBPB	chr1:72863451-72863893	Hela-S3	cervix:	n/a	chr1:72863747-72863760 chr1:72863625-72863634 chr1:72863624-72863635
16	CEBPB	chr1:72748554-72748740	HepG2	liver:	n/a	n/a
17	CEBPB	chr1:72832124-72832535	HepG2	liver:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
18	CEBPB	chr1:72812174-72812494	HepG2	liver:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
19	CEBPB	chr1:72812157-72812489	Hela-S3	cervix:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
20	CEBPB	chr1:72879047-72879244	K562	blood:	n/a	chr1:72879141-72879154 chr1:72879142-72879153 chr1:72879143-72879152
21	CEBPB	chr1:72814338-72814482	A549	lung:	n/a	n/a
22	CEBPB	chr1:72750450-72750705	HepG2	liver:	n/a	chr1:72750584-72750595 chr1:72750585-72750596
23	CEBPB	chr1:72832060-72832541	ECC-1	luminal epithelium:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
24	CEBPB	chr1:72748450-72748905	IMR90	lung:	n/a	chr1:72748863-72748876
25	CEBPB	chr1:72812222-72812489	A549	lung:	n/a	chr1:72812301-72812312 chr1:72812343-72812354
26	CEBPB	chr1:72832052-72832580	ECC-1	luminal epithelium:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
27	CEBPB	chr1:72749367-72749678	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr1:72878983-72879304	IMR90	lung:	n/a	chr1:72879141-72879154 chr1:72879142-72879153 chr1:72879143-72879152
29	CEBPB	chr1:72750011-72750992	IMR90	lung:	n/a	chr1:72750584-72750595 chr1:72750585-72750596 chr1:72750147-72750158
30	CEBPB	chr1:72863538-72863792	H1-hESC	embryonic stem cell:	n/a	chr1:72863747-72863760 chr1:72863625-72863634 chr1:72863624-72863635
31	CEBPB	chr1:72832103-72832583	Hela-S3	cervix:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
32	CEBPB	chr1:72864339-72864539	A549	lung:	n/a	n/a
33	CEBPB	chr1:72749276-72749833	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr1:72878418-72878650	HepG2	liver:	n/a	chr1:72878524-72878535
35	CEBPB	chr1:72748537-72748783	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr1:72832149-72832526	IMR90	lung:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
37	CEBPB	chr1:72832224-72832511	A549	lung:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
38	CEBPB	chr1:72755092-72755159	HepG2	liver:	n/a	chr1:72755122-72755131 chr1:72755120-72755131
39	CEBPB	chr1:72864245-72864573	IMR90	lung:	n/a	n/a
40	CEBPB	chr1:72864290-72864529	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:72878986-72879303	Hela-S3	cervix:	n/a	chr1:72879141-72879154 chr1:72879142-72879153 chr1:72879143-72879152
42	CEBPB	chr1:72863442-72863818	IMR90	lung:	n/a	chr1:72863747-72863760 chr1:72863625-72863634 chr1:72863624-72863635
43	CEBPB	chr1:72814314-72814570	IMR90	lung:	n/a	n/a
44	CEBPB	chr1:72879000-72879263	H1-hESC	embryonic stem cell:	n/a	chr1:72879141-72879154 chr1:72879142-72879153 chr1:72879143-72879152
45	CEBPB	chr1:72746375-72746702	IMR90	lung:	n/a	n/a
46	CEBPB	chr1:72762099-72762426	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr1:72823103-72823425	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr1:72748420-72750957	Hela-S3	cervix:	n/a	chr1:72750584-72750595 chr1:72748863-72748876 chr1:72750585-72750596 chr1:72750147-72750158
49	CEBPB	chr1:72832206-72832459	MCF-7	breast:	n/a	chr1:72832336-72832347 chr1:72832334-72832345 chr1:72832336-72832345
50	CEBPB	chr1:72818172-72818482	IMR90	lung:	n/a	chr1:72818339-72818350

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:72749275-72749325	GM12878	blood:	n/a
2	chr1:72749275-72749325	GM12878	blood:	n/a
3	chr1:72885180-72885230	HRE	kidney:	n/a
4	chr1:72748610-72748660	AG04450	lung:	fetal
5	chr1:72749581-72749631	HCF	heart:	n/a
6	chr1:72748389-72748439	BJ	skin:	n/a
7	chr1:72749735-72749785	A549	lung:	n/a
8	chr1:72747802-72747852	BJ	skin:	n/a
9	chr1:72750241-72750291	HepG2	liver:	n/a
10	chr1:72750671-72750721	NB4	blood:	n/a
11	chr1:72749880-72749930	HRCEpiC	kidney:	n/a
12	chr1:72747802-72747852	HRCEpiC	kidney:	n/a
13	chr1:72753076-72753126	GM12892	blood:	n/a
14	chr1:72748610-72748660	H1-hESC	embryonic stem cell:	embryo
15	chr1:72748610-72748660	HIPEpiC	eye:	n/a
16	chr1:72750124-72750174	ovcar-3	ovarian:	n/a
17	chr1:72885180-72885230	NHBE	bronchial:	n/a
18	chr1:72749735-72749785	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:72885079-72885129	AG09319	gingival:	n/a
20	chr1:72748610-72748660	PANC-1	pancreas:	n/a
21	chr1:72749735-72749785	AG10803	skin:	n/a
22	chr1:72749015-72749065	A549	lung:	n/a
23	chr1:72748124-72748174	T-47D	breast:	n/a
24	chr1:72749735-72749785	Jurkat	blood:	n/a
25	chr1:72748124-72748174	SK-N-SH	brain:	n/a
26	chr1:72750241-72750291	HNPCEpiC	eye:	n/a
27	chr1:72748124-72748174	HCF	heart:	n/a
28	chr1:72749735-72749785	PrEC	prostate:	n/a
29	chr1:72747802-72747852	SKMC	muscle:	n/a
30	chr1:72750502-72750552	BE2_C	brain:	n/a
31	chr1:72749275-72749325	U87	brain:	n/a
32	chr1:72884990-72885040	AG10803	skin:	n/a
