Variant report

Variant	esv1792405
Chromosome Location	chr1:86814270-86825639
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	CEBPB	chr1:86817785-86817986	K562	blood:	n/a	n/a
2	CEBPB	chr1:86817767-86818125	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:86822191-86822196	K562	blood:	n/a	n/a
4	CEBPB	chr1:86817853-86818061	HepG2	liver:	n/a	n/a
5	CEBPB	chr1:86817806-86818107	A549	lung:	n/a	n/a
6	CEBPB	chr1:86817786-86818113	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr1:86822020-86822170	SAEC	small airway:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
8	CTCF	chr1:86821980-86822130	HEK293	kidney:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
9	CTCF	chr1:86821940-86822090	Caco-2	colon:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
10	CTCF	chr1:86821960-86822110	AG04450	lung:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
11	CTCF	chr1:86821960-86822110	SAEC	small airway:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
12	CTCF	chr1:86822081-86822129	MCF-7	breast:	n/a	n/a
13	CTCF	chr1:86822003-86822114	LNCaP	prostate:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
14	CTCF	chr1:86822040-86822190	HMEC	breast:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
15	CTCF	chr1:86822000-86822150	AG09309	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
16	CTCF	chr1:86822039-86822132	NHEK	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
17	CTCF	chr1:86822055-86822176	Fibrobl	skin:	n/a	n/a
18	CTCF	chr1:86821960-86822110	HMF	breast:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
19	CTCF	chr1:86821940-86822090	HBMEC	blood vessel:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
20	CTCF	chr1:86821995-86822102	HUVEC	blood vessel:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
21	CTCF	chr1:86821940-86822090	AG10803	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
22	CTCF	chr1:86821900-86822050	RPTEC	kidney:	n/a	n/a
23	CTCF	chr1:86822000-86822150	BE2_C	brain:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
24	CTCF	chr1:86822040-86822190	HEEpiC	esophagus:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
25	CTCF	chr1:86821940-86822090	BJ	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
26	CTCF	chr1:86822000-86822150	SK-N-SH_RA	brain:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
27	CTCF	chr1:86821992-86822118	Hela-S3	cervix:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
28	CTCF	chr1:86821960-86822110	AG04449	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
29	CTCF	chr1:86822019-86822161	MCF-7	breast:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
30	CTCF	chr1:86821960-86822110	HFF	foreskin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
31	CTCF	chr1:86822086-86822124	GM19238	blood:	n/a	n/a
32	CTCF	chr1:86821980-86822130	HFF-Myc	foreskin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
33	CTCF	chr1:86822023-86822100	Spleen_OC	spleen:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
34	CTCF	chr1:86822080-86822230	HVMF	connective:	n/a	n/a
35	CTCF	chr1:86821980-86822130	BE2_C	brain:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
36	CTCF	chr1:86822070-86822157	MCF-7	breast:	n/a	n/a
37	CTCF	chr1:86822020-86822170	HMEC	breast:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
38	CTCF	chr1:86821980-86822130	HRE	kidney:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
39	CTCF	chr1:86821994-86822129	GM12878	blood:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
40	CTCF	chr1:86821988-86822147	HepG2	liver:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
41	CTCF	chr1:86821961-86822133	HepG2	liver:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
