Variant report

Variant	nsv948978
Chromosome Location	chr10:813426-1019115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4088)
CpG islands
(count:5437)
Chromatin interactive
region (count:321)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:4088 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:952663-952668	K562	blood:	n/a	n/a
2	ARID3A	chr10:975612-976178	K562	blood:	n/a	n/a
3	ARID3A	chr10:834600-835039	HepG2	liver:	n/a	chr10:834754-834770
4	ARID3A	chr10:977720-977747	K562	blood:	n/a	n/a
5	ARID3A	chr10:967804-967954	K562	blood:	n/a	n/a
6	ARID3A	chr10:840593-840806	HepG2	liver:	n/a	n/a
7	ARID3A	chr10:1016027-1017475	HepG2	liver:	n/a	n/a
8	ARID3A	chr10:977654-977803	HepG2	liver:	n/a	n/a
9	ATF1	chr10:916788-916805	K562	blood:	n/a	n/a
10	ATF1	chr10:977597-977929	K562	blood:	n/a	n/a
11	ATF2	chr10:897794-898328	GM12878	blood:	n/a	n/a
12	ATF2	chr10:977473-977853	GM12878	blood:	n/a	n/a
13	ATF2	chr10:897850-898486	GM12878	blood:	n/a	n/a
14	ATF3	chr10:1009570-1009894	K562	blood:	n/a	n/a
15	ATF3	chr10:835269-835673	A549	lung:	n/a	n/a
16	ATF3	chr10:1015490-1015684	K562	blood:	n/a	n/a
17	BACH1	chr10:947299-947597	K562	blood:	n/a	n/a
18	BACH1	chr10:950640-950905	K562	blood:	n/a	n/a
19	BACH1	chr10:830736-831092	H1-hESC	embryonic stem cell:	n/a	chr10:830863-830877
20	BACH1	chr10:976720-976818	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr10:967719-967950	K562	blood:	n/a	n/a
22	BACH1	chr10:950622-950871	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr10:835339-835594	K562	blood:	n/a	n/a
24	BACH1	chr10:976057-976295	K562	blood:	n/a	n/a
25	BACH1	chr10:834956-835728	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr10:864426-864693	GM12878	blood:	n/a	n/a
27	BATF	chr10:982609-982943	GM12878	blood:	n/a	n/a
28	BATF	chr10:989748-990049	GM12878	blood:	n/a	n/a
29	BATF	chr10:864445-864780	GM12878	blood:	n/a	n/a
30	BATF	chr10:982588-982952	GM12878	blood:	n/a	n/a
31	BCL11A	chr10:897831-898188	GM12878	blood:	n/a	n/a
32	BCL3	chr10:848783-849025	GM12878	blood:	n/a	n/a
33	BCL3	chr10:857352-857584	GM12878	blood:	n/a	n/a
34	BCL3	chr10:857311-857602	GM12878	blood:	n/a	n/a
35	BCL3	chr10:837478-837818	GM12878	blood:	n/a	n/a
36	BCL3	chr10:911059-911458	GM12878	blood:	n/a	n/a
37	BCL3	chr10:851319-851820	GM12878	blood:	n/a	n/a
38	BCL3	chr10:837596-837974	GM12878	blood:	n/a	n/a
39	BCL3	chr10:850707-851034	GM12878	blood:	n/a	n/a
40	BCL3	chr10:850410-851109	K562	blood:	n/a	n/a
41	BCL3	chr10:835049-835724	A549	lung:	n/a	chr10:835215-835224 chr10:835319-835332 chr10:835073-835082 chr10:835063-835076
42	BCLAF1	chr10:976320-976797	GM12878	blood:	n/a	n/a
43	BCLAF1	chr10:975826-976665	GM12878	blood:	n/a	n/a
44	BCLAF1	chr10:897823-898237	GM12878	blood:	n/a	n/a
45	BCLAF1	chr10:897748-898331	GM12878	blood:	n/a	n/a
46	BHLHE40	chr10:1017670-1017832	K562	blood:	n/a	n/a
47	BHLHE40	chr10:977582-978159	GM12878	blood:	n/a	n/a
48	BHLHE40	chr10:982650-982975	GM12878	blood:	n/a	n/a
49	BHLHE40	chr10:917007-917199	GM12878	blood:	n/a	n/a
50	BHLHE40	chr10:834946-835733	K562	blood:	n/a	n/a

