Variant report

Variant	nsv884444
Chromosome Location	chr6:31756670-31768217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1214)
CpG islands
(count:4644)
Chromatin interactive
region (count:55)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1214 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31759119-31759394	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:31759069-31759416	K562	blood:	n/a	n/a
3	ARID3A	chr6:31763502-31763947	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:31763554-31764074	K562	blood:	n/a	n/a
5	ARID3A	chr6:31761944-31762639	K562	blood:	n/a	n/a
6	ATF2	chr6:31763566-31764057	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr6:31763619-31764006	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr6:31757039-31757512	GM12878	blood:	n/a	n/a
9	ATF3	chr6:31763079-31763875	K562	blood:	n/a	chr6:31763644-31763653
10	ATF3	chr6:31763531-31763886	A549	lung:	n/a	chr6:31763644-31763653
11	ATF3	chr6:31763328-31763991	K562	blood:	n/a	chr6:31763644-31763653
12	BACH1	chr6:31762945-31763355	K562	blood:	n/a	n/a
13	BACH1	chr6:31763634-31763834	K562	blood:	n/a	n/a
14	BATF	chr6:31757156-31757438	GM12878	blood:	n/a	n/a
15	BATF	chr6:31757142-31757413	GM12878	blood:	n/a	n/a
16	BATF	chr6:31763618-31763815	GM12878	blood:	n/a	n/a
17	BCL11A	chr6:31757133-31757472	GM12878	blood:	n/a	n/a
18	BCL11A	chr6:31757072-31757527	GM12878	blood:	n/a	n/a
19	BCL3	chr6:31763260-31763930	GM12878	blood:	n/a	chr6:31763469-31763482 chr6:31763390-31763403 chr6:31763475-31763488 chr6:31763803-31763816 chr6:31763526-31763539
20	BCL3	chr6:31762535-31764219	K562	blood:	n/a	chr6:31763469-31763482 chr6:31763390-31763403 chr6:31763475-31763488 chr6:31763803-31763816 chr6:31763526-31763539
21	BCL3	chr6:31763225-31763562	A549	lung:	n/a	chr6:31763469-31763482 chr6:31763390-31763403 chr6:31763475-31763488 chr6:31763526-31763539
22	BCLAF1	chr6:31763200-31764057	K562	blood:	n/a	chr6:31763469-31763482 chr6:31763390-31763403 chr6:31763475-31763488 chr6:31763803-31763816 chr6:31763526-31763539
23	BCLAF1	chr6:31763162-31763979	GM12878	blood:	n/a	chr6:31763469-31763482 chr6:31763390-31763403 chr6:31763475-31763488 chr6:31763803-31763816 chr6:31763526-31763539
24	BCLAF1	chr6:31762987-31764044	GM12878	blood:	n/a	chr6:31763469-31763482 chr6:31763390-31763403 chr6:31763475-31763488 chr6:31763803-31763816 chr6:31763526-31763539
25	BCLAF1	chr6:31763029-31764091	K562	blood:	n/a	chr6:31763469-31763482 chr6:31763390-31763403 chr6:31763475-31763488 chr6:31763803-31763816 chr6:31763526-31763539
26	BCLAF1	chr6:31757086-31757555	GM12878	blood:	n/a	n/a
27	BHLHE40	chr6:31762008-31764113	K562	blood:	n/a	chr6:31763475-31763491 chr6:31763368-31763384 chr6:31763467-31763483
28	BHLHE40	chr6:31763314-31764058	GM12878	blood:	n/a	chr6:31763475-31763491 chr6:31763368-31763384 chr6:31763467-31763483
29	BHLHE40	chr6:31763273-31763916	HepG2	liver:	n/a	chr6:31763475-31763491 chr6:31763368-31763384 chr6:31763467-31763483
30	BHLHE40	chr6:31762386-31762600	HepG2	liver:	n/a	n/a
31	BHLHE40	chr6:31759175-31759452	K562	blood:	n/a	n/a
32	BRCA1	chr6:31763007-31763305	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr6:31763367-31763932	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr6:31763593-31763894	HepG2	liver:	n/a	n/a
35	BRCA1	chr6:31763685-31764054	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr6:31763118-31763294	HepG2	liver:	n/a	n/a
37	CBX3	chr6:31762834-31764422	K562	blood:	n/a	n/a
38	CBX3	chr6:31762810-31764194	K562	blood:	n/a	n/a
39	CBX3	chr6:31761898-31762762	K562	blood:	n/a	n/a
40	CCNT2	chr6:31762037-31762879	K562	blood:	n/a	chr6:31762577-31762586 chr6:31762207-31762227
41	CCNT2	chr6:31763079-31764065	K562	blood:	n/a	n/a
42	CEBPB	chr6:31763462-31763978	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr6:31763691-31763701	K562	blood:	n/a	n/a
44	CEBPB	chr6:31762231-31762580	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr6:31762166-31762548	K562	blood:	n/a	n/a
