Variant report

Variant	nsv544690
Chromosome Location	chr22:34231732-34553006
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2517)
CpG islands
(count:671)
Chromatin interactive
region (count:80)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2517 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:34305041-34305352	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:34260707-34261720	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:34263027-34263505	HepG2	liver:	n/a	n/a
4	ARID3A	chr22:34397243-34397472	HepG2	liver:	n/a	n/a
5	ARID3A	chr22:34392790-34393312	HepG2	liver:	n/a	n/a
6	ARID3A	chr22:34317112-34317421	HepG2	liver:	n/a	n/a
7	ARID3A	chr22:34319612-34319925	HepG2	liver:	n/a	n/a
8	ATF2	chr22:34498637-34498966	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr22:34237716-34238353	GM12878	blood:	n/a	n/a
10	ATF2	chr22:34237683-34238915	GM12878	blood:	n/a	n/a
11	ATF2	chr22:34292873-34293362	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr22:34291937-34293362	GM12878	blood:	n/a	n/a
13	ATF2	chr22:34267833-34268333	GM12878	blood:	n/a	n/a
14	ATF2	chr22:34267904-34268303	GM12878	blood:	n/a	n/a
15	ATF2	chr22:34292032-34292987	GM12878	blood:	n/a	n/a
16	ATF3	chr22:34451806-34452138	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr22:34316855-34317451	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr22:34244328-34244642	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr22:34381644-34381723	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr22:34382949-34383312	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr22:34267545-34267589	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr22:34287933-34288315	GM12878	blood:	n/a	n/a
23	BATF	chr22:34291932-34292403	GM12878	blood:	n/a	chr22:34292191-34292202
24	BATF	chr22:34237726-34237991	GM12878	blood:	n/a	n/a
25	BATF	chr22:34244253-34244653	GM12878	blood:	n/a	chr22:34244450-34244461
26	BATF	chr22:34279533-34279901	GM12878	blood:	n/a	chr22:34279726-34279737
27	BATF	chr22:34292525-34293380	GM12878	blood:	n/a	chr22:34292610-34292623
28	BATF	chr22:34293029-34293343	GM12878	blood:	n/a	n/a
29	BATF	chr22:34287968-34288282	GM12878	blood:	n/a	n/a
30	BATF	chr22:34279594-34279893	GM12878	blood:	n/a	chr22:34279726-34279737
31	BCL11A	chr22:34287951-34288299	GM12878	blood:	n/a	n/a
32	BCL11A	chr22:34279521-34279833	GM12878	blood:	n/a	n/a
33	BCL11A	chr22:34279585-34279869	GM12878	blood:	n/a	n/a
34	BCL3	chr22:34287946-34288297	GM12878	blood:	n/a	n/a
35	BCL3	chr22:34279570-34279880	GM12878	blood:	n/a	n/a
36	BCLAF1	chr22:34238364-34238878	GM12878	blood:	n/a	n/a
37	BCLAF1	chr22:34291980-34293379	GM12878	blood:	n/a	chr22:34293008-34293017
38	BCLAF1	chr22:34313700-34314146	GM12878	blood:	n/a	n/a
39	BCLAF1	chr22:34317824-34318158	GM12878	blood:	n/a	chr22:34317845-34317858 chr22:34318074-34318087
40	BCLAF1	chr22:34292647-34293357	GM12878	blood:	n/a	chr22:34293008-34293017
