Variant report

Variant	esv3344959
Chromosome Location	chr6:109760484-109763032
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:863)
CpG islands
(count:488)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:863 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:109761101-109761402	K562	blood:	n/a	n/a
2	ARID3A	chr6:109761923-109762202	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:109761655-109761701	HepG2	liver:	n/a	n/a
4	ATF2	chr6:109761789-109762235	GM12878	blood:	n/a	n/a
5	ATF2	chr6:109762084-109762607	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:109762430-109762621	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:109761471-109762144	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCLAF1	chr6:109761528-109762774	GM12878	blood:	n/a	chr6:109761582-109761595 chr6:109762470-109762479 chr6:109761562-109761571 chr6:109761860-109761869 chr6:109761847-109761860
9	BHLHE40	chr6:109761538-109762725	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:109761593-109762442	K562	blood:	n/a	n/a
11	BHLHE40	chr6:109761432-109762376	GM12878	blood:	n/a	n/a
12	BRCA1	chr6:109761865-109762065	HepG2	liver:	n/a	n/a
13	CBX3	chr6:109761235-109762357	K562	blood:	n/a	n/a
14	CBX3	chr6:109762397-109762885	K562	blood:	n/a	n/a
15	CCNT2	chr6:109761378-109762585	K562	blood:	n/a	n/a
16	CEBPB	chr6:109761946-109762146	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr6:109761617-109761676	K562	blood:	n/a	n/a
18	CEBPB	chr6:109761521-109762127	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr6:109762405-109762744	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:109761629-109762781	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:109762459-109762642	K562	blood:	n/a	n/a
22	CEBPB	chr6:109761774-109762748	HepG2	liver:	n/a	n/a
23	CEBPB	chr6:109762401-109762747	A549	lung:	n/a	n/a
24	CEBPB	chr6:109762451-109762672	HepG2	liver:	n/a	n/a
25	CEBPD	chr6:109761875-109762205	HepG2	liver:	n/a	n/a
26	CHD1	chr6:109761726-109762942	GM12878	blood:	n/a	n/a
27	CHD1	chr6:109762084-109762447	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr6:109761719-109762906	GM12878	blood:	n/a	n/a
29	CHD2	chr6:109762388-109762932	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr6:109761688-109762702	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr6:109761586-109762167	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr6:109761454-109762680	HepG2	liver:	n/a	n/a
33	CHD2	chr6:109761573-109762291	K562	blood:	n/a	n/a
34	CREB1	chr6:109761563-109762178	A549	lung:	n/a	n/a
35	CREB1	chr6:109761432-109762195	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTBP2	chr6:109761688-109762934	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr6:109762540-109762690	HCT-116	colon:	n/a	n/a
38	CTCF	chr6:109762440-109762590	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr6:109761940-109762090	GM12878	blood:	n/a	chr6:109762019-109762029 chr6:109762017-109762030 chr6:109762017-109762026 chr6:109762014-109762032
40	CTCF	chr6:109761980-109762130	GM12872	blood:	n/a	chr6:109762019-109762029 chr6:109762017-109762030 chr6:109762017-109762026 chr6:109762014-109762032
41	CTCF	chr6:109762500-109762650	GM12871	blood:	n/a	n/a
42	CTCF	chr6:109762480-109762630	GM06990	blood:	n/a	n/a
43	CTCF	chr6:109762520-109762670	HVMF	connective:	n/a	n/a
44	CTCF	chr6:109761960-109762110	BE2_C	brain:	n/a	chr6:109762019-109762029 chr6:109762017-109762030 chr6:109762017-109762026 chr6:109762014-109762032
45	CTCF	chr6:109761920-109762070	SAEC	small airway:	n/a	chr6:109762019-109762029 chr6:109762017-109762030 chr6:109762017-109762026 chr6:109762014-109762032
46	CTCF	chr6:109762560-109762710	GM12865	blood:	n/a	n/a
47	CTCF	chr6:109762540-109762690	AG04449	skin:	n/a	n/a
48	CTCF	chr6:109761960-109762110	BJ	skin:	n/a	chr6:109762019-109762029 chr6:109762017-109762030 chr6:109762017-109762026 chr6:109762014-109762032
49	CTCF	chr6:109762520-109762670	MCF-7	breast:	n/a	n/a
50	CTCF	chr6:109761949-109762092	GM13977	blood:	n/a	chr6:109762019-109762029 chr6:109762017-109762030 chr6:109762017-109762026 chr6:109762014-109762032

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:109761938-109761988	HNPCEpiC	eye:	n/a
2	chr6:109760831-109760881	Hepatocyte	liver:	n/a
