Variant report

Variant	esv3518965
Chromosome Location	chr10:19786251-20061305
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1220)
CpG islands
(count:488)
Chromatin interactive
region (count:24)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr10:19927475-19927788	HepG2	liver:	n/a	n/a
2	ARID3A	chr10:19945416-19945759	HepG2	liver:	n/a	n/a
3	ARID3A	chr10:19928010-19928135	HepG2	liver:	n/a	n/a
4	ATF1	chr10:20019092-20019388	K562	blood:	n/a	n/a
5	ATF1	chr10:20031092-20031318	K562	blood:	n/a	n/a
6	ATF1	chr10:20024073-20024273	K562	blood:	n/a	n/a
7	ATF1	chr10:19798150-19798313	K562	blood:	n/a	n/a
8	ATF1	chr10:19792017-19792188	K562	blood:	n/a	n/a
9	BACH1	chr10:19836112-19836113	K562	blood:	n/a	n/a
10	BACH1	chr10:19867582-19867705	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr10:19807634-19807887	GM12878	blood:	n/a	chr10:19807691-19807699
12	BATF	chr10:20058387-20058638	GM12878	blood:	n/a	n/a
13	BATF	chr10:20035644-20035814	GM12878	blood:	n/a	n/a
14	BATF	chr10:20058390-20058625	GM12878	blood:	n/a	n/a
15	BATF	chr10:20035664-20035859	GM12878	blood:	n/a	n/a
16	BCL11A	chr10:20058379-20058635	GM12878	blood:	n/a	n/a
17	BCL11A	chr10:20058400-20058555	GM12878	blood:	n/a	n/a
18	BCL11A	chr10:20035672-20035886	GM12878	blood:	n/a	n/a
19	BCL11A	chr10:19807647-19807851	GM12878	blood:	n/a	n/a
20	BCL11A	chr10:20035655-20035827	GM12878	blood:	n/a	n/a
21	BCL11A	chr10:20036910-20037233	GM12878	blood:	n/a	n/a
22	BHLHE40	chr10:20035652-20035896	HepG2	liver:	n/a	n/a
23	BHLHE40	chr10:20036959-20037247	HepG2	liver:	n/a	n/a
24	BRCA1	chr10:19884779-19884781	HepG2	liver:	n/a	n/a
25	CEBPB	chr10:19825248-19825603	HepG2	liver:	n/a	n/a
26	CEBPB	chr10:19859105-19859419	A549	lung:	n/a	chr10:19859255-19859268 chr10:19859256-19859267 chr10:19859255-19859266 chr10:19859255-19859268 chr10:19859308-19859319
27	CEBPB	chr10:19940513-19940808	K562	blood:	n/a	chr10:19940638-19940649
28	CEBPB	chr10:19936373-19936835	MCF-7	breast:	n/a	chr10:19936565-19936576 chr10:19936564-19936575 chr10:19936566-19936575
29	CEBPB	chr10:19940438-19941029	IMR90	lung:	n/a	chr10:19940638-19940649
30	CEBPB	chr10:20038058-20038599	Hela-S3	cervix:	n/a	chr10:20038189-20038200
31	CEBPB	chr10:19876127-19876402	MCF-7	breast:	n/a	chr10:19876303-19876314
32	CEBPB	chr10:19877274-19877779	HepG2	liver:	n/a	n/a
33	CEBPB	chr10:19835213-19835386	H1-hESC	embryonic stem cell:	n/a	chr10:19835318-19835331 chr10:19835318-19835329 chr10:19835320-19835331 chr10:19835318-19835331
34	CEBPB	chr10:19859013-19859499	Hela-S3	cervix:	n/a	chr10:19859255-19859268 chr10:19859256-19859267 chr10:19859255-19859266 chr10:19859255-19859268 chr10:19859308-19859319
35	CEBPB	chr10:19996466-19996579	A549	lung:	n/a	chr10:19996526-19996537 chr10:19996526-19996539
36	CEBPB	chr10:19918561-19918761	HepG2	liver:	n/a	chr10:19918689-19918700 chr10:19918691-19918702
37	CEBPB	chr10:20023681-20023947	HepG2	liver:	n/a	n/a
38	CEBPB	chr10:19940455-19941127	HepG2	liver:	n/a	chr10:19940638-19940649
39	CEBPB	chr10:20038066-20038352	A549	lung:	n/a	chr10:20038189-20038200
40	CEBPB	chr10:20038015-20038653	IMR90	lung:	n/a	chr10:20038189-20038200
41	CEBPB	chr10:19877458-19877820	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr10:19945429-19945775	IMR90	lung:	n/a	n/a
43	CEBPB	chr10:20038151-20038314	H1-hESC	embryonic stem cell:	n/a	chr10:20038189-20038200
44	CEBPB	chr10:19825290-19825489	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr10:20040519-20040846	IMR90	lung:	n/a	chr10:20040659-20040670
46	CEBPB	chr10:19923178-19923460	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr10:19859211-19859370	H1-hESC	embryonic stem cell:	n/a	chr10:19859255-19859268 chr10:19859256-19859267 chr10:19859255-19859266 chr10:19859255-19859268 chr10:19859308-19859319
48	CEBPB	chr10:19936432-19936660	IMR90	lung:	n/a	chr10:19936565-19936576 chr10:19936564-19936575 chr10:19936566-19936575
49	CEBPB	chr10:19927464-19927923	MCF-7	breast:	n/a	chr10:19927714-19927725
