Variant report

Variant	esv3390652
Chromosome Location	chr22:33452977-33455825
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:168)
CpG islands
(count:733)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:168 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr22:33454325-33454803	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr22:33454252-33454424	H1-hESC	embryonic stem cell:	n/a	n/a
3	CCNT2	chr22:33454020-33454464	K562	blood:	n/a	n/a
4	CEBPB	chr22:33454297-33454465	HepG2	liver:	n/a	n/a
5	CEBPD	chr22:33454190-33454501	HepG2	liver:	n/a	n/a
6	CEBPD	chr22:33454274-33454591	HepG2	liver:	n/a	n/a
7	CHD1	chr22:33454164-33454361	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD1	chr22:33453606-33453754	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr22:33454233-33454295	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr22:33454300-33454450	GM12866	blood:	n/a	n/a
11	CTCF	chr22:33454074-33454700	A549	lung:	n/a	n/a
12	CTCF	chr22:33454304-33454471	MCF-7	breast:	n/a	n/a
13	CTCF	chr22:33454240-33454390	HEK293	kidney:	n/a	n/a
14	CTCF	chr22:33453940-33454090	A549	lung:	n/a	n/a
15	CTCF	chr22:33454280-33454430	SAEC	small airway:	n/a	n/a
16	CTCF	chr22:33454205-33454451	HepG2	liver:	n/a	n/a
17	CTCF	chr22:33454280-33454430	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr22:33454294-33454445	GM13977	blood:	n/a	n/a
19	CTCF	chr22:33454308-33454457	Fibrobl	skin:	n/a	n/a
20	CTCF	chr22:33454240-33454390	GM12874	blood:	n/a	n/a
21	CTCF	chr22:33454150-33454516	HepG2	liver:	n/a	n/a
22	CTCF	chr22:33454280-33454430	GM12864	blood:	n/a	n/a
23	CTCF	chr22:33454280-33454430	K562	blood:	n/a	n/a
24	CTCF	chr22:33454312-33454475	Spleen_OC	spleen:	n/a	n/a
25	CTCF	chr22:33454319-33454431	MCF-7	breast:	n/a	n/a
26	CTCF	chr22:33454165-33454597	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr22:33454300-33454450	HMEC	breast:	n/a	n/a
28	CTCF	chr22:33454284-33454499	NHEK	skin:	n/a	n/a
29	CTCF	chr22:33454282-33454479	Medullo	brain:	n/a	n/a
30	CTCF	chr22:33454100-33454250	GM12864	blood:	n/a	n/a
31	CTCF	chr22:33454260-33454410	GM12871	blood:	n/a	n/a
32	CTCF	chr22:33454266-33454475	IMR90	lung:	n/a	n/a
33	CTCF	chr22:33454324-33454452	Gliobla	brain:	n/a	n/a
34	CTCF	chr22:33454340-33454490	GM12866	blood:	n/a	n/a
35	CTCF	chr22:33454300-33454450	GM12865	blood:	n/a	n/a
36	CTCF	chr22:33454393-33454414	LNCaP	prostate:	n/a	n/a
37	CTCF	chr22:33454200-33454350	GM12867	blood:	n/a	n/a
38	CTCF	chr22:33454268-33454504	A549	lung:	n/a	n/a
39	CTCF	chr22:33454280-33454430	GM12869	blood:	n/a	n/a
40	CTCF	chr22:33454300-33454450	GM12871	blood:	n/a	n/a
41	CTCF	chr22:33454274-33454453	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr22:33454266-33454450	SK-N-SH_RA	brain:	n/a	n/a
43	CTCF	chr22:33454273-33454506	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr22:33454320-33454470	GM12868	blood:	n/a	n/a
45	CTCF	chr22:33454334-33454482	K562	blood:	n/a	n/a
46	CTCF	chr22:33453920-33454070	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr22:33454040-33454190	GM12868	blood:	n/a	n/a
