Variant report

Variant	esv3453694
Chromosome Location	chr1:86821560-86823342
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	chr1:86822191-86822196	K562	blood:	n/a	n/a
2	CTCF	chr1:86822055-86822176	Fibrobl	skin:	n/a	n/a
3	CTCF	chr1:86821988-86822147	HepG2	liver:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
4	CTCF	chr1:86822009-86822127	GM12878	blood:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
5	CTCF	chr1:86822060-86822210	A549	lung:	n/a	n/a
6	CTCF	chr1:86822100-86822250	HAc	cerebellar:	n/a	n/a
7	CTCF	chr1:86821995-86822102	HUVEC	blood vessel:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
8	CTCF	chr1:86822040-86822190	HMEC	breast:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
9	CTCF	chr1:86821940-86822090	HPAF	blood vessel:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
10	CTCF	chr1:86821960-86822110	SAEC	small airway:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
11	CTCF	chr1:86822003-86822114	LNCaP	prostate:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
12	CTCF	chr1:86821960-86822110	WERI-Rb-1	eye:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
13	CTCF	chr1:86822081-86822129	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:86822000-86822150	HCM	heart:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
15	CTCF	chr1:86821980-86822130	HRPEpiC	eye:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
16	CTCF	chr1:86821900-86822050	RPTEC	kidney:	n/a	n/a
17	CTCF	chr1:86821972-86822152	K562	blood:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
18	CTCF	chr1:86822000-86822150	AG09309	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
19	CTCF	chr1:86822023-86822100	Spleen_OC	spleen:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
20	CTCF	chr1:86821960-86822110	HMF	breast:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
21	CTCF	chr1:86821961-86822133	HepG2	liver:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
22	CTCF	chr1:86821940-86822090	Caco-2	colon:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
23	CTCF	chr1:86821960-86822110	AG10803	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
24	CTCF	chr1:86821980-86822130	BJ	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
25	CTCF	chr1:86821912-86822172	H1-hESC	embryonic stem cell:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
26	CTCF	chr1:86821992-86822118	Hela-S3	cervix:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
27	CTCF	chr1:86822070-86822157	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:86821980-86822130	HRE	kidney:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
29	CTCF	chr1:86821960-86822110	NHDF-neo	bronchial:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
30	CTCF	chr1:86821980-86822130	HPAF	blood vessel:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
31	CTCF	chr1:86821960-86822110	HCT-116	colon:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
32	CTCF	chr1:86821940-86822090	HCFaa	heart:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
33	CTCF	chr1:86821940-86822090	HBMEC	blood vessel:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
34	CTCF	chr1:86822035-86822113	Pancreas_OC	pancreas:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
35	CTCF	chr1:86821994-86822129	GM12878	blood:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
36	CTCF	chr1:86822000-86822150	AG09319	gingival:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
37	CTCF	chr1:86822000-86822150	BE2_C	brain:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
38	CTCF	chr1:86822020-86822170	NHLF	lung:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
39	CTCF	chr1:86822039-86822132	NHEK	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
40	CTCF	chr1:86821980-86822130	BE2_C	brain:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
41	CTCF	chr1:86822020-86822170	HMEC	breast:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
42	CTCF	chr1:86821960-86822110	HFF-Myc	foreskin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
43	CTCF	chr1:86822000-86822150	SK-N-SH_RA	brain:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
44	CTCF	chr1:86822048-86822164	A549	lung:	n/a	chr1:86822049-86822067
45	CTCF	chr1:86821980-86822130	RPTEC	kidney:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
46	CTCF	chr1:86821960-86822110	HFF	foreskin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
47	CTCF	chr1:86821840-86821990	NHLF	lung:	n/a	n/a
48	CTCF	chr1:86821960-86822110	AG04449	skin:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
49	CTCF	chr1:86822000-86822150	HPF	lung:	n/a	chr1:86822044-86822065 chr1:86822049-86822067
50	CTCF	chr1:86822020-86822170	HBMEC	blood vessel:	n/a	chr1:86822044-86822065 chr1:86822049-86822067

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:86360058..86360590-chr1:86821594..86822114,2	MCF-7	breast:
2	chr1:86821077..86823352-chr1:86861196..86863227,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COL24A1-3	chr1:86822259-86822285	NONHSAT004266