50	CEBPB	chr10:19936293-19936803	MCF-7	breast:	n/a	chr10:19936565-19936576 chr10:19936564-19936575 chr10:19936566-19936575

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:20019641-20019691	NT2-D1	testis:	n/a
2	chr10:20009221-20009271	SK-N-MC	brain:	n/a
3	chr10:20019641-20019691	NH-A	brain:	n/a
4	chr10:19918310-19918360	ProgFib	skin:	n/a
5	chr10:20009221-20009271	HPAEpiC	pulmonary alveolar:	n/a
6	chr10:19918310-19918360	HNPCEpiC	eye:	n/a
7	chr10:19972179-19972229	H1-hESC	embryonic stem cell:	embryo
8	chr10:19946093-19946143	H1-hESC	embryonic stem cell:	embryo
9	chr10:20017996-20018046	ProgFib	skin:	n/a
10	chr10:19918310-19918360	AG04450	lung:	fetal
11	chr10:20009221-20009271	HEEpiC	esophagus:	n/a
12	chr10:20019641-20019691	GM19239	blood:	n/a
13	chr10:20019641-20019691	HCF	heart:	n/a
14	chr10:19918310-19918360	AG10803	skin:	n/a
15	chr10:19918310-19918360	HL-60	blood:	n/a
16	chr10:19946093-19946143	Hela-S3	cervix:	n/a
17	chr10:20019641-20019691	HMEC	breast:	n/a
18	chr10:19972179-19972229	PrEC	prostate:	n/a
19	chr10:20009221-20009271	AG04449	skin:	fetal
20	chr10:19918310-19918360	HEEpiC	esophagus:	n/a
21	chr10:20023014-20023064	AG04450	lung:	fetal
22	chr10:19972179-19972229	NH-A	brain:	n/a
23	chr10:19946093-19946143	SK-N-SH_RA	brain:	n/a
24	chr10:19946093-19946143	GM12892	blood:	n/a
25	chr10:19946093-19946143	IMR90	lung:	fetal
26	chr10:19993393-19993443	PANC-1	pancreas:	n/a
27	chr10:19993393-19993443	HRPEpiC	eye:	n/a
28	chr10:19918310-19918360	SK-N-SH	brain:	n/a
29	chr10:20019641-20019691	MCF-7	breast:	n/a
30	chr10:20023014-20023064	PANC-1	pancreas:	n/a
31	chr10:19946093-19946143	HEK293	kidney:	embryo
32	chr10:19972179-19972229	LNCaP	prostate:	n/a
33	chr10:19918310-19918360	A549	lung:	n/a
34	chr10:19993393-19993443	HRCEpiC	kidney:	n/a
35	chr10:19993393-19993443	MCF-7	breast:	n/a
36	chr10:20019641-20019691	U87	brain:	n/a
37	chr10:19972179-19972229	CMK	blood:	n/a
38	chr10:19918310-19918360	NB4	blood:	n/a
39	chr10:19946093-19946143	AG10803	skin:	n/a
40	chr10:19993393-19993443	NT2-D1	testis:	n/a
41	chr10:19918310-19918360	AG09319	gingival:	n/a
42	chr10:19993393-19993443	RPTEC	kidney:	n/a
43	chr10:20017996-20018046	HNPCEpiC	eye:	n/a
44	chr10:19918310-19918360	AoSMC	blood vessel:	n/a
45	chr10:19946093-19946143	GM19239	blood:	n/a
46	chr10:19972179-19972229	HCM	heart:	n/a
47	chr10:20023014-20023064	GM12878	blood:	n/a
48	chr10:19918310-19918360	Hepatocyte	liver:	n/a
49	chr10:20023014-20023064	NH-A	brain:	n/a
50	chr10:19993393-19993443	T-47D	breast:	n/a

(count:24 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:19874981..19877744-chr10:19939869..19941893,2	MCF-7	breast:
2	chr10:19874981..19877744-chr10:19939869..19941893,2	MCF-7	breast:
3	chr10:19784572..19786146-chr10:19787649..19789922,2	MCF-7	breast:
4	chr1:114251553..114252290-chr10:19972729..19973619,2	MCF-7	breast:
5	chr10:19813535..19816224-chr10:19819107..19822084,2	MCF-7	breast:
6	chr10:19814024..19815559-chr10:19817040..19818969,2	K562	blood:
7	chr10:20045444..20047121-chr10:20048455..20050479,2	MCF-7	breast:
8	chr10:19928272..19930845-chr10:19944987..19947653,2	K562	blood:
9	chr10:20019487..20021486-chr10:20023021..20025929,2	K562	blood:
10	chr10:19943628..19945748-chr10:19960912..19962861,2	K562	blood:
11	chr10:19806044..19808111-chr10:19811941..19813567,2	K562	blood:
12	chr10:19814024..19815559-chr10:19817040..19818969,2	K562	blood:
13	chr10:19785625..19787709-chr10:19788365..19791040,2	MCF-7	breast:
14	chr10:19813535..19816224-chr10:19819107..19822084,2	MCF-7	breast:
15	chr10:19884872..19887449-chr10:19896760..19899723,2	MCF-7	breast:
16	chr10:20045444..20047121-chr10:20048455..20050479,2	MCF-7	breast:
17	chr10:19776078..19778713-chr10:19790449..19792992,2	K562	blood:
18	chr10:19928272..19930845-chr10:19944987..19947653,2	K562	blood:
19	chr10:19785625..19787709-chr10:19788365..19791040,2	MCF-7	breast:
