Variant report

Variant	nsv823353
Chromosome Location	chr1:84464183-84465098
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:285)
CpG islands
(count:305)
Chromatin interactive
region (count:3)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:285 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:84464866-84465021	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:84464757-84464865	K562	blood:	n/a	n/a
3	BACH1	chr1:84464671-84464855	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr1:84464367-84465447	K562	blood:	n/a	n/a
5	BHLHE40	chr1:84464733-84465164	GM12878	blood:	n/a	n/a
6	BHLHE40	chr1:84464677-84465244	HepG2	liver:	n/a	n/a
7	BRCA1	chr1:84464862-84464916	HepG2	liver:	n/a	n/a
8	BRCA1	chr1:84464930-84465017	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr1:84464831-84465146	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr1:84464810-84465043	K562	blood:	n/a	n/a
11	CCNT2	chr1:84464659-84465225	K562	blood:	n/a	n/a
12	CHD1	chr1:84464729-84465131	GM12878	blood:	n/a	n/a
13	CHD1	chr1:84464441-84465805	IMR90	lung:	n/a	n/a
14	CHD1	chr1:84464514-84465452	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr1:84464791-84465284	K562	blood:	n/a	n/a
16	CHD2	chr1:84464727-84465111	HepG2	liver:	n/a	n/a
17	CHD2	chr1:84464557-84465409	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr1:84464853-84465169	Hela-S3	cervix:	n/a	n/a
19	CREB1	chr1:84464417-84465246	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr1:84464601-84465298	A549	lung:	n/a	n/a
21	CTBP2	chr1:84464401-84465401	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr1:84464140-84464290	AG04449	skin:	n/a	n/a
23	CTCF	chr1:84464240-84464390	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr1:84464256-84464275	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:84464180-84464330	AG09309	skin:	n/a	n/a
26	CTCF	chr1:84464200-84464350	BJ	skin:	n/a	n/a
27	CTCF	chr1:84464200-84464350	HMEC	breast:	n/a	n/a
28	CTCF	chr1:84464240-84464390	AG04449	skin:	n/a	n/a
29	CTCF	chr1:84464153-84464379	K562	blood:	n/a	n/a
30	CTCF	chr1:84464160-84464310	GM12874	blood:	n/a	n/a
31	CTCF	chr1:84464740-84464890	AG04449	skin:	n/a	n/a
32	CTCF	chr1:84464160-84464310	AG09319	gingival:	n/a	n/a
33	CTCF	chr1:84465080-84465230	GM12871	blood:	n/a	n/a
34	CTCF	chr1:84464200-84464350	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr1:84464200-84464350	NHLF	lung:	n/a	n/a
36	CTCF	chr1:84465020-84465170	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr1:84464160-84464310	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr1:84464160-84464310	GM12864	blood:	n/a	n/a
39	CTCF	chr1:84464375-84464438	GM12891	blood:	n/a	n/a
40	CTCF	chr1:84464220-84464370	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr1:84464291-84464301	MCF-7	breast:	n/a	n/a
42	CTCF	chr1:84464402-84464412	Fibrobl	skin:	n/a	n/a
43	CTCF	chr1:84464180-84464330	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr1:84465018-84465264	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr1:84464140-84464290	HMF	breast:	n/a	n/a
46	CTCF	chr1:84464195-84464398	Fibrobl	skin:	n/a	n/a
47	CTCF	chr1:84464180-84464330	AG10803	skin:	n/a	n/a
48	CTCF	chr1:84464833-84464899	Fibrobl	skin:	n/a	n/a
49	CTCF	chr1:84464140-84464290	HRE	kidney:	n/a	n/a
50	CTCF	chr1:84464180-84464330	HPF	lung:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:84464326-84464376	HCPEpiC	choroid plexus:	n/a
2	chr1:84464645-84464695	AG09319	gingival:	n/a
3	chr1:84464326-84464376	HCF	heart:	n/a
4	chr1:84464326-84464376	GM19239	blood:	n/a
5	chr1:84464224-84464274	HL-60	blood:	n/a
6	chr1:84464645-84464695	SK-N-SH_RA	brain:	n/a
7	chr1:84464224-84464274	GM12878	blood:	n/a
8	chr1:84464326-84464376	AG10803	skin:	n/a
9	chr1:84465055-84465105	BE2_C	brain:	n/a
10	chr1:84465009-84465059	HMEC	breast:	n/a
11	chr1:84464326-84464376	SK-N-SH_RA	brain:	n/a
12	chr1:84464224-84464274	PANC-1	pancreas:	n/a
13	chr1:84464645-84464695	SK-N-MC	brain:	n/a
14	chr1:84465009-84465059	A549	lung:	n/a
15	chr1:84465055-84465105	HL-60	blood:	n/a
16	chr1:84464224-84464274	NHDF-neo	bronchial:	n/a
17	chr1:84464326-84464376	HPAEpiC	pulmonary alveolar:	n/a
18	chr1:84464224-84464274	K562	blood:	n/a
19	chr1:84464645-84464695	NB4	blood:	n/a
20	chr1:84465055-84465105	AG09309	skin:	n/a
21	chr1:84465055-84465105	NT2-D1	testis:	n/a