41	BCLAF1	chr22:34237755-34238277	GM12878	blood:	n/a	n/a
42	BCLAF1	chr22:34313588-34314217	GM12878	blood:	n/a	n/a
43	BCLAF1	chr22:34285684-34286171	GM12878	blood:	n/a	n/a
44	BHLHE40	chr22:34317091-34317261	K562	blood:	n/a	n/a
45	BHLHE40	chr22:34315460-34315917	GM12878	blood:	n/a	n/a
46	BHLHE40	chr22:34311539-34311573	GM12878	blood:	n/a	n/a
47	BHLHE40	chr22:34310393-34310509	GM12878	blood:	n/a	n/a
48	BHLHE40	chr22:34316935-34317323	GM12878	blood:	n/a	n/a
49	BHLHE40	chr22:34291793-34292391	GM12878	blood:	n/a	n/a
50	BHLHE40	chr22:34313741-34314093	GM12878	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34316977-34317027	Jurkat	blood:	n/a
2	chr22:34316977-34317027	HCPEpiC	choroid plexus:	n/a
3	chr22:34316977-34317027	HepG2	liver:	n/a
4	chr22:34317024-34317074	HCF	heart:	n/a
5	chr22:34316977-34317027	HRCEpiC	kidney:	n/a
6	chr22:34316977-34317027	GM12892	blood:	n/a
7	chr22:34319904-34319954	A549	lung:	n/a
8	chr22:34316655-34316705	Caco-2	colon:	n/a
9	chr22:34317024-34317074	GM19239	blood:	n/a
10	chr22:34317552-34317602	AG09309	skin:	n/a
11	chr22:34316977-34317027	HCM	heart:	n/a
12	chr22:34317552-34317602	H1-hESC	embryonic stem cell:	embryo
13	chr22:34316316-34316366	RPTEC	kidney:	n/a
14	chr22:34318327-34318377	HRE	kidney:	n/a
15	chr22:34318614-34318664	SKMC	muscle:	n/a
16	chr22:34313250-34313300	T-47D	breast:	n/a
17	chr22:34314305-34314355	HEK293	kidney:	embryo
18	chr22:34314305-34314355	HL-60	blood:	n/a
19	chr22:34314305-34314355	AG04449	skin:	fetal
20	chr22:34316655-34316705	HAEpiC	amniotic membrane:	n/a
21	chr22:34316316-34316366	Caco-2	colon:	n/a
22	chr22:34318614-34318664	BJ	skin:	n/a
23	chr22:34316655-34316705	MCF10A-Er-Src	breast:	n/a
24	chr22:34314305-34314355	U87	brain:	n/a
25	chr22:34383032-34383082	NHBE	bronchial:	n/a
26	chr22:34313250-34313300	HCT-116	colon:	n/a
27	chr22:34316316-34316366	HCM	heart:	n/a
28	chr22:34316316-34316366	MCF10A-Er-Src	breast:	n/a
29	chr22:34383032-34383082	GM12891	blood:	n/a
30	chr22:34316316-34316366	SK-N-MC	brain:	n/a
31	chr22:34316977-34317027	PrEC	prostate:	n/a
32	chr22:34383032-34383082	Hela-S3	cervix:	n/a
33	chr22:34317552-34317602	Caco-2	colon:	n/a
34	chr22:34316977-34317027	HRE	kidney:	n/a
35	chr22:34313250-34313300	Jurkat	blood:	n/a
36	chr22:34317024-34317074	GM12878	blood:	n/a
37	chr22:34317024-34317074	HAEpiC	amniotic membrane:	n/a
38	chr22:34317552-34317602	GM19239	blood:	n/a
39	chr22:34317024-34317074	LNCaP	prostate:	n/a
40	chr22:34318327-34318377	NT2-D1	testis:	n/a
41	chr22:34316977-34317027	HEEpiC	esophagus:	n/a
42	chr22:34318614-34318664	HIPEpiC	eye:	n/a
43	chr22:34316655-34316705	SKMC	muscle:	n/a
44	chr22:34316316-34316366	Jurkat	blood:	n/a
45	chr22:34314305-34314355	HNPCEpiC	eye:	n/a
46	chr22:34383032-34383082	BJ	skin:	n/a
47	chr22:34317024-34317074	SAEC	small airway:	n/a
48	chr22:34314305-34314355	CMK	blood:	n/a
49	chr22:34318327-34318377	AG04449	skin:	fetal
50	chr22:34317024-34317074	SK-N-SH_RA	brain:	n/a