20	chr10:19943628..19945748-chr10:19960912..19962861,2	K562	blood:
21	chr10:19806044..19808111-chr10:19811941..19813567,2	K562	blood:
22	chr10:20059859..20061809-chr10:20063253..20064764,2	K562	blood:
23	chr10:19781369..19782958-chr10:19786296..19789278,2	MCF-7	breast:
24	chr10:20020129..20021732-chr10:20034774..20036880,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C10orf112-1	chr10:19981239-19981290	NONHSAT011665
2	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1
3	lnc-NEBL-3	chr10:20057340-20057485	NONHSAT011672
4	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.2
5	lnc-NEBL-2	chr10:20010626-20011154	ENSG00000233968.1
6	lnc-NEBL-3	chr10:20051265-20051357	NONHSAT011670
7	lnc-NEBL-3	chr10:20050632-20051160	NONHSAT011671
8	lnc-NEBL-3	chr10:20057340-20057485	NONHSAT011670
9	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.1
10	lnc-NEBL-3	chr10:20057340-20057485	NONHSAT011671
11	lnc-NEBL-3	chr10:20051049-20051160	NONHSAT011670
12	lnc-NEBL-3	chr10:20045734-20045825	ucscGeneNc_uc001iqf_2
13	lnc-NEBL-3	chr10:20051265-20051357	ucscGeneNc_uc001iqf_2
14	lnc-NEBL-3	chr10:20051049-20051160	ucscGeneNc_uc001iqf_2
15	lnc-NEBL-2	chr10:20010907-20011154	ENSG00000233968.1
16	lnc-NEBL-3	chr10:20039270-20040223	ucscGeneNc_uc001iqf_2
17	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.2
18	lnc-NEBL-3	chr10:20050913-20051160	NONHSAT011672
19	lnc-NEBL-2	chr10:20011259-20011517	ENSG00000233968.1
20	lnc-NEBL-3	chr10:20045734-20045825	NONHSAT011670
21	lnc-NEBL-2	chr10:19999257-20000217	ENSG00000233968.1
22	lnc-NEBL-3	chr10:20039263-20040223	NONHSAT011670
23	lnc-C10orf112-1	chr10:19981387-19981483	NONHSAT011665
24	lnc-NEBL-3	chr10:20051265-20051523	NONHSAT011672
25	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.1
26	lnc-PLXDC2-4	chr10:19887176-19887391	NONHSAT011663
27	lnc-NEBL-3	chr10:20057340-20057485	ucscGeneNc_uc001iqf_2
28	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.2
29	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1
30	lnc-NEBL-3	chr10:20051265-20051357	NONHSAT011671
31	lnc-NEBL-2	chr10:20013856-20013910	ENSG00000233968.1
32	lnc-NEBL-3	chr10:20053862-20053916	NONHSAT011672
33	lnc-NEBL-2	chr10:20010517-20011154	ENSG00000233968.2
34	lnc-NEBL-2	chr10:20017334-20017479	ENSG00000233968.1
35	lnc-NEBL-2	chr10:20011259-20011351	ENSG00000233968.1
36	lnc-NEBL-2	chr10:20011043-20011154	ENSG00000233968.1
37	lnc-NEBL-2	chr10:20005728-20005819	ENSG00000233968.1
38	lnc-NEBL-3	chr10:20053862-20053916	NONHSAT011671

No data

Variant related genes	Relation type
MALRD1	TF binding region
RNA5SP303	TF binding region
MTND2P16	TF binding region
ENSG00000233968	TF binding region
ENSG00000200545	TF binding region
MALRD1	CpG island
RNA5SP303	CpG island
MTND2P16	CpG island
ENSG00000233968	CpG island
ENSG00000200545	CpG island
ENSG00000200545	chromatin interactions
ENSG00000204740	chromatin interactions
ENSG00000230818	chromatin interactions
ENSG00000239539	chromatin interactions

Extended variants
information (count: 12128 )
Associated
traits (count: 48 )

Variant overlapped rSNPs/rCNVs (count:12128 , 50 per page) page: 1 2 3 4 5 6 7 ... 243

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569617809	chr10:19786294-19786295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs79711815	chr10:19786338-19786339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs149872224	chr10:19786378-19786379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs564186593	chr10:19786442-19786443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567579160	chr10:19786570-19786571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs534902705	chr10:19786595-19786596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs552935888	chr10:19786655-19786656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs571396987	chr10:19786681-19786682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs185720594	