Variant report

Variant	nsv895996
Chromosome Location	chr10:110739765-110991026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr10:110822054-110822512	GM12878	blood:	n/a	n/a
2	ATF2	chr10:110822004-110822546	GM12878	blood:	n/a	n/a
3	BACH1	chr10:110962081-110962083	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr10:110789641-110790009	GM12878	blood:	n/a	chr10:110789877-110789886
5	BCL11A	chr10:110789702-110789967	GM12878	blood:	n/a	chr10:110789894-110789903
6	BCL11A	chr10:110965722-110965968	GM12878	blood:	n/a	n/a
7	BCL3	chr10:110965656-110966031	GM12878	blood:	n/a	n/a
8	BCLAF1	chr10:110789732-110789946	GM12878	blood:	n/a	chr10:110789894-110789903
9	CEBPB	chr10:110822162-110822463	IMR90	lung:	n/a	n/a
10	CEBPB	chr10:110963404-110963714	IMR90	lung:	n/a	n/a
11	CEBPB	chr10:110875582-110875736	H1-hESC	embryonic stem cell:	n/a	chr10:110875710-110875723
12	CEBPB	chr10:110887763-110888031	HepG2	liver:	n/a	chr10:110887931-110887942
13	CEBPB	chr10:110943073-110943417	IMR90	lung:	n/a	n/a
14	CEBPB	chr10:110810360-110810672	HepG2	liver:	n/a	chr10:110810481-110810492
15	CEBPB	chr10:110806245-110806445	HepG2	liver:	n/a	chr10:110806360-110806371
16	CEBPB	chr10:110806187-110806422	A549	lung:	n/a	chr10:110806360-110806371
17	CEBPB	chr10:110903762-110903848	HepG2	liver:	n/a	chr10:110903779-110903792 chr10:110903779-110903790
18	CEBPB	chr10:110778780-110779016	A549	lung:	n/a	chr10:110778873-110778886
19	CEBPB	chr10:110778732-110779120	IMR90	lung:	n/a	chr10:110778873-110778886
20	CEBPB	chr10:110951009-110951335	IMR90	lung:	n/a	chr10:110951178-110951189
21	CEBPB	chr10:110752721-110752754	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr10:110947314-110947879	IMR90	lung:	n/a	n/a
23	CEBPB	chr10:110965666-110966667	IMR90	lung:	n/a	n/a
24	CEBPB	chr10:110835498-110835735	HepG2	liver:	n/a	chr10:110835654-110835663 chr10:110835654-110835663
25	CEBPB	chr10:110740473-110740646	HepG2	liver:	n/a	chr10:110740560-110740573 chr10:110740560-110740571 chr10:110740561-110740572
26	CEBPB	chr10:110951036-110951329	HepG2	liver:	n/a	chr10:110951178-110951189
27	CEBPB	chr10:110841702-110841925	HepG2	liver:	n/a	n/a
28	CHD2	chr10:110864739-110864742	K562	blood:	n/a	n/a
29	CTCF	chr10:110885969-110886100	Medullo	brain:	n/a	n/a
30	CTCF	chr10:110778600-110778750	HVMF	connective:	n/a	n/a
31	CTCF	chr10:110831380-110831530	SK-N-SH_RA	brain:	n/a	n/a
32	CTCF	chr10:110778700-110778850	HFF	foreskin:	n/a	chr10:110778828-110778849 chr10:110778834-110778850
33	CTCF	chr10:110778823-110778892	Pancreas_OC	pancreas:	n/a	chr10:110778828-110778849 chr10:110778834-110778850
34	CTCF	chr10:110803188-110803218	GM20000	blood:	n/a	n/a
35	CTCF	chr10:110885940-110886090	Caco-2	colon:	n/a	n/a
36	CTCF	chr10:110778760-110778910	GM12874	blood:	n/a	chr10:110778828-110778849 chr10:110778834-110778850
37	CTCF	chr10:110778760-110778910	HBMEC	blood vessel:	n/a	chr10:110778828-110778849 chr10:110778834-110778850
38	CTCF	chr10:110885900-110886050	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr10:110831300-110831450	BE2_C	brain:	n/a	n/a
40	CTCF	chr10:110885901-110886160	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr10:110885980-110886130	HMF	breast:	n/a	n/a
42	CTCF	chr10:110778776-110778932	GM10248	blood:	n/a	chr10:110778828-110778849 chr10:110778834-110778850
43	CTCF	chr10:110886001-110886089	Gliobla	brain:	n/a	n/a
44	CTCF	chr10:110778780-110778930	SK-N-SH_RA	brain:	n/a	chr10:110778828-110778849 chr10:110778834-110778850
45	CTCF	chr10:110885940-110886090	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr10:110885920-110886070	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr10:110831427-110831535	GM12878	blood:	n/a	n/a
48	CTCF	chr10:110885920-110886070	HVMF	connective:	n/a	n/a
49	CTCF	chr10:110885817-110886144	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr10:110983436-110983590	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:110946662-110946712	Caco-2	colon:	n/a
2	chr10:110741628-110741678	ovcar-3	ovarian:	n/a
3	chr10:110946662-110946712	HCT-116	colon:	n/a
4	chr10:110741628-110741678	BJ	skin:	n/a
