Variant report

Variant	nsv966098
Chromosome Location	chr22:29069640-29088208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:453)
CpG islands
(count:551)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:453 , 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	chr22:29071147-29071157	K562	blood:	n/a	n/a
2	ATF1	chr22:29076933-29077144	K562	blood:	n/a	n/a
3	ATF2	chr22:29069985-29070415	GM12878	blood:	n/a	n/a
4	ATF3	chr22:29076874-29077103	K562	blood:	n/a	n/a
5	BACH1	chr22:29075695-29076206	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr22:29075339-29075367	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr22:29088114-29088341	GM12878	blood:	n/a	n/a
8	BATF	chr22:29072176-29072389	GM12878	blood:	n/a	n/a
9	BATF	chr22:29084039-29084373	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	BCL11A	chr22:29085983-29086182	GM12878	blood:	n/a	n/a
13	BCL11A	chr22:29070081-29070349	GM12878	blood:	n/a	n/a
14	BCL11A	chr22:29076664-29076907	GM12878	blood:	n/a	n/a
15	BCL11A	chr22:29072214-29072534	GM12878	blood:	n/a	n/a
16	BCL3	chr22:29070034-29070394	GM12878	blood:	n/a	n/a
17	BHLHE40	chr22:29075834-29076370	HepG2	liver:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
18	BHLHE40	chr22:29076849-29076985	HepG2	liver:	n/a	n/a
19	BHLHE40	chr22:29076134-29076273	A549	lung:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
20	BHLHE40	chr22:29076012-29076324	GM12878	blood:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
21	BHLHE40	chr22:29075875-29076373	K562	blood:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
22	BRCA1	chr22:29075353-29075356	GM12878	blood:	n/a	n/a
23	CBX3	chr22:29070039-29070343	K562	blood:	n/a	chr22:29070074-29070085
24	CCNT2	chr22:29075326-29075382	K562	blood:	n/a	n/a
25	CEBPB	chr22:29076791-29077162	HepG2	liver:	n/a	chr22:29076972-29076983
26	CEBPB	chr22:29076789-29077167	Hela-S3	cervix:	n/a	chr22:29076972-29076983
27	CEBPB	chr22:29076886-29077036	K562	blood:	n/a	chr22:29076972-29076983
28	CEBPB	chr22:29076766-29077109	K562	blood:	n/a	chr22:29076972-29076983
29	CEBPB	chr22:29076904-29077084	HepG2	liver:	n/a	chr22:29076972-29076983
30	CEBPB	chr22:29069964-29070527	GM12878	blood:	n/a	n/a
31	CEBPB	chr22:29076953-29076998	H1-hESC	embryonic stem cell:	n/a	chr22:29076972-29076983
32	CEBPB	chr22:29076789-29077168	HepG2	liver:	n/a	chr22:29076972-29076983
33	CEBPB	chr22:29076785-29077169	IMR90	lung:	n/a	chr22:29076972-29076983
34	CEBPB	chr22:29076869-29077080	HepG2	liver:	n/a	chr22:29076972-29076983
35	CEBPB	chr22:29076790-29077167	K562	blood:	n/a	chr22:29076972-29076983
36	CEBPB	chr22:29076789-29077165	A549	lung:	n/a	chr22:29076972-29076983
37	CEBPD	chr22:29075821-29076234	HepG2	liver:	n/a	n/a
38	CHD2	chr22:29075341-29075521	K562	blood:	n/a	n/a
39	CHD2	chr22:29075282-29075552	Hela-S3	cervix:	n/a	n/a
40	CREB1	chr22:29075618-29076123	HepG2	liver:	n/a	n/a
41	CREB1	chr22:29075608-29076170	A549	lung:	n/a	n/a
42	CTCF	chr22:29078468-29078509	GM13976	blood:	n/a	n/a
43	CTCF	chr22:29075836-29076027	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr22:29075864-29076010	GM13977	blood:	n/a	n/a
45	CTCF	chr22:29075930-29075935	LNCaP	prostate:	n/a	n/a
46	CTCF	chr22:29075837-29075995	GM13976	blood:	n/a	n/a
47	CTCF	chr22:29075941-29076035	GM10266	blood:	n/a	n/a
48	CTCF	chr22:29075841-29075970	LNCaP	prostate:	n/a	n/a
49	CTCF	chr22:29075840-29075990	GM12864	blood:	n/a	n/a
50	CTCF	chr22:29075836-29076061	Spleen_OC	spleen:	n/a	n/a

