Variant report

Variant	nsv541002
Chromosome Location	chr11:35101282-35224624
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3848)
CpG islands
(count:1831)
Chromatin interactive
region (count:86)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:3848 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:35194753-35195096	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:35212245-35212521	HepG2	liver:	n/a	n/a
3	ATF1	chr11:35120645-35121044	K562	blood:	n/a	n/a
4	ATF1	chr11:35125408-35125579	K562	blood:	n/a	n/a
5	ATF1	chr11:35182060-35182303	K562	blood:	n/a	n/a
6	ATF1	chr11:35166888-35167161	K562	blood:	n/a	n/a
7	ATF1	chr11:35104027-35104396	K562	blood:	n/a	n/a
8	ATF1	chr11:35133237-35133513	K562	blood:	n/a	n/a
9	ATF1	chr11:35162652-35162835	K562	blood:	n/a	n/a
10	ATF1	chr11:35164287-35164318	K562	blood:	n/a	n/a
11	ATF1	chr11:35168376-35168687	K562	blood:	n/a	n/a
12	ATF1	chr11:35122859-35123088	K562	blood:	n/a	n/a
13	ATF1	chr11:35132632-35132924	K562	blood:	n/a	n/a
14	ATF2	chr11:35111179-35111661	GM12878	blood:	n/a	n/a
15	ATF2	chr11:35187309-35188167	GM12878	blood:	n/a	n/a
16	ATF2	chr11:35166629-35167313	GM12878	blood:	n/a	n/a
17	ATF2	chr11:35187310-35187972	GM12878	blood:	n/a	n/a
18	ATF2	chr11:35103848-35104479	GM12878	blood:	n/a	n/a
19	ATF2	chr11:35104016-35104542	GM12878	blood:	n/a	n/a
20	ATF2	chr11:35109087-35109714	GM12878	blood:	n/a	n/a
21	ATF2	chr11:35208765-35209181	GM12878	blood:	n/a	n/a
22	ATF2	chr11:35140337-35140923	GM12878	blood:	n/a	n/a
23	ATF2	chr11:35140329-35140826	GM12878	blood:	n/a	n/a
24	ATF2	chr11:35111140-35111947	GM12878	blood:	n/a	n/a
25	ATF2	chr11:35167420-35168628	GM12878	blood:	n/a	n/a
26	ATF2	chr11:35109062-35110065	GM12878	blood:	n/a	n/a
27	ATF2	chr11:35147513-35148569	GM12878	blood:	n/a	n/a
28	ATF2	chr11:35147745-35149600	GM12878	blood:	n/a	n/a
29	ATF2	chr11:35104602-35105713	GM12878	blood:	n/a	n/a
30	ATF2	chr11:35104643-35105435	GM12878	blood:	n/a	n/a
31	ATF2	chr11:35167580-35168640	GM12878	blood:	n/a	n/a
32	ATF2	chr11:35148675-35149703	GM12878	blood:	n/a	n/a
33	ATF2	chr11:35152590-35153181	GM12878	blood:	n/a	n/a
34	ATF2	chr11:35143863-35144425	GM12878	blood:	n/a	n/a
35	ATF2	chr11:35165372-35166426	GM12878	blood:	n/a	n/a
36	ATF2	chr11:35166448-35167418	GM12878	blood:	n/a	n/a
37	ATF2	chr11:35165624-35166332	GM12878	blood:	n/a	n/a
38	ATF3	chr11:35188083-35188607	A549	lung:	n/a	n/a
39	ATF3	chr11:35176584-35176795	K562	blood:	n/a	n/a
40	BACH1	chr11:35202998-35203161	K562	blood:	n/a	n/a
41	BACH1	chr11:35173481-35173712	H1-hESC	embryonic stem cell:	n/a	n/a
42	BATF	chr11:35140450-35140835	GM12878	blood:	n/a	n/a
43	BATF	chr11:35208723-35209029	GM12878	blood:	n/a	chr11:35208842-35208853
44	BATF	chr11:35165661-35166245	GM12878	blood:	n/a	chr11:35165967-35165978
45	BATF	chr11:35148056-35148539	GM12878	blood:	n/a	n/a
46	BATF	chr11:35150354-35150628	GM12878	blood:	n/a	n/a
47	BATF	chr11:35157164-35157464	GM12878	blood:	n/a	chr11:35157283-35157294 chr11:35157313-35157324 chr11:35157314-35157324
48	BATF	chr11:35193580-35193816	GM12878	blood:	n/a	n/a
49	BATF	chr11:35208829-35209017	GM12878	blood:	n/a	chr11:35208842-35208853
50	BATF	chr11:35167514-35168067	GM12878	blood:	n/a	chr11:35167751-35167761 chr11:35167750-35167761 chr11:35167875-35167884

(count:1831 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:35167041-35167091	IMR90	lung:	fetal
2	chr11:35167041-35167091	IMR90	lung:	fetal
3	chr11:35159087-35159137	HRPEpiC	eye:	n/a
4	chr11:35105199-35105249	SK-N-SH	brain:	n/a
5	chr11:35186440-35186490	MCF10A-Er-Src	breast:	n/a
6	chr11:35160400-35160450	GM19239	blood:	n/a
7	chr11:35158283-35158333	NH-A	brain:	n/a
8	chr11:35105199-35105249	HNPCEpiC	eye:	n/a
9	chr11:35161229-35161279	GM12878	blood:	n/a
10	chr11:35105199-35105249	HRPEpiC	eye:	n/a
11	chr11:35105199-35105249	Caco-2	colon:	n/a
12	chr11:35198201-35198251	HUVEC	blood vessel:	n/a
13	chr11:35159382-35159432	HRPEpiC	eye:	n/a
14	chr11:35158283-35158333	GM06990	blood:	n/a
15	chr11:35159136-35159186	HNPCEpiC	eye:	n/a
16	chr11:35160462-35160512	HMEC	breast:	n/a
17	chr11:35161345-35161395	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:35159136-35159186	H1-hESC	embryonic stem cell:	embryo
19	chr11:35159087-35159137	HNPCEpiC	eye:	n/a
