Variant report

Variant	nsv1059314
Chromosome Location	chr22:31893613-31936088
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:296)
CpG islands
(count:61)
Chromatin interactive
region (count:23)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:296 , 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	ARID3A	chr22:31926449-31927040	HepG2	liver:	n/a	n/a
2	ATF2	chr22:31934659-31935425	GM12878	blood:	n/a	n/a
3	ATF2	chr22:31932812-31933569	GM12878	blood:	n/a	n/a
4	ATF2	chr22:31932852-31933662	GM12878	blood:	n/a	n/a
5	ATF2	chr22:31934714-31935235	GM12878	blood:	n/a	n/a
6	BATF	chr22:31932933-31933569	GM12878	blood:	n/a	n/a
7	BATF	chr22:31932926-31933388	GM12878	blood:	n/a	n/a
8	BATF	chr22:31916048-31916368	GM12878	blood:	n/a	n/a
9	BATF	chr22:31893442-31893799	GM12878	blood:	n/a	n/a
10	BATF	chr22:31916079-31916329	GM12878	blood:	n/a	n/a
11	BATF	chr22:31934780-31935139	GM12878	blood:	n/a	n/a
12	BCL11A	chr22:31934808-31935153	GM12878	blood:	n/a	n/a
13	BCL11A	chr22:31932986-31933351	GM12878	blood:	n/a	n/a
14	BCL3	chr22:31932953-31933350	GM12878	blood:	n/a	n/a
15	BCL3	chr22:31928591-31928965	GM12878	blood:	n/a	n/a
16	BCLAF1	chr22:31932863-31933451	GM12878	blood:	n/a	n/a
17	BCLAF1	chr22:31934748-31935242	GM12878	blood:	n/a	n/a
18	BCLAF1	chr22:31934354-31935291	GM12878	blood:	n/a	n/a
19	BCLAF1	chr22:31932868-31933326	GM12878	blood:	n/a	n/a
20	BHLHE40	chr22:31934815-31935180	GM12878	blood:	n/a	n/a
21	CEBPB	chr22:31934488-31935305	GM12878	blood:	n/a	n/a
22	CEBPB	chr22:31921448-31921784	MCF-7	breast:	n/a	chr22:31921653-31921664
23	CEBPB	chr22:31926493-31927001	IMR90	lung:	n/a	n/a
24	CEBPB	chr22:31926498-31926727	HepG2	liver:	n/a	n/a
25	CEBPB	chr22:31921507-31921779	IMR90	lung:	n/a	chr22:31921653-31921664
26	CEBPB	chr22:31900299-31900814	IMR90	lung:	n/a	n/a
27	CEBPB	chr22:31921493-31921769	HepG2	liver:	n/a	chr22:31921653-31921664
28	CEBPB	chr22:31921516-31921764	A549	lung:	n/a	chr22:31921653-31921664
29	CEBPB	chr22:31921591-31921766	H1-hESC	embryonic stem cell:	n/a	chr22:31921653-31921664
30	CEBPB	chr22:31921636-31921697	K562	blood:	n/a	chr22:31921653-31921664
31	CEBPB	chr22:31900440-31900533	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr22:31934730-31935160	GM12878	blood:	n/a	n/a
33	CREB1	chr22:31932767-31933714	GM12878	blood:	n/a	n/a
34	CREB1	chr22:31934640-31935386	GM12878	blood:	n/a	n/a
35	CREB1	chr22:31932905-31933605	GM12878	blood:	n/a	n/a
36	CREB1	chr22:31893219-31894054	GM12878	blood:	n/a	n/a
37	CREB1	chr22:31893409-31893973	GM12878	blood:	n/a	n/a
38	CREB1	chr22:31934655-31935251	GM12878	blood:	n/a	n/a
39	CTCF	chr22:31929328-31929418	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr22:31906423-31906530	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr22:31898029-31898099	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr22:31928340-31928490	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr22:31928260-31928410	AG04449	skin:	n/a	n/a
44	CUX1	chr22:31893438-31893656	GM12878	blood:	n/a	n/a
45	CUX1	chr22:31924685-31924782	GM12878	blood:	n/a	n/a
46	E2F4	chr22:31926749-31927028	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr22:31932949-31933373	GM12878	blood:	n/a	n/a
48	EBF1	chr22:31932934-31933419	GM12878	blood:	n/a	n/a
49	EBF1	chr22:31934822-31935103	GM12878	blood:	n/a	n/a
50	EBF1	chr22:31932039-31932318	GM12878	blood:	n/a	chr22:31932163-31932172 chr22:31932162-31932173 chr22:31932161-31932174 chr22:31932162-31932172

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:31897078-31897128	U87	brain:	n/a
2	chr22:31897078-31897128	NHBE	bronchial:	n/a
3	chr22:31897078-31897128	Caco-2	colon:	n/a
4	chr22:31897078-31897128	SK-N-SH_RA	brain:	n/a
5	chr22:31897078-31897128	PFSK-1	brain:	n/a
6	chr22:31897078-31897128	RPTEC	kidney:	n/a
7	chr22:31897078-31897128	HCT-116	colon:	n/a
8	chr22:31897078-31897128	AG09319	gingival:	n/a
9	chr22:31897078-31897128	AG04449	skin:	fetal
10	chr22:31897078-31897128	NHDF-neo	bronchial:	n/a
11	chr22:31897078-31897128	T-47D	breast:	n/a
12	chr22:31897078-31897128	IMR90	lung:	fetal
13	chr22:31897078-31897128	AG09309	skin:	n/a
14	chr22:31897078-31897128	SAEC	small airway:	n/a
15	chr22:31897078-31897128	SK-N-MC	brain:	n/a