46	CEBPB	chr6:31763492-31764085	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr6:31763559-31764206	K562	blood:	n/a	n/a
48	CEBPB	chr6:31761944-31762625	K562	blood:	n/a	n/a
49	CEBPD	chr6:31763438-31763647	HepG2	liver:	n/a	n/a
50	CEBPD	chr6:31763272-31763929	HepG2	liver:	n/a	n/a

(count:4644 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31764656-31764706	AG04450	lung:	fetal
2	chr6:31759486-31759536	NB4	blood:	n/a
3	chr6:31760796-31760846	HL-60	blood:	n/a
4	chr6:31765083-31765133	Caco-2	colon:	n/a
5	chr6:31762723-31762773	GM19239	blood:	n/a
6	chr6:31759834-31759884	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:31760383-31760433	HCT-116	colon:	n/a
8	chr6:31762630-31762680	HIPEpiC	eye:	n/a
9	chr6:31764656-31764706	AG04450	lung:	fetal
10	chr6:31759486-31759536	NB4	blood:	n/a
11	chr6:31760796-31760846	HL-60	blood:	n/a
12	chr6:31765083-31765133	Caco-2	colon:	n/a
13	chr6:31762723-31762773	GM19239	blood:	n/a
14	chr6:31759834-31759884	HPAEpiC	pulmonary alveolar:	n/a
15	chr6:31760383-31760433	HCT-116	colon:	n/a
16	chr6:31762630-31762680	HIPEpiC	eye:	n/a
17	chr6:31762630-31762680	NT2-D1	testis:	n/a
18	chr6:31763282-31763332	NB4	blood:	n/a
19	chr6:31762555-31762605	HEK293	kidney:	embryo
20	chr6:31762442-31762492	HEEpiC	esophagus:	n/a
21	chr6:31763282-31763332	LNCaP	prostate:	n/a
22	chr6:31760767-31760817	ovcar-3	ovarian:	n/a
23	chr6:31761055-31761105	H1-hESC	embryonic stem cell:	embryo
24	chr6:31760767-31760817	GM19239	blood:	n/a
25	chr6:31760006-31760056	HEEpiC	esophagus:	n/a
26	chr6:31763551-31763601	PFSK-1	brain:	n/a
27	chr6:31767074-31767124	ProgFib	skin:	n/a
28	chr6:31763470-31763520	HCM	heart:	n/a
29	chr6:31762688-31762738	Hepatocyte	liver:	n/a
30	chr6:31760767-31760817	PFSK-1	brain:	n/a
31	chr6:31760608-31760658	NHDF-neo	bronchial:	n/a
32	chr6:31759513-31759563	LNCaP	prostate:	n/a
33	chr6:31760288-31760338	ProgFib	skin:	n/a
34	chr6:31767750-31767800	ECC-1	luminal epithelium:	n/a
35	chr6:31762776-31762826	SK-N-SH_RA	brain:	n/a
36	chr6:31762630-31762680	HAEpiC	amniotic membrane:	n/a
37	chr6:31760047-31760097	HUVEC	blood vessel:	n/a
38	chr6:31762555-31762605	HCF	heart:	n/a
39	chr6:31765195-31765245	HCM	heart:	n/a
40	chr6:31763377-31763427	GM12891	blood:	n/a
41	chr6:31765195-31765245	AoSMC	blood vessel:	n/a
42	chr6:31762555-31762605	ECC-1	luminal epithelium:	n/a
43	chr6:31760345-31760395	NHDF-neo	bronchial:	n/a
44	chr6:31765083-31765133	GM19239	blood:	n/a
45	chr6:31759412-31759462	CMK	blood:	n/a
46	chr6:31760593-31760643	GM12878	blood:	n/a
47	chr6:31765634-31765684	HCF	heart:	n/a
48	chr6:31765567-31765617	H1-hESC	embryonic stem cell:	embryo
49	chr6:31764656-31764706	AoSMC	blood vessel:	n/a
50	chr6:31758897-31758947	AG10803	skin:	n/a

(count:55 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:31758631..31763066-chr6:31827655..31831615,4	K562	blood:
2	chr6:31706414..31709644-chr6:31760309..31763318,4	MCF-7	breast:
3	chr6:31685559..31688052-chr6:31762150..31763709,2	MCF-7	breast:
4	chr6:31707530..31710458-chr6:31763602..31765832,2	MCF-7	breast:
5	chr6:31759098..31761444-chr6:32081984..32084051,2	K562	blood:
6	chr6:31762216..31763831-chr6:31854405..31856951,2	MCF-7	breast:
7	chr6:31626696..31628687-chr6:31762053..31764771,3	MCF-7	breast:
8	chr6:31760037..31761914-chr6:31767619..31769119,2	MCF-7	breast:
9	chr6:31758779..31760923-chr6:31939769..31942169,2	K562	blood:
10	chr6:31761659..31764051-chr6:31869423..31871582,3	K562	blood:
11	chr6:31763803..31765429-chr6:31940244..31942129,2	K562	blood:
12	chr6:31684792..31688095-chr6:31761930..31764765,3	MCF-7	breast:
13	chr6:31741149..31744902-chr6:31760858..31763694,5	MCF-7	breast:
14	chr6:31754468..31756767-chr6:31794972..31797010,2	MCF-7	breast:
15	chr6:31767528..31770908-chr6:31772125..31775627,6	MCF-7	breast:
16	chr6:31619065..31621303-chr6:31762386..31764649,2	MCF-7	breast:
17	chr6:31761659..31763884-chr6:31868027..31870923,3	K562	blood:
18	chr6:31764746..31766452-chr6:31831134..31833580,2	K562	blood:
