Variant report

Variant	esv2754129
Chromosome Location	chr1:76489579-76529279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:313)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:76525298-76525542	HepG2	liver:	n/a	n/a
2	ATF1	chr1:76498047-76498053	K562	blood:	n/a	n/a
3	BACH1	chr1:76511892-76511893	K562	blood:	n/a	n/a
4	BCL3	chr1:76517845-76518261	GM12878	blood:	n/a	n/a
5	BCL3	chr1:76525123-76525625	A549	lung:	n/a	n/a
6	CBX3	chr1:76490205-76490683	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:76525156-76525679	A549	lung:	n/a	n/a
8	CEBPB	chr1:76496325-76496364	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr1:76518638-76519295	H1-hESC	embryonic stem cell:	n/a	n/a
10	CREB1	chr1:76518573-76519120	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTBP2	chr1:76518634-76519100	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr1:76500820-76500970	AoAF	blood vessel:	n/a	n/a
13	CTCF	chr1:76500880-76501030	NHEK	skin:	n/a	n/a
14	CTCF	chr1:76500855-76501024	K562	blood:	n/a	n/a
15	CTCF	chr1:76500840-76500990	HEEpiC	esophagus:	n/a	n/a
16	CTCF	chr1:76500840-76500990	GM12865	blood:	n/a	n/a
17	CTCF	chr1:76500900-76501050	BJ	skin:	n/a	n/a
18	CTCF	chr1:76500940-76501090	HA-sp	spinal cord:	n/a	n/a
19	CTCF	chr1:76500880-76501030	AG09319	gingival:	n/a	n/a
20	CTCF	chr1:76500840-76500990	HL-60	blood:	n/a	n/a
21	CTCF	chr1:76500840-76500990	HVMF	connective:	n/a	n/a
22	CTCF	chr1:76500880-76501030	HPF	lung:	n/a	n/a
23	CTCF	chr1:76500820-76500970	HVMF	connective:	n/a	n/a
24	CTCF	chr1:76500880-76501030	HRE	kidney:	n/a	n/a
25	CTCF	chr1:76500860-76501010	BJ	skin:	n/a	n/a
26	CTCF	chr1:76500037-76501352	SK-N-SH	brain:	n/a	n/a
27	CTCF	chr1:76500900-76501050	MCF-7	breast:	n/a	n/a
28	CTCF	chr1:76500802-76501051	HepG2	liver:	n/a	n/a
29	CTCF	chr1:76500900-76501050	HMEC	breast:	n/a	n/a
30	CTCF	chr1:76500860-76501010	GM12873	blood:	n/a	n/a
31	CTCF	chr1:76500844-76501106	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr1:76500866-76501037	GM12878	blood:	n/a	n/a
33	CTCF	chr1:76500900-76501050	GM12868	blood:	n/a	n/a
34	CTCF	chr1:76500828-76501058	Gliobla	brain:	n/a	n/a
35	CTCF	chr1:76500820-76500970	HCFaa	heart:	n/a	n/a
36	CTCF	chr1:76500800-76500950	HCM	heart:	n/a	n/a
37	CTCF	chr1:76500900-76501050	GM12871	blood:	n/a	n/a
38	CTCF	chr1:76500829-76501049	LNCaP	prostate:	n/a	n/a
39	CTCF	chr1:76500860-76501010	NHLF	lung:	n/a	n/a
40	CTCF	chr1:76500900-76501050	HMF	breast:	n/a	n/a
41	CTCF	chr1:76500840-76500990	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr1:76500880-76501030	HUVEC	blood vessel:	n/a	n/a
43	CTCF	chr1:76500840-76500990	GM12874	blood:	n/a	n/a
44	CTCF	chr1:76500826-76501062	Medullo	brain:	n/a	n/a
45	CTCF	chr1:76500860-76501010	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr1:76500806-76501108	IMR90	lung:	n/a	n/a
47	CTCF	chr1:76500765-76501114	GM12878	blood:	n/a	n/a
48	CTCF	chr1:76500840-76500990	GM12875	blood:	n/a	n/a
49	CTCF	chr1:76500800-76500950	SAEC	small airway:	n/a	n/a
50	CTCF	chr1:76500907-76500972	Spleen_OC	spleen:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:76518896-76518946	HMEC	breast:	n/a
2	chr1:76518896-76518946	HCT-116	colon:	n/a
3	chr1:76489892-76489942	SK-N-MC	brain:	n/a
4	chr1:76518896-76518946	BE2_C	brain:	n/a
5	chr1:76489892-76489942	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:76518896-76518946	ovcar-3	ovarian:	n/a
7	chr1:76489892-76489942	U87	brain:	n/a
8	chr1:76489892-76489942	NHDF-neo	bronchial:	n/a
9	chr1:76518896-76518946	A549	lung:	n/a
10	chr1:76489892-76489942	NHBE	bronchial:	n/a
11	chr1:76518896-76518946	HIPEpiC	eye:	n/a
12	chr1:76518896-76518946	HAEpiC	amniotic membrane:	n/a
13	chr1:76518896-76518946	GM06990	blood:	n/a
14	chr1:76518896-76518946	Caco-2	colon:	n/a
15	chr1:76518896-76518946	MCF-7	breast:	n/a
16	chr1:76489892-76489942	HRPEpiC	eye:	n/a
17	chr1:76489892-76489942	PrEC	prostate:	n/a
18	chr1:76489892-76489942	MCF10A-Er-Src	breast:	n/a
19	chr1:76489892-76489942	HCPEpiC	choroid plexus:	n/a
20	chr1:76489892-76489942	NT2-D1	testis:	n/a
21	chr1:76489892-76489942	AG09319	gingival:	n/a
22	chr1:76489892-76489942	AoSMC	blood vessel:	n/a
23	chr1:76489892-76489942	HepG2	liver:	n/a
24	chr1:76518896-76518946	Hela-S3	cervix:	n/a
25	chr1:76518896-76518946	HPAEpiC	pulmonary alveolar:	n/a
26	chr1:76489892-76489942	HMEC	breast:	n/a
27	chr1:76518896-76518946	IMR90	lung:	fetal
28	chr1:76489892-76489942	SKMC	muscle:	n/a
29	chr1:76489892-76489942	HCT-116	colon:	n/a
30	chr1:76518896-76518946	HEK293	kidney:	embryo
31	chr1:76518896-76518946	CMK	blood:	n/a
32	chr1:76489892-76489942	Hela-S3	cervix:	n/a
33	chr1:76518896-76518946	AG09319	gingival:	n/a
34	chr1:76489892-76489942	NH-A	brain:	n/a
35	chr1:76518896-76518946	HUVEC	blood vessel:	n/a
