Variant report

Variant	esv3407216
Chromosome Location	chr10:116580587-116583135
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:626)
CpG islands
(count:611)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:116582532-116582797	HepG2	liver:	n/a	n/a
2	BACH1	chr10:116581091-116581507	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr10:116581320-116581682	GM12878	blood:	n/a	chr10:116581564-116581577
4	BCLAF1	chr10:116581091-116581650	GM12878	blood:	n/a	chr10:116581564-116581577
5	BHLHE40	chr10:116581215-116581604	GM12878	blood:	n/a	n/a
6	BHLHE40	chr10:116581237-116581877	K562	blood:	n/a	chr10:116581809-116581825 chr10:116581749-116581765 chr10:116581760-116581776 chr10:116581763-116581779
7	BRCA1	chr10:116581416-116581586	HepG2	liver:	n/a	n/a
8	BRCA1	chr10:116580611-116580929	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	chr10:116582256-116582736	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr10:116582180-116582938	IMR90	lung:	n/a	n/a
13	CEBPB	chr10:116581096-116581668	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr10:116582627-116582869	HepG2	liver:	n/a	n/a
15	CEBPB	chr10:116580521-116580887	Hela-S3	cervix:	n/a	chr10:116580606-116580617
16	CEBPB	chr10:116582606-116582939	A549	lung:	n/a	n/a
17	CEBPB	chr10:116582208-116583193	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr10:116581544-116581570	HepG2	liver:	n/a	n/a
19	CEBPB	chr10:116582497-116583034	A549	lung:	n/a	n/a
20	CEBPB	chr10:116582219-116582907	K562	blood:	n/a	n/a
21	CEBPB	chr10:116582520-116583228	MCF-7	breast:	n/a	n/a
22	CHD1	chr10:116580993-116583316	IMR90	lung:	n/a	chr10:116581716-116581726
23	CHD1	chr10:116581223-116583093	GM12878	blood:	n/a	chr10:116581716-116581726
24	CHD1	chr10:116581639-116582386	H1-hESC	embryonic stem cell:	n/a	chr10:116581716-116581726
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	chr10:116581263-116581463	K562	blood:	n/a	n/a
28	CHD2	chr10:116581616-116581803	HepG2	liver:	n/a	chr10:116581716-116581726
29	CHD2	chr10:116582464-116582656	GM12878	blood:	n/a	n/a
30	CREB1	chr10:116581276-116581700	A549	lung:	n/a	n/a
31	CTBP2	chr10:116581441-116582211	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr10:116581380-116581530	GM12870	blood:	n/a	n/a
33	CTCF	chr10:116581460-116581610	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr10:116581400-116581550	GM12872	blood:	n/a	n/a
35	CTCF	chr10:116581440-116581590	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr10:116581217-116581831	Spleen_OC	spleen:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
37	CTCF	chr10:116581278-116581626	GM12878	blood:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
38	CTCF	chr10:116581640-116581790	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr10:116581080-116581230	MCF-7	breast:	n/a	chr10:116581103-116581111
40	CTCF	chr10:116581380-116581530	AG09309	skin:	n/a	n/a
41	CTCF	chr10:116581063-116582779	SK-N-SH	brain:	n/a	chr10:116582127-116582140 chr10:116581357-116581370 chr10:116581354-116581372 chr10:116581103-116581111
42	CTCF	chr10:116581420-116581570	HMF	breast:	n/a	n/a
43	CTCF	chr10:116581380-116581530	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr10:116581296-116581637	K562	blood:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
45	CTCF	chr10:116581239-116581598	SK-N-SH_RA	brain:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