48	CTCF	chr22:33454280-33454430	HepG2	liver:	n/a	n/a
49	CTCF	chr22:33453440-33453590	HepG2	liver:	n/a	n/a
50	CTCF	chr22:33454363-33454439	GM19239	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:33453893-33453943	SKMC	muscle:	n/a
2	chr22:33453893-33453943	SKMC	muscle:	n/a
3	chr22:33454491-33454541	Jurkat	blood:	n/a
4	chr22:33454616-33454666	AG10803	skin:	n/a
5	chr22:33454324-33454374	PrEC	prostate:	n/a
6	chr22:33454444-33454494	LNCaP	prostate:	n/a
7	chr22:33454616-33454666	K562	blood:	n/a
8	chr22:33454616-33454666	HRCEpiC	kidney:	n/a
9	chr22:33454491-33454541	IMR90	lung:	fetal
10	chr22:33454632-33454682	BE2_C	brain:	n/a
11	chr22:33454491-33454541	Caco-2	colon:	n/a
12	chr22:33454632-33454682	HIPEpiC	eye:	n/a
13	chr22:33454564-33454614	GM06990	blood:	n/a
14	chr22:33453994-33454044	HNPCEpiC	eye:	n/a
15	chr22:33454444-33454494	Hela-S3	cervix:	n/a
16	chr22:33454491-33454541	HL-60	blood:	n/a
17	chr22:33454564-33454614	PANC-1	pancreas:	n/a
18	chr22:33454324-33454374	SKMC	muscle:	n/a
19	chr22:33454209-33454259	HL-60	blood:	n/a
20	chr22:33454616-33454666	SK-N-MC	brain:	n/a
21	chr22:33454504-33454554	HAEpiC	amniotic membrane:	n/a
22	chr22:33453022-33453072	PFSK-1	brain:	n/a
23	chr22:33453994-33454044	HAEpiC	amniotic membrane:	n/a
24	chr22:33454491-33454541	PFSK-1	brain:	n/a
25	chr22:33454632-33454682	AoSMC	blood vessel:	n/a
26	chr22:33453022-33453072	GM06990	blood:	n/a
27	chr22:33453893-33453943	HRPEpiC	eye:	n/a
28	chr22:33454564-33454614	H1-hESC	embryonic stem cell:	embryo
29	chr22:33454209-33454259	GM06990	blood:	n/a
30	chr22:33454616-33454666	A549	lung:	n/a
31	chr22:33453994-33454044	ECC-1	luminal epithelium:	n/a
32	chr22:33454209-33454259	Caco-2	colon:	n/a
33	chr22:33453022-33453072	GM19239	blood:	n/a
34	chr22:33453893-33453943	U87	brain:	n/a
35	chr22:33454444-33454494	NB4	blood:	n/a
36	chr22:33454209-33454259	HUVEC	blood vessel:	n/a
37	chr22:33454444-33454494	AG04450	lung:	fetal
38	chr22:33454491-33454541	RPTEC	kidney:	n/a
39	chr22:33454504-33454554	GM12878	blood:	n/a
40	chr22:33454324-33454374	HAEpiC	amniotic membrane:	n/a
41	chr22:33454632-33454682	CMK	blood:	n/a
42	chr22:33454623-33454673	GM12892	blood:	n/a
43	chr22:33453994-33454044	GM12892	blood:	n/a
44	chr22:33453893-33453943	AG09309	skin:	n/a
45	chr22:33454623-33454673	IMR90	lung:	fetal
46	chr22:33454632-33454682	HCPEpiC	choroid plexus:	n/a
47	chr22:33454616-33454666	NHDF-neo	bronchial:	n/a
48	chr22:33454324-33454374	ECC-1	luminal epithelium:	n/a
49	chr22:33454564-33454614	HCF	heart:	n/a
50	chr22:33454491-33454541	CMK	blood:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:33450128..33453064-chr22:33538436..33541136,2	MCF-7	breast:
2	22:33030812-33041554..22:33452523-33459358	GM12878	blood:
3	22:32846948-32860159..22:33452523-33459358	Hela-S3	cervix:
4	chr22:32523564..32526507-chr22:33453978..33455661,2	MCF-7	breast:
5	22:32360288-32405313..22:33452523-33459358	H1-hESC	embryonic stem cell:	embryo

