Variant report

Variant	esv1814163
Chromosome Location	chr10:116519705-116582581
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1313)
CpG islands
(count:1162)
Chromatin interactive
region (count:31)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1313 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:116546209-116546472	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:116546208-116546488	K562	blood:	n/a	n/a
3	ARID3A	chr10:116582532-116582797	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:116539550-116539739	HepG2	liver:	n/a	n/a
5	ATF2	chr10:116570558-116571153	GM12878	blood:	n/a	n/a
6	ATF2	chr10:116570638-116571113	GM12878	blood:	n/a	n/a
7	ATF3	chr10:116539376-116540077	A549	lung:	n/a	n/a
8	ATF3	chr10:116539430-116540360	A549	lung:	n/a	n/a
9	BACH1	chr10:116581091-116581507	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr10:116527410-116527614	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr10:116540069-116540343	GM12878	blood:	n/a	chr10:116540218-116540229
12	BATF	chr10:116561175-116561459	GM12878	blood:	n/a	n/a
13	BATF	chr10:116562009-116562225	GM12878	blood:	n/a	n/a
14	BCL11A	chr10:116561112-116561422	GM12878	blood:	n/a	n/a
15	BCL3	chr10:116539380-116540153	A549	lung:	n/a	n/a
16	BCL3	chr10:116539343-116540260	A549	lung:	n/a	n/a
17	BCL3	chr10:116581320-116581682	GM12878	blood:	n/a	chr10:116581564-116581577
18	BCLAF1	chr10:116581091-116581650	GM12878	blood:	n/a	chr10:116581564-116581577
19	BHLHE40	chr10:116581215-116581604	GM12878	blood:	n/a	n/a
20	BHLHE40	chr10:116546232-116546402	GM12878	blood:	n/a	n/a
21	BHLHE40	chr10:116581237-116581877	K562	blood:	n/a	chr10:116581809-116581825 chr10:116581749-116581765 chr10:116581760-116581776 chr10:116581763-116581779
22	BRCA1	chr10:116580611-116580929	Hela-S3	cervix:	n/a	n/a
23	BRCA1	chr10:116539546-116540067	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr10:116527383-116527509	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr10:116579101-116579527	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr10:116581416-116581586	HepG2	liver:	n/a	n/a
27	CBX3	chr10:116581162-116581461	K562	blood:	n/a	n/a
28	CCNT2	chr10:116581247-116582165	K562	blood:	n/a	n/a
29	CEBPB	chr10:116580521-116580887	Hela-S3	cervix:	n/a	chr10:116580606-116580617
30	CEBPB	chr10:116579078-116579518	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr10:116532206-116532408	IMR90	lung:	n/a	n/a
32	CEBPB	chr10:116582219-116582907	K562	blood:	n/a	n/a
33	CEBPB	chr10:116539532-116539917	MCF-7	breast:	n/a	n/a
34	CEBPB	chr10:116582180-116582938	IMR90	lung:	n/a	n/a
35	CEBPB	chr10:116546255-116546566	Hela-S3	cervix:	n/a	chr10:116546443-116546456
36	CEBPB	chr10:116539515-116540003	MCF-7	breast:	n/a	n/a
37	CEBPB	chr10:116566465-116567260	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr10:116581544-116581570	HepG2	liver:	n/a	n/a
39	CEBPB	chr10:116539492-116539905	IMR90	lung:	n/a	n/a
40	CEBPB	chr10:116539359-116540144	A549	lung:	n/a	n/a
41	CEBPB	chr10:116539436-116540144	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:116581096-116581668	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr10:116539459-116540005	A549	lung:	n/a	n/a
44	CEBPB	chr10:116582497-116583034	A549	lung:	n/a	n/a
45	CEBPB	chr10:116546292-116546580	A549	lung:	n/a	chr10:116546443-116546456
46	CEBPB	chr10:116538612-116538620	IMR90	lung:	n/a	n/a
47	CEBPB	chr10:116582256-116582736	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr10:116559582-116559596	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr10:116559583-116559661	IMR90	lung:	n/a	n/a
50	CEBPB	chr10:116539137-116540864	HCT-116	colon:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:116581808-116581858	NB4	blood:	n/a
2	chr10:116530809-116530859	BE2_C	brain:	n/a
3	chr10:116581183-116581233	HCF	heart:	n/a
4	chr10:116581808-116581858	NB4	blood:	n/a
5	chr10:116530809-116530859	BE2_C	brain:	n/a
6	chr10:116581183-116581233	HCF	heart:	n/a
7	chr10:116582469-116582519	NHBE	bronchial:	n/a
8	chr10:116581305-116581355	HEK293	kidney:	embryo
9	chr10:116581808-116581858	LNCaP	prostate:	n/a
10	chr10:116530809-116530859	IMR90	lung:	fetal
11	chr10:116528187-116528237	IMR90	lung:	fetal
12	chr10:116528228-116528278	BE2_C	brain:	n/a
13	chr10:116582469-116582519	HRE	kidney:	n/a
14	chr10:116528363-116528413	HCM	heart:	n/a
15	chr10:116528228-116528278	BJ	skin:	n/a
16	chr10:116581305-116581355	ProgFib	skin:	n/a
17	chr10:116581808-116581858	HepG2	liver:	n/a
