Variant report

Variant	nsv817417
Chromosome Location	chr22:29998464-30035142
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1551)
CpG islands
(count:915)
Chromatin interactive
region (count:32)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1551 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:29999369-29999506	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:29999159-29999616	K562	blood:	n/a	chr22:29999225-29999240
3	ATF1	chr22:29999113-29999668	K562	blood:	n/a	n/a
4	ATF2	chr22:29999237-29999535	GM12878	blood:	n/a	n/a
5	ATF2	chr22:29999217-29999588	GM12878	blood:	n/a	n/a
6	ATF3	chr22:30018029-30018545	A549	lung:	n/a	n/a
7	ATF3	chr22:30017908-30018534	A549	lung:	n/a	n/a
8	ATF3	chr22:29999232-29999626	K562	blood:	n/a	chr22:29999557-29999566
9	ATF3	chr22:29999382-29999689	K562	blood:	n/a	chr22:29999557-29999566
10	BACH1	chr22:29999147-29999764	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr22:30014184-30014487	GM12878	blood:	n/a	n/a
12	BCL3	chr22:30017900-30018585	A549	lung:	n/a	n/a
13	BCLAF1	chr22:29999465-30000097	GM12878	blood:	n/a	chr22:29999873-29999886
14	BHLHE40	chr22:29999295-29999823	GM12878	blood:	n/a	chr22:29999508-29999524 chr22:29999769-29999785
15	BHLHE40	chr22:29999130-29999695	K562	blood:	n/a	chr22:29999508-29999524
16	BHLHE40	chr22:30021689-30021932	GM12878	blood:	n/a	n/a
17	BHLHE40	chr22:30021663-30021734	K562	blood:	n/a	n/a
18	BRCA1	chr22:29999206-29999683	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr22:29999951-29999970	HepG2	liver:	n/a	n/a
20	BRCA1	chr22:29999750-29999851	GM12878	blood:	n/a	n/a
21	BRCA1	chr22:29999296-29999482	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr22:29999002-29999651	K562	blood:	n/a	n/a
23	CBX3	chr22:30017681-30018651	HCT-116	colon:	n/a	n/a
24	CCNT2	chr22:29999365-30000009	K562	blood:	n/a	n/a
25	CCNT2	chr22:30027823-30027903	K562	blood:	n/a	n/a
26	CEBPB	chr22:30018069-30018495	A549	lung:	n/a	chr22:30018082-30018094
27	CEBPB	chr22:30014379-30014694	A549	lung:	n/a	n/a
28	CEBPB	chr22:30013942-30014734	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr22:30014006-30014672	MCF-7	breast:	n/a	n/a
30	CEBPB	chr22:30022543-30022944	IMR90	lung:	n/a	n/a
31	CEBPB	chr22:30013967-30014775	HCT-116	colon:	n/a	n/a
32	CEBPB	chr22:30017638-30018689	HCT-116	colon:	n/a	chr22:30018536-30018549 chr22:30018082-30018094
33	CEBPB	chr22:30022486-30022961	ECC-1	luminal epithelium:	n/a	n/a
34	CEBPB	chr22:30022545-30022959	MCF-7	breast:	n/a	n/a
35	CEBPB	chr22:30022488-30022952	MCF-7	breast:	n/a	n/a
36	CEBPB	chr22:30022609-30022930	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr22:30018025-30018508	IMR90	lung:	n/a	chr22:30018082-30018094
38	CEBPB	chr22:30022594-30022894	A549	lung:	n/a	n/a
39	CEBPB	chr22:30022538-30023017	A549	lung:	n/a	n/a
40	CEBPB	chr22:30014319-30014542	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr22:30014320-30014654	IMR90	lung:	n/a	n/a
42	CEBPB	chr22:30017973-30018638	ECC-1	luminal epithelium:	n/a	chr22:30018536-30018549 chr22:30018082-30018094
43	CEBPB	chr22:30022616-30022918	HepG2	liver:	n/a	n/a
44	CEBPB	chr22:30013916-30014697	ECC-1	luminal epithelium:	n/a	n/a
45	CEBPB	chr22:29999269-29999655	Hela-S3	cervix:	n/a	chr22:29999437-29999445
46	CEBPB	chr22:30014189-30014791	A549	lung:	n/a	n/a
47	CEBPB	chr22:30020457-30020695	IMR90	lung:	n/a	n/a
48	CEBPB	chr22:30018047-30018320	A549	lung:	n/a	chr22:30018082-30018094
49	CEBPB	chr22:30022574-30022910	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr22:30017997-30018459	ECC-1	luminal epithelium:	n/a	chr22:30018082-30018094

