Variant report

Variant	esv3407090
Chromosome Location	chr8:95960201-95962949
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:732)
Chromatin interactive
region (count:24)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 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	chr8:95961531-95961983	HepG2	liver:	n/a	n/a
2	ATF3	chr8:95961656-95961784	GM12878	blood:	n/a	n/a
3	ATF3	chr8:95961544-95961786	HepG2	liver:	n/a	n/a
4	ATF3	chr8:95961614-95961871	K562	blood:	n/a	n/a
5	ATF3	chr8:95961572-95961885	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr8:95960641-95960846	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr8:95961350-95961874	GM12878	blood:	n/a	chr8:95961484-95961497
8	BCLAF1	chr8:95961521-95961973	GM12878	blood:	n/a	chr8:95961890-95961903
9	BHLHE40	chr8:95961666-95961897	A549	lung:	n/a	chr8:95961730-95961739 chr8:95961861-95961877 chr8:95961729-95961738 chr8:95961729-95961738
10	BHLHE40	chr8:95961434-95962708	HepG2	liver:	n/a	chr8:95961730-95961739 chr8:95961861-95961877 chr8:95961525-95961541 chr8:95961729-95961738 chr8:95961518-95961534 chr8:95961729-95961738
11	BHLHE40	chr8:95960749-95960846	K562	blood:	n/a	chr8:95960754-95960770
12	BHLHE40	chr8:95961454-95961999	GM12878	blood:	n/a	chr8:95961730-95961739 chr8:95961861-95961877 chr8:95961525-95961541 chr8:95961729-95961738 chr8:95961518-95961534 chr8:95961729-95961738
13	BHLHE40	chr8:95961415-95962767	K562	blood:	n/a	chr8:95961730-95961739 chr8:95961861-95961877 chr8:95961525-95961541 chr8:95961729-95961738 chr8:95961518-95961534 chr8:95961729-95961738
14	BRCA1	chr8:95960640-95960644	GM12878	blood:	n/a	n/a
15	BRCA1	chr8:95961774-95962163	HepG2	liver:	n/a	n/a
16	CCNT2	chr8:95960684-95962473	K562	blood:	n/a	chr8:95962064-95962073 chr8:95961866-95961875
17	CEBPB	chr8:95961604-95961753	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPD	chr8:95961668-95961872	HepG2	liver:	n/a	n/a
19	CEBPD	chr8:95961444-95961944	HepG2	liver:	n/a	n/a
20	CHD1	chr8:95961943-95962463	GM12878	blood:	n/a	n/a
21	CHD1	chr8:95960513-95960570	GM12878	blood:	n/a	n/a
22	CHD1	chr8:95961842-95962143	H1-hESC	embryonic stem cell:	n/a	n/a
23	CHD1	chr8:95960743-95960968	H1-hESC	embryonic stem cell:	n/a	n/a
24	CHD2	chr8:95961734-95962448	HepG2	liver:	n/a	n/a
25	CHD2	chr8:95962164-95962408	K562	blood:	n/a	n/a
26	CHD2	chr8:95960915-95960925	K562	blood:	n/a	n/a
27	CHD2	chr8:95961567-95961907	K562	blood:	n/a	n/a
28	CHD2	chr8:95961617-95962563	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr8:95961506-95961932	GM12878	blood:	n/a	n/a
30	CREB1	chr8:95961397-95961900	H1-hESC	embryonic stem cell:	n/a	n/a
31	CREB1	chr8:95961515-95961825	A549	lung:	n/a	n/a
32	CREB1	chr8:95961298-95961953	A549	lung:	n/a	n/a
33	CTBP2	chr8:95961223-95961988	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr8:95961753-95961769	GM12878	blood:	n/a	n/a
35	CTCF	chr8:95961880-95962030	GM12871	blood:	n/a	chr8:95961884-95961897
36	CTCF	chr8:95960980-95961130	AG04449	skin:	n/a	n/a
37	CTCF	chr8:95962220-95962370	HepG2	liver:	n/a	n/a
38	CTCF	chr8:95961740-95961890	BJ	skin:	n/a	n/a
39	CTCF	chr8:95962080-95962230	GM12864	blood:	n/a	chr8:95962199-95962207 chr8:95962138-95962151
40	CTCF	chr8:95961340-95961490	GM12864	blood:	n/a	n/a
41	CTCF	chr8:95961940-95962090	HMEC	breast:	n/a	n/a
42	CTCF	chr8:95961980-95962130	HCPEpiC	choroid plexus:	n/a	n/a
43	CUX1	chr8:95960401-95960485	K562	blood:	n/a	n/a
44	CUX1	chr8:95961461-95961703	GM12878	blood:	n/a	n/a
45	CUX1	chr8:95962117-95962147	K562	blood:	n/a	n/a
46	E2F4	chr8:95961441-95962415	K562	blood:	n/a	chr8:95962356-95962368 chr8:95961526-95961536
47	E2F4	chr8:95961591-95961899	GM12878	blood:	n/a	n/a
48	E2F4	chr8:95961514-95962264	MCF10A-Er-Src	breast:	n/a	chr8:95961526-95961536
49	E2F6	chr8:95961416-95962497	K562	blood:	n/a	chr8:95962356-95962368 chr8:95961526-95961536
50	E2F6	chr8:95962077-95962410	K562	blood:	n/a	chr8:95962356-95962368

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:95960752-95960802	ProgFib	skin:	n/a
2	chr8:95960752-95960802	RPTEC	kidney:	n/a
3	chr8:95961757-95961807	AG09309	skin:	n/a
4	chr8:95960752-95960802	SK-N-MC	brain:	n/a
5	chr8:95960752-95960802	SKMC	muscle:	n/a
6	chr8:95962371-95962421	AG10803	skin:	n/a
7	chr8:95962371-95962421	K562	blood:	n/a
8	chr8:95961618-95961668	GM19239	blood:	n/a
