Variant report

Variant	esv3361413
Chromosome Location	chr8:86374200-86377398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:483)
CpG islands
(count:488)
Chromatin interactive
region (count:10)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:483 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86375408-86375608	K562	blood:	n/a	n/a
2	ATF2	chr8:86375277-86375647	GM12878	blood:	n/a	n/a
3	BACH1	chr8:86375517-86375618	K562	blood:	n/a	n/a
4	BACH1	chr8:86376436-86376638	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr8:86375322-86375896	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:86373952-86374352	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCLAF1	chr8:86375357-86375764	GM12878	blood:	n/a	n/a
8	BHLHE40	chr8:86375361-86375709	GM12878	blood:	n/a	n/a
9	BHLHE40	chr8:86376459-86376495	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:86375452-86375647	K562	blood:	n/a	n/a
11	CCNT2	chr8:86375511-86375657	K562	blood:	n/a	n/a
12	CCNT2	chr8:86376240-86376362	K562	blood:	n/a	n/a
13	CEBPZ	chr8:86374687-86374690	HepG2	liver:	n/a	n/a
14	CHD1	chr8:86376351-86376654	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr8:86375451-86375973	Hela-S3	cervix:	n/a	chr8:86375783-86375790
16	CHD2	chr8:86375400-86375871	H1-hESC	embryonic stem cell:	n/a	chr8:86375783-86375790
17	CHD2	chr8:86375482-86375688	K562	blood:	n/a	n/a
18	CHD2	chr8:86376556-86376599	HepG2	liver:	n/a	n/a
19	CHD2	chr8:86375434-86375666	GM12878	blood:	n/a	n/a
20	CREB1	chr8:86375406-86375740	A549	lung:	n/a	n/a
21	CTBP2	chr8:86376244-86376655	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr8:86375760-86375910	GM12869	blood:	n/a	n/a
23	CTCF	chr8:86375378-86375779	K562	blood:	n/a	chr8:86375565-86375578
24	CTCF	chr8:86375520-86375670	HCFaa	heart:	n/a	chr8:86375565-86375578
25	CTCF	chr8:86376440-86376590	GM12872	blood:	n/a	n/a
26	CTCF	chr8:86376355-86376360	GM12892	blood:	n/a	n/a
27	CTCF	chr8:86375520-86375670	BE2_C	brain:	n/a	chr8:86375565-86375578
28	CTCF	chr8:86376420-86376570	GM12873	blood:	n/a	n/a
29	CTCF	chr8:86375500-86375650	AG09319	gingival:	n/a	chr8:86375565-86375578
30	CTCF	chr8:86375500-86375650	WERI-Rb-1	eye:	n/a	chr8:86375565-86375578
31	CTCF	chr8:86375427-86375682	LNCaP	prostate:	n/a	chr8:86375565-86375578
32	CTCF	chr8:86375500-86375650	GM12872	blood:	n/a	chr8:86375565-86375578
33	CTCF	chr8:86375907-86375918	GM20000	blood:	n/a	n/a
34	CTCF	chr8:86375422-86375769	HepG2	liver:	n/a	chr8:86375565-86375578
35	CTCF	chr8:86375402-86375780	H1-hESC	embryonic stem cell:	n/a	chr8:86375565-86375578
36	CTCF	chr8:86374080-86374230	HCT-116	colon:	n/a	n/a
37	CTCF	chr8:86375520-86375670	GM12873	blood:	n/a	chr8:86375565-86375578
38	CTCF	chr8:86375520-86375670	GM12869	blood:	n/a	chr8:86375565-86375578
39	CTCF	chr8:86375780-86375930	GM12874	blood:	n/a	n/a
40	CTCF	chr8:86375407-86375738	A549	lung:	n/a	chr8:86375565-86375578
41	CTCF	chr8:86375460-86375710	A549	lung:	n/a	chr8:86375565-86375578
42	CTCF	chr8:86375413-86375892	HCT-116	colon:	n/a	chr8:86375565-86375578
43	CTCF	chr8:86375540-86375690	HEK293	kidney:	n/a	chr8:86375565-86375578
44	CTCF	chr8:86375407-86375728	GM19239	blood:	n/a	chr8:86375565-86375578
45	CTCF	chr8:86376340-86376490	GM12870	blood:	n/a	n/a
46	CTCF	chr8:86375480-86375630	AG04450	lung:	n/a	chr8:86375565-86375578
47	CTCF	chr8:86375427-86375686	GM10248	blood:	n/a	chr8:86375565-86375578
48	CTCF	chr8:86375437-86375703	Hela-S3	cervix:	n/a	chr8:86375565-86375578
49	CTCF	chr8:86376080-86376230	GM12870	blood:	n/a	n/a
50	CTCF	chr8:86375520-86375670	GM12866	blood:	n/a	chr8:86375565-86375578

