Variant report

Variant	nsv540645
Chromosome Location	chr10:57470352-58026988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:963)
CpG islands
(count:245)
Chromatin interactive
region (count:34)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr10:57507840-57507889	K562	blood:	n/a	n/a
2	ATF2	chr10:57901748-57902579	GM12878	blood:	n/a	n/a
3	BACH1	chr10:57816600-57816618	K562	blood:	n/a	n/a
4	BACH1	chr10:57696199-57696273	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr10:57518771-57519015	GM12878	blood:	n/a	chr10:57518959-57518970
6	BATF	chr10:57518775-57519069	GM12878	blood:	n/a	chr10:57518959-57518970
7	BATF	chr10:57941408-57941722	GM12878	blood:	n/a	n/a
8	BATF	chr10:57941419-57941655	GM12878	blood:	n/a	n/a
9	BCL11A	chr10:57518766-57519117	GM12878	blood:	n/a	n/a
10	BCLAF1	chr10:57901793-57902423	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:57875201-57875212	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:57850862-57850948	HepG2	liver:	n/a	n/a
13	CEBPB	chr10:57493945-57494290	A549	lung:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
14	CEBPB	chr10:57879199-57879468	K562	blood:	n/a	chr10:57879342-57879355 chr10:57879342-57879355 chr10:57879343-57879354
15	CEBPB	chr10:57873585-57873881	HepG2	liver:	n/a	chr10:57873712-57873723
16	CEBPB	chr10:57703351-57703618	K562	blood:	n/a	chr10:57703483-57703496 chr10:57703485-57703494 chr10:57703480-57703497 chr10:57703485-57703496
17	CEBPB	chr10:57483521-57483980	HepG2	liver:	n/a	chr10:57483842-57483853
18	CEBPB	chr10:57904709-57905039	HepG2	liver:	n/a	chr10:57904866-57904877
19	CEBPB	chr10:57512602-57512721	A549	lung:	n/a	n/a
20	CEBPB	chr10:57844017-57844042	K562	blood:	n/a	n/a
21	CEBPB	chr10:57883123-57883361	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr10:57552760-57553149	A549	lung:	n/a	n/a
23	CEBPB	chr10:57904714-57905021	IMR90	lung:	n/a	chr10:57904866-57904877
24	CEBPB	chr10:57771890-57772244	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr10:57728587-57729655	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr10:58000458-58000612	K562	blood:	n/a	chr10:58000485-58000496 chr10:58000483-58000496
27	CEBPB	chr10:57494052-57494186	H1-hESC	embryonic stem cell:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
28	CEBPB	chr10:57635106-57635391	HepG2	liver:	n/a	chr10:57635230-57635241
29	CEBPB	chr10:57852160-57852447	HepG2	liver:	n/a	chr10:57852267-57852278 chr10:57852266-57852279 chr10:57852266-57852279 chr10:57852265-57852282
30	CEBPB	chr10:57748347-57748542	HepG2	liver:	n/a	chr10:57748421-57748432
31	CEBPB	chr10:58000286-58000636	Hela-S3	cervix:	n/a	chr10:58000485-58000496 chr10:58000483-58000496
32	CEBPB	chr10:57512468-57512713	K562	blood:	n/a	n/a
33	CEBPB	chr10:57873576-57873887	A549	lung:	n/a	chr10:57873712-57873723
34	CEBPB	chr10:57637025-57637307	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:57879224-57879458	A549	lung:	n/a	chr10:57879342-57879355 chr10:57879342-57879355 chr10:57879343-57879354
36	CEBPB	chr10:57728750-57729056	MCF-7	breast:	n/a	n/a
37	CEBPB	chr10:57483591-57483950	A549	lung:	n/a	chr10:57483842-57483853
38	CEBPB	chr10:57552815-57553184	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr10:57493950-57494263	IMR90	lung:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118
40	CEBPB	chr10:57728652-57729024	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr10:57879198-57879474	HepG2	liver:	n/a	chr10:57879342-57879355 chr10:57879342-57879355 chr10:57879343-57879354
42	CEBPB	chr10:57771861-57772274	MCF-7	breast:	n/a	n/a
43	CEBPB	chr10:57507027-57507291	HepG2	liver:	n/a	n/a
44	CEBPB	chr10:57843892-57844145	HepG2	liver:	n/a	chr10:57843968-57843977 chr10:57843966-57843977 chr10:57843968-57843977 chr10:57843967-57843978 chr10:57843968-57843977 chr10:57843968-57843977
45	CEBPB	chr10:57830325-57830474	A549	lung:	n/a	n/a
46	CEBPB	chr10:57506975-57507448	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr10:57560874-57561053	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr10:57495562-57495924	HepG2	liver:	n/a	n/a
49	CEBPB	chr10:57483653-57483898	IMR90	lung:	n/a	chr10:57483842-57483853
50	CEBPB	chr10:57493973-57494246	HepG2	liver:	n/a	chr10:57494109-57494118 chr10:57494109-57494118 chr10:57494107-57494118 chr10:57494109-57494118

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:57915076-57915126	BE2_C	brain:	n/a
2	chr10:57915076-57915126	BE2_C	brain:	n/a
3	chr10:57659566-57659616	LNCaP	prostate:	n/a
4	chr10:57915132-57915182	HEEpiC	esophagus:	n/a
5	chr10:57659702-57659752	HRE	kidney:	n/a
6	chr10:57659702-57659752	HEEpiC	esophagus:	n/a
7	chr10:57915132-57915182	AG04450	lung:	fetal
8	chr10:57659702-57659752	HMEC	breast:	n/a
9	chr10:57915076-57915126	SK-N-SH	brain:	n/a
10	chr10:57915132-57915182	ovcar-3	ovarian:	n/a
11	chr10:57659566-57659616	HCM	heart:	n/a