9	chr8:95962367-95962417	HL-60	blood:	n/a
10	chr8:95961492-95961542	K562	blood:	n/a
11	chr8:95962463-95962513	HepG2	liver:	n/a
12	chr8:95960752-95960802	K562	blood:	n/a
13	chr8:95962463-95962513	BE2_C	brain:	n/a
14	chr8:95961759-95961809	IMR90	lung:	fetal
15	chr8:95961556-95961606	HCM	heart:	n/a
16	chr8:95961556-95961606	HMEC	breast:	n/a
17	chr8:95962084-95962134	ProgFib	skin:	n/a
18	chr8:95961757-95961807	HAEpiC	amniotic membrane:	n/a
19	chr8:95961618-95961668	NHDF-neo	bronchial:	n/a
20	chr8:95962352-95962402	SAEC	small airway:	n/a
21	chr8:95962352-95962402	NH-A	brain:	n/a
22	chr8:95961618-95961668	HepG2	liver:	n/a
23	chr8:95961556-95961606	MCF-7	breast:	n/a
24	chr8:95961759-95961809	NB4	blood:	n/a
25	chr8:95961759-95961809	BE2_C	brain:	n/a
26	chr8:95961492-95961542	AG09319	gingival:	n/a
27	chr8:95961757-95961807	BJ	skin:	n/a
28	chr8:95962383-95962433	NHDF-neo	bronchial:	n/a
29	chr8:95960752-95960802	SK-N-SH_RA	brain:	n/a
30	chr8:95962463-95962513	H1-hESC	embryonic stem cell:	embryo
31	chr8:95961757-95961807	NT2-D1	testis:	n/a
32	chr8:95961492-95961542	NHBE	bronchial:	n/a
33	chr8:95962352-95962402	HCT-116	colon:	n/a
34	chr8:95962371-95962421	PFSK-1	brain:	n/a
35	chr8:95962367-95962417	A549	lung:	n/a
36	chr8:95962352-95962402	HEEpiC	esophagus:	n/a
37	chr8:95961757-95961807	Hela-S3	cervix:	n/a
38	chr8:95960752-95960802	HMEC	breast:	n/a
39	chr8:95962463-95962513	AG04449	skin:	fetal
40	chr8:95961618-95961668	HCF	heart:	n/a
41	chr8:95961492-95961542	BE2_C	brain:	n/a
42	chr8:95962352-95962402	HCM	heart:	n/a
43	chr8:95962367-95962417	MCF-7	breast:	n/a
44	chr8:95962463-95962513	HL-60	blood:	n/a
45	chr8:95962463-95962513	HAEpiC	amniotic membrane:	n/a
46	chr8:95961556-95961606	HL-60	blood:	n/a
47	chr8:95961556-95961606	CMK	blood:	n/a
48	chr8:95961757-95961807	GM12891	blood:	n/a
49	chr8:95960752-95960802	Hepatocyte	liver:	n/a
50	chr8:95962352-95962402	RPTEC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:95908275..95911187-chr8:95962763..95964938,2	K562	blood:
2	chr8:95958215..95960553-chr8:96082467..96084119,2	MCF-7	breast:
3	chr8:95913634..95919106-chr8:95960002..95963177,4	MCF-7	breast:
4	chr8:95959016..95961570-chr8:96028062..96029955,2	MCF-7	breast:
5	chr8:95956652..95964127-chr8:96035798..96039465,14	MCF-7	breast:
6	chr8:95962222..95963809-chr8:96146177..96149016,2	MCF-7	breast:
7	chr8:95958416..95961526-chr8:96166017..96168571,3	MCF-7	breast:
8	chr8:95905045..95910108-chr8:95959761..95963234,8	MCF-7	breast:
9	chr8:95958816..95960482-chr8:96125143..96126685,2	MCF-7	breast:
10	chr8:95960109..95960976-chr8:96036356..96037275,2	MCF-7	breast:
11	chr8:95959784..95963292-chr8:96036254..96039616,3	K562	blood:
12	chr8:95959198..95962585-chr8:96144089..96147312,4	MCF-7	breast:
13	chr8:95958803..95961918-chr8:96144805..96148535,6	MCF-7	breast:
14	chr8:95959150..95962570-chr8:95985356..95988577,4	MCF-7	breast:
15	chr8:95958396..95961086-chr8:96079770..96081416,2	MCF-7	breast:
16	chr8:95962646..95965102-chr8:96032516..96035099,2	MCF-7	breast:
17	chr8:95960086..95962162-chr8:96280907..96282894,2	MCF-7	breast:
18	chr8:95918169..95919782-chr8:95960752..95962481,2	MCF-7	breast:
19	chr8:95959920..95961566-chr8:96108874..96111712,2	MCF-7	breast:
20	chr8:95961511..95965084-chr8:95968441..95972141,5	K562	blood:
21	chr8:95905670..95907596-chr8:95958575..95960918,2	K562	blood:
22	chr8:95959680..95964310-chr8:96036583..96039456,6	MCF-7	breast:
23	chr8:95960008..95964622-chr8:95970124..95974538,6	MCF-7	breast:
24	chr8:95907370..95909639-chr8:95961818..95964122,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTS8-1	chr8:95962265-95962587	ENSG00000253878.1
2	lnc-INTS8-1	chr8:95962453-95962587	ENSG00000253878.1

No data

Variant related genes	Relation type
TP53INP1	TF binding region
ENSG00000253878	TF binding region
TP53INP1	CpG island
ENSG00000253878	CpG island
ENSG00000156172	chromatin interactions
ENSG00000175305	chromatin interactions
ENSG00000238791	chromatin interactions
ENSG00000156170	chromatin interactions
ENSG00000253773	chromatin interactions
ENSG00000175895	chromatin interactions
ENSG00000253528	chromatin interactions

Extended variants
information (count: 86 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:86 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557679218	chr8:95960269-95960270	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
