Variant report

Variant	esv3440277
Chromosome Location	chr22:34315777-34318325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:459)
CpG islands
(count:305)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:459 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:34317112-34317421	HepG2	liver:	n/a	n/a
2	BACH1	chr22:34316855-34317451	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCLAF1	chr22:34317824-34318158	GM12878	blood:	n/a	chr22:34317845-34317858 chr22:34318074-34318087
4	BHLHE40	chr22:34316935-34317323	GM12878	blood:	n/a	n/a
5	BHLHE40	chr22:34317091-34317261	K562	blood:	n/a	n/a
6	BHLHE40	chr22:34315460-34315917	GM12878	blood:	n/a	n/a
7	BRCA1	chr22:34317873-34318071	H1-hESC	embryonic stem cell:	n/a	n/a
8	CCNT2	chr22:34316791-34317414	K562	blood:	n/a	chr22:34317308-34317317
9	CEBPB	chr22:34317260-34317440	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr22:34317864-34318034	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPD	chr22:34316769-34317086	HepG2	liver:	n/a	n/a
12	CHD1	chr22:34315321-34315814	GM12878	blood:	n/a	chr22:34315519-34315529
13	CHD1	chr22:34315387-34316282	H1-hESC	embryonic stem cell:	n/a	chr22:34315519-34315529
14	CHD1	chr22:34317876-34318123	H1-hESC	embryonic stem cell:	n/a	n/a
15	CHD2	chr22:34316198-34316291	GM12878	blood:	n/a	n/a
16	CHD2	chr22:34317010-34317362	GM12878	blood:	n/a	n/a
17	CHD2	chr22:34317067-34317068	K562	blood:	n/a	n/a
18	CHD2	chr22:34317059-34317386	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr22:34317201-34317356	HepG2	liver:	n/a	n/a
20	CHD2	chr22:34317839-34318540	GM12878	blood:	n/a	n/a
21	CHD2	chr22:34317821-34318591	H1-hESC	embryonic stem cell:	n/a	n/a
22	CREB1	chr22:34316919-34317327	A549	lung:	n/a	n/a
23	CTBP2	chr22:34317076-34318704	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr22:34316956-34317025	GM19240	blood:	n/a	n/a
25	CTCF	chr22:34315800-34315950	BJ	skin:	n/a	n/a
26	CTCF	chr22:34317153-34317276	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr22:34315990-34316029	Fibrobl	skin:	n/a	n/a
28	CTCF	chr22:34317200-34317350	GM06990	blood:	n/a	n/a
29	CTCF	chr22:34315860-34316010	GM12864	blood:	n/a	n/a
30	CTCF	chr22:34316218-34316262	GM12892	blood:	n/a	n/a
31	CTCF	chr22:34315899-34316093	GM12892	blood:	n/a	n/a
32	CTCF	chr22:34315880-34316030	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr22:34316868-34317146	GM12878	blood:	n/a	n/a
34	CTCF	chr22:34315894-34315897	GM12892	blood:	n/a	n/a
35	CTCF	chr22:34316032-34316033	Fibrobl	skin:	n/a	n/a
36	CTCF	chr22:34315800-34315950	AG04449	skin:	n/a	n/a
37	CTCF	chr22:34317260-34317410	SAEC	small airway:	n/a	n/a
38	CTCF	chr22:34315800-34315950	GM06990	blood:	n/a	n/a
39	CTCF	chr22:34316948-34317029	GM12892	blood:	n/a	n/a
40	CTCF	chr22:34315900-34316050	GM12869	blood:	n/a	n/a
41	CTCF	chr22:34316956-34317024	GM12891	blood:	n/a	n/a
42	CTCF	chr22:34316620-34316770	GM12865	blood:	n/a	n/a
43	CTCF	chr22:34317860-34318010	AG04449	skin:	n/a	n/a
44	CTCF	chr22:34317900-34318050	HCPEpiC	choroid plexus:	n/a	n/a
