Variant report

Variant	nsv831321
Chromosome Location	chr8:58086885-58237744
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1312)
CpG islands
(count:3543)
Chromatin interactive
region (count:43)
LncRNA
region (count:50)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1312 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:58122168-58122783	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:58137879-58138528	HepG2	liver:	n/a	n/a
3	ATF1	chr8:58142984-58143184	K562	blood:	n/a	n/a
4	ATF1	chr8:58122169-58123010	K562	blood:	n/a	n/a
5	ATF2	chr8:58163182-58163690	GM12878	blood:	n/a	n/a
6	ATF2	chr8:58164849-58165716	GM12878	blood:	n/a	n/a
7	ATF3	chr8:58137924-58138390	A549	lung:	n/a	n/a
8	BACH1	chr8:58122347-58122997	K562	blood:	n/a	n/a
9	BATF	chr8:58164916-58165854	GM12878	blood:	n/a	n/a
10	BATF	chr8:58163305-58163642	GM12878	blood:	n/a	n/a
11	BATF	chr8:58163276-58163662	GM12878	blood:	n/a	n/a
12	BATF	chr8:58156932-58157184	GM12878	blood:	n/a	chr8:58157088-58157098
13	BATF	chr8:58156891-58157182	GM12878	blood:	n/a	chr8:58157088-58157098 chr8:58156907-58156915
14	BCL3	chr8:58161874-58162566	GM12878	blood:	n/a	n/a
15	BCL3	chr8:58161749-58162514	GM12878	blood:	n/a	n/a
16	BCLAF1	chr8:58164899-58165684	GM12878	blood:	n/a	chr8:58165328-58165337
17	BHLHE40	chr8:58105853-58106191	K562	blood:	n/a	n/a
18	BHLHE40	chr8:58122112-58123036	K562	blood:	n/a	n/a
19	BHLHE40	chr8:58189904-58189917	GM12878	blood:	n/a	n/a
20	BHLHE40	chr8:58163280-58163709	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:58162469-58162481	K562	blood:	n/a	n/a
22	BHLHE40	chr8:58159213-58159482	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:58118159-58118698	K562	blood:	n/a	n/a
24	BHLHE40	chr8:58164961-58165519	GM12878	blood:	n/a	n/a
25	BHLHE40	chr8:58127590-58127948	K562	blood:	n/a	n/a
26	BHLHE40	chr8:58137964-58138275	HepG2	liver:	n/a	n/a
27	BRCA1	chr8:58122208-58123016	GM12878	blood:	n/a	n/a
28	BRCA1	chr8:58127563-58127875	GM12878	blood:	n/a	n/a
29	BRCA1	chr8:58162132-58162328	GM12878	blood:	n/a	n/a
30	BRCA1	chr8:58118301-58118654	GM12878	blood:	n/a	n/a
31	BRCA1	chr8:58122170-58122971	HepG2	liver:	n/a	n/a
32	BRCA1	chr8:58127438-58127751	HepG2	liver:	n/a	n/a
33	CBX3	chr8:58105849-58106177	K562	blood:	n/a	n/a
34	CCNT2	chr8:58105900-58106102	K562	blood:	n/a	n/a
35	CEBPB	chr8:58118292-58118614	HepG2	liver:	n/a	chr8:58118437-58118448
36	CEBPB	chr8:58135434-58135802	A549	lung:	n/a	chr8:58135609-58135620
37	CEBPB	chr8:58135407-58135877	A549	lung:	n/a	chr8:58135609-58135620
38	CEBPB	chr8:58138094-58138305	HepG2	liver:	n/a	n/a
39	CEBPB	chr8:58137871-58138537	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr8:58122125-58123045	K562	blood:	n/a	n/a
41	CEBPB	chr8:58135416-58135803	HepG2	liver:	n/a	chr8:58135609-58135620
42	CEBPB	chr8:58135419-58135810	K562	blood:	n/a	chr8:58135609-58135620
43	CEBPB	chr8:58138061-58138288	A549	lung:	n/a	n/a
44	CEBPB	chr8:58138106-58138233	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:58148436-58148762	A549	lung:	n/a	chr8:58148597-58148608 chr8:58148610-58148621
46	CEBPB	chr8:58135434-58135730	K562	blood:	n/a	chr8:58135609-58135620
47	CEBPB	chr8:58144842-58145071	A549	lung:	n/a	chr8:58144923-58144934
48	CEBPB	chr8:58135455-58135719	HepG2	liver:	n/a	chr8:58135609-58135620
49	CEBPB	chr8:58148423-58148803	Hela-S3	cervix:	n/a	chr8:58148597-58148608 chr8:58148610-58148621
50	CEBPB	chr8:58135395-58135845	MCF-7	breast:	n/a	chr8:58135609-58135620

(count:3543 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:58117541-58117591	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:58130323-58130373	PFSK-1	brain:	n/a
3	chr8:58168222-58168272	Jurkat	blood:	n/a
4	chr8:58192883-58192933	Hela-S3	cervix:	n/a
5	chr8:58191969-58192019	HCPEpiC	choroid plexus:	n/a
6	chr8:58117541-58117591	HPAEpiC	pulmonary alveolar:	n/a
7	chr8:58130323-58130373	PFSK-1	brain:	n/a
8	chr8:58168222-58168272	Jurkat	blood:	n/a
9	chr8:58192883-58192933	Hela-S3	cervix:	n/a
10	chr8:58191969-58192019	HCPEpiC	choroid plexus:	n/a