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

Extended variants
information (count: 89 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187766850	chr1:86821560-86821561	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs543460361	chr1:86821571-86821572	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs143652796	chr1:86821603-86821604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs529250057	chr1:86821739-86821740	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs17129092	chr1:86821746-86821747	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs559622197	chr1:86821754-86821755	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs528291050	chr1:86821877-86821878	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551429908	chr1:86821892-86821893	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564834154	chr1:86821900-86821901	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs200180150	chr1:86821906-86821907	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs369360481	chr1:86821910-86821911	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs68126437	chr1:86821911-86821912	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs201948631	chr1:86821914-86821915	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs200426377	chr1:86821915-86821916	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs398053190	chr1:86821918-86821919	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs530487083	chr1:86821922-86821923	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550203032	chr1:86821925-86821926	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs79579195	chr1:86821927-86821928	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs535776774	chr1:86821945-86821946	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs549279405	chr1:86821952-86821953	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs1182099	chr1:86821974-86821975	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs534906791	chr1:86821975-86821976	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558190061	chr1:86822040-86822041	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs57534123	chr1:86822042-86822043	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555093268	chr1:86822064-86822065	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs574817136	chr1:86822088-86822089	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs374484026	chr1:86822092-86822093	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs142356442	chr1:86822109-86822110	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs199702607	chr1:86822116-86822117	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs138813020	chr1:86822123-86822124	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs573966982	chr1:86822162-86822163	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs368562180	chr1:86822169-86822170	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs542908890	chr1:86822170-86822171	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs368185410	chr1:86822179-86822180	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs117798340	chr1:86822204-86822205	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs192480175	chr1:86822205-86822206	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs544887352	chr1:86822215-86822216	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs368679168	chr1:86822216-86822217	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs149805854	chr1:86822220-86822221	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs147025866	chr1:86822221-86822222	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs372029682	chr1:86822223-86822224	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs11810074	chr1:86822226-86822227	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs530569725	chr1:86822229-86822230	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs385437	chr1:86822231-86822232	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs142772711	chr1:86822245-86822246	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs114962597	chr1:86822246-86822247	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs112831254	chr1:86822280-86822281	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs139812168	chr1:86822287-86822288	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs376732664	chr1:86822289-86822290	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200753122	chr1:86822294-86822295	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86806400-86823600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr1:86808600-86842800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:86813800-86836400	Weak transcription	Lung	lung
4	chr1:86813800-86842600	Weak transcription	Fetal Heart	heart
5	chr1:86815200-86860200	Weak transcription	Fetal Brain Male	brain
6	chr1:86816000-86842400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:86816200-86824200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr1:86816200-86826200	Weak transcription	A549	lung
9	chr1:86817200-86843800	Weak transcription	Small Intestine	intestine
10	chr1:86817400-86824400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr1:86817400-86824400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:86817400-86826000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr1:86817400-86826000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr1:86817400-86826200	Strong transcription	HUVEC	blood vessel
15	chr1:86817600-86825200	Strong transcription	Primary T cells fromperipheralblood	blood
16	chr1:86817600-86825400	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr1:86817600-86826000	Strong transcription	Primary T helper cells PMA-I stimulated	--
18	chr1:86817600-86826200	Strong transcription	Primary T helper cells fromperipheralblood	blood
19	chr1:86817600-86843000	Weak transcription	Brain Cingulate Gyrus	brain
20	chr1:86817800-86828000	Weak transcription	Fetal Stomach	stomach
21	chr1:86817800-86828000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr1:86817800-86835400	Weak transcription	Esophagus	oesophagus
23	chr1:86817800-86840000	Weak transcription	GM12878-XiMat	blood
24	chr1:86817800-86842400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr1:86818000-86822200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr1:86818000-86822400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr1:86818000-86842600	Weak transcription	Fetal Intestine Small	intestine
28	chr1:86818000-86843200	Weak transcription	Pancreas	Pancrea
29	chr1:86818000-86851600	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr1:86818200-86841000	Weak transcription	Fetal Kidney	kidney
31	chr1:86818400-86823400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr1:86818400-86824000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr1:86818600-86822400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr1:86818600-86822400	Strong transcription	Primary B cells from peripheral blood	blood
35	chr1:86818800-86823600	Strong transcription	Primary T cells from cord blood	blood
36	chr1:86819000-86824000	Strong transcription	Fetal Intestine Large	intestine
37	chr1:86819000-86838400	Weak transcription	NHDF-Ad	bronchial
38	chr1:86819800-86821600	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr1:86819800-86822200	Weak transcription	Aorta	Aorta
40	chr1:86819800-86823200	Weak transcription	Colonic Mucosa	Colon
41	chr1:86819800-86824000	Weak transcription	Right Ventricle	heart
42	chr1:86819800-86828000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr1:86819800-86830200	Weak transcription	Spleen	Spleen
44	chr1:86819800-86839400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr1:86819800-86839400	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr1:86819800-86840200	Weak transcription	Brain Angular Gyrus	brain
47	chr1:86819800-86840200	Weak transcription	HMEC	breast
48	chr1:86819800-86842200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr1:86819800-86842600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr1:86819800-86843000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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