Variant report

Variant	nsv975355
Chromosome Location	chr11:33725252-33729708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:303)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:303 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:33725848-33726047	HepG2	liver:	n/a	n/a
2	BRCA1	chr11:33727190-33727229	GM12878	blood:	n/a	n/a
3	CEBPB	chr11:33725342-33725724	IMR90	lung:	n/a	n/a
4	CEBPB	chr11:33728185-33728436	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:33729556-33729671	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr11:33728163-33728493	HepG2	liver:	n/a	n/a
7	CEBPB	chr11:33725314-33725635	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr11:33725367-33725610	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr11:33725860-33726010	HCM	heart:	n/a	n/a
10	CTCF	chr11:33725860-33726010	HVMF	connective:	n/a	n/a
11	CTCF	chr11:33725400-33725550	AoAF	blood vessel:	n/a	n/a
12	CTCF	chr11:33725840-33725990	HPF	lung:	n/a	n/a
13	CTCF	chr11:33725880-33726030	AG04450	lung:	n/a	n/a
14	CTCF	chr11:33725820-33725970	BJ	skin:	n/a	n/a
15	CTCF	chr11:33725860-33726010	GM12873	blood:	n/a	n/a
16	CTCF	chr11:33725860-33726010	AG09319	gingival:	n/a	n/a
17	CTCF	chr11:33725840-33725990	HUVEC	blood vessel:	n/a	n/a
18	CTCF	chr11:33725880-33726030	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr11:33725860-33726010	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr11:33725640-33725930	A549	lung:	n/a	n/a
21	CTCF	chr11:33725900-33726050	HRPEpiC	eye:	n/a	n/a
22	CTCF	chr11:33725860-33726010	GM12874	blood:	n/a	n/a
23	CTCF	chr11:33725860-33726010	AG04449	skin:	n/a	n/a
24	CTCF	chr11:33725740-33725890	GM12864	blood:	n/a	n/a
25	CTCF	chr11:33725900-33726050	SK-N-SH_RA	brain:	n/a	n/a
26	CTCF	chr11:33725360-33725510	AoAF	blood vessel:	n/a	n/a
27	CTCF	chr11:33725880-33726030	HRE	kidney:	n/a	n/a
28	CTCF	chr11:33725880-33726030	HCT-116	colon:	n/a	n/a
29	CTCF	chr11:33725900-33726050	AG09319	gingival:	n/a	n/a
30	CTCF	chr11:33725900-33726050	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr11:33725860-33726010	HMEC	breast:	n/a	n/a
32	CTCF	chr11:33725500-33725650	HPF	lung:	n/a	n/a
33	CTCF	chr11:33725860-33726010	GM12872	blood:	n/a	n/a
34	CTCF	chr11:33725880-33726030	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr11:33725860-33726010	HEK293	kidney:	n/a	n/a
36	CTCF	chr11:33725880-33726030	NHLF	lung:	n/a	n/a
37	CTCF	chr11:33725900-33726050	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr11:33725900-33726050	GM12878	blood:	n/a	n/a
39	CTCF	chr11:33725900-33726050	HMF	breast:	n/a	n/a
40	CTCF	chr11:33725900-33726050	MCF-7	breast:	n/a	n/a
41	CTCF	chr11:33725860-33726010	K562	blood:	n/a	n/a
42	CTCF	chr11:33725880-33726030	BJ	skin:	n/a	n/a
43	CTCF	chr11:33725860-33726010	SK-N-SH_RA	brain:	n/a	n/a
44	CTCF	chr11:33725840-33725990	AG10803	skin:	n/a	n/a
45	CTCF	chr11:33725820-33725970	AG10803	skin:	n/a	n/a
46	CTCF	chr11:33725880-33726030	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr11:33725880-33726030	HPF	lung:	n/a	n/a
48	CTCF	chr11:33725780-33725930	HAc	cerebellar:	n/a	n/a
49	CTCF	chr11:33725380-33725530	HMEC	breast:	n/a	n/a
50	CTCF	chr11:33725960-33726110	HA-sp	spinal cord:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:33729190-33729240	AG04450	lung:	fetal
2	chr11:33729190-33729240	HIPEpiC	eye:	n/a
3	chr11:33729190-33729240	BJ	skin:	n/a
4	chr11:33729190-33729240	GM19239	blood:	n/a