(count:915 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29999883-29999933	NT2-D1	testis:	n/a
2	chr22:29999883-29999933	A549	lung:	n/a
3	chr22:29999402-29999452	GM12892	blood:	n/a
4	chr22:29999457-29999507	AG04450	lung:	fetal
5	chr22:29999554-29999604	PrEC	prostate:	n/a
6	chr22:29999883-29999933	HCPEpiC	choroid plexus:	n/a
7	chr22:29999205-29999255	HEEpiC	esophagus:	n/a
8	chr22:29999326-29999376	MCF10A-Er-Src	breast:	n/a
9	chr22:30000107-30000157	T-47D	breast:	n/a
10	chr22:29999397-29999447	PFSK-1	brain:	n/a
11	chr22:29999516-29999566	BE2_C	brain:	n/a
12	chr22:29999407-29999457	NHBE	bronchial:	n/a
13	chr22:30000107-30000157	Caco-2	colon:	n/a
14	chr22:29999118-29999168	NHBE	bronchial:	n/a
15	chr22:29999883-29999933	HUVEC	blood vessel:	n/a
16	chr22:30000194-30000244	NHBE	bronchial:	n/a
17	chr22:29999516-29999566	MCF-7	breast:	n/a
18	chr22:29999407-29999457	GM12892	blood:	n/a
19	chr22:29999326-29999376	RPTEC	kidney:	n/a
20	chr22:29999516-29999566	LNCaP	prostate:	n/a
21	chr22:29999407-29999457	ECC-1	luminal epithelium:	n/a
22	chr22:30000107-30000157	AG09309	skin:	n/a
23	chr22:29999554-29999604	HMEC	breast:	n/a
24	chr22:29999402-29999452	PFSK-1	brain:	n/a
25	chr22:29999457-29999507	SKMC	muscle:	n/a
26	chr22:30003603-30003653	HEEpiC	esophagus:	n/a
27	chr22:29999407-29999457	AG09319	gingival:	n/a
28	chr22:29999402-29999452	IMR90	lung:	fetal
29	chr22:29999457-29999507	CMK	blood:	n/a
30	chr22:30003603-30003653	NH-A	brain:	n/a
31	chr22:29999444-29999494	HNPCEpiC	eye:	n/a
32	chr22:29999444-29999494	NHDF-neo	bronchial:	n/a
33	chr22:29999457-29999507	PANC-1	pancreas:	n/a
34	chr22:30000194-30000244	SK-N-SH	brain:	n/a
35	chr22:29999516-29999566	HEK293	kidney:	embryo
36	chr22:29999457-29999507	HMEC	breast:	n/a
37	chr22:29999444-29999494	LNCaP	prostate:	n/a
38	chr22:29999402-29999452	NHDF-neo	bronchial:	n/a
39	chr22:29999205-29999255	RPTEC	kidney:	n/a
40	chr22:29999883-29999933	SK-N-SH	brain:	n/a
41	chr22:29999444-29999494	BE2_C	brain:	n/a
42	chr22:30003603-30003653	HCM	heart:	n/a
43	chr22:29999969-30000019	Hepatocyte	liver:	n/a
44	chr22:29999407-29999457	SKMC	muscle:	n/a
45	chr22:29999326-29999376	HCF	heart:	n/a
46	chr22:29999402-29999452	HEEpiC	esophagus:	n/a
47	chr22:29999883-29999933	BE2_C	brain:	n/a
48	chr22:29999516-29999566	SAEC	small airway:	n/a
49	chr22:29999883-29999933	CMK	blood:	n/a