18	chr10:116528187-116528237	HPAEpiC	pulmonary alveolar:	n/a
19	chr10:116527201-116527251	HRCEpiC	kidney:	n/a
20	chr10:116582297-116582347	AoSMC	blood vessel:	n/a
21	chr10:116581829-116581879	HepG2	liver:	n/a
22	chr10:116530809-116530859	HCPEpiC	choroid plexus:	n/a
23	chr10:116528228-116528278	Hepatocyte	liver:	n/a
24	chr10:116581358-116581408	PANC-1	pancreas:	n/a
25	chr10:116528187-116528237	MCF-7	breast:	n/a
26	chr10:116582297-116582347	GM06990	blood:	n/a
27	chr10:116581112-116581162	Jurkat	blood:	n/a
28	chr10:116528581-116528631	AoSMC	blood vessel:	n/a
29	chr10:116530809-116530859	Jurkat	blood:	n/a
30	chr10:116581344-116581394	HRPEpiC	eye:	n/a
31	chr10:116581248-116581298	HEEpiC	esophagus:	n/a
32	chr10:116530809-116530859	HCT-116	colon:	n/a
33	chr10:116581183-116581233	NB4	blood:	n/a
34	chr10:116581183-116581233	HNPCEpiC	eye:	n/a
35	chr10:116581305-116581355	PANC-1	pancreas:	n/a
36	chr10:116528318-116528368	K562	blood:	n/a
37	chr10:116528187-116528237	SK-N-MC	brain:	n/a
38	chr10:116582469-116582519	NB4	blood:	n/a
39	chr10:116582469-116582519	SK-N-SH	brain:	n/a
40	chr10:116581344-116581394	HepG2	liver:	n/a
41	chr10:116528187-116528237	GM06990	blood:	n/a
42	chr10:116581183-116581233	AG09309	skin:	n/a
43	chr10:116581183-116581233	HCPEpiC	choroid plexus:	n/a
44	chr10:116527795-116527845	HEEpiC	esophagus:	n/a
45	chr10:116582469-116582519	SK-N-MC	brain:	n/a
46	chr10:116581344-116581394	HUVEC	blood vessel:	n/a
47	chr10:116581248-116581298	SK-N-MC	brain:	n/a
48	chr10:116528581-116528631	HAEpiC	amniotic membrane:	n/a
49	chr10:116581248-116581298	NHBE	bronchial:	n/a
50	chr10:116581808-116581858	AoSMC	blood vessel:	n/a

(count:31 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:116469822..116472730-chr10:116527178..116529089,2	MCF-7	breast:
2	chr10:116575612..116578929-chr10:116581323..116583414,4	MCF-7	breast:
3	chr10:116310327..116310900-chr10:116545935..116546455,2	MCF-7	breast:
4	chr10:116520053..116522860-chr10:116528096..116531529,3	K562	blood:
5	chr10:116531753..116534346-chr10:116628137..116630750,2	K562	blood:
6	chr10:116567584..116574580-chr10:116575101..116583231,11	MCF-7	breast:
7	chr10:116524589..116526478-chr10:116585947..116587960,2	K562	blood:
8	chr10:116564843..116568193-chr10:116577870..116580490,3	MCF-7	breast:
9	chr10:116463343..116464122-chr10:116545816..116546627,2	MCF-7	breast:
10	chr10:116510537..116513350-chr10:116526093..116528633,2	MCF-7	breast:
11	chr10:116579148..116581126-chr10:116581176..116582786,3	MCF-7	breast:
12	chr10:116528299..116531150-chr10:116536234..116538726,2	MCF-7	breast:
13	chr10:116526447..116528712-chr10:116580718..116582885,3	MCF-7	breast:
14	chr10:116529761..116532511-chr10:116581268..116583823,3	MCF-7	breast:
15	chr10:116575494..116578184-chr10:116579422..116580946,2	K562	blood:
16	chr10:116580811..116581705-chr8:27631902..27632494,2	Hela-S3	cervix:
17	chr10:116575494..116578184-chr10:116579422..116580946,2	K562	blood:
18	chr10:116520053..116522860-chr10:116528096..116531529,3	K562	blood:
19	chr10:116581616..116582495-chr7:115851052..115851797,2	Hela-S3	cervix:
20	chr10:116581424..116582241-chr6:24720620..24721196,2	Hela-S3	cervix:
21	chr10:116564843..116568193-chr10:116577870..116580490,3	MCF-7	breast:
22	chr10:116296905..116298827-chr10:116577093..116580051,2	MCF-7	breast:
23	chr10:116484261..116485769-chr10:116537705..116539311,2	MCF-7	breast:
24	chr10:116284639..116286631-chr10:116544810..116546439,2	MCF-7	breast:
25	chr10:116567584..116574580-chr10:116575101..116583231,11	MCF-7	breast:
26	chr10:116512788..116514605-chr10:116528016..116530958,2	MCF-7	breast:
27	chr10:116574613..116576880-chr10:116580074..116582189,2	MCF-7	breast:
28	chr10:116546305..116546864-chr10:116581188..116581980,2	MCF-7	breast:
29	chr10:116483992..116485637-chr10:116525925..116527534,2	MCF-7	breast:
30	chr10:116577691..116581134-chr10:116581459..116583772,3	MCF-7	breast:
31	chr10:116528299..116531150-chr10:116536234..116538726,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM160B1-1	chr10:116538334-116539662	NONHSAT016463
2	lnc-FAM160B1-1	chr10:116535701-116535920	NONHSAT016463
3	lnc-FAM160B1-4	chr10:116527700-116528317	ucscGeneNc_uc001lca_1
4	lnc-FAM160B1-1	chr10:116524547-116524751	NONHSAT016463
5	lnc-ABLIM1-1	chr10:116581032-116581425	NONHSAT016464
6	lnc-FAM160B1-1	chr10:116524547-116524751	ENSG00000228484
7	lnc-ABLIM1-1	chr10:116552407-116552431	NONHSAT016464
8	lnc-FAM160B1-3	chr10:116570684-116570929	NONHSAT016465
9	lnc-FAM160B1-1	chr10:116537710-116538327	NONHSAT016463
