Variant report

Variant	nsv825208
Chromosome Location	chr10:965883-1004836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1130)
CpG islands
(count:856)
Chromatin interactive
region (count:89)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1130 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:967804-967954	K562	blood:	n/a	n/a
2	ARID3A	chr10:977720-977747	K562	blood:	n/a	n/a
3	ARID3A	chr10:975612-976178	K562	blood:	n/a	n/a
4	ARID3A	chr10:977654-977803	HepG2	liver:	n/a	n/a
5	ATF1	chr10:977597-977929	K562	blood:	n/a	n/a
6	ATF2	chr10:977473-977853	GM12878	blood:	n/a	n/a
7	BACH1	chr10:976057-976295	K562	blood:	n/a	n/a
8	BACH1	chr10:976720-976818	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr10:967719-967950	K562	blood:	n/a	n/a
10	BATF	chr10:982609-982943	GM12878	blood:	n/a	n/a
11	BATF	chr10:982588-982952	GM12878	blood:	n/a	n/a
12	BATF	chr10:989748-990049	GM12878	blood:	n/a	n/a
13	BCLAF1	chr10:975826-976665	GM12878	blood:	n/a	n/a
14	BCLAF1	chr10:976320-976797	GM12878	blood:	n/a	n/a
15	BHLHE40	chr10:975896-976809	GM12878	blood:	n/a	n/a
16	BHLHE40	chr10:977582-978159	GM12878	blood:	n/a	n/a
17	BHLHE40	chr10:995462-995623	K562	blood:	n/a	n/a
18	BHLHE40	chr10:982650-982975	GM12878	blood:	n/a	n/a
19	BHLHE40	chr10:990467-990813	GM12878	blood:	n/a	n/a
20	BHLHE40	chr10:990466-990731	K562	blood:	n/a	n/a
21	BHLHE40	chr10:982217-982270	K562	blood:	n/a	n/a
22	BHLHE40	chr10:976476-976810	K562	blood:	n/a	n/a
23	BHLHE40	chr10:977609-978009	HepG2	liver:	n/a	n/a
24	BHLHE40	chr10:977554-978115	K562	blood:	n/a	n/a
25	BHLHE40	chr10:967653-968020	K562	blood:	n/a	n/a
26	BRCA1	chr10:977585-977787	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr10:977564-977827	GM12878	blood:	n/a	n/a
28	BRCA1	chr10:977555-977858	Hela-S3	cervix:	n/a	n/a
29	CCNT2	chr10:976675-978128	K562	blood:	n/a	n/a
30	CCNT2	chr10:1001902-1001966	K562	blood:	n/a	n/a
31	CEBPB	chr10:980445-980512	H1-hESC	embryonic stem cell:	n/a	chr10:980489-980498 chr10:980488-980499 chr10:980487-980498
32	CEBPB	chr10:980375-980636	K562	blood:	n/a	chr10:980489-980498 chr10:980488-980499 chr10:980487-980498
33	CEBPB	chr10:976002-976201	K562	blood:	n/a	n/a
34	CEBPB	chr10:992848-992874	HepG2	liver:	n/a	n/a
35	CEBPB	chr10:980436-980636	A549	lung:	n/a	chr10:980489-980498 chr10:980488-980499 chr10:980487-980498
36	CEBPB	chr10:980342-980737	HepG2	liver:	n/a	chr10:980489-980498 chr10:980488-980499 chr10:980487-980498
37	CEBPB	chr10:977550-977764	K562	blood:	n/a	n/a
38	CEBPB	chr10:977555-977810	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr10:980353-980643	IMR90	lung:	n/a	chr10:980489-980498 chr10:980488-980499 chr10:980487-980498
40	CEBPB	chr10:967649-967927	K562	blood:	n/a	chr10:967658-967669
41	CEBPB	chr10:977648-977792	A549	lung:	n/a	n/a
42	CEBPB	chr10:990364-990590	HepG2	liver:	n/a	n/a
43	CEBPB	chr10:977489-977746	HepG2	liver:	n/a	n/a
44	CHD1	chr10:976545-976804	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr10:975406-978308	IMR90	lung:	n/a	chr10:977804-977814 chr10:977690-977700
46	CHD1	chr10:975847-976842	GM12878	blood:	n/a	n/a
47	CHD2	chr10:976657-976885	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr10:990445-990652	GM12878	blood:	n/a	n/a
49	CHD2	chr10:977494-977954	GM12878	blood:	n/a	chr10:977804-977814 chr10:977690-977700
50	CHD2	chr10:977519-977905	HepG2	liver:	n/a	chr10:977804-977814 chr10:977690-977700

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:978077-978127	AG04449	skin:	fetal
2	chr10:976940-976990	HUVEC	blood vessel:	n/a
3	chr10:978077-978127	AG04449	skin:	fetal
4	chr10:976940-976990	HUVEC	blood vessel:	n/a
5	chr10:994943-994993	HRPEpiC	eye:	n/a
6	chr10:995290-995340	HCM	heart:	n/a
7	chr10:976548-976598	HCPEpiC	choroid plexus:	n/a
8	chr10:995095-995145	U87	brain:	n/a
9	chr10:994943-994993	HIPEpiC	eye:	n/a
10	chr10:978077-978127	HCPEpiC	choroid plexus:	n/a
11	chr10:995095-995145	NT2-D1	testis:	n/a
12	chr10:974338-974388	AG04450	lung:	fetal
13	chr10:977622-977672	SK-N-SH	brain:	n/a
14	chr10:978077-978127	HepG2	liver:	n/a
15	chr10:980765-980815	HNPCEpiC	eye:	n/a
16	chr10:994943-994993	LNCaP	prostate:	n/a
17	chr10:976594-976644	ECC-1	luminal epithelium:	n/a
18	chr10:1000575-1000625	HEEpiC	esophagus:	n/a