22	chr1:84465009-84465059	HEK293	kidney:	embryo
23	chr1:84464645-84464695	Jurkat	blood:	n/a
24	chr1:84465009-84465059	RPTEC	kidney:	n/a
25	chr1:84465055-84465105	HNPCEpiC	eye:	n/a
26	chr1:84464645-84464695	HIPEpiC	eye:	n/a
27	chr1:84465055-84465105	AG10803	skin:	n/a
28	chr1:84465009-84465059	NHBE	bronchial:	n/a
29	chr1:84465009-84465059	HCT-116	colon:	n/a
30	chr1:84465055-84465105	T-47D	breast:	n/a
31	chr1:84464645-84464695	HCF	heart:	n/a
32	chr1:84465055-84465105	HEK293	kidney:	embryo
33	chr1:84464326-84464376	Jurkat	blood:	n/a
34	chr1:84464224-84464274	GM19239	blood:	n/a
35	chr1:84464224-84464274	U87	brain:	n/a
36	chr1:84465055-84465105	ProgFib	skin:	n/a
37	chr1:84464645-84464695	CMK	blood:	n/a
38	chr1:84464645-84464695	Hepatocyte	liver:	n/a
39	chr1:84465055-84465105	SKMC	muscle:	n/a
40	chr1:84464326-84464376	GM06990	blood:	n/a
41	chr1:84464326-84464376	HepG2	liver:	n/a
42	chr1:84465055-84465105	HRE	kidney:	n/a
43	chr1:84464224-84464274	HMEC	breast:	n/a
44	chr1:84464645-84464695	GM06990	blood:	n/a
45	chr1:84464224-84464274	SAEC	small airway:	n/a
46	chr1:84465009-84465059	IMR90	lung:	fetal
47	chr1:84464645-84464695	HEEpiC	esophagus:	n/a
48	chr1:84465009-84465059	SK-N-SH	brain:	n/a
49	chr1:84465009-84465059	Caco-2	colon:	n/a
50	chr1:84464645-84464695	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:84463410..84466364-chr1:84542152..84546505,5	K562	blood:
2	chr1:84464994..84466919-chr1:84468968..84470510,3	K562	blood:
3	chr1:84464864..84467059-chr1:84542152..84543740,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTLL7-1	chr1:84464970-84465750	XLOC_000888

No data

Variant related genes	Relation type
TTLL7	TF binding region
TTLL7	CpG island
ENSG00000142875	chromatin interactions
ENSG00000271576	chromatin interactions

Extended variants
information (count: 34 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1952065	chr1:84464205-84464206	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs189994954	chr1:84464227-84464228	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs181118925	chr1:84464233-84464234	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs375385945	chr1:84464255-84464256	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs539441659	chr1:84464256-84464257	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs71652661	chr1:84464281-84464282	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs556285468	chr1:84464289-84464290	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs61766894	chr1:84464322-84464323	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs576083281	chr1:84464357-84464358	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs542028901	chr1:84464385-84464386	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs555508160	chr1:84464392-84464393	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs572428889	chr1:84464411-84464412	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs12126397	chr1:84464418-84464419	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs547408111	chr1:84464433-84464434	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs1871925	chr1:84464468-84464469	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs532982142	chr1:84464478-84464479	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543045223	chr1:84464498-84464499	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs563374273	chr1:84464540-84464541	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528953615	chr1:84464546-84464547	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs549213661	chr1:84464670-84464671	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs559560112	chr1:84464740-84464741	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs369080572	chr1:84464742-84464743	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs536971037	chr1:84464782-84464783	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs186510580	chr1:84464803-84464804	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs373559053	chr1:84464805-84464806	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs571448255	chr1:84464840-84464841	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs151257524	chr1:84464900-84464901	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs549726371	chr1:84465025-84465026	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs569832278	chr1:84465026-84465027	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs575633	chr1:84465036-84465037	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs555421603	chr1:84465045-84465046	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs575577	chr1:84465057-84465058	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs200749210	chr1:84465068-84465069	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs1536165	chr1:84465073-84465074	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
