Variant report

Variant	nsv522714
Chromosome Location	chr22:29612508-29630337
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:253)
CpG islands
(count:0)
Chromatin interactive
region (count:26)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr22:29628218-29628633	GM12878	blood:	n/a	n/a
2	BCL3	chr22:29627837-29628113	GM12878	blood:	n/a	n/a
3	BCL3	chr22:29627387-29627732	GM12878	blood:	n/a	n/a
4	BHLHE40	chr22:29621739-29621873	K562	blood:	n/a	chr22:29621804-29621820
5	BHLHE40	chr22:29616972-29617209	K562	blood:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
6	BHLHE40	chr22:29617036-29617131	HepG2	liver:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
7	BHLHE40	chr22:29616987-29617222	GM12878	blood:	n/a	chr22:29617116-29617125 chr22:29617116-29617125 chr22:29617115-29617124 chr22:29617114-29617127
8	CEBPB	chr22:29613333-29613598	A549	lung:	n/a	chr22:29613465-29613476
9	CEBPB	chr22:29613330-29613589	Hela-S3	cervix:	n/a	chr22:29613465-29613476
10	CEBPB	chr22:29613324-29613524	HepG2	liver:	n/a	chr22:29613465-29613476
11	CEBPB	chr22:29613270-29613658	IMR90	lung:	n/a	chr22:29613465-29613476
12	CEBPB	chr22:29613260-29613667	HepG2	liver:	n/a	chr22:29613465-29613476
13	CEBPB	chr22:29613288-29613671	MCF-7	breast:	n/a	chr22:29613465-29613476
14	CEBPB	chr22:29613294-29613677	HepG2	liver:	n/a	chr22:29613465-29613476
15	CEBPB	chr22:29613260-29613670	HepG2	liver:	n/a	chr22:29613465-29613476
16	CEBPD	chr22:29613362-29613544	HepG2	liver:	n/a	n/a
17	CEBPD	chr22:29613360-29613608	HepG2	liver:	n/a	n/a
18	CHD2	chr22:29613530-29613531	GM12878	blood:	n/a	n/a
19	CHD2	chr22:29628513-29628664	GM12878	blood:	n/a	n/a
20	CHD2	chr22:29616489-29616785	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr22:29616440-29616590	AG04450	lung:	n/a	n/a
22	CTCF	chr22:29616424-29616573	LNCaP	prostate:	n/a	n/a
23	CTCF	chr22:29616479-29616572	MCF-7	breast:	n/a	n/a
24	CTCF	chr22:29616400-29616550	Caco-2	colon:	n/a	n/a
25	CTCF	chr22:29621760-29621910	HCFaa	heart:	n/a	n/a
26	CTCF	chr22:29616454-29616552	HepG2	liver:	n/a	n/a
27	CTCF	chr22:29616481-29616587	MCF-7	breast:	n/a	n/a
28	CTCF	chr22:29616465-29616557	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr22:29628480-29628630	HepG2	liver:	n/a	n/a
30	CTCF	chr22:29616496-29616556	MCF-7	breast:	n/a	n/a
31	CTCF	chr22:29616527-29616533	MCF-7	breast:	n/a	n/a
32	CTCF	chr22:29616501-29616526	MCF-7	breast:	n/a	n/a
33	CTCF	chr22:29621860-29622010	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr22:29616507-29616554	MCF-7	breast:	n/a	n/a
35	CTCF	chr22:29621840-29621990	NHEK	skin:	n/a	n/a
36	CTCF	chr22:29616380-29616530	HepG2	liver:	n/a	n/a
37	CTCF	chr22:29621800-29621950	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr22:29613300-29613450	HepG2	liver:	n/a	n/a
39	EBF1	chr22:29613035-29613228	GM12878	blood:	n/a	chr22:29613150-29613161 chr22:29613173-29613184
40	EBF1	chr22:29613260-29613555	GM12878	blood:	n/a	n/a
41	EBF1	chr22:29627246-29627303	GM12878	blood:	n/a	chr22:29627287-29627298
42	ELF1	chr22:29629970-29630362	GM12878	blood:	n/a	n/a
43	ELF1	chr22:29616716-29617186	GM12878	blood:	n/a	n/a
44	ELF1	chr22:29628582-29628856	HepG2	liver:	n/a	n/a
45	ELF1	chr22:29628595-29628929	GM12878	blood:	n/a	n/a
46	ELF1	chr22:29621413-29622207	GM12878	blood:	n/a	chr22:29621471-29621482
47	ELF1	chr22:29629256-29629664	GM12878	blood:	n/a	n/a
48	EP300	chr22:29613356-29613623	HepG2	liver:	n/a	n/a
49	EP300	chr22:29613302-29613590	HepG2	liver:	n/a	n/a
50	FOS	chr22:29621820-29621866	MCF10A-Er-Src	breast:	n/a	chr22:29621853-29621860 chr22:29621852-29621861 chr22:29621853-29621861