19	chr6:31764901..31767310-chr6:31801623..31804190,2	MCF-7	breast:
20	chr6:31648224..31648787-chr6:31758999..31759731,2	MCF-7	breast:
21	chr6:31760815..31765798-chr6:31772413..31777523,17	MCF-7	breast:
22	chr6:31759482..31765185-chr6:31781824..31784897,13	MCF-7	breast:
23	chr6:31761979..31764717-chr6:31829414..31832230,4	MCF-7	breast:
24	chr6:31762749..31764673-chr6:32143789..32146313,2	K562	blood:
25	chr6:31761655..31763549-chr6:31865451..31867211,2	MCF-7	breast:
26	chr6:31763546..31764167-chr6:31782631..31783559,2	K562	blood:
27	chr6:31649204..31651280-chr6:31762211..31763800,2	MCF-7	breast:
28	chr6:31761963..31763938-chr6:32162269..32164335,2	MCF-7	breast:
29	chr6:31760851..31764032-chr6:31800769..31804370,7	MCF-7	breast:
30	chr6:31429705..31431328-chr6:31762595..31764431,2	K562	blood:
31	chr6:31767775..31769625-chr6:31827147..31829502,2	K562	blood:
32	chr6:31763649..31765429-chr6:31938517..31942129,4	K562	blood:
33	chr6:31702768..31704359-chr6:31759116..31761149,2	MCF-7	breast:
34	chr6:31762561..31765176-chr6:31866590..31868817,2	MCF-7	breast:
35	chr6:31763762..31765403-chr6:31864017..31865779,2	MCF-7	breast:
36	chr6:31764794..31767222-chr6:31789462..31791730,2	MCF-7	breast:
37	chr6:31758020..31763887-chr6:31863868..31868391,6	K562	blood:
38	chr6:31647614..31649375-chr6:31762314..31763878,2	MCF-7	breast:
39	chr15:90808542..90809340-chr6:31762980..31763831,2	Hela-S3	cervix:
40	chr6:31587253..31589657-chr6:31761134..31763419,2	MCF-7	breast:
41	chr6:31620215..31622719-chr6:31761944..31763523,2	MCF-7	breast:
42	chr6:31756951..31764627-chr6:31780500..31799197,32	MCF-7	breast:
43	chr6:31667922..31671961-chr6:31761581..31764967,5	MCF-7	breast:
44	chr6:31764734..31766726-chr6:31783206..31784816,2	MCF-7	breast:
45	chr6:31761456..31762985-chr6:31846516..31848351,2	K562	blood:
46	chr6:31695390..31696984-chr6:31762234..31763768,2	MCF-7	breast:
47	chr6:31743360..31746217-chr6:31755901..31759903,4	MCF-7	breast:
48	chr6:31761672..31765296-chr6:31772847..31776146,6	MCF-7	breast:
49	chr6:31696888..31697817-chr6:31762900..31763783,2	K562	blood:
50	chr6:31761047..31764270-chr6:31827785..31831725,4	MCF-7	breast:

No data

Variant related genes	Relation type
VARS	TF binding region
VARS	CpG island
ENSG00000204439	chromatin interactions
ENSG00000204396	chromatin interactions
ENSG00000255152	chromatin interactions
ENSG00000204392	chromatin interactions
ENSG00000204427	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000204388	chromatin interactions
ENSG00000204308	chromatin interactions
ENSG00000213719	chromatin interactions
ENSG00000204385	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000182768	chromatin interactions
ENSG00000213654	chromatin interactions
ENSG00000227198	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000204444	chromatin interactions
ENSG00000201823	chromatin interactions
ENSG00000204428	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000264672	chromatin interactions
ENSG00000233902	chromatin interactions
ENSG00000168477	chromatin interactions
ENSG00000204387	chromatin interactions
ENSG00000204410	chromatin interactions
ENSG00000204310	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000204463	chromatin interactions
ENSG00000206337	chromatin interactions
ENSG00000204389	chromatin interactions
ENSG00000204371	chromatin interactions
ENSG00000204420	chromatin interactions
ENSG00000266776	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000108389	chromatin interactions
ENSG00000204394	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000166278	chromatin interactions

Extended variants