33	chr1:72749015-72749065	HMEC	breast:	n/a
34	chr1:72747802-72747852	HUVEC	blood vessel:	n/a
35	chr1:72885079-72885129	GM19239	blood:	n/a
36	chr1:72747802-72747852	HEK293	kidney:	embryo
37	chr1:72748607-72748657	HCF	heart:	n/a
38	chr1:72748139-72748189	ECC-1	luminal epithelium:	n/a
39	chr1:72885180-72885230	HepG2	liver:	n/a
40	chr1:72884990-72885040	HCM	heart:	n/a
41	chr1:72749735-72749785	HepG2	liver:	n/a
42	chr1:72884990-72885040	GM12878	blood:	n/a
43	chr1:72747802-72747852	IMR90	lung:	fetal
44	chr1:72885079-72885129	AG04449	skin:	fetal
45	chr1:72748610-72748660	AG09309	skin:	n/a
46	chr1:72884990-72885040	Jurkat	blood:	n/a
47	chr1:72884990-72885040	ECC-1	luminal epithelium:	n/a
48	chr1:72748124-72748174	Jurkat	blood:	n/a
49	chr1:72885180-72885230	SK-N-SH_RA	brain:	n/a
50	chr1:72749735-72749785	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:72748974..72749649-chr17:56420933..56421808,2	NB4	blood:
2	chr1:72748841..72749750-chr13:47370740..47371446,2	NB4	blood:
3	chr1:72863619..72864264-chr11:65396606..65397388,2	MCF-7	breast:
4	chr1:72752065..72752600-chr8:87527466..87528155,2	MCF-7	breast:

Variant related genes	Relation type
RPL31P12	TF binding region
NEGR1	TF binding region
RPL31P12	CpG island
NEGR1	CpG island
ENSG00000139684	chromatin interactions

Extended variants
information (count: 1652 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1652 , 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	rs562301421	chr1:72742417-72742418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs543085395	chr1:72742435-72742436	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562566334	chr1:72742494-72742495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs531418311	chr1:72742504-72742505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141574529	chr1:72742583-72742584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184234020	chr1:72742590-72742591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147175062	chr1:72742610-72742611	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527576040	chr1:72742611-72742612	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547116785	chr1:72742632-72742633	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567239649	chr1:72742652-72742653	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376738766	chr1:72742685-72742686	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs529781346	chr1:72742687-72742688	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549873066	chr1:72742715-72742716	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs569737130	chr1:72742729-72742730	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538450858	chr1:72742755-72742756	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369473058	chr1:72742765-72742766	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs111349598	chr1:72742773-72742774	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115092312	chr1:72742783-72742784	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs193188737	chr1:72742848-72742849	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs115304318	chr1:72742852-72742853	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs542620319	chr1:72742942-72742943	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs17092532	chr1:72742962-72742963	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs547596451	chr1:72743110-72743111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576077580	chr1:72743115-72743116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373676974	chr1:72743141-72743142	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140096797	chr1:72743204-72743205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs111589182	chr1:72743206-72743207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544847662	chr1:72743220-72743221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs184656815	chr1:72743234-72743235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs527613239	chr1:72743317-72743318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140259114	chr1:72743372-72743373	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs200047719	chr1:72743375-72743376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560998856	chr1:72743403-72743404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529710808	chr1:72743414-72743415	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs144224593	chr1:72743471-72743472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs368341295	chr1:72743487-72743488	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569770260	chr1:72743539-72743540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375185997	chr1:72743569-72743570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369316354	chr1:72743594-72743595	