42	CTCF	chr1:86822035-86822113	Pancreas_OC	pancreas:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
43	CTCF	chr1:86821980-86822130	HRPEpiC	eye:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
44	CTCF	chr1:86822022-86822126	LNCaP	prostate:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
45	CTCF	chr1:86822000-86822150	AG09319	gingival:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
46	CTCF	chr1:86821960-86822110	NHDF-neo	bronchial:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
47	CTCF	chr1:86822020-86822170	HCM	heart:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
48	CTCF	chr1:86822040-86822190	ProgFib	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
49	CTCF	chr1:86822100-86822250	HAc	cerebellar:	n/a	n/a
50	CTCF	chr1:86821960-86822110	AG10803	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:86819371-86819421	SK-N-SH	brain:	n/a
2	chr1:86819371-86819421	AG04449	skin:	fetal
3	chr1:86819371-86819421	GM06990	blood:	n/a
4	chr1:86819371-86819421	NT2-D1	testis:	n/a
5	chr1:86819371-86819421	NHBE	bronchial:	n/a
6	chr1:86819371-86819421	GM12878	blood:	n/a
7	chr1:86819371-86819421	ovcar-3	ovarian:	n/a
8	chr1:86819371-86819421	HUVEC	blood vessel:	n/a
9	chr1:86819371-86819421	GM12891	blood:	n/a
10	chr1:86819371-86819421	PrEC	prostate:	n/a
11	chr1:86819371-86819421	AG10803	skin:	n/a
12	chr1:86819371-86819421	ProgFib	skin:	n/a
13	chr1:86819371-86819421	Jurkat	blood:	n/a
14	chr1:86819371-86819421	NH-A	brain:	n/a
15	chr1:86819371-86819421	HEEpiC	esophagus:	n/a
16	chr1:86819371-86819421	HL-60	blood:	n/a
17	chr1:86819371-86819421	HEK293	kidney:	embryo
18	chr1:86819371-86819421	MCF10A-Er-Src	breast:	n/a
19	chr1:86819371-86819421	NHDF-neo	bronchial:	n/a
20	chr1:86819371-86819421	AG09309	skin:	n/a
21	chr1:86819371-86819421	GM19239	blood:	n/a
22	chr1:86819371-86819421	HCT-116	colon:	n/a
23	chr1:86819371-86819421	GM12892	blood:	n/a
24	chr1:86819371-86819421	AG04450	lung:	fetal
25	chr1:86819371-86819421	HCM	heart:	n/a
26	chr1:86819371-86819421	Caco-2	colon:	n/a
27	chr1:86819371-86819421	ECC-1	luminal epithelium:	n/a
28	chr1:86819371-86819421	A549	lung:	n/a
29	chr1:86819371-86819421	PFSK-1	brain:	n/a
30	chr1:86819371-86819421	BJ	skin:	n/a
31	chr1:86819371-86819421	HPAEpiC	pulmonary alveolar:	n/a
32	chr1:86819371-86819421	T-47D	breast:	n/a
33	chr1:86819371-86819421	H1-hESC	embryonic stem cell:	embryo
34	chr1:86819371-86819421	AG09319	gingival:	n/a
35	chr1:86819371-86819421	Hepatocyte	liver:	n/a
36	chr1:86819371-86819421	SK-N-SH_RA	brain:	n/a
37	chr1:86819371-86819421	HIPEpiC	eye:	n/a
38	chr1:86819371-86819421	HCF	heart:	n/a
39	chr1:86819371-86819421	Hela-S3	cervix:	n/a
40	chr1:86819371-86819421	HRE	kidney:	n/a
41	chr1:86819371-86819421	PANC-1	pancreas:	n/a
42	chr1:86819371-86819421	IMR90	lung:	fetal
43	chr1:86819371-86819421	SK-N-MC	brain:	n/a
44	chr1:86819371-86819421	SKMC	muscle:	n/a
45	chr1:86819371-86819421	HCPEpiC	choroid plexus:	n/a
46	chr1:86819371-86819421	BE2_C	brain:	n/a
47	chr1:86819371-86819421	HRPEpiC	eye:	n/a
48	chr1:86819371-86819421	SAEC	small airway:	n/a
49	chr1:86819371-86819421	NB4	blood:	n/a
50	chr1:86819371-86819421	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:86360058..86360590-chr1:86821594..86822114,2	MCF-7	breast:
2	chr1:86817766..86820014-chr1:86820204..86822305,3	K562	blood:
3	chr1:86821077..86823352-chr1:86861196..86863227,2	K562	blood:
4	chr1:86817633..86819266-chr1:86820612..86822159,2	K562	blood:
5	chr1:86823768..86826042-chr1:86827235..86830172,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL24A1-3	chr1:86823623-86823788	NONHSAT004267
2	lnc-COL24A1-3	chr1:86824470-86824574	NONHSAT004267
3	lnc-COL24A1-3	chr1:86824470-86824574	NONHSAT004266
4	lnc-COL24A1-3	chr1:86822259-86822285	NONHSAT004266

