Variant report

Variant	esv1832454
Chromosome Location	chr22:29074021-29094885
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:418)
CpG islands
(count:427)
Chromatin interactive
region (count:5)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:418 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr22:29076933-29077144	K562	blood:	n/a	n/a
2	ATF3	chr22:29076874-29077103	K562	blood:	n/a	n/a
3	BACH1	chr22:29075339-29075367	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr22:29075695-29076206	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr22:29084039-29084373	GM12878	blood:	n/a	n/a
6	BATF	chr22:29088114-29088341	GM12878	blood:	n/a	n/a
7	BATF	chr22:29088557-29088776	GM12878	blood:	n/a	n/a
8	BCL11A	chr22:29076664-29076907	GM12878	blood:	n/a	n/a
9	BCL11A	chr22:29085983-29086182	GM12878	blood:	n/a	n/a
10	BCL11A	chr22:29079431-29079609	GM12878	blood:	n/a	n/a
11	BCL11A	chr22:29088139-29088370	GM12878	blood:	n/a	chr22:29088204-29088212
12	BHLHE40	chr22:29076849-29076985	HepG2	liver:	n/a	n/a
13	BHLHE40	chr22:29075875-29076373	K562	blood:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
14	BHLHE40	chr22:29076134-29076273	A549	lung:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
15	BHLHE40	chr22:29076012-29076324	GM12878	blood:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
16	BHLHE40	chr22:29075834-29076370	HepG2	liver:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
17	BRCA1	chr22:29075353-29075356	GM12878	blood:	n/a	n/a
18	CCNT2	chr22:29075326-29075382	K562	blood:	n/a	n/a
19	CEBPB	chr22:29076790-29077167	K562	blood:	n/a	chr22:29076972-29076983
20	CEBPB	chr22:29076766-29077109	K562	blood:	n/a	chr22:29076972-29076983
21	CEBPB	chr22:29076791-29077162	HepG2	liver:	n/a	chr22:29076972-29076983
22	CEBPB	chr22:29076789-29077168	HepG2	liver:	n/a	chr22:29076972-29076983
23	CEBPB	chr22:29076789-29077167	Hela-S3	cervix:	n/a	chr22:29076972-29076983
24	CEBPB	chr22:29076789-29077165	A549	lung:	n/a	chr22:29076972-29076983
25	CEBPB	chr22:29076886-29077036	K562	blood:	n/a	chr22:29076972-29076983
26	CEBPB	chr22:29076869-29077080	HepG2	liver:	n/a	chr22:29076972-29076983
27	CEBPB	chr22:29076904-29077084	HepG2	liver:	n/a	chr22:29076972-29076983
28	CEBPB	chr22:29076953-29076998	H1-hESC	embryonic stem cell:	n/a	chr22:29076972-29076983
29	CEBPB	chr22:29076785-29077169	IMR90	lung:	n/a	chr22:29076972-29076983
30	CEBPD	chr22:29075821-29076234	HepG2	liver:	n/a	n/a
31	CHD2	chr22:29075341-29075521	K562	blood:	n/a	n/a
32	CHD2	chr22:29075282-29075552	Hela-S3	cervix:	n/a	n/a
33	CREB1	chr22:29075608-29076170	A549	lung:	n/a	n/a
34	CREB1	chr22:29075618-29076123	HepG2	liver:	n/a	n/a
35	CTCF	chr22:29075941-29076035	GM10266	blood:	n/a	n/a
36	CTCF	chr22:29075840-29075990	GM12864	blood:	n/a	n/a
37	CTCF	chr22:29075938-29075985	LNCaP	prostate:	n/a	n/a
38	CTCF	chr22:29075836-29076061	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr22:29075841-29075970	LNCaP	prostate:	n/a	n/a
40	CTCF	chr22:29079560-29079710	GM12870	blood:	n/a	n/a
41	CTCF	chr22:29075930-29075935	LNCaP	prostate:	n/a	n/a
42	CTCF	chr22:29075836-29076027	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr22:29075380-29075530	GM12868	blood:	n/a	n/a
44	CTCF	chr22:29080765-29080844	Lung_OC	lung:	n/a	n/a