2	rs577412625	chr8:95960274-95960275	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
3	rs540001009	chr8:95960282-95960283	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
4	rs732665	chr8:95960334-95960335	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
5	rs558402010	chr8:95960409-95960410	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs572121171	chr8:95960445-95960446	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
7	rs540696759	chr8:95960447-95960448	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
8	rs560551574	chr8:95960490-95960491	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
9	rs61663478	chr8:95960511-95960512	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs78634159	chr8:95960559-95960560	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
11	rs536004179	chr8:95960585-95960586	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
12	rs138143359	chr8:95960593-95960594	Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
13	rs556222345	chr8:95960603-95960604	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
14	rs559256927	chr8:95960617-95960618	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs542806391	chr8:95960641-95960642	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs528591815	chr8:95960647-95960648	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs143644610	chr8:95960672-95960673	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs373839020	chr8:95960683-95960684	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs537439842	chr8:95960690-95960691	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs551322521	chr8:95960695-95960696	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs571108003	chr8:95960699-95960700	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs1320164	chr8:95960767-95960768	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs145919038	chr8:95960770-95960771	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs181090585	chr8:95960774-95960775	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs896853	chr8:95960855-95960856	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs896852	chr8:95960886-95960887	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs574141454	chr8:95960905-95960906	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs2879813	chr8:95960947-95960948	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs563104575	chr8:95961009-95961010	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs577090123	chr8:95961012-95961013	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs545733063	chr8:95961019-95961020	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs560984954	chr8:95961021-95961022	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs559512134	chr8:95961025-95961026	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs370843658	chr8:95961057-95961058	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs548749470	chr8:95961058-95961059	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs562144264	chr8:95961082-95961083	Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs561010086	chr8:95961363-95961364	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs572827485	chr8:95961370-95961371	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs540255710	chr8:95961372-95961373	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs4436093	chr8:95961387-95961388	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs185136740	chr8:95961459-95961460	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs189548874	chr8:95961553-95961554	Active TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs570726961	chr8:95961565-95961566	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs533678578	chr8:95961599-95961600	Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs35943357	chr8:95961618-95961619	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs10097617	chr8:95961626-95961627	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs34043642	chr8:95961691-95961692	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs377231776	chr8:95961745-95961746	Active TSS Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs10108430	chr8:95961794-95961795	Active TSS Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs535648671	chr8:95961823-95961824	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