3	chr6:109761938-109761988	AG10803	skin:	n/a
4	chr6:109760819-109760869	Jurkat	blood:	n/a
5	chr6:109760831-109760881	H1-hESC	embryonic stem cell:	embryo
6	chr6:109760831-109760881	ovcar-3	ovarian:	n/a
7	chr6:109760831-109760881	T-47D	breast:	n/a
8	chr6:109760831-109760881	GM06990	blood:	n/a
9	chr6:109762635-109762685	SK-N-SH	brain:	n/a
10	chr6:109761667-109761717	BE2_C	brain:	n/a
11	chr6:109762418-109762468	PANC-1	pancreas:	n/a
12	chr6:109762382-109762432	HRCEpiC	kidney:	n/a
13	chr6:109762418-109762468	SK-N-MC	brain:	n/a
14	chr6:109762158-109762208	AG04449	skin:	fetal
15	chr6:109761938-109761988	IMR90	lung:	fetal
16	chr6:109761938-109761988	HIPEpiC	eye:	n/a
17	chr6:109761938-109761988	HCM	heart:	n/a
18	chr6:109762635-109762685	H1-hESC	embryonic stem cell:	embryo
19	chr6:109760819-109760869	T-47D	breast:	n/a
20	chr6:109761938-109761988	BE2_C	brain:	n/a
21	chr6:109762418-109762468	HL-60	blood:	n/a
22	chr6:109761667-109761717	HNPCEpiC	eye:	n/a
23	chr6:109762418-109762468	NT2-D1	testis:	n/a
24	chr6:109762158-109762208	NH-A	brain:	n/a
25	chr6:109762635-109762685	HPAEpiC	pulmonary alveolar:	n/a
26	chr6:109762418-109762468	SK-N-SH_RA	brain:	n/a
27	chr6:109761667-109761717	GM06990	blood:	n/a
28	chr6:109762158-109762208	BE2_C	brain:	n/a
29	chr6:109762158-109762208	HCM	heart:	n/a
30	chr6:109760831-109760881	HCPEpiC	choroid plexus:	n/a
31	chr6:109762635-109762685	HAEpiC	amniotic membrane:	n/a
32	chr6:109760831-109760881	PrEC	prostate:	n/a
33	chr6:109761667-109761717	HCF	heart:	n/a
34	chr6:109761667-109761717	RPTEC	kidney:	n/a
35	chr6:109761938-109761988	NT2-D1	testis:	n/a
36	chr6:109762635-109762685	GM12878	blood:	n/a
37	chr6:109760819-109760869	MCF-7	breast:	n/a
38	chr6:109762158-109762208	HAEpiC	amniotic membrane:	n/a
39	chr6:109762418-109762468	Jurkat	blood:	n/a
40	chr6:109762418-109762468	HEK293	kidney:	embryo
41	chr6:109762635-109762685	HIPEpiC	eye:	n/a
42	chr6:109760831-109760881	HPAEpiC	pulmonary alveolar:	n/a
43	chr6:109761667-109761717	AG04449	skin:	fetal
44	chr6:109760831-109760881	ECC-1	luminal epithelium:	n/a
45	chr6:109762382-109762432	PFSK-1	brain:	n/a
46	chr6:109762158-109762208	AoSMC	blood vessel:	n/a
47	chr6:109761667-109761717	PFSK-1	brain:	n/a
48	chr6:109762382-109762432	GM06990	blood:	n/a
49	chr6:109762158-109762208	HUVEC	blood vessel:	n/a
50	chr6:109762635-109762685	GM12891	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:109414651..109418067-chr6:109760738..109763991,4	MCF-7	breast:
2	chr6:109747606..109757389-chr6:109757828..109761794,11	K562	blood:
3	chr6:109702383..109706611-chr6:109760202..109762116,4	K562	blood:
4	chr6:109759628..109764398-chr6:109803414..109806709,4	K562	blood:
5	chr6:109699708..109703613-chr6:109762807..109765058,4	K562	blood:
6	chr6:109415348..109417479-chr6:109760287..109762549,2	K562	blood:
7	chr6:109702022..109707287-chr6:109760251..109763953,8	MCF-7	breast:
8	chr6:109702065..109705528-chr6:109760483..109765471,8	MCF-7	breast:
9	chr6:109759652..109764361-chr6:109800705..109806354,8	K562	blood:
10	chr6:109752212..109757242-chr6:109759553..109764133,7	MCF-7	breast:
11	chr6:109703212..109703944-chr6:109761595..109762112,2	K562	blood:
12	chr6:108880181..108882285-chr6:109761167..109763162,2	MCF-7	breast:
13	chr6:109747606..109750215-chr6:109758639..109760987,2	K562	blood:
14	chr6:109760146..109763576-chr6:109804047..109805770,3	MCF-7	breast:
15	chr6:109760182..109762059-chr6:109802883..109805670,2	MCF-7	breast:

No data

Variant related genes	Relation type
SMPD2	TF binding region
PPIL6	TF binding region
SMPD2	CpG island
PPIL6	CpG island
ENSG00000118689	chromatin interactions
ENSG00000112365	chromatin interactions
ENSG00000185250	chromatin interactions
ENSG00000080546	chromatin interactions
ENSG00000239160	chromatin interactions
ENSG00000183137	chromatin interactions
ENSG00000260273	chromatin interactions
ENSG00000135535	chromatin interactions

Extended variants