19	chr10:977622-977672	T-47D	breast:	n/a
20	chr10:978077-978127	RPTEC	kidney:	n/a
21	chr10:994943-994993	GM19239	blood:	n/a
22	chr10:980765-980815	HEEpiC	esophagus:	n/a
23	chr10:994943-994993	AoSMC	blood vessel:	n/a
24	chr10:1000300-1000350	NB4	blood:	n/a
25	chr10:976548-976598	K562	blood:	n/a
26	chr10:978019-978069	NHBE	bronchial:	n/a
27	chr10:1000300-1000350	NHDF-neo	bronchial:	n/a
28	chr10:980765-980815	Hepatocyte	liver:	n/a
29	chr10:1000300-1000350	HUVEC	blood vessel:	n/a
30	chr10:977622-977672	AoSMC	blood vessel:	n/a
31	chr10:974338-974388	Caco-2	colon:	n/a
32	chr10:995095-995145	T-47D	breast:	n/a
33	chr10:1000575-1000625	NHDF-neo	bronchial:	n/a
34	chr10:978019-978069	HMEC	breast:	n/a
35	chr10:978077-978127	HAEpiC	amniotic membrane:	n/a
36	chr10:1000575-1000625	AG04449	skin:	fetal
37	chr10:974338-974388	HRPEpiC	eye:	n/a
38	chr10:968280-968330	HIPEpiC	eye:	n/a
39	chr10:980765-980815	SK-N-SH	brain:	n/a
40	chr10:978019-978069	RPTEC	kidney:	n/a
41	chr10:978077-978127	AG10803	skin:	n/a
42	chr10:978077-978127	SK-N-SH	brain:	n/a
43	chr10:995095-995145	SK-N-SH_RA	brain:	n/a
44	chr10:1000300-1000350	MCF-7	breast:	n/a
45	chr10:995095-995145	PFSK-1	brain:	n/a
46	chr10:978077-978127	LNCaP	prostate:	n/a
47	chr10:994943-994993	HRCEpiC	kidney:	n/a
48	chr10:994943-994993	SKMC	muscle:	n/a
49	chr10:1000300-1000350	HCT-116	colon:	n/a
50	chr10:978019-978069	HNPCEpiC	eye:	n/a

(count:89 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:980826..983608-chr10:1003068..1004956,2	K562	blood:
2	chr10:974758..976966-chr10:1110782..1112393,2	MCF-7	breast:
3	chr10:988532..990709-chr10:1000522..1003406,2	MCF-7	breast:
4	chr10:975330..979257-chr10:1093215..1097529,5	K562	blood:
5	chr10:969504..972308-chr10:1100615..1103813,3	MCF-7	breast:
6	chr10:1002020..1004924-chr10:1009202..1011501,2	MCF-7	breast:
7	chr10:968194..970356-chr10:1031851..1035420,3	K562	blood:
8	chr10:949389..951942-chr10:967681..970288,3	MCF-7	breast:
9	chr10:976263..979384-chr10:986596..991037,4	MCF-7	breast:
10	chr10:980753..982426-chr17:57919026..57921181,2	MCF-7	breast:
11	chr10:976647..980794-chr10:1093154..1097319,8	MCF-7	breast:
12	chr10:991162..993286-chr10:1002150..1004961,2	K562	blood:
13	chr10:982121..984896-chr10:984955..986688,2	K562	blood:
14	chr10:976152..979108-chr10:1085303..1088696,4	MCF-7	breast:
15	chr10:968856..970673-chr10:1033223..1035399,2	K562	blood:
16	chr10:963108..967368-chr10:972053..975262,4	MCF-7	breast:
17	chr10:957384..959889-chr10:967554..970347,2	MCF-7	breast:
18	chr10:963108..967368-chr10:972053..975262,4	MCF-7	breast:
19	chr10:988056..990097-chr10:1030417..1032200,2	K562	blood:
20	chr10:956864..959449-chr10:987864..990001,2	K562	blood:
21	chr10:976344..979673-chr10:1032747..1036349,14	K562	blood:
22	chr10:975799..978442-chr10:1098842..1102725,4	MCF-7	breast:
23	chr10:949318..951166-chr10:969815..971426,2	MCF-7	breast:
24	chr10:980826..983608-chr10:1003068..1004956,2	K562	blood:
25	chr10:969783..971974-chr10:1038430..1041356,2	K562	blood:
26	chr10:983720..986820-chr10:989199..992227,3	MCF-7	breast:
27	chr10:981472..983740-chr10:1094452..1096792,3	MCF-7	breast:
28	chr10:1003784..1006528-chr10:1035596..1037131,2	K562	blood:
29	chr10:974670..978531-chr10:1101117..1104171,5	K562	blood:
30	chr10:983875..986452-chr10:1011606..1014374,2	K562	blood:
31	chr10:974439..980732-chr10:1030011..1038533,28	MCF-7	breast:
32	chr10:975582..978698-chr10:1119494..1122267,3	MCF-7	breast:
33	chr10:974834..978758-chr10:991717..994316,3	MCF-7	breast:
34	chr10:964099..966900-chr10:967663..969499,2	MCF-7	breast:
35	chr10:976200..979208-chr10:1093606..1097726,5	MCF-7	breast:
36	chr10:986490..989100-chr10:1016201..1018491,2	MCF-7	breast:
37	chr10:981522..983775-chr10:1008969..1010630,2	K562	blood:
38	chr10:955784..957552-chr10:964009..966938,2	K562	blood:
39	chr10:977031..978658-chr10:1101205..1103073,2	K562	blood:
40	chr10:976974..978781-chr10:992429..995773,3	MCF-7	breast:
41	chr10:974339..976019-chr10:1070236..1073056,2	MCF-7	breast:
42	chr10:1004224..1005982-chr10:1009154..1011697,2	K562	blood:
43	chr10:983630..985701-chr10:1101739..1103467,2	MCF-7	breast:
44	chr10:986549..990201-chr10:1030700..1035554,4	K562	blood:
45	chr10:967396..974147-chr10:1032852..1035834,6	MCF-7	breast:
46	chr10:1000614..1004584-chr10:1019814..1022762,4	K562	blood:
47	chr10:988532..990709-chr10:1000522..1003406,2	MCF-7	breast:
48	chr10:972336..974147-chr10:1040690..1042738,2	K562	blood:
49	chr10:1002935..1005856-chr10:1082299..1084442,2	MCF-7	breast:
50	chr10:993243..997969-chr10:1000077..1005831,6	K562	blood:

(count:12 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1524 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:1524 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192135018	chr10:965907-965908	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs547021881	chr10:965918-965919	Weak transcription Enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs566865077	chr10:966014-966015	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs147248172	chr10:966041-966042	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs551681199	chr10:966078-966079	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs571536587	chr10:966079-966080	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs115289566	chr10:966104-966105	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs529621294	chr10:966130-966131	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs369361577	chr10:966164-966165	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs114024818	chr10:966191-966192	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs568059315	chr10:966200-966201	Weak transcription Enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs184274214	chr10:966208-966209	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs552589441	chr10:966221-966222	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs188611074	chr10:966241-966242	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139730934	chr10:966296-966297	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs181167500	chr10:966325-966326	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs539066164	chr10:966329-966330	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs575808208	chr10:966337-966338	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs117165645	chr10:966355-966356	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs561322005	chr10:966367-966368	Weak transcription Strong transcription Enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs530257307	chr10:966408-966409	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs149798101	chr10:966450-966451	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs12570439	chr10:966451-966452	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs375247073	chr10:966500-966501	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560501849	chr10:966511-966512	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs111256604	chr10:966522-966523	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs183788221	chr10:966533-966534	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145783501	chr10:966539-966540	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs571572689	chr10:966582-966583	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs530667424	chr10:966620-966621	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs550798567	chr10:966649-966650	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs112446413	chr10:966661-966662	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs567339713	chr10:966665-966666	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs569216717	chr10:966669-966670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs549413656	chr10:966699-966700	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs573787403	chr10:966740-966741	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs148974839	chr10:966760-966761	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs566197950	chr10:966777-966778	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs116474248	chr10:966787-966788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189298008	chr10:966841-966842	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs538144573	chr10:966861-966862	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575940459	chr10:966913-966914	