11	chr8:58191969-58192019	MCF10A-Er-Src	breast:	n/a
12	chr8:58122850-58122900	GM12878	blood:	n/a
13	chr8:58173601-58173651	Jurkat	blood:	n/a
14	chr8:58106094-58106144	NT2-D1	testis:	n/a
15	chr8:58124249-58124299	Caco-2	colon:	n/a
16	chr8:58128724-58128774	SK-N-SH_RA	brain:	n/a
17	chr8:58117687-58117737	HCT-116	colon:	n/a
18	chr8:58106598-58106648	Hela-S3	cervix:	n/a
19	chr8:58130323-58130373	GM12891	blood:	n/a
20	chr8:58131602-58131652	HepG2	liver:	n/a
21	chr8:58173162-58173212	RPTEC	kidney:	n/a
22	chr8:58188909-58188959	HCM	heart:	n/a
23	chr8:58117541-58117591	AG09319	gingival:	n/a
24	chr8:58106094-58106144	AG04449	skin:	fetal
25	chr8:58106155-58106205	AG04449	skin:	fetal
26	chr8:58191969-58192019	AG04449	skin:	fetal
27	chr8:58172571-58172621	AoSMC	blood vessel:	n/a
28	chr8:58120465-58120515	ProgFib	skin:	n/a
29	chr8:58172855-58172905	GM19239	blood:	n/a
30	chr8:58119141-58119191	NH-A	brain:	n/a
31	chr8:58106155-58106205	SK-N-MC	brain:	n/a
32	chr8:58138048-58138098	A549	lung:	n/a
33	chr8:58130041-58130091	HAEpiC	amniotic membrane:	n/a
34	chr8:58114915-58114965	HRPEpiC	eye:	n/a
35	chr8:58174422-58174472	NT2-D1	testis:	n/a
36	chr8:58117541-58117591	HepG2	liver:	n/a
37	chr8:58130467-58130517	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:58118711-58118761	NH-A	brain:	n/a
39	chr8:58172855-58172905	NT2-D1	testis:	n/a
40	chr8:58173601-58173651	HPAEpiC	pulmonary alveolar:	n/a
41	chr8:58106520-58106570	HL-60	blood:	n/a
42	chr8:58116908-58116958	HNPCEpiC	eye:	n/a
43	chr8:58191610-58191660	ovcar-3	ovarian:	n/a
44	chr8:58132287-58132337	SKMC	muscle:	n/a
45	chr8:58119141-58119191	PANC-1	pancreas:	n/a
46	chr8:58122850-58122900	HCT-116	colon:	n/a
47	chr8:58177661-58177711	Caco-2	colon:	n/a
48	chr8:58190903-58190953	U87	brain:	n/a
49	chr8:58172571-58172621	GM12892	blood:	n/a
50	chr8:58117794-58117844	NHDF-neo	bronchial:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
2	chr8:58137967..58139990-chr8:58271314..58273259,2	MCF-7	breast:
3	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
4	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
5	chr8:58122191..58122786-chr8:58255142..58256110,2	K562	blood:
6	chr8:58145565..58149221-chr8:58153371..58158136,4	K562	blood:
7	chr8:58155473..58158296-chr8:58162081..58163594,2	K562	blood:
8	chr8:58116819..58119579-chr8:58126200..58127971,2	K562	blood:
9	chr8:58094506..58095013-chr8:58135741..58136318,2	MCF-7	breast:
10	chr8:58143846..58145924-chr8:58146772..58148988,2	K562	blood:
11	chr8:58143846..58145924-chr8:58146772..58148988,2	K562	blood:
12	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
13	chr8:58137340..58139312-chr8:58141710..58144515,2	MCF-7	breast:
14	chr8:58098067..58099836-chr8:58101928..58103636,2	K562	blood:
15	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
16	chr8:58157176..58158882-chr8:58160639..58162485,2	K562	blood:
17	chr8:58157176..58158882-chr8:58160639..58162485,2	K562	blood:
18	chr8:58094799..58095495-chr8:58255642..58256690,5	MCF-7	breast:
19	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
20	chr8:58111629..58114368-chr8:58116589..58119919,3	K562	blood:
21	chr8:58145565..58148679-chr8:58153371..58155909,3	K562	blood:
22	chr8:58134015..58136749-chr8:58138139..58140095,2	K562	blood:
23	chr8:58129429..58131931-chr8:58132415..58133992,2	K562	blood:
24	chr8:58155473..58158296-chr8:58162081..58163594,2	K562	blood:
25	chr8:58134015..58136749-chr8:58138139..58140095,2	K562	blood:
26	chr8:58083900..58086328-chr8:58091891..58093782,2	K562	blood:
27	chr8:58129899..58132563-chr8:58137038..58139171,2	K562	blood:
28	chr8:58094506..58095013-chr8:58135741..58136318,2	MCF-7	breast:
29	chr8:58116442..58118477-chr8:58121162..58123026,3	K562	blood:
30	chr8:58137340..58139312-chr8:58141710..58144515,2	MCF-7	breast:
31	chr8:58190918..58193705-chr8:58197368..58198890,2	K562	blood:
32	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:
33	chr8:58094338..58095391-chr8:58255624..58256416,4	MCF-7	breast:
34	chr8:58135656..58136628-chr8:58255573..58256399,7	MCF-7	breast:
35	chr8:58121826..58122902-chr8:58255580..58256503,3	MCF-7	breast:
36	chr8:58145565..58148679-chr8:58153371..58155909,3	K562	blood:
37	chr8:58127588..58129747-chr8:58135062..58137669,2	K562	blood:
38	chr8:58104914..58107604-chr8:58109994..58112221,3	K562	blood:
39	chr8:58117787..58118343-chr8:58127587..58128273,3	K562	blood:
40	chr8:58098067..58099836-chr8:58101928..58103636,2	K562	blood:
41	chr8:58111742..58114368-chr8:58116589..58118815,2	K562	blood:
42	chr8:58145565..58149221-chr8:58153371..58158136,4	K562	blood:
43	chr8:58116966..58119487-chr8:58121967..58124287,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM110B-8	chr8:58131093-58131254	ENSG00000253301.1
2	lnc-FAM110B-13	chr8:58156865-58157483	NONHSAT126745
3	lnc-FAM110B-8	chr8:58106149-58106248	ENSG00000253301.1
4	lnc-FAM110B-8	chr8:58134728-58134830	NONHSAT126741
5	lnc-FAM110B-8	chr8:58131969-58132182	NONHSAT126741
6	lnc-FAM110B-8	chr8:58131969-58132082	ENSG00000253301.1
7	lnc-FAM110B-8	chr8:58132670-58132854	NONHSAT126742
8	lnc-FAM110B-7	chr8:58174093-58175676	NR_038874
9	lnc-FAM110B-8	chr8:58133958-58134166	NONHSAT126741
10	lnc-FAM110B-8	chr8:58131162-58131254	ENSG00000253301.1
11	lnc-FAM110B-8	chr8:58133148-58133297	ENSG00000253301.1
12	lnc-FAM110B-7	chr8:58174093-58175676	ENSG00000253614
13	lnc-FAM110B-8	chr8:58131969-58132126	ENSG00000253301.1
14	lnc-FAM110B-8	chr8:58133958-58134166	ENSG00000253301.1
15	lnc-FAM110B-8	chr8:58142104-58142287	ENSG00000253301.1
16	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
17	lnc-FAM110B-8	chr8:58131648-58131697	ENSG00000253301.1
18	lnc-FAM110B-8	chr8:58143951-58145195	ENSG00000253301.1
19	lnc-FAM110B-8	chr8:58120568-58120763	ENSG00000253301.1
20	lnc-FAM110B-7	chr8:58177900-58179172	ENSG00000253614
21	lnc-FAM110B-7	chr8:58173785-58173898	NR_038874
22	lnc-FAM110B-8	chr8:58132670-58132854	NONHSAT126741
23	lnc-FAM110B-8	chr8:58131615-58131697	ENSG00000253301.1
24	lnc-FAM110B-8	chr8:58142009-58146182	NONHSAT126744
25	lnc-FAM110B-8	chr8:58142104-58142287	NONHSAT126741
26	lnc-FAM110B-8	chr8:58121058-58121191	ENSG00000253301.1
27	lnc-FAM110B-8	chr8:58131648-58131697	NONHSAT126741
28	lnc-FAM110B-8	chr8:58131938-58132182	ENSG00000253301.1
29	lnc-FAM110B-8	chr8:58131969-58132182	ENSG00000253301.1
30	lnc-FAM110B-8	chr8:58134728-58134830	ENSG00000253301.1
31	lnc-FAM110B-8	chr8:58135154-58135255	ENSG00000253301.1
32	lnc-FAM110B-8	chr8:58135154-58135255	NONHSAT126742
33	lnc-FAM110B-8	chr8:58136443-58136530	NONHSAT126744
34	lnc-FAM110B-7	chr8:58173785-58173898	ENSG00000253614
35	lnc-FAM110B-8	chr8:58106179-58106275	ENSG00000253301.1
36	lnc-FAM110B-8	chr8:58143951-58145388	NONHSAT126741
37	lnc-FAM110B-8	chr8:58135154-58135255	ENSG00000253301.1
38	lnc-FAM110B-8	chr8:58142104-58142573	NONHSAT126742
39	lnc-FAM110B-8	chr8:58139050-58139184	NONHSAT126742
40	lnc-FAM110B-8	chr8:58132670-58132854	ENSG00000253301.1
41	lnc-FAM110B-7	chr8:58177900-58179170	NR_038874
42	lnc-FAM110B-8	chr8:58131885-58132182	NONHSAT126742
43	lnc-FAM110B-8	chr8:58135154-58135255	NONHSAT126741
44	lnc-FAM110B-8	chr8:58106444-58106570	ENSG00000253301.1
45	lnc-FAM110B-8	chr8:58152654-58152857	ENSG00000253301.1
46	lnc-FAM110B-13	chr8:58153517-58153779	NONHSAT126745
47	lnc-FAM110B-8	chr8:58142104-58142287	ENSG00000253301.1
48	lnc-FAM110B-8	chr8:58130835-58130911	ENSG00000253301.1
49	lnc-FAM110B-8	chr8:58132670-58132854	ENSG00000253301.1
50	lnc-FAM110B-8	chr8:58132670-58132795	ENSG00000253301.1

No data

Variant related genes	Relation type
ENSG00000253614	TF binding region
RNU6-596P	TF binding region
ENSG00000220984	TF binding region
ENSG00000253301	TF binding region
LINC00588	TF binding region
ENSG00000251142	TF binding region
ENSG00000253614	CpG island
RNU6-596P	CpG island
ENSG00000220984	CpG island
ENSG00000253301	CpG island
LINC00588	CpG island
ENSG00000251142	CpG island
ENSG00000253301	chromatin interactions
ENSG00000253871	chromatin interactions
ENSG00000215117	chromatin interactions

Extended variants