(count:551 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29073496-29073546	LNCaP	prostate:	n/a
2	chr22:29076383-29076433	HEEpiC	esophagus:	n/a
3	chr22:29073496-29073546	LNCaP	prostate:	n/a
4	chr22:29076383-29076433	HEEpiC	esophagus:	n/a
5	chr22:29074955-29075005	MCF-7	breast:	n/a
6	chr22:29075247-29075297	HCT-116	colon:	n/a
7	chr22:29073496-29073546	BE2_C	brain:	n/a
8	chr22:29076113-29076163	GM19239	blood:	n/a
9	chr22:29072190-29072240	Caco-2	colon:	n/a
10	chr22:29076175-29076225	Jurkat	blood:	n/a
11	chr22:29075247-29075297	AoSMC	blood vessel:	n/a
12	chr22:29075159-29075209	RPTEC	kidney:	n/a
13	chr22:29076175-29076225	T-47D	breast:	n/a
14	chr22:29076383-29076433	MCF10A-Er-Src	breast:	n/a
15	chr22:29072190-29072240	MCF10A-Er-Src	breast:	n/a
16	chr22:29075159-29075209	PrEC	prostate:	n/a
17	chr22:29073496-29073546	Hepatocyte	liver:	n/a
18	chr22:29075247-29075297	PANC-1	pancreas:	n/a
19	chr22:29076113-29076163	IMR90	lung:	fetal
20	chr22:29076383-29076433	PFSK-1	brain:	n/a
21	chr22:29073496-29073546	GM06990	blood:	n/a
22	chr22:29074955-29075005	SK-N-MC	brain:	n/a
23	chr22:29072190-29072240	SKMC	muscle:	n/a
24	chr22:29074955-29075005	HRPEpiC	eye:	n/a
25	chr22:29076175-29076225	SKMC	muscle:	n/a
26	chr22:29076113-29076163	AG09319	gingival:	n/a
27	chr22:29073496-29073546	HRE	kidney:	n/a
28	chr22:29076113-29076163	BE2_C	brain:	n/a
29	chr22:29072190-29072240	SK-N-MC	brain:	n/a
30	chr22:29073496-29073546	T-47D	breast:	n/a
31	chr22:29072190-29072240	PrEC	prostate:	n/a
32	chr22:29076175-29076225	AG09309	skin:	n/a
33	chr22:29076113-29076163	PrEC	prostate:	n/a
34	chr22:29076175-29076225	HRPEpiC	eye:	n/a
35	chr22:29075247-29075297	SK-N-SH_RA	brain:	n/a
36	chr22:29078644-29078694	GM12891	blood:	n/a
37	chr22:29074955-29075005	HCF	heart:	n/a
38	chr22:29073496-29073546	AG04450	lung:	fetal
39	chr22:29078644-29078694	HAEpiC	amniotic membrane:	n/a
40	chr22:29076175-29076225	BJ	skin:	n/a
41	chr22:29076383-29076433	GM12891	blood:	n/a
42	chr22:29073496-29073546	RPTEC	kidney:	n/a
43	chr22:29074955-29075005	SK-N-SH_RA	brain:	n/a
44	chr22:29078644-29078694	NT2-D1	testis:	n/a
45	chr22:29076383-29076433	IMR90	lung:	fetal
46	chr22:29076113-29076163	AG09309	skin:	n/a
47	chr22:29076113-29076163	PANC-1	pancreas:	n/a
48	chr22:29078644-29078694	T-47D	breast:	n/a
49	chr22:29076383-29076433	HNPCEpiC	eye:	n/a
50	chr22:29072190-29072240	ECC-1	luminal epithelium:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:29068301..29072007-chr22:29167336..29171119,3	K562	blood:
2	chr22:29051030..29053991-chr22:29069549..29071319,2	K562	blood:
3	chr22:29069948..29071525-chr22:29073386..29075260,2	K562	blood:
4	chr22:29068475..29070803-chr22:29136306..29139155,2	K562	blood:
5	chr22:29069948..29071525-chr22:29073386..29075260,2	K562	blood:
6	chr22:29074345..29076106-chr22:29137826..29140000,2	K562	blood:
7	chr22:29071306..29073725-chr22:29073922..29075807,2	K562	blood:

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

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

No data

Variant related genes	Relation type
TTC28	TF binding region
CHEK2	TF binding region
TTC28	CpG island
CHEK2	CpG island
ENSG00000100209	chromatin interactions
ENSG00000100154	chromatin interactions
ENSG00000159873	chromatin interactions
ENSG00000183765	chromatin interactions