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs542672181	chr10:966930-966931	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538149958	chr10:966955-966956	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs555182854	chr10:966976-966977	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs146624889	chr10:966980-966981	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182301114	chr10:966988-966989	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs540803998	chr10:967016-967017	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs574587310	chr10:967039-967040	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141434545	chr10:967073-967074	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1406 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:927600-972600	Weak transcription	Hela-S3	cervix
2	chr10:928000-966400	Weak transcription	Small Intestine	intestine
3	chr10:929400-975800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr10:929400-976400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr10:931600-967400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr10:940000-970200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr10:940200-967600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr10:946000-966600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr10:947800-975400	Weak transcription	Fetal Brain Male	brain
10	chr10:949600-974600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr10:951000-975400	Weak transcription	Fetal Kidney	kidney
12	chr10:952600-967800	Weak transcription	Brain Angular Gyrus	brain
13	chr10:952600-971000	Weak transcription	Brain Substantia Nigra	brain
14	chr10:952600-975400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr10:952800-966000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr10:953000-967400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr10:953000-974400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
18	chr10:954600-975000	Weak transcription	Stomach Smooth Muscle	stomach
19	chr10:954800-967600	Weak transcription	NHDF-Ad	bronchial
20	chr10:954800-973600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chr10:955000-967600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr10:955000-968200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr10:955000-974600	Weak transcription	Colonic Mucosa	Colon
24	chr10:956000-967400	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr10:956200-966000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr10:956200-972400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr10:956600-967400	Weak transcription	Colon Smooth Muscle	Colon
28	chr10:956800-970000	Weak transcription	Brain Germinal Matrix	brain
29	chr10:956800-975400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr10:956800-975600	Weak transcription	Fetal Brain Female	brain
31	chr10:956800-976400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr10:957000-967400	Weak transcription	Brain Hippocampus Middle	brain
33	chr10:957000-967400	Weak transcription	Ovary	ovary
34	chr10:957000-967800	Weak transcription	Esophagus	oesophagus
35	chr10:957000-970600	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr10:957200-966000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr10:957200-967400	Weak transcription	HSMMtube	muscle
38	chr10:957600-966800	Weak transcription	NH-A	brain
39	chr10:957600-975200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr10:957800-970000	Weak transcription	Brain Anterior Caudate	brain
41	chr10:958000-967400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
42	chr10:958000-967400	Weak transcription	Liver	Liver
43	chr10:958000-967400	Weak transcription	NHLF	lung
44	chr10:958000-967600	Weak transcription	Duodenum Mucosa	Duodenum
45	chr10:958000-967600	Weak transcription	Fetal Lung	lung
46	chr10:958000-967800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr10:958000-967800	Weak transcription	Placenta	Placenta
48	chr10:958000-967800	Weak transcription	Lung	lung
49	chr10:958000-968000	Weak transcription	Fetal Intestine Large	intestine
50	chr10:958000-970400	Weak transcription	Spleen	Spleen

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