Variant report

Variant	nsv1018483
Chromosome Location	chr8:86142258-86547831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3672)
CpG islands
(count:3969)
Chromatin interactive
region (count:203)
LncRNA
region (count:36)
Mature miRNA
region (count: 0)
miRNA target
sites (count:5)

(count:3672 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:86295505-86295821	K562	blood:	n/a	n/a
2	ARID3A	chr8:86169715-86169909	K562	blood:	n/a	n/a
3	ARID3A	chr8:86180047-86180413	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:86157652-86158712	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:86375408-86375608	K562	blood:	n/a	n/a
6	ARID3A	chr8:86158415-86158709	K562	blood:	n/a	n/a
7	ARID3A	chr8:86290333-86290829	K562	blood:	n/a	n/a
8	ARID3A	chr8:86277502-86277804	HepG2	liver:	n/a	n/a
9	ARID3A	chr8:86459249-86459549	HepG2	liver:	n/a	n/a
10	ARID3A	chr8:86202468-86202617	K562	blood:	n/a	n/a
11	ARID3A	chr8:86176898-86177188	K562	blood:	n/a	n/a
12	ARID3A	chr8:86291587-86291777	K562	blood:	n/a	n/a
13	ARID3A	chr8:86464069-86464458	HepG2	liver:	n/a	n/a
14	ARID3A	chr8:86363787-86364168	HepG2	liver:	n/a	n/a
15	ARID3A	chr8:86258991-86259361	HepG2	liver:	n/a	n/a
16	ATF1	chr8:86290328-86290675	K562	blood:	n/a	n/a
17	ATF1	chr8:86322674-86323117	K562	blood:	n/a	n/a
18	ATF1	chr8:86291509-86291829	K562	blood:	n/a	n/a
19	ATF2	chr8:86375277-86375647	GM12878	blood:	n/a	n/a
20	ATF2	chr8:86456763-86457418	GM12878	blood:	n/a	n/a
21	ATF2	chr8:86157875-86158542	GM12878	blood:	n/a	n/a
22	ATF2	chr8:86456835-86457349	GM12878	blood:	n/a	n/a
23	ATF2	chr8:86379099-86379380	GM12878	blood:	n/a	n/a
24	ATF3	chr8:86209644-86209936	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF3	chr8:86176921-86177222	K562	blood:	n/a	n/a
26	ATF3	chr8:86494789-86495026	K562	blood:	n/a	n/a
27	ATF3	chr8:86209670-86209992	K562	blood:	n/a	n/a
28	BACH1	chr8:86445039-86445121	K562	blood:	n/a	n/a
29	BACH1	chr8:86350837-86350999	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr8:86373952-86374352	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr8:86375517-86375618	K562	blood:	n/a	n/a
32	BACH1	chr8:86157639-86158022	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr8:86477707-86478028	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr8:86469052-86469363	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr8:86403854-86404118	H1-hESC	embryonic stem cell:	n/a	n/a
36	BACH1	chr8:86376436-86376638	H1-hESC	embryonic stem cell:	n/a	n/a
37	BACH1	chr8:86477700-86478018	K562	blood:	n/a	n/a
38	BACH1	chr8:86375322-86375896	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr8:86403885-86404059	K562	blood:	n/a	n/a
40	BACH1	chr8:86380185-86380380	H1-hESC	embryonic stem cell:	n/a	n/a
41	BATF	chr8:86456746-86457294	GM12878	blood:	n/a	n/a
42	BATF	chr8:86414365-86414644	GM12878	blood:	n/a	chr8:86414511-86414522 chr8:86414512-86414522
43	BATF	chr8:86208534-86208968	GM12878	blood:	n/a	n/a
44	BATF	chr8:86251720-86251890	GM12878	blood:	n/a	n/a
45	BATF	chr8:86407687-86407926	GM12878	blood:	n/a	chr8:86407879-86407890
46	BATF	chr8:86407688-86408006	GM12878	blood:	n/a	chr8:86407879-86407890
47	BATF	chr8:86456863-86457355	GM12878	blood:	n/a	n/a
48	BATF	chr8:86208270-86208976	GM12878	blood:	n/a	n/a
49	BATF	chr8:86414421-86414607	GM12878	blood:	n/a	chr8:86414511-86414522 chr8:86414512-86414522
50	BCL11A	chr8:86456931-86457329	GM12878	blood:	n/a	n/a

