Variant report

Variant	esv2753756
Chromosome Location	chr10:985264-1052950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1860)
CpG islands
(count:2136)
Chromatin interactive
region (count:172)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1860 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:1034162-1034648	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:1030018-1030553	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:1016027-1017475	HepG2	liver:	n/a	n/a
4	ARID3A	chr10:1035974-1036196	HepG2	liver:	n/a	n/a
5	ARID3A	chr10:1048542-1048707	HepG2	liver:	n/a	n/a
6	ARID3A	chr10:1034095-1034579	K562	blood:	n/a	n/a
7	ARID3A	chr10:1019922-1020290	HepG2	liver:	n/a	n/a
8	ATF1	chr10:1032320-1032640	K562	blood:	n/a	n/a
9	ATF1	chr10:1034082-1034516	K562	blood:	n/a	n/a
10	ATF2	chr10:1019961-1020367	GM12878	blood:	n/a	n/a
11	ATF2	chr10:1020013-1020380	GM12878	blood:	n/a	n/a
12	ATF2	chr10:1034004-1034948	GM12878	blood:	n/a	n/a
13	ATF2	chr10:1033975-1034607	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr10:1038400-1038963	GM12878	blood:	n/a	n/a
15	ATF2	chr10:1034018-1034530	GM12878	blood:	n/a	n/a
16	ATF3	chr10:1015490-1015684	K562	blood:	n/a	n/a
17	ATF3	chr10:1009570-1009894	K562	blood:	n/a	n/a
18	ATF3	chr10:1032387-1032656	K562	blood:	n/a	n/a
19	ATF3	chr10:1034045-1034513	K562	blood:	n/a	chr10:1034312-1034332
20	BACH1	chr10:1033795-1034044	K562	blood:	n/a	n/a
21	BACH1	chr10:1033729-1034885	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr10:1020093-1020177	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr10:1034256-1034350	K562	blood:	n/a	n/a
24	BATF	chr10:989748-990049	GM12878	blood:	n/a	n/a
25	BATF	chr10:1019992-1020322	GM12878	blood:	n/a	n/a
26	BATF	chr10:1034872-1035161	GM12878	blood:	n/a	chr10:1035022-1035033
27	BATF	chr10:1034107-1034594	GM12878	blood:	n/a	n/a
28	BATF	chr10:1032411-1032694	GM12878	blood:	n/a	chr10:1032548-1032559
29	BCL11A	chr10:1020141-1020398	GM12878	blood:	n/a	chr10:1020236-1020245
30	BCL11A	chr10:1038544-1038736	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:1019946-1020339	GM12878	blood:	n/a	chr10:1019984-1019992 chr10:1020236-1020245
32	BCL11A	chr10:1038464-1038821	GM12878	blood:	n/a	n/a
33	BCL3	chr10:1020022-1020432	GM12878	blood:	n/a	chr10:1020236-1020245
34	BCL3	chr10:1033878-1034563	A549	lung:	n/a	chr10:1034316-1034325
35	BCL3	chr10:1034100-1034715	A549	lung:	n/a	chr10:1034579-1034592 chr10:1034316-1034325
36	BCLAF1	chr10:1034030-1034567	K562	blood:	n/a	chr10:1034316-1034325
37	BCLAF1	chr10:1033922-1034983	GM12878	blood:	n/a	chr10:1034579-1034592 chr10:1034316-1034325
38	BCLAF1	chr10:1033990-1034773	GM12878	blood:	n/a	chr10:1034579-1034592 chr10:1034316-1034325
39	BHLHE40	chr10:1019884-1020287	HepG2	liver:	n/a	n/a
40	BHLHE40	chr10:1014440-1014729	K562	blood:	n/a	n/a
41	BHLHE40	chr10:1035382-1035383	GM12878	blood:	n/a	n/a
42	BHLHE40	chr10:1032914-1033160	K562	blood:	n/a	n/a
43	BHLHE40	chr10:1018772-1019068	GM12878	blood:	n/a	chr10:1019006-1019022
44	BHLHE40	chr10:1032356-1032659	K562	blood:	n/a	n/a
45	BHLHE40	chr10:1016187-1017356	HepG2	liver:	n/a	n/a
46	BHLHE40	chr10:1034145-1034594	HepG2	liver:	n/a	n/a
47	BHLHE40	chr10:1033530-1035006	K562	blood:	n/a	n/a
48	BHLHE40	chr10:990466-990731	K562	blood:	n/a	n/a
49	BHLHE40	chr10:1019571-1020585	GM12878	blood:	n/a	n/a
50	BHLHE40	chr10:1038483-1039064	GM12878	blood:	n/a	n/a