45	CTCF	chr22:29078468-29078509	GM13976	blood:	n/a	n/a
46	CTCF	chr22:29094104-29094212	LNCaP	prostate:	n/a	n/a
47	CTCF	chr22:29075841-29076004	GM12892	blood:	n/a	n/a
48	CTCF	chr22:29075837-29075995	GM13976	blood:	n/a	n/a
49	CTCF	chr22:29075860-29075946	GM12891	blood:	n/a	n/a
50	CTCF	chr22:29075864-29076010	GM13977	blood:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29078644-29078694	AG09319	gingival:	n/a
2	chr22:29075159-29075209	A549	lung:	n/a
3	chr22:29076113-29076163	Jurkat	blood:	n/a
4	chr22:29075247-29075297	HL-60	blood:	n/a
5	chr22:29078644-29078694	PrEC	prostate:	n/a
6	chr22:29074955-29075005	SKMC	muscle:	n/a
7	chr22:29074955-29075005	SK-N-MC	brain:	n/a
8	chr22:29075247-29075297	HepG2	liver:	n/a
9	chr22:29075247-29075297	AG04449	skin:	fetal
10	chr22:29076113-29076163	HRE	kidney:	n/a
11	chr22:29075159-29075209	HIPEpiC	eye:	n/a
12	chr22:29076175-29076225	AoSMC	blood vessel:	n/a
13	chr22:29076113-29076163	IMR90	lung:	fetal
14	chr22:29078644-29078694	T-47D	breast:	n/a
15	chr22:29075159-29075209	HAEpiC	amniotic membrane:	n/a
16	chr22:29078644-29078694	ovcar-3	ovarian:	n/a
17	chr22:29078644-29078694	HNPCEpiC	eye:	n/a
18	chr22:29074955-29075005	GM12891	blood:	n/a
19	chr22:29076383-29076433	A549	lung:	n/a
20	chr22:29076113-29076163	Caco-2	colon:	n/a
21	chr22:29075247-29075297	GM19239	blood:	n/a
22	chr22:29076175-29076225	AG04449	skin:	fetal
23	chr22:29075247-29075297	BE2_C	brain:	n/a
24	chr22:29075159-29075209	AG04449	skin:	fetal
25	chr22:29074955-29075005	HEEpiC	esophagus:	n/a
26	chr22:29078644-29078694	SK-N-SH_RA	brain:	n/a
27	chr22:29076175-29076225	PrEC	prostate:	n/a
28	chr22:29078644-29078694	AoSMC	blood vessel:	n/a
29	chr22:29076383-29076433	U87	brain:	n/a
30	chr22:29076175-29076225	Jurkat	blood:	n/a
31	chr22:29075159-29075209	HepG2	liver:	n/a
32	chr22:29076383-29076433	GM12878	blood:	n/a
33	chr22:29076175-29076225	BE2_C	brain:	n/a
34	chr22:29076175-29076225	BJ	skin:	n/a
35	chr22:29075247-29075297	LNCaP	prostate:	n/a
36	chr22:29074955-29075005	H1-hESC	embryonic stem cell:	embryo
37	chr22:29074955-29075005	PANC-1	pancreas:	n/a
38	chr22:29078644-29078694	HRE	kidney:	n/a
39	chr22:29075159-29075209	Caco-2	colon:	n/a
40	chr22:29078644-29078694	NHBE	bronchial:	n/a
41	chr22:29076113-29076163	HCPEpiC	choroid plexus:	n/a
42	chr22:29075159-29075209	GM12891	blood:	n/a
43	chr22:29078644-29078694	IMR90	lung:	fetal
44	chr22:29075159-29075209	PANC-1	pancreas:	n/a
45	chr22:29075159-29075209	BE2_C	brain:	n/a
46	chr22:29074955-29075005	NHBE	bronchial:	n/a
47	chr22:29076383-29076433	HL-60	blood:	n/a
48	chr22:29076383-29076433	ovcar-3	ovarian:	n/a
49	chr22:29076113-29076163	HCF	heart:	n/a
50	chr22:29076383-29076433	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr22:29074345..29076106-chr22:29137826..29140000,2	K562	blood:
2	chr22:29090716..29093047-chr22:29154418..29156765,2	K562	blood:
3	chr22:29093925..29096043-chr22:29097734..29099299,2	K562	blood:
4	chr22:29069948..29071525-chr22:29073386..29075260,2	K562	blood:
5	chr22:29094612..29096688-chr22:29136318..29138280,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TTC28-1	chr22:29083737-29083974	NONHSAT084651
2	lnc-TTC28-1	chr22:29085123-29085398	NONHSAT084651