(count:3969 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86157836-86157886	AG10803	skin:	n/a
2	chr8:86353723-86353773	MCF10A-Er-Src	breast:	n/a
3	chr8:86351018-86351068	NHBE	bronchial:	n/a
4	chr8:86350568-86350618	AoSMC	blood vessel:	n/a
5	chr8:86157836-86157886	AG10803	skin:	n/a
6	chr8:86353723-86353773	MCF10A-Er-Src	breast:	n/a
7	chr8:86351018-86351068	NHBE	bronchial:	n/a
8	chr8:86350568-86350618	AoSMC	blood vessel:	n/a
9	chr8:86350913-86350963	SK-N-SH_RA	brain:	n/a
10	chr8:86157641-86157691	ProgFib	skin:	n/a
11	chr8:86230419-86230469	AG04449	skin:	fetal
12	chr8:86154580-86154630	ovcar-3	ovarian:	n/a
13	chr8:86371819-86371869	CMK	blood:	n/a
14	chr8:86157641-86157691	Caco-2	colon:	n/a
15	chr8:86157410-86157460	HCPEpiC	choroid plexus:	n/a
16	chr8:86353723-86353773	CMK	blood:	n/a
17	chr8:86350592-86350642	HEK293	kidney:	embryo
18	chr8:86375919-86375969	SK-N-SH	brain:	n/a
19	chr8:86379678-86379728	NHDF-neo	bronchial:	n/a
20	chr8:86189883-86189933	MCF-7	breast:	n/a
21	chr8:86376088-86376138	Jurkat	blood:	n/a
22	chr8:86393055-86393105	HEK293	kidney:	embryo
23	chr8:86186217-86186267	NH-A	brain:	n/a
24	chr8:86158305-86158355	HRCEpiC	kidney:	n/a
25	chr8:86414553-86414603	HepG2	liver:	n/a
26	chr8:86255139-86255189	PrEC	prostate:	n/a
27	chr8:86230419-86230469	HPAEpiC	pulmonary alveolar:	n/a
28	chr8:86291640-86291690	HIPEpiC	eye:	n/a
29	chr8:86157935-86157985	SK-N-MC	brain:	n/a
30	chr8:86157410-86157460	PANC-1	pancreas:	n/a
31	chr8:86352350-86352400	HCT-116	colon:	n/a
32	chr8:86350889-86350939	AG04449	skin:	fetal
33	chr8:86157838-86157888	NT2-D1	testis:	n/a
34	chr8:86376277-86376327	MCF-7	breast:	n/a
35	chr8:86376842-86376892	Hepatocyte	liver:	n/a
36	chr8:86347111-86347161	NHBE	bronchial:	n/a
37	chr8:86157735-86157785	LNCaP	prostate:	n/a
38	chr8:86351067-86351117	IMR90	lung:	fetal
39	chr8:86157410-86157460	BJ	skin:	n/a
40	chr8:86157838-86157888	PFSK-1	brain:	n/a
41	chr8:86351195-86351245	SAEC	small airway:	n/a
42	chr8:86290878-86290928	HRPEpiC	eye:	n/a
43	chr8:86186217-86186267	CMK	blood:	n/a
44	chr8:86189690-86189740	PANC-1	pancreas:	n/a
45	chr8:86189883-86189933	HCT-116	colon:	n/a
46	chr8:86157838-86157888	GM12892	blood:	n/a
47	chr8:86251915-86251965	NH-A	brain:	n/a
48	chr8:86349742-86349792	HEK293	kidney:	embryo
49	chr8:86189690-86189740	HRPEpiC	eye:	n/a
50	chr8:86290432-86290482	HCPEpiC	choroid plexus:	n/a