information (count: 94 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:94 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs375588271	chr6:109760563-109760564	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs540715323	chr6:109760583-109760584	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs143076835	chr6:109760586-109760587	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs558334415	chr6:109760617-109760618	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs575054328	chr6:109760684-109760685	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs543912141	chr6:109760717-109760718	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs185390692	chr6:109760742-109760743	Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs574005438	chr6:109760810-109760811	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs371568774	chr6:109760815-109760816	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
10	rs563784628	chr6:109760822-109760823	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs148226848	chr6:109760893-109760894	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs528789710	chr6:109760917-109760918	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs552054232	chr6:109760940-109760941	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs565497639	chr6:109760941-109760942	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs374414274	chr6:109760981-109760982	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs531101709	chr6:109761007-109761008	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs188312538	chr6:109761032-109761033	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs180825156	chr6:109761169-109761170	Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs117406850	chr6:109761303-109761304	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs552602971	chr6:109761333-109761334	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs563161054	chr6:109761341-109761342	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs142756236	chr6:109761353-109761354	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs566086061	chr6:109761354-109761355	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs185579631	chr6:109761361-109761362	Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs558395975	chr6:109761409-109761410	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs4945831	chr6:109761437-109761438	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs537621977	chr6:109761458-109761459	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs557460599	chr6:109761483-109761484	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs188478136	chr6:109761516-109761517	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs140277965	chr6:109761545-109761546	Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs112826718	chr6:109761607-109761608	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs553403944	chr6:109761615-109761616	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs370996850	chr6:109761629-109761630	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
34	rs374376223	chr6:109761653-109761654	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
35	rs367562291	chr6:109761661-109761662	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
36	rs371321942	chr6:109761699-109761700	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
37	rs113984319	chr6:109761760-109761761	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs541955468	chr6:109761770-109761771	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs565558655	chr6:109761796-109761797	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs873419	chr6:109761855-109761856	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs531172504	chr6:109761869-109761870	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs544470120	chr6:109761931-109761932	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs375876394	chr6:109761940-109761941	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs181183799	chr6:109761966-109761967	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
45	rs529756695	chr6:109761976-109761977	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
46	rs546635102	chr6:109761996-109761997	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
47	rs150353891	chr6:109762007-109762008	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
48	rs111369755	chr6:109762027-109762028	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
49	rs115963563	chr6:109762067-109762068	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
