Variant report

Variant	nsv1041443
Chromosome Location	chr10:45247484-45359231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1133)
CpG islands
(count:611)
Chromatin interactive
region (count:61)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1133 , 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	chr10:45353231-45353390	K562	blood:	n/a	n/a
2	ATF1	chr10:45284313-45284641	K562	blood:	n/a	n/a
3	ATF2	chr10:45353031-45353569	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr10:45320128-45320341	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr10:45353142-45353592	H1-hESC	embryonic stem cell:	n/a	chr10:45353244-45353258
6	BACH1	chr10:45305172-45305309	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr10:45299606-45299615	K562	blood:	n/a	n/a
8	BACH1	chr10:45353406-45353571	K562	blood:	n/a	n/a
9	BCL11A	chr10:45353248-45353459	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCLAF1	chr10:45353153-45353511	GM12878	blood:	n/a	n/a
11	BHLHE40	chr10:45353265-45353562	GM12878	blood:	n/a	n/a
12	BHLHE40	chr10:45316732-45317038	K562	blood:	n/a	n/a
13	BHLHE40	chr10:45281024-45281155	K562	blood:	n/a	chr10:45281073-45281082 chr10:45281071-45281080 chr10:45281072-45281081 chr10:45281066-45281087 chr10:45281072-45281081 chr10:45281070-45281083
14	BHLHE40	chr10:45353269-45353487	K562	blood:	n/a	n/a
15	BHLHE40	chr10:45263065-45263128	K562	blood:	n/a	n/a
16	BHLHE40	chr10:45320033-45320161	K562	blood:	n/a	n/a
17	BHLHE40	chr10:45284232-45284511	K562	blood:	n/a	n/a
18	BHLHE40	chr10:45316768-45317065	HepG2	liver:	n/a	n/a
19	BRCA1	chr10:45323848-45323869	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr10:45317191-45317198	HepG2	liver:	n/a	n/a
21	BRCA1	chr10:45353094-45353455	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr10:45297411-45297826	MCF-7	breast:	n/a	n/a
23	CEBPB	chr10:45346038-45346267	A549	lung:	n/a	chr10:45346135-45346144 chr10:45346135-45346144 chr10:45346134-45346145 chr10:45346135-45346144 chr10:45346133-45346144 chr10:45346133-45346146 chr10:45346135-45346144
24	CEBPB	chr10:45353142-45353614	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr10:45291482-45291748	A549	lung:	n/a	chr10:45291656-45291667
26	CEBPB	chr10:45284306-45284404	IMR90	lung:	n/a	n/a
27	CEBPB	chr10:45294259-45294568	HepG2	liver:	n/a	chr10:45294421-45294432
28	CEBPB	chr10:45251683-45252022	IMR90	lung:	n/a	n/a
29	CEBPB	chr10:45277676-45277830	HepG2	liver:	n/a	chr10:45277784-45277795
30	CEBPB	chr10:45291507-45291802	HepG2	liver:	n/a	chr10:45291656-45291667
31	CEBPB	chr10:45351884-45352061	K562	blood:	n/a	chr10:45352018-45352029 chr10:45352018-45352029
32	CEBPB	chr10:45294263-45294553	IMR90	lung:	n/a	chr10:45294421-45294432
33	CEBPB	chr10:45291498-45291799	IMR90	lung:	n/a	chr10:45291656-45291667
34	CEBPB	chr10:45266543-45266695	HepG2	liver:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
35	CEBPB	chr10:45248271-45248670	MCF-7	breast:	n/a	chr10:45248346-45248358
36	CEBPB	chr10:45284290-45284604	K562	blood:	n/a	n/a
37	CEBPB	chr10:45323362-45323726	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:45281919-45282355	IMR90	lung:	n/a	n/a
39	CEBPB	chr10:45277736-45277852	A549	lung:	n/a	chr10:45277784-45277795
40	CEBPB	chr10:45308006-45308303	IMR90	lung:	n/a	chr10:45308145-45308156
41	CEBPB	chr10:45308055-45308266	HepG2	liver:	n/a	chr10:45308145-45308156
42	CEBPB	chr10:45297390-45297826	ECC-1	luminal epithelium:	n/a	n/a
43	CEBPB	chr10:45346019-45346217	HepG2	liver:	n/a	chr10:45346135-45346144 chr10:45346135-45346144 chr10:45346134-45346145 chr10:45346135-45346144 chr10:45346133-45346144 chr10:45346133-45346146 chr10:45346135-45346144
44	CEBPB	chr10:45322765-45323115	HepG2	liver:	n/a	n/a
45	CEBPB	chr10:45284223-45284595	K562	blood:	n/a	n/a
46	CEBPB	chr10:45323342-45323756	MCF-7	breast:	n/a	n/a
47	CEBPB	chr10:45291597-45291775	K562	blood:	n/a	chr10:45291656-45291667
48	CEBPB	chr10:45308030-45308247	A549	lung:	n/a	chr10:45308145-45308156