45	CTCF	chr22:34315840-34315990	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr22:34315920-34316070	GM12864	blood:	n/a	n/a
47	CTCF	chr22:34317960-34318110	GM12873	blood:	n/a	n/a
48	CTCF	chr22:34317220-34317370	AG04449	skin:	n/a	n/a
49	CTCF	chr22:34315923-34315968	GM19240	blood:	n/a	n/a
50	CTCF	chr22:34315436-34316329	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:34316316-34316366	NT2-D1	testis:	n/a
2	chr22:34316655-34316705	BJ	skin:	n/a
3	chr22:34316655-34316705	AoSMC	blood vessel:	n/a
4	chr22:34317024-34317074	AG09319	gingival:	n/a
5	chr22:34317024-34317074	ovcar-3	ovarian:	n/a
6	chr22:34316977-34317027	HEK293	kidney:	embryo
7	chr22:34317024-34317074	AG04450	lung:	fetal
8	chr22:34316655-34316705	HEK293	kidney:	embryo
9	chr22:34317552-34317602	NH-A	brain:	n/a
10	chr22:34316977-34317027	H1-hESC	embryonic stem cell:	embryo
11	chr22:34316316-34316366	AG04449	skin:	fetal
12	chr22:34317024-34317074	NB4	blood:	n/a
13	chr22:34316316-34316366	HCT-116	colon:	n/a
14	chr22:34316977-34317027	IMR90	lung:	fetal
15	chr22:34317552-34317602	NHDF-neo	bronchial:	n/a
16	chr22:34317552-34317602	GM12891	blood:	n/a
17	chr22:34316655-34316705	T-47D	breast:	n/a
18	chr22:34316655-34316705	PrEC	prostate:	n/a
19	chr22:34316316-34316366	MCF-7	breast:	n/a
20	chr22:34316655-34316705	MCF10A-Er-Src	breast:	n/a
21	chr22:34316316-34316366	HMEC	breast:	n/a
22	chr22:34316316-34316366	SK-N-SH_RA	brain:	n/a
23	chr22:34316655-34316705	GM12892	blood:	n/a
24	chr22:34317024-34317074	GM12878	blood:	n/a
25	chr22:34316655-34316705	A549	lung:	n/a
26	chr22:34316655-34316705	PANC-1	pancreas:	n/a
27	chr22:34317552-34317602	RPTEC	kidney:	n/a
28	chr22:34316316-34316366	K562	blood:	n/a
29	chr22:34317024-34317074	HNPCEpiC	eye:	n/a
30	chr22:34316316-34316366	LNCaP	prostate:	n/a
31	chr22:34316977-34317027	CMK	blood:	n/a
32	chr22:34316977-34317027	HUVEC	blood vessel:	n/a
33	chr22:34316316-34316366	GM19239	blood:	n/a
34	chr22:34317552-34317602	HCPEpiC	choroid plexus:	n/a
35	chr22:34317552-34317602	HPAEpiC	pulmonary alveolar:	n/a
36	chr22:34316977-34317027	NHDF-neo	bronchial:	n/a
37	chr22:34316977-34317027	Hepatocyte	liver:	n/a
38	chr22:34316977-34317027	Hela-S3	cervix:	n/a
39	chr22:34317024-34317074	K562	blood:	n/a
40	chr22:34317024-34317074	HUVEC	blood vessel:	n/a
41	chr22:34316977-34317027	GM12878	blood:	n/a
42	chr22:34316977-34317027	HPAEpiC	pulmonary alveolar:	n/a
43	chr22:34316977-34317027	AG10803	skin:	n/a
44	chr22:34316977-34317027	Caco-2	colon:	n/a
45	chr22:34316655-34316705	GM06990	blood:	n/a
46	chr22:34316977-34317027	HCF	heart:	n/a
47	chr22:34317024-34317074	HepG2	liver:	n/a
48	chr22:34317552-34317602	HCF	heart:	n/a
49	chr22:34317024-34317074	SAEC	small airway:	n/a
50	chr22:34317552-34317602	MCF10A-Er-Src	breast:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:34297092..34298993-chr22:34314365..34316257,2	MCF-7	breast:
2	chr22:34283913..34285789-chr22:34315526..34317915,2	MCF-7	breast:
3	chr22:34255666..34258346-chr22:34316396..34318049,2	MCF-7	breast:
4	chr22:34269243..34272868-chr22:34312880..34316299,3	MCF-7	breast:

No data

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

Extended variants
information (count: 68 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:68 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs576978602	chr22:34315794-34315795	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs77908284	chr22:34315796-34315797	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs534182173	chr22:34315843-34315844	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs372798550	chr22:34315996-34315997	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs374159324	chr22:34315997-34315998	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs572984967	chr22:34316042-34316043	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs143403352	chr22:34316049-34316050	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs3210587	chr22:34316077-34316078	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs530725597	chr22:34316094-34316095	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540474112	chr22:34316099-34316100	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs185068235	chr22:34316171-34316172	Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532396916	chr22:34316226-34316227	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs552623718	chr22:34316255-34316256	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs114106875	chr22:34316297-34316298	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs535216289	chr22:34316299-34316300	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532736408	chr22:34316355-34316356	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs568730001	chr22:34316370-34316371	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs537756491	chr22:34316381-34316382	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs372136992	chr22:34316483-34316484	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs557715847	chr22:34316488-34316489	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs113084764	chr22:34316508-34316509	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs576893278	chr22:34316567-34316568	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs539481544	chr22:34316570-34316571	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs553030892	chr22:34316579-34316580	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs572856214	chr22:34316581-34316582	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs537834683	chr22:34316635-34316636	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs551778913	chr22:34316741-34316742	Weak transcription Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs189581879	chr22:34316830-34316831	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs561752351	chr22:34316936-34316937	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs142702048	chr22:34317001-34317002	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs544076142	chr22:34317034-34317035	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs8141308	chr22:34317080-34317081	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs564071803	chr22:34317081-34317082	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs111583533	chr22:34317122-34317123	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs532361663	chr22:34317142-34317143	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs552334684	chr22:34317212-34317213	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs559750746	chr22:34317260-34317261	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs191643203	chr22:34317272-34317273	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs369327782	chr22:34317296-34317297	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs571647766	chr22:34317301-34317302	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs62225076	chr22:34317375-34317376	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs568693151	chr22:34317394-34317395	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs537676314	chr22:34317406-34317407	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs548658678	chr22:34317411-34317412	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs75758906	chr22:34317415-34317416	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs571210031	chr22:34317546-34317547	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs2267328	chr22:34317623-34317624	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs116949899	chr22:34317668-34317669	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs566528930	chr22:34317709-34317710	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs535222711	chr22:34317724-34317725	Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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

Chromatin state (count:400 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:34313600-34315800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr22:34313600-34315800	Flanking Active TSS	Fetal Brain Female	brain
3	chr22:34313600-34319000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr22:34313800-34315800	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr22:34313800-34316400	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr22:34313800-34319200	Active TSS	H9 Cell Line	embryonic stem cell
7	chr22:34314000-34319000	Active TSS	Right Atrium	heart
8	chr22:34314200-34316200	Active TSS	Fetal Kidney	kidney
9	chr22:34314200-34316400	Active TSS	Brain Angular Gyrus	brain
10	chr22:34314200-34318400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr22:34314200-34319000	Active TSS	Left Ventricle	heart
12	chr22:34314400-34316000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
13	chr22:34314400-34316400	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr22:34314600-34316000	Flanking Active TSS	Ovary	ovary
15	chr22:34314600-34316400	Active TSS	Rectal Smooth Muscle	rectum
16	chr22:34314600-34316400	Active TSS	HSMMtube	muscle
17	chr22:34314800-34315800	Flanking Active TSS	Primary B cells from peripheral blood	blood
18	chr22:34314800-34315800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
19	chr22:34314800-34316000	Active TSS	Fetal Heart	heart
20	chr22:34314800-34316000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
21	chr22:34314800-34316200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
22	chr22:34314800-34316400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
23	chr22:34314800-34318600	Active TSS	Gastric	stomach
24	chr22:34315000-34315800	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
25	chr22:34315000-34315800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr22:34315000-34315800	Flanking Active TSS	Duodenum Mucosa	Duodenum
27	chr22:34315000-34315800	Flanking Active TSS	NHEK	skin
28	chr22:34315000-34316000	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
29	chr22:34315000-34316400	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr22:34315000-34316400	Active TSS	Fetal Intestine Large	intestine
31	chr22:34315000-34316400	Active TSS	Fetal Intestine Small	intestine
32	chr22:34315000-34316400	Active TSS	Rectal Mucosa Donor 29	rectum
33	chr22:34315000-34316400	Active TSS	GM12878-XiMat	blood
34	chr22:34315000-34319200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr22:34315000-34319200	Active TSS	Psoas Muscle	Psoas
36	chr22:34315200-34315800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
37	chr22:34315200-34315800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr22:34315200-34315800	Flanking Active TSS	Liver	Liver
39	chr22:34315200-34315800	Flanking Active TSS	Brain Substantia Nigra	brain
40	chr22:34315200-34315800	Flanking Active TSS	Fetal Lung	lung
41	chr22:34315200-34315800	Flanking Active TSS	NH-A	brain
42	chr22:34315200-34315800	Flanking Active TSS	Osteobl	bone
43	chr22:34315200-34316000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
44	chr22:34315200-34316000	Flanking Active TSS	Stomach Smooth Muscle	stomach
45	chr22:34315200-34316200	Flanking Active TSS	HMEC	breast
46	chr22:34315200-34316400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr22:34315200-34316400	Active TSS	NHDF-Ad	bronchial
48	chr22:34315200-34318600	Active TSS	HSMM	muscle
49	chr22:34315200-34318800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr22:34315200-34318800	Active TSS	Pancreatic Islets	Pancreatic Islet

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