Variant report

Variant	nsv508497
Chromosome Location	chr8:10680621-10750255
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10697291-10697370	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:10696393-10696785	HepG2	liver:	n/a	n/a
3	ATF1	chr8:10733780-10734065	K562	blood:	n/a	n/a
4	ATF1	chr8:10697184-10697696	K562	blood:	n/a	chr8:10697396-10697410
5	ATF1	chr8:10722294-10722314	K562	blood:	n/a	n/a
6	ATF2	chr8:10697128-10697561	GM12878	blood:	n/a	chr8:10697398-10697409 chr8:10697396-10697410
7	ATF2	chr8:10697121-10697646	H1-hESC	embryonic stem cell:	n/a	chr8:10697398-10697409 chr8:10697396-10697410
8	ATF2	chr8:10697142-10697894	GM12878	blood:	n/a	chr8:10697398-10697409 chr8:10697396-10697410
9	ATF3	chr8:10697122-10697570	HepG2	liver:	n/a	chr8:10697399-10697419 chr8:10697398-10697411 chr8:10697399-10697407 chr8:10697396-10697409 chr8:10697396-10697407 chr8:10697400-10697407 chr8:10697397-10697407 chr8:10697398-10697409 chr8:10697388-10697408 chr8:10697396-10697411 chr8:10697398-10697409 chr8:10697188-10697199
10	ATF3	chr8:10697179-10697527	HepG2	liver:	n/a	chr8:10697399-10697419 chr8:10697398-10697411 chr8:10697399-10697407 chr8:10697396-10697409 chr8:10697396-10697407 chr8:10697400-10697407 chr8:10697397-10697407 chr8:10697398-10697409 chr8:10697388-10697408 chr8:10697396-10697411 chr8:10697398-10697409 chr8:10697188-10697199
11	ATF3	chr8:10697078-10697557	K562	blood:	n/a	chr8:10697399-10697419 chr8:10697398-10697411 chr8:10697399-10697407 chr8:10697396-10697409 chr8:10697396-10697407 chr8:10697400-10697407 chr8:10697397-10697407 chr8:10697398-10697409 chr8:10697388-10697408 chr8:10697396-10697411 chr8:10697398-10697409 chr8:10697188-10697199
12	ATF3	chr8:10697132-10697785	GM12878	blood:	n/a	chr8:10697399-10697419 chr8:10697398-10697411 chr8:10697399-10697407 chr8:10697396-10697409 chr8:10697396-10697407 chr8:10697400-10697407 chr8:10697397-10697407 chr8:10697398-10697409 chr8:10697388-10697408 chr8:10697396-10697411 chr8:10697398-10697409 chr8:10697188-10697199
13	ATF3	chr8:10697125-10697572	H1-hESC	embryonic stem cell:	n/a	chr8:10697399-10697419 chr8:10697398-10697411 chr8:10697399-10697407 chr8:10697396-10697409 chr8:10697396-10697407 chr8:10697400-10697407 chr8:10697397-10697407 chr8:10697398-10697409 chr8:10697388-10697408 chr8:10697396-10697411 chr8:10697398-10697409 chr8:10697188-10697199
14	ATF3	chr8:10697260-10697540	GM12878	blood:	n/a	chr8:10697399-10697419 chr8:10697398-10697411 chr8:10697399-10697407 chr8:10697396-10697409 chr8:10697396-10697407 chr8:10697400-10697407 chr8:10697397-10697407 chr8:10697398-10697409 chr8:10697388-10697408 chr8:10697396-10697411 chr8:10697398-10697409
15	ATF3	chr8:10697124-10697566	H1-hESC	embryonic stem cell:	n/a	chr8:10697399-10697419 chr8:10697398-10697411 chr8:10697399-10697407 chr8:10697396-10697409 chr8:10697396-10697407 chr8:10697400-10697407 chr8:10697397-10697407 chr8:10697398-10697409 chr8:10697388-10697408 chr8:10697396-10697411 chr8:10697398-10697409 chr8:10697188-10697199
16	ATF3	chr8:10697192-10697596	K562	blood:	n/a	chr8:10697399-10697419 chr8:10697398-10697411 chr8:10697399-10697407 chr8:10697396-10697409 chr8:10697396-10697407 chr8:10697400-10697407 chr8:10697397-10697407 chr8:10697398-10697409 chr8:10697388-10697408 chr8:10697396-10697411 chr8:10697398-10697409
17	BACH1	chr8:10709219-10709600	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCLAF1	chr8:10696343-10696842	GM12878	blood:	n/a	chr8:10696686-10696694
19	BHLHE40	chr8:10733794-10734097	K562	blood:	n/a	n/a
20	BHLHE40	chr8:10744698-10745016	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:10696305-10698013	GM12878	blood:	n/a	chr8:10697375-10697391 chr8:10697367-10697383
