Variant report

Variant	nsv886676
Chromosome Location	chr6:133111706-133168582
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2439)
CpG islands
(count:2325)
Chromatin interactive
region (count:144)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2439 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:133119218-133120465	K562	blood:	n/a	n/a
2	ARID3A	chr6:133119116-133119709	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:133119955-133120501	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:133164461-133164874	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:133151397-133151695	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:133144140-133144418	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:133151422-133151653	K562	blood:	n/a	n/a
8	ARID3A	chr6:133135176-133136074	K562	blood:	n/a	n/a
9	ARID3A	chr6:133133546-133134814	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:133135183-133135945	HepG2	liver:	n/a	n/a
11	ATF1	chr6:133154119-133154349	K562	blood:	n/a	n/a
12	ATF1	chr6:133144166-133144463	K562	blood:	n/a	n/a
13	ATF2	chr6:133135112-133136032	GM12878	blood:	n/a	n/a
14	ATF2	chr6:133139322-133140019	GM12878	blood:	n/a	n/a
15	ATF2	chr6:133138596-133141032	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr6:133135064-133136140	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr6:133141042-133141394	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr6:133133920-133136221	GM12878	blood:	n/a	n/a
19	ATF2	chr6:133137549-133138050	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr6:133140542-133141381	GM12878	blood:	n/a	n/a
21	ATF2	chr6:133135123-133137131	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr6:133119779-133120460	GM12878	blood:	n/a	n/a
23	ATF2	chr6:133141648-133142284	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:133134163-133135006	GM12878	blood:	n/a	n/a
25	ATF2	chr6:133137238-133138580	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr6:133140519-133141387	GM12878	blood:	n/a	n/a
27	ATF2	chr6:133138592-133141523	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:133136568-133136991	H1-hESC	embryonic stem cell:	n/a	n/a
29	ATF2	chr6:133120008-133120354	GM12878	blood:	n/a	n/a
30	ATF3	chr6:133135100-133135580	A549	lung:	n/a	n/a
31	ATF3	chr6:133135099-133135938	A549	lung:	n/a	n/a
32	ATF3	chr6:133135201-133135832	K562	blood:	n/a	n/a
33	BACH1	chr6:133133404-133133766	K562	blood:	n/a	n/a
34	BACH1	chr6:133119509-133119733	H1-hESC	embryonic stem cell:	n/a	n/a
35	BACH1	chr6:133141800-133142743	K562	blood:	n/a	n/a
36	BACH1	chr6:133135475-133135974	K562	blood:	n/a	n/a
37	BATF	chr6:133134664-133135001	GM12878	blood:	n/a	n/a
38	BATF	chr6:133134714-133135000	GM12878	blood:	n/a	n/a
39	BATF	chr6:133120048-133120330	GM12878	blood:	n/a	n/a
40	BATF	chr6:133133912-133134498	GM12878	blood:	n/a	chr6:133134171-133134182
41	BCL11A	chr6:133135567-133135850	GM12878	blood:	n/a	n/a
42	BCL11A	chr6:133135530-133135950	GM12878	blood:	n/a	n/a
43	BCL11A	chr6:133134668-133135043	GM12878	blood:	n/a	n/a
44	BCL3	chr6:133135314-133135961	GM12878	blood:	n/a	n/a
45	BCL3	chr6:133141639-133142381	A549	lung:	n/a	n/a
46	BCL3	chr6:133139176-133142713	A549	lung:	n/a	chr6:133140480-133140489
47	BCL3	chr6:133141699-133142239	GM12878	blood:	n/a	n/a
48	BCL3	chr6:133140179-133141582	GM12878	blood:	n/a	chr6:133140480-133140489
49	BCL3	chr6:133138857-133140029	K562	blood:	n/a	n/a
50	BCL3	chr6:133140220-133141232	K562	blood:	n/a	chr6:133140480-133140489

(count:2325 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:133135579-133135629	IMR90	lung:	fetal
2	chr6:133135564-133135614	GM19239	blood:	n/a
3	chr6:133137827-133137877	Hela-S3	cervix:	n/a
4	chr6:133136015-133136065	SAEC	small airway:	n/a
5	chr6:133135557-133135607	SK-N-SH_RA	brain:	n/a
6	chr6:133137893-133137943	HCF	heart:	n/a
7	chr6:133135524-133135574	NHBE	bronchial:	n/a
8	chr6:133135579-133135629	IMR90	lung:	fetal
9	chr6:133135564-133135614	GM19239	blood:	n/a
10	chr6:133137827-133137877	Hela-S3	cervix:	n/a
11	chr6:133136015-133136065	SAEC	small airway:	n/a
12	chr6:133135557-133135607	SK-N-SH_RA	brain:	n/a
13	chr6:133137893-133137943	HCF	heart:	n/a
