Variant report

Variant	nsv518081
Chromosome Location	chr10:116576189-116582502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:657)
CpG islands
(count:610)
Chromatin interactive
region (count:12)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:657 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr10:116581091-116581507	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr10:116581320-116581682	GM12878	blood:	n/a	chr10:116581564-116581577
3	BCLAF1	chr10:116581091-116581650	GM12878	blood:	n/a	chr10:116581564-116581577
4	BHLHE40	chr10:116581215-116581604	GM12878	blood:	n/a	n/a
5	BHLHE40	chr10:116581237-116581877	K562	blood:	n/a	chr10:116581809-116581825 chr10:116581749-116581765 chr10:116581760-116581776 chr10:116581763-116581779
6	BRCA1	chr10:116580611-116580929	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr10:116581416-116581586	HepG2	liver:	n/a	n/a
8	BRCA1	chr10:116579101-116579527	Hela-S3	cervix:	n/a	n/a
9	CBX3	chr10:116581162-116581461	K562	blood:	n/a	n/a
10	CCNT2	chr10:116581247-116582165	K562	blood:	n/a	n/a
11	CEBPB	chr10:116582219-116582907	K562	blood:	n/a	n/a
12	CEBPB	chr10:116582497-116583034	A549	lung:	n/a	n/a
13	CEBPB	chr10:116582180-116582938	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:116581544-116581570	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:116581096-116581668	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr10:116580521-116580887	Hela-S3	cervix:	n/a	chr10:116580606-116580617
17	CEBPB	chr10:116579078-116579518	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr10:116582208-116583193	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr10:116582256-116582736	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr10:116581223-116583093	GM12878	blood:	n/a	chr10:116581716-116581726
21	CHD1	chr10:116581639-116582386	H1-hESC	embryonic stem cell:	n/a	chr10:116581716-116581726
22	CHD1	chr10:116580993-116583316	IMR90	lung:	n/a	chr10:116581716-116581726
23	CHD2	chr10:116582464-116582656	GM12878	blood:	n/a	n/a
24	CHD2	chr10:116581263-116581463	K562	blood:	n/a	n/a
25	CHD2	chr10:116581136-116581770	GM12878	blood:	n/a	chr10:116581716-116581726
26	CHD2	chr10:116581215-116581806	Hela-S3	cervix:	n/a	chr10:116581716-116581726
27	CHD2	chr10:116581616-116581803	HepG2	liver:	n/a	chr10:116581716-116581726
28	CREB1	chr10:116581276-116581700	A549	lung:	n/a	n/a
29	CTBP2	chr10:116581441-116582211	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr10:116581317-116581649	Pancreas_OC	pancreas:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
31	CTCF	chr10:116581380-116581530	HAc	cerebellar:	n/a	n/a
32	CTCF	chr10:116581420-116581570	GM12866	blood:	n/a	n/a
33	CTCF	chr10:116581250-116581627	MCF-7	breast:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
34	CTCF	chr10:116581760-116581910	HepG2	liver:	n/a	n/a
35	CTCF	chr10:116581440-116581590	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr10:116581742-116581917	GM19240	blood:	n/a	n/a
37	CTCF	chr10:116576200-116576350	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr10:116576200-116576350	HEK293	kidney:	n/a	n/a
39	CTCF	chr10:116581836-116581936	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr10:116581460-116581610	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr10:116582300-116582450	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr10:116581803-116581936	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr10:116581420-116581570	GM12865	blood:	n/a	n/a
44	CTCF	chr10:116581319-116581596	LNCaP	prostate:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
45	CTCF	chr10:116581277-116581630	Hela-S3	cervix:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
46	CTCF	chr10:116581170-116581707	K562	blood:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
47	CTCF	chr10:116581322-116581657	NHEK	skin:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
48	CTCF	chr10:116581200-116581350	AG04450	lung:	n/a	n/a
49	CTCF	chr10:116581420-116581570	GM12871	blood:	n/a	n/a
50	CTCF	chr10:116581440-116581590	HL-60	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:116581344-116581394	RPTEC	kidney:	n/a
2	chr10:116581112-116581162	SK-N-SH_RA	brain:	n/a
3	chr10:116581248-116581298	HUVEC	blood vessel:	n/a
4	chr10:116581248-116581298	AG04450	lung:	fetal
5	chr10:116581183-116581233	GM12891	blood:	n/a
6	chr10:116581829-116581879	HRCEpiC	kidney:	n/a
7	chr10:116581344-116581394	SKMC	muscle:	n/a
8	chr10:116581248-116581298	U87	brain:	n/a
9	chr10:116581248-116581298	K562	blood:	n/a
10	chr10:116582469-116582519	HEEpiC	esophagus:	n/a
11	chr10:116581808-116581858	AG09319	gingival:	n/a
12	chr10:116581829-116581879	HUVEC	blood vessel:	n/a
13	chr10:116582469-116582519	SK-N-SH_RA	brain:	n/a
14	chr10:116581358-116581408	HEEpiC	esophagus:	n/a
15	chr10:116582297-116582347	AG10803	skin:	n/a
16	chr10:116581183-116581233	RPTEC	kidney:	n/a
17	chr10:116581112-116581162	GM06990	blood:	n/a
18	chr10:116581248-116581298	BE2_C	brain:	n/a
19	chr10:116581183-116581233	BJ	skin:	n/a
20	chr10:116581344-116581394	HRPEpiC	eye:	n/a
21	chr10:116581112-116581162	HCPEpiC	choroid plexus:	n/a
22	chr10:116581183-116581233	HAEpiC	amniotic membrane:	n/a
23	chr10:116581112-116581162	PFSK-1	brain:	n/a
24	chr10:116581248-116581298	Caco-2	colon:	n/a
25	chr10:116582469-116582519	HRCEpiC	kidney:	n/a
26	chr10:116581248-116581298	AG09319	gingival:	n/a
27	chr10:116581829-116581879	HIPEpiC	eye:	n/a
28	chr10:116581344-116581394	GM12892	blood:	n/a