5	chr10:110946662-110946712	CMK	blood:	n/a
6	chr10:110741628-110741678	AG09309	skin:	n/a
7	chr10:110946662-110946712	LNCaP	prostate:	n/a
8	chr10:110741628-110741678	GM19239	blood:	n/a
9	chr10:110946662-110946712	ProgFib	skin:	n/a
10	chr10:110741628-110741678	SK-N-SH_RA	brain:	n/a
11	chr10:110741628-110741678	RPTEC	kidney:	n/a
12	chr10:110946662-110946712	NT2-D1	testis:	n/a
13	chr10:110946662-110946712	A549	lung:	n/a
14	chr10:110741628-110741678	HCT-116	colon:	n/a
15	chr10:110741628-110741678	ECC-1	luminal epithelium:	n/a
16	chr10:110946662-110946712	NB4	blood:	n/a
17	chr10:110946662-110946712	GM06990	blood:	n/a
18	chr10:110946662-110946712	GM12878	blood:	n/a
19	chr10:110741628-110741678	AG09319	gingival:	n/a
20	chr10:110741628-110741678	HPAEpiC	pulmonary alveolar:	n/a
21	chr10:110946662-110946712	GM12891	blood:	n/a
22	chr10:110741628-110741678	PrEC	prostate:	n/a
23	chr10:110741628-110741678	HAEpiC	amniotic membrane:	n/a
24	chr10:110741628-110741678	GM12891	blood:	n/a
25	chr10:110741628-110741678	LNCaP	prostate:	n/a
26	chr10:110741628-110741678	AG04449	skin:	fetal
27	chr10:110741628-110741678	SK-N-SH	brain:	n/a
28	chr10:110741628-110741678	HRPEpiC	eye:	n/a
29	chr10:110946662-110946712	NH-A	brain:	n/a
30	chr10:110741628-110741678	Jurkat	blood:	n/a
31	chr10:110946662-110946712	HEEpiC	esophagus:	n/a
32	chr10:110946662-110946712	HL-60	blood:	n/a
33	chr10:110946662-110946712	PrEC	prostate:	n/a
34	chr10:110741628-110741678	HCF	heart:	n/a
35	chr10:110946662-110946712	AG04450	lung:	fetal
36	chr10:110946662-110946712	HRCEpiC	kidney:	n/a
37	chr10:110946662-110946712	ECC-1	luminal epithelium:	n/a
38	chr10:110741628-110741678	A549	lung:	n/a
39	chr10:110741628-110741678	NHBE	bronchial:	n/a
40	chr10:110946662-110946712	GM12892	blood:	n/a
41	chr10:110741628-110741678	HNPCEpiC	eye:	n/a
42	chr10:110741628-110741678	PFSK-1	brain:	n/a
43	chr10:110741628-110741678	GM12878	blood:	n/a
44	chr10:110741628-110741678	ProgFib	skin:	n/a
45	chr10:110946662-110946712	U87	brain:	n/a
46	chr10:110741628-110741678	H1-hESC	embryonic stem cell:	embryo
47	chr10:110741628-110741678	HRE	kidney:	n/a
48	chr10:110946662-110946712	HUVEC	blood vessel:	n/a
49	chr10:110741628-110741678	NT2-D1	testis:	n/a
50	chr10:110741628-110741678	MCF-7	breast:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:110778371..110779098-chr10:111625911..111626776,3	MCF-7	breast:
2	chr10:110947357..110950585-chr10:110952313..110955318,3	K562	blood:
3	chr10:110947357..110950585-chr10:110952313..110955318,3	K562	blood:
4	chr10:110909632..110912318-chr10:110918760..110920466,2	MCF-7	breast:
5	chr10:110909632..110912318-chr10:110918760..110920466,2	MCF-7	breast:
6	chr10:110778372..110779316-chr10:111186907..111187555,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADD3-2	chr10:110748587-110748683	XLOC_008609
2	lnc-ADD3-1	chr10:110759920-110759969	XLOC_008610
3	lnc-ADD3-2	chr10:110759882-110759905	XLOC_008609
4	lnc-ADD3-1	chr10:110778428-110778745	XLOC_008610
5	lnc-ADD3-10	chr10:110749872-110749959	l_372_chr10:110721109-110768632_testes
6	lnc-ADD3-10	chr10:110768418-110768632	l_372_chr10:110721109-110768632_testes

No data

Variant related genes	Relation type
RNU5B-6P	TF binding region
RNU5B-6P	CpG island
RNF138	miRNA target sites
STAG2	miRNA target sites
IRAK2	miRNA target sites
STAM2	miRNA target sites

Extended variants
information (count: 4145 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:4145 , 50 per page) page: 1 2 3 4 5 6 7 ... 83