chr10:19786684-19786685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs16918871	chr10:19786687-19786688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs576431277	chr10:19786688-19786689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543415503	chr10:19786716-19786717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555331944	chr10:19786717-19786718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371873594	chr10:19786725-19786726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs574042871	chr10:19786733-19786734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149056722	chr10:19786759-19786760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190645063	chr10:19786880-19786881	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559731654	chr10:19786889-19786890	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs3852461	chr10:19787002-19787003	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs145906672	chr10:19787010-19787011	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs116001411	chr10:19787018-19787019	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530583051	chr10:19787020-19787021	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs16918877	chr10:19787037-19787038	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs181940880	chr10:19787060-19787061	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs528421835	chr10:19787065-19787066	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs117598916	chr10:19787106-19787107	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34678835	chr10:19787121-19787122	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs538847615	chr10:19787155-19787156	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs550442351	chr10:19787157-19787158	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs565062481	chr10:19787166-19787167	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147811985	chr10:19787171-19787172	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs532361372	chr10:19787195-19787196	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141344386	chr10:19787223-19787224	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367700873	chr10:19787240-19787241	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs34048344	chr10:19787356-19787357	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs77726240	chr10:19787382-19787383	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555370536	chr10:19787392-19787393	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs369888696	chr10:19787402-19787403	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs147001449	chr10:19787411-19787412	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12256835	chr10:19787418-19787419	Enhancers Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs187028362	chr10:19787429-19787430	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs578150983	chr10:19787439-19787440	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545595686	chr10:19787496-19787497	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563724836	chr10:19787502-19787503	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575455761	chr10:19787510-19787511	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542720685	chr10:19787565-19787566	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188958508	chr10:19787570-19787571	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181358022	chr10:19787636-19787637	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185630336	chr10:19787639-19787640	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148066660	chr10:19787672-19787673	Enhancers Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:48)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Breast cancer	17133270	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