Extended variants
information (count: 835 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:835 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9625526	chr22:29069642-29069643	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550417045	chr22:29069722-29069723	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs150764826	chr22:29069740-29069741	ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs565724179	chr22:29069814-29069815	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538941217	chr22:29069893-29069894	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs373619992	chr22:29069999-29070000	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs534529620	chr22:29070169-29070170	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs182154181	chr22:29070170-29070171	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs186851432	chr22:29070176-29070177	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs139138158	chr22:29070192-29070193	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs536303354	chr22:29070213-29070214	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs376957990	chr22:29070246-29070247	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs73881117	chr22:29070251-29070252	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs75068042	chr22:29070254-29070255	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs74430658	chr22:29070256-29070257	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs115560662	chr22:29070279-29070280	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs73881118	chr22:29070297-29070298	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs558800033	chr22:29070336-29070337	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs577005637	chr22:29070361-29070362	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs551644797	chr22:29070372-29070373	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs190867484	chr22:29070437-29070438	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs5997385	chr22:29070466-29070467	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572216161	chr22:29070522-29070523	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs542676416	chr22:29070524-29070525	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs368691043	chr22:29070579-29070580	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs200248476	chr22:29070582-29070583	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs558533207	chr22:29070722-29070723	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs531707499	chr22:29070723-29070724	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs543793713	chr22:29070778-29070779	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs188058811	chr22:29070784-29070785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs532651636	chr22:29070791-29070792	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs576374758	chr22:29070792-29070793	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs79014481	chr22:29070805-29070806	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34351638	chr22:29070806-29070807	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs76933776	chr22:29070807-29070808	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs77753006	chr22:29070808-29070809	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs398036762	chr22:29070824-29070825	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs201826518	chr22:29070827-29070828	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs193080428	chr22:29070841-29070842	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs548022357	chr22:29070857-29070858	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs566244347	chr22:29070879-29070880	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs5762740	chr22:29070910-29070911	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs529838489	chr22:29070958-29070959	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs185283743	chr22:29070988-29070989	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs569585241	chr22:29071002-29071003	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs554845405	chr22:29071111-29071112	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs537041508	chr22:29071144-29071145	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558625764	chr22:29071147-29071148	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs535814416	chr22:29071148-29071149	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs372145907	chr22:29071151-29071152	Weak transcription Bivalent Enhancer 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
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

Chromatin state (count:587 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29046400-29073800	Weak transcription	Ovary	ovary
2	chr22:29052600-29074600	Weak transcription	Colon Smooth Muscle	Colon
3	chr22:29056800-29074600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr22:29057600-29070200	Weak transcription	Fetal Stomach	stomach
5	chr22:29058000-29070200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr22:29064600-29074800	Weak transcription	Left Ventricle	heart
7	chr22:29064800-29069800	Weak transcription	HUVEC	blood vessel
8	chr22:29067000-29069800	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr22:29067000-29074400	Weak transcription	Fetal Lung	lung
10	chr22:29067200-29073800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr22:29067200-29074400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr22:29067600-29074400	Weak transcription	Fetal Brain Female	brain
13	chr22:29067800-29074400	Weak transcription	HepG2	liver
14	chr22:29068600-29069800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr22:29068600-29069800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
16	chr22:29068800-29069800	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
17	chr22:29068800-29069800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr22:29068800-29070800	Bivalent Enhancer	Dnd41	blood
19	chr22:29068800-29071400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
20	chr22:29068800-29071400	Bivalent Enhancer	Primary T killer memory cells from peripheral blood	blood
21	chr22:29068800-29071400	Enhancers	GM12878-XiMat	blood
22	chr22:29069200-29071000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr22:29069400-29070000	Bivalent Enhancer	Primary T cells from cord blood	blood
24	chr22:29069400-29070800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr22:29069400-29071000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr22:29069400-29071200	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
27	chr22:29069400-29071200	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
28	chr22:29069400-29071400	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
29	chr22:29069600-29069800	Flanking Bivalent TSS/Enh	Primary B cells from cord blood	blood
30	chr22:29069600-29069800	Flanking Bivalent TSS/Enh	Primary T helper naive cells from peripheral blood	blood
31	chr22:29069600-29070000	Weak transcription	NHDF-Ad	bronchial
32	chr22:29069600-29070600	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr22:29069600-29070800	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chr22:29069600-29071000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
35	chr22:29069600-29071400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr22:29069600-29071400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr22:29069800-29070000	Enhancers	HUVEC	blood vessel
38	chr22:29069800-29070600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr22:29069800-29070600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
40	chr22:29069800-29070600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr22:29069800-29070600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr22:29069800-29070600	Enhancers	K562	blood
43	chr22:29069800-29071000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
44	chr22:29069800-29071000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr22:29069800-29071200	Enhancers	Primary B cells from peripheral blood	blood
46	chr22:29069800-29071400	Bivalent Enhancer	Primary B cells from cord blood	blood
47	chr22:29069800-29071400	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
48	chr22:29069800-29072600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr22:29070000-29070400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr22:29070000-29070400	Enhancers	Primary T cells from cord blood	blood

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