16	chr22:31897078-31897128	HUVEC	blood vessel:	n/a
17	chr22:31897078-31897128	PrEC	prostate:	n/a
18	chr22:31897078-31897128	BJ	skin:	n/a
19	chr22:31897078-31897128	ECC-1	luminal epithelium:	n/a
20	chr22:31897078-31897128	H1-hESC	embryonic stem cell:	embryo
21	chr22:31897078-31897128	HIPEpiC	eye:	n/a
22	chr22:31897078-31897128	ProgFib	skin:	n/a
23	chr22:31897078-31897128	HepG2	liver:	n/a
24	chr22:31897078-31897128	Jurkat	blood:	n/a
25	chr22:31897078-31897128	HL-60	blood:	n/a
26	chr22:31897078-31897128	MCF-7	breast:	n/a
27	chr22:31897078-31897128	AG04450	lung:	fetal
28	chr22:31897078-31897128	AoSMC	blood vessel:	n/a
29	chr22:31897078-31897128	SK-N-SH	brain:	n/a
30	chr22:31897078-31897128	CMK	blood:	n/a
31	chr22:31897078-31897128	BE2_C	brain:	n/a
32	chr22:31897078-31897128	SKMC	muscle:	n/a
33	chr22:31897078-31897128	NB4	blood:	n/a
34	chr22:31897078-31897128	HMEC	breast:	n/a
35	chr22:31897078-31897128	NT2-D1	testis:	n/a
36	chr22:31897078-31897128	K562	blood:	n/a
37	chr22:31897078-31897128	HAEpiC	amniotic membrane:	n/a
38	chr22:31897078-31897128	HEEpiC	esophagus:	n/a
39	chr22:31897078-31897128	Hela-S3	cervix:	n/a
40	chr22:31897078-31897128	HCM	heart:	n/a
41	chr22:31897078-31897128	AG10803	skin:	n/a
42	chr22:31897078-31897128	HNPCEpiC	eye:	n/a
43	chr22:31897078-31897128	GM12878	blood:	n/a
44	chr22:31897078-31897128	HCPEpiC	choroid plexus:	n/a
45	chr22:31897078-31897128	PANC-1	pancreas:	n/a
46	chr22:31897078-31897128	HRCEpiC	kidney:	n/a
47	chr22:31897078-31897128	HRPEpiC	eye:	n/a
48	chr22:31897078-31897128	HRE	kidney:	n/a
49	chr22:31897078-31897128	ovcar-3	ovarian:	n/a
50	chr22:31897078-31897128	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	22:31930706-31935473..22:32012966-32043914	GM12878	blood:
2	chr22:31895925..31897585-chr22:31899327..31902230,2	K562	blood:
3	chr22:31915170..31916943-chr22:31918334..31921689,3	K562	blood:
4	chr22:31926551..31928354-chr22:31935476..31937024,2	K562	blood:
5	chr22:31928865..31930656-chr22:31938813..31940821,2	MCF-7	breast:
6	chr22:31892695..31894776-chr22:32016253..32018919,2	K562	blood:
7	22:31936007-31936880..22:32338420-32342898	K562	blood:
8	22:31864703-31891033..22:31930706-31935473	GM12878	blood:
9	chr22:31895644..31897585-chr22:31899488..31902230,2	K562	blood:
10	chr22:31915170..31916943-chr22:31918334..31921689,3	K562	blood:
11	chr22:31892433..31894421-chr22:31898516..31901632,3	K562	blood:
12	chr22:31892596..31895248-chr22:31897166..31900535,3	MCF-7	breast:
13	chr22:31907252..31908998-chr22:32028816..32030585,2	MCF-7	breast:
14	chr22:31892881..31894794-chr22:31897314..31900016,2	K562	blood:
15	chr22:31895925..31897585-chr22:31899327..31902230,2	K562	blood:
16	chr22:31892596..31895248-chr22:31897166..31900535,3	MCF-7	breast:
17	chr22:31926551..31928354-chr22:31935476..31937024,2	K562	blood:
18	chr22:31901562..31903154-chr22:32024706..32027058,2	MCF-7	breast:
19	chr22:31892881..31894794-chr22:31897314..31900016,2	K562	blood:
20	chr22:31890839..31893648-chr22:31927423..31929799,2	MCF-7	breast:
21	chr22:31884404..31886896-chr22:31898271..31902090,3	MCF-7	breast:
22	chr22:31883080..31888273-chr22:31897152..31901136,10	MCF-7	breast:
23	chr22:31895644..31897585-chr22:31899488..31902230,2	K562	blood:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SFI1-2	chr22:31924676-31924852	NONHSAT084896
2	lnc-SFI1-2	chr22:31904241-31904362	NONHSAT084895
3	lnc-SFI1-2	chr22:31924676-31925053	NONHSAT084895
4	lnc-EIF4ENIF1-5	chr22:31934338-31934575	NONHSAT084898
5	lnc-SFI1-2	chr22:31917221-31917306	NONHSAT084896
6	lnc-EIF4ENIF1-4	chr22:31917185-31917578	NONHSAT084897
7	lnc-SFI1-2	chr22:31904241-31904362	NONHSAT084896

No data

Variant related genes	Relation type
ENSG00000229169	TF binding region
EIF4ENIF1	TF binding region
H2AFZP6	TF binding region
SFI1	TF binding region
ENSG00000229169	CpG island
EIF4ENIF1	CpG island
H2AFZP6	CpG island
SFI1	CpG island
ENSG00000241878	chromatin interactions
ENSG00000128245	chromatin interactions
ENSG00000128254	chromatin interactions
ENSG00000198089	chromatin interactions
ENSG00000184708	chromatin interactions
ENSG00000199248	chromatin interactions

Extended variants