(count:2136 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:1037934-1037984	SAEC	small airway:	n/a
2	chr10:1037934-1037984	SAEC	small airway:	n/a
3	chr10:994943-994993	ECC-1	luminal epithelium:	n/a
4	chr10:1021712-1021762	GM12878	blood:	n/a
5	chr10:1034318-1034368	MCF-7	breast:	n/a
6	chr10:995290-995340	LNCaP	prostate:	n/a
7	chr10:994943-994993	HAEpiC	amniotic membrane:	n/a
8	chr10:1034168-1034218	AG09309	skin:	n/a
9	chr10:1025639-1025689	HAEpiC	amniotic membrane:	n/a
10	chr10:1022615-1022665	HCM	heart:	n/a
11	chr10:1011381-1011431	K562	blood:	n/a
12	chr10:1022615-1022665	HUVEC	blood vessel:	n/a
13	chr10:1011248-1011298	GM12878	blood:	n/a
14	chr10:1000300-1000350	ProgFib	skin:	n/a
15	chr10:1043368-1043418	Caco-2	colon:	n/a
16	chr10:995095-995145	GM19239	blood:	n/a
17	chr10:1034166-1034216	BJ	skin:	n/a
18	chr10:1043368-1043418	LNCaP	prostate:	n/a
19	chr10:1034318-1034368	HEEpiC	esophagus:	n/a
20	chr10:1043382-1043432	PrEC	prostate:	n/a
21	chr10:1033901-1033951	Hela-S3	cervix:	n/a
22	chr10:995290-995340	CMK	blood:	n/a
23	chr10:1037934-1037984	PFSK-1	brain:	n/a
24	chr10:1019161-1019211	ovcar-3	ovarian:	n/a
25	chr10:1034473-1034523	HEK293	kidney:	embryo
26	chr10:1011142-1011192	GM12878	blood:	n/a
27	chr10:1000575-1000625	GM06990	blood:	n/a
28	chr10:1034166-1034216	Hela-S3	cervix:	n/a
29	chr10:1034030-1034080	NB4	blood:	n/a
30	chr10:1016695-1016745	NH-A	brain:	n/a
31	chr10:1021712-1021762	PFSK-1	brain:	n/a
32	chr10:1019026-1019076	HCM	heart:	n/a
33	chr10:1043407-1043457	Jurkat	blood:	n/a
34	chr10:995290-995340	GM19239	blood:	n/a
35	chr10:1000575-1000625	AG04450	lung:	fetal
36	chr10:1034293-1034343	HRE	kidney:	n/a
37	chr10:1025639-1025689	K562	blood:	n/a
38	chr10:1019161-1019211	NB4	blood:	n/a
39	chr10:1033349-1033399	IMR90	lung:	fetal
40	chr10:1022108-1022158	NHBE	bronchial:	n/a
41	chr10:1025639-1025689	BE2_C	brain:	n/a
42	chr10:1021712-1021762	SKMC	muscle:	n/a
43	chr10:1034293-1034343	IMR90	lung:	fetal
44	chr10:1011381-1011431	BJ	skin:	n/a
45	chr10:1034168-1034218	LNCaP	prostate:	n/a
46	chr10:1034338-1034388	NH-A	brain:	n/a
47	chr10:1043382-1043432	HUVEC	blood vessel:	n/a
48	chr10:1034401-1034451	NHDF-neo	bronchial:	n/a
49	chr10:1034166-1034216	NH-A	brain:	n/a
50	chr10:1011381-1011431	HAEpiC	amniotic membrane:	n/a

