Variant report

Variant	esv3356829
Chromosome Location	chr11:71933329-71936177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:711)
CpG islands
(count:672)
Chromatin interactive
region (count:32)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:711 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71934520-71934741	HepG2	liver:	n/a	chr11:71934635-71934651
2	ARID3A	chr11:71934226-71934702	K562	blood:	n/a	chr11:71934635-71934651
3	ARID3A	chr11:71935316-71935332	HepG2	liver:	n/a	n/a
4	ATF2	chr11:71933938-71934596	GM12878	blood:	n/a	n/a
5	ATF2	chr11:71934385-71934745	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr11:71933856-71934677	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr11:71934546-71934672	K562	blood:	n/a	n/a
8	BCLAF1	chr11:71934932-71935319	GM12878	blood:	n/a	chr11:71934983-71934996
9	BCLAF1	chr11:71934051-71934574	GM12878	blood:	n/a	chr11:71934557-71934566 chr11:71934311-71934320 chr11:71934314-71934327 chr11:71934405-71934414
10	BHLHE40	chr11:71933338-71933388	K562	blood:	n/a	n/a
11	BHLHE40	chr11:71934179-71934761	K562	blood:	n/a	chr11:71934552-71934568 chr11:71934420-71934436
12	BHLHE40	chr11:71934999-71935134	K562	blood:	n/a	n/a
13	BHLHE40	chr11:71933635-71933803	K562	blood:	n/a	n/a
14	BHLHE40	chr11:71934071-71934744	GM12878	blood:	n/a	chr11:71934552-71934568 chr11:71934420-71934436
15	BHLHE40	chr11:71933540-71933802	HepG2	liver:	n/a	n/a
16	BRCA1	chr11:71934131-71934729	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr11:71935281-71935519	H1-hESC	embryonic stem cell:	n/a	n/a
18	CBX3	chr11:71934087-71934776	K562	blood:	n/a	n/a
19	CCNT2	chr11:71933585-71935323	K562	blood:	n/a	chr11:71933680-71933700 chr11:71934318-71934327
20	CCNT2	chr11:71935571-71936374	K562	blood:	n/a	chr11:71935741-71935750 chr11:71935780-71935789
21	CEBPB	chr11:71934068-71934510	Hela-S3	cervix:	n/a	n/a
22	CEBPD	chr11:71934027-71934459	HepG2	liver:	n/a	n/a
23	CEBPD	chr11:71934643-71934847	HepG2	liver:	n/a	n/a
24	CHD1	chr11:71933897-71935936	GM12878	blood:	n/a	chr11:71934835-71934845 chr11:71934840-71934850 chr11:71934293-71934300
25	CHD2	chr11:71934965-71935281	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr11:71934556-71934755	K562	blood:	n/a	n/a
27	CHD2	chr11:71934030-71935955	GM12878	blood:	n/a	chr11:71934835-71934845 chr11:71934840-71934850 chr11:71934293-71934300
28	CHD2	chr11:71933847-71936905	Hela-S3	cervix:	n/a	chr11:71934835-71934845 chr11:71934840-71934850 chr11:71934293-71934300
29	CHD2	chr11:71935606-71935930	HepG2	liver:	n/a	n/a
30	CHD2	chr11:71934966-71935929	K562	blood:	n/a	n/a
31	CHD2	chr11:71935000-71935287	HepG2	liver:	n/a	n/a
32	CHD2	chr11:71934299-71934342	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr11:71935631-71935801	H1-hESC	embryonic stem cell:	n/a	n/a
34	CREB1	chr11:71934067-71934748	GM12878	blood:	n/a	n/a
35	CREB1	chr11:71934089-71934761	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr11:71934267-71934878	H1-hESC	embryonic stem cell:	n/a	n/a
37	CREB1	chr11:71935617-71936254	A549	lung:	n/a	n/a
38	CREB1	chr11:71934151-71934426	A549	lung:	n/a	n/a
39	CREB1	chr11:71934018-71936020	HepG2	liver:	n/a	n/a
40	CREB1	chr11:71933949-71935375	A549	lung:	n/a	n/a
41	CTBP2	chr11:71934196-71934777	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr11:71934240-71934390	HEEpiC	esophagus:	n/a	chr11:71934306-71934316
43	CTCF	chr11:71934320-71934470	HFF-Myc	foreskin:	n/a	chr11:71934439-71934452
44	CTCF	chr11:71934260-71934410	K562	blood:	n/a	chr11:71934306-71934316
45	CTCF	chr11:71934104-71934513	GM12878	blood:	n/a	chr11:71934306-71934316 chr11:71934439-71934452
46	CTCF	chr11:71934200-71934350	HRPEpiC	eye:	n/a	chr11:71934306-71934316
47	CTCF	chr11:71934260-71934410	SAEC	small airway:	n/a	chr11:71934306-71934316
48	CTCF	chr11:71934840-71934990	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr11:71934054-71934560	K562	blood:	n/a	chr11:71934306-71934316 chr11:71934439-71934452
50	CTCF	chr11:71934240-71934390	AoAF	blood vessel:	n/a	chr11:71934306-71934316

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71934705-71934755	Caco-2	colon:	n/a
2	chr11:71934705-71934755	Caco-2	colon:	n/a
3	chr11:71934276-71934326	GM12891	blood:	n/a
4	chr11:71934510-71934560	NH-A	brain:	n/a
5	chr11:71934705-71934755	CMK	blood:	n/a
6	chr11:71935686-71935736	AoSMC	blood vessel:	n/a
7	chr11:71934510-71934560	HL-60	blood:	n/a
8	chr11:71934705-71934755	AG04449	skin:	fetal
