Variant report

Variant	esv1851921
Chromosome Location	chr1:84678418-84715634
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:327)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:327 , 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	ATF1	chr1:84691434-84691612	K562	blood:	n/a	n/a
2	ATF1	chr1:84713080-84713702	K562	blood:	n/a	n/a
3	ATF3	chr1:84712947-84713599	A549	lung:	n/a	n/a
4	ATF3	chr1:84712971-84713766	HCT-116	colon:	n/a	n/a
5	ATF3	chr1:84713134-84713579	K562	blood:	n/a	n/a
6	BCL3	chr1:84712912-84713611	A549	lung:	n/a	n/a
7	BCL3	chr1:84712879-84713635	A549	lung:	n/a	n/a
8	BHLHE40	chr1:84713184-84713547	K562	blood:	n/a	n/a
9	CBX3	chr1:84688887-84689091	K562	blood:	n/a	n/a
10	CBX3	chr1:84712907-84713811	HCT-116	colon:	n/a	n/a
11	CBX3	chr1:84712916-84713748	HCT-116	colon:	n/a	n/a
12	CCNT2	chr1:84713360-84713562	K562	blood:	n/a	n/a
13	CCNT2	chr1:84711404-84711593	K562	blood:	n/a	n/a
14	CEBPB	chr1:84713119-84713844	A549	lung:	n/a	n/a
15	CEBPB	chr1:84713110-84713757	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr1:84712970-84713972	A549	lung:	n/a	n/a
17	CEBPB	chr1:84713685-84713834	K562	blood:	n/a	n/a
18	CEBPB	chr1:84713298-84713479	K562	blood:	n/a	n/a
19	CEBPB	chr1:84712503-84712775	A549	lung:	n/a	n/a
20	CEBPB	chr1:84712526-84712776	IMR90	lung:	n/a	n/a
21	CEBPB	chr1:84713194-84713861	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:84712408-84712879	A549	lung:	n/a	n/a
23	CEBPD	chr1:84713288-84713673	K562	blood:	n/a	n/a
24	CEBPD	chr1:84713264-84713696	K562	blood:	n/a	n/a
25	CHD1	chr1:84712968-84713901	IMR90	lung:	n/a	n/a
26	CHD2	chr1:84713269-84713513	Hela-S3	cervix:	n/a	n/a
27	CREB1	chr1:84713192-84713612	A549	lung:	n/a	n/a
28	CREB1	chr1:84713174-84713510	GM12878	blood:	n/a	n/a
29	CREB1	chr1:84713035-84713385	A549	lung:	n/a	n/a
30	CTCF	chr1:84689820-84689970	MCF-7	breast:	n/a	n/a
31	CTCF	chr1:84689854-84689970	NHEK	skin:	n/a	n/a
32	CTCF	chr1:84711158-84711313	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr1:84689840-84689990	HEEpiC	esophagus:	n/a	n/a
34	CTCF	chr1:84689760-84689910	GM12865	blood:	n/a	n/a
35	CTCF	chr1:84689760-84689910	GM12873	blood:	n/a	n/a
36	CTCF	chr1:84713240-84713390	HCT-116	colon:	n/a	n/a
37	CTCF	chr1:84689892-84689996	Fibrobl	skin:	n/a	n/a
38	CTCF	chr1:84689820-84689970	GM12870	blood:	n/a	n/a
39	CTCF	chr1:84689820-84689970	HEK293	kidney:	n/a	n/a
40	CTCF	chr1:84689800-84689950	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr1:84689820-84689970	A549	lung:	n/a	n/a
42	CTCF	chr1:84689901-84689906	MCF-7	breast:	n/a	n/a
43	CTCF	chr1:84689820-84689970	AG09319	gingival:	n/a	n/a
44	CTCF	chr1:84689860-84689953	MCF-7	breast:	n/a	n/a
45	CTCF	chr1:84689800-84689950	WI-38	lung:	n/a	n/a
46	CTCF	chr1:84689840-84689990	HCT-116	colon:	n/a	n/a
47	CTCF	chr1:84689920-84690070	GM12865	blood:	n/a	n/a
48	CTCF	chr1:84689880-84690030	HEK293	kidney:	n/a	n/a
49	CTCF	chr1:84689900-84690050	RPTEC	kidney:	n/a	n/a