(count:5437 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:849032-849082	HCPEpiC	choroid plexus:	n/a
2	chr10:860862-860912	ProgFib	skin:	n/a
3	chr10:931643-931693	HEEpiC	esophagus:	n/a
4	chr10:831835-831885	MCF10A-Er-Src	breast:	n/a
5	chr10:817083-817133	PrEC	prostate:	n/a
6	chr10:835505-835555	ProgFib	skin:	n/a
7	chr10:858817-858867	Hela-S3	cervix:	n/a
8	chr10:995095-995145	Hela-S3	cervix:	n/a
9	chr10:849032-849082	HCPEpiC	choroid plexus:	n/a
10	chr10:860862-860912	ProgFib	skin:	n/a
11	chr10:931643-931693	HEEpiC	esophagus:	n/a
12	chr10:831835-831885	MCF10A-Er-Src	breast:	n/a
13	chr10:817083-817133	PrEC	prostate:	n/a
14	chr10:835505-835555	ProgFib	skin:	n/a
15	chr10:858817-858867	Hela-S3	cervix:	n/a
16	chr10:995095-995145	Hela-S3	cervix:	n/a
17	chr10:853153-853203	HepG2	liver:	n/a
18	chr10:829463-829513	NT2-D1	testis:	n/a
19	chr10:867221-867271	SKMC	muscle:	n/a
20	chr10:1011381-1011431	PFSK-1	brain:	n/a
21	chr10:855796-855846	BE2_C	brain:	n/a
22	chr10:995095-995145	HL-60	blood:	n/a
23	chr10:835505-835555	PrEC	prostate:	n/a
24	chr10:976548-976598	GM19239	blood:	n/a
25	chr10:1000575-1000625	NB4	blood:	n/a
26	chr10:855060-855110	BE2_C	brain:	n/a
27	chr10:820321-820371	MCF10A-Er-Src	breast:	n/a
28	chr10:855060-855110	Caco-2	colon:	n/a
29	chr10:932596-932646	HEEpiC	esophagus:	n/a
30	chr10:853153-853203	PFSK-1	brain:	n/a
31	chr10:851439-851489	MCF-7	breast:	n/a
32	chr10:976594-976644	HEK293	kidney:	embryo
33	chr10:820206-820256	HCM	heart:	n/a
34	chr10:821124-821174	NH-A	brain:	n/a
35	chr10:823151-823201	MCF-7	breast:	n/a
36	chr10:820027-820077	HL-60	blood:	n/a
37	chr10:932596-932646	NHDF-neo	bronchial:	n/a
38	chr10:851439-851489	Hepatocyte	liver:	n/a
39	chr10:932596-932646	HAEpiC	amniotic membrane:	n/a
40	chr10:822873-822923	AG04449	skin:	fetal
41	chr10:834503-834553	Jurkat	blood:	n/a
42	chr10:839865-839915	GM06990	blood:	n/a
43	chr10:858817-858867	NT2-D1	testis:	n/a
44	chr10:830689-830739	HCM	heart:	n/a
45	chr10:833290-833340	NHBE	bronchial:	n/a
46	chr10:867221-867271	NHBE	bronchial:	n/a
47	chr10:931793-931843	HCF	heart:	n/a
48	chr10:924646-924696	AG09309	skin:	n/a
49	chr10:830689-830739	A549	lung:	n/a
50	chr10:820321-820371	MCF-7	breast:	n/a