information (count: 1628 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5753659	chr22:31893613-31893614	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138748894	chr22:31893642-31893643	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs541492785	chr22:31893645-31893646	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs199862315	chr22:31893651-31893652	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs60809082	chr22:31893654-31893655	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs398061886	chr22:31893669-31893670	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs143489432	chr22:31893671-31893672	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs530108122	chr22:31893677-31893678	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs550208002	chr22:31893725-31893726	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs563925427	chr22:31893726-31893727	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs9609297	chr22:31893731-31893732	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs552462140	chr22:31893732-31893733	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs183833415	chr22:31893745-31893746	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs188105310	chr22:31893753-31893754	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs180846652	chr22:31893761-31893762	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs567065967	chr22:31893784-31893785	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs535807587	chr22:31893799-31893800	Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs185848878	chr22:31893829-31893830	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs545969996	chr22:31893897-31893898	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs576220446	chr22:31893910-31893911	Weak transcription ZNF genes & repeats Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs71319198	chr22:31894002-31894003	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs148014585	chr22:31894046-31894047	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs190322639	chr22:31894051-31894052	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs9621273	chr22:31894062-31894063	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs531694185	chr22:31894063-31894064	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111553097	chr22:31894107-31894108	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs376851517	chr22:31894122-31894123	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555060695	chr22:31894149-31894150	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138677784	chr22:31894150-31894151	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs543811239	chr22:31894178-31894179	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs563690466	chr22:31894182-31894183	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113953412	chr22:31894196-31894197	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532436791	chr22:31894205-31894206	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs546457181	chr22:31894215-31894216	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9619204	chr22:31894225-31894226	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9609299	chr22:31894237-31894238	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs367717531	chr22:31894253-31894254	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs35517776	chr22:31894263-31894264	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545390259	chr22:31894289-31894290	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs548386561	chr22:31894291-31894292	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2413053	chr22:31894310-31894311	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs548105837	chr22:31894316-31894317	Weak transcription Enhancers Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529751827	chr22:31894436-31894437	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549497748	chr22:31894447-31894448	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569608823	chr22:31894457-31894458	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs538302434	chr22:31894493-31894494	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs182088146	chr22:31894515-31894516	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565845176	chr22:31894532-31894533	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369153391	chr22:31894543-31894544	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35069980	chr22:31894635-31894636	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