50	CTCF	chr1:84711076-84711320	GM12878	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:84709527-84709577	CMK	blood:	n/a
2	chr1:84709527-84709577	SAEC	small airway:	n/a
3	chr1:84709527-84709577	HNPCEpiC	eye:	n/a
4	chr1:84709527-84709577	AG04449	skin:	fetal
5	chr1:84709527-84709577	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:84709527-84709577	GM19239	blood:	n/a
7	chr1:84709527-84709577	H1-hESC	embryonic stem cell:	embryo
8	chr1:84709527-84709577	PANC-1	pancreas:	n/a
9	chr1:84709527-84709577	NH-A	brain:	n/a
10	chr1:84709527-84709577	AG09319	gingival:	n/a
11	chr1:84709527-84709577	HCPEpiC	choroid plexus:	n/a
12	chr1:84709527-84709577	HepG2	liver:	n/a
13	chr1:84709527-84709577	HMEC	breast:	n/a
14	chr1:84709527-84709577	HEEpiC	esophagus:	n/a
15	chr1:84709527-84709577	U87	brain:	n/a
16	chr1:84709527-84709577	HCT-116	colon:	n/a
17	chr1:84709527-84709577	Hepatocyte	liver:	n/a
18	chr1:84709527-84709577	GM06990	blood:	n/a
19	chr1:84709527-84709577	GM12878	blood:	n/a
20	chr1:84709527-84709577	PrEC	prostate:	n/a
21	chr1:84709527-84709577	IMR90	lung:	fetal
22	chr1:84709527-84709577	Hela-S3	cervix:	n/a
23	chr1:84709527-84709577	T-47D	breast:	n/a
24	chr1:84709527-84709577	NB4	blood:	n/a
25	chr1:84709527-84709577	AG09309	skin:	n/a
26	chr1:84709527-84709577	BE2_C	brain:	n/a
27	chr1:84709527-84709577	A549	lung:	n/a
28	chr1:84709527-84709577	HRE	kidney:	n/a
29	chr1:84709527-84709577	ECC-1	luminal epithelium:	n/a
30	chr1:84709527-84709577	MCF10A-Er-Src	breast:	n/a
31	chr1:84709527-84709577	HCF	heart:	n/a
32	chr1:84709527-84709577	HAEpiC	amniotic membrane:	n/a
33	chr1:84709527-84709577	NHDF-neo	bronchial:	n/a
34	chr1:84709527-84709577	SK-N-SH	brain:	n/a
35	chr1:84709527-84709577	Caco-2	colon:	n/a
36	chr1:84709527-84709577	AG04450	lung:	fetal
37	chr1:84709527-84709577	SK-N-SH_RA	brain:	n/a
38	chr1:84709527-84709577	PFSK-1	brain:	n/a
39	chr1:84709527-84709577	HCM	heart:	n/a
40	chr1:84709527-84709577	GM12892	blood:	n/a
41	chr1:84709527-84709577	HRCEpiC	kidney:	n/a
42	chr1:84709527-84709577	K562	blood:	n/a
43	chr1:84709527-84709577	LNCaP	prostate:	n/a
44	chr1:84709527-84709577	HEK293	kidney:	embryo
45	chr1:84709527-84709577	GM12891	blood:	n/a
46	chr1:84709527-84709577	AoSMC	blood vessel:	n/a
47	chr1:84709527-84709577	SKMC	muscle:	n/a
48	chr1:84709527-84709577	ProgFib	skin:	n/a
49	chr1:84709527-84709577	HL-60	blood:	n/a
50	chr1:84709527-84709577	AG10803	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:84699628..84701684-chr1:84763119..84765204,2	MCF-7	breast:
2	chr1:84703877..84705548-chr1:84707085..84709584,2	K562	blood:
3	chr1:84707348..84709881-chr1:84716416..84718748,2	K562	blood:
4	chr1:84671668..84674166-chr1:84678982..84681039,2	MCF-7	breast:
5	chr1:84708889..84710683-chr1:84712706..84714926,2	MCF-7	breast:
6	chr1:84701446..84703629-chr1:84722658..84725060,2	MCF-7	breast:
7	chr1:84703877..84705548-chr1:84707085..84709584,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACB-5	chr1:84710017-84710260	NONHSAT004193