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr8:86211093..86212034-chr8:86283049..86283804,4	MCF-7	breast:
2	chr8:86348746..86351284-chr8:86374911..86377490,2	MCF-7	breast:
3	chr8:86209797..86210360-chr8:87056059..87056917,2	MCF-7	breast:
4	chr8:86376072..86377713-chr8:86460075..86462237,2	MCF-7	breast:
5	chr8:86209220..86210007-chr8:87100560..87101317,2	MCF-7	breast:
6	chr8:85542893..85545480-chr8:86287576..86290240,2	MCF-7	breast:
7	chr8:86209312..86210314-chr8:87045120..87046083,5	MCF-7	breast:
8	chr8:86146124..86147928-chr8:86175921..86177921,2	K562	blood:
9	chr8:86209418..86210324-chr8:87100237..87101601,6	K562	blood:
10	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
11	chr8:86132601..86133518-chr8:86202049..86203190,16	MCF-7	breast:
12	chr8:86447479..86449343-chr8:86449929..86452624,2	MCF-7	breast:
13	chr8:86525634..86527923-chr8:86533854..86535632,2	MCF-7	breast:
14	chr8:86364193..86367420-chr8:86983302..86985481,3	MCF-7	breast:
15	chr8:86383914..86386781-chr8:86392186..86393964,2	MCF-7	breast:
16	chr8:86451147..86453927-chr8:86454865..86457122,2	MCF-7	breast:
17	chr8:86157167..86159112-chr8:86171678..86174510,2	K562	blood:
18	chr8:86374416..86376946-chr8:86448157..86452576,4	MCF-7	breast:
19	chr8:86372586..86374669-chr8:86379787..86381546,2	MCF-7	breast:
20	chr1:144931784..144933992-chr8:86374827..86377261,2	MCF-7	breast:
21	chr8:86375875..86379086-chr8:86380688..86384617,3	MCF-7	breast:
22	chr8:86146124..86147928-chr8:86175921..86177921,2	K562	blood:
23	chr8:86211093..86212034-chr8:86283049..86283804,4	MCF-7	breast:
24	chr8:86376103..86378213-chr8:86422646..86424905,3	MCF-7	breast:
25	chr8:86448503..86451342-chr8:86452814..86454465,2	MCF-7	breast:
26	chr8:86360412..86362696-chr8:87043331..87045552,2	MCF-7	breast:
27	chr17:56933457..56934374-chr8:86363652..86364173,2	MCF-7	breast:
28	chr8:86153495..86155437-chr8:86156348..86158559,3	MCF-7	breast:
29	chr8:86379732..86382227-chr8:86385483..86388148,2	K562	blood:
30	chr8:43092411..43092911-chr8:86471290..86472121,2	MCF-7	breast:
31	chr8:86494376..86498242-chr8:86499635..86502661,3	MCF-7	breast:
32	chr8:86372586..86374669-chr8:86379787..86381546,2	MCF-7	breast:
33	chr8:86404163..86406491-chr8:86406532..86408170,2	MCF-7	breast:
34	chr8:86170519..86173141-chr8:86177699..86180911,3	K562	blood:
35	chr8:86156067..86157846-chr8:86165485..86167515,2	K562	blood:
36	chr8:86403779..86406429-chr8:86407390..86409709,2	MCF-7	breast:
37	chr8:86145854..86147928-chr8:86176421..86178334,2	K562	blood:
38	chr8:86475952..86478807-chr8:86480492..86482472,2	MCF-7	breast:
39	chr8:86126895..86128516-chr8:86206289..86209119,2	K562	blood:
40	chr8:86373635..86376461-chr8:86417769..86420196,2	MCF-7	breast:
41	chr8:86363504..86364383-chr8:86986429..86987168,3	MCF-7	breast:
42	chr8:86406517..86409106-chr8:86411209..86414222,3	MCF-7	breast:
43	chr8:86132667..86134494-chr8:86156330..86158323,2	K562	blood:
44	chr8:86375429..86377548-chr8:86385406..86389030,6	MCF-7	breast:
45	chr8:86466130..86468882-chr8:86474529..86476271,2	MCF-7	breast:
46	chr8:86457982..86459592-chr8:86459757..86463318,3	MCF-7	breast:
47	chr5:177630888..177633321-chr8:86308842..86311326,2	MCF-7	breast:
48	chr8:86209691..86210223-chr8:86364003..86364752,2	MCF-7	breast:
49	chr8:86454738..86456401-chr8:86461305..86463210,2	MCF-7	breast:
50	chr20:59055461..59055980-chr8:86363823..86364460,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
2	lnc-CA1-1	chr8:86354276-86354466	ENSG00000253549.1
3	lnc-RP11-219B4.5.1-1	chr8:86155574-86155917	NONHSAT127522
4	lnc-CA2-2	chr8:86436806-86437088	ENSG00000254380
5	lnc-CA1-1	chr8:86375161-86375283	ENSG00000253549.1
6	lnc-CA1-1	chr8:86374965-86375030	NONHSAT127529
7	lnc-CA13-1	chr8:86142314-86142429	NONHSAT127521
8	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
9	lnc-RP11-219B4.6.1-1	chr8:86245754-86245849	NONHSAT127524
10	lnc-CA2-1	chr8:86445765-86445878	XLOC_006865
11	lnc-CA1-1	chr8:86375661-86375942	NONHSAT127529
12	lnc-CA1-1	chr8:86354080-86354466	ENSG00000253549.1
13	lnc-RP11-219B4.6.1-1	chr8:86254978-86255054	NONHSAT127524
14	lnc-CA1-1	chr8:86376457-86376562	ENSG00000253549.1
15	lnc-CA2-2	chr8:86436090-86436470	XLOC_006864
16	lnc-REXO1L1-3	chr8:86508349-86508606	NONHSAT127537
17	lnc-RP11-219B4.6.1-1	chr8:86253644-86253888	NONHSAT127525
18	lnc-CA2-3	chr8:86447984-86448189	FPKM1_group_31645_transcript_1
19	lnc-CA1-1	chr8:86354387-86354466	NONHSAT127529
20	lnc-CA1-1	chr8:86356236-86356349	NONHSAT127527
21	lnc-RP11-219B4.6.1-1	chr8:86254978-86255029	NONHSAT127525
22	lnc-CA2-2	chr8:86452574-86452740	ENSG00000254380
23	lnc-CA1-1	chr8:86368852-86369092	ENSG00000253549.1
24	lnc-CA13-1	chr8:86142522-86142565	NONHSAT127521
25	lnc-CA2-2	chr8:86413304-86413414	XLOC_006864
26	lnc-CA1-1	chr8:86376811-86377144	ENSG00000253549.1
27	lnc-CA1-1	chr8:86375161-86375671	NONHSAT127527
28	lnc-CA2-3	chr8:86444927-86444978	FPKM1_group_31645_transcript_1
29	lnc-CA1-1	chr8:86354135-86354466	NONHSAT127527
30	lnc-RP11-219B4.5.1-1	chr8:86157624-86157946	NONHSAT127522
31	lnc-REXO1L1-3	chr8:86509528-86509569	NONHSAT127537
32	lnc-RP11-219B4.6.1-1	chr8:86244600-86244781	NONHSAT127524
33	lnc-CA2-1	chr8:86446631-86446811	XLOC_006865
34	lnc-CA1-1	chr8:86374965-86375030	ENSG00000253549.1
35	lnc-CA1-1	chr8:86374965-86375030	NONHSAT127527
36	lnc-CA2-2	chr8:86436128-86436354	ENSG00000254380

