Variant report

Variant	esv1831483
Chromosome Location	chr10:1021156-1062915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1794)
CpG islands
(count:1526)
Chromatin interactive
region (count:110)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1794 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:1035974-1036196	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:1055274-1055344	K562	blood:	n/a	n/a
3	ARID3A	chr10:1034095-1034579	K562	blood:	n/a	n/a
4	ARID3A	chr10:1048542-1048707	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:1034162-1034648	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:1030018-1030553	HepG2	liver:	n/a	n/a
7	ATF1	chr10:1055216-1055507	K562	blood:	n/a	n/a
8	ATF1	chr10:1034082-1034516	K562	blood:	n/a	n/a
9	ATF1	chr10:1032320-1032640	K562	blood:	n/a	n/a
10	ATF2	chr10:1034004-1034948	GM12878	blood:	n/a	n/a
11	ATF2	chr10:1033975-1034607	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr10:1034018-1034530	GM12878	blood:	n/a	n/a
13	ATF2	chr10:1038400-1038963	GM12878	blood:	n/a	n/a
14	ATF3	chr10:1034045-1034513	K562	blood:	n/a	chr10:1034312-1034332
15	ATF3	chr10:1032387-1032656	K562	blood:	n/a	n/a
16	BACH1	chr10:1033729-1034885	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr10:1033795-1034044	K562	blood:	n/a	n/a
18	BACH1	chr10:1034256-1034350	K562	blood:	n/a	n/a
19	BATF	chr10:1032411-1032694	GM12878	blood:	n/a	chr10:1032548-1032559
20	BATF	chr10:1034872-1035161	GM12878	blood:	n/a	chr10:1035022-1035033
21	BATF	chr10:1034107-1034594	GM12878	blood:	n/a	n/a
22	BCL11A	chr10:1038544-1038736	GM12878	blood:	n/a	n/a
23	BCL11A	chr10:1038464-1038821	GM12878	blood:	n/a	n/a
24	BCL3	chr10:1058081-1058469	GM12878	blood:	n/a	n/a
25	BCL3	chr10:1058472-1058834	GM12878	blood:	n/a	n/a
26	BCL3	chr10:1034100-1034715	A549	lung:	n/a	chr10:1034579-1034592 chr10:1034316-1034325
27	BCL3	chr10:1033878-1034563	A549	lung:	n/a	chr10:1034316-1034325
28	BCL3	chr10:1058115-1058429	GM12878	blood:	n/a	n/a
29	BCLAF1	chr10:1033922-1034983	GM12878	blood:	n/a	chr10:1034579-1034592 chr10:1034316-1034325
30	BCLAF1	chr10:1034030-1034567	K562	blood:	n/a	chr10:1034316-1034325
31	BCLAF1	chr10:1033990-1034773	GM12878	blood:	n/a	chr10:1034579-1034592 chr10:1034316-1034325
32	BHLHE40	chr10:1033788-1034753	GM12878	blood:	n/a	n/a
33	BHLHE40	chr10:1038483-1039064	GM12878	blood:	n/a	n/a
34	BHLHE40	chr10:1035382-1035383	GM12878	blood:	n/a	n/a
35	BHLHE40	chr10:1055165-1055482	K562	blood:	n/a	n/a
36	BHLHE40	chr10:1034145-1034594	HepG2	liver:	n/a	n/a
37	BHLHE40	chr10:1032356-1032659	K562	blood:	n/a	n/a
38	BHLHE40	chr10:1033530-1035006	K562	blood:	n/a	n/a
39	BHLHE40	chr10:1032914-1033160	K562	blood:	n/a	n/a
40	BRCA1	chr10:1029872-1030642	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr10:1034096-1034517	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr10:1034182-1034573	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr10:1034240-1034564	HepG2	liver:	n/a	n/a
44	CBX3	chr10:1024671-1025246	HCT-116	colon:	n/a	n/a
45	CBX3	chr10:1034109-1034429	K562	blood:	n/a	n/a
46	CBX3	chr10:1026443-1026801	K562	blood:	n/a	n/a
47	CBX3	chr10:1026389-1026851	K562	blood:	n/a	n/a
48	CBX3	chr10:1034022-1034707	K562	blood:	n/a	n/a
49	CBX3	chr10:1024697-1025191	K562	blood:	n/a	n/a
50	CBX3	chr10:1024732-1025187	K562	blood:	n/a	n/a

