Variant report

Variant	esv3356283
Chromosome Location	chr22:31089477-31092325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:288)
CpG islands
(count:550)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr22:31090028-31090338	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr22:31090018-31090411	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr22:31090926-31091161	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr22:31090133-31090640	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr22:31090815-31091164	K562	blood:	n/a	n/a
6	BHLHE40	chr22:31090209-31091189	GM12878	blood:	n/a	n/a
7	BHLHE40	chr22:31091537-31091847	HepG2	liver:	n/a	n/a
8	CCNT2	chr22:31090951-31091431	K562	blood:	n/a	n/a
9	CEBPB	chr22:31090056-31090384	Hela-S3	cervix:	n/a	n/a
10	CHD1	chr22:31090073-31090273	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr22:31090826-31090873	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr22:31090132-31090365	H1-hESC	embryonic stem cell:	n/a	chr22:31090348-31090358
13	CHD2	chr22:31090850-31091044	GM12878	blood:	n/a	n/a
14	CHD2	chr22:31090167-31090551	GM12878	blood:	n/a	chr22:31090348-31090358
15	CHD2	chr22:31090259-31090525	Hela-S3	cervix:	n/a	chr22:31090348-31090358
16	CHD2	chr22:31091046-31091074	HepG2	liver:	n/a	n/a
17	CREB1	chr22:31090058-31090413	A549	lung:	n/a	n/a
18	CTCF	chr22:31090260-31090410	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr22:31090367-31090377	NHEK	skin:	n/a	n/a
20	CTCF	chr22:31089340-31089490	GM12872	blood:	n/a	n/a
21	CTCF	chr22:31091386-31091454	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr22:31090280-31090430	A549	lung:	n/a	n/a
23	CTCF	chr22:31090920-31091070	NHEK	skin:	n/a	n/a
24	CTCF	chr22:31090928-31091021	GM19239	blood:	n/a	n/a
25	CTCF	chr22:31090964-31090965	MCF-7	breast:	n/a	n/a
26	CTCF	chr22:31090961-31091037	LNCaP	prostate:	n/a	n/a
27	CTCF	chr22:31090966-31091030	MCF-7	breast:	n/a	n/a
28	CTCF	chr22:31090260-31090410	HBMEC	blood vessel:	n/a	n/a
29	CTCF	chr22:31090960-31091110	BJ	skin:	n/a	n/a
30	CTCF	chr22:31090389-31090399	GM19240	blood:	n/a	n/a
31	CTCF	chr22:31090940-31091090	GM12864	blood:	n/a	n/a
32	CTCF	chr22:31090980-31091130	GM12875	blood:	n/a	n/a
33	CTCF	chr22:31090898-31091082	MCF-7	breast:	n/a	n/a
34	CTCF	chr22:31090880-31091030	GM12875	blood:	n/a	n/a
35	CTCF	chr22:31091000-31091150	Caco-2	colon:	n/a	n/a
36	CTCF	chr22:31090216-31090601	GM12878	blood:	n/a	n/a
37	CTCF	chr22:31090920-31091070	GM12868	blood:	n/a	n/a
38	CTCF	chr22:31090381-31090419	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr22:31090382-31090402	NHEK	skin:	n/a	n/a
40	CTCF	chr22:31090860-31091010	BE2_C	brain:	n/a	n/a
41	CTCF	chr22:31090268-31090430	GM19238	blood:	n/a	n/a
42	CTCF	chr22:31090275-31090392	MCF-7	breast:	n/a	n/a
43	CTCF	chr22:31090220-31090370	AG04449	skin:	n/a	n/a
44	CTCF	chr22:31090960-31091110	GM12873	blood:	n/a	n/a
45	CTCF	chr22:31090240-31090390	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr22:31090160-31090310	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr22:31090940-31091090	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr22:31090940-31091090	MCF-7	breast:	n/a	n/a
49	CTCF	chr22:31090400-31090550	GM06990	blood:	n/a	n/a
50	CTCF	chr22:31090960-31091110	SK-N-SH_RA	brain:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:31090071-31090121	HMEC	breast:	n/a
2	chr22:31090071-31090121	HMEC	breast:	n/a
3	chr22:31090201-31090251	SK-N-SH	brain:	n/a
4	chr22:31090747-31090797	PrEC	prostate:	n/a
5	chr22:31090201-31090251	HRPEpiC	eye:	n/a
6	chr22:31090223-31090273	HIPEpiC	eye:	n/a
7	chr22:31090201-31090251	PFSK-1	brain:	n/a
8	chr22:31090071-31090121	HCPEpiC	choroid plexus:	n/a
9	chr22:31090747-31090797	HepG2	liver:	n/a
10	chr22:31091262-31091312	AG10803	skin:	n/a
11	chr22:31091262-31091312	HAEpiC	amniotic membrane:	n/a
12	chr22:31090725-31090775	HAEpiC	amniotic membrane:	n/a
13	chr22:31090740-31090790	AG09319	gingival:	n/a
14	chr22:31090201-31090251	HNPCEpiC	eye:	n/a
15	chr22:31091262-31091312	HL-60	blood:	n/a
16	chr22:31090071-31090121	SK-N-SH	brain:	n/a
17	chr22:31090740-31090790	HRCEpiC	kidney:	n/a
18	chr22:31090747-31090797	ProgFib	skin:	n/a
19	chr22:31090071-31090121	RPTEC	kidney:	n/a
20	chr22:31090201-31090251	IMR90	lung:	fetal
21	chr22:31090352-31090402	HCPEpiC	choroid plexus:	n/a
22	chr22:31090740-31090790	PFSK-1	brain:	n/a
23	chr22:31090201-31090251	LNCaP	prostate:	n/a
24	chr22:31090071-31090121	GM12892	blood:	n/a
25	chr22:31090071-31090121	GM12878	blood:	n/a
26	chr22:31090352-31090402	AG10803	skin:	n/a
27	chr22:31090201-31090251	HMEC	breast:	n/a
28	chr22:31090071-31090121	NHBE	bronchial:	n/a
29	chr22:31091262-31091312	ECC-1	luminal epithelium:	n/a
30	chr22:31090740-31090790	HAEpiC	amniotic membrane:	n/a
31	chr22:31090352-31090402	NHBE	bronchial:	n/a
32	chr22:31090725-31090775	HPAEpiC	pulmonary alveolar:	n/a
33	chr22:31090223-31090273	SK-N-MC	brain:	n/a
34	chr22:31091550-31091600	T-47D	breast:	n/a
35	chr22:31091550-31091600	GM12892	blood:	n/a
36	chr22:31090071-31090121	HepG2	liver:	n/a
37	chr22:31090201-31090251	PANC-1	pancreas:	n/a
38	chr22:31090740-31090790	H1-hESC	embryonic stem cell:	embryo
39	chr22:31090740-31090790	AG04449	skin:	fetal