9	chr11:71935846-71935896	LNCaP	prostate:	n/a
10	chr11:71935199-71935249	NHDF-neo	bronchial:	n/a
11	chr11:71935881-71935931	AG04450	lung:	fetal
12	chr11:71935881-71935931	BJ	skin:	n/a
13	chr11:71935881-71935931	HIPEpiC	eye:	n/a
14	chr11:71934660-71934710	A549	lung:	n/a
15	chr11:71935692-71935742	MCF10A-Er-Src	breast:	n/a
16	chr11:71935881-71935931	NH-A	brain:	n/a
17	chr11:71934276-71934326	GM19239	blood:	n/a
18	chr11:71934660-71934710	HIPEpiC	eye:	n/a
19	chr11:71935686-71935736	HCT-116	colon:	n/a
20	chr11:71935849-71935899	AG04450	lung:	fetal
21	chr11:71934276-71934326	PrEC	prostate:	n/a
22	chr11:71934510-71934560	GM19239	blood:	n/a
23	chr11:71935881-71935931	HNPCEpiC	eye:	n/a
24	chr11:71935692-71935742	HRCEpiC	kidney:	n/a
25	chr11:71934705-71934755	AG10803	skin:	n/a
26	chr11:71935686-71935736	HMEC	breast:	n/a
27	chr11:71934705-71934755	AG09319	gingival:	n/a
28	chr11:71935881-71935931	SK-N-SH	brain:	n/a
29	chr11:71934705-71934755	HL-60	blood:	n/a
30	chr11:71935846-71935896	ECC-1	luminal epithelium:	n/a
31	chr11:71935881-71935931	SK-N-SH_RA	brain:	n/a
32	chr11:71935849-71935899	ProgFib	skin:	n/a
33	chr11:71935353-71935403	HCM	heart:	n/a
34	chr11:71934510-71934560	AG09319	gingival:	n/a
35	chr11:71935353-71935403	HMEC	breast:	n/a
36	chr11:71935846-71935896	HL-60	blood:	n/a
37	chr11:71934705-71934755	HCPEpiC	choroid plexus:	n/a
38	chr11:71934705-71934755	AG04450	lung:	fetal
39	chr11:71934705-71934755	MCF-7	breast:	n/a
40	chr11:71934276-71934326	AG09309	skin:	n/a
41	chr11:71935353-71935403	HPAEpiC	pulmonary alveolar:	n/a
42	chr11:71935881-71935931	HEEpiC	esophagus:	n/a
43	chr11:71935199-71935249	HCF	heart:	n/a
44	chr11:71935199-71935249	PrEC	prostate:	n/a
45	chr11:71935686-71935736	HRE	kidney:	n/a
46	chr11:71935849-71935899	PrEC	prostate:	n/a
47	chr11:71935846-71935896	SK-N-SH	brain:	n/a
48	chr11:71934660-71934710	NHBE	bronchial:	n/a
49	chr11:71935199-71935249	IMR90	lung:	fetal
50	chr11:71935686-71935736	NHBE	bronchial:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:71933813..71936010-chr11:72394188..72397078,2	MCF-7	breast:
2	chr11:71748920..71751712-chr11:71934433..71936381,2	K562	blood:
3	chr11:71929797..71931441-chr11:71932339..71934152,2	MCF-7	breast:
4	chr11:71734724..71737619-chr11:71934939..71936763,2	MCF-7	breast:
5	chr11:71821560..71824482-chr11:71933153..71936536,4	MCF-7	breast:
6	chr11:71933506..71936425-chr8:101962971..101964656,2	MCF-7	breast:
7	chr11:71935149..71936719-chr11:72144197..72145744,2	K562	blood:
8	chr11:71928745..71931355-chr11:71933643..71936077,2	MCF-7	breast:
9	chr11:71901671..71903414-chr11:71935255..71937663,2	K562	blood:
10	chr11:71902919..71905831-chr11:71935320..71937132,2	MCF-7	breast:
11	chr11:71750373..71752525-chr11:71933775..71937280,4	MCF-7	breast:
12	chr11:71933976..71935544-chr6:30710899..30712644,2	MCF-7	breast:
13	chr11:71790877..71793243-chr11:71934127..71937254,3	K562	blood:
14	chr11:71903106..71905888-chr11:71932566..71934811,2	K562	blood:
15	chr11:71899963..71900919-chr11:71934256..71934793,2	Hela-S3	cervix:
16	chr11:71926160..71927705-chr11:71931885..71934510,2	MCF-7	breast:
17	chr11:71927693..71930362-chr11:71935799..71938358,2	MCF-7	breast:
18	chr11:71749038..71754852-chr11:71933473..71937860,9	MCF-7	breast:
19	chr11:71820588..71822402-chr11:71934430..71936040,2	K562	blood:
20	chr11:71812032..71815862-chr11:71933743..71937376,6	MCF-7	breast:
21	chr11:71935409..71935957-chr11:72144881..72145767,2	MCF-7	breast:
22	chr11:71822132..71825937-chr11:71933388..71938158,5	MCF-7	breast:
23	chr11:71932379..71935171-chr11:72141438..72143643,2	K562	blood:
24	chr11:71823487..71825907-chr11:71932451..71935590,3	K562	blood:
25	chr11:71901535..71906562-chr11:71933469..71937383,8	MCF-7	breast:
26	chr11:71928000..71929697-chr11:71932021..71933671,2	MCF-7	breast:
27	chr11:71812576..71816251-chr11:71934138..71937267,4	MCF-7	breast:
28	chr11:71705470..71708103-chr11:71933163..71935736,2	K562	blood:
29	chr11:71935078..71937662-chr11:71961584..71963637,2	MCF-7	breast:
30	chr11:71933747..71936558-chr11:71962323..71967146,4	K562	blood:
31	chr11:71794597..71796676-chr11:71933862..71937757,3	K562	blood:
32	chr11:71933144..71936187-chr11:72142812..72145474,4	MCF-7	breast:

No data

Variant related genes	Relation type
INPPL1	TF binding region
INPPL1	CpG island
ENSG00000164924	chromatin interactions
ENSG00000110203	chromatin interactions
ENSG00000110200	chromatin interactions