10	lnc-FAM160B1-1	chr10:116535701-116535920	ENSG00000228484
11	lnc-FAM160B1-1	chr10:116537710-116539662	ENSG00000228484
12	lnc-FAM160B1-4	chr10:116525691-116525910	ucscGeneNc_uc001lca_1
13	lnc-FAM160B1-3	chr10:116569134-116569386	NONHSAT016465

No data

Variant related genes	Relation type
FAM160B1	TF binding region
ENSG00000228484	TF binding region
TAF9BP2	TF binding region
FAM160B1	CpG island
ENSG00000228484	CpG island
TAF9BP2	CpG island
ENSG00000099204	chromatin interactions
ENSG00000215760	chromatin interactions
ENSG00000112308	chromatin interactions
ENSG00000151553	chromatin interactions
ENSG00000171320	chromatin interactions
UTP15	miRNA target sites
ASCC3	miRNA target sites

Extended variants
information (count: 2363 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:2363 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571387324	chr10:116519751-116519752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs533530696	chr10:116519823-116519824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145616990	chr10:116519911-116519912	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs190909873	chr10:116519915-116519916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183236305	chr10:116519962-116519963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs553767047	chr10:116519980-116519981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188160490	chr10:116519982-116519983	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs567535756	chr10:116520015-116520016	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs537875103	chr10:116520031-116520032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556207849	chr10:116520049-116520050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113303502	chr10:116520075-116520076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73373774	chr10:116520125-116520126	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs141062346	chr10:116520139-116520140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376885872	chr10:116520164-116520165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573903656	chr10:116520167-116520168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs3981296	chr10:116520197-116520198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs58286785	chr10:116520199-116520200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs71007490	chr10:116520203-116520204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs80214827	chr10:116520208-116520209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542548397	chr10:116520213-116520214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561265800	chr10:116520251-116520252	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs531306578	chr10:116520264-116520265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs543457396	chr10:116520280-116520281	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368565154	chr10:116520294-116520295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs553242029	chr10:116520311-116520312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564933927	chr10:116520332-116520333	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532250518	chr10:116520370-116520371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs547519965	chr10:116520465-116520466	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182879121	chr10:116520508-116520509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs117773512	chr10:116520536-116520537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs549388250	chr10:116520573-116520574	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs567968551	chr10:116520621-116520622	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs537810736	chr10:116520778-116520779	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs542255700	chr10:116520849-116520850	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs540870778	chr10:116520871-116520872	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs144603460	chr10:116520894-116520895	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs187555933	chr10:116520932-116520933	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs538741874	chr10:116520936-116520937	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs139024248	chr10:116520937-116520938	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs808300	chr10:116520963-116520964	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs147884530	