49	CEBPB	chr10:45266517-45266742	K562	blood:	n/a	chr10:45266601-45266614 chr10:45266602-45266613 chr10:45266601-45266614 chr10:45266601-45266614
50	CEBPB	chr10:45276653-45276925	IMR90	lung:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:45282107-45282157	SKMC	muscle:	n/a
2	chr10:45282107-45282157	SKMC	muscle:	n/a
3	chr10:45353344-45353394	NHBE	bronchial:	n/a
4	chr10:45270290-45270340	AG09309	skin:	n/a
5	chr10:45324653-45324703	Hela-S3	cervix:	n/a
6	chr10:45282107-45282157	SK-N-MC	brain:	n/a
7	chr10:45324653-45324703	SK-N-MC	brain:	n/a
8	chr10:45357075-45357125	HAEpiC	amniotic membrane:	n/a
9	chr10:45306728-45306778	SK-N-SH_RA	brain:	n/a
10	chr10:45248889-45248939	HNPCEpiC	eye:	n/a
11	chr10:45298460-45298510	HepG2	liver:	n/a
12	chr10:45306728-45306778	SKMC	muscle:	n/a
13	chr10:45352772-45352822	SKMC	muscle:	n/a
14	chr10:45353344-45353394	H1-hESC	embryonic stem cell:	embryo
15	chr10:45353344-45353394	SKMC	muscle:	n/a
16	chr10:45353344-45353394	HRCEpiC	kidney:	n/a
17	chr10:45357075-45357125	HCPEpiC	choroid plexus:	n/a
18	chr10:45306728-45306778	BJ	skin:	n/a
19	chr10:45352772-45352822	MCF-7	breast:	n/a
20	chr10:45324653-45324703	HAEpiC	amniotic membrane:	n/a
21	chr10:45324999-45325049	HCPEpiC	choroid plexus:	n/a
22	chr10:45282107-45282157	HPAEpiC	pulmonary alveolar:	n/a
23	chr10:45298460-45298510	HCT-116	colon:	n/a
24	chr10:45306728-45306778	HEK293	kidney:	embryo
25	chr10:45324999-45325049	NH-A	brain:	n/a
26	chr10:45306728-45306778	GM12892	blood:	n/a
27	chr10:45324653-45324703	BJ	skin:	n/a
28	chr10:45248889-45248939	HRCEpiC	kidney:	n/a
29	chr10:45282107-45282157	GM12892	blood:	n/a
30	chr10:45270290-45270340	NT2-D1	testis:	n/a
31	chr10:45353344-45353394	HEEpiC	esophagus:	n/a
32	chr10:45270290-45270340	AG04450	lung:	fetal
33	chr10:45282107-45282157	AG09309	skin:	n/a
34	chr10:45248889-45248939	HCM	heart:	n/a
35	chr10:45248889-45248939	MCF-7	breast:	n/a
36	chr10:45248889-45248939	IMR90	lung:	fetal
37	chr10:45248889-45248939	H1-hESC	embryonic stem cell:	embryo
38	chr10:45352772-45352822	HEK293	kidney:	embryo
39	chr10:45353344-45353394	SAEC	small airway:	n/a
40	chr10:45298460-45298510	HAEpiC	amniotic membrane:	n/a
41	chr10:45353344-45353394	AG10803	skin:	n/a
42	chr10:45352772-45352822	PANC-1	pancreas:	n/a
43	chr10:45282107-45282157	HCT-116	colon:	n/a
44	chr10:45357075-45357125	PFSK-1	brain:	n/a
45	chr10:45270290-45270340	AG10803	skin:	n/a
46	chr10:45324653-45324703	GM12878	blood:	n/a
47	chr10:45282107-45282157	T-47D	breast:	n/a
48	chr10:45352772-45352822	NB4	blood:	n/a
49	chr10:45357075-45357125	GM06990	blood:	n/a
50	chr10:45270290-45270340	CMK	blood:	n/a

(count:61 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
2	chr10:44806565..44809195-chr10:45358624..45361285,2	MCF-7	breast:
3	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
4	chr10:45323438..45325285-chr10:45357392..45360351,2	MCF-7	breast:
5	chr10:45359136..45362011-chr10:45365608..45368022,2	MCF-7	breast:
6	chr10:45289285..45290810-chr10:45339377..45341494,2	K562	blood:
7	chr10:45315653..45316627-chr10:45360108..45360667,2	MCF-7	breast:
8	chr10:45358763..45359359-chr10:45420588..45421166,2	MCF-7	breast:
9	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
10	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
11	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
12	chr10:45259585..45261390-chr10:45269370..45271263,2	MCF-7	breast:
13	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
14	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
15	chr10:45219309..45221498-chr10:45248045..45250477,2	MCF-7	breast:
16	chr10:45280392..45282397-chr10:45283199..45285809,2	MCF-7	breast:
17	chr10:45358806..45362184-chr10:45374031..45377195,7	MCF-7	breast:
18	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
19	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
20	chr10:45322078..45324747-chr10:45339592..45342919,3	MCF-7	breast:
21	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
22	chr10:45299556..45301491-chr10:45302567..45305313,2	MCF-7	breast:
23	chr10:45316115..45319026-chr10:45322828..45325403,2	MCF-7	breast:
24	chr10:45314626..45316368-chr10:45319725..45322021,2	K562	blood:
25	chr10:45345447..45347889-chr10:45348586..45350625,2	MCF-7	breast:
26	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
27	chr10:45351801..45354236-chr10:45357437..45359701,2	MCF-7	breast:
28	chr10:45290179..45292610-chr10:45294237..45296557,2	K562	blood:
29	chr10:45284435..45287035-chr10:45287547..45289345,3	MCF-7	breast:
30	chr10:45343728..45347558-chr10:45349566..45353071,5	K562	blood:
31	chr10:45346108..45348016-chr10:45358744..45360566,2	MCF-7	breast:
32	chr10:44838214..44839988-chr10:45358990..45361761,2	MCF-7	breast:
33	chr10:45346108..45348016-chr10:45358744..45360566,2	MCF-7	breast:
34	chr10:45316144..45319215-chr10:45321479..45323724,3	MCF-7	breast:
35	chr10:45359058..45361978-chr10:45470827..45473686,2	K562	blood:
36	chr10:45348502..45349200-chr7:103463744..103464468,2	MCF-7	breast:
37	chr10:45358904..45360461-chr10:45469985..45472068,2	MCF-7	breast:
38	chr10:45313542..45315605-chr10:45324228..45326274,2	MCF-7	breast:
39	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
40	chr10:44889278..44891908-chr10:45358859..45361394,2	MCF-7	breast:
41	chr10:45228558..45230518-chr10:45348231..45349134,6	MCF-7	breast:
42	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
43	chr10:44881926..44882676-chr10:45348263..45349209,2	MCF-7	breast:
44	chr10:45352445..45354314-chr10:45358197..45360590,2	K562	blood:
45	chr10:45336364..45339014-chr10:45360151..45362117,2	MCF-7	breast:
46	chr10:45348548..45350169-chr10:45351123..45353396,2	MCF-7	breast:
47	chr10:45315813..45316747-chr10:45352848..45353822,2	MCF-7	breast:
48	chr10:45298059..45299757-chr10:45299870..45301378,2	K562	blood:
49	chr10:45252118..45254825-chr10:45257063..45259616,2	MCF-7	breast:
50	chr10:45201624..45204188-chr10:45255999..45258220,2	MCF-7	breast:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf10-2	chr10:45320950-45321029	ENSG00000224812
2	lnc-TMEM72-2	chr10:45301891-45303671	NONHSAT013040
3	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812.2
4	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812.2
5	lnc-C10orf10-2	chr10:45320950-45321029	ENSG00000224812.2
6	lnc-C10orf10-2	chr10:45321600-45321816	ENSG00000224812.2
7	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812.2
8	lnc-C10orf10-2	chr10:45306472-45307631	ENSG00000224812
9	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812.2
10	lnc-C10orf10-2	chr10:45324620-45324729	NONHSAT013044
11	lnc-C10orf10-2	chr10:45324023-45324287	NONHSAT013044
12	lnc-C10orf10-2	chr10:45326448-45326693	ENSG00000224812
13	lnc-C10orf10-2	chr10:45318638-45318736	ENSG00000224812
14	lnc-C10orf10-2	chr10:45321600-45321818	ENSG00000224812
15	lnc-C10orf10-2	chr10:45322733-45324287	NONHSAT013043
16	lnc-C10orf10-5	chr10:45270071-45272253	ucscGeneNc_uc001jcf_1
17	lnc-C10orf10-2	chr10:45329514-45330767	ENSG00000224812

No data

Variant related genes	Relation type
EIF2AP4	TF binding region
EIF2AP4	CpG island
ENSG00000107562	chromatin interactions
MALT1	miRNA target sites
YOD1	miRNA target sites

Extended variants
information (count: 4421 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:4421 , 50 per page) page: 1 2 3 4 5 6 7 ... 89