(count:172 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr10:988532..990709-chr10:1000522..1003406,2	MCF-7	breast:
2	chr10:1014806..1016425-chr10:1022937..1025172,2	MCF-7	breast:
3	chr10:986490..989100-chr10:1016201..1018491,2	MCF-7	breast:
4	chr10:1015119..1019104-chr10:1032459..1035516,7	MCF-7	breast:
5	chr10:1011250..1013274-chr10:1018564..1020381,2	K562	blood:
6	chr10:1038435..1041115-chr10:1083089..1086536,3	K562	blood:
7	chr10:993234..997786-chr10:1013619..1016483,4	MCF-7	breast:
8	chr10:1013251..1015818-chr10:1022738..1024636,2	K562	blood:
9	chr10:1031711..1035740-chr10:1100728..1103796,4	K562	blood:
10	chr10:1028166..1030337-chr10:1039910..1042809,2	MCF-7	breast:
11	chr10:1014806..1016425-chr10:1022937..1025172,2	MCF-7	breast:
12	chr10:974439..980732-chr10:1030011..1038533,28	MCF-7	breast:
13	chr10:1017304..1018070-chr10:1030124..1030639,2	MCF-7	breast:
14	chr10:1009296..1011482-chr10:1012719..1015110,2	MCF-7	breast:
15	chr10:1040702..1042841-chr10:1100328..1103891,3	K562	blood:
16	chr10:986461..988686-chr10:1017171..1019953,2	MCF-7	breast:
17	chr10:1013235..1016804-chr10:1032534..1035039,3	K562	blood:
18	chr10:972336..974147-chr10:1040690..1042738,2	K562	blood:
19	chr10:982121..984896-chr10:984955..986688,2	K562	blood:
20	chr10:976040..979233-chr10:1016379..1022615,6	MCF-7	breast:
21	chr10:986461..988686-chr10:1017171..1019953,2	MCF-7	breast:
22	chr10:1017049..1018015-chr10:1034396..1035314,2	MCF-7	breast:
23	chr10:1030088..1034279-chr10:1100732..1103594,4	MCF-7	breast:
24	chr10:1019010..1021511-chr10:1021947..1027823,6	MCF-7	breast:
25	chr10:1017304..1018070-chr10:1030124..1030639,2	MCF-7	breast:
26	chr10:1015182..1016794-chr10:1031895..1033943,2	K562	blood:
27	chr10:1020473..1022394-chr10:1030542..1032536,2	K562	blood:
28	chr10:1019967..1021680-chr10:1093563..1096115,2	MCF-7	breast:
29	chr10:949273..951052-chr10:1017196..1019797,2	K562	blood:
30	chr10:1032470..1034485-chr10:1092422..1096343,5	MCF-7	breast:
31	chr10:1001054..1003663-chr10:1008457..1009991,2	MCF-7	breast:
32	chr10:1018775..1022710-chr10:1032776..1036101,4	K562	blood:
33	chr10:981522..983775-chr10:1008969..1010630,2	K562	blood:
34	chr10:980826..983608-chr10:1003068..1004956,2	K562	blood:
35	chr10:995726..997603-chr10:1033507..1035656,2	K562	blood:
36	chr10:1016732..1019141-chr10:1025032..1027093,3	MCF-7	breast:
37	chr10:975132..982582-chr10:1010670..1022073,17	MCF-7	breast:
38	chr10:1024974..1028277-chr10:1028484..1030664,3	MCF-7	breast:
39	chr10:979434..982350-chr10:995576..997645,2	MCF-7	breast:
40	chr10:1005925..1008895-chr10:1011879..1014677,2	MCF-7	breast:
41	chr10:1006827..1010625-chr10:1012447..1015815,4	K562	blood:
42	chr10:1039855..1042712-chr10:1046941..1050374,3	MCF-7	breast:
43	chr10:1016732..1019141-chr10:1025032..1027093,3	MCF-7	breast:
44	chr10:993403..996250-chr10:1036309..1038565,2	K562	blood:
45	chr10:973639..977569-chr10:1043188..1045496,3	MCF-7	breast:
46	chr10:976344..979673-chr10:1032747..1036349,14	K562	blood:
47	chr10:1000614..1004584-chr10:1019814..1022762,4	K562	blood:
48	chr10:1005925..1008895-chr10:1011879..1014677,2	MCF-7	breast:
49	chr10:992595..994110-chr10:1032273..1033999,2	K562	blood:
50	chr10:1019010..1021511-chr10:1021947..1027823,6	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LARP4B-2	chr10:988075-988179	NONHSAT010884
2	lnc-LARP4B-2	chr10:988421-988583	NONHSAT010884
3	lnc-GTPBP4-3	chr10:988420-988683	ENSG00000229869.1
4	lnc-AL359878.1-1	chr10:997609-997718	NONHSAT010887
5	lnc-GTPBP4-3	chr10:988127-988179	ENSG00000229869.1
6	lnc-GTPBP4-3	chr10:988420-988828	NONHSAT010883
7	lnc-GTPBP4-3	chr10:987882-988179	NONHSAT010883
8	lnc-AL359878.1-1	chr10:999388-1000122	NONHSAT010887