20	chr11:35173592-35173642	NHDF-neo	bronchial:	n/a
21	chr11:35159087-35159137	HRE	kidney:	n/a
22	chr11:35160330-35160380	MCF-7	breast:	n/a
23	chr11:35161183-35161233	HNPCEpiC	eye:	n/a
24	chr11:35195513-35195563	HCPEpiC	choroid plexus:	n/a
25	chr11:35173592-35173642	Jurkat	blood:	n/a
26	chr11:35188437-35188487	AG09309	skin:	n/a
27	chr11:35159382-35159432	NH-A	brain:	n/a
28	chr11:35105199-35105249	SKMC	muscle:	n/a
29	chr11:35160330-35160380	HNPCEpiC	eye:	n/a
30	chr11:35167041-35167091	AG04450	lung:	fetal
31	chr11:35161183-35161233	HRPEpiC	eye:	n/a
32	chr11:35160498-35160548	AG04450	lung:	fetal
33	chr11:35160330-35160380	SAEC	small airway:	n/a
34	chr11:35161900-35161950	HIPEpiC	eye:	n/a
35	chr11:35160498-35160548	GM12892	blood:	n/a
36	chr11:35160330-35160380	Hepatocyte	liver:	n/a
37	chr11:35160462-35160512	PrEC	prostate:	n/a
38	chr11:35160892-35160942	BE2_C	brain:	n/a
39	chr11:35161900-35161950	SAEC	small airway:	n/a
40	chr11:35160843-35160893	ovcar-3	ovarian:	n/a
41	chr11:35138084-35138134	NT2-D1	testis:	n/a
42	chr11:35186440-35186490	BE2_C	brain:	n/a
43	chr11:35160709-35160759	NHBE	bronchial:	n/a
44	chr11:35160462-35160512	BJ	skin:	n/a
45	chr11:35201133-35201183	HCM	heart:	n/a
46	chr11:35160330-35160380	NHBE	bronchial:	n/a
47	chr11:35164485-35164535	RPTEC	kidney:	n/a
48	chr11:35160330-35160380	AG09319	gingival:	n/a
49	chr11:35160462-35160512	ovcar-3	ovarian:	n/a
50	chr11:35160498-35160548	NH-A	brain:	n/a

(count:86 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr11:35135735..35137455-chr11:35149991..35152217,2	K562	blood:
2	chr11:35119423..35121112-chr11:35124669..35126752,2	MCF-7	breast:
3	chr11:35109556..35112078-chr11:35117913..35120120,2	MCF-7	breast:
4	chr11:35186531..35188215-chr11:35413426..35415708,2	MCF-7	breast:
5	chr11:35160364..35160882-chr15:75932271..75932998,2	Hela-S3	cervix:
6	chr11:35193443..35196303-chr11:35198924..35201669,2	MCF-7	breast:
7	chr1:11968192..11969146-chr11:35160267..35160843,2	Hela-S3	cervix:
8	chr11:35101233..35103768-chr11:35185557..35187275,2	MCF-7	breast:
9	chr1:154154871..154155752-chr11:35160501..35161403,2	Hela-S3	cervix:
10	chr11:35101233..35103768-chr11:35185557..35187275,2	MCF-7	breast:
11	chr11:35186608..35189447-chr11:35199235..35201624,2	MCF-7	breast:
12	chr11:35160028..35162902-chr11:35183937..35186481,3	MCF-7	breast:
13	chr11:35184295..35186190-chr11:35191742..35193747,2	MCF-7	breast:
14	chr11:35160960..35162794-chr11:35186248..35188654,2	MCF-7	breast:
15	chr11:35160584..35161366-chr17:72983348..72984211,2	Hela-S3	cervix:
16	chr11:35224481..35226874-chr11:35226876..35229247,2	MCF-7	breast:
17	chr11:35208907..35210567-chr11:35212909..35215234,2	MCF-7	breast:
18	chr11:35118109..35120819-chr11:35160068..35162189,2	MCF-7	breast:
19	chr11:35121360..35123846-chr11:35132606..35135309,2	K562	blood:
20	chr11:34938093..34939698-chr11:35166380..35168722,2	MCF-7	breast:
21	chr11:35183121..35185456-chr11:35188061..35190243,2	MCF-7	breast:
22	chr11:35135157..35136854-chr11:35159646..35161211,2	MCF-7	breast:
23	chr11:35195238..35197148-chr11:35385944..35388591,2	MCF-7	breast:
24	chr11:35137747..35140053-chr11:35157394..35160229,2	MCF-7	breast:
25	chr11:35208296..35211320-chr11:35214358..35217497,3	K562	blood:
26	chr11:35172301..35174738-chr11:35189496..35192114,2	MCF-7	breast:
27	chr11:35170246..35172817-chr11:35174979..35176507,2	MCF-7	breast:
28	chr11:35160324..35161311-chr3:14444116..14444878,2	Hela-S3	cervix:
29	chr11:35170246..35172817-chr11:35174979..35176507,2	MCF-7	breast:
30	chr11:35208907..35210567-chr11:35212909..35215234,2	MCF-7	breast:
31	chr11:35132300..35135003-chr11:35146023..35147940,2	MCF-7	breast:
32	chr11:35121360..35123846-chr11:35132606..35135309,2	K562	blood:
33	chr11:35169325..35170963-chr11:35175287..35177044,2	K562	blood:
34	chr11:35186608..35189447-chr11:35199235..35201624,2	MCF-7	breast:
35	chr11:35122584..35124925-chr11:35126765..35129371,2	MCF-7	breast:
36	chr11:35184295..35186190-chr11:35191742..35193747,2	MCF-7	breast:
37	chr11:35119495..35120096-chr11:35412276..35412995,2	MCF-7	breast:
38	chr11:35188706..35190323-chr11:35204261..35206876,2	K562	blood:
39	chr11:35159898..35160664-chr9:96928460..96928999,2	Hela-S3	cervix:
40	chr11:35183121..35185456-chr11:35188061..35190243,2	MCF-7	breast:
41	chr11:35163163..35167316-chr11:35171190..35174236,4	K562	blood:
42	chr11:35160374..35163354-chr11:35164253..35168964,4	K562	blood:
43	chr1:153606580..153607386-chr11:35159581..35160522,2	Hela-S3	cervix:
44	chr11:35187046..35189640-chr11:35384110..35385949,2	MCF-7	breast:
45	chr11:35026967..35028548-chr11:35162664..35165084,2	MCF-7	breast:
46	chr11:35104262..35106718-chr11:35159601..35161198,2	MCF-7	breast:
47	chr11:35155392..35158105-chr11:35159031..35160697,2	MCF-7	breast:
48	chr11:35160506..35161348-chr5:172198026..172198579,2	Hela-S3	cervix:
49	chr1:207503349..207504173-chr11:35160887..35161695,2	Hela-S3	cervix:
50	chr11:35199491..35202638-chr11:35207456..35210593,3	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDHX-3	chr11:35107760-35107870	NONHSAT018772
2	lnc-SLC1A2-2	chr11:35157893-35158084	XLOC_009416
3	lnc-PDHX-4	chr11:35219416-35220102	NONHSAT018780
4	lnc-PDHX-3	chr11:35108965-35110133	NONHSAT018772
5	lnc-PDHX-3	chr11:35112276-35112331	NONHSAT018772
6	lnc-PDHX-5	chr11:35223168-35223334	NONHSAT018782
7	lnc-CD44-4	chr11:35124735-35124991	NONHSAT018773
8	lnc-PDHX-5	chr11:35222691-35222742	NONHSAT018781
9	lnc-SLC1A2-2	chr11:35157781-35158173	ENSG00000255521.1
10	lnc-PDHX-3	chr11:35119168-35119365	NONHSAT018768
11	lnc-PDHX-3	chr11:35140600-35142723	NONHSAT018772
12	lnc-SLC1A2-2	chr11:35154202-35154687	ENSG00000255521.1
13	lnc-SLC1A2-2	chr11:35159245-35159273	ENSG00000255521.1
14	lnc-SLC1A2-2	chr11:35150431-35150467	XLOC_009416
15	lnc-PDHX-5	chr11:35211473-35211612	NONHSAT018779
16	lnc-CD44-3	chr11:35132621-35132927	NONHSAT018774
17	lnc-PDHX-3	chr11:35119065-35120242	NONHSAT018772
18	lnc-CD44-5	chr11:35103203-35103622	NONHSAT018771
19	lnc-SLC1A2-2	chr11:35159245-35159579	ENSG00000255521.1
20	lnc-SLC1A2-2	chr11:35157893-35158173	ENSG00000255521.1
21	lnc-PDHX-3	chr11:35109985-35110151	NONHSAT018768
22	lnc-PDHX-4	chr11:35218709-35219340	NONHSAT018780
23	lnc-PDHX-5	chr11:35223215-35223334	NONHSAT018781

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CD44	hsa-miR-520c-3p	chr11:35211491-35211514
2	CD44	hsa-miR-373-3p	chr11:35211492-35211514

Variant related genes	Relation type
ENSG00000269766	TF binding region
CD44	TF binding region
ENSG00000255521	TF binding region
ENSG00000269766	CpG island
CD44	CpG island
ENSG00000255521	CpG island
ENSG00000026508	chromatin interactions
ENSG00000160741	chromatin interactions
ENSG00000143549	chromatin interactions
ENSG00000177971	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000255521	chromatin interactions
ENSG00000128886	chromatin interactions
ENSG00000232519	chromatin interactions
ENSG00000271853	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000110435	chromatin interactions
ENSG00000131389	chromatin interactions
ENSG00000160813	chromatin interactions
ENSG00000120129	chromatin interactions
ENSG00000269946	chromatin interactions
ENSG00000197837	chromatin interactions
ENSG00000272030	chromatin interactions
ENSG00000065243	chromatin interactions
ENSG00000109089	chromatin interactions
ENSG00000269766	chromatin interactions
ENSG00000125459	chromatin interactions
POU2F1	miRNA target sites

Extended variants
information (count: 5004 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:5004 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555360026	chr11:35101285-35101286	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs16926815	chr11:35101399-35101400	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs368354163	chr11:35101412-35101413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116047068	chr11:35101423-35101424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs375335492	chr11:35101424-35101425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560112038	chr11:35101433-35101434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182129745	chr11:35101446-35101447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186811497	chr11:35101464-35101465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs353610	chr11:35101496-35101497	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs528872051	chr11:35101497-35101498	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371111617	