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
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
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
Multiple myeloma	16461302	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
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 myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:460 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95933400-95960600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:95957000-95960400	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:95957200-95960400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr8:95957200-95960600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:95957200-95960600	Weak transcription	Gastric	stomach
6	chr8:95957400-95960400	Weak transcription	Esophagus	oesophagus
7	chr8:95957800-95963400	Active TSS	Pancreas	Pancrea
8	chr8:95958000-95962600	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr8:95958400-95960600	Weak transcription	Spleen	Spleen
10	chr8:95958400-95960800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
11	chr8:95958600-95960600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
12	chr8:95959000-95960400	Flanking Active TSS	Primary hematopoietic stem cells	blood
13	chr8:95959000-95960400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
14	chr8:95959000-95960600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:95959000-95960600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
16	chr8:95959000-95960800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr8:95959000-95960800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr8:95959000-95960800	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr8:95959000-95961000	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr8:95959000-95962200	Active TSS	Rectal Smooth Muscle	rectum
21	chr8:95959200-95960400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr8:95959200-95960400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:95959200-95960800	Flanking Active TSS	Primary T cells fromperipheralblood	blood
24	chr8:95959200-95960800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr8:95959200-95960800	Flanking Active TSS	Fetal Thymus	thymus
26	chr8:95959200-95960800	Flanking Active TSS	Osteobl	bone
27	chr8:95959200-95961000	Flanking Active TSS	Primary T cells from cord blood	blood
28	chr8:95959200-95961000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
29	chr8:95959200-95961800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr8:95959400-95960400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:95959400-95960400	Flanking Active TSS	Colon Smooth Muscle	Colon
32	chr8:95959400-95960600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr8:95959400-95960800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr8:95959400-95960800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
35	chr8:95959400-95960800	Flanking Active TSS	Primary B cells from peripheral blood	blood
36	chr8:95959400-95961800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr8:95959400-95961800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr8:95959400-95962400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr8:95959400-95962400	Active TSS	Right Atrium	heart
40	chr8:95959600-95960400	Flanking Active TSS	HUVEC	blood vessel
41	chr8:95959600-95960600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
42	chr8:95959600-95960600	Flanking Active TSS	Brain Hippocampus Middle	brain
43	chr8:95959600-95960800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
44	chr8:95959600-95960800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
45	chr8:95959600-95960800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
46	chr8:95959600-95960800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
47	chr8:95959600-95961000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
48	chr8:95959600-95961600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr8:95959800-95960400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
50	chr8:95959800-95960400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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