No data

Variant related genes	Relation type
CHEK2	TF binding region
TTC28	TF binding region
CHEK2	CpG island
TTC28	CpG island
ENSG00000100209	chromatin interactions
ENSG00000183765	chromatin interactions

Extended variants
information (count: 919 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:919 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530025319	chr22:29074038-29074039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs191212920	chr22:29074056-29074057	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551296509	chr22:29074059-29074060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs183716355	chr22:29074060-29074061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs148910858	chr22:29074116-29074117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547093226	chr22:29074120-29074121	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200656425	chr22:29074180-29074181	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs181196837	chr22:29074211-29074212	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199729583	chr22:29074219-29074220	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200692685	chr22:29074235-29074236	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs201710771	chr22:29074248-29074249	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199863284	chr22:29074257-29074258	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs535469384	chr22:29074263-29074264	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs148045949	chr22:29074288-29074289	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190513125	chr22:29074291-29074292	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12166744	chr22:29074294-29074295	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs200814808	chr22:29074311-29074312	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540082506	chr22:29074327-29074328	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs182173452	chr22:29074332-29074333	Enhancers Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573082804	chr22:29074358-29074359	Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs117959254	chr22:29074382-29074383	Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555037764	chr22:29074394-29074395	Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs111983983	chr22:29074398-29074399	Enhancers Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs563650471	chr22:29074417-29074418	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543868679	chr22:29074437-29074438	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs562464645	chr22:29074533-29074534	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs577876425	chr22:29074560-29074561	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs145971580	chr22:29074618-29074619	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs560417158	chr22:29074638-29074639	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs138563917	chr22:29074652-29074653	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs185119603	chr22:29074657-29074658	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs374150110	chr22:29074737-29074738	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs562158677	chr22:29074739-29074740	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs529339846	chr22:29074756-29074757	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs377193203	chr22:29074772-29074773	Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs185641388	chr22:29074800-29074801	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs550705636	chr22:29074813-29074814	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs542951030	chr22:29074894-29074895	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs569197070	chr22:29074911-29074912	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs201040484	chr22:29074914-29074915	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs559331123	chr22:29074933-29074934	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs112998088	chr22:29074934-29074935	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs111592014	chr22:29074944-29074945	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs539775819	chr22:29074948-29074949	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189997351	chr22:29074963-29074964	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs528060990	chr22:29074966-29074967	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs112062536	chr22:29074972-29074973	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566766503	chr22:29074974-29074975	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs62235680	chr22:29074976-29074977	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs9613664	chr22:29074987-29074988	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Ovine squamous-cell carcinoma	17599052	CNVD
Cat eye syndrome	16708226	CNVD
Olfactory neuroblastoma	18408657	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20616022	CNVD
Breast cancer	21486468	CNVD
Ovarian cancer	21486468	CNVD

Chromatin state (count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29052600-29074600	Weak transcription	Colon Smooth Muscle	Colon
2	chr22:29056800-29074600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr22:29064600-29074800	Weak transcription	Left Ventricle	heart
4	chr22:29067000-29074400	Weak transcription	Fetal Lung	lung
5	chr22:29067200-29074400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr22:29067600-29074400	Weak transcription	Fetal Brain Female	brain
7	chr22:29067800-29074400	Weak transcription	HepG2	liver
8	chr22:29070600-29074400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr22:29070600-29074400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr22:29070600-29074400	Weak transcription	HUVEC	blood vessel
11	chr22:29070600-29074600	Weak transcription	K562	blood
12	chr22:29070600-29074600	Weak transcription	NHLF	lung
13	chr22:29070600-29074600	Weak transcription	Osteobl	bone
14	chr22:29071400-29074400	Weak transcription	NHDF-Ad	bronchial
15	chr22:29071400-29074800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr22:29071800-29074200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr22:29071800-29074600	Weak transcription	A549	lung
18	chr22:29073200-29074600	Weak transcription	Fetal Muscle Leg	muscle
19	chr22:29073800-29074200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr22:29073800-29074400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr22:29073800-29074400	Enhancers	Ovary	ovary
22	chr22:29074000-29074200	Weak transcription	Fetal Stomach	stomach
23	chr22:29074000-29074600	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr22:29074200-29074400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr22:29074200-29075000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr22:29074200-29076400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr22:29074400-29074600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr22:29074400-29074600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr22:29074400-29074600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr22:29074400-29074600	Flanking Active TSS	Fetal Lung	lung
31	chr22:29074400-29074600	Enhancers	Fetal Stomach	stomach
32	chr22:29074400-29074600	Flanking Active TSS	Ovary	ovary
33	chr22:29074400-29074600	Flanking Active TSS	HepG2	liver
34	chr22:29074400-29074600	Flanking Active TSS	HUVEC	blood vessel
35	chr22:29074400-29074800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr22:29074400-29074800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr22:29074400-29074800	Enhancers	Fetal Brain Male	brain
38	chr22:29074400-29074800	Enhancers	Fetal Muscle Trunk	muscle
39	chr22:29074400-29074800	Enhancers	Placenta	Placenta
40	chr22:29074400-29074800	Enhancers	Right Ventricle	heart
41	chr22:29074400-29074800	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr22:29074400-29075000	Active TSS	iPS-20b Cell Line	embryonic stem cell
43	chr22:29074400-29075000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr22:29074400-29075000	Active TSS	Brain Germinal Matrix	brain
45	chr22:29074400-29075200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
46	chr22:29074400-29076400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr22:29074400-29076400	Active TSS	Brain Angular Gyrus	brain
48	chr22:29074400-29076400	Active TSS	Fetal Brain Female	brain
49	chr22:29074400-29076400	Active TSS	Hela-S3	cervix
50	chr22:29074400-29076400	Active TSS	NHDF-Ad	bronchial

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