14	chr6:133135524-133135574	NHBE	bronchial:	n/a
15	chr6:133135579-133135629	Hela-S3	cervix:	n/a
16	chr6:133122955-133123005	AG04450	lung:	fetal
17	chr6:133137167-133137217	HUVEC	blood vessel:	n/a
18	chr6:133135438-133135488	HCPEpiC	choroid plexus:	n/a
19	chr6:133136317-133136367	Hela-S3	cervix:	n/a
20	chr6:133120269-133120319	HIPEpiC	eye:	n/a
21	chr6:133122955-133123005	AoSMC	blood vessel:	n/a
22	chr6:133120269-133120319	AG09309	skin:	n/a
23	chr6:133120269-133120319	HCT-116	colon:	n/a
24	chr6:133135579-133135629	HRE	kidney:	n/a
25	chr6:133131884-133131934	HAEpiC	amniotic membrane:	n/a
26	chr6:133136135-133136185	HepG2	liver:	n/a
27	chr6:133119484-133119534	HRPEpiC	eye:	n/a
28	chr6:133120269-133120319	SK-N-MC	brain:	n/a
29	chr6:133138210-133138260	CMK	blood:	n/a
30	chr6:133137893-133137943	PrEC	prostate:	n/a
31	chr6:133119641-133119691	ProgFib	skin:	n/a
32	chr6:133135438-133135488	Hela-S3	cervix:	n/a
33	chr6:133138210-133138260	HEK293	kidney:	embryo
34	chr6:133135492-133135542	NHDF-neo	bronchial:	n/a
35	chr6:133134704-133134754	HCM	heart:	n/a
36	chr6:133137167-133137217	HAEpiC	amniotic membrane:	n/a
37	chr6:133119641-133119691	NHDF-neo	bronchial:	n/a
38	chr6:133131884-133131934	Hepatocyte	liver:	n/a
39	chr6:133135492-133135542	HNPCEpiC	eye:	n/a
40	chr6:133119734-133119784	NT2-D1	testis:	n/a
41	chr6:133135564-133135614	HEK293	kidney:	embryo
42	chr6:133135579-133135629	HIPEpiC	eye:	n/a
43	chr6:133137827-133137877	Hepatocyte	liver:	n/a
44	chr6:133116721-133116771	HNPCEpiC	eye:	n/a
45	chr6:133135438-133135488	RPTEC	kidney:	n/a
46	chr6:133122955-133123005	HRPEpiC	eye:	n/a
47	chr6:133137827-133137877	HAEpiC	amniotic membrane:	n/a
48	chr6:133137167-133137217	AG09309	skin:	n/a
49	chr6:133136015-133136065	NB4	blood:	n/a
50	chr6:133136347-133136397	T-47D	breast:	n/a

(count:144 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:52312335..52312919-chr6:133119372..133120190,2	HCT-116	colon:
2	chr1:159894871..159895411-chr6:133135389..133136277,2	Hela-S3	cervix:
3	chr6:133142863..133144465-chr9:131937930..131940573,2	MCF-7	breast:
4	chr14:69259781..69261291-chr6:133134489..133136848,2	MCF-7	breast:
5	chr6:132833194..132835178-chr6:133134140..133136704,2	MCF-7	breast:
6	chr6:133133823..133137064-chr6:133152471..133155832,4	K562	blood:
7	chr19:58873348..58874285-chr6:133135194..133136031,2	Hela-S3	cervix:
8	chr17:41393352..41393896-chr6:133154227..133154728,3	Hela-S3	cervix:
9	chr6:133104366..133109365-chr6:133114099..133117737,7	K562	blood:
10	chr20:52224699..52226307-chr6:133135521..133137429,2	MCF-7	breast:
11	chr6:133146833..133149424-chr6:133152798..133154698,2	K562	blood:
12	chr6:133125209..133127039-chr6:133127242..133130510,3	MCF-7	breast:
13	chr11:18417141..18419717-chr6:133139653..133142088,2	K562	blood:
14	chr6:133140432..133142390-chr6:133219540..133222428,2	MCF-7	breast:
15	chr6:133140486..133142664-chr6:133322602..133325155,3	K562	blood:
16	chr6:133142048..133144415-chr6:133161174..133163996,2	MCF-7	breast:
17	chr6:133142164..133143821-chr6:133206466..133209266,2	MCF-7	breast:
18	chr6:132774346..132776472-chr6:133129139..133131123,2	MCF-7	breast:
19	chr6:133150152..133152401-chr6:133214566..133217408,2	MCF-7	breast:
20	chr6:132935279..132937061-chr6:133139072..133141964,2	K562	blood:
21	chr19:1478974..1479621-chr6:133135658..133136245,2	Hela-S3	cervix:
22	chr6:133132887..133135811-chr6:134273188..134277510,5	K562	blood:
23	chr6:133122629..133124869-chr6:133126190..133128532,2	MCF-7	breast:
24	chr6:133151095..133151913-chr6:133282483..133283322,2	MCF-7	breast:
25	chr6:133134186..133135888-chr6:133168555..133170762,2	K562	blood:
26	chr6:133135683..133136351-chr9:130547259..130548177,2	Hela-S3	cervix:
27	chr1:33429448..33430407-chr6:133134991..133135963,2	Hela-S3	cervix:
28	chr6:133151125..133151898-chr6:133283825..133285077,5	MCF-7	breast:
29	chr6:133083233..133085227-chr6:133144108..133145647,2	K562	blood:
30	chr6:133151304..133151920-chr6:133833595..133834151,2	MCF-7	breast:
31	chr6:133135224..133137195-chr7:86974442..86977103,2	MCF-7	breast:
32	chr6:133151099..133152076-chr6:133282420..133283410,5	MCF-7	breast:
33	chr6:132832870..132835344-chr6:133122954..133125013,2	MCF-7	breast:
34	chr1:853806..855355-chr6:133134480..133137289,2	MCF-7	breast:
35	chr17:79479507..79480059-chr6:133135411..133136304,2	HCT-116	colon:
36	chr6:133140267..133142584-chr6:133384243..133385857,2	MCF-7	breast:
37	chr6:133151897..133155334-chr6:133156928..133160559,4	K562	blood:
38	chr6:133142048..133144415-chr6:133161174..133163996,2	MCF-7	breast:
39	chr6:133111344..133113707-chr6:133142113..133144354,2	K562	blood:
40	chr11:122932373..122933017-chr6:133135657..133136205,2	Hela-S3	cervix:
41	chr15:34330929..34333080-chr6:133140289..133142201,2	MCF-7	breast:
42	chr6:132832429..132834669-chr6:133134284..133137002,3	K562	blood:
43	chr6:133118544..133124606-chr6:133132137..133138834,13	MCF-7	breast:
44	chr6:133093368..133095334-chr6:133141299..133145047,3	K562	blood:
45	chr15:63449130..63449939-chr6:133135315..133135869,2	Hela-S3	cervix:
46	chr6:132965299..132967214-chr6:133134332..133136020,2	K562	blood:
47	chr6:132832857..132835191-chr6:133139455..133141127,3	K562	blood:
48	chr6:133135395..133135910-chr9:102668805..102669502,2	MCF-7	breast:
49	chr6:133132907..133137002-chr6:133163874..133168278,4	MCF-7	breast:
50	chr6:133139605..133142425-chr6:133167716..133170536,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf192-1	chr6:133134432-133134602	XLOC_005834
2	lnc-C6orf192-1	chr6:133125837-133126090	XLOC_005834
3	lnc-C6orf192-1	chr6:133125513-133125727	XLOC_005834

No data

Variant related genes	Relation type
SNORD101	TF binding region
RPS12	TF binding region
SNORA33	TF binding region
SLC18B1	TF binding region
SNORD100	TF binding region
SNORD101	CpG island
RPS12	CpG island
SNORA33	CpG island
SLC18B1	CpG island
SNORD100	CpG island
ENSG00000238059	chromatin interactions
ENSG00000085365	chromatin interactions
ENSG00000268050	chromatin interactions
ENSG00000271488	chromatin interactions
ENSG00000112306	chromatin interactions
ENSG00000158710	chromatin interactions
ENSG00000028839	chromatin interactions
ENSG00000005469	chromatin interactions
ENSG00000106399	chromatin interactions
ENSG00000185088	chromatin interactions
ENSG00000223764	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000268230	chromatin interactions
ENSG00000146410	chromatin interactions
ENSG00000269054	chromatin interactions
ENSG00000234484	chromatin interactions
ENSG00000146409	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000012048	chromatin interactions
ENSG00000227954	chromatin interactions
ENSG00000136807	chromatin interactions
ENSG00000131725	chromatin interactions
ENSG00000206754	chromatin interactions
ENSG00000136631	chromatin interactions
ENSG00000170190	chromatin interactions
ENSG00000174586	chromatin interactions
ENSG00000116514	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000169857	chromatin interactions
ENSG00000152818	chromatin interactions
ENSG00000185650	chromatin interactions
ENSG00000182165	chromatin interactions
ENSG00000137936	chromatin interactions
ENSG00000266070	chromatin interactions
ENSG00000235415	chromatin interactions
ENSG00000109971	chromatin interactions
ENSG00000079950	chromatin interactions
ENSG00000095066	chromatin interactions
ENSG00000273015	chromatin interactions
ENSG00000219545	chromatin interactions
ENSG00000112303	chromatin interactions
ENSG00000255145	chromatin interactions
ENSG00000204055	chromatin interactions
ENSG00000218194	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000187595	chromatin interactions
ENSG00000200534	chromatin interactions
ENSG00000134333	chromatin interactions
ENSG00000258429	chromatin interactions
ENSG00000072786	chromatin interactions
ENSG00000104885	chromatin interactions
ENSG00000119559	chromatin interactions
ENSG00000221500	chromatin interactions
ENSG00000188483	chromatin interactions
ENSG00000237110	chromatin interactions
ENSG00000245556	chromatin interactions
ENSG00000164091	chromatin interactions
ENSG00000093134	chromatin interactions
ENSG00000100207	chromatin interactions
ENSG00000146399	chromatin interactions
ENSG00000136874	chromatin interactions
SFRS5	miRNA target sites
LPP	miRNA target sites
SMAD5	miRNA target sites

Extended variants