No data

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

Extended variants
information (count: 2955 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:2955 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10904585	chr10:985264-985265	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs182551281	chr10:985266-985267	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550198675	chr10:985299-985300	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs187163637	chr10:985410-985411	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529630074	chr10:985445-985446	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs74953165	chr10:985550-985551	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs146528488	chr10:985596-985597	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs370169119	chr10:985642-985643	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs190337057	chr10:985644-985645	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140435844	chr10:985650-985651	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs181484668	chr10:985735-985736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs569408639	chr10:985749-985750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538320093	chr10:985791-985792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs549283756	chr10:985811-985812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs554734927	chr10:985823-985824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185730083	chr10:985838-985839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150409194	chr10:985863-985864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553233239	chr10:985874-985875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs11253523	chr10:985896-985897	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
20	rs544845739	chr10:985934-985935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564725367	chr10:985935-985936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs78277855	chr10:985952-985953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377510655	chr10:985953-985954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs77119794	chr10:985958-985959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575023790	chr10:986020-986021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149164898	chr10:986028-986029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564052779	chr10:986034-986035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560788285	chr10:986088-986089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs190186121	chr10:986118-986119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376227322	chr10:986143-986144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182372363	chr10:986146-986147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs560806564	chr10:986149-986150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs532839389	chr10:986193-986194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370695716	chr10:986199-986200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs552832033	chr10:986203-986204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186250426	chr10:986245-986246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551450557	chr10:986253-986254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531904891	chr10:986299-986300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs548669902	chr10:986339-986340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568412559	chr10:986362-986363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs534246531	chr10:986385-986386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs58731075	chr10:986413-986414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10795300	chr10:986429-986430	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs566466070	chr10:986433-986434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538526498	chr10:986443-986444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537555369	chr10:986444-986445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190774530	chr10:986456-986457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11253524	chr10:986459-986460	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs567667108	chr10:986460-986461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs554654514	chr10:986495-986496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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

Chromatin state (count:1772 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:978200-985400	Weak transcription	Brain Angular Gyrus	brain
2	chr10:978400-985800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr10:984600-985800	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr10:984800-985400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr10:984800-985600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:984800-985600	Enhancers	Primary hematopoietic stem cells	blood
7	chr10:984800-985600	Enhancers	Primary T helper cells fromperipheralblood	blood
8	chr10:984800-985800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chr10:984800-985800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr10:984800-985800	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr10:984800-985800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
12	chr10:984800-985800	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chr10:985000-985400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
14	chr10:985000-985400	Enhancers	Fetal Muscle Leg	muscle
15	chr10:985000-985600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
16	chr10:985000-985600	Enhancers	Spleen	Spleen
17	chr10:985000-985800	Enhancers	Primary T cells fromperipheralblood	blood
18	chr10:985000-985800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr10:985000-985800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr10:985000-985800	Enhancers	Fetal Thymus	thymus
21	chr10:985000-985800	Enhancers	Dnd41	blood
22	chr10:985200-985600	Flanking Active TSS	Primary T cells from cord blood	blood
23	chr10:985200-985600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr10:985200-985600	Enhancers	Thymus	Thymus
25	chr10:985200-990200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr10:985400-990000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
27	chr10:985400-990400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr10:985600-985800	Enhancers	Primary T cells from cord blood	blood
29	chr10:985600-989600	Weak transcription	Primary hematopoietic stem cells	blood
30	chr10:985600-989600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr10:985600-989800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr10:985600-989800	Weak transcription	Spleen	Spleen
33	chr10:985600-990200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
34	chr10:985600-990200	Weak transcription	Primary T helper cells fromperipheralblood	blood
35	chr10:985600-990400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr10:985800-990000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
37	chr10:985800-990200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr10:985800-990200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
39	chr10:985800-990200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr10:985800-990200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr10:985800-990400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
42	chr10:985800-990400	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr10:986800-987000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr10:989200-989400	Enhancers	GM12878-XiMat	blood
45	chr10:989200-989600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr10:989400-990200	Enhancers	Duodenum Mucosa	Duodenum
47	chr10:989400-990600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
48	chr10:989400-990800	Flanking Active TSS	GM12878-XiMat	blood
49	chr10:989400-991000	Enhancers	Primary B cells from peripheral blood	blood
50	chr10:989600-989800	Enhancers	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links