(count:80 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr22:34315414..34317058-chr22:34327574..34329120,2	MCF-7	breast:
2	chr22:34261283..34264105-chr22:34285527..34288136,2	MCF-7	breast:
3	chr22:34255666..34258346-chr22:34316396..34318049,2	MCF-7	breast:
4	chr22:34265653..34267240-chr22:34270322..34272194,2	MCF-7	breast:
5	chr22:34319140..34320261-chr22:34501294..34502117,5	MCF-7	breast:
6	chr22:34248231..34249994-chr22:34261049..34263874,2	MCF-7	breast:
7	chr22:34296334..34297959-chr22:34304595..34307456,3	MCF-7	breast:
8	chr22:34262180..34264985-chr22:34291444..34294296,2	MCF-7	breast:
9	chr22:34264153..34267717-chr22:34273021..34274940,3	MCF-7	breast:
10	chr22:34306645..34309140-chr22:34317602..34320390,2	MCF-7	breast:
11	chr22:34243203..34243910-chr9:5087187..5087998,2	MCF-7	breast:
12	chr22:34270428..34272649-chr22:34273804..34275941,2	MCF-7	breast:
13	chr22:34256859..34259072-chr22:34312887..34314818,2	MCF-7	breast:
14	chr22:34451500..34452493-chr22:34500977..34502467,14	MCF-7	breast:
15	chr22:34304733..34311493-chr22:34313014..34317407,8	MCF-7	breast:
16	chr22:34153944..34154522-chr22:34255921..34256610,2	MCF-7	breast:
17	chr22:34248614..34251924-chr22:34259957..34262591,3	MCF-7	breast:
18	chr22:34255630..34257426-chr22:34307549..34309607,2	MCF-7	breast:
19	chr22:34451450..34452355-chr22:34506974..34507926,4	MCF-7	breast:
20	chr22:34260736..34263686-chr22:34313890..34318281,7	MCF-7	breast:
21	chr22:34255630..34257426-chr22:34307549..34309607,2	MCF-7	breast:
22	chr22:34296673..34299632-chr22:34313962..34315661,2	MCF-7	breast:
23	chr22:34312443..34314367-chr22:35604933..35607464,2	K562	blood:
24	chr22:34319321..34320710-chr22:34415195..34416586,9	MCF-7	breast:
25	chr22:34264153..34267717-chr22:34273021..34274940,3	MCF-7	breast:
26	chr22:34269817..34272444-chr22:34314882..34316654,2	MCF-7	breast:
27	chr22:34255666..34258346-chr22:34316396..34318049,2	MCF-7	breast:
28	chr22:34296334..34297959-chr22:34304595..34307456,3	MCF-7	breast:
29	chr22:34279207..34280839-chr22:34295025..34297477,2	MCF-7	breast:
30	chr22:34314379..34318265-chr22:34319808..34323706,4	MCF-7	breast:
31	chr22:34287867..34289464-chr22:34291655..34293352,2	MCF-7	breast:
32	chr22:34296231..34298036-chr22:34317275..34319526,2	MCF-7	breast:
33	chr22:34247616..34248584-chr22:34315645..34316533,2	MCF-7	breast:
34	chr22:34300595..34304253-chr22:34306616..34309764,3	MCF-7	breast:
35	chr22:34270457..34273179-chr22:34316799..34318425,2	MCF-7	breast:
36	chr22:34409232..34410755-chr22:34412827..34414607,2	MCF-7	breast:
37	chr22:34245347..34248923-chr22:34315491..34319689,7	MCF-7	breast:
38	chr22:34300595..34304253-chr22:34306616..34309764,3	MCF-7	breast:
39	chr22:34319140..34320261-chr22:34501294..34502117,5	MCF-7	breast:
40	chr22:34246562..34250566-chr22:34253925..34258689,11	MCF-7	breast:
41	chr22:34247996..34248570-chr22:34261032..34261815,2	MCF-7	breast:
42	chr22:34451604..34452439-chr22:34501272..34502065,4	MCF-7	breast:
43	chr22:34259639..34261419-chr22:34267116..34269181,2	MCF-7	breast:
44	chr22:34262180..34264985-chr22:34291444..34294296,2	MCF-7	breast:
45	chr22:34248240..34252170-chr22:34315347..34319641,4	MCF-7	breast:
46	chr22:34287867..34289464-chr22:34291655..34293352,2	MCF-7	breast:
47	chr22:34319321..34320710-chr22:34415195..34416586,9	MCF-7	breast:
48	chr22:34451500..34452493-chr22:34500977..34502467,14	MCF-7	breast:
49	chr22:34261283..34264105-chr22:34285527..34288136,2	MCF-7	breast:
50	chr22:34317156..34319746-chr22:34329020..34331193,2	MCF-7	breast:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ISX-3	chr22:34496347-34496430	ENSG00000236052
2	lnc-ISX-3	chr22:34479958-34480016	ENSG00000236052
3	lnc-ISX-3	chr22:34547854-34547916	ENSG00000236052
4	lnc-ISX-9	chr22:34486267-34491188	NONHSAT085023
5	lnc-TIMP3-8	chr22:34318410-34318754	ENSG00000273082.1
6	lnc-ISX-10	chr22:34478438-34478641	uc_458_+
7	lnc-LARGE-6	chr22:34478438-34478641	uc_458_-
8	lnc-ISX-3	chr22:34413462-34413516	ENSG00000236052