information (count: 2545 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2545 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7770641	chr6:133111706-133111707	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181386642	chr6:133111751-133111752	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs112983766	chr6:133111872-133111873	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs370233916	chr6:133111884-133111885	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs377676263	chr6:133111893-133111894	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs79224753	chr6:133111913-133111914	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs534715527	chr6:133111924-133111925	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs185281072	chr6:133111996-133111997	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs72996126	chr6:133111999-133112000	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs543547507	chr6:133112057-133112058	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs189854282	chr6:133112126-133112127	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs140524209	chr6:133112143-133112144	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs562437542	chr6:133112202-133112203	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs543156745	chr6:133112418-133112419	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs79335067	chr6:133112458-133112459	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs76508361	chr6:133112467-133112468	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs577243903	chr6:133112483-133112484	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs569952856	chr6:133112526-133112527	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs183245144	chr6:133112583-133112584	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs141151138	chr6:133112616-133112617	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs544587775	chr6:133112715-133112716	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs115103406	chr6:133112750-133112751	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs549620888	chr6:133112783-133112784	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs569686420	chr6:133112793-133112794	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs17606700	chr6:133112822-133112823	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs535718804	chr6:133112828-133112829	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs58155972	chr6:133112840-133112841	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs565674427	chr6:133112888-133112889	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs374120096	chr6:133112924-133112925	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs118117902	chr6:133112970-133112971	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs557779709	chr6:133113020-133113021	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs577603773	chr6:133113027-133113028	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs7738256	chr6:133113066-133113067	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs186484572	chr6:133113083-133113084	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs535277540	chr6:133113088-133113089	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs529464281	chr6:133113089-133113090	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs551324567	chr6:133113091-133113092	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs191468755	chr6:133113104-133113105	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs183569285	chr6:133113136-133113137	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs188503918	chr6:133113195-133113196	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs386705996	chr6:133113221-133113222	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs182694001	chr6:133113222-133113223	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs7738569	chr6:133113237-133113238	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs186475882	chr6:133113262-133113263	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs142922162	chr6:133113326-133113327	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs553756627	