22	BHLHE40	chr8:10734300-10734588	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:10713932-10713944	GM12878	blood:	n/a	n/a
24	BHLHE40	chr8:10696968-10697822	HepG2	liver:	n/a	chr8:10697375-10697391 chr8:10697367-10697383
25	BHLHE40	chr8:10696344-10697885	K562	blood:	n/a	chr8:10697375-10697391 chr8:10697367-10697383
26	BHLHE40	chr8:10682842-10683140	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:10708116-10708434	GM12878	blood:	n/a	n/a
28	BRCA1	chr8:10697206-10697857	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr8:10696526-10696677	GM12878	blood:	n/a	n/a
30	BRCA1	chr8:10682855-10683017	GM12878	blood:	n/a	n/a
31	BRCA1	chr8:10696572-10696725	HepG2	liver:	n/a	n/a
32	BRCA1	chr8:10696372-10696808	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr8:10697211-10697471	HepG2	liver:	n/a	n/a
34	BRCA1	chr8:10697253-10697570	GM12878	blood:	n/a	n/a
35	BRCA1	chr8:10697238-10697731	H1-hESC	embryonic stem cell:	n/a	n/a
36	CBX3	chr8:10697135-10697883	K562	blood:	n/a	n/a
37	CBX3	chr8:10707934-10708310	K562	blood:	n/a	n/a
38	CCNT2	chr8:10696697-10697605	K562	blood:	n/a	n/a
39	CEBPB	chr8:10697193-10697743	Hela-S3	cervix:	n/a	chr8:10697549-10697557
40	CEBPB	chr8:10696818-10696934	HepG2	liver:	n/a	n/a
41	CEBPB	chr8:10700842-10701340	HepG2	liver:	n/a	chr8:10700989-10701000
42	CEBPB	chr8:10682886-10683181	A549	lung:	n/a	n/a
43	CEBPB	chr8:10702789-10702979	A549	lung:	n/a	chr8:10702809-10702820
44	CEBPB	chr8:10700849-10701087	H1-hESC	embryonic stem cell:	n/a	chr8:10700989-10701000
45	CEBPB	chr8:10684321-10684419	K562	blood:	n/a	n/a
46	CEBPB	chr8:10697270-10697470	HepG2	liver:	n/a	n/a
47	CEBPB	chr8:10700845-10701141	K562	blood:	n/a	chr8:10700989-10701000
48	CEBPB	chr8:10682862-10683216	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr8:10700867-10701158	IMR90	lung:	n/a	chr8:10700989-10701000
50	CEBPB	chr8:10700841-10701144	A549	lung:	n/a	chr8:10700989-10701000

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10695457-10695507	AG10803	skin:	n/a
2	chr8:10695457-10695507	AG10803	skin:	n/a
3	chr8:10709415-10709465	NB4	blood:	n/a
4	chr8:10736649-10736699	NT2-D1	testis:	n/a
5	chr8:10695457-10695507	HRE	kidney:	n/a
6	chr8:10683044-10683094	IMR90	lung:	fetal
7	chr8:10701153-10701203	A549	lung:	n/a
8	chr8:10736649-10736699	LNCaP	prostate:	n/a
9	chr8:10697698-10697748	NB4	blood:	n/a
10	chr8:10683266-10683316	SAEC	small airway:	n/a
11	chr8:10717687-10717737	HepG2	liver:	n/a
12	chr8:10683266-10683316	NHBE	bronchial:	n/a
13	chr8:10697633-10697683	HRPEpiC	eye:	n/a
14	chr8:10701153-10701203	U87	brain:	n/a
15	chr8:10686070-10686120	HEK293	kidney:	embryo
16	chr8:10695457-10695507	HUVEC	blood vessel:	n/a
17	chr8:10696571-10696621	PrEC	prostate:	n/a
18	chr8:10697698-10697748	HCPEpiC	choroid plexus:	n/a
19	chr8:10697017-10697067	U87	brain:	n/a
20	chr8:10736649-10736699	AoSMC	blood vessel:	n/a
21	chr8:10696689-10696739	T-47D	breast:	n/a
22	chr8:10696571-10696621	HRE	kidney:	n/a
23	chr8:10695457-10695507	RPTEC	kidney:	n/a
24	chr8:10686070-10686120	MCF-7	breast:	n/a
25	chr8:10708248-10708298	Caco-2	colon:	n/a
26	chr8:10697633-10697683	SK-N-SH_RA	brain:	n/a
27	chr8:10708248-10708298	HRPEpiC	eye:	n/a
28	chr8:10683188-10683238	Caco-2	colon:	n/a
29	chr8:10697540-10697590	NB4	blood:	n/a
30	chr8:10697546-10697596	AG09309	skin:	n/a
31	chr8:10697540-10697590	NHDF-neo	bronchial:	n/a
32	chr8:10696639-10696689	GM12892	blood:	n/a
33	chr8:10683167-10683217	ovcar-3	ovarian:	n/a
34	chr8:10697365-10697415	IMR90	lung:	fetal
35	chr8:10697633-10697683	SK-N-MC	brain:	n/a
36	chr8:10701153-10701203	HUVEC	blood vessel:	n/a