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
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84460000-84465600	Active TSS	Brain Anterior Caudate	brain
2	chr1:84461200-84465600	Active TSS	Brain Cingulate Gyrus	brain
3	chr1:84461800-84465600	Active TSS	Brain Inferior Temporal Lobe	brain
4	chr1:84461800-84465800	Active TSS	Aorta	Aorta
5	chr1:84461800-84465800	Active TSS	Brain Substantia Nigra	brain
6	chr1:84462000-84465600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
7	chr1:84462000-84466000	Active TSS	Brain Hippocampus Middle	brain
8	chr1:84462000-84467000	Active TSS	Brain Angular Gyrus	brain
9	chr1:84463000-84464200	Active TSS	Brain Germinal Matrix	brain
10	chr1:84463000-84465800	Active TSS	NHLF	lung
11	chr1:84463400-84464200	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
12	chr1:84463400-84465600	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr1:84463600-84464200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
14	chr1:84463600-84464400	Active TSS	Fetal Brain Male	brain
15	chr1:84463600-84466400	Active TSS	Stomach Smooth Muscle	stomach
16	chr1:84463800-84464200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
17	chr1:84463800-84464200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
18	chr1:84463800-84464200	Active TSS	Fetal Muscle Trunk	muscle
19	chr1:84463800-84464200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
20	chr1:84463800-84464400	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
21	chr1:84463800-84464400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr1:84463800-84464400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr1:84463800-84465000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr1:84463800-84465400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr1:84463800-84465400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr1:84463800-84465400	Active TSS	NHEK	skin
27	chr1:84463800-84465600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
28	chr1:84463800-84465600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
29	chr1:84463800-84465600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr1:84463800-84465600	Active TSS	Right Atrium	heart
31	chr1:84463800-84465600	Active TSS	Right Ventricle	heart
32	chr1:84463800-84465800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
33	chr1:84463800-84465800	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
34	chr1:84464000-84464200	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr1:84464000-84464200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr1:84464000-84464200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr1:84464000-84464200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr1:84464000-84464200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
39	chr1:84464000-84464200	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
40	chr1:84464000-84464200	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr1:84464000-84464200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
42	chr1:84464000-84464200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr1:84464000-84464200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr1:84464000-84464200	Bivalent Enhancer	Primary B cells from cord blood	blood
45	chr1:84464000-84464200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr1:84464000-84464200	Flanking Active TSS	Primary hematopoietic stem cells	blood
47	chr1:84464000-84464200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
48	chr1:84464000-84464200	Bivalent/Poised TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
49	chr1:84464000-84464200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr1:84464000-84464200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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