Variant report

Variant	nsv890340
Chromosome Location	chr8:9029413-9121398
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:632)
CpG islands
(count:734)
Chromatin interactive
region (count:36)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:632 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:9060202-9060298	K562	blood:	n/a	n/a
2	ARID3A	chr8:9106581-9106674	K562	blood:	n/a	n/a
3	ARID3A	chr8:9075293-9075305	K562	blood:	n/a	n/a
4	ARID3A	chr8:9029209-9030373	K562	blood:	n/a	chr8:9029830-9029846
5	ATF1	chr8:9112997-9113254	K562	blood:	n/a	n/a
6	ATF1	chr8:9106470-9106696	K562	blood:	n/a	n/a
7	ATF1	chr8:9029238-9029565	K562	blood:	n/a	n/a
8	ATF1	chr8:9036682-9037019	K562	blood:	n/a	n/a
9	ATF1	chr8:9117581-9118000	K562	blood:	n/a	n/a
10	ATF1	chr8:9029870-9030322	K562	blood:	n/a	n/a
11	ATF2	chr8:9106397-9106813	GM12878	blood:	n/a	n/a
12	ATF2	chr8:9106362-9106824	GM12878	blood:	n/a	n/a
13	ATF3	chr8:9029942-9030356	K562	blood:	n/a	n/a
14	BACH1	chr8:9068025-9068192	K562	blood:	n/a	n/a
15	BACH1	chr8:9029223-9030347	K562	blood:	n/a	n/a
16	BATF	chr8:9106307-9106946	GM12878	blood:	n/a	chr8:9106632-9106643 chr8:9106633-9106643
17	BATF	chr8:9106372-9106826	GM12878	blood:	n/a	chr8:9106632-9106643 chr8:9106633-9106643
18	BCL11A	chr8:9106380-9106943	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
19	BCL11A	chr8:9106430-9106921	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
20	BCLAF1	chr8:9106457-9106732	GM12878	blood:	n/a	chr8:9106636-9106645 chr8:9106635-9106644
21	BHLHE40	chr8:9068120-9068123	K562	blood:	n/a	n/a
22	BHLHE40	chr8:9029724-9030795	K562	blood:	n/a	n/a
23	BHLHE40	chr8:9029318-9029521	K562	blood:	n/a	n/a
24	BHLHE40	chr8:9117711-9118064	K562	blood:	n/a	n/a
25	BHLHE40	chr8:9110181-9110378	K562	blood:	n/a	n/a
26	BHLHE40	chr8:9110246-9110274	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:9090326-9090623	K562	blood:	n/a	n/a
28	BHLHE40	chr8:9110612-9110648	K562	blood:	n/a	n/a
29	BHLHE40	chr8:9095362-9095700	K562	blood:	n/a	n/a
30	BHLHE40	chr8:9112909-9113255	K562	blood:	n/a	n/a
31	BHLHE40	chr8:9031847-9031860	K562	blood:	n/a	n/a
32	BHLHE40	chr8:9106199-9106847	GM12878	blood:	n/a	n/a
33	CBX3	chr8:9082474-9083014	HCT-116	colon:	n/a	n/a
34	CBX3	chr8:9030003-9030803	K562	blood:	n/a	n/a
35	CCNT2	chr8:9029977-9030328	K562	blood:	n/a	n/a
36	CCNT2	chr8:9029350-9029636	K562	blood:	n/a	n/a
37	CEBPB	chr8:9117691-9118023	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr8:9100544-9100750	IMR90	lung:	n/a	chr8:9100620-9100631
39	CEBPB	chr8:9044944-9045778	IMR90	lung:	n/a	chr8:9045122-9045131 chr8:9045122-9045131 chr8:9045120-9045131 chr8:9045120-9045133 chr8:9045122-9045131
40	CEBPB	chr8:9100618-9100654	H1-hESC	embryonic stem cell:	n/a	chr8:9100620-9100631
41	CEBPB	chr8:9045415-9045898	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chr8:9117674-9117963	K562	blood:	n/a	n/a
43	CEBPB	chr8:9045458-9045853	MCF-7	breast:	n/a	n/a
44	CEBPB	chr8:9100552-9100824	A549	lung:	n/a	chr8:9100620-9100631
45	CEBPB	chr8:9092228-9092358	K562	blood:	n/a	n/a
46	CEBPB	chr8:9121074-9121429	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:9044831-9045896	A549	lung:	n/a	chr8:9045122-9045131 chr8:9045122-9045131 chr8:9045120-9045131 chr8:9045120-9045133 chr8:9045122-9045131
48	CEBPB	chr8:9044930-9045342	MCF-7	breast:	n/a	chr8:9045122-9045131 chr8:9045122-9045131 chr8:9045120-9045131 chr8:9045120-9045133 chr8:9045122-9045131
49	CEBPB	chr8:9044895-9046045	HCT-116	colon:	n/a	chr8:9045122-9045131 chr8:9045122-9045131 chr8:9045120-9045131 chr8:9045120-9045133 chr8:9045122-9045131
50	CEBPB	chr8:9117816-9117945	HepG2	liver:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:9046478-9046528	HNPCEpiC	eye:	n/a
2	chr8:9046480-9046530	K562	blood:	n/a
3	chr8:9046478-9046528	HNPCEpiC	eye:	n/a
4	chr8:9046480-9046530	K562	blood:	n/a
5	chr8:9045328-9045378	K562	blood:	n/a
6	chr8:9106953-9107003	RPTEC	kidney:	n/a