(count:321 , 50 per page) page: 1 2 3 4 5 6 7

No.	Distal block	Cell Line	Cell type
1	chr10:974758..976966-chr10:1110782..1112393,2	MCF-7	breast:
2	chr10:990098..992111-chr10:1033029..1035814,2	MCF-7	breast:
3	chr10:961541..964198-chr10:975771..977663,3	MCF-7	breast:
4	chr10:974439..980732-chr10:1030011..1038533,28	MCF-7	breast:
5	chr10:989315..991705-chr10:1095222..1096768,2	MCF-7	breast:
6	chr10:916687..920893-chr10:921035..925677,5	K562	blood:
7	chr10:852322..854745-chr10:858049..860254,2	K562	blood:
8	chr10:862973..864664-chr10:865575..868933,3	K562	blood:
9	chr10:892068..894386-chr10:1102064..1103667,2	MCF-7	breast:
10	chr10:1015119..1019104-chr10:1032459..1035516,7	MCF-7	breast:
11	chr10:976263..979384-chr10:986596..991037,4	MCF-7	breast:
12	chr10:819060..821540-chr10:825309..827354,2	MCF-7	breast:
13	chr10:977686..978278-chr3:23958133..23959063,2	HCT-116	colon:
14	chr10:877019..880477-chr10:881479..884204,3	K562	blood:
15	chr10:924774..927126-chr10:932557..935160,2	K562	blood:
16	chr10:864445..868005-chr10:868654..872720,4	MCF-7	breast:
17	chr10:978959..981256-chr10:1013885..1016544,2	K562	blood:
18	chr10:1009125..1012338-chr10:1015177..1017521,3	K562	blood:
19	chr10:954912..957818-chr10:959546..962502,2	K562	blood:
20	chr10:974758..977274-chr10:1018618..1021450,2	K562	blood:
21	chr10:936128..938846-chr10:942658..944551,2	K562	blood:
22	chr10:851217..854668-chr10:856285..859147,3	MCF-7	breast:
23	chr10:976152..979108-chr10:1085303..1088696,4	MCF-7	breast:
24	chr10:918117..920893-chr10:922741..925677,3	K562	blood:
25	chr10:903990..906276-chr10:933287..935164,2	K562	blood:
26	chr10:878636..882956-chr10:886285..890248,4	MCF-7	breast:
27	chr10:862973..864664-chr10:865575..868933,3	K562	blood:
28	chr10:1015043..1019353-chr10:1030351..1034278,6	MCF-7	breast:
29	chr10:908934..911082-chr10:916897..919212,2	MCF-7	breast:
30	chr10:1006112..1009530-chr10:1011286..1014390,5	K562	blood:
31	chr10:957384..959889-chr10:967554..970347,2	MCF-7	breast:
32	chr10:976200..979208-chr10:1093606..1097726,5	MCF-7	breast:
33	chr10:817104..818718-chr10:820025..821722,2	MCF-7	breast:
34	chr10:833990..835898-chr10:1099433..1102164,2	K562	blood:
35	chr10:963108..967368-chr10:972053..975262,4	MCF-7	breast:
36	chr10:924622..926459-chr10:931314..932954,2	MCF-7	breast:
37	chr10:1006925..1008811-chr10:1092405..1095339,2	MCF-7	breast:
38	chr10:979434..982350-chr10:995576..997645,2	MCF-7	breast:
39	chr10:1017049..1018015-chr10:1034396..1035314,2	MCF-7	breast:
40	chr10:556641..557560-chr10:835088..835885,2	K562	blood:
41	chr10:962348..963924-chr10:1102137..1103921,2	K562	blood:
42	chr10:907666..909265-chr10:909779..913077,3	MCF-7	breast:
43	chr10:956864..959449-chr10:987864..990001,2	K562	blood:
44	chr10:893412..896074-chr10:1094765..1097365,2	MCF-7	breast:
45	chr10:890079..892207-chr10:894846..896504,2	K562	blood:
46	chr10:854955..857145-chr10:859946..862172,2	MCF-7	breast:
47	chr10:975799..978442-chr10:1098842..1102725,4	MCF-7	breast:
48	chr10:1016935..1018860-chr10:1032660..1034729,2	K562	blood:
49	chr10:947556..951451-chr10:951605..956878,5	K562	blood:
50	chr10:949273..951052-chr10:1017196..1019797,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL359878.1-1	chr10:999388-1000122	NONHSAT010887
2	lnc-GTPBP4-3	chr10:987882-988179	NONHSAT010883
3	lnc-GTPBP4-3	chr10:978420-978683	NONHSAT010879
4	lnc-LARP4B-2	chr10:988075-988179	NONHSAT010884
5	lnc-GTPBP4-3	chr10:978127-978179	NONHSAT010879
6	lnc-AL359878.1-2	chr10:958175-958406	expReg_chr10_76_-
7	lnc-LARP4B-2	chr10:988421-988583	NONHSAT010884
8	lnc-AL359878.1-1	chr10:997609-997718	NONHSAT010887
9	lnc-GTPBP4-3	chr10:988127-988179	ENSG00000229869.1
10	lnc-GTPBP4-3	chr10:978966-979055	ENSG00000229869.1
11	lnc-GTPBP4-3	chr10:988420-988828	NONHSAT010883
12	lnc-GTPBP4-3	chr10:968966-969055	NONHSAT010879
13	lnc-GTPBP4-3	chr10:988420-988683	ENSG00000229869.1

No data

Variant related genes	Relation type
ENSG00000229869	TF binding region
LARP4B	TF binding region
ENSG00000229869	CpG island
LARP4B	CpG island
ENSG00000229869	chromatin interactions
ENSG00000238924	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000067064	chromatin interactions
ENSG00000107937	chromatin interactions
ENSG00000107929	chromatin interactions
ENSG00000198646	chromatin interactions
ENSG00000165476	chromatin interactions
ENSG00000148377	chromatin interactions
ENSG00000197885	chromatin interactions
ENSG00000205740	chromatin interactions
ENSG00000015171	chromatin interactions
ENSG00000047056	chromatin interactions
ENSG00000174748	chromatin interactions
ENSG00000151240	chromatin interactions