No data

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:29621556..29624508-chr22:29627726..29630197,3	K562	blood:
2	chr22:29616773..29618442-chr22:29619234..29622066,2	MCF-7	breast:
3	chr22:29619234..29621532-chr22:29627625..29630372,2	MCF-7	breast:
4	chr22:29618425..29620618-chr22:29628418..29631413,2	K562	blood:
5	chr22:29612161..29619581-chr22:29619796..29623989,9	K562	blood:
6	chr22:29616773..29618442-chr22:29619234..29622066,2	MCF-7	breast:
7	chr22:29601808..29604222-chr22:29612669..29614934,2	MCF-7	breast:
8	chr22:29611701..29614819-chr22:29620518..29622673,3	K562	blood:
9	chr22:29622067..29623775-chr22:29624148..29626498,2	K562	blood:
10	chr22:29622067..29623775-chr22:29624148..29626498,2	K562	blood:
11	chr22:29600453..29603035-chr22:29615819..29618230,2	K562	blood:
12	chr22:29612019..29613931-chr22:29615202..29617842,2	MCF-7	breast:
13	chr22:29611701..29614819-chr22:29620518..29622673,3	K562	blood:
14	chr22:29617687..29619581-chr22:29621568..29623250,2	K562	blood:
15	chr22:29612167..29614111-chr22:29627917..29629464,2	K562	blood:
16	chr22:29602636..29604550-chr22:29611942..29613555,2	K562	blood:
17	chr22:29612161..29619581-chr22:29619796..29623989,9	K562	blood:
18	chr22:29619482..29621531-chr22:29625031..29626896,2	K562	blood:
19	chr22:29619482..29621531-chr22:29625031..29626896,2	K562	blood:
20	chr22:29609378..29611506-chr22:29620734..29622343,2	MCF-7	breast:
21	chr22:29617283..29619466-chr22:29651521..29653548,2	K562	blood:
22	chr22:29616106..29618160-chr22:29628448..29630302,2	K562	blood:
23	chr22:29612019..29613931-chr22:29615202..29617842,2	MCF-7	breast:
24	chr22:29601210..29603979-chr22:29627327..29629637,2	K562	blood:
25	chr22:29617687..29619581-chr22:29621568..29623250,2	K562	blood:
26	chr22:29616331..29618039-chr22:29656036..29658500,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EWSR1-4	chr22:29627671-29629457	NONHSAT084681
2	lnc-EWSR1-4	chr22:29629603-29629851	NONHSAT084681
3	lnc-EWSR1-3	chr22:29620225-29620479	expReg_chr22_2008_+

No data

Variant related genes	Relation type
EMID1	TF binding region
ENSG00000186998	chromatin interactions
ENSG00000237015	chromatin interactions