(count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:1034293-1034343	K562	blood:	n/a
2	chr10:1034293-1034343	K562	blood:	n/a
3	chr10:1021712-1021762	CMK	blood:	n/a
4	chr10:1034473-1034523	MCF10A-Er-Src	breast:	n/a
5	chr10:1037934-1037984	SK-N-MC	brain:	n/a
6	chr10:1033901-1033951	AG09309	skin:	n/a
7	chr10:1034473-1034523	HCF	heart:	n/a
8	chr10:1034293-1034343	HIPEpiC	eye:	n/a
9	chr10:1034284-1034334	NT2-D1	testis:	n/a
10	chr10:1034318-1034368	AoSMC	blood vessel:	n/a
11	chr10:1034166-1034216	NB4	blood:	n/a
12	chr10:1058092-1058142	LNCaP	prostate:	n/a
13	chr10:1058036-1058086	BE2_C	brain:	n/a
14	chr10:1058036-1058086	MCF10A-Er-Src	breast:	n/a
15	chr10:1033349-1033399	HRCEpiC	kidney:	n/a
16	chr10:1034677-1034727	NT2-D1	testis:	n/a
17	chr10:1022108-1022158	HCT-116	colon:	n/a
18	chr10:1034318-1034368	LNCaP	prostate:	n/a
19	chr10:1034677-1034727	HL-60	blood:	n/a
20	chr10:1031432-1031482	SAEC	small airway:	n/a
21	chr10:1043407-1043457	GM19239	blood:	n/a
22	chr10:1034168-1034218	AoSMC	blood vessel:	n/a
23	chr10:1034318-1034368	Hela-S3	cervix:	n/a
24	chr10:1037934-1037984	HCT-116	colon:	n/a
25	chr10:1034473-1034523	NB4	blood:	n/a
26	chr10:1034473-1034523	HEK293	kidney:	embryo
27	chr10:1034030-1034080	HEEpiC	esophagus:	n/a
28	chr10:1034168-1034218	GM12891	blood:	n/a
29	chr10:1058036-1058086	RPTEC	kidney:	n/a
30	chr10:1022108-1022158	AG10803	skin:	n/a
31	chr10:1034338-1034388	Caco-2	colon:	n/a
32	chr10:1025639-1025689	HEEpiC	esophagus:	n/a
33	chr10:1034338-1034388	SK-N-SH_RA	brain:	n/a
34	chr10:1043382-1043432	NHBE	bronchial:	n/a
35	chr10:1022108-1022158	SK-N-MC	brain:	n/a
36	chr10:1031432-1031482	Caco-2	colon:	n/a
37	chr10:1034166-1034216	HPAEpiC	pulmonary alveolar:	n/a
38	chr10:1034401-1034451	RPTEC	kidney:	n/a
39	chr10:1022615-1022665	HUVEC	blood vessel:	n/a
40	chr10:1034168-1034218	NB4	blood:	n/a
41	chr10:1034401-1034451	K562	blood:	n/a
42	chr10:1034338-1034388	HAEpiC	amniotic membrane:	n/a
43	chr10:1034166-1034216	A549	lung:	n/a
44	chr10:1034030-1034080	MCF10A-Er-Src	breast:	n/a
45	chr10:1033901-1033951	BJ	skin:	n/a
46	chr10:1034030-1034080	HCM	heart:	n/a
47	chr10:1021712-1021762	HEEpiC	esophagus:	n/a
48	chr10:1043382-1043432	HCF	heart:	n/a
49	chr10:1025639-1025689	PFSK-1	brain:	n/a
50	chr10:1034473-1034523	HIPEpiC	eye:	n/a