40	chr22:31091550-31091600	PANC-1	pancreas:	n/a
41	chr22:31090223-31090273	SK-N-SH_RA	brain:	n/a
42	chr22:31090223-31090273	T-47D	breast:	n/a
43	chr22:31090725-31090775	HRPEpiC	eye:	n/a
44	chr22:31090352-31090402	AG04450	lung:	fetal
45	chr22:31091262-31091312	HRCEpiC	kidney:	n/a
46	chr22:31090352-31090402	HCF	heart:	n/a
47	chr22:31090747-31090797	HPAEpiC	pulmonary alveolar:	n/a
48	chr22:31091550-31091600	AG04450	lung:	fetal
49	chr22:31090223-31090273	HRE	kidney:	n/a
50	chr22:31090740-31090790	SK-N-SH	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:31031588..31032094-chr22:31090123..31090949,2	MCF-7	breast:
2	chr22:30820440..30822751-chr22:31090157..31092444,2	MCF-7	breast:
3	chr22:31057579..31060597-chr22:31088878..31091753,3	MCF-7	breast:
4	chr22:31062803..31066328-chr22:31088733..31092098,4	MCF-7	breast:
5	chr22:31062708..31065866-chr22:31088934..31092028,6	MCF-7	breast:
6	chr22:31090489..31091184-chr8:687600..688120,2	MCF-7	breast:

No data

Variant related genes	Relation type
OSBP2	TF binding region
OSBP2	CpG island
ENSG00000100036	chromatin interactions
ENSG00000237647	chromatin interactions
ENSG00000104714	chromatin interactions
ENSG00000167065	chromatin interactions
ENSG00000242114	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5994333	chr22:31089543-31089544	Weak transcription Bivalent/Poised TSS Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs186815598	chr22:31089710-31089711	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs547411192	chr22:31089721-31089722	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs547001678	chr22:31089756-31089757	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs375120998	chr22:31089773-31089774	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368202793	chr22:31089774-31089775	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs566777536	chr22:31089782-31089783	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs529356265	chr22:31089797-31089798	Weak transcription Enhancers Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs116428241	chr22:31089816-31089817	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs569427330	chr22:31089831-31089832	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs372364316	chr22:31089847-31089848	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs191754938	chr22:31089909-31089910	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571997909	chr22:31089912-31089913	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534245751	chr22:31089938-31089939	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201775325	chr22:31089958-31089959	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs397951804	chr22:31089971-31089972	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs552899736	chr22:31090003-31090004	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200529884	chr22:31090013-31090014	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs532801857	chr22:31090052-31090053	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs111265481	chr22:31090067-31090068	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs67289012	chr22:31090068-31090069	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs111696013	chr22:31090071-31090072	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs572759413	chr22:31090077-31090078	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs114356320	chr22:31090164-31090165	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs78160826	chr22:31090183-31090184	Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs375975281	chr22:31090224-31090225	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs79925406	chr22:31090244-31090245	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs558578607	chr22:31090245-31090246	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs538364972	chr22:31090266-31090267	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs569016755	chr22:31090314-31090315	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs560499637	chr22:31090331-31090332	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs537812548	chr22:31090355-31090356	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs554564058	chr22:31090370-31090371	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs181340992	chr22:31090374-31090375	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs574519471	chr22:31090390-31090391	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs368529570	chr22:31090394-31090395	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs531927235	chr22:31090406-31090407	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs557937551	chr22:31090428-31090429	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs74322462	chr22:31090450-31090451	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs186485235	chr22:31090482-31090483	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs534465362	chr22:31090506-31090507	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs547778438	chr22:31090510-31090511	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs566457269	chr22:31090524-31090525	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs554208222	chr22:31090567-31090568	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs11387475	chr22:31090571-31090572	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs11912993	chr22:31090582-31090583	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs564754571	chr22:31090611-31090612	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs72436834	chr22:31090616-31090617	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs368086078	chr22:31090617-31090618	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs75060437	chr22:31090619-31090620	Bivalent/Poised TSS Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Velocardiofacial syndrome	20111667	CNVD