chr11:35101529-35101530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs190932509	chr11:35101534-35101535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148764642	chr11:35101577-35101578	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs114621322	chr11:35101613-35101614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs537851098	chr11:35101647-35101648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368823470	chr11:35101654-35101655	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs353609	chr11:35101696-35101697	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs353608	chr11:35101738-35101739	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs547466659	chr11:35101821-35101822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151315434	chr11:35101920-35101921	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139040535	chr11:35101922-35101923	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149890428	chr11:35101943-35101944	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs184118705	chr11:35102023-35102024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs538103873	chr11:35102027-35102028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs569457858	chr11:35102033-35102034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558123495	chr11:35102080-35102081	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs373614752	chr11:35102088-35102089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs111885579	chr11:35102132-35102133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs367711972	chr11:35102215-35102216	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs35910659	chr11:35102236-35102237	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs536968220	chr11:35102241-35102242	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs188327689	chr11:35102259-35102260	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs146419594	chr11:35102332-35102333	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs541875751	chr11:35102340-35102341	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs353607	chr11:35102366-35102367	Weak transcription Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs573191393	chr11:35102410-35102411	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs140938168	chr11:35102419-35102420	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs562454651	chr11:35102449-35102450	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs140090239	chr11:35102458-35102459	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs531215908	chr11:35102471-35102472	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs376178100	chr11:35102483-35102484	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs551657562	chr11:35102530-35102531	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs565267919	chr11:35102533-35102534	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs533902385	chr11:35102589-35102590	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs144649546	chr11:35102635-35102636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs193198307	chr11:35102691-35102692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs184698753	chr11:35102735-35102736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs536703837	chr11:35102748-35102749	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550017805	chr11:35102793-35102794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369877841	chr11:35102807-35102808	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	16783165	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Potocki-Shaffer syndrome	19222835	CNVD
WAGR syndrome	19222835	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
Aniridia syndrome	21572526	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Retinoblastoma	22278416	CNVD
Denys-drash syndrome	21085971	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
WAGR syndrome	16773131	CNVD
Disorders of sex development	22290220	CNVD
Aniridia syndrome	17204608	CNVD
Mental retardation	17204608	CNVD
WAGR syndrome	19617690	CNVD
genitourinary abnormalities	17204608	CNVD
Breast cancer	16397240	CNVD
Mental retardation	16773131	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17160897	CNVD