(count:110 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr10:1034212..1034872-chr3:48956219..48957108,3	Hela-S3	cervix:
2	chr10:1061106..1063843-chr10:1063922..1066024,3	K562	blood:
3	chr10:1041791..1044346-chr10:1102809..1104842,2	MCF-7	breast:
4	chr10:1040702..1042841-chr10:1100328..1103891,3	K562	blood:
5	chr10:1028166..1030337-chr10:1039910..1042809,2	MCF-7	breast:
6	chr10:1038435..1041115-chr10:1083089..1086536,3	K562	blood:
7	chr10:1054711..1057336-chr10:1093694..1095483,2	MCF-7	breast:
8	chr10:1048891..1050643-chr10:1061683..1063902,2	K562	blood:
9	chr10:1053366..1056481-chr10:1086210..1089642,3	K562	blood:
10	chr10:1031655..1033355-chr10:1053764..1056440,2	K562	blood:
11	chr10:1020473..1022394-chr10:1030542..1032536,2	K562	blood:
12	chr10:1037288..1039582-chr10:1100848..1103600,2	K562	blood:
13	chr10:1019010..1021511-chr10:1021947..1027823,6	MCF-7	breast:
14	chr10:976344..979673-chr10:1032747..1036349,14	K562	blood:
15	chr10:1028166..1030337-chr10:1039910..1042809,2	MCF-7	breast:
16	chr10:993403..996250-chr10:1036309..1038565,2	K562	blood:
17	chr10:1013251..1015818-chr10:1022738..1024636,2	K562	blood:
18	chr10:1037105..1038655-chr10:1093115..1095926,2	K562	blood:
19	chr10:1053366..1056354-chr10:1087658..1089642,2	K562	blood:
20	chr10:974451..976397-chr10:1027362..1028867,2	MCF-7	breast:
21	chr10:1053179..1055951-chr10:1060885..1063576,2	MCF-7	breast:
22	chr10:1033201..1035981-chr10:1054777..1056323,2	MCF-7	breast:
23	chr10:1052939..1055149-chr10:1088165..1090086,2	MCF-7	breast:
24	chr10:1039038..1043366-chr10:1094125..1096899,4	K562	blood:
25	chr10:1053992..1056284-chr10:1061634..1063262,2	K562	blood:
26	chr10:1032021..1036235-chr10:1037103..1040442,8	MCF-7	breast:
27	chr10:972336..974147-chr10:1040690..1042738,2	K562	blood:
28	chr10:1034172..1034811-chr11:65686147..65686698,2	Hela-S3	cervix:
29	chr10:1049830..1051331-chr10:1051501..1053237,2	MCF-7	breast:
30	chr10:1053992..1056284-chr10:1061634..1063262,2	K562	blood:
31	chr10:1017304..1018070-chr10:1030124..1030639,2	MCF-7	breast:
32	chr10:1010243..1012883-chr10:1030629..1033582,2	K562	blood:
33	chr10:974636..980819-chr10:1029938..1037009,15	MCF-7	breast:
34	chr10:988056..990097-chr10:1030417..1032200,2	K562	blood:
35	chr10:1034367..1036220-chr10:1101305..1103834,2	MCF-7	breast:
36	chr10:1032460..1036223-chr10:1037053..1039174,5	K562	blood:
37	chr10:1039855..1042712-chr10:1046941..1050374,3	MCF-7	breast:
38	chr10:1015043..1019353-chr10:1030351..1034278,6	MCF-7	breast:
39	chr10:1031655..1033355-chr10:1053764..1056440,2	K562	blood:
40	chr10:1048578..1051233-chr10:1058068..1059841,2	MCF-7	breast:
41	chr10:1053179..1055951-chr10:1060885..1063576,2	MCF-7	breast:
42	chr10:1052653..1055132-chr10:1094709..1096832,2	K562	blood:
43	chr10:1048891..1050643-chr10:1061683..1063902,2	K562	blood:
44	chr10:1024974..1028277-chr10:1028484..1030664,3	MCF-7	breast:
45	chr10:1033196..1035740-chr10:1100283..1103390,4	K562	blood:
46	chr10:1033868..1034831-chr2:114647091..114647827,2	HCT-116	colon:
47	chr10:1019761..1022243-chr10:1028840..1032476,4	MCF-7	breast:
48	chr10:968239..971005-chr10:1062615..1065271,2	MCF-7	breast:
49	chr10:1000614..1004584-chr10:1019814..1022470,3	K562	blood:
50	chr10:1000614..1004584-chr10:1019814..1022762,4	K562	blood:

No data

Variant related genes	Relation type
ENSG00000205740	TF binding region
GTPBP4	TF binding region
ENSG00000205740	CpG island
GTPBP4	CpG island
ENSG00000067064	chromatin interactions
ENSG00000107929	chromatin interactions
ENSG00000148377	chromatin interactions
ENSG00000270019	chromatin interactions
ENSG00000047056	chromatin interactions
ENSG00000175573	chromatin interactions
ENSG00000107937	chromatin interactions
ENSG00000221883	chromatin interactions
ENSG00000238924	chromatin interactions
ENSG00000177479	chromatin interactions
ENSG00000205740	chromatin interactions
ENSG00000115091	chromatin interactions
ENSG00000229869	chromatin interactions

