Variant report

Variant	esv1832155
Chromosome Location	chr6:147554900-147715464
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1435)
CpG islands
(count:245)
Chromatin interactive
region (count:170)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:1435 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:147712124-147712420	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:147642433-147642696	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:147704126-147704442	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:147704152-147704396	K562	blood:	n/a	n/a
5	ATF1	chr6:147563836-147563881	K562	blood:	n/a	n/a
6	ATF3	chr6:147613024-147613310	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:147668403-147668878	K562	blood:	n/a	n/a
8	BACH1	chr6:147619572-147619745	K562	blood:	n/a	n/a
9	BACH1	chr6:147568452-147568564	K562	blood:	n/a	n/a
10	BACH1	chr6:147700286-147700486	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:147689088-147689285	K562	blood:	n/a	n/a
12	BACH1	chr6:147643267-147643332	K562	blood:	n/a	n/a
13	BACH1	chr6:147619125-147619346	K562	blood:	n/a	n/a
14	BACH1	chr6:147562497-147562531	K562	blood:	n/a	n/a
15	BACH1	chr6:147622318-147622405	K562	blood:	n/a	n/a
16	BACH1	chr6:147691714-147691717	K562	blood:	n/a	n/a
17	BATF	chr6:147643559-147643930	GM12878	blood:	n/a	chr6:147643753-147643762
18	BATF	chr6:147706532-147706728	GM12878	blood:	n/a	n/a
19	BATF	chr6:147643614-147643982	GM12878	blood:	n/a	chr6:147643753-147643762
20	BCL11A	chr6:147706516-147706817	GM12878	blood:	n/a	n/a
21	BCL3	chr6:147666819-147668873	K562	blood:	n/a	n/a
22	BCL3	chr6:147673487-147674459	K562	blood:	n/a	n/a
23	BCL3	chr6:147666121-147666736	K562	blood:	n/a	n/a
24	BHLHE40	chr6:147705956-147706203	GM12878	blood:	n/a	n/a
25	BHLHE40	chr6:147712247-147712297	GM12878	blood:	n/a	n/a
26	CBX3	chr6:147618203-147618656	K562	blood:	n/a	n/a
27	CBX3	chr6:147625161-147625767	K562	blood:	n/a	n/a
28	CBX3	chr6:147619319-147620023	K562	blood:	n/a	n/a
29	CBX3	chr6:147617302-147617677	K562	blood:	n/a	n/a
30	CBX3	chr6:147572073-147572608	K562	blood:	n/a	n/a
31	CBX3	chr6:147571248-147571606	K562	blood:	n/a	n/a
32	CBX3	chr6:147573399-147574012	K562	blood:	n/a	n/a
33	CCNT2	chr6:147603738-147603823	K562	blood:	n/a	n/a
34	CCNT2	chr6:147620532-147620627	K562	blood:	n/a	n/a
35	CCNT2	chr6:147599902-147599989	K562	blood:	n/a	n/a
36	CCNT2	chr6:147659167-147659323	K562	blood:	n/a	n/a
37	CCNT2	chr6:147706073-147706272	K562	blood:	n/a	n/a
38	CCNT2	chr6:147622425-147622612	K562	blood:	n/a	n/a
39	CCNT2	chr6:147667511-147667654	K562	blood:	n/a	n/a
40	CCNT2	chr6:147667909-147668231	K562	blood:	n/a	n/a
41	CCNT2	chr6:147557534-147557539	K562	blood:	n/a	n/a
42	CCNT2	chr6:147653145-147653160	K562	blood:	n/a	n/a
43	CCNT2	chr6:147600749-147600984	K562	blood:	n/a	n/a
44	CCNT2	chr6:147670514-147670836	K562	blood:	n/a	n/a
45	CCNT2	chr6:147713782-147714282	K562	blood:	n/a	n/a
46	CEBPB	chr6:147600568-147600905	K562	blood:	n/a	chr6:147600719-147600732 chr6:147600720-147600731
47	CEBPB	chr6:147643695-147643974	Hela-S3	cervix:	n/a	chr6:147643837-147643850 chr6:147643837-147643848 chr6:147643837-147643850 chr6:147643838-147643849 chr6:147643839-147643848
48	CEBPB	chr6:147712117-147712383	HepG2	liver:	n/a	chr6:147712205-147712218
49	CEBPB	chr6:147635413-147635716	HepG2	liver:	n/a	n/a
50	CEBPB	chr6:147600547-147600913	IMR90	lung:	n/a	chr6:147600719-147600732 chr6:147600720-147600731