information (count: 355 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:355 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549704529	chr6:31756687-31756688	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs192791820	chr6:31756737-31756738	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs564547444	chr6:31756744-31756745	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs553292624	chr6:31756759-31756760	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs183763957	chr6:31756762-31756763	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs546932483	chr6:31756763-31756764	Weak transcription Strong transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs115050884	chr6:31756802-31756803	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs55761205	chr6:31756803-31756804	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs188097087	chr6:31756856-31756857	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs192546132	chr6:31756982-31756983	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs201078154	chr6:31757028-31757029	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs56291059	chr6:31757045-31757046	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs114778939	chr6:31757190-31757191	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs557944148	chr6:31757270-31757271	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs570484849	chr6:31757400-31757401	Strong transcription Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs117678546	chr6:31757401-31757402	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs552928558	chr6:31757419-31757420	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs184771143	chr6:31757442-31757443	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs574388410	chr6:31757492-31757493	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs140088572	chr6:31757540-31757541	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs189158375	chr6:31757568-31757569	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs575634772	chr6:31757573-31757574	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs557963596	chr6:31757661-31757662	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs181648263	chr6:31757665-31757666	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs540419645	chr6:31757726-31757727	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs373624594	chr6:31757732-31757733	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs575080628	chr6:31757766-31757767	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs562105211	chr6:31757770-31757771	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs377137424	chr6:31757790-31757791	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs142006308	chr6:31757791-31757792	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs186708406	chr6:31757802-31757803	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs569173765	chr6:31757844-31757845	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs533455198	chr6:31757874-31757875	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs536213828	chr6:31757882-31757883	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs551510538	chr6:31757896-31757897	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs566998234	chr6:31758002-31758003	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs4959081	chr6:31758050-31758051	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs4959019	chr6:31758064-31758065	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs369565743	chr6:31758090-31758091	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs189537173	chr6:31758145-31758146	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs552825228	chr6:31758163-31758164	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs568028252	chr6:31758190-31758191	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs535415487	chr6:31758195-31758196	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs181081265	chr6:31758241-31758242	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs546123534	chr6:31758309-31758310	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs557930223	chr6:31758443-31758444	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs572995806	chr6:31758458-31758459	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs185098101	chr6:31758501-31758502	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs189563889	chr6:31758521-31758522	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs573812028	chr6:31758569-31758570	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1126 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31745000-31760200	Weak transcription	Psoas Muscle	Psoas