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147837609	chr1:72743703-72743704	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549074576	chr1:72743745-72743746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs10493497	chr1:72743768-72743769	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs114832991	chr1:72743790-72743791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567822541	chr1:72743791-72743792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188609774	chr1:72743824-72743825	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556278394	chr1:72743831-72743832	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs576168082	chr1:72743892-72743893	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538729420	chr1:72743908-72743909	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs558360747	chr1:72743930-72743931	Weak transcription Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs1194260	chr1:72743949-72743950	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
abnormal development	18461090	CNVD
Ewing''s sarcoma	17952124	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Poland''s syndrome	22110015	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Effusion lymphoma	18079361	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:801 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:72737600-72744200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr1:72738000-72744200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr1:72738000-72745800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr1:72739000-72744400	Weak transcription	Rectal Smooth Muscle	rectum
5	chr1:72741800-72742800	Weak transcription	Brain Angular Gyrus	brain
6	chr1:72742200-72744000	Enhancers	Colon Smooth Muscle	Colon
7	chr1:72742400-72742600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:72742600-72742800	Weak transcription	Brain Cingulate Gyrus	brain
9	chr1:72742600-72742800	Enhancers	Brain Substantia Nigra	brain
10	chr1:72742600-72743000	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
11	chr1:72742800-72743000	Enhancers	Brain Angular Gyrus	brain
12	chr1:72742800-72743000	Enhancers	Brain Cingulate Gyrus	brain
13	chr1:72742800-72743200	Enhancers	Dnd41	blood
14	chr1:72742800-72744000	Weak transcription	Brain Substantia Nigra	brain
15	chr1:72742800-72745800	Weak transcription	Brain Anterior Caudate	brain
16	chr1:72743000-72745000	Weak transcription	Brain Angular Gyrus	brain
17	chr1:72743000-72745000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:72743000-72745800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr1:72743200-72743600	Weak transcription	Dnd41	blood
20	chr1:72743600-72745800	Enhancers	Dnd41	blood
21	chr1:72743800-72744200	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr1:72743800-72751600	Active TSS	Brain Inferior Temporal Lobe	brain
23	chr1:72744000-72744200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr1:72744000-72745000	Weak transcription	Colon Smooth Muscle	Colon
25	chr1:72744000-72745200	Enhancers	Brain Substantia Nigra	brain
26	chr1:72744200-72744400	Enhancers	NHDF-Ad	bronchial
27	chr1:72744200-72744600	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr1:72744200-72744800	Active TSS	Stomach Smooth Muscle	stomach
29	chr1:72744200-72744800	Enhancers	HUVEC	blood vessel
30	chr1:72744200-72745400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr1:72744200-72745800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr1:72744200-72746000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr1:72744400-72744600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:72744400-72745000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr1:72744400-72745800	Weak transcription	NHDF-Ad	bronchial
36	chr1:72744400-72746400	Enhancers	Rectal Smooth Muscle	rectum
37	chr1:72744600-72744800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr1:72744600-72745200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr1:72744600-72745600	Enhancers	Osteobl	bone
40	chr1:72744600-72745800	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr1:72744800-72745000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:72744800-72745000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr1:72744800-72745000	Flanking Active TSS	Stomach Smooth Muscle	stomach
44	chr1:72744800-72745000	Enhancers	NHLF	lung
45	chr1:72744800-72745200	Flanking Active TSS	HUVEC	blood vessel
46	chr1:72744800-72746000	Enhancers	HSMM	muscle
47	chr1:72745000-72745200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr1:72745000-72745200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
49	chr1:72745000-72745200	Enhancers	Fetal Brain Male	brain
50	chr1:72745000-72745600	Enhancers	Duodenum Smooth Muscle	Duodenum

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