50	rs1048210	chr6:109762092-109762093	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	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
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Basal cell lymphoma	17170743	CNVD
Prostate cancer	16573809	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Autism	17483303	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
abnormal development	18461090	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Systemic lupus erythematosus	19220326	CNVD
Cancer	17160897	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Acute lymphoblastic leukemia	17229543	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:492 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:109721200-109760600	Weak transcription	Fetal Brain Female	brain
2	chr6:109725800-109760800	Weak transcription	Brain Anterior Caudate	brain
3	chr6:109736600-109760800	Weak transcription	Brain Angular Gyrus	brain
4	chr6:109745600-109760800	Weak transcription	Gastric	stomach
5	chr6:109750800-109760800	Weak transcription	Brain Substantia Nigra	brain
6	chr6:109751000-109760800	Weak transcription	Right Atrium	heart
7	chr6:109751200-109761400	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr6:109751400-109760800	Weak transcription	Fetal Stomach	stomach
9	chr6:109753800-109760800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr6:109754000-109760800	Weak transcription	Pancreas	Pancrea
11	chr6:109754800-109760600	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr6:109756000-109760800	Weak transcription	Spleen	Spleen
13	chr6:109756400-109760600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:109756800-109761400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:109757200-109760600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:109758600-109760800	Weak transcription	Primary hematopoietic stem cells	blood
17	chr6:109758600-109760800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
18	chr6:109758800-109760600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr6:109758800-109760600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:109759200-109760800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr6:109760000-109760600	Enhancers	Stomach Mucosa	stomach
22	chr6:109760200-109760600	Enhancers	HSMM	muscle
23	chr6:109760200-109760600	Enhancers	HSMMtube	muscle
24	chr6:109760200-109760600	Enhancers	Osteobl	bone
25	chr6:109760200-109760800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr6:109760200-109760800	Active TSS	Hela-S3	cervix
27	chr6:109760200-109761600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
28	chr6:109760200-109763200	Active TSS	A549	lung
29	chr6:109760400-109760600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:109760400-109760600	Enhancers	Adipose Nuclei	Adipose
31	chr6:109760400-109760600	Enhancers	Placenta	Placenta
32	chr6:109760400-109760600	Enhancers	NHEK	skin
33	chr6:109760400-109760800	Active TSS	Fetal Kidney	kidney
34	chr6:109760400-109760800	Enhancers	Fetal Muscle Trunk	muscle
35	chr6:109760400-109760800	Enhancers	Fetal Muscle Leg	muscle
36	chr6:109760400-109760800	Enhancers	K562	blood
37	chr6:109760400-109761000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr6:109760400-109761600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr6:109760400-109762400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:109760400-109762400	Active TSS	Duodenum Mucosa	Duodenum
41	chr6:109760400-109762600	Active TSS	Ovary	ovary
42	chr6:109760400-109762600	Active TSS	Rectal Smooth Muscle	rectum
43	chr6:109760400-109762800	Active TSS	Fetal Intestine Small	intestine
44	chr6:109760400-109763400	Active TSS	Pancreatic Islets	Pancreatic Islet
45	chr6:109760600-109760800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
46	chr6:109760600-109760800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:109760600-109760800	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr6:109760600-109760800	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr6:109760600-109760800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr6:109760600-109760800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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