chr6:133113364-133113365	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs369727965	chr6:133113365-133113366	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs138994218	chr6:133113368-133113369	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs555565026	chr6:133113375-133113376	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs551822588	chr6:133113380-133113381	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1577 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133083800-133118200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr6:133085000-133114600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
3	chr6:133085000-133119000	Weak transcription	Thymus	Thymus
4	chr6:133085200-133112200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:133085200-133119400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:133085400-133114400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr6:133085600-133118800	Weak transcription	Colon Smooth Muscle	Colon
8	chr6:133085800-133119000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr6:133086000-133112800	Weak transcription	Hela-S3	cervix
10	chr6:133086000-133113800	Weak transcription	NHEK	skin
11	chr6:133086000-133118800	Weak transcription	Fetal Kidney	kidney
12	chr6:133088600-133114600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr6:133089400-133111800	Weak transcription	Lung	lung
14	chr6:133089400-133119400	Weak transcription	Gastric	stomach
15	chr6:133089600-133111800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:133089600-133118800	Weak transcription	Fetal Heart	heart
17	chr6:133089600-133119000	Weak transcription	Primary hematopoietic stem cells	blood
18	chr6:133089600-133119200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr6:133089600-133119200	Weak transcription	Right Ventricle	heart
20	chr6:133089600-133119200	Weak transcription	Stomach Mucosa	stomach
21	chr6:133089600-133119400	Weak transcription	Pancreas	Pancrea
22	chr6:133089800-133118200	Weak transcription	Fetal Brain Male	brain
23	chr6:133089800-133118800	Weak transcription	Brain Angular Gyrus	brain
24	chr6:133090000-133118800	Weak transcription	HepG2	liver
25	chr6:133090400-133114200	Strong transcription	Primary T helper cells fromperipheralblood	blood
26	chr6:133091800-133119000	Weak transcription	Psoas Muscle	Psoas
27	chr6:133098400-133119000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:133098400-133119000	Weak transcription	Brain Substantia Nigra	brain
29	chr6:133098600-133118800	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr6:133099000-133113000	Strong transcription	Fetal Intestine Large	intestine
31	chr6:133100400-133112000	Weak transcription	Adipose Nuclei	Adipose
32	chr6:133100400-133114000	Weak transcription	Spleen	Spleen
33	chr6:133100400-133114200	Weak transcription	Fetal Brain Female	brain
34	chr6:133100400-133114400	Weak transcription	Brain Hippocampus Middle	brain
35	chr6:133100400-133118600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr6:133100400-133118800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr6:133100400-133119000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr6:133100600-133113600	Weak transcription	HMEC	breast
39	chr6:133100600-133114600	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr6:133100600-133114600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr6:133100600-133118000	Weak transcription	Small Intestine	intestine
42	chr6:133100600-133118200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr6:133100600-133118800	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr6:133100600-133118800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:133100600-133118800	Weak transcription	Rectal Smooth Muscle	rectum
46	chr6:133100600-133119000	Weak transcription	Aorta	Aorta
47	chr6:133100600-133119000	Weak transcription	Fetal Thymus	thymus
48	chr6:133100600-133119000	Weak transcription	Skeletal Muscle Female	skeletal muscle
49	chr6:133101000-133118800	Weak transcription	Liver	Liver
50	chr6:133103000-133119000	Weak transcription	Fetal Muscle Trunk	muscle

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