7	chr8:9040449-9040499	AG09319	gingival:	n/a
8	chr8:9046478-9046528	NH-A	brain:	n/a
9	chr8:9095150-9095200	Hela-S3	cervix:	n/a
10	chr8:9046478-9046528	PFSK-1	brain:	n/a
11	chr8:9095150-9095200	NH-A	brain:	n/a
12	chr8:9046480-9046530	ProgFib	skin:	n/a
13	chr8:9106953-9107003	HL-60	blood:	n/a
14	chr8:9045328-9045378	Caco-2	colon:	n/a
15	chr8:9046480-9046530	PFSK-1	brain:	n/a
16	chr8:9048528-9048578	PrEC	prostate:	n/a
17	chr8:9046418-9046468	HCT-116	colon:	n/a
18	chr8:9055850-9055900	HCF	heart:	n/a
19	chr8:9107382-9107432	Hela-S3	cervix:	n/a
20	chr8:9107382-9107432	CMK	blood:	n/a
21	chr8:9045558-9045608	NH-A	brain:	n/a
22	chr8:9046480-9046530	Jurkat	blood:	n/a
23	chr8:9095150-9095200	BJ	skin:	n/a
24	chr8:9046418-9046468	MCF10A-Er-Src	breast:	n/a
25	chr8:9029456-9029506	NB4	blood:	n/a
26	chr8:9029456-9029506	PANC-1	pancreas:	n/a
27	chr8:9048528-9048578	H1-hESC	embryonic stem cell:	embryo
28	chr8:9046418-9046468	HEK293	kidney:	embryo
29	chr8:9029456-9029506	HCM	heart:	n/a
30	chr8:9046480-9046530	HEK293	kidney:	embryo
31	chr8:9048528-9048578	NH-A	brain:	n/a
32	chr8:9040449-9040499	Jurkat	blood:	n/a
33	chr8:9046478-9046528	GM12878	blood:	n/a
34	chr8:9046418-9046468	NHDF-neo	bronchial:	n/a
35	chr8:9046480-9046530	MCF-7	breast:	n/a
36	chr8:9046478-9046528	HRCEpiC	kidney:	n/a
37	chr8:9045328-9045378	HCPEpiC	choroid plexus:	n/a
38	chr8:9029456-9029506	GM12878	blood:	n/a
39	chr8:9046418-9046468	K562	blood:	n/a
40	chr8:9045558-9045608	NB4	blood:	n/a
41	chr8:9106953-9107003	NT2-D1	testis:	n/a
42	chr8:9046478-9046528	AG09309	skin:	n/a
43	chr8:9106953-9107003	Jurkat	blood:	n/a
44	chr8:9046478-9046528	LNCaP	prostate:	n/a
45	chr8:9046418-9046468	SKMC	muscle:	n/a
46	chr8:9046480-9046530	AG04450	lung:	fetal
47	chr8:9045328-9045378	NHDF-neo	bronchial:	n/a
48	chr8:9095150-9095200	PFSK-1	brain:	n/a
49	chr8:9046418-9046468	CMK	blood:	n/a
50	chr8:9048528-9048578	MCF10A-Er-Src	breast:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:9069999..9071504-chr8:9082002..9084260,2	K562	blood:
2	chr8:9026002..9027691-chr8:9032014..9033553,2	K562	blood:
3	chr8:9112030..9114953-chr8:9119545..9121234,2	K562	blood:
4	chr8:9055363..9058285-chr8:9064246..9065769,2	K562	blood:
5	chr8:9104792..9106778-chr8:9108609..9110525,2	K562	blood:
6	chr8:9024883..9027420-chr8:9028031..9029548,2	K562	blood:
7	chr8:9025233..9028612-chr8:9030173..9035326,5	K562	blood:
8	chr8:9075405..9078700-chr8:9080220..9082269,4	K562	blood:
9	chr8:9104792..9106778-chr8:9108609..9110525,2	K562	blood:
10	chr8:9094088..9097084-chr8:9119791..9121846,2	K562	blood:
11	chr8:9069999..9071504-chr8:9082002..9084260,2	K562	blood:
12	chr8:9056772..9059082-chr8:9087003..9089013,2	K562	blood:
13	chr8:9094088..9097084-chr8:9119791..9121846,2	K562	blood:
14	chr8:9019289..9020816-chr8:9034682..9036513,2	K562	blood:
15	chr8:9090534..9092903-chr8:9095758..9098005,2	MCF-7	breast:
16	chr8:9028683..9031216-chr8:9032072..9035247,3	K562	blood:
17	chr8:9040629..9042906-chr8:9043135..9044982,2	K562	blood:
18	chr8:9061535..9063157-chr8:9069276..9071088,2	MCF-7	breast:
19	chr8:9103215..9105968-chr8:9109700..9112241,2	K562	blood:
20	chr8:9048360..9049931-chr8:9051500..9053085,2	K562	blood:
21	chr8:9048939..9051745-chr8:9268709..9271649,2	K562	blood:
22	chr8:9056772..9059082-chr8:9087003..9089013,2	K562	blood:
23	chr8:9075405..9078700-chr8:9080220..9082269,4	K562	blood:
24	chr8:9095921..9098459-chr8:9104554..9106558,2	K562	blood:
25	chr8:9061535..9063157-chr8:9069276..9071088,2	MCF-7	breast:
26	chr8:9048360..9049861-chr8:9051500..9053163,2	K562	blood:
27	chr8:9040629..9042906-chr8:9043135..9044982,2	K562	blood:
28	chr8:9095921..9098459-chr8:9104554..9106558,2	K562	blood:
29	chr8:9112030..9114953-chr8:9119545..9121234,2	K562	blood:
30	chr8:9090534..9092903-chr8:9095758..9098005,2	MCF-7	breast:
31	chr8:9055363..9058285-chr8:9064246..9065769,2	K562	blood:
32	chr8:9048360..9049861-chr8:9051500..9053163,2	K562	blood:
33	chr8:9103215..9105968-chr8:9109700..9112241,2	K562	blood:
34	chr8:9098947..9101284-chr8:9104230..9106988,2	K562	blood:
35	chr8:9048360..9049931-chr8:9051500..9053085,2	K562	blood:
36	chr8:9028683..9031216-chr8:9032072..9035247,3	K562	blood:

(count:46 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-10A14.4.1-2	chr8:9056378-9056501	NONHSAT124930
2	lnc-PPP1R3B-2	chr8:9117538-9117805	XLOC_006999
3	lnc-RP11-10A14.4.1-2	chr8:9060009-9060363	XLOC_006705
4	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	ENSG00000248538
5	lnc-RP11-10A14.4.1-2	chr8:9049886-9050069	l_3542_chr8:9046697-9051717_testes
6	lnc-PPP1R3B-2	chr8:9117538-9117805	ENSG00000253887
7	lnc-RP11-10A14.4.1-2	chr8:9060009-9060347	ENSG00000248538
8	lnc-RP11-10A14.4.1-2	chr8:9059902-9060000	ENSG00000248538
9	lnc-RP11-10A14.4.1-6	chr8:9084120-9084517	l_3543_chr8:9084119-9097777_placenta
10	lnc-RP11-10A14.4.1-2	chr8:9051072-9051274	l_3542_chr8:9046697-9051717_testes
11	lnc-PPP1R3B-2	chr8:9117538-9117788	XLOC_006999
12	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	XLOC_006705
13	lnc-PPP1R3B-2	chr8:9112859-9113012	ENSG00000253887
14	lnc-RP11-10A14.4.1-2	chr8:9051691-9051717	l_3542_chr8:9046697-9051717_testes
15	lnc-RP11-10A14.4.1-2	chr8:9046698-9046837	l_3542_chr8:9046697-9051717_testes
16	lnc-PPP1R3B-2	chr8:9117538-9117805	XLOC_006999
17	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	ENSG00000248538
18	lnc-RP11-10A14.4.1-2	chr8:9059902-9060357	NONHSAT124931
19	lnc-RP11-10A14.4.1-6	chr8:9097312-9097798	l_3543_chr8:9084119-9097777_placenta
20	lnc-RP11-10A14.4.1-5	chr8:9090523-9090959	NONHSAT124932
21	lnc-RP11-10A14.4.1-6	chr8:9088317-9088952	l_3543_chr8:9084119-9097777_placenta
22	lnc-RP11-10A14.4.1-2	chr8:9056378-9056501	NONHSAT124931
23	lnc-RP11-10A14.4.1-2	chr8:9046512-9046556	XLOC_006705
24	lnc-RP11-10A14.4.1-2	chr8:9046858-9047096	ENSG00000248538
25	lnc-RP11-10A14.4.1-2	chr8:9046860-9047096	NONHSAT124925
26	lnc-RP11-10A14.4.1-6	chr8:9093844-9093911	l_3543_chr8:9084119-9097777_placenta
27	lnc-RP11-10A14.4.1-2	chr8:9046858-9047096	XLOC_006705
28	lnc-PPP1R3B-1	chr8:9037761-9038032	ENSG00000253252.2
29	lnc-RP11-10A14.4.1-2	chr8:9060009-9060357	NONHSAT124930
30	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	XLOC_006705
31	lnc-PPP1R3B-2	chr8:9112315-9112398	XLOC_006999
32	lnc-RP11-10A14.4.1-2	chr8:9047015-9047096	ENSG00000248538
33	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	NONHSAT124925
34	lnc-RP11-10A14.4.1-2	chr8:9056434-9056501	ENSG00000248538
35	lnc-RP11-10A14.4.1-2	chr8:9046509-9046556	NONHSAT124925
36	lnc-RP11-10A14.4.1-2	chr8:9060009-9060364	ENSG00000248538
37	lnc-RP11-10A14.4.1-2	chr8:9046856-9047096	ENSG00000248538
38	lnc-RP11-10A14.4.1-2	chr8:9046521-9046556	ENSG00000248538
39	lnc-PPP1R3B-1	chr8:9039974-9040029	ENSG00000253252.2
40	lnc-RP11-10A14.4.1-2	chr8:9046509-9046556	XLOC_006705
41	lnc-RP11-10A14.4.1-2	chr8:9046858-9047107	XLOC_006705
42	lnc-PPP1R3B-2	chr8:9112893-9113012	XLOC_006999
43	lnc-RP11-10A14.4.1-2	chr8:9060009-9060366	XLOC_006705
44	lnc-RP11-10A14.4.1-2	chr8:9060009-9060368	NONHSAT124925
45	lnc-RP11-10A14.4.1-2	chr8:9051468-9051542	ENSG00000248538
46	lnc-PPP1R3B-2	chr8:9115957-9116369	XLOC_006999

No data

Variant related genes	Relation type
ENSG00000254091	TF binding region
ENSG00000253887	TF binding region
ENSG00000253252	TF binding region
ENSG00000248538	TF binding region
ENSG00000254235	TF binding region
ENSG00000254091	CpG island
ENSG00000253887	CpG island
ENSG00000253252	CpG island
ENSG00000248538	CpG island
ENSG00000254235	CpG island
ENSG00000254235	chromatin interactions

Extended variants
information (count: 5254 )
Associated
traits (count: 138 )