36	chr1:76518896-76518946	MCF10A-Er-Src	breast:	n/a
37	chr1:76518896-76518946	H1-hESC	embryonic stem cell:	embryo
38	chr1:76518896-76518946	NB4	blood:	n/a
39	chr1:76518896-76518946	SK-N-SH_RA	brain:	n/a
40	chr1:76518896-76518946	AG10803	skin:	n/a
41	chr1:76489892-76489942	LNCaP	prostate:	n/a
42	chr1:76518896-76518946	BJ	skin:	n/a
43	chr1:76518896-76518946	GM12891	blood:	n/a
44	chr1:76518896-76518946	HCPEpiC	choroid plexus:	n/a
45	chr1:76489892-76489942	HL-60	blood:	n/a
46	chr1:76489892-76489942	HEK293	kidney:	embryo
47	chr1:76518896-76518946	SKMC	muscle:	n/a
48	chr1:76489892-76489942	MCF-7	breast:	n/a
49	chr1:76518896-76518946	SAEC	small airway:	n/a
50	chr1:76518896-76518946	HNPCEpiC	eye:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:76492764..76495132-chr1:76495850..76497868,2	K562	blood:
2	chr1:76528266..76531083-chr1:76533694..76535257,2	MCF-7	breast:
3	chr1:76492764..76495132-chr1:76495850..76497868,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ST6GALNAC3-1	chr1:76521433-76521898	NONHSAT004011
2	lnc-ST6GALNAC3-1	chr1:76507405-76507583	NONHSAT004009
3	lnc-ST6GALNAC3-1	chr1:76507376-76507583	ENSG00000230027
4	lnc-ST6GALNAC3-1	chr1:76521198-76521376	NONHSAT004010
5	lnc-ST6GALNAC3-1	chr1:76507405-76507583	NONHSAT004010

No data

Variant related genes	Relation type
ENSG00000230027	TF binding region
ENSG00000230027	CpG island

Extended variants
information (count: 1440 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1440 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550466215	chr1:76489591-76489592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs17097917	chr1:76489615-76489616	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs571912081	chr1:76489617-76489618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114927261	chr1:76489642-76489643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188376586	chr1:76489679-76489680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs534496521	chr1:76489695-76489696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs11162069	chr1:76489779-76489780	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs74646162	chr1:76489839-76489840	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs147126704	chr1:76489865-76489866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551465918	chr1:76489893-76489894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs76261991	chr1:76489967-76489968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537065200	chr1:76489987-76489988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs12035171	chr1:76490088-76490089	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs180739269	chr1:76490124-76490125	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs574651663	chr1:76490129-76490130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376263941	chr1:76490134-76490135	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs6676370	chr1:76490185-76490186	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs371366356	chr1:76490203-76490204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs10493578	chr1:76490234-76490235	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs17599188	chr1:76490262-76490263	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs138323783	chr1:76490295-76490296	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs112562216	chr1:76490304-76490305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12028029	chr1:76490316-76490317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs576072690	chr1:76490392-76490393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs4035040	chr1:76490412-76490413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17097922	chr1:76490425-76490426	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs563928512	chr1:76490440-76490441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561576072	chr1:76490441-76490442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs373867897	chr1:76490473-76490474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529582621	chr1:76490478-76490479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377700586	chr1:76490479-76490480	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs371289929	chr1:76490537-76490538	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1819691	chr1:76490562-76490563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs144327292	chr1:76490565-76490566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569801854	chr1:76490598-76490599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs540056601	chr1:76490601-76490602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs537173803	chr1:76490642-76490643	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs367979549	chr1:76490643-76490644	