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Lung cancer	18438408	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Intracranial aneurysm	16715129	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16616336	CNVD
T-cell lymphomas	19863542	CNVD
Esophageal cancer	21851588	CNVD
small cell lung cancer	20016488	CNVD
Epilepsy	22083797	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:926 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19778400-19787400	Weak transcription	Fetal Lung	lung
2	chr10:19778400-19787400	Weak transcription	Fetal Muscle Leg	muscle
3	chr10:19778400-19790600	Weak transcription	Fetal Brain Male	brain
4	chr10:19778600-19795800	Weak transcription	Aorta	Aorta
5	chr10:19779000-19790000	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr10:19779200-19789600	Weak transcription	Stomach Smooth Muscle	stomach
7	chr10:19780200-19796400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr10:19783200-19789400	Weak transcription	HepG2	liver
9	chr10:19783200-19791600	Weak transcription	Fetal Stomach	stomach
10	chr10:19783400-19786800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr10:19783400-19787400	Weak transcription	Duodenum Mucosa	Duodenum
12	chr10:19783400-19799400	Weak transcription	Ovary	ovary
13	chr10:19783600-19787800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr10:19784200-19787400	Weak transcription	Fetal Intestine Large	intestine
15	chr10:19784200-19795800	Weak transcription	Fetal Intestine Small	intestine
16	chr10:19786800-19788600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr10:19786800-19788600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr10:19786800-19788800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr10:19787200-19788200	Enhancers	NHEK	skin
20	chr10:19787400-19787600	Enhancers	Fetal Muscle Leg	muscle
21	chr10:19787400-19787800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr10:19787400-19788000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr10:19787400-19788000	Enhancers	Adipose Nuclei	Adipose
24	chr10:19787400-19788000	Enhancers	Fetal Lung	lung
25	chr10:19787400-19790400	Strong transcription	Fetal Intestine Large	intestine
26	chr10:19787400-19790600	Strong transcription	Duodenum Mucosa	Duodenum
27	chr10:19787800-19788600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr10:19788200-19790000	Weak transcription	NHEK	skin
29	chr10:19788600-19795600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr10:19788600-19798600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr10:19788800-19794200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr10:19790000-19790200	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr10:19790000-19790200	Enhancers	NHEK	skin
34	chr10:19790400-19794200	Weak transcription	Fetal Intestine Large	intestine
35	chr10:19790600-19792400	Weak transcription	Duodenum Mucosa	Duodenum
36	chr10:19792400-19793400	Strong transcription	Duodenum Mucosa	Duodenum
37	chr10:19793400-19804800	Weak transcription	Duodenum Mucosa	Duodenum
38	chr10:19794200-19795400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr10:19794200-19796200	Strong transcription	Fetal Intestine Large	intestine
40	chr10:19794400-19795000	Enhancers	Adipose Nuclei	Adipose
41	chr10:19794600-19795200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr10:19795800-19796200	ZNF genes & repeats	Aorta	Aorta
43	chr10:19795800-19796200	ZNF genes & repeats	Fetal Intestine Small	intestine
44	chr10:19796000-19796200	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr10:19796200-19796600	Weak transcription	Fetal Intestine Small	intestine
46	chr10:19796200-19805200	Weak transcription	Fetal Intestine Large	intestine
47	chr10:19796200-19839400	Weak transcription	Aorta	Aorta
48	chr10:19796800-19798800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr10:19798400-19798800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr10:19798400-19799200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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