No data

Variant related genes	Relation type
LARGE	TF binding region
ENSG00000273082	TF binding region
ENSG00000236052	TF binding region
LARGE	CpG island
ENSG00000273082	CpG island
ENSG00000236052	CpG island
ENSG00000273082	chromatin interactions
ENSG00000236052	chromatin interactions
ENSG00000133424	chromatin interactions

Extended variants
information (count: 7927 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:7927 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116050591	chr22:34231744-34231745	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs558807449	chr22:34231770-34231771	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs532817470	chr22:34231811-34231812	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs566425579	chr22:34231849-34231850	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs139568146	chr22:34231858-34231859	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs149335199	chr22:34231863-34231864	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs376280699	chr22:34231909-34231910	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs114360351	chr22:34231920-34231921	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189302735	chr22:34232071-34232072	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs542735648	chr22:34232079-34232080	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs562701611	chr22:34232111-34232112	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs144592912	chr22:34232136-34232137	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs10707505	chr22:34232205-34232206	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs535482703	chr22:34232286-34232287	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs115274673	chr22:34232318-34232319	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs148724848	chr22:34232346-34232347	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs528008857	chr22:34232352-34232353	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs547332917	chr22:34232412-34232413	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs76599351	chr22:34232457-34232458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529770471	chr22:34232483-34232484	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17808887	chr22:34232605-34232606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569810970	chr22:34232606-34232607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11914199	chr22:34232616-34232617	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs113692321	chr22:34232660-34232661	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs565949342	chr22:34232668-34232669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534629157	chr22:34232705-34232706	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs554109027	chr22:34232713-34232714	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573706282	chr22:34232786-34232787	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11411468	chr22:34232792-34232793	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374334783	chr22:34232899-34232900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs8142645	chr22:34232903-34232904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556236121	chr22:34232935-34232936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs762835	chr22:34232951-34232952	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs545565155	chr22:34232970-34232971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs12483818	chr22:34233005-34233006	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs572670316	chr22:34233033-34233034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs147865908	chr22:34233058-34233059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs560829929	chr22:34233098-34233099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139979631	chr22:34233160-34233161	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192637331	chr22:34233179-34233180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147768340	chr22:34233210-34233211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs145444205	chr22:34233235-34233236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532279705	chr22:34233245-34233246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs10551521	chr22:34233246-34233247	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73154509	chr22:34233247-34233248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554910437	chr22:34233248-34233249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs9621778	chr22:34233257-34233258	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397838427	chr22:34233267-34233268	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs74267812	chr22:34233268-34233269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112550660	chr22:34233287-34233288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
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
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
Endometrioid adenocarcinoma	16974079	CNVD
Acute myeloid leukemia	20729466	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	19384346	CNVD
Myelofibrosis	22110671	CNVD
muscular dystrophy type 1D	21248746	CNVD
Leukoplakia	24403051	CNVD
Ovarian neoplasms	16753589	CNVD
Deafness	17160897	CNVD
Bipolar disorder	19114987	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Prostate cancer	22341455	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bladder cancer	21909424	CNVD

Chromatin state (count:3379 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34200600-34234200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr22:34213200-34232200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr22:34219800-34231800	Weak transcription	Aorta	Aorta
4	chr22:34224800-34232000	Weak transcription	Fetal Intestine Small	intestine
5	chr22:34226600-34246200	Weak transcription	Duodenum Mucosa	Duodenum
6	chr22:34228600-34232200	Weak transcription	Spleen	Spleen
7	chr22:34228600-34234000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr22:34228600-34234800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr22:34228800-34240000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr22:34229000-34232200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr22:34229000-34232200	Weak transcription	Lung	lung
12	chr22:34229000-34232200	Weak transcription	Pancreas	Pancrea
13	chr22:34229000-34233400	Weak transcription	Ovary	ovary
14	chr22:34229000-34233600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr22:34229000-34233800	Weak transcription	Brain Anterior Caudate	brain
16	chr22:34229000-34234600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr22:34229600-34232200	Weak transcription	Gastric	stomach
18	chr22:34230000-34234200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr22:34230200-34234000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr22:34230600-34232600	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr22:34230600-34232600	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr22:34230800-34232000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr22:34230800-34232000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr22:34230800-34232200	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr22:34230800-34232400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
26	chr22:34230800-34232400	Enhancers	Fetal Stomach	stomach
27	chr22:34230800-34232600	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr22:34230800-34232800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr22:34230800-34234000	Enhancers	H9 Cell Line	embryonic stem cell
30	chr22:34230800-34234200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr22:34230800-34234400	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr22:34231000-34231800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr22:34231000-34232200	Enhancers	Fetal Brain Male	brain
34	chr22:34231000-34232200	Enhancers	Fetal Brain Female	brain
35	chr22:34231000-34232200	Enhancers	Rectal Smooth Muscle	rectum
36	chr22:34231000-34232400	Enhancers	Colon Smooth Muscle	Colon
37	chr22:34231000-34233000	Enhancers	Skeletal Muscle Male	skeletal muscle
38	chr22:34231000-34236000	Enhancers	Skeletal Muscle Female	skeletal muscle
39	chr22:34231200-34232200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr22:34231200-34232200	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr22:34231200-34232800	Enhancers	Brain Hippocampus Middle	brain
42	chr22:34231200-34233000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr22:34231200-34233200	Enhancers	Fetal Muscle Leg	muscle
44	chr22:34231200-34233600	Enhancers	Psoas Muscle	Psoas
45	chr22:34231200-34234000	Enhancers	Right Ventricle	heart
46	chr22:34231400-34231800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr22:34231400-34231800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr22:34231400-34231800	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr22:34231400-34231800	Enhancers	Fetal Intestine Large	intestine
50	chr22:34231400-34232000	Enhancers	Esophagus	oesophagus

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