No data

Variant related genes	Relation type
SYN3	TF binding region
SYN3	CpG island
ENSG00000184459	chromatin interactions
ENSG00000230866	chromatin interactions
ENSG00000240647	chromatin interactions
ENSG00000251890	chromatin interactions
ENSG00000237439	chromatin interactions

Extended variants
information (count: 80 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:80 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180852320	chr22:33452983-33452984	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs538551402	chr22:33453023-33453024	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs185067588	chr22:33453074-33453075	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs60297889	chr22:33453128-33453129	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs533677701	chr22:33453133-33453134	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs112713620	chr22:33453164-33453165	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs567284204	chr22:33453180-33453181	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs57574537	chr22:33453215-33453216	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs572293941	chr22:33453227-33453228	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs556896178	chr22:33453240-33453241	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs192101326	chr22:33453255-33453256	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs184000083	chr22:33453270-33453271	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs558929416	chr22:33453320-33453321	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs572405855	chr22:33453350-33453351	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs188495677	chr22:33453368-33453369	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs561308662	chr22:33453382-33453383	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs574497022	chr22:33453387-33453388	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs5754399	chr22:33453422-33453423	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs148249800	chr22:33453479-33453480	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs13057166	chr22:33453533-33453534	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551079502	chr22:33453558-33453559	Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs141379178	chr22:33453607-33453608	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs564966364	chr22:33453616-33453617	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs527346255	chr22:33453701-33453702	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs73164310	chr22:33453831-33453832	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs567222905	chr22:33453840-33453841	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs368577675	chr22:33453864-33453865	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs574855439	chr22:33453880-33453881	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs549841125	chr22:33453884-33453885	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs570358152	chr22:33453907-33453908	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs138221731	chr22:33453973-33453974	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs576089653	chr22:33453984-33453985	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs559075980	chr22:33454054-33454055	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs572575119	chr22:33454092-33454093	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs143715995	chr22:33454105-33454106	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs535072158	chr22:33454202-33454203	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs554654079	chr22:33454283-33454284	Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs138116184	chr22:33454426-33454427	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs13057853	chr22:33454441-33454442	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs7364306	chr22:33454483-33454484	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs9607008	chr22:33454503-33454504	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs576269664	chr22:33454545-33454546	Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs544990994	chr22:33454623-33454624	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
44	rs144307013	chr22:33454633-33454634	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs565060935	chr22:33454786-33454787	Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs191976121	chr22:33454917-33454918	Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs62232761	chr22:33454920-33454921	Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs182921827	chr22:33454921-33454922	Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs529859658	chr22:33454940-33454941	Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs376001093	chr22:33454985-33454986	Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

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

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:33449400-33453600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
2	chr22:33450800-33454600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
3	chr22:33451200-33453000	Active TSS	Fetal Brain Female	brain
4	chr22:33451200-33454800	Bivalent/Poised TSS	Brain Angular Gyrus	brain
5	chr22:33452000-33453200	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
6	chr22:33452200-33453000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
7	chr22:33452200-33453200	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
8	chr22:33452200-33454800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
9	chr22:33452400-33453000	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
10	chr22:33452400-33453000	Flanking Active TSS	HepG2	liver
11	chr22:33452400-33453400	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
12	chr22:33452400-33453400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
13	chr22:33452400-33453800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr22:33452600-33454600	Bivalent/Poised TSS	Brain Anterior Caudate	brain
15	chr22:33452800-33453000	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
16	chr22:33452800-33453000	Flanking Bivalent TSS/Enh	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr22:33452800-33453000	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr22:33452800-33453200	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
19	chr22:33452800-33453400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr22:33452800-33454000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr22:33452800-33454000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
22	chr22:33452800-33454000	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
23	chr22:33452800-33454200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
24	chr22:33452800-33454800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
25	chr22:33453000-33453200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
26	chr22:33453000-33453200	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr22:33453000-33453200	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
28	chr22:33453000-33453200	Bivalent/Poised TSS	Brain Germinal Matrix	brain
29	chr22:33453000-33453400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
30	chr22:33453000-33453400	Active TSS	HepG2	liver
31	chr22:33453000-33453600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr22:33453000-33453800	Flanking Bivalent TSS/Enh	Fetal Brain Male	brain
33	chr22:33453000-33454000	Bivalent/Poised TSS	Fetal Brain Female	brain
34	chr22:33453000-33454400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr22:33453200-33453400	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
36	chr22:33453200-33453400	Bivalent Enhancer	Fetal Stomach	stomach
37	chr22:33453200-33453600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
38	chr22:33453200-33453600	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr22:33453200-33453600	Bivalent Enhancer	Brain Germinal Matrix	brain
40	chr22:33453200-33453800	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
41	chr22:33453200-33453800	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
42	chr22:33453200-33454000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
43	chr22:33453400-33453600	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr22:33453400-33453600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr22:33453400-33453600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr22:33453400-33453600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr22:33453400-33453600	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
48	chr22:33453400-33453600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
49	chr22:33453400-33453600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
50	chr22:33453400-33453800	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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