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3737307	chr10:45247493-45247494	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375091027	chr10:45247519-45247520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs1325162	chr10:45247539-45247540	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs577423579	chr10:45247693-45247694	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs538151695	chr10:45247708-45247709	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs117436931	chr10:45247709-45247710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182093949	chr10:45247712-45247713	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187092936	chr10:45247769-45247770	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11239235	chr10:45247900-45247901	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs572586327	chr10:45247901-45247902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546137040	chr10:45247917-45247918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564326751	chr10:45247964-45247965	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530586898	chr10:45247976-45247977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114034639	chr10:45247977-45247978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192765821	chr10:45248037-45248038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375930162	chr10:45248064-45248065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs529812519	chr10:45248143-45248144	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs377271802	chr10:45248149-45248150	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs75858594	chr10:45248150-45248151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111898604	chr10:45248151-45248152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372703110	chr10:45248157-45248158	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs547999366	chr10:45248161-45248162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs17156883	chr10:45248168-45248169	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs533648283	chr10:45248170-45248171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs113587698	chr10:45248175-45248176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs570340806	chr10:45248183-45248184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs184837934	chr10:45248187-45248188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556555768	chr10:45248201-45248202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575231600	chr10:45248221-45248222	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs10900108	chr10:45248254-45248255	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs10900109	chr10:45248263-45248264	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs572525050	chr10:45248386-45248387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567050677	chr10:45248392-45248393	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs188544412	chr10:45248448-45248449	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117791427	chr10:45248483-45248484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1771982	chr10:45248484-45248485	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs79928351	chr10:45248510-45248511	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs562409340	chr10:45248512-45248513	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529950211	chr10:45248541-45248542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111982525	chr10:45248553-45248554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs376584168	chr10:45248577-45248578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559915168	chr10:45248610-45248611	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs527519392	chr10:45248644-45248645	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs537098182	chr10:45248652-45248653	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs1749327	chr10:45248711-45248712	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs34904482	chr10:45248743-45248744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs75037973	chr10:45248759-45248760	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs537414348	chr10:45248770-45248771	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs139743469	chr10:45248777-45248778	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs73289710	chr10:45248788-45248789	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Lung cancer	18438408	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