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34534012	chr10:110741622-110741623	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549140464	chr10:110741629-110741630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566123020	chr10:110741690-110741691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs139250015	chr10:110741700-110741701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs558160915	chr10:110741720-110741721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571662814	chr10:110741738-110741739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537397682	chr10:110741745-110741746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs557500010	chr10:110741861-110741862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114939728	chr10:110741877-110741878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs542864063	chr10:110741904-110741905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs553159716	chr10:110741913-110741914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs79921434	chr10:110741955-110741956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149972966	chr10:110741978-110741979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368208737	chr10:110741979-110741980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs530425523	chr10:110741980-110741981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs543763039	chr10:110742042-110742043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145249795	chr10:110742062-110742063	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529769676	chr10:110742100-110742101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547015795	chr10:110742156-110742157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542882130	chr10:110742166-110742167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs568356798	chr10:110742237-110742238	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs183312582	chr10:110742246-110742247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566305979	chr10:110742319-110742320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs118157913	chr10:110742322-110742323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs376218997	chr10:110742327-110742328	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113387508	chr10:110742330-110742331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149157231	chr10:110742337-110742338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs368162699	chr10:110742394-110742395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35928290	chr10:110742433-110742434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs34479412	chr10:110742437-110742438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35641922	chr10:110742452-110742453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537458222	chr10:110742455-110742456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs550966136	chr10:110742456-110742457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs34435720	chr10:110742461-110742462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs35487018	chr10:110742473-110742474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567643591	chr10:110742478-110742479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34359125	chr10:110742563-110742564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs536777263	chr10:110742576-110742577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35825823	chr10:110742580-110742581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142411984	chr10:110742582-110742583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187996908	chr10:110742601-110742602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575394012	chr10:110742607-110742608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs558820036	chr10:110742665-110742666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78247582	chr10:110742699-110742700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550950794	chr10:110742802-110742803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542671754	chr10:110742820-110742821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs560587302	chr10:110742835-110742836	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs574086218	chr10:110742898-110742899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs80197413	chr10:110742927-110742928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540009791	chr10:110742968-110742969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Autism	22495311	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