ENSG00000110195	chromatin interactions
ENSG00000184154	chromatin interactions
ENSG00000137331	chromatin interactions
ENSG00000137497	chromatin interactions
ENSG00000165457	chromatin interactions
ENSG00000256007	chromatin interactions
ENSG00000137522	chromatin interactions
ENSG00000149357	chromatin interactions
ENSG00000238768	chromatin interactions
ENSG00000162129	chromatin interactions
ENSG00000228286	chromatin interactions

Extended variants
information (count: 88 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:88 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138877984	chr11:71933337-71933338	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
2	rs180801872	chr11:71933364-71933365	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs540589729	chr11:71933389-71933390	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs185498603	chr11:71933468-71933469	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs532432883	chr11:71933483-71933484	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
6	rs190985983	chr11:71933578-71933579	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs140619680	chr11:71933593-71933594	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs145670947	chr11:71933602-71933603	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs535128028	chr11:71933605-71933606	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs566564501	chr11:71933611-71933612	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs138219891	chr11:71933646-71933647	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs552218118	chr11:71933669-71933670	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs375274955	chr11:71933717-71933718	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs570711660	chr11:71933736-71933737	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs556885036	chr11:71933748-71933749	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
16	rs575483759	chr11:71933776-71933777	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
17	rs537883957	chr11:71933789-71933790	Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
18	rs567314192	chr11:71933879-71933880	Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
19	rs114665398	chr11:71933940-71933941	Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
20	rs77348083	chr11:71933991-71933992	Flanking Active TSS Enhancers Active TSS	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
21	rs535556204	chr11:71934004-71934005	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
22	rs142816319	chr11:71934063-71934064	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
23	rs557579609	chr11:71934103-71934104	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
24	rs370766560	chr11:71934106-71934107	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
25	rs374823253	chr11:71934148-71934149	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
26	rs573382056	chr11:71934169-71934170	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
27	rs540804371	chr11:71934188-71934189	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
28	rs565479190	chr11:71934204-71934205	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
29	rs577462087	chr11:71934205-71934206	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
30	rs572692930	chr11:71934216-71934217	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
31	rs553008673	chr11:71934221-71934222	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
32	rs562552052	chr11:71934257-71934258	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
33	rs530002189	chr11:71934313-71934314	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
34	rs563074172	chr11:71934337-71934338	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
35	rs560614300	chr11:71934340-71934341	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
36	rs527528285	chr11:71934360-71934361	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
37	rs552340484	chr11:71934383-71934384	Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
38	rs12280967	chr11:71934418-71934419	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
39	rs531642016	chr11:71934426-71934427	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
40	rs376068530	chr11:71934432-71934433	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
41	rs78176749	chr11:71934447-71934448	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