Mental retardation	21062444	CNVD
Cancer	21183584	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22241247	CNVD
Intellectual disability	21811512	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Obesity	21956041	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21785460	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21948486	CNVD
Dysmorphic features	21948486	CNVD
Epilepsy	21948486	CNVD
Glioblastoma multiforme	22122801	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD

Chromatin state (count:964 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45238000-45247800	Weak transcription	Pancreas	Pancrea
2	chr10:45241600-45248600	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr10:45245000-45251400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr10:45245200-45247800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr10:45245400-45247800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr10:45245400-45248600	Weak transcription	HMEC	breast
7	chr10:45246400-45247800	Weak transcription	Fetal Kidney	kidney
8	chr10:45246800-45248600	Enhancers	Osteobl	bone
9	chr10:45247000-45247600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr10:45247200-45247600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr10:45247200-45248600	Weak transcription	Aorta	Aorta
12	chr10:45247400-45249400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr10:45247400-45249600	Enhancers	NHDF-Ad	bronchial
14	chr10:45247600-45249200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr10:45247600-45249200	Enhancers	Muscle Satellite Cultured Cells	--
16	chr10:45247600-45249600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr10:45247600-45249600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr10:45247600-45249800	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr10:45247800-45248000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr10:45247800-45248800	Enhancers	NHLF	lung
21	chr10:45247800-45249200	Enhancers	HSMM	muscle
22	chr10:45247800-45249400	Enhancers	Fetal Kidney	kidney
23	chr10:45247800-45249400	Enhancers	HSMMtube	muscle
24	chr10:45247800-45249600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr10:45247800-45249600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr10:45247800-45249600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr10:45247800-45249600	Enhancers	Colon Smooth Muscle	Colon
28	chr10:45247800-45249600	Enhancers	Ovary	ovary
29	chr10:45247800-45249600	Enhancers	Pancreas	Pancrea
30	chr10:45247800-45249600	Enhancers	Rectal Smooth Muscle	rectum
31	chr10:45247800-45249600	Enhancers	HUVEC	blood vessel
32	chr10:45247800-45249600	Enhancers	NH-A	brain
33	chr10:45248000-45248400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr10:45248000-45248400	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr10:45248000-45249000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
36	chr10:45248000-45249000	Enhancers	Stomach Smooth Muscle	stomach
37	chr10:45248000-45249600	Enhancers	Fetal Stomach	stomach
38	chr10:45248200-45249400	Enhancers	Fetal Heart	heart
39	chr10:45248400-45249200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr10:45248600-45248800	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr10:45248600-45248800	Enhancers	Fetal Muscle Leg	muscle
42	chr10:45248600-45249000	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr10:45248600-45249000	Flanking Active TSS	Osteobl	bone
44	chr10:45248600-45249200	Enhancers	Aorta	Aorta
45	chr10:45248600-45249200	Enhancers	HMEC	breast
46	chr10:45248800-45249200	Flanking Active TSS	NHLF	lung
47	chr10:45248800-45249600	Enhancers	Gastric	stomach
48	chr10:45248800-45249600	Enhancers	Lung	lung
49	chr10:45249000-45249600	Enhancers	Osteobl	bone
50	chr10:45249200-45249600	Enhancers	NHLF	lung

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