High-grade prostatic intraepithelial neoplasia	16573809	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
renal hypoplasia	20603712	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Myxofibrosarcoma	16751306	CNVD
Cornelia de Lange syndrome	24599119	CNVD
T-cell lymphomas	19863542	CNVD
Breast cancer	16397240	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	16616336	CNVD
Chronic lymphocytic leukemia	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21364760	CNVD
Barrett''s syndrome	19417022	CNVD
Sezary syndrome	18413736	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	20962326	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:110741600-110742000	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr10:110741600-110742000	Enhancers	Fetal Stomach	stomach
3	chr10:110741600-110742200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr10:110741600-110742600	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr10:110741800-110742200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr10:110742000-110742400	Weak transcription	Fetal Stomach	stomach
7	chr10:110742400-110742600	Enhancers	Fetal Stomach	stomach
8	chr10:110742600-110744600	Weak transcription	Fetal Stomach	stomach
9	chr10:110744600-110747200	Enhancers	Fetal Stomach	stomach
10	chr10:110745000-110745200	Enhancers	Rectal Smooth Muscle	rectum
11	chr10:110745800-110746000	Enhancers	Rectal Smooth Muscle	rectum
12	chr10:110746200-110747000	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr10:110746200-110747400	Enhancers	HSMMtube	muscle
14	chr10:110747000-110747200	Enhancers	Fetal Brain Male	brain
15	chr10:110747200-110749200	Weak transcription	Fetal Stomach	stomach
16	chr10:110747400-110748600	Weak transcription	Fetal Brain Male	brain
17	chr10:110748600-110750400	Enhancers	Fetal Brain Male	brain
18	chr10:110749200-110750400	Enhancers	Fetal Stomach	stomach
19	chr10:110749400-110749600	Enhancers	Fetal Lung	lung
20	chr10:110749400-110750400	Enhancers	Fetal Brain Female	brain
21	chr10:110749600-110750200	Enhancers	Colon Smooth Muscle	Colon
22	chr10:110749600-110750400	Enhancers	Brain Germinal Matrix	brain
23	chr10:110750200-110750400	Enhancers	Fetal Lung	lung
24	chr10:110778400-110779200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr10:110778400-110779400	Enhancers	Adipose Nuclei	Adipose
26	chr10:110779000-110779400	Enhancers	Fetal Stomach	stomach
27	chr10:110779400-110782000	Weak transcription	Adipose Nuclei	Adipose
28	chr10:110782000-110782400	Enhancers	Adipose Nuclei	Adipose
29	chr10:110782400-110786400	Weak transcription	Adipose Nuclei	Adipose
30	chr10:110786400-110786600	Enhancers	Pancreas	Pancrea
31	chr10:110786400-110788600	Enhancers	Adipose Nuclei	Adipose
32	chr10:110788600-110789000	Enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr10:110789000-110789400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr10:110789400-110790000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr10:110789800-110790200	Enhancers	Fetal Brain Male	brain
36	chr10:110790200-110790600	Weak transcription	Fetal Brain Male	brain
37	chr10:110790600-110791200	Enhancers	Fetal Brain Male	brain
38	chr10:110800400-110800600	ZNF genes & repeats	Spleen	Spleen
39	chr10:110800400-110800800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr10:110800800-110807600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr10:110807600-110807800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr10:110823400-110824000	Enhancers	Muscle Satellite Cultured Cells	--
43	chr10:110824400-110824800	Enhancers	Fetal Brain Male	brain
44	chr10:110824800-110825600	Weak transcription	Fetal Brain Male	brain
45	chr10:110825600-110826600	Enhancers	Fetal Brain Male	brain
46	chr10:110826600-110827400	Enhancers	Fetal Intestine Large	intestine
47	chr10:110826600-110831000	Weak transcription	Fetal Brain Male	brain
48	chr10:110831000-110831800	Enhancers	Fetal Brain Male	brain
49	chr10:110845200-110845800	ZNF genes & repeats	Pancreas	Pancrea
50	chr10:110845800-110848600	Weak transcription	Pancreas	Pancrea

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