29	chr10:116581344-116581394	HMEC	breast:	n/a
30	chr10:116581808-116581858	AG10803	skin:	n/a
31	chr10:116581829-116581879	GM12892	blood:	n/a
32	chr10:116582469-116582519	PrEC	prostate:	n/a
33	chr10:116581808-116581858	PrEC	prostate:	n/a
34	chr10:116581305-116581355	MCF10A-Er-Src	breast:	n/a
35	chr10:116581808-116581858	NB4	blood:	n/a
36	chr10:116581305-116581355	SK-N-SH_RA	brain:	n/a
37	chr10:116581183-116581233	HRCEpiC	kidney:	n/a
38	chr10:116582297-116582347	AG04449	skin:	fetal
39	chr10:116581183-116581233	PrEC	prostate:	n/a
40	chr10:116581248-116581298	ECC-1	luminal epithelium:	n/a
41	chr10:116581829-116581879	PANC-1	pancreas:	n/a
42	chr10:116581358-116581408	GM12892	blood:	n/a
43	chr10:116581248-116581298	HEEpiC	esophagus:	n/a
44	chr10:116581305-116581355	AG04449	skin:	fetal
45	chr10:116581808-116581858	MCF-7	breast:	n/a
46	chr10:116582469-116582519	HMEC	breast:	n/a
47	chr10:116581358-116581408	BE2_C	brain:	n/a
48	chr10:116581344-116581394	HIPEpiC	eye:	n/a
49	chr10:116581248-116581298	PFSK-1	brain:	n/a
50	chr10:116581829-116581879	AoSMC	blood vessel:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:116580811..116581705-chr8:27631902..27632494,2	Hela-S3	cervix:
2	chr10:116581616..116582495-chr7:115851052..115851797,2	Hela-S3	cervix:
3	chr10:116575494..116578184-chr10:116579422..116580946,2	K562	blood:
4	chr10:116296905..116298827-chr10:116577093..116580051,2	MCF-7	breast:
5	chr10:116574613..116576880-chr10:116580074..116582189,2	MCF-7	breast:
6	chr10:116581424..116582241-chr6:24720620..24721196,2	Hela-S3	cervix:
7	chr10:116577691..116581134-chr10:116581459..116583772,3	MCF-7	breast:
8	chr10:116575494..116578184-chr10:116579422..116580946,2	K562	blood:
9	chr10:116579148..116581126-chr10:116581176..116582786,3	MCF-7	breast:
10	chr10:116575612..116578929-chr10:116581323..116583414,4	MCF-7	breast:
11	chr10:116564843..116568193-chr10:116577870..116580490,3	MCF-7	breast:
12	chr10:116567584..116574580-chr10:116575101..116583231,11	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABLIM1-1	chr10:116581032-116581425	NONHSAT016464

No data

Variant related genes	Relation type
FAM160B1	TF binding region
FAM160B1	CpG island
ENSG00000215760	chromatin interactions
ENSG00000151553	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000171320	chromatin interactions

Extended variants
information (count: 225 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:225 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11196926	chr10:116576189-116576190	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs528022644	chr10:116576196-116576197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs186799434	chr10:116576212-116576213	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs12771956	chr10:116576228-116576229	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs189202354	chr10:116576239-116576240	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs550289278	chr10:116576241-116576242	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs546176937	chr10:116576263-116576264	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs144959948	chr10:116576271-116576272	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs74608802	chr10:116576299-116576300	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs181961781	chr10:116576331-116576332	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs552505669	chr10:116576384-116576385	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs557090840	chr10:116576427-116576428	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs536567222	chr10:116576433-116576434	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs7081975	chr10:116576445-116576446	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs376621090	chr10:116576495-116576496	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575639850	chr10:116576502-116576503	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs543054316	chr10:116576561-116576562	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs71473065	chr10:116576570-116576571	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs571254780	chr10:116576580-116576581	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs61532025	chr10:116576586-116576587	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs377609951	chr10:116576587-116576588	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs564633228	chr10:116576642-116576643	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs117091368	chr10:116576645-116576646	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs142000321	chr10:116576689-116576690	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs148124095	chr10:116576784-116576785	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs4752255	chr10:116576790-116576791	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs543353660	chr10:116576805-116576806	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs561609882	chr10:116576815-116576816	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531736077	chr10:116576928-116576929	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs550228547	chr10:116576998-116576999	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs148714676	chr10:116577010-116577011	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs531168105	chr10:116577021-116577022	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs546045705	chr10:116577025-116577026	