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs187430017	chr1:76490654-76490655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548741985	chr1:76490659-76490660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs567592038	chr1:76490665-76490666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148762898	chr1:76490666-76490667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs557238077	chr1:76490671-76490672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191808628	chr1:76490676-76490677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199862507	chr1:76490696-76490697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572240478	chr1:76490705-76490706	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs77894124	chr1:76490711-76490712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560361095	chr1:76490736-76490737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs539659763	chr1:76490739-76490740	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113183603	chr1:76490793-76490794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20393555	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76484800-76489600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:76487400-76491000	Enhancers	Fetal Lung	lung
3	chr1:76488200-76491800	Enhancers	Primary T cells from cord blood	blood
4	chr1:76488400-76490400	Enhancers	Placenta Amnion	Placenta Amnion
5	chr1:76488600-76490200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:76488600-76490400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr1:76488800-76490600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr1:76489000-76490000	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr1:76489000-76490400	Enhancers	Primary hematopoietic stem cells	blood
10	chr1:76489000-76490600	Enhancers	NHEK	skin
11	chr1:76489200-76490200	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr1:76489200-76490400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr1:76489200-76490600	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr1:76489200-76490600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr1:76489200-76490800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
16	chr1:76489200-76490800	Enhancers	HMEC	breast
17	chr1:76489400-76489800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr1:76489400-76489800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
19	chr1:76489400-76489800	Enhancers	Left Ventricle	heart
20	chr1:76489400-76490600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr1:76489400-76490800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr1:76489400-76490800	Enhancers	Fetal Heart	heart
23	chr1:76489600-76490400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr1:76489600-76490400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr1:76489600-76490400	Enhancers	Rectal Mucosa Donor 31	rectum
26	chr1:76489600-76490400	Enhancers	NH-A	brain
27	chr1:76489600-76491200	Enhancers	Fetal Stomach	stomach
28	chr1:76489800-76490400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
29	chr1:76489800-76490600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr1:76489800-76491000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr1:76489800-76491000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr1:76489800-76502800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr1:76490200-76490600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr1:76491000-76491200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
35	chr1:76491000-76492200	Weak transcription	Fetal Lung	lung
36	chr1:76491200-76491400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
37	chr1:76491800-76497400	Weak transcription	Primary T cells from cord blood	blood
38	chr1:76492200-76492600	Enhancers	Fetal Lung	lung
39	chr1:76492600-76503400	Weak transcription	Fetal Lung	lung
40	chr1:76493000-76494000	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr1:76494000-76495400	Weak transcription	Primary monocytes fromperipheralblood	blood
42	chr1:76494600-76494800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr1:76495400-76495800	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr1:76497400-76499000	Enhancers	Primary T cells from cord blood	blood
45	chr1:76498200-76498800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:76498200-76499200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:76498400-76498600	Enhancers	H9 Cell Line	embryonic stem cell
48	chr1:76498600-76502000	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr1:76500200-76503000	Weak transcription	Fetal Kidney	kidney
50	chr1:76501600-76503400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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