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86376277-86376327	NHBE	bronchial:	n/a
2	chr8:86376306-86376356	H1-hESC	embryonic stem cell:	embryo
3	chr8:86376842-86376892	HNPCEpiC	eye:	n/a
4	chr8:86375450-86375500	PANC-1	pancreas:	n/a
5	chr8:86376489-86376539	GM12891	blood:	n/a
6	chr8:86376306-86376356	SKMC	muscle:	n/a
7	chr8:86376088-86376138	Caco-2	colon:	n/a
8	chr8:86376277-86376327	CMK	blood:	n/a
9	chr8:86376842-86376892	ovcar-3	ovarian:	n/a
10	chr8:86375919-86375969	Hela-S3	cervix:	n/a
11	chr8:86375450-86375500	HIPEpiC	eye:	n/a
12	chr8:86376277-86376327	AG10803	skin:	n/a
13	chr8:86375919-86375969	HRPEpiC	eye:	n/a
14	chr8:86375450-86375500	Jurkat	blood:	n/a
15	chr8:86376489-86376539	SK-N-SH	brain:	n/a
16	chr8:86376489-86376539	SK-N-SH_RA	brain:	n/a
17	chr8:86376489-86376539	ovcar-3	ovarian:	n/a
18	chr8:86376489-86376539	NHDF-neo	bronchial:	n/a
19	chr8:86376088-86376138	GM12878	blood:	n/a
20	chr8:86376088-86376138	CMK	blood:	n/a
21	chr8:86376306-86376356	NB4	blood:	n/a
22	chr8:86376306-86376356	CMK	blood:	n/a
23	chr8:86376088-86376138	NHDF-neo	bronchial:	n/a
24	chr8:86376489-86376539	AoSMC	blood vessel:	n/a
25	chr8:86375450-86375500	U87	brain:	n/a
26	chr8:86375501-86375551	SAEC	small airway:	n/a
27	chr8:86376489-86376539	LNCaP	prostate:	n/a
28	chr8:86375501-86375551	HCT-116	colon:	n/a
29	chr8:86376088-86376138	HEK293	kidney:	embryo
30	chr8:86375501-86375551	ProgFib	skin:	n/a
31	chr8:86376489-86376539	NH-A	brain:	n/a
32	chr8:86376088-86376138	NH-A	brain:	n/a
33	chr8:86375919-86375969	SK-N-SH	brain:	n/a
34	chr8:86375919-86375969	ProgFib	skin:	n/a
35	chr8:86376489-86376539	HCT-116	colon:	n/a
36	chr8:86376277-86376327	ECC-1	luminal epithelium:	n/a
37	chr8:86376842-86376892	GM19239	blood:	n/a
38	chr8:86376306-86376356	NH-A	brain:	n/a
39	chr8:86375450-86375500	H1-hESC	embryonic stem cell:	embryo
40	chr8:86376842-86376892	ECC-1	luminal epithelium:	n/a
41	chr8:86376489-86376539	AG09309	skin:	n/a
42	chr8:86375450-86375500	NHDF-neo	bronchial:	n/a
43	chr8:86376489-86376539	IMR90	lung:	fetal
44	chr8:86375501-86375551	H1-hESC	embryonic stem cell:	embryo
45	chr8:86376277-86376327	AoSMC	blood vessel:	n/a
46	chr8:86376088-86376138	HEEpiC	esophagus:	n/a
47	chr8:86375450-86375500	PFSK-1	brain:	n/a
48	chr8:86376489-86376539	HNPCEpiC	eye:	n/a
49	chr8:86375501-86375551	SK-N-MC	brain:	n/a
50	chr8:86376306-86376356	HL-60	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:86363678..86364494-chr8:86374198..86374980,2	MCF-7	breast:
2	chr8:86375382..86376006-chr8:87045172..87046083,3	MCF-7	breast:
3	chr22:36782277..36784307-chr8:86374266..86376495,2	MCF-7	breast:
4	chr8:86372586..86374669-chr8:86379787..86381546,2	MCF-7	breast:
5	chr8:86211076..86211587-chr8:86373603..86374373,2	MCF-7	breast:
6	chr8:86348746..86351284-chr8:86374911..86377490,2	MCF-7	breast:
7	chr8:86373353..86377706-chr8:86848632..86856784,15	MCF-7	breast:
8	chr1:144931784..144933992-chr8:86374827..86377261,2	MCF-7	breast:
9	chr8:86373793..86376899-chr8:86998896..87001584,3	MCF-7	breast:
10	chr8:86372229..86378702-chr8:86846475..86858080,32	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CA1-1	chr8:86374965-86375030	NONHSAT127527
2	lnc-CA1-1	chr8:86375161-86375671	NONHSAT127527
3	lnc-CA1-1	chr8:86375161-86375283	ENSG00000253549.1
4	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
5	lnc-CA1-1	chr8:86376811-86377144	ENSG00000253549.1
6	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
7	lnc-CA1-1	chr8:86376457-86376562	ENSG00000253549.1
8	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
9	lnc-CA1-1	chr8:86374965-86375030	NONHSAT127529
10	lnc-CA1-1	chr8:86375661-86375942	NONHSAT127529

No data

Variant related genes	Relation type
ENSG00000253549	TF binding region
CA2	TF binding region
ENSG00000253549	CpG island
CA2	CpG island
ENSG00000164879	chromatin interactions
ENSG00000253154	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000147614	chromatin interactions
ENSG00000100345	chromatin interactions