50	chr22:29999883-29999933	HMEC	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:30013839..30015515-chr22:30021150..30023734,2	MCF-7	breast:
2	chr22:29998526..30000327-chr22:30030498..30033329,2	MCF-7	breast:
3	chr22:30013839..30015515-chr22:30021150..30023734,2	MCF-7	breast:
4	chr22:29999599..30001910-chr22:30007013..30009061,2	K562	blood:
5	chr22:29998126..30001095-chr22:30001149..30002674,2	MCF-7	breast:
6	chr22:29999342..30001478-chr22:30003978..30005588,2	MCF-7	breast:
7	chr22:29999342..30001478-chr22:30003978..30005588,2	MCF-7	breast:
8	chr22:30013978..30015955-chr22:30016681..30018575,2	K562	blood:
9	chr22:29998884..29999633-chr3:23958298..23958926,2	NB4	blood:
10	chr22:30019747..30021747-chr22:30036683..30039570,2	MCF-7	breast:
11	chr22:30021415..30023125-chr22:30030680..30033150,2	K562	blood:
12	chr22:30007746..30010687-chr22:30014931..30018872,3	K562	blood:
13	chr22:30000016..30001666-chr22:30003377..30005707,2	K562	blood:
14	chr22:30002736..30005272-chr22:30005511..30007524,2	K562	blood:
15	chr22:29999797..30002683-chr22:30006391..30009061,4	K562	blood:
16	chr22:30006178..30007796-chr22:30012477..30014335,2	MCF-7	breast:
17	chr22:30019261..30020777-chr22:30025452..30026983,2	K562	blood:
18	chr22:30013978..30015955-chr22:30016681..30018575,2	K562	blood:
19	chr22:30010110..30012415-chr22:30019753..30021534,2	K562	blood:
20	chr13:52026823..52027558-chr22:29999049..30000022,2	HCT-116	colon:
21	chr22:30021415..30023125-chr22:30030680..30033150,2	K562	blood:
22	chr22:29975560..29978145-chr22:29998416..30001350,4	MCF-7	breast:
23	chr22:30031527..30032428-chr22:30484594..30485517,5	K562	blood:
24	chr22:29975483..29978642-chr22:29996311..30000725,6	MCF-7	breast:
25	chr22:30019261..30020777-chr22:30025452..30026983,2	K562	blood:
26	chr22:30001741..30005693-chr22:30010044..30012563,3	K562	blood:
27	chr22:29997853..30001127-chr22:30012116..30016282,4	MCF-7	breast:
28	chr22:30007746..30010687-chr22:30014931..30018872,3	K562	blood:
29	chr22:30006178..30007796-chr22:30012477..30014335,2	MCF-7	breast:
30	chr22:30010110..30012415-chr22:30019753..30021534,2	K562	blood:
31	chr22:30002723..30005398-chr22:30022131..30024031,2	MCF-7	breast:
32	chr22:29991169..29993450-chr22:30000929..30002699,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CABP7-2	chr22:30004889-30005490	NONHSAT084715
2	lnc-NEFH-1	chr22:29999564-29999811	NONHSAT084713
3	lnc-NEFH-1	chr22:29999564-29999796	NONHSAT084714