Variant overlapped rSNPs/rCNVs (count:5254 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs435581	chr8:9029413-9029414	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544363409	chr8:9029416-9029417	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs138512540	chr8:9029417-9029418	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs74394293	chr8:9029426-9029427	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs536342105	chr8:9029437-9029438	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs530605492	chr8:9029456-9029457	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs147297914	chr8:9029465-9029466	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs567473072	chr8:9029472-9029473	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs529967917	chr8:9029488-9029489	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs549408412	chr8:9029503-9029504	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs564642091	chr8:9029548-9029549	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs533343590	chr8:9029553-9029554	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs140845097	chr8:9029554-9029555	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs189589493	chr8:9029569-9029570	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs571837595	chr8:9029586-9029587	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs537267861	chr8:9029592-9029593	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs557495305	chr8:9029603-9029604	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs78990023	chr8:9029604-9029605	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs374343236	chr8:9029609-9029610	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs542864249	chr8:9029671-9029672	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs77110146	chr8:9029680-9029681	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs371761713	chr8:9029694-9029695	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs182777430	chr8:9029702-9029703	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs146923523	chr8:9029756-9029757	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs572494562	chr8:9029775-9029776	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs544735347	chr8:9029791-9029792	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs371575172	chr8:9029814-9029815	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs112993388	chr8:9029821-9029822	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs375389974	chr8:9029889-9029890	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs575274868	chr8:9029914-9029915	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs544093548	chr8:9029919-9029920	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs112313694	chr8:9029931-9029932	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs571970224	chr8:9029934-9029935	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs561097448	chr8:9029966-9029967	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs192268531	chr8:9029996-9029997	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs546915408	chr8:9030006-9030007	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs554404131	chr8:9030008-9030009	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs3748138	chr8:9030034-9030035	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs143092120	chr8:9030049-9030050	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs184049304	chr8:9030055-9030056	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs150842112	chr8:9030069-9030070	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs115550370	chr8:9030079-9030080	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs3748137	chr8:9030103-9030104	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs567842482	chr8:9030130-9030131	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs536587252	chr8:9030143-9030144	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs187375441	chr8:9030149-9030150	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs3748136	chr8:9030160-9030161	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs572535742	chr8:9030178-9030179	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs574210728	chr8:9030179-9030180	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs9721365	chr8:9030193-9030194	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:138)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:802 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9009400-9039000	Weak transcription	Pancreas	Pancrea