Extended variants
information (count: 8821 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:8821 , 50 per page) page: 1 2 3 4 5 6 7 ... 177

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11253424	chr10:813426-813427	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs564392631	chr10:813435-813436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs143297011	chr10:813436-813437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564055210	chr10:813505-813506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138920212	chr10:813520-813521	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549587226	chr10:813541-813542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs371104966	chr10:813545-813546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs533110657	chr10:813620-813621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142140583	chr10:813627-813628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528608034	chr10:813636-813637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs10904560	chr10:813646-813647	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs571678326	chr10:813659-813660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs192631772	chr10:813669-813670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs145838578	chr10:813698-813699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs60463454	chr10:813759-813760	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184774792	chr10:813763-813764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577313924	chr10:814154-814155	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs556774200	chr10:814204-814205	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs9971028	chr10:814216-814217	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs563120943	chr10:814217-814218	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs117664895	chr10:814273-814274	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564162947	chr10:814286-814287	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532810060	chr10:814373-814374	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs74564208	chr10:814380-814381	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs187646529	chr10:814391-814392	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs368274613	chr10:814394-814395	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs117064272	chr10:814401-814402	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192557506	chr10:814435-814436	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs528321093	chr10:814443-814444	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571818448	chr10:814479-814480	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs565372168	chr10:814580-814581	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200108031	chr10:814602-814603	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185554689	chr10:814622-814623	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554016621	chr10:814648-814649	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs7084171	chr10:814653-814654	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs139471992	chr10:814660-814661	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs555331011	chr10:814681-814682	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539984759	chr10:814684-814685	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs534551176	chr10:814685-814686	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs149260108	chr10:814756-814757	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189444196	chr10:814770-814771	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs35146578	chr10:814777-814778	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs397847390	chr10:814794-814795	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs35015317	chr10:814795-814796	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs536725959	chr10:814822-814823	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556938341	chr10:814841-814842	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34122579	chr10:814903-814904	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs74341803	chr10:814974-814975	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs398074843	chr10:814979-814980	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562177004	chr10:815033-815034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
Obesity	19966786	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Pancreatic cancer	17952125	CNVD
Autism	22495311	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Acute lymphoblastic leukemia	20724749	CNVD

Chromatin state (count:6171 , 50 per page) page: 1 2 3 4 5 6 7 ... 124

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:813400-813800	Enhancers	Pancreas	Pancrea
2	chr10:817000-817400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr10:817000-817400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:817200-817400	ZNF genes & repeats	Spleen	Spleen
5	chr10:817200-817600	Enhancers	Placenta	Placenta
6	chr10:817400-818000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr10:817400-820800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr10:817400-821800	Weak transcription	Spleen	Spleen
9	chr10:818000-818600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr10:818200-818400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr10:818200-818600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr10:818400-830600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr10:818600-821000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr10:818600-821600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr10:818800-819600	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr10:819400-819800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr10:820800-821000	Enhancers	Fetal Brain Male	brain
18	chr10:820800-821200	Enhancers	Stomach Smooth Muscle	stomach
19	chr10:820800-822400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr10:821000-821200	Enhancers	Muscle Satellite Cultured Cells	--
21	chr10:821000-821200	Enhancers	Skeletal Muscle Male	skeletal muscle
22	chr10:821000-821200	Bivalent Enhancer	Osteobl	bone
23	chr10:821000-821400	Enhancers	Colon Smooth Muscle	Colon
24	chr10:821000-821800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr10:821000-821800	Enhancers	A549	lung
26	chr10:821000-822000	Enhancers	Esophagus	oesophagus
27	chr10:821200-821400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr10:821200-821600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr10:821200-821600	Flanking Active TSS	Osteobl	bone
30	chr10:821200-821800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr10:821200-821800	Active TSS	Rectal Smooth Muscle	rectum
32	chr10:821200-821800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
33	chr10:821200-821800	Enhancers	HSMMtube	muscle
34	chr10:821200-822000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr10:821200-822000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr10:821200-822000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
37	chr10:821200-822000	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr10:821200-822000	Flanking Active TSS	Stomach Smooth Muscle	stomach
39	chr10:821200-822000	Enhancers	NH-A	brain
40	chr10:821400-821600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr10:821400-821600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr10:821400-821800	Enhancers	Hela-S3	cervix
43	chr10:821400-821800	Enhancers	HMEC	breast
44	chr10:821400-822000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr10:821400-822000	Enhancers	HUVEC	blood vessel
46	chr10:821400-824000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
47	chr10:821600-821800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr10:821600-821800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr10:821600-821800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr10:821600-821800	Enhancers	Fetal Brain Male	brain

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