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:147605330-147605380	HL-60	blood:	n/a
2	chr6:147605330-147605380	HL-60	blood:	n/a
3	chr6:147705971-147706021	HMEC	breast:	n/a
4	chr6:147705971-147706021	Caco-2	colon:	n/a
5	chr6:147643548-147643598	NHDF-neo	bronchial:	n/a
6	chr6:147705971-147706021	HepG2	liver:	n/a
7	chr6:147705971-147706021	PrEC	prostate:	n/a
8	chr6:147570728-147570778	GM19239	blood:	n/a
9	chr6:147705971-147706021	HCF	heart:	n/a
10	chr6:147570728-147570778	MCF-7	breast:	n/a
11	chr6:147705971-147706021	HUVEC	blood vessel:	n/a
12	chr6:147705971-147706021	SK-N-SH_RA	brain:	n/a
13	chr6:147643548-147643598	HUVEC	blood vessel:	n/a
14	chr6:147705971-147706021	ProgFib	skin:	n/a
15	chr6:147570728-147570778	LNCaP	prostate:	n/a
16	chr6:147570728-147570778	GM12878	blood:	n/a
17	chr6:147570728-147570778	PANC-1	pancreas:	n/a
18	chr6:147705971-147706021	AG09309	skin:	n/a
19	chr6:147605330-147605380	IMR90	lung:	fetal
20	chr6:147570728-147570778	HCT-116	colon:	n/a
21	chr6:147643548-147643598	GM19239	blood:	n/a
22	chr6:147643548-147643598	PrEC	prostate:	n/a
23	chr6:147643548-147643598	NH-A	brain:	n/a
24	chr6:147570728-147570778	HepG2	liver:	n/a
25	chr6:147643548-147643598	AG04449	skin:	fetal
26	chr6:147605330-147605380	AoSMC	blood vessel:	n/a
27	chr6:147605330-147605380	HCM	heart:	n/a
28	chr6:147605330-147605380	NHBE	bronchial:	n/a
29	chr6:147705971-147706021	CMK	blood:	n/a
30	chr6:147643548-147643598	AG09319	gingival:	n/a
31	chr6:147605330-147605380	CMK	blood:	n/a
32	chr6:147605330-147605380	AG09319	gingival:	n/a
33	chr6:147705971-147706021	HCPEpiC	choroid plexus:	n/a
34	chr6:147643548-147643598	Jurkat	blood:	n/a
35	chr6:147605330-147605380	T-47D	breast:	n/a
36	chr6:147570728-147570778	A549	lung:	n/a
37	chr6:147605330-147605380	HepG2	liver:	n/a
38	chr6:147605330-147605380	NT2-D1	testis:	n/a
39	chr6:147643548-147643598	HL-60	blood:	n/a
40	chr6:147570728-147570778	K562	blood:	n/a
41	chr6:147705971-147706021	U87	brain:	n/a
42	chr6:147705971-147706021	MCF10A-Er-Src	breast:	n/a
43	chr6:147570728-147570778	RPTEC	kidney:	n/a
44	chr6:147570728-147570778	T-47D	breast:	n/a
45	chr6:147643548-147643598	A549	lung:	n/a
46	chr6:147605330-147605380	AG04450	lung:	fetal
47	chr6:147570728-147570778	HCF	heart:	n/a
48	chr6:147605330-147605380	GM06990	blood:	n/a
49	chr6:147705971-147706021	Hepatocyte	liver:	n/a
50	chr6:147705971-147706021	ECC-1	luminal epithelium:	n/a