5	chr11:33729190-33729240	GM06990	blood:	n/a
6	chr11:33729190-33729240	HCPEpiC	choroid plexus:	n/a
7	chr11:33729190-33729240	ECC-1	luminal epithelium:	n/a
8	chr11:33729190-33729240	SK-N-SH_RA	brain:	n/a
9	chr11:33729190-33729240	AG10803	skin:	n/a
10	chr11:33729190-33729240	NT2-D1	testis:	n/a
11	chr11:33729190-33729240	GM12878	blood:	n/a
12	chr11:33729190-33729240	Hepatocyte	liver:	n/a
13	chr11:33729190-33729240	LNCaP	prostate:	n/a
14	chr11:33729190-33729240	HRCEpiC	kidney:	n/a
15	chr11:33729190-33729240	HUVEC	blood vessel:	n/a
16	chr11:33729190-33729240	AG09309	skin:	n/a
17	chr11:33729190-33729240	HRPEpiC	eye:	n/a
18	chr11:33729190-33729240	PrEC	prostate:	n/a
19	chr11:33729190-33729240	SK-N-SH	brain:	n/a
20	chr11:33729190-33729240	AoSMC	blood vessel:	n/a
21	chr11:33729190-33729240	HRE	kidney:	n/a
22	chr11:33729190-33729240	NHDF-neo	bronchial:	n/a
23	chr11:33729190-33729240	SK-N-MC	brain:	n/a
24	chr11:33729190-33729240	IMR90	lung:	fetal
25	chr11:33729190-33729240	Hela-S3	cervix:	n/a
26	chr11:33729190-33729240	H1-hESC	embryonic stem cell:	embryo
27	chr11:33729190-33729240	T-47D	breast:	n/a
28	chr11:33729190-33729240	HEEpiC	esophagus:	n/a
29	chr11:33729190-33729240	HAEpiC	amniotic membrane:	n/a
30	chr11:33729190-33729240	PFSK-1	brain:	n/a
31	chr11:33729190-33729240	RPTEC	kidney:	n/a
32	chr11:33729190-33729240	AG04449	skin:	fetal
33	chr11:33729190-33729240	A549	lung:	n/a
34	chr11:33729190-33729240	NH-A	brain:	n/a
35	chr11:33729190-33729240	GM12891	blood:	n/a
36	chr11:33729190-33729240	MCF-7	breast:	n/a
37	chr11:33729190-33729240	U87	brain:	n/a
38	chr11:33729190-33729240	ProgFib	skin:	n/a
39	chr11:33729190-33729240	NB4	blood:	n/a
40	chr11:33729190-33729240	HepG2	liver:	n/a
41	chr11:33729190-33729240	HMEC	breast:	n/a
42	chr11:33729190-33729240	HEK293	kidney:	embryo
43	chr11:33729190-33729240	PANC-1	pancreas:	n/a
44	chr11:33729190-33729240	HPAEpiC	pulmonary alveolar:	n/a
45	chr11:33729190-33729240	HCF	heart:	n/a
46	chr11:33729190-33729240	MCF10A-Er-Src	breast:	n/a
47	chr11:33729190-33729240	SKMC	muscle:	n/a
48	chr11:33729190-33729240	K562	blood:	n/a
49	chr11:33729190-33729240	Jurkat	blood:	n/a
50	chr11:33729190-33729240	Caco-2	colon:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:33722219..33726232-chr11:33726761..33732163,6	K562	blood:
2	chr11:33722652..33724426-chr11:33725685..33727649,2	MCF-7	breast:
3	chr11:33726536..33728687-chr11:33732022..33734323,2	K562	blood:
4	chr11:33722379..33724106-chr11:33727718..33730003,2	K562	blood:
5	chr11:33724538..33726806-chr11:33736477..33738773,2	MCF-7	breast:
6	chr11:33722219..33726232-chr11:33726761..33732163,6	K562	blood:
7	chr11:33729551..33732086-chr11:33743744..33746634,3	K562	blood:
8	chr11:33714211..33716994-chr11:33723846..33727009,3	MCF-7	breast:
9	chr11:33720026..33726393-chr11:33756116..33759860,12	MCF-7	breast:
10	chr11:33722591..33725977-chr11:33729219..33731745,3	MCF-7	breast:
11	chr11:33728871..33731814-chr11:33757804..33759607,3	MCF-7	breast:
12	chr11:33722397..33723935-chr11:33724881..33726688,2	K562	blood:
13	chr11:33722591..33725977-chr11:33729219..33731745,3	MCF-7	breast:
14	chr11:33721709..33724293-chr11:33724908..33726754,2	K562	blood:
15	chr11:33727421..33729812-chr11:33757140..33760586,3	K562	blood:
16	chr11:33719802..33725980-chr11:33755197..33760109,10	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C11orf91-1	chr11:33724567-33725791	NONHSAT018710