Cancer	21183584	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
WAGR syndrome	22470819	CNVD
Neurodevelopmental disorder	22521361	CNVD
Denys-drash syndrome	19566914	CNVD
Familial wilms tumor	19566914	CNVD
Frasier syndrome	19566914	CNVD
Non-small cell lung cancer	21829676	CNVD
WAGR syndrome	20603712	CNVD
Autism	17322880	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Breast cancer	16620391	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Lung squamous cell carcinoma	20842114	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:4680 , 50 per page) page: 1 2 3 4 5 6 7 ... 94

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:35097600-35101400	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
2	chr11:35097600-35103800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr11:35097600-35106400	Enhancers	Primary B cells from peripheral blood	blood
4	chr11:35097800-35102400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr11:35097800-35106600	Enhancers	Fetal Thymus	thymus
6	chr11:35098000-35101400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr11:35098200-35101400	Enhancers	Primary hematopoietic stem cells	blood
8	chr11:35098200-35101800	Enhancers	Thymus	Thymus
9	chr11:35098200-35102400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr11:35098400-35101400	Enhancers	HMEC	breast
11	chr11:35098600-35101400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr11:35098600-35101400	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr11:35098600-35103200	Weak transcription	Adipose Nuclei	Adipose
14	chr11:35098800-35103400	Weak transcription	Pancreas	Pancrea
15	chr11:35098800-35103600	Weak transcription	Skeletal Muscle Male	skeletal muscle
16	chr11:35098800-35103800	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr11:35098800-35104000	Weak transcription	Psoas Muscle	Psoas
18	chr11:35098800-35104000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr11:35098800-35104000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr11:35098800-35105400	Weak transcription	Small Intestine	intestine
21	chr11:35099000-35101400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr11:35099200-35101400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
23	chr11:35099200-35101400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr11:35099400-35101400	Enhancers	Duodenum Mucosa	Duodenum
25	chr11:35099400-35103800	Weak transcription	K562	blood
26	chr11:35099400-35104400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr11:35099600-35103800	Enhancers	Primary T cells fromperipheralblood	blood
28	chr11:35099600-35104000	Enhancers	Primary T killer memory cells from peripheral blood	blood
29	chr11:35099800-35104000	Weak transcription	Stomach Mucosa	stomach
30	chr11:35099800-35104200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr11:35100000-35101400	Enhancers	Muscle Satellite Cultured Cells	--
32	chr11:35100000-35102800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr11:35100000-35103800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr11:35100000-35103800	Enhancers	Primary T helper cells fromperipheralblood	blood
35	chr11:35100000-35103800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr11:35100000-35103800	Weak transcription	A549	lung
37	chr11:35100000-35103800	Weak transcription	HSMM	muscle
38	chr11:35100000-35103800	Weak transcription	NH-A	brain
39	chr11:35100200-35102200	Enhancers	Dnd41	blood
40	chr11:35100200-35103200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr11:35100200-35103200	Weak transcription	NHDF-Ad	bronchial
42	chr11:35100200-35103600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr11:35100200-35103800	Enhancers	Primary T cells from cord blood	blood
44	chr11:35100200-35103800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr11:35100200-35103800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr11:35100200-35103800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:35100200-35103800	Weak transcription	Esophagus	oesophagus
48	chr11:35100200-35103800	Enhancers	GM12878-XiMat	blood
49	chr11:35100200-35104000	Enhancers	Primary B cells from cord blood	blood
50	chr11:35100400-35102600	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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