Extended variants
information (count: 115 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:115 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72682966	chr8:86374208-86374209	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs150743480	chr8:86374222-86374223	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs371784277	chr8:86374245-86374246	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs556169905	chr8:86374304-86374305	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs369185748	chr8:86374343-86374344	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs541931987	chr8:86374370-86374371	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs139096299	chr8:86374433-86374434	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs530309311	chr8:86374452-86374453	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs149868238	chr8:86374484-86374485	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs540608193	chr8:86374544-86374545	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs372990501	chr8:86374621-86374622	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs532619917	chr8:86374634-86374635	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs186544199	chr8:86374643-86374644	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs576791646	chr8:86374650-86374651	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs535070627	chr8:86374656-86374657	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs3758078	chr8:86374664-86374665	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs189832245	chr8:86374690-86374691	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs548661434	chr8:86374723-86374724	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs6994366	chr8:86374765-86374766	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs145945011	chr8:86374770-86374771	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs547231793	chr8:86374815-86374816	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs570783984	chr8:86374824-86374825	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs375178819	chr8:86374831-86374832	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs539653634	chr8:86374896-86374897	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs377382183	chr8:86374937-86374938	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs576162910	chr8:86374939-86374940	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs180714443	chr8:86374981-86374982	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
28	rs370787616	chr8:86375004-86375005	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
29	rs186349539	chr8:86375019-86375020	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
30	rs190699020	chr8:86375061-86375062	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs560452440	chr8:86375081-86375082	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs560649758	chr8:86375088-86375089	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs139744733	chr8:86375122-86375123	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs117460621	chr8:86375127-86375128	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs75827641	chr8:86375143-86375144	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs144484838	chr8:86375175-86375176	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
37	rs562591120	chr8:86375182-86375183	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
38	rs368536377	chr8:86375203-86375204	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
39	rs183704345	chr8:86375205-86375206	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
40	rs548248502	chr8:86375248-86375249	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
41	rs188536081	chr8:86375274-86375275	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
42	rs527758423	chr8:86375286-86375287	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
43	rs191828008	chr8:86375307-86375308	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
44	rs117219547	chr8:86375312-86375313	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
45	rs539774287	chr8:86375336-86375337	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
46	rs113908603	chr8:86375347-86375348	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
47	rs146646049	chr8:86375349-86375350	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
48	rs77250341	chr8:86375406-86375407	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
49	rs535438531	chr8:86375469-86375470	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
50	rs115206105	chr8:86375478-86375479	Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86354400-86375400	Weak transcription	Psoas Muscle	Psoas
2	chr8:86358400-86375600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr8:86366600-86375000	Weak transcription	HMEC	breast
4	chr8:86366600-86375200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr8:86366800-86375200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr8:86366800-86375200	Weak transcription	NHEK	skin
7	chr8:86367600-86375600	Weak transcription	Gastric	stomach
8	chr8:86368400-86375400	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr8:86368600-86375600	Weak transcription	Esophagus	oesophagus
10	chr8:86369200-86375400	Enhancers	Primary B cells from cord blood	blood
11	chr8:86370400-86375400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr8:86371800-86374200	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr8:86371800-86375200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr8:86371800-86375200	Weak transcription	Colon Smooth Muscle	Colon
15	chr8:86372000-86375400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:86372200-86375200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr8:86372200-86375200	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr8:86372200-86375400	Weak transcription	Primary T cells from cord blood	blood
19	chr8:86372200-86375400	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr8:86372400-86374800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr8:86372400-86375200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:86372600-86374600	Weak transcription	Primary hematopoietic stem cells	blood
23	chr8:86373000-86374400	Enhancers	Monocytes-CD14+_RO01746	blood
24	chr8:86373400-86374800	Weak transcription	Primary B cells from peripheral blood	blood
25	chr8:86373600-86374400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr8:86373600-86374600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:86373600-86374600	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr8:86373600-86374800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr8:86373800-86374400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:86373800-86375200	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr8:86373800-86375200	Enhancers	Brain Angular Gyrus	brain
32	chr8:86373800-86375200	Enhancers	Brain Anterior Caudate	brain
33	chr8:86373800-86375200	Enhancers	Brain Hippocampus Middle	brain
34	chr8:86373800-86375400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr8:86373800-86375400	Enhancers	Fetal Lung	lung
36	chr8:86374000-86374200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr8:86374000-86374200	Enhancers	Colonic Mucosa	Colon
38	chr8:86374000-86374400	Enhancers	Fetal Intestine Small	intestine
39	chr8:86374000-86374600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr8:86374000-86374600	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
41	chr8:86374000-86374600	Flanking Active TSS	Liver	Liver
42	chr8:86374000-86375000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr8:86374000-86375000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr8:86374000-86375200	Enhancers	H9 Cell Line	embryonic stem cell
45	chr8:86374000-86375200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr8:86374000-86375200	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr8:86374000-86375200	Enhancers	Brain Substantia Nigra	brain
48	chr8:86374000-86375200	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr8:86374000-86375400	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr8:86374000-86375400	Enhancers	Adipose Nuclei	Adipose

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