46	CTCF	chr10:116581188-116581714	A549	lung:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
47	CTCF	chr10:116581460-116581610	BE2_C	brain:	n/a	n/a
48	CTCF	chr10:116581809-116581863	Gliobla	brain:	n/a	n/a
49	CTCF	chr10:116581340-116581490	RPTEC	kidney:	n/a	chr10:116581357-116581370 chr10:116581354-116581372
50	CTCF	chr10:116581400-116581550	AG09319	gingival:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:116581305-116581355	GM06990	blood:	n/a
2	chr10:116581305-116581355	GM06990	blood:	n/a
3	chr10:116581829-116581879	SK-N-MC	brain:	n/a
4	chr10:116581829-116581879	NHDF-neo	bronchial:	n/a
5	chr10:116581344-116581394	NB4	blood:	n/a
6	chr10:116581183-116581233	HIPEpiC	eye:	n/a
7	chr10:116581248-116581298	RPTEC	kidney:	n/a
8	chr10:116581344-116581394	MCF-7	breast:	n/a
9	chr10:116581183-116581233	AG10803	skin:	n/a
10	chr10:116581248-116581298	SK-N-MC	brain:	n/a
11	chr10:116581808-116581858	ovcar-3	ovarian:	n/a
12	chr10:116581248-116581298	AG09319	gingival:	n/a
13	chr10:116581183-116581233	NH-A	brain:	n/a
14	chr10:116582469-116582519	CMK	blood:	n/a
15	chr10:116581305-116581355	HRPEpiC	eye:	n/a
16	chr10:116581183-116581233	MCF-7	breast:	n/a
17	chr10:116581358-116581408	SK-N-MC	brain:	n/a
18	chr10:116581305-116581355	GM12878	blood:	n/a
19	chr10:116581305-116581355	Jurkat	blood:	n/a
20	chr10:116581829-116581879	AoSMC	blood vessel:	n/a
21	chr10:116581808-116581858	BJ	skin:	n/a
22	chr10:116581344-116581394	HCT-116	colon:	n/a
23	chr10:116581358-116581408	AG04450	lung:	fetal
24	chr10:116581248-116581298	HCF	heart:	n/a
25	chr10:116581808-116581858	SAEC	small airway:	n/a
26	chr10:116582297-116582347	HCF	heart:	n/a
27	chr10:116581829-116581879	HCF	heart:	n/a
28	chr10:116581344-116581394	HRCEpiC	kidney:	n/a
29	chr10:116581305-116581355	SK-N-SH	brain:	n/a
30	chr10:116581808-116581858	H1-hESC	embryonic stem cell:	embryo
31	chr10:116581305-116581355	PrEC	prostate:	n/a
32	chr10:116581358-116581408	AG10803	skin:	n/a
33	chr10:116581829-116581879	HRE	kidney:	n/a
34	chr10:116581305-116581355	HCF	heart:	n/a
35	chr10:116581248-116581298	HEK293	kidney:	embryo
36	chr10:116581248-116581298	AG04450	lung:	fetal
37	chr10:116581808-116581858	Hela-S3	cervix:	n/a
38	chr10:116581829-116581879	BE2_C	brain:	n/a
39	chr10:116581829-116581879	HRPEpiC	eye:	n/a
40	chr10:116581344-116581394	HEK293	kidney:	embryo
41	chr10:116582469-116582519	HMEC	breast:	n/a
42	chr10:116581829-116581879	HUVEC	blood vessel:	n/a
43	chr10:116581829-116581879	GM12892	blood:	n/a
44	chr10:116582469-116582519	LNCaP	prostate:	n/a
45	chr10:116581183-116581233	HEK293	kidney:	embryo
46	chr10:116581183-116581233	RPTEC	kidney:	n/a
47	chr10:116581829-116581879	CMK	blood:	n/a
48	chr10:116582297-116582347	HEEpiC	esophagus:	n/a
49	chr10:116581358-116581408	GM12878	blood:	n/a
50	chr10:116581248-116581298	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr10:116581424..116582241-chr6:24720620..24721196,2	Hela-S3	cervix:
2	chr10:116567584..116574580-chr10:116575101..116583231,11	MCF-7	breast:
3	chr10:116580811..116581705-chr8:27631902..27632494,2	Hela-S3	cervix:
4	chr10:116579148..116581126-chr10:116581176..116582786,3	MCF-7	breast:
5	chr10:116575494..116578184-chr10:116579422..116580946,2	K562	blood:
6	chr10:116577691..116581134-chr10:116581459..116583772,3	MCF-7	breast:
7	chr10:116581616..116582495-chr7:115851052..115851797,2	Hela-S3	cervix:

(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
ENSG00000171320	chromatin interactions
ENSG00000151553	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000215760	chromatin interactions

Extended variants
information (count: 73 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544192389	chr10:116580588-116580589	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs10450384	chr10:116580591-116580592	Weak transcription Active TSS Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs532996568	chr10:116580623-116580624	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs141392294	chr10:116580754-116580755	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs566609447	chr10:116580791-116580792	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs72833130	chr10:116580794-116580795	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs546825331	chr10:116580802-116580803	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs145167292	chr10:116580838-116580839	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs535768852	chr10:116580842-116580843	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs192740495	chr10:116580868-116580869	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs138788223	chr10:116580936-116580937	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs185189428	chr10:116580983-116580984	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs113167463	chr10:116581009-116581010	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs189064735	chr10:116581047-116581048	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	Overlapped CNVs	n/a
15	rs116905900	chr10:116581209-116581210	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs533958189	chr10:116581262-116581263	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs555614445	chr10:116581356-116581357	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs573954580	chr10:116581365-116581366	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs544520169	chr10:116581379-116581380	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs562464564	chr10:116581399-116581400	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs808271	chr10:116581411-116581412	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs369559357	chr10:116581422-116581423	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs577562489	chr10:116581455-116581456	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs545017628	chr10:116581459-116581460	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs808270	chr10:116581486-116581487	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs559976929	chr10:116581542-116581543	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs527401571	chr10:116581561-116581562	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs546763945	chr10:116581580-116581581	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs561951534	chr10:116581596-116581597	Active TSS Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs529507099	chr10:116581658-116581659	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs181836930	chr10:116581661-116581662	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs569578360	chr10:116581711-116581712	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs539425596	chr10:116581792-116581793	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs551784914	chr10:116581831-116581832	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs2984930	chr10:116581887-116581888	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs2984931	chr10:116581935-116581936	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs2984932	chr10:116581959-116581960	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs2760668	chr10:116582017-116582018	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs11196929	chr10:116582080-116582081	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs534308761	chr10:116582143-116582144	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs113254458	chr10:116582187-116582188	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs555553085	chr10:116582189-116582190	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs573890592	chr10:116582202-116582203	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs538078094	chr10:116582211-116582212	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs556162324	chr10:116582221-116582222	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs577903678	chr10:116582228-116582229	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs544645684	chr10:116582241-116582242	Active TSS Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs563571871	chr10:116582281-116582282	Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs140445059	chr10:116582297-116582298	Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530671608	chr10:116582333-116582334	Active TSS Flanking Active TSS	Chromatin interactive region	1 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:305 , 50 per page) page: 1 2 3 4 5 6 7

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	chr10:116576000-116581000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr10:116576000-116581000	Weak transcription	NHDF-Ad	bronchial
7	chr10:116576200-116581000	Weak transcription	Primary monocytes fromperipheralblood	blood
8	chr10:116578800-116580600	Enhancers	Hela-S3	cervix
9	chr10:116579000-116580600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr10:116579000-116580600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr10:116579200-116580600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr10:116579400-116580600	Weak transcription	A549	lung
13	chr10:116579400-116580600	Weak transcription	NH-A	brain
14	chr10:116579400-116581000	Enhancers	Liver	Liver
15	chr10:116579400-116583600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr10:116579600-116580600	Weak transcription	GM12878-XiMat	blood
17	chr10:116579600-116581000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr10:116579800-116580600	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr10:116579800-116580600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr10:116579800-116580800	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr10:116579800-116583600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr10:116580000-116580600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr10:116580000-116580600	Enhancers	Adipose Nuclei	Adipose
24	chr10:116580200-116580600	Active TSS	Osteobl	bone
25	chr10:116580200-116582200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr10:116580400-116580600	Enhancers	Dnd41	blood
27	chr10:116580400-116580600	Enhancers	HUVEC	blood vessel
28	chr10:116580400-116580600	Enhancers	NHEK	skin
29	chr10:116580400-116581000	Enhancers	Primary T cells fromperipheralblood	blood
30	chr10:116580400-116581200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr10:116580600-116580800	Enhancers	Primary T cells from cord blood	blood
32	chr10:116580600-116580800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
33	chr10:116580600-116580800	Flanking Active TSS	Adipose Nuclei	Adipose
34	chr10:116580600-116580800	Enhancers	Stomach Mucosa	stomach
35	chr10:116580600-116580800	Flanking Active TSS	A549	lung
36	chr10:116580600-116580800	Flanking Active TSS	Hela-S3	cervix
37	chr10:116580600-116580800	Enhancers	NH-A	brain
38	chr10:116580600-116581000	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr10:116580600-116581000	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr10:116580600-116581000	Enhancers	Primary T helper cells PMA-I stimulated	--
41	chr10:116580600-116581000	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr10:116580600-116581000	Active TSS	Muscle Satellite Cultured Cells	--
43	chr10:116580600-116581000	Enhancers	Colon Smooth Muscle	Colon
44	chr10:116580600-116581000	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr10:116580600-116581200	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr10:116580600-116581200	Enhancers	Primary hematopoietic stem cells	blood
47	chr10:116580600-116581200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
48	chr10:116580600-116581200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr10:116580600-116581200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr10:116580600-116581200	Flanking Active TSS	Osteobl	bone

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