37	chr8:10686070-10686120	GM12891	blood:	n/a
38	chr8:10717687-10717737	ECC-1	luminal epithelium:	n/a
39	chr8:10696571-10696621	LNCaP	prostate:	n/a
40	chr8:10695457-10695507	GM06990	blood:	n/a
41	chr8:10686070-10686120	SKMC	muscle:	n/a
42	chr8:10683139-10683189	GM12891	blood:	n/a
43	chr8:10697350-10697400	NHDF-neo	bronchial:	n/a
44	chr8:10697633-10697683	AG10803	skin:	n/a
45	chr8:10694831-10694881	MCF10A-Er-Src	breast:	n/a
46	chr8:10697350-10697400	NT2-D1	testis:	n/a
47	chr8:10736649-10736699	SK-N-SH_RA	brain:	n/a
48	chr8:10683044-10683094	NH-A	brain:	n/a
49	chr8:10697698-10697748	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:10698115-10698165	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:10528112..10530692-chr8:10696880..10699073,2	K562	blood:
2	chr8:10442713..10444669-chr8:10687154..10689359,2	K562	blood:
3	chr8:10683525..10686850-chr8:10694502..10697878,5	K562	blood:
4	chr8:10687103..10689280-chr8:10695921..10698730,3	MCF-7	breast:
5	chr8:10736875..10738986-chr8:10748805..10751252,2	MCF-7	breast:
6	chr8:10735412..10737707-chr8:10739403..10741216,2	K562	blood:
7	chr8:10694766..10696620-chr8:10707984..10711858,3	K562	blood:
8	chr8:10696105..10699610-chr8:10701195..10704333,4	K562	blood:
9	chr8:10742152..10743978-chr8:10754413..10756262,2	K562	blood:
10	chr8:10444435..10445487-chr8:10682600..10683390,5	MCF-7	breast:
11	chr8:10696188..10698315-chr8:10720440..10722479,2	K562	blood:
12	chr8:10712367..10714043-chr8:10772145..10774622,2	K562	blood:
13	chr8:10713177..10714693-chr8:10715821..10718106,2	K562	blood:
14	chr8:10690421..10694581-chr8:10695821..10698975,5	MCF-7	breast:
15	chr8:10709949..10712901-chr8:10721572..10724488,2	K562	blood:
16	chr8:10694766..10696620-chr8:10707984..10711858,3	K562	blood:
17	chr8:10695083..10698096-chr8:10698399..10704123,5	MCF-7	breast:
18	chr8:10421700..10424416-chr8:10707916..10710717,2	K562	blood:
19	chr8:10697642..10700130-chr8:10739492..10741230,2	MCF-7	breast:
20	chr8:10695510..10697955-chr8:10737190..10739802,3	K562	blood:
21	chr8:10444970..10445545-chr8:10682548..10683133,2	K562	blood:
22	chr8:10704113..10707157-chr8:10708528..10711302,3	K562	blood:
23	chr8:10698588..10701340-chr8:10707877..10710220,2	MCF-7	breast:
24	chr8:10687156..10690707-chr8:10693616..10698468,7	K562	blood:
25	chr8:10709949..10712901-chr8:10721572..10724488,2	K562	blood:
26	chr7:6048462..6049308-chr8:10696898..10697687,2	Hela-S3	cervix:
27	chr8:10711587..10713736-chr8:10731150..10732656,2	K562	blood:
28	chr8:10582499..10584929-chr8:10712844..10715124,2	K562	blood:
29	chr8:10675871..10677525-chr8:10687580..10689455,2	MCF-7	breast:
30	chr8:10695954..10697810-chr8:10705274..10708188,2	K562	blood:
31	chr8:10700359..10702352-chr8:10709225..10710771,2	K562	blood:
32	chr8:10696353..10698510-chr8:10723072..10725077,2	K562	blood:
33	chr8:10737387..10739768-chr8:10741802..10743720,2	K562	blood:
34	chr8:10704113..10707157-chr8:10708528..10711302,3	K562	blood:
35	chr8:10707686..10708314-chr8:11136770..11137601,3	MCF-7	breast:
36	chr8:10739545..10741704-chr8:10806254..10808140,2	K562	blood:
37	chr8:10698588..10701340-chr8:10707877..10710220,2	MCF-7	breast:
38	chr8:10694381..10696683-chr8:10699083..10701009,2	K562	blood:
39	chr8:10683001..10685748-chr8:10686026..10689497,3	K562	blood:
40	chr8:10687146..10690339-chr8:10690695..10692954,3	K562	blood:
41	chr8:10713177..10714693-chr8:10715821..10718106,2	K562	blood:
42	chr8:10692044..10695028-chr8:10695086..10697405,2	MCF-7	breast:
43	chr8:10444886..10445502-chr8:10682512..10683360,2	MCF-7	breast:
44	chr8:10674954..10678350-chr8:10693952..10697087,3	K562	blood:
45	chr8:10711587..10713736-chr8:10731150..10732656,2	K562	blood:
46	chr8:10407992..10408718-chr8:10682226..10683074,2	MCF-7	breast:
47	chr8:10674524..10677009-chr8:10677940..10680830,2	K562	blood:
48	chr8:10683547..10686608-chr8:10694341..10697878,5	K562	blood:
49	chr8:10734114..10739768-chr8:10740375..10743720,5	K562	blood:
50	chr8:10447726..10448226-chr8:10680360..10680981,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf74-2	chr8:10703728-10704018	NONHSAT125020
2	lnc-C8orf74-5	chr8:10741138-10741453	l_3549_chr8:10734846-10741453_testes
3	lnc-C8orf74-2	chr8:10697463-10697586	NONHSAT125020
4	lnc-C8orf74-5	chr8:10735041-10735080	l_3549_chr8:10734846-10741453_testes
5	lnc-C8orf74-2	chr8:10703728-10704011	ENSG00000253695.1
6	lnc-C8orf74-2	chr8:10699143-10699244	NONHSAT125020
7	lnc-C8orf74-5	chr8:10734847-10734996	l_3549_chr8:10734846-10741453_testes
8	lnc-C8orf74-3	chr8:10708201-10708241	XLOC_006709
9	lnc-C8orf74-2	chr8:10699143-10699244	ENSG00000253695.1
10	lnc-C8orf74-3	chr8:10713726-10714106	XLOC_006709
11	lnc-C8orf74-5	chr8:10736553-10736654	l_3549_chr8:10734846-10741453_testes
12	lnc-C8orf74-2	chr8:10698071-10698138	NONHSAT125020
13	lnc-C8orf74-3	chr8:10714568-10714730	XLOC_006709
14	lnc-C8orf74-2	chr8:10699143-10699244	NONHSAT125021
15	lnc-PINX1-2	chr8:10713595-10716946	NONHSAT125023
16	lnc-C8orf74-5	chr8:10735481-10735548	l_3549_chr8:10734846-10741453_testes
17	lnc-C8orf74-2	chr8:10698086-10698138	ENSG00000253695.1
18	lnc-C8orf74-3	chr8:10713900-10714089	XLOC_006709
19	lnc-C8orf74-2	chr8:10703679-10705076	NONHSAT125021
20	lnc-C8orf74-2	chr8:10698086-10698138	NONHSAT125021

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1322	chr8:10682885-10682903	MIMAT0005953

Variant related genes	Relation type
SOX7	TF binding region
PINX1	TF binding region
ENSG00000253695	TF binding region
ENSG00000258724	TF binding region
SOX7	CpG island
PINX1	CpG island
ENSG00000253695	CpG island
ENSG00000258724	CpG island
ENSG00000106305	chromatin interactions
ENSG00000122512	chromatin interactions
ENSG00000258724	chromatin interactions
ENSG00000157653	chromatin interactions
ENSG00000148229	chromatin interactions
ENSG00000254093	chromatin interactions
ENSG00000171060	chromatin interactions
ENSG00000253695	chromatin interactions

Extended variants
information (count: 3392 )
Associated
traits (count: 142 )

Variant overlapped rSNPs/rCNVs (count:3392 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532235454	chr8:10680649-10680650	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189613294	chr8:10680695-10680696	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs576097475	chr8:10680716-10680717	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs193247891	chr8:10680725-10680726	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs139884359	chr8:10680734-10680735	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535660544	chr8:10680757-10680758	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149840713	chr8:10680778-10680779	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs73208793	chr8:10680785-10680786	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs36080074	chr8:10680806-10680807	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs397746307	chr8:10680809-10680810	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs76926466	chr8:10680828-10680829	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185271468	chr8:10680853-10680854	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs532481813	chr8:10680873-10680874	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376401347	chr8:10680881-10680882	