Medulloblastoma	21979893	CNVD
sporadic solitary meningiomas	19589153	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Congenital heart defect	22511896	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Seminomas	18059402	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Metachromatic leukodystrophy	18421352	CNVD
Basal cell lymphoma	17170743	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Breast cancer	21858162	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Ovarian cancer	22174824	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	21251322	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Cancer	21183584	CNVD
Renal cell carcinoma	18765545	CNVD
Schizophrenia	19521646	CNVD
Schizophrenia	18990708	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Hepatocellular carcinoma	16750200	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31077400-31089800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr22:31077400-31090000	Weak transcription	Fetal Heart	heart
3	chr22:31077600-31090000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr22:31086000-31089800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr22:31087600-31090000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr22:31087800-31089800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr22:31087800-31090000	Weak transcription	NHDF-Ad	bronchial
8	chr22:31089200-31089800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr22:31089200-31089800	Enhancers	Brain Germinal Matrix	brain
10	chr22:31089200-31089800	Enhancers	Fetal Brain Female	brain
11	chr22:31089200-31090000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr22:31089200-31090000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr22:31089400-31089600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
14	chr22:31089400-31089600	Bivalent/Poised TSS	Primary B cells from cord blood	blood
15	chr22:31089400-31089800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr22:31089400-31089800	Enhancers	Brain Anterior Caudate	brain
17	chr22:31089400-31090000	Enhancers	Primary T helper cells PMA-I stimulated	--
18	chr22:31089400-31090000	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr22:31089400-31091600	Active TSS	Fetal Kidney	kidney
20	chr22:31089600-31089800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
21	chr22:31089600-31089800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr22:31089600-31089800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr22:31089600-31090000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
24	chr22:31089600-31090000	Enhancers	Primary hematopoietic stem cells	blood
25	chr22:31089600-31090000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chr22:31089600-31090000	Enhancers	GM12878-XiMat	blood
27	chr22:31089800-31090000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr22:31089800-31090000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr22:31089800-31090000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr22:31089800-31090000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
31	chr22:31089800-31090000	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr22:31089800-31090000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
33	chr22:31089800-31090000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
34	chr22:31089800-31090000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr22:31089800-31090000	Enhancers	Muscle Satellite Cultured Cells	--
36	chr22:31089800-31090000	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr22:31089800-31090000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr22:31089800-31090000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr22:31089800-31090000	Enhancers	Liver	Liver
40	chr22:31089800-31090000	Enhancers	Brain Angular Gyrus	brain
41	chr22:31089800-31090000	Active TSS	Brain Anterior Caudate	brain
42	chr22:31089800-31090000	Weak transcription	Brain Germinal Matrix	brain
43	chr22:31089800-31090000	Enhancers	Colonic Mucosa	Colon
44	chr22:31089800-31090000	Enhancers	Colon Smooth Muscle	Colon
45	chr22:31089800-31090000	Enhancers	Duodenum Mucosa	Duodenum
46	chr22:31089800-31090000	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
47	chr22:31089800-31090000	Enhancers	Esophagus	oesophagus
48	chr22:31089800-31090000	Enhancers	Fetal Intestine Small	intestine
49	chr22:31089800-31090000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr22:31089800-31090000	Enhancers	Ovary	ovary

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