42	rs74635729	chr11:71934452-71934453	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
43	rs371803974	chr11:71934468-71934469	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
44	rs535417342	chr11:71934484-71934485	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
45	rs553616982	chr11:71934504-71934505	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
46	rs375734646	chr11:71934516-71934517	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
47	rs565755741	chr11:71934517-71934518	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
48	rs377649389	chr11:71934557-71934558	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
49	rs534173553	chr11:71934558-71934559	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a
50	rs575049026	chr11:71934667-71934668	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	15 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71928000-71933600	Weak transcription	Pancreas	Pancrea
2	chr11:71929400-71933400	Weak transcription	Primary T cells from cord blood	blood
3	chr11:71929600-71933600	Weak transcription	Colonic Mucosa	Colon
4	chr11:71929800-71933400	Weak transcription	Lung	lung
5	chr11:71929800-71933600	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr11:71931600-71933600	Enhancers	Fetal Muscle Leg	muscle
7	chr11:71931600-71933800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr11:71931800-71933400	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr11:71931800-71933600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr11:71931800-71933600	Enhancers	Adipose Nuclei	Adipose
11	chr11:71932200-71933600	Enhancers	Primary hematopoietic stem cells	blood
12	chr11:71932200-71933600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr11:71932200-71933600	Enhancers	Fetal Muscle Trunk	muscle
14	chr11:71932200-71933800	Enhancers	Placenta	Placenta
15	chr11:71932400-71933400	Weak transcription	Thymus	Thymus
16	chr11:71932400-71933600	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr11:71932400-71933600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr11:71932400-71933600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr11:71932400-71934000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr11:71932400-71934200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
21	chr11:71932600-71933400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr11:71932600-71933400	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr11:71932600-71933400	Enhancers	Stomach Smooth Muscle	stomach
24	chr11:71932600-71933400	Enhancers	K562	blood
25	chr11:71932600-71933600	Enhancers	Duodenum Mucosa	Duodenum
26	chr11:71932600-71933800	Enhancers	H1 Cell Line	embryonic stem cell
27	chr11:71932600-71933800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr11:71932600-71933800	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr11:71932800-71933400	Enhancers	Brain Anterior Caudate	brain
30	chr11:71932800-71933600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr11:71932800-71933600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr11:71932800-71933600	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr11:71932800-71933600	Enhancers	Liver	Liver
34	chr11:71932800-71933600	Enhancers	Brain Substantia Nigra	brain
35	chr11:71932800-71933600	Enhancers	Duodenum Smooth Muscle	Duodenum
36	chr11:71932800-71933600	Enhancers	Fetal Lung	lung
37	chr11:71932800-71933800	Enhancers	Fetal Intestine Large	intestine
38	chr11:71932800-71933800	Enhancers	Fetal Stomach	stomach
39	chr11:71932800-71934000	Flanking Active TSS	GM12878-XiMat	blood
40	chr11:71932800-71934200	Flanking Active TSS	Primary B cells from cord blood	blood
41	chr11:71933000-71933400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr11:71933000-71933400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:71933000-71933400	Enhancers	Colon Smooth Muscle	Colon
44	chr11:71933000-71933400	Weak transcription	Right Atrium	heart
45	chr11:71933000-71933600	Enhancers	Primary B cells from peripheral blood	blood
46	chr11:71933000-71933600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr11:71933000-71933600	Enhancers	Spleen	Spleen
48	chr11:71933000-71933800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:71933000-71933800	Enhancers	Brain Hippocampus Middle	brain
50	chr11:71933000-71933800	Enhancers	Fetal Thymus	thymus

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