No data

Variant related genes	Relation type
RPEP4	TF binding region
NF2	TF binding region
RPEP4	CpG island
NF2	CpG island
ENSG00000197885	chromatin interactions
ENSG00000186575	chromatin interactions
ENSG00000236778	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000184117	chromatin interactions
ENSG00000233010	chromatin interactions
ENSG00000174748	chromatin interactions

Extended variants
information (count: 1222 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188051396	chr22:29998516-29998517	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs572480137	chr22:29998639-29998640	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542775628	chr22:29998667-29998668	Weak transcription Active TSS Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571330743	chr22:29998711-29998712	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs148459689	chr22:29998820-29998821	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs60091951	chr22:29998830-29998831	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs142608565	chr22:29998833-29998834	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs565169860	chr22:29998852-29998853	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs532484321	chr22:29998863-29998864	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs185174462	chr22:29998865-29998866	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs565761453	chr22:29998870-29998871	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190365260	chr22:29998891-29998892	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs533201506	chr22:29998913-29998914	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs569264303	chr22:29998926-29998927	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs536644603	chr22:29998956-29998957	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs113869485	chr22:29998965-29998966	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs182551418	chr22:29998972-29998973	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs577898203	chr22:29998975-29998976	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs554057011	chr22:29998977-29998978	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs111546722	chr22:29998983-29998984	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs186575833	chr22:29998998-29998999	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs368745480	chr22:29999057-29999058	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs147596838	chr22:29999066-29999067	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs549757204	chr22:29999074-29999075	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs9625839	chr22:29999088-29999089	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs9614001	chr22:29999108-29999109	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs543067023	chr22:29999188-29999189	Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs142062896	chr22:29999206-29999207	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs1800538	chr22:29999236-29999237	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs144246747	chr22:29999242-29999243	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs11090574	chr22:29999309-29999310	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs59243127	chr22:29999340-29999341	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs559560319	chr22:29999344-29999345	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs397832686	chr22:29999345-29999346	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs541678066	chr22:29999349-29999350	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs57056994	chr22:29999350-29999351	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs112049943	chr22:29999358-29999359	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs559461077	chr22:29999387-29999388	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs140062784	chr22:29999413-29999414	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs529863911	chr22:29999428-29999429	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs552077586	chr22:29999458-29999459	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs569400926	chr22:29999493-29999494	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs530551700	chr22:29999499-29999500	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs112995186	chr22:29999518-29999519	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs551731219	chr22:29999523-29999524	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs570135699	chr22:29999584-29999585	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
47	rs539283977	chr22:29999599-29999600	Active TSS Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	Overlapped CNVs	n/a
48	rs571842282	chr22:29999647-29999648	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
49	rs554177413	chr22:29999658-29999659	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	Overlapped CNVs	n/a
50	rs56733822	chr22:29999742-29999743	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:70)

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
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	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
Gastrointestinal stromal cancer	20877625	CNVD
Myelofibrosis	22110671	CNVD
Non-small cell lung cancer	21829676	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
Melanoma	17363583	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:1799 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29977600-29998800	Weak transcription	Right Atrium	heart
2	chr22:29985200-29999000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr22:29985200-29999000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr22:29990200-29999000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr22:29992800-29999000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr22:29993400-29999000	Weak transcription	HSMMtube	muscle
7	chr22:29993600-29999000	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr22:29995000-29998600	Weak transcription	Duodenum Mucosa	Duodenum
9	chr22:29995000-29999000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr22:29995000-29999000	Weak transcription	Colon Smooth Muscle	Colon
11	chr22:29995000-29999000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr22:29995000-29999000	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr22:29995400-29999000	Weak transcription	Fetal Intestine Large	intestine
14	chr22:29997000-29999000	Weak transcription	Placenta	Placenta
15	chr22:29997600-29998600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr22:29997600-29999000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr22:29997600-29999000	Enhancers	Fetal Muscle Trunk	muscle
18	chr22:29997800-29998800	Enhancers	A549	lung
19	chr22:29997800-29999000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr22:29997800-29999000	Enhancers	Fetal Muscle Leg	muscle
21	chr22:29997800-29999000	Weak transcription	K562	blood
22	chr22:29998000-29998600	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr22:29998000-29998600	Enhancers	Hela-S3	cervix
24	chr22:29998000-29999000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr22:29998000-29999000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr22:29998000-29999000	Weak transcription	Fetal Intestine Small	intestine
27	chr22:29998000-29999000	Weak transcription	NH-A	brain
28	chr22:29998000-29999000	Weak transcription	NHEK	skin
29	chr22:29998200-29998800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr22:29998400-29998600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr22:29998400-29998600	Enhancers	Dnd41	blood
32	chr22:29998400-29998600	Enhancers	GM12878-XiMat	blood
33	chr22:29998400-29999000	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr22:29998400-30000200	Active TSS	Primary T killer memory cells from peripheral blood	blood
35	chr22:29998400-30001200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr22:29998600-29998800	Enhancers	Primary T cells fromperipheralblood	blood
37	chr22:29998600-29998800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr22:29998600-29998800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr22:29998600-29998800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr22:29998600-29998800	Weak transcription	Brain Anterior Caudate	brain
41	chr22:29998600-29998800	Flanking Active TSS	Dnd41	blood
42	chr22:29998600-29998800	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr22:29998600-29999000	Enhancers	Primary monocytes fromperipheralblood	blood
44	chr22:29998600-29999000	Enhancers	Primary B cells from peripheral blood	blood
45	chr22:29998600-29999000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
46	chr22:29998600-29999000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr22:29998600-29999000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr22:29998600-29999000	Enhancers	Duodenum Mucosa	Duodenum
49	chr22:29998600-29999000	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr22:29998600-29999000	Enhancers	Spleen	Spleen

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