2	chr8:9026200-9030200	Weak transcription	Fetal Lung	lung
3	chr8:9028000-9029600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:9028000-9030000	Weak transcription	Fetal Heart	heart
5	chr8:9028400-9045200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:9029000-9030400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr8:9029000-9030400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:9029000-9030600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr8:9029000-9030600	Flanking Active TSS	K562	blood
10	chr8:9029200-9029800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:9029200-9030400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr8:9029200-9030400	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr8:9029400-9029800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:9029400-9030400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr8:9029400-9030400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr8:9029600-9030000	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr8:9029600-9030200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr8:9029600-9030200	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr8:9029600-9030400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr8:9029600-9030600	Enhancers	H9 Cell Line	embryonic stem cell
21	chr8:9029600-9030600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr8:9029600-9030600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr8:9029800-9030400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr8:9029800-9030600	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr8:9029800-9034800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:9030000-9030400	Enhancers	Fetal Heart	heart
27	chr8:9030000-9034600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr8:9030200-9030600	Enhancers	Fetal Lung	lung
29	chr8:9030200-9030600	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr8:9030200-9030800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
31	chr8:9030200-9036400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr8:9030200-9040200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr8:9030400-9034000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr8:9030400-9034800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr8:9030400-9034800	Weak transcription	H1 Cell Line	embryonic stem cell
36	chr8:9030400-9038800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr8:9030400-9040000	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr8:9030400-9040200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
39	chr8:9030600-9031600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr8:9030600-9032400	Enhancers	K562	blood
41	chr8:9031600-9033800	Strong transcription	HUES6 Cell Line	embryonic stem cell
42	chr8:9032400-9034800	Weak transcription	K562	blood
43	chr8:9033800-9034800	Weak transcription	HUES6 Cell Line	embryonic stem cell
44	chr8:9034000-9034800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr8:9034600-9035000	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr8:9034800-9035000	Enhancers	Left Ventricle	heart
47	chr8:9034800-9035000	Enhancers	K562	blood
48	chr8:9034800-9035200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr8:9034800-9035200	Enhancers	H1 Cell Line	embryonic stem cell
50	chr8:9034800-9035200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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