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552245564	chr8:10680885-10680886	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368855246	chr8:10680896-10680897	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113142854	chr8:10680928-10680929	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536020052	chr8:10680929-10680930	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370783284	chr8:10680957-10680958	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs531710670	chr8:10680971-10680972	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141954932	chr8:10681007-10681008	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs150462634	chr8:10681027-10681028	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs553848658	chr8:10681028-10681029	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs117263379	chr8:10681032-10681033	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs533818854	chr8:10681080-10681081	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547615284	chr8:10681093-10681094	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115871379	chr8:10681128-10681129	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539581744	chr8:10681139-10681140	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs575518078	chr8:10681151-10681152	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs144228426	chr8:10681198-10681199	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575972775	chr8:10681206-10681207	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs147793165	chr8:10681212-10681213	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73208794	chr8:10681248-10681249	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs117502369	chr8:10681249-10681250	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114540864	chr8:10681273-10681274	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs551652123	chr8:10681275-10681276	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577021411	chr8:10681292-10681293	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545924248	chr8:10681316-10681317	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562627207	chr8:10681323-10681324	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531678227	chr8:10681330-10681331	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs28549373	chr8:10681353-10681354	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs181327812	chr8:10681373-10681374	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527591206	chr8:10681392-10681393	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs148840987	chr8:10681409-10681410	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs570706161	chr8:10681415-10681416	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs533135628	chr8:10681435-10681436	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183875511	chr8:10681443-10681444	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs143500644	chr8:10681468-10681469	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535171446	chr8:10681478-10681479	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555352887	chr8:10681497-10681498	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:142)

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
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
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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD
Renal cell carcinoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1311 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10647000-10681200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr8:10648200-10683400	Weak transcription	Brain Angular Gyrus	brain