12	chr10:57659702-57659752	HL-60	blood:	n/a
13	chr10:57915076-57915126	K562	blood:	n/a
14	chr10:57915076-57915126	GM12878	blood:	n/a
15	chr10:57659702-57659752	SK-N-MC	brain:	n/a
16	chr10:57659566-57659616	SK-N-SH_RA	brain:	n/a
17	chr10:57659566-57659616	HEEpiC	esophagus:	n/a
18	chr10:57659702-57659752	PANC-1	pancreas:	n/a
19	chr10:57915076-57915126	SK-N-MC	brain:	n/a
20	chr10:57659566-57659616	RPTEC	kidney:	n/a
21	chr10:57659566-57659616	HRCEpiC	kidney:	n/a
22	chr10:57659702-57659752	HRPEpiC	eye:	n/a
23	chr10:57915076-57915126	PFSK-1	brain:	n/a
24	chr10:57659566-57659616	HL-60	blood:	n/a
25	chr10:57915076-57915126	HMEC	breast:	n/a
26	chr10:57915132-57915182	HCM	heart:	n/a
27	chr10:57915076-57915126	NHDF-neo	bronchial:	n/a
28	chr10:57915076-57915126	AG09319	gingival:	n/a
29	chr10:57659566-57659616	HAEpiC	amniotic membrane:	n/a
30	chr10:57915132-57915182	HMEC	breast:	n/a
31	chr10:57915132-57915182	HRCEpiC	kidney:	n/a
32	chr10:57659702-57659752	A549	lung:	n/a
33	chr10:57915076-57915126	HCPEpiC	choroid plexus:	n/a
34	chr10:57659702-57659752	IMR90	lung:	fetal
35	chr10:57659566-57659616	SK-N-SH	brain:	n/a
36	chr10:57915132-57915182	GM12892	blood:	n/a
37	chr10:57659702-57659752	GM12891	blood:	n/a
38	chr10:57915132-57915182	ECC-1	luminal epithelium:	n/a
39	chr10:57915132-57915182	H1-hESC	embryonic stem cell:	embryo
40	chr10:57915076-57915126	BJ	skin:	n/a
41	chr10:57659566-57659616	ovcar-3	ovarian:	n/a
42	chr10:57915132-57915182	SK-N-SH_RA	brain:	n/a
43	chr10:57915132-57915182	NH-A	brain:	n/a
44	chr10:57659702-57659752	PFSK-1	brain:	n/a
45	chr10:57659566-57659616	Hepatocyte	liver:	n/a
46	chr10:57915132-57915182	AG09309	skin:	n/a
47	chr10:57659702-57659752	CMK	blood:	n/a
48	chr10:57659566-57659616	IMR90	lung:	fetal
49	chr10:57659702-57659752	HepG2	liver:	n/a
50	chr10:57915076-57915126	AG10803	skin:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:55961337..55963211-chr10:57586910..57589588,2	K562	blood:
2	chr10:57475413..57477793-chr10:57482048..57484055,2	K562	blood:
3	chr10:57717449..57719826-chr10:58113141..58115181,2	K562	blood:
4	chr10:57810927..57812454-chr10:57820002..57821661,2	K562	blood:
5	chr10:57909018..57911218-chr10:57914611..57917570,2	K562	blood:
6	chr10:57927604..57930485-chr10:57936536..57938322,2	K562	blood:
7	chr10:57810927..57812454-chr10:57820002..57821661,2	K562	blood:
8	chr10:57748719..57749535-chr10:57876195..57877022,4	MCF-7	breast:
9	chr10:57824291..57825869-chr10:57827938..57830838,2	MCF-7	breast:
10	chr10:57930488..57932712-chr10:57934430..57936445,2	K562	blood:
11	chr10:58004930..58006745-chr10:58107564..58110540,2	K562	blood:
12	chr10:57714459..57717334-chr10:57718560..57721356,2	K562	blood:
13	chr10:57746592..57749487-chr10:57834078..57836757,2	K562	blood:
14	chr10:57824291..57825869-chr10:57827938..57830838,2	MCF-7	breast:
15	chr10:57714459..57717334-chr10:57718560..57721356,2	K562	blood:
16	chr10:57689140..57691906-chr10:57693909..57695941,3	K562	blood:
17	chr10:57859224..57862107-chr10:57868320..57870697,2	K562	blood:
18	chr10:57747558..57749260-chr10:57921516..57923175,2	MCF-7	breast:
19	chr10:57747558..57749260-chr10:57921516..57923175,2	MCF-7	breast:
20	chr10:57930488..57932712-chr10:57934430..57936445,2	K562	blood:
21	chr10:57746592..57749487-chr10:57834078..57836757,2	K562	blood:
22	chr10:57755531..57757629-chr14:20811264..20812832,2	MCF-7	breast:
23	chr10:57757077..57758579-chr10:57764722..57766777,2	MCF-7	breast:
24	chr10:57927604..57930485-chr10:57936536..57938322,2	K562	blood:
25	chr10:57748719..57749535-chr10:57876195..57877022,4	MCF-7	breast:
26	chr10:57986919..57989468-chr10:57989725..57991743,2	K562	blood:
27	chr10:57909018..57911218-chr10:57914611..57917570,2	K562	blood:
28	chr10:57624031..57627084-chr10:57627386..57630706,3	K562	blood:
29	chr10:57624031..57627084-chr10:57627386..57630706,3	K562	blood:
30	chr10:57859224..57862107-chr10:57868320..57870697,2	K562	blood:
31	chr10:57757077..57758579-chr10:57764722..57766777,2	MCF-7	breast:
32	chr10:57475413..57477793-chr10:57482048..57484055,2	K562	blood:
33	chr10:57986919..57989468-chr10:57989725..57991743,2	K562	blood:
34	chr10:57689140..57691906-chr10:57693909..57695941,3	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTRNR2L5-6	chr10:57742833-57743287	l_316_chr10:57728954-57743287_hela
2	lnc-MTRNR2L5-5	chr10:57506311-57506668	NONHSAT013465
3	lnc-ZWINT-1	chr10:57914592-57914731	NONHSAT013466
4	lnc-MTRNR2L5-6	chr10:57742028-57742255	l_316_chr10:57728954-57743287_hela
5	lnc-ZWINT-1	chr10:57911541-57911756	NONHSAT013466
6	lnc-ZWINT-1	chr10:57914592-57914605	FPKM1_group_3344_transcript_1
7	lnc-ZWINT-1	chr10:57914593-57914731	XLOC_008828
8	lnc-ZWINT-1	chr10:57911541-57911756	FPKM1_group_3344_transcript_1
9	lnc-ZWINT-1	chr10:57911542-57911756	XLOC_008828