(count:170 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr6:147600867..147603452-chr6:147606920..147609139,2	K562	blood:
2	chr6:147660277..147661948-chr6:147667119..147669406,3	K562	blood:
3	chr6:147178646..147179531-chr6:147606189..147606807,2	MCF-7	breast:
4	chr6:147178386..147179221-chr6:147703832..147704746,2	K562	blood:
5	chr6:147636247..147638976-chr6:147647521..147649974,3	K562	blood:
6	chr6:147598044..147601159-chr6:147601266..147602927,3	K562	blood:
7	chr6:147605533..147608299-chr6:147613299..147616141,2	K562	blood:
8	chr6:147643796..147646367-chr6:147650099..147652941,2	K562	blood:
9	chr6:147563079..147565638-chr6:147567520..147569543,2	K562	blood:
10	chr6:147689027..147691902-chr6:147709302..147712120,2	K562	blood:
11	chr6:147664249..147666005-chr6:147673962..147676762,2	K562	blood:
12	chr6:147627048..147629299-chr6:147632371..147635278,3	K562	blood:
13	chr6:147632934..147634936-chr6:147640228..147643160,2	MCF-7	breast:
14	chr6:147583523..147585752-chr6:147591147..147593959,2	K562	blood:
15	chr6:147619344..147621259-chr6:147622624..147624192,2	K562	blood:
16	chr6:147712156..147712687-chr6:148291545..148292366,2	MCF-7	breast:
17	chr6:147633394..147635714-chr6:147648364..147650085,2	K562	blood:
18	chr6:147703869..147707372-chr6:147716822..147719564,3	K562	blood:
19	chr6:147685432..147688337-chr6:147695787..147697611,2	K562	blood:
20	chr6:147588082..147592199-chr6:147598950..147601651,3	K562	blood:
21	chr6:147636564..147639299-chr6:147639869..147642721,3	K562	blood:
22	chr6:147704406..147707731-chr6:147708554..147712454,8	K562	blood:
23	chr6:147564930..147567300-chr6:147589285..147591858,2	K562	blood:
24	chr6:147565658..147568685-chr6:147568738..147571330,4	K562	blood:
25	chr6:147205531..147207061-chr6:147703036..147705763,2	K562	blood:
26	chr6:147674142..147676430-chr6:147682128..147684419,2	K562	blood:
27	chr6:147638465..147640199-chr6:147644851..147646514,2	MCF-7	breast:
28	chr6:147578196..147582032-chr6:147582354..147586233,5	K562	blood:
29	chr6:147562403..147564458-chr6:147565957..147567500,2	K562	blood:
30	chr6:147685644..147688085-chr6:147690225..147693015,3	K562	blood:
31	chr6:147579954..147581876-chr6:147584142..147585790,2	K562	blood:
32	chr6:147223283..147224171-chr6:147605957..147606781,4	MCF-7	breast:
33	chr6:147583523..147585752-chr6:147591147..147593959,2	K562	blood:
34	chr6:147565658..147568685-chr6:147568738..147571330,4	K562	blood:
35	chr6:147689027..147691902-chr6:147709302..147712120,2	K562	blood:
36	chr6:147632716..147635508-chr6:147662008..147664678,2	K562	blood:
37	chr6:147685432..147688337-chr6:147695787..147697611,2	K562	blood:
38	chr6:147570173..147572962-chr6:147576488..147578515,2	K562	blood:
39	chr6:147640420..147643294-chr6:147648350..147651490,3	K562	blood:
40	chr6:147605533..147608299-chr6:147613299..147616141,2	K562	blood:
41	chr6:147596142..147599213-chr6:147600887..147603555,4	K562	blood:
42	chr6:147223830..147226657-chr6:147694168..147696836,2	K562	blood:
43	chr6:147598437..147600865-chr6:147608002..147611556,3	K562	blood:
44	chr6:147544721..147547282-chr6:147606691..147608691,2	K562	blood:
45	chr6:147685644..147688085-chr6:147690225..147693015,3	K562	blood:
46	chr6:147644229..147646379-chr6:147656668..147659345,2	K562	blood:
47	chr6:147627048..147629299-chr6:147632371..147635278,3	K562	blood:
48	chr6:147633394..147635714-chr6:147648364..147650085,2	K562	blood:
49	chr6:147628339..147630746-chr6:147632929..147635838,2	K562	blood:
50	chr6:147674544..147676430-chr6:147682128..147684379,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STXBP5-1	chr6:147710198-147711601	ENSG00000225135
2	lnc-STXBP5-1	chr6:147708800-147708872	ENSG00000225135
3	lnc-STXBP5-3	chr6:147708957-147709300	expReg_chr6_10989_+
4	lnc-SAMD5-3	chr6:147566472-147566951	expReg_chr6_10923_+

No data

(count:3 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	STXBP5	hsa-miR-21-5p	chr6:147706426-147706447
2	STXBP5	hsa-miR-21-5p	chr6:147636655-147636676
3	STXBP5	hsa-miR-21-5p	chr6:147708269-147708290

Variant related genes	Relation type
STXBP5	TF binding region
ENSG00000225135	TF binding region
STXBP5	CpG island
ENSG00000225135	CpG island
ENSG00000125846	chromatin interactions
ENSG00000225135	chromatin interactions
ENSG00000136826	chromatin interactions
ENSG00000233452	chromatin interactions
ENSG00000164506	chromatin interactions