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PRKACB	hsa-miR-93-5p	chr1:84702387-84702393
2	PRKACB	hsa-miR-19b-3p	chr1:84701025-84701031
3	PRKACB	hsa-miR-93-5p	chr1:84702372-84702394
4	PRKACB	hsa-miR-19b-3p	chr1:84702375-84702399

Variant related genes	Relation type
ENSG00000226970	TF binding region
ENSG00000226970	CpG island
ENSG00000203943	chromatin interactions
ENSG00000226970	chromatin interactions

Extended variants
information (count: 1406 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:1406 , 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	rs2134647	chr1:84678418-84678419	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs145888887	chr1:84678441-84678442	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs374159900	chr1:84678465-84678466	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190513184	chr1:84678545-84678546	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148557028	chr1:84678565-84678566	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560745655	chr1:84678665-84678666	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532192213	chr1:84678683-84678684	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs41301170	chr1:84678761-84678762	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs35719070	chr1:84678792-84678793	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573876666	chr1:84678795-84678796	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537548845	chr1:84678833-84678834	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs41301172	chr1:84678918-84678919	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs145590021	chr1:84678972-84678973	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs568179476	chr1:84679012-84679013	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs41301174	chr1:84679016-84679017	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs368045938	chr1:84679019-84679020	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562654790	chr1:84679053-84679054	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553694167	chr1:84679055-84679056	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs41301176	chr1:84679138-84679139	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs193114038	chr1:84679157-84679158	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558530019	chr1:84679178-84679179	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575564982	chr1:84679191-84679192	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371385131	chr1:84679270-84679271	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375082965	chr1:84679284-84679285	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs544393765	chr1:84679448-84679449	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs561418198	chr1:84679456-84679457	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368094879	chr1:84679499-84679500	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs147687515	chr1:84679512-84679513	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs540818824	chr1:84679585-84679586	Weak transcription Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560806825	chr1:84679619-84679620	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs532866623	chr1:84679630-84679631	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551495799	chr1:84679653-84679654	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552858520	chr1:84679675-84679676	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs112103042	chr1:84679718-84679719	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531304964	chr1:84679737-84679738	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs117750049	chr1:84679778-84679779	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568129167	chr1:84679811-84679812	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372018748	chr1:84679822-84679823	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs142401084	chr1:84679823-84679824	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs376344710	chr1:84679825-84679826	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs369887968	chr1:84679833-84679834	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs17857047	chr1:84679851-84679852	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs373556199	chr1:84679865-84679866	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549575163	chr1:84679889-84679890	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376696327	chr1:84679943-84679944	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs143624941	chr1:84679969-84679970	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371312432	chr1:84679973-84679974	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373976154	chr1:84679990-84679991	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs200388700	chr1:84679999-84680000	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs373825392	chr1:84680008-84680009	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	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
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
Ewing''s sarcoma	17952124	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 endocrine tumor	17639061	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	16397240	CNVD

Chromatin state (count:775 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84652400-84689800	Weak transcription	Aorta	Aorta
2	chr1:84657600-84708000	Weak transcription	Left Ventricle	heart
3	chr1:84659000-84685000	Weak transcription	Rectal Smooth Muscle	rectum
4	chr1:84659000-84700600	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr1:84659000-84700800	Weak transcription	Colon Smooth Muscle	Colon
6	chr1:84659200-84688400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr1:84659400-84685400	Weak transcription	Stomach Smooth Muscle	stomach
8	chr1:84659800-84701400	Weak transcription	NHLF	lung
9	chr1:84660600-84683200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:84660600-84686200	Weak transcription	Fetal Intestine Small	intestine
11	chr1:84660800-84688400	Weak transcription	Fetal Brain Male	brain
12	chr1:84663200-84684600	Weak transcription	Hela-S3	cervix
13	chr1:84665200-84700800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:84665400-84684000	Weak transcription	Brain Hippocampus Middle	brain
15	chr1:84665400-84684600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr1:84665400-84685200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:84665400-84687600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr1:84665400-84700600	Weak transcription	Colonic Mucosa	Colon
19	chr1:84665400-84701000	Weak transcription	Fetal Kidney	kidney
20	chr1:84665600-84684800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr1:84665800-84680200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr1:84665800-84681800	Weak transcription	Fetal Muscle Leg	muscle
23	chr1:84665800-84684400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr1:84666000-84679600	Weak transcription	Thymus	Thymus
25	chr1:84666000-84689800	Weak transcription	Fetal Stomach	stomach
26	chr1:84666200-84682600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr1:84666200-84683800	Weak transcription	Fetal Lung	lung
28	chr1:84666800-84710200	Weak transcription	HSMMtube	muscle
29	chr1:84667600-84680600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr1:84668200-84690000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr1:84669800-84683000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr1:84670200-84682600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr1:84670800-84683400	Weak transcription	Esophagus	oesophagus
34	chr1:84672400-84683800	Weak transcription	Brain Cingulate Gyrus	brain
35	chr1:84672400-84684200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr1:84672600-84679800	Weak transcription	Adipose Nuclei	Adipose
37	chr1:84672600-84683000	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr1:84672600-84683000	Weak transcription	Ovary	ovary
39	chr1:84672600-84683200	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr1:84672600-84683400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr1:84672600-84685200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr1:84672600-84685200	Weak transcription	Fetal Intestine Large	intestine
43	chr1:84672600-84687400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
44	chr1:84672600-84689800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:84672600-84700600	Weak transcription	Brain Anterior Caudate	brain
46	chr1:84672600-84701000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:84672600-84711200	Weak transcription	Brain Substantia Nigra	brain
48	chr1:84672800-84684200	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr1:84672800-84685000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr1:84673000-84680400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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