No data

(count:5 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CA13	hsa-miR-18a-5p	chr8:86196024-86196049
2	CA2	hsa-miR-26b-5p	chr8:86393132-86393151
3	CA13	hsa-miR-19b-3p	chr8:86194067-86194089
4	CA2	hsa-miR-26a-5p	chr8:86393131-86393151
5	CA13	hsa-miR-374b-5p	chr8:86196014-86196038

Variant related genes	Relation type
ENSG00000254380	TF binding region
ENSG00000253680	TF binding region
ENSG00000253549	TF binding region
CA3	TF binding region
CA2	TF binding region
CA1	TF binding region
CA13	TF binding region
ENSG00000258256	TF binding region
ENSG00000257962	TF binding region
ENSG00000254380	CpG island
ENSG00000253680	CpG island
ENSG00000253549	CpG island
CA3	CpG island
CA2	CpG island
CA1	CpG island
CA13	CpG island
ENSG00000258256	CpG island
ENSG00000257962	CpG island
ENSG00000176731	chromatin interactions
ENSG00000104267	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000147613	chromatin interactions
ENSG00000197451	chromatin interactions
ENSG00000257962	chromatin interactions
ENSG00000253549	chromatin interactions
ENSG00000253154	chromatin interactions
ENSG00000258256	chromatin interactions
ENSG00000254380	chromatin interactions
ENSG00000254231	chromatin interactions
ENSG00000260493	chromatin interactions
ENSG00000101104	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000133740	chromatin interactions
ENSG00000123124	chromatin interactions
ENSG00000147614	chromatin interactions
ENSG00000185015	chromatin interactions
ENSG00000100345	chromatin interactions
ENSG00000133742	chromatin interactions
ENSG00000254208	chromatin interactions
ENSG00000164879	chromatin interactions

Extended variants
information (count: 12833 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:12833 , 50 per page) page: 1 2 3 4 5 6 7 ... 257