information (count: 4666 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4666 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544541191	chr8:58086897-58086898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs561127029	chr8:58086922-58086923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7823911	chr8:58086926-58086927	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs371710732	chr8:58086979-58086980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs142626982	chr8:58086992-58086993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs559952299	chr8:58086993-58086994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532235728	chr8:58086995-58086996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551881004	chr8:58087008-58087009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs113514794	chr8:58087169-58087170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs145876118	chr8:58092659-58092660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552073248	chr8:58092663-58092664	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs28408204	chr8:58092674-58092675	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs28578130	chr8:58092725-58092726	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557454981	chr8:58092728-58092729	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs574189045	chr8:58092735-58092736	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs28548459	chr8:58092852-58092853	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs575400751	chr8:58092853-58092854	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs28690714	chr8:58092861-58092862	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs377732671	chr8:58092902-58092903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs560603575	chr8:58092920-58092921	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs529785906	chr8:58092926-58092927	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs539840873	chr8:58092958-58092959	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs560130634	chr8:58092971-58092972	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs542172980	chr8:58094354-58094355	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs561854317	chr8:58094355-58094356	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs372954588	chr8:58094435-58094436	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs57238808	chr8:58094450-58094451	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs75857502	chr8:58094451-58094452	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs367974648	chr8:58094452-58094453	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs527446058	chr8:58094463-58094464	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561071556	chr8:58094473-58094474	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs185811346	chr8:58094476-58094477	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs190324695	chr8:58094526-58094527	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs193195710	chr8:58094533-58094534	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs371061814	chr8:58094564-58094565	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs552137204	chr8:58094590-58094591	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs568941235	chr8:58094594-58094595	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150861969	chr8:58094613-58094614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs373109401	chr8:58094658-58094659	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs548441813	chr8:58094673-58094674	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs184326201	chr8:58094685-58094686	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs200218277	chr8:58094715-58094716	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs534353265	chr8:58094718-58094719	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554116050	chr8:58094729-58094730	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs188563457	chr8:58094768-58094769	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs539574131	chr8:58094798-58094799	