Extended variants
information (count: 795 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9625736	chr22:29612508-29612509	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552284678	chr22:29612516-29612517	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs200941856	chr22:29612542-29612543	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs538828162	chr22:29612568-29612569	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs112653836	chr22:29612652-29612653	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554460534	chr22:29612679-29612680	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs185150265	chr22:29612703-29612704	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs536652423	chr22:29612705-29612706	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs132382	chr22:29612736-29612737	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs576020161	chr22:29612773-29612774	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs543546629	chr22:29612849-29612850	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs532351747	chr22:29612853-29612854	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs558608092	chr22:29612856-29612857	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs189807415	chr22:29612860-29612861	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs540833859	chr22:29612883-29612884	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs371502588	chr22:29612901-29612902	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs574598746	chr22:29612933-29612934	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs55676901	chr22:29612934-29612935	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs16987275	chr22:29612948-29612949	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs545766576	chr22:29612985-29612986	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs530496484	chr22:29612996-29612997	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs112521948	chr22:29613001-29613002	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs111849223	chr22:29613012-29613013	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs540236042	chr22:29613020-29613021	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs564135814	chr22:29613026-29613027	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs531792457	chr22:29613097-29613098	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs73882500	chr22:29613120-29613121	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542018734	chr22:29613149-29613150	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs5752881	chr22:29613177-29613178	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560149537	chr22:29613244-29613245	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs369447175	chr22:29613367-29613368	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs9620871	chr22:29613368-29613369	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs566259385	chr22:29613371-29613372	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs115798235	chr22:29613375-29613376	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs386820571	chr22:29613439-29613440	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs7284245	chr22:29613441-29613442	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs9620872	chr22:29613451-29613452	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs558642805	chr22:29613517-29613518	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs132383	chr22:29613520-29613521	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs534822261	chr22:29613529-29613530	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138080837	chr22:29613580-29613581	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181054392	chr22:29613583-29613584	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149528292	chr22:29613585-29613586	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs563544484	chr22:29613595-29613596	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs575325463	chr22:29613624-29613625	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs545775165	chr22:29613637-29613638	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs36047619	chr22:29613654-29613655	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs564173110	chr22:29613764-29613765	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs187275965	chr22:29613772-29613773	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs111523929	chr22:29613785-29613786	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
abnormal development	18461090	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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	17322880	CNVD
Breast cancer	20409316	CNVD
Neurofibromatosis type 2	19566914	CNVD
Autism	19384346	CNVD

Chromatin state (count:413 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29602800-29616000	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr22:29602800-29616000	Weak transcription	Ovary	ovary
3	chr22:29603800-29612600	Weak transcription	Brain Angular Gyrus	brain
4	chr22:29604000-29616200	Weak transcription	Thymus	Thymus
5	chr22:29604800-29612600	Weak transcription	Brain Cingulate Gyrus	brain
6	chr22:29605000-29619400	Weak transcription	Colonic Mucosa	Colon
7	chr22:29605400-29612600	Weak transcription	Fetal Muscle Trunk	muscle
8	chr22:29605400-29614400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr22:29605400-29616000	Weak transcription	Lung	lung
10	chr22:29605800-29612800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
11	chr22:29606000-29612600	Weak transcription	Brain Hippocampus Middle	brain
12	chr22:29606200-29616000	Strong transcription	Fetal Intestine Large	intestine
13	chr22:29607200-29612600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr22:29607600-29615000	Enhancers	Fetal Brain Male	brain
15	chr22:29607600-29615200	Weak transcription	Gastric	stomach
16	chr22:29607600-29616000	Strong transcription	Fetal Intestine Small	intestine
17	chr22:29607600-29621000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr22:29607600-29621000	Weak transcription	Esophagus	oesophagus
19	chr22:29607800-29614000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr22:29607800-29616000	Weak transcription	Duodenum Mucosa	Duodenum
21	chr22:29608600-29615200	Strong transcription	Dnd41	blood
22	chr22:29609200-29616400	Weak transcription	Fetal Kidney	kidney
23	chr22:29609400-29615400	Strong transcription	Fetal Stomach	stomach
24	chr22:29610000-29615600	Genic enhancers	Spleen	Spleen
25	chr22:29610400-29613000	Weak transcription	Fetal Muscle Leg	muscle
26	chr22:29611000-29613000	Strong transcription	Fetal Brain Female	brain
27	chr22:29611000-29613600	Enhancers	GM12878-XiMat	blood
28	chr22:29611400-29612600	Strong transcription	Brain Germinal Matrix	brain
29	chr22:29611400-29616000	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr22:29611600-29612600	Strong transcription	Fetal Lung	lung
31	chr22:29611600-29616000	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr22:29611600-29616000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr22:29611600-29616200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr22:29611600-29620800	Weak transcription	Primary hematopoietic stem cells	blood
35	chr22:29611800-29613400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
36	chr22:29611800-29613800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr22:29611800-29614400	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr22:29611800-29616000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr22:29611800-29621400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr22:29612000-29612800	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr22:29612200-29614000	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr22:29612200-29614600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr22:29612200-29614800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr22:29612200-29614800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
45	chr22:29612200-29614800	Enhancers	Pancreas	Pancrea
46	chr22:29612400-29612600	Enhancers	Brain Anterior Caudate	brain
47	chr22:29612400-29613200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr22:29612400-29614000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr22:29612400-29621200	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr22:29612600-29612800	Enhancers	Fetal Muscle Trunk	muscle

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