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7856-5p	chr1:86823348-86823368	MIMAT0030431

Variant related genes	Relation type
ODF2L	TF binding region
ODF2L	CpG island
ENSG00000122417	chromatin interactions

Extended variants
information (count: 412 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12742411	chr1:86814270-86814271	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs180852119	chr1:86814306-86814307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs113732309	chr1:86814368-86814369	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186066009	chr1:86814411-86814412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144355767	chr1:86814444-86814445	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs555592277	chr1:86814453-86814454	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs376059730	chr1:86814470-86814471	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs373791078	chr1:86814505-86814506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566039482	chr1:86814506-86814507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs534876020	chr1:86814521-86814522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192094466	chr1:86814564-86814565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs272491	chr1:86814688-86814689	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs272492	chr1:86814743-86814744	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557188411	chr1:86814868-86814869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11476580	chr1:86814921-86814922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573951538	chr1:86814962-86814963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543047752	chr1:86814981-86814982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs559646162	chr1:86814984-86814985	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545224502	chr1:86814988-86814989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs423991	chr1:86815022-86815023	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs183985623	chr1:86815264-86815265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550617436	chr1:86815279-86815280	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17129078	chr1:86815303-86815304	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs272493	chr1:86815319-86815320	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs546226945	chr1:86815346-86815347	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35261823	chr1:86815379-86815380	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs535013679	chr1:86815434-86815435	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76940920	chr1:86815490-86815491	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188483287	chr1:86815522-86815523	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs147170768	chr1:86815524-86815525	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs557380394	chr1:86815560-86815561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536972499	chr1:86815572-86815573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190711130	chr1:86815581-86815582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115313988	chr1:86815583-86815584	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573155176	chr1:86815659-86815660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs545358293	chr1:86815744-86815745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565049673	chr1:86815760-86815761	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575370909	chr1:86815829-86815830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544083650	chr1:86815862-86815863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182899058	chr1:86815897-86815898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529783612	chr1:86815938-86815939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546166453	chr1:86815969-86815970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35166283	chr1:86815976-86815977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559750102	chr1:86816035-86816036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4497186	chr1:86816036-86816037	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs552022471	chr1:86816040-86816041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs144285412	chr1:86816103-86816104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537612466	chr1:86816127-86816128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs550934539	chr1:86816176-86816177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187222035	chr1:86816181-86816182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Cancer	22429812	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17133270	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86805400-86817400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr1:86806400-86823600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:86808600-86842800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:86810400-86819200	Weak transcription	NHLF	lung
5	chr1:86810600-86816200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:86810600-86819200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr1:86810800-86815800	Enhancers	HUVEC	blood vessel
8	chr1:86810800-86817400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr1:86810800-86818600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:86810800-86819400	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr1:86811000-86816400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr1:86811000-86817400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:86811000-86817800	Weak transcription	Adipose Nuclei	Adipose
14	chr1:86811200-86815400	Weak transcription	Aorta	Aorta
15	chr1:86811200-86818800	Weak transcription	Fetal Thymus	thymus
16	chr1:86811200-86819000	Weak transcription	Fetal Lung	lung
17	chr1:86811400-86817400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr1:86811400-86817600	Weak transcription	Primary T cells from cord blood	blood
19	chr1:86811600-86819000	Weak transcription	Brain Angular Gyrus	brain
20	chr1:86812000-86818400	Weak transcription	NH-A	brain
21	chr1:86812000-86819200	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr1:86812600-86817600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:86813000-86819200	Weak transcription	Left Ventricle	heart
24	chr1:86813200-86816400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:86813200-86819200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr1:86813600-86818000	Weak transcription	HSMM	muscle
27	chr1:86813600-86819400	Weak transcription	Osteobl	bone
28	chr1:86813800-86817600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr1:86813800-86836400	Weak transcription	Lung	lung
30	chr1:86813800-86842600	Weak transcription	Fetal Heart	heart
31	chr1:86814000-86817200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:86814000-86817600	Weak transcription	NHDF-Ad	bronchial
33	chr1:86814800-86817400	Weak transcription	Dnd41	blood
34	chr1:86815000-86817600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr1:86815000-86819000	Weak transcription	Fetal Intestine Large	intestine
36	chr1:86815200-86817600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr1:86815200-86819000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr1:86815200-86860200	Weak transcription	Fetal Brain Male	brain
39	chr1:86815400-86815600	Enhancers	Aorta	Aorta
40	chr1:86815400-86817600	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr1:86815600-86817400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr1:86815600-86819400	Weak transcription	Aorta	Aorta
43	chr1:86815800-86817400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
44	chr1:86815800-86817400	Weak transcription	HUVEC	blood vessel
45	chr1:86815800-86817600	Weak transcription	Liver	Liver
46	chr1:86815800-86817800	Weak transcription	HUES64 Cell Line	embryonic stem cell
47	chr1:86816000-86817600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr1:86816000-86817600	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr1:86816000-86817600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr1:86816000-86817600	Weak transcription	Rectal Mucosa Donor 29	rectum

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