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545770539	chr8:86142258-86142259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs547508014	chr8:86142263-86142264	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs150252022	chr8:86142454-86142455	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs564189885	chr8:86142457-86142458	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs187799636	chr8:86142572-86142573	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs139135672	chr8:86142610-86142611	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs143151978	chr8:86142638-86142639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2291786	chr8:86142725-86142726	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs554840108	chr8:86142855-86142856	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs574561595	chr8:86142889-86142890	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs574817699	chr8:86142918-86142919	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs540223417	chr8:86142926-86142927	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs374958854	chr8:86142951-86142952	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs561424248	chr8:86143012-86143013	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs147446292	chr8:86143021-86143022	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs369053344	chr8:86143029-86143030	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs577239560	chr8:86143082-86143083	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs192014834	chr8:86143137-86143138	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs79619336	chr8:86143163-86143164	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576284548	chr8:86143198-86143199	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs542189296	chr8:86143319-86143320	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs372508347	chr8:86143327-86143328	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs531642213	chr8:86143360-86143361	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183939072	chr8:86143367-86143368	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs527288174	chr8:86143488-86143489	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs187517764	chr8:86143490-86143491	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs564228102	chr8:86143506-86143507	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs191981936	chr8:86143568-86143569	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs184491668	chr8:86143574-86143575	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs376045220	chr8:86143640-86143641	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs543185188	chr8:86143650-86143651	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs59170491	chr8:86143684-86143685	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs187332422	chr8:86143692-86143693	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs149528906	chr8:86143736-86143737	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs79865282	chr8:86143738-86143739	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534221319	chr8:86143754-86143755	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs35878177	chr8:86143772-86143773	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs553848676	chr8:86143779-86143780	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs7829240	chr8:86143794-86143795	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs532675686	chr8:86143846-86143847	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs113708178	chr8:86143848-86143849	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs6986747	chr8:86143851-86143852	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs542003136	chr8:86143860-86143861	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs192886462	chr8:86143979-86143980	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs184420554	chr8:86144005-86144006	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs541035666	chr8:86144020-86144021	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs373192653	chr8:86144085-86144086	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566190521	chr8:86144093-86144094	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs563960312	chr8:86144126-86144127	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs200615722	chr8:86144175-86144176	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Gastric cancer	22014070	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Hepatocellular carcinoma	22267523	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:3578 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86133000-86143200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr8:86133000-86145800	Weak transcription	Gastric	stomach
3	chr8:86133800-86157200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:86134600-86157200	Weak transcription	Right Atrium	heart
5	chr8:86135200-86147000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr8:86135200-86155200	Weak transcription	Primary B cells from cord blood	blood
7	chr8:86135400-86151400	Weak transcription	HepG2	liver
8	chr8:86136000-86157200	Weak transcription	Liver	Liver
9	chr8:86136200-86157000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr8:86136400-86145800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr8:86136400-86157000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr8:86137400-86147000	Weak transcription	Fetal Intestine Large	intestine
13	chr8:86138200-86145800	Weak transcription	Fetal Intestine Small	intestine
14	chr8:86139600-86157200	Weak transcription	Pancreas	Pancrea
15	chr8:86141400-86143200	Enhancers	GM12878-XiMat	blood
16	chr8:86142000-86143200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr8:86142000-86143400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:86142200-86142800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:86142600-86157200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr8:86143200-86143400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:86143400-86146000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:86143600-86157000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr8:86145000-86157200	Weak transcription	Ovary	ovary
24	chr8:86145600-86151400	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr8:86145600-86157400	Weak transcription	Brain Angular Gyrus	brain
26	chr8:86145800-86146000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr8:86145800-86146200	ZNF genes & repeats	Gastric	stomach
28	chr8:86145800-86146400	Strong transcription	Fetal Intestine Small	intestine
29	chr8:86146000-86146200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr8:86146000-86146200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:86146000-86146200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr8:86146000-86146200	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
33	chr8:86146000-86146200	Enhancers	Stomach Mucosa	stomach
34	chr8:86146000-86146400	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr8:86146200-86146400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr8:86146200-86146600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr8:86146200-86146800	Weak transcription	Stomach Mucosa	stomach
38	chr8:86146200-86152600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr8:86146200-86156400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
40	chr8:86146200-86157200	Weak transcription	Gastric	stomach
41	chr8:86146400-86149000	Weak transcription	Fetal Intestine Small	intestine
42	chr8:86146400-86152400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr8:86146800-86148600	Enhancers	Stomach Mucosa	stomach
44	chr8:86147000-86147400	Enhancers	K562	blood
45	chr8:86147000-86149000	Enhancers	Duodenum Mucosa	Duodenum
46	chr8:86147000-86150800	Enhancers	Fetal Intestine Large	intestine
47	chr8:86147400-86147600	Enhancers	Small Intestine	intestine
48	chr8:86147600-86149200	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr8:86147600-86151800	Weak transcription	Small Intestine	intestine
50	chr8:86147800-86148000	Enhancers	Esophagus	oesophagus

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