10	lnc-MTRNR2L5-6	chr10:57728955-57729220	l_316_chr10:57728954-57743287_hela
11	lnc-MTRNR2L5-6	chr10:57732679-57732829	l_316_chr10:57728954-57743287_hela

No data

Variant related genes	Relation type
ENSG00000270541	TF binding region
ENSG00000270541	CpG island
ENSG00000259001	chromatin interactions
ENSG00000129484	chromatin interactions
TAF5L	miRNA target sites

Extended variants
information (count: 4618 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4618 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572079330	chr10:57483405-57483406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs75320408	chr10:57483425-57483426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78315358	chr10:57483442-57483443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548175080	chr10:57483451-57483452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148968965	chr10:57483495-57483496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs143761697	chr10:57483500-57483501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186740544	chr10:57483505-57483506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77466294	chr10:57483641-57483642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs10740625	chr10:57483653-57483654	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs568572990	chr10:57483661-57483662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190644884	chr10:57483665-57483666	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547550453	chr10:57483736-57483737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs118116270	chr10:57483770-57483771	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539832492	chr10:57483823-57483824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376329909	chr10:57483843-57483844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs78578490	chr10:57483918-57483919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535408280	chr10:57483954-57483955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555503671	chr10:57483966-57483967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181793674	chr10:57483998-57483999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs565024663	chr10:57496601-57496602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs147887493	chr10:57496653-57496654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs577064829	chr10:57496664-57496665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528302058	chr10:57496669-57496670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551454536	chr10:57496683-57496684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185925263	chr10:57496692-57496693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544401128	chr10:57496721-57496722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188820805	chr10:57496725-57496726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7923740	chr10:57496774-57496775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116024120	chr10:57496807-57496808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs570336450	chr10:57496822-57496823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs552519652	chr10:57496831-57496832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs376731799	chr10:57496854-57496855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533062913	chr10:57496874-57496875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113498491	chr10:57496875-57496876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12356396	chr10:57496882-57496883	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs181720071	chr10:57496975-57496976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs141422070	chr10:57497017-57497018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187332845	chr10:57497039-57497040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147017115	chr10:57497046-57497047	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1917824	chr10:57497070-57497071	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs376890217	chr10:57497143-57497144	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573724441	chr10:57497146-57497147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542495937	chr10:57497212-57497213	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74664521	chr10:57497329-57497330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs528244685	chr10:57497347-57497348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192241771	chr10:57497410-57497411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7074747	chr10:57497418-57497419	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs138084713	chr10:57497428-57497429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs10733937	chr10:57497439-57497440	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76591239	chr10:57497444-57497445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Pancreatic endocrine tumor	17639061	CNVD