No data

Variant related genes	Relation type
C11orf91	TF binding region
C11orf91	CpG island
ENSG00000085063	chromatin interactions
ENSG00000205177	chromatin interactions

Extended variants
information (count: 182 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:182 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553132200	chr11:33725292-33725293	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs572972301	chr11:33725307-33725308	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs541886702	chr11:33725334-33725335	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs555361149	chr11:33725340-33725341	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs139205836	chr11:33725351-33725352	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs564828161	chr11:33725353-33725354	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs376030631	chr11:33725357-33725358	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs149759939	chr11:33725366-33725367	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs564138996	chr11:33725374-33725375	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs190331319	chr11:33725384-33725385	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs540038846	chr11:33725398-33725399	Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs112739416	chr11:33725435-33725436	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs529309614	chr11:33725463-33725464	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs548970580	chr11:33725464-33725465	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs569207862	chr11:33725499-33725500	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs139612286	chr11:33725509-33725510	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs552086469	chr11:33725511-33725512	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs144332932	chr11:33725542-33725543	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs534450498	chr11:33725551-33725552	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
20	rs181152494	chr11:33725589-33725590	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs566580758	chr11:33725593-33725594	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs535493370	chr11:33725640-33725641	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs73481002	chr11:33725737-33725738	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs111350654	chr11:33725742-33725743	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs537424942	chr11:33725747-33725748	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs143165441	chr11:33725757-33725758	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs58634493	chr11:33725759-33725760	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs531082156	chr11:33725777-33725778	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs558082049	chr11:33725779-33725780	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs529415307	chr11:33725802-33725803	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs190358780	chr11:33725809-33725810	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs540049316	chr11:33725846-33725847	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs73482903	chr11:33725880-33725881	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs146600210	chr11:33725927-33725928	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs542680180	chr11:33725934-33725935	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs112851123	chr11:33725968-33725969	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs60513302	chr11:33725992-33725993	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs143346574	chr11:33726028-33726029	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs565612441	chr11:33726030-33726031	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs527948089	chr11:33726031-33726032	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs1738549	chr11:33726035-33726036	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs539604875	chr11:33726062-33726063	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs7943851	chr11:33726066-33726067	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs185478880	chr11:33726085-33726086	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs151313805	chr11:33726087-33726088	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs567645545	chr11:33726107-33726108	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs12420931	chr11:33726149-33726150	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs150294211	chr11:33726196-33726197	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs1546727	chr11:33726222-33726223	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs114518661	chr11:33726228-33726229	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Breast cancer	21364760	CNVD
Glioblastoma multiforme	22286061	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:33718400-33725800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr11:33722400-33728800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr11:33722800-33725600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr11:33722800-33728600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr11:33722800-33730600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr11:33723000-33725800	Enhancers	Duodenum Mucosa	Duodenum
7	chr11:33723000-33726000	Enhancers	Fetal Intestine Small	intestine
8	chr11:33723000-33726000	Enhancers	Small Intestine	intestine
9	chr11:33723000-33726400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:33723000-33726400	Enhancers	Fetal Intestine Large	intestine
11	chr11:33723000-33730600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr11:33723000-33746000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr11:33723200-33725400	Weak transcription	Fetal Muscle Trunk	muscle
14	chr11:33723200-33726000	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr11:33723200-33726000	Enhancers	HSMM	muscle
16	chr11:33723200-33726400	Enhancers	Colonic Mucosa	Colon
17	chr11:33723200-33726600	Weak transcription	Aorta	Aorta
18	chr11:33723200-33726800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr11:33723200-33726800	Weak transcription	Ovary	ovary
20	chr11:33723200-33728200	Weak transcription	GM12878-XiMat	blood
21	chr11:33723200-33728400	Enhancers	Brain Angular Gyrus	brain
22	chr11:33723200-33728800	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr11:33723200-33729600	Weak transcription	HUES64 Cell Line	embryonic stem cell
24	chr11:33723200-33730200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
25	chr11:33723200-33730200	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr11:33723200-33730200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr11:33723200-33730400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr11:33723200-33730600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr11:33723200-33730600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:33723200-33730600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
31	chr11:33723200-33731000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr11:33723200-33731200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr11:33723200-33737400	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr11:33723200-33744400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
35	chr11:33723200-33744400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
36	chr11:33723400-33725400	Enhancers	NHLF	lung
37	chr11:33723400-33725600	Enhancers	Skeletal Muscle Female	skeletal muscle
38	chr11:33723400-33726000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr11:33723400-33726400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr11:33723400-33726800	Weak transcription	Primary T cells from cord blood	blood
41	chr11:33723400-33726800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr11:33723400-33728200	Weak transcription	Stomach Smooth Muscle	stomach
43	chr11:33723400-33728600	Enhancers	Brain Hippocampus Middle	brain
44	chr11:33723400-33728800	Enhancers	Brain Substantia Nigra	brain
45	chr11:33723400-33729600	Weak transcription	Primary T helper cells PMA-I stimulated	--
46	chr11:33723400-33730200	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr11:33723400-33730200	Weak transcription	Rectal Smooth Muscle	rectum
48	chr11:33723400-33731000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr11:33723400-33731200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr11:33723400-33735000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood

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