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	17142309	CNVD
Autism	22543975	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:966 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:31891600-31893800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr22:31891800-31893800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr22:31891800-31893800	Active TSS	Fetal Lung	lung
4	chr22:31892000-31893800	Active TSS	Fetal Heart	heart
5	chr22:31892200-31893800	Active TSS	Primary T cells fromperipheralblood	blood
6	chr22:31892600-31893800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
7	chr22:31892800-31894200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
8	chr22:31893000-31893800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr22:31893000-31893800	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
10	chr22:31893000-31893800	Flanking Active TSS	HMEC	breast
11	chr22:31893000-31905200	Weak transcription	Aorta	Aorta
12	chr22:31893200-31893800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr22:31893200-31893800	Enhancers	Spleen	Spleen
14	chr22:31893200-31894000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
15	chr22:31893200-31894000	ZNF genes & repeats	Primary hematopoietic stem cells	blood
16	chr22:31893200-31894000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
17	chr22:31893200-31894200	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr22:31893200-31903600	Weak transcription	Left Ventricle	heart
19	chr22:31893200-31912200	Weak transcription	Small Intestine	intestine
20	chr22:31893200-31934800	Weak transcription	Ovary	ovary
21	chr22:31893400-31893800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
22	chr22:31893400-31893800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr22:31893400-31893800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
24	chr22:31893400-31893800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
25	chr22:31893400-31893800	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr22:31893400-31893800	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr22:31893400-31893800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr22:31893400-31893800	Enhancers	Brain Cingulate Gyrus	brain
29	chr22:31893400-31893800	Enhancers	Colon Smooth Muscle	Colon
30	chr22:31893400-31893800	ZNF genes & repeats	Fetal Muscle Leg	muscle
31	chr22:31893400-31893800	Flanking Active TSS	Fetal Thymus	thymus
32	chr22:31893400-31893800	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr22:31893400-31893800	Enhancers	Sigmoid Colon	Sigmoid Colon
34	chr22:31893400-31893800	Flanking Active TSS	Thymus	Thymus
35	chr22:31893400-31893800	Flanking Active TSS	Hela-S3	cervix
36	chr22:31893400-31894000	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr22:31893400-31894000	Flanking Active TSS	Primary T cells from cord blood	blood
38	chr22:31893400-31894000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
39	chr22:31893400-31894000	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
40	chr22:31893400-31894000	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
41	chr22:31893400-31894000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
42	chr22:31893400-31894000	Enhancers	Brain Substantia Nigra	brain
43	chr22:31893400-31894000	Transcr. at gene 5' and 3'	Dnd41	blood
44	chr22:31893400-31894000	Active TSS	NH-A	brain
45	chr22:31893400-31894200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr22:31893400-31896600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr22:31893400-31897400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr22:31893400-31900000	Weak transcription	HSMM	muscle
49	chr22:31893400-31905200	Weak transcription	Fetal Intestine Large	intestine
50	chr22:31893400-31907200	Weak transcription	Fetal Intestine Small	intestine

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