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
Thoracic aortic aneurysm	21092924	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
Esophageal cancer	21851588	CNVD
Prostate cancer	18632612	CNVD
Autism	18414403	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
T-cell lymphomas	19863542	CNVD
Testicular germ cell tumor	18059402	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
Obesity	21956041	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Metanephric adenoma	20802469	CNVD
Autism	20841430	CNVD
Mental retardation	17124404	CNVD
Epilepsy	20923578	CNVD
Prostate cancer	16573809	CNVD
Schizophrenia	19329560	CNVD
Heart failure	18772530	CNVD
Heart failure	18854381	CNVD
Hyperglycemia	19060297	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Glioblastoma multiforme	22286061	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Usher syndrome	20538994	CNVD
Glioblastoma multiforme	17002787	CNVD
Autism	20858243	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	17426248	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	18511947	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:313 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:57483400-57484000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr10:57496600-57497000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr10:57496600-57497000	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr10:57496600-57497000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr10:57496600-57497000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr10:57496600-57497200	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr10:57496600-57497200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr10:57496600-57497400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr10:57497000-57499600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr10:57497000-57499600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:57497200-57499600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr10:57497400-57499600	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr10:57499400-57500200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr10:57499600-57499800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr10:57499600-57499800	Enhancers	Pancreas	Pancrea
16	chr10:57499600-57500000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr10:57499600-57500400	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr10:57499600-57500400	Enhancers	Fetal Heart	heart
19	chr10:57499600-57500800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr10:57499600-57501000	Enhancers	Liver	Liver
21	chr10:57499800-57500200	Enhancers	HepG2	liver
22	chr10:57500000-57500200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr10:57500800-57506800	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr10:57501000-57506200	Weak transcription	Liver	Liver
25	chr10:57506200-57507400	Enhancers	Liver	Liver
26	chr10:57506400-57507600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr10:57506600-57507600	Enhancers	H1 Cell Line	embryonic stem cell
28	chr10:57506600-57507600	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chr10:57506800-57507400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr10:57506800-57507400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr10:57506800-57507400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr10:57506800-57507600	Enhancers	H9 Cell Line	embryonic stem cell
33	chr10:57506800-57507600	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chr10:57506800-57507600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr10:57506800-57507800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr10:57507000-57507600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr10:57527800-57528400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr10:57528000-57528400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr10:57528000-57528400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr10:57546000-57546400	Enhancers	Liver	Liver
41	chr10:57546400-57546600	Flanking Active TSS	Liver	Liver
42	chr10:57546600-57546800	Enhancers	Liver	Liver
43	chr10:57556800-57557800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr10:57557000-57557200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr10:57557000-57557800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr10:57557200-57558000	Enhancers	HUES64 Cell Line	embryonic stem cell
47	chr10:57557800-57558000	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr10:57559400-57559600	Enhancers	Fetal Brain Male	brain
49	chr10:57559600-57560400	Weak transcription	Fetal Brain Male	brain
50	chr10:57559800-57560200	Enhancers	Liver	Liver

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links