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs538879041	chr10:116577119-116577120	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs141249475	chr10:116577121-116577122	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs565867521	chr10:116577131-116577132	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs4752256	chr10:116577161-116577162	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs554431513	chr10:116577162-116577163	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569660727	chr10:116577166-116577167	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs536626303	chr10:116577173-116577174	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs558164714	chr10:116577208-116577209	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576829506	chr10:116577209-116577210	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs541125319	chr10:116577254-116577255	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554032032	chr10:116577261-116577262	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs572591931	chr10:116577285-116577286	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs543291954	chr10:116577363-116577364	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs561545871	chr10:116577382-116577383	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs532080230	chr10:116577387-116577388	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs200572638	chr10:116577391-116577392	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs373338605	chr10:116577392-116577393	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Barrett''s syndrome	19417022	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neuroticism	17667963	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	17133270	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116569800-116580600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr10:116571000-116580600	Weak transcription	Primary hematopoietic stem cells	blood
3	chr10:116572200-116580600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr10:116572200-116580800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr10:116575200-116576200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr10:116575200-116578200	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr10:116575600-116576200	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr10:116575600-116576800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr10:116575800-116576200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr10:116575800-116579400	Weak transcription	Liver	Liver
11	chr10:116576000-116576200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr10:116576000-116576200	Enhancers	Osteobl	bone
13	chr10:116576000-116581000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr10:116576000-116581000	Weak transcription	NHDF-Ad	bronchial
15	chr10:116576200-116579000	Weak transcription	Osteobl	bone
16	chr10:116576200-116579600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr10:116576200-116581000	Weak transcription	Primary monocytes fromperipheralblood	blood
18	chr10:116576400-116579600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:116576800-116579000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr10:116577800-116579000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr10:116578200-116579200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr10:116578800-116580600	Enhancers	Hela-S3	cervix
23	chr10:116579000-116579200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr10:116579000-116579200	Enhancers	NH-A	brain
25	chr10:116579000-116579400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr10:116579000-116579400	Active TSS	Osteobl	bone
27	chr10:116579000-116579600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr10:116579000-116579600	Enhancers	GM12878-XiMat	blood
29	chr10:116579000-116580600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr10:116579000-116580600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr10:116579200-116579400	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr10:116579200-116579400	Enhancers	A549	lung
33	chr10:116579200-116580600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr10:116579400-116579800	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr10:116579400-116579800	Flanking Active TSS	Osteobl	bone
36	chr10:116579400-116580600	Weak transcription	A549	lung
37	chr10:116579400-116580600	Weak transcription	NH-A	brain
38	chr10:116579400-116581000	Enhancers	Liver	Liver
39	chr10:116579400-116583600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr10:116579600-116579800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr10:116579600-116579800	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr10:116579600-116580000	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr10:116579600-116580600	Weak transcription	GM12878-XiMat	blood
44	chr10:116579600-116581000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr10:116579800-116580000	Enhancers	Muscle Satellite Cultured Cells	--
46	chr10:116579800-116580000	Active TSS	Osteobl	bone
47	chr10:116579800-116580600	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr10:116579800-116580600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr10:116579800-116580800	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr10:116579800-116583600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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