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs139560975	chr8:58094823-58094824	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs576078680	chr8:58094868-58094869	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs541860468	chr8:58094894-58094895	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs561971371	chr8:58094896-58094897	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Sezary syndrome	18413736	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Recurrent pregnancy loss	19789632	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58086000-58087200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:58086600-58087000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:58105400-58105600	Enhancers	K562	blood
4	chr8:58105600-58106000	Flanking Active TSS	K562	blood
5	chr8:58105800-58106000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr8:58106000-58106200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:58106000-58107200	Active TSS	K562	blood
8	chr8:58106200-58114800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:58111800-58112200	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr8:58114800-58115400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr8:58115400-58118200	Weak transcription	Right Atrium	heart
12	chr8:58116000-58117400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr8:58116200-58117000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr8:58116200-58117200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr8:58116400-58117000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:58116400-58117000	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
18	chr8:58116400-58117200	ZNF genes & repeats	Spleen	Spleen
19	chr8:58116400-58117400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr8:58116400-58118000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
21	chr8:58116600-58116800	ZNF genes & repeats	Brain Hippocampus Middle	brain
22	chr8:58116600-58117000	Enhancers	Gastric	stomach
23	chr8:58116600-58117200	ZNF genes & repeats	Fetal Kidney	kidney
24	chr8:58116600-58117200	ZNF genes & repeats	Pancreas	Pancrea
25	chr8:58116600-58117600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr8:58116600-58118800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr8:58116800-58118200	Weak transcription	Brain Hippocampus Middle	brain
28	chr8:58117000-58118200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr8:58117000-58118200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:58117000-58118200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr8:58117000-58118200	Weak transcription	Gastric	stomach
32	chr8:58117000-58119000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr8:58117200-58118200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr8:58117200-58118200	Weak transcription	Fetal Kidney	kidney
35	chr8:58117400-58118200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr8:58117800-58118800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
37	chr8:58118000-58118800	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
38	chr8:58118000-58118800	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr8:58118000-58118800	ZNF genes & repeats	Brain Germinal Matrix	brain
40	chr8:58118000-58118800	ZNF genes & repeats	Pancreas	Pancrea
41	chr8:58118200-58118400	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
42	chr8:58118200-58118600	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
43	chr8:58118200-58118600	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Large	intestine
45	chr8:58118200-58118600	ZNF genes & repeats	Fetal Intestine Small	intestine
46	chr8:58118200-58118600	ZNF genes & repeats	Fetal Muscle Trunk	muscle
47	chr8:58118200-58118600	ZNF genes & repeats	Placenta	Placenta
48	chr8:58118200-58118600	Flanking Bivalent TSS/Enh	Stomach Smooth Muscle	stomach
49	chr8:58118200-58118600	ZNF genes & repeats	NHEK	skin
50	chr8:58118200-58118800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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