chr10:116520967-116520968	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs140484700	chr10:116521023-116521024	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs562630488	chr10:116521025-116521026	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs80330493	chr10:116521026-116521027	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs398046260	chr10:116521037-116521038	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs397725863	chr10:116521038-116521039	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs554533198	chr10:116521067-116521068	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs576424552	chr10:116521127-116521128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs74158052	chr10:116521129-116521130	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs79950178	chr10:116521160-116521161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:116513800-116527000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr10:116515000-116527400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:116515400-116521200	Weak transcription	Right Ventricle	heart
4	chr10:116515600-116521000	Weak transcription	Right Atrium	heart
5	chr10:116515600-116524400	Weak transcription	Adipose Nuclei	Adipose
6	chr10:116515600-116526200	Weak transcription	Fetal Intestine Small	intestine
7	chr10:116516600-116521800	Enhancers	Fetal Heart	heart
8	chr10:116517200-116521000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr10:116517800-116520800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr10:116518000-116521000	Weak transcription	Left Ventricle	heart
11	chr10:116518000-116526400	Weak transcription	Brain Anterior Caudate	brain
12	chr10:116518400-116521000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:116518400-116526400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr10:116518600-116519800	Weak transcription	Brain Cingulate Gyrus	brain
15	chr10:116518600-116521000	Weak transcription	Brain Hippocampus Middle	brain
16	chr10:116519600-116520400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr10:116519800-116520000	Enhancers	Brain Cingulate Gyrus	brain
18	chr10:116520000-116520600	Weak transcription	Brain Cingulate Gyrus	brain
19	chr10:116520400-116521800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr10:116520600-116521600	Enhancers	Brain Cingulate Gyrus	brain
21	chr10:116520800-116521400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr10:116521000-116521400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr10:116521000-116521600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr10:116521000-116521600	Enhancers	Left Ventricle	heart
25	chr10:116521000-116521600	Enhancers	Right Atrium	heart
26	chr10:116521000-116521800	Enhancers	Brain Hippocampus Middle	brain
27	chr10:116521200-116521400	Enhancers	Brain Inferior Temporal Lobe	brain
28	chr10:116521200-116521600	Enhancers	Right Ventricle	heart
29	chr10:116521400-116525000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr10:116521400-116525600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr10:116521600-116522600	Weak transcription	Left Ventricle	heart
32	chr10:116521600-116524600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr10:116521600-116525600	Weak transcription	Right Atrium	heart
34	chr10:116521600-116526200	Weak transcription	Right Ventricle	heart
35	chr10:116521800-116522600	Weak transcription	Fetal Heart	heart
36	chr10:116521800-116525600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr10:116522600-116522800	Genic enhancers	Fetal Heart	heart
38	chr10:116522600-116523400	Enhancers	Left Ventricle	heart
39	chr10:116522800-116524400	Weak transcription	Fetal Heart	heart
40	chr10:116523200-116523600	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr10:116523400-116524200	Weak transcription	Left Ventricle	heart
42	chr10:116523600-116523800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr10:116523800-116525600	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr10:116524200-116525000	Enhancers	Left Ventricle	heart
45	chr10:116524400-116526000	Enhancers	Adipose Nuclei	Adipose
46	chr10:116524400-116526000	Enhancers	Fetal Heart	heart
47	chr10:116524600-116524800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr10:116524600-116524800	Enhancers	Aorta	Aorta
49	chr10:116524600-116524800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr10:116524600-116524800	Enhancers	Pancreas	Pancrea

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