2	chr6:31745000-31762400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr6:31745200-31760400	Weak transcription	Fetal Brain Male	brain
4	chr6:31745200-31761000	Strong transcription	Fetal Stomach	stomach
5	chr6:31745400-31761600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:31745400-31762800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr6:31745600-31758800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:31745600-31759400	Strong transcription	Dnd41	blood
9	chr6:31745600-31760400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr6:31745600-31760400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:31745600-31760600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr6:31745600-31760800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr6:31745600-31760800	Strong transcription	HUES6 Cell Line	embryonic stem cell
14	chr6:31745600-31760800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr6:31745600-31760800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr6:31745600-31762200	Weak transcription	Primary neutrophils fromperipheralblood	blood
17	chr6:31745800-31757000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:31745800-31758600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr6:31745800-31760800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
20	chr6:31745800-31760800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:31745800-31761000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:31745800-31762000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr6:31745800-31762000	Weak transcription	Fetal Kidney	kidney
24	chr6:31746000-31761800	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr6:31746000-31761800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr6:31746200-31759200	Strong transcription	Fetal Muscle Trunk	muscle
27	chr6:31746200-31760600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
28	chr6:31746200-31760800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr6:31746400-31761000	Strong transcription	Fetal Intestine Small	intestine
30	chr6:31746600-31760400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr6:31750000-31762400	Weak transcription	Right Atrium	heart
32	chr6:31750200-31759200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr6:31752400-31759400	Weak transcription	Small Intestine	intestine
34	chr6:31753200-31757000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr6:31753200-31761800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr6:31753400-31757000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
37	chr6:31753400-31757000	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:31753400-31757000	Weak transcription	Stomach Mucosa	stomach
39	chr6:31753400-31757000	Weak transcription	NH-A	brain
40	chr6:31753400-31757200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr6:31753400-31757200	Weak transcription	NHDF-Ad	bronchial
42	chr6:31753400-31759000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
43	chr6:31753400-31759400	Weak transcription	Aorta	Aorta
44	chr6:31753400-31759400	Weak transcription	HUVEC	blood vessel
45	chr6:31753400-31759800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr6:31753400-31760400	Weak transcription	Ovary	ovary
47	chr6:31753400-31762400	Weak transcription	Rectal Smooth Muscle	rectum
48	chr6:31753600-31757000	Weak transcription	Liver	Liver
49	chr6:31753600-31757000	Weak transcription	HMEC	breast
50	chr6:31753600-31757200	Weak transcription	H9 Cell Line	embryonic stem cell

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