Extended variants
information (count: 5595 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:5595 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2053459	chr6:147554900-147554901	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114249469	chr6:147554916-147554917	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567403667	chr6:147554969-147554970	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs576562871	chr6:147554972-147554973	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549762749	chr6:147554975-147554976	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569278885	chr6:147555006-147555007	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538222614	chr6:147555020-147555021	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545288373	chr6:147555025-147555026	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558455029	chr6:147555039-147555040	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565626931	chr6:147555073-147555074	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73582526	chr6:147555080-147555081	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554420394	chr6:147555216-147555217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs371652844	chr6:147555260-147555261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546367081	chr6:147555271-147555272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147268854	chr6:147555278-147555279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563046779	chr6:147555370-147555371	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs117101404	chr6:147555378-147555379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs557414018	chr6:147555408-147555409	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs78641828	chr6:147555420-147555421	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs111942278	chr6:147555425-147555426	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs531984801	chr6:147555448-147555449	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374849457	chr6:147555455-147555456	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs376969191	chr6:147555499-147555500	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs546204872	chr6:147555521-147555522	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs560130165	chr6:147555531-147555532	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs528780172	chr6:147555537-147555538	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs73788842	chr6:147555598-147555599	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs139110377	chr6:147555622-147555623	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs186865882	chr6:147555623-147555624	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs191303462	chr6:147555630-147555631	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs549491350	chr6:147555644-147555645	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs183220887	chr6:147555661-147555662	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs186789570	chr6:147555698-147555699	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs191262011	chr6:147555756-147555757	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs565967462	chr6:147555795-147555796	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs116522499	chr6:147555816-147555817	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs143111371	chr6:147555821-147555822	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs568134189	chr6:147555828-147555829	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs537229144	chr6:147555846-147555847	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs73788844	chr6:147555851-147555852	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs577409320	chr6:147555931-147555932	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs527789534	chr6:147555942-147555943	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs76147314	chr6:147555995-147555996	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs553358735	chr6:147556044-147556045	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs547527100	chr6:147556086-147556087	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs573493043	chr6:147556095-147556096	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs542126413	chr6:147556128-147556129	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs560945475	chr6:147556195-147556196	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562331968	chr6:147556206-147556207	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs142102687	chr6:147556220-147556221	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3359 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147526000-147572200	Weak transcription	Lung	lung
2	chr6:147527200-147557800	Weak transcription	Fetal Stomach	stomach
3	chr6:147527200-147570000	Weak transcription	Left Ventricle	heart
4	chr6:147527200-147572000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:147527200-147572200	Weak transcription	Esophagus	oesophagus
6	chr6:147527400-147558800	Weak transcription	Primary B cells from cord blood	blood
7	chr6:147527400-147563800	Weak transcription	NH-A	brain
8	chr6:147527400-147566800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
9	chr6:147527400-147576400	Weak transcription	HSMMtube	muscle
10	chr6:147527600-147559600	Weak transcription	Colon Smooth Muscle	Colon
11	chr6:147527800-147586800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr6:147528800-147565800	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr6:147528800-147572000	Weak transcription	A549	lung
14	chr6:147529000-147572200	Weak transcription	Aorta	Aorta
15	chr6:147529400-147571800	Weak transcription	Fetal Brain Male	brain
16	chr6:147530000-147572000	Weak transcription	NHEK	skin
17	chr6:147533200-147572200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr6:147534000-147572200	Weak transcription	Brain Cingulate Gyrus	brain
19	chr6:147535800-147557600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:147537600-147572200	Weak transcription	Ovary	ovary
21	chr6:147537800-147571600	Weak transcription	Fetal Muscle Trunk	muscle
22	chr6:147538200-147572200	Weak transcription	Spleen	Spleen
23	chr6:147538400-147572200	Weak transcription	Fetal Lung	lung
24	chr6:147538800-147572200	Weak transcription	Placenta	Placenta
25	chr6:147540200-147559200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr6:147540200-147569600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr6:147540200-147572000	Weak transcription	Thymus	Thymus
28	chr6:147540800-147561800	Weak transcription	Fetal Kidney	kidney
29	chr6:147542400-147590800	Weak transcription	Placenta Amnion	Placenta Amnion
30	chr6:147543800-147556400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:147543800-147556800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr6:147543800-147556800	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr6:147543800-147557600	Weak transcription	Primary monocytes fromperipheralblood	blood
34	chr6:147543800-147557800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr6:147543800-147557800	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr6:147543800-147559000	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr6:147543800-147560600	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:147543800-147561800	Weak transcription	Adipose Nuclei	Adipose
39	chr6:147543800-147562000	Weak transcription	NHLF	lung
40	chr6:147543800-147562600	Weak transcription	Brain Hippocampus Middle	brain
41	chr6:147543800-147563600	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr6:147543800-147566200	Weak transcription	Stomach Mucosa	stomach
43	chr6:147543800-147572200	Weak transcription	Rectal Smooth Muscle	rectum
44	chr6:147543800-147588800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr6:147544000-147559200	Weak transcription	Fetal Intestine Small	intestine
46	chr6:147544000-147561800	Weak transcription	Duodenum Mucosa	Duodenum
47	chr6:147544000-147572200	Weak transcription	GM12878-XiMat	blood
48	chr6:147544200-147559400	Weak transcription	Fetal Thymus	thymus
49	chr6:147544200-147566800	Weak transcription	Pancreas	Pancrea
50	chr6:147544200-147574200	Weak transcription	H9 Cell Line	embryonic stem cell

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