3	chr8:10657400-10681400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr8:10657400-10685800	Weak transcription	Psoas Muscle	Psoas
5	chr8:10657600-10681800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr8:10659600-10682400	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr8:10663000-10681200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
8	chr8:10663000-10681400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr8:10663000-10696200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr8:10665400-10680800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr8:10665800-10688200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chr8:10666400-10695200	Strong transcription	Primary T cells from cord blood	blood
13	chr8:10666800-10692400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr8:10667600-10693200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr8:10668400-10682400	Weak transcription	Colonic Mucosa	Colon
16	chr8:10668400-10696200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr8:10668600-10681400	Weak transcription	A549	lung
18	chr8:10669200-10692800	Strong transcription	Primary B cells from cord blood	blood
19	chr8:10669400-10692200	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr8:10669600-10691800	Strong transcription	GM12878-XiMat	blood
21	chr8:10669600-10692800	Strong transcription	Primary T helper cells PMA-I stimulated	--
22	chr8:10670200-10680800	Weak transcription	Placenta	Placenta
23	chr8:10670200-10692000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr8:10670400-10692800	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr8:10671000-10681000	Weak transcription	Osteobl	bone
26	chr8:10671400-10692000	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr8:10672000-10681200	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr8:10673000-10686800	Strong transcription	Fetal Thymus	thymus
29	chr8:10673000-10692000	Strong transcription	Primary B cells from peripheral blood	blood
30	chr8:10673200-10682600	Weak transcription	Fetal Brain Male	brain
31	chr8:10673200-10683000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr8:10673200-10686600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr8:10673200-10692200	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr8:10673200-10692400	Strong transcription	HUES6 Cell Line	embryonic stem cell
35	chr8:10673400-10684600	Weak transcription	Small Intestine	intestine
36	chr8:10673800-10683400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:10673800-10684000	Weak transcription	Primary neutrophils fromperipheralblood	blood
38	chr8:10673800-10692000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr8:10674000-10690200	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr8:10674200-10681400	Weak transcription	Fetal Kidney	kidney
41	chr8:10674400-10692000	Strong transcription	Stomach Smooth Muscle	stomach
42	chr8:10674400-10692800	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr8:10674600-10692000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr8:10674600-10692000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr8:10674600-10692000	Strong transcription	Fetal Muscle Leg	muscle
46	chr8:10674600-10692200	Strong transcription	HUES64 Cell Line	embryonic stem cell
47	chr8:10674600-10692200	Strong transcription	Duodenum Smooth Muscle	Duodenum
48	chr8:10674600-10693200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
49	chr8:10674800-10696200	Weak transcription	Stomach Mucosa	stomach
50	chr8:10675000-10681800	Weak transcription	Right Ventricle	heart

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