Extended variants
information (count: 2128 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2128 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571054573	chr10:1021209-1021210	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs542471355	chr10:1021244-1021245	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs559162474	chr10:1021288-1021289	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs1250896	chr10:1021289-1021290	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs117732138	chr10:1021310-1021311	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs116783704	chr10:1021331-1021332	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs530600506	chr10:1021363-1021364	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs550598994	chr10:1021371-1021372	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs567232730	chr10:1021395-1021396	Enhancers Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs184159420	chr10:1021431-1021432	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs553701375	chr10:1021445-1021446	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs12359796	chr10:1021479-1021480	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs538844910	chr10:1021501-1021502	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs559071582	chr10:1021513-1021514	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs569711627	chr10:1021514-1021515	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs373210673	chr10:1021516-1021517	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
17	rs575668222	chr10:1021521-1021522	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
18	rs544249878	chr10:1021526-1021527	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs188712113	chr10:1021527-1021528	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs574482346	chr10:1021558-1021559	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs193219140	chr10:1021618-1021619	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs574339672	chr10:1021643-1021644	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs555350339	chr10:1021670-1021671	Enhancers Weak transcription Strong transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs544897586	chr10:1021709-1021710	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs4880747	chr10:1021712-1021713	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs183442733	chr10:1021713-1021714	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs4881545	chr10:1021716-1021717	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs372227685	chr10:1021718-1021719	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs530633089	chr10:1021723-1021724	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs187385364	chr10:1021741-1021742	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs112302392	chr10:1021765-1021766	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs112620894	chr10:1021766-1021767	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs547354124	chr10:1021767-1021768	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs567071256	chr10:1021771-1021772	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs539288018	chr10:1021782-1021783	Enhancers Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs558884977	chr10:1021845-1021846	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs569390114	chr10:1021854-1021855	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs537987920	chr10:1021858-1021859	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs11598980	chr10:1021864-1021865	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs574519447	chr10:1021894-1021895	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs540216964	chr10:1021898-1021899	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs554108815	chr10:1021905-1021906	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs184161231	chr10:1021910-1021911	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs28684619	chr10:1021917-1021918	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs376164165	chr10:1021929-1021930	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs545248362	chr10:1021930-1021931	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs564974496	chr10:1021932-1021933	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs575508186	chr10:1021935-1021936	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs544353538	chr10:1021949-1021950	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs560952603	chr10:1021953-1021954	Weak transcription Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Cancer	20164920	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	20409316	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pilocytic astrocytoma	18622384	CNVD
Pilomyxoid astrocytoma	18622384	CNVD
Breast cancer	17133270	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Cancer	21129771	CNVD
Sudden cardiac death	19188705	CNVD
Digeorge syndrome	22283845	CNVD
Colorectal cancer	20709793	CNVD
Wilms tumour	19047088	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21183584	CNVD
Barakat syndrome	22470819	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	21720365	CNVD
Autism	18414403	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22032731	CNVD
Medulloblastoma	16783165	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Phyllodes tumor	17334353	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Melanoma	17363583	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21785460	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Glioblastoma multiforme	21525872	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:1452 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:998800-1026200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr10:1014800-1022400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr10:1016000-1021600	Enhancers	Stomach Mucosa	stomach
4	chr10:1017000-1022400	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr10:1017000-1022600	Weak transcription	Ovary	ovary
6	chr10:1017600-1023800	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr10:1017800-1021400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr10:1017800-1022600	Weak transcription	HSMM	muscle
9	chr10:1017800-1022600	Weak transcription	NHLF	lung
10	chr10:1017800-1023600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr10:1017800-1024600	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr10:1017800-1024800	Weak transcription	Brain Cingulate Gyrus	brain
13	chr10:1018000-1021200	Enhancers	HepG2	liver
14	chr10:1018000-1022400	Weak transcription	Fetal Muscle Leg	muscle
15	chr10:1018000-1022400	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr10:1018000-1023800	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr10:1018000-1024400	Weak transcription	Adipose Nuclei	Adipose
18	chr10:1018400-1025000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr10:1019200-1022000	Weak transcription	Lung	lung
20	chr10:1019200-1022200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr10:1019400-1030800	Weak transcription	Gastric	stomach
22	chr10:1020000-1021800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr10:1020200-1025000	Weak transcription	Osteobl	bone
24	chr10:1020600-1024600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr10:1020800-1022600	Weak transcription	Fetal Intestine Large	intestine
26	chr10:1021000-1022000	Weak transcription	Fetal Intestine Small	intestine
27	chr10:1021000-1022400	Weak transcription	Pancreas	Pancrea
28	chr10:1021000-1022800	Weak transcription	Fetal Lung	lung
29	chr10:1021400-1023600	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr10:1021600-1029400	Weak transcription	Stomach Mucosa	stomach
31	chr10:1021800-1022200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr10:1022000-1022200	Enhancers	Lung	lung
33	chr10:1022000-1023000	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr10:1022000-1023000	ZNF genes & repeats	Fetal Intestine Small	intestine
35	chr10:1022000-1023200	ZNF genes & repeats	Fetal Stomach	stomach
36	chr10:1022200-1022800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr10:1022200-1023400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr10:1022200-1024000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr10:1022400-1022600	Strong transcription	Fetal Muscle Leg	muscle
40	chr10:1022400-1022600	Weak transcription	A549	lung
41	chr10:1022400-1022800	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
42	chr10:1022400-1023000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
43	chr10:1022400-1023000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr10:1022400-1023000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr10:1022400-1023000	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
46	chr10:1022400-1023000	Enhancers	Pancreas	Pancrea
47	chr10:1022600-1022800	ZNF genes & repeats	Fetal Intestine Large	intestine
48	chr10:1022600-1022800	ZNF genes & repeats	HSMM	muscle
49	chr10:1022600-1023000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
50	chr10:1022600-1023000	ZNF genes & repeats	Fetal Muscle Leg	muscle

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