Variant report

Variant	esv1828355
Chromosome Location	chr22:29072426-29095085
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:428)
CpG islands
(count:489)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:428 , 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	chr22:29088114-29088341	GM12878	blood:	n/a	n/a
6	BATF	chr22:29088557-29088776	GM12878	blood:	n/a	n/a
7	BATF	chr22:29084039-29084373	GM12878	blood:	n/a	n/a
8	BCL11A	chr22:29072214-29072534	GM12878	blood:	n/a	n/a
9	BCL11A	chr22:29079431-29079609	GM12878	blood:	n/a	n/a
10	BCL11A	chr22:29085983-29086182	GM12878	blood:	n/a	n/a
11	BCL11A	chr22:29076664-29076907	GM12878	blood:	n/a	n/a
12	BCL11A	chr22:29088139-29088370	GM12878	blood:	n/a	chr22:29088204-29088212
13	BHLHE40	chr22:29075834-29076370	HepG2	liver:	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	chr22:29075875-29076373	K562	blood:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
16	BHLHE40	chr22:29076012-29076324	GM12878	blood:	n/a	chr22:29076201-29076210 chr22:29076201-29076210 chr22:29076202-29076211
17	BHLHE40	chr22:29076849-29076985	HepG2	liver:	n/a	n/a
18	BRCA1	chr22:29075353-29075356	GM12878	blood:	n/a	n/a
19	CCNT2	chr22:29075326-29075382	K562	blood:	n/a	n/a
20	CEBPB	chr22:29076789-29077167	Hela-S3	cervix:	n/a	chr22:29076972-29076983
21	CEBPB	chr22:29076953-29076998	H1-hESC	embryonic stem cell:	n/a	chr22:29076972-29076983
22	CEBPB	chr22:29076789-29077168	HepG2	liver:	n/a	chr22:29076972-29076983
23	CEBPB	chr22:29076791-29077162	HepG2	liver:	n/a	chr22:29076972-29076983
24	CEBPB	chr22:29076904-29077084	HepG2	liver:	n/a	chr22:29076972-29076983
25	CEBPB	chr22:29076785-29077169	IMR90	lung:	n/a	chr22:29076972-29076983
26	CEBPB	chr22:29076766-29077109	K562	blood:	n/a	chr22:29076972-29076983
27	CEBPB	chr22:29076790-29077167	K562	blood:	n/a	chr22:29076972-29076983
28	CEBPB	chr22:29076886-29077036	K562	blood:	n/a	chr22:29076972-29076983
29	CEBPB	chr22:29076869-29077080	HepG2	liver:	n/a	chr22:29076972-29076983
30	CEBPB	chr22:29076789-29077165	A549	lung:	n/a	chr22:29076972-29076983
31	CEBPD	chr22:29075821-29076234	HepG2	liver:	n/a	n/a
32	CHD2	chr22:29075341-29075521	K562	blood:	n/a	n/a
33	CHD2	chr22:29075282-29075552	Hela-S3	cervix:	n/a	n/a
34	CREB1	chr22:29075608-29076170	A549	lung:	n/a	n/a
35	CREB1	chr22:29075618-29076123	HepG2	liver:	n/a	n/a
36	CTCF	chr22:29075930-29075935	LNCaP	prostate:	n/a	n/a
37	CTCF	chr22:29075864-29076010	GM13977	blood:	n/a	n/a
38	CTCF	chr22:29075836-29076061	Spleen_OC	spleen:	n/a	n/a
39	CTCF	chr22:29075841-29076004	GM12892	blood:	n/a	n/a
40	CTCF	chr22:29075380-29075530	GM12868	blood:	n/a	n/a
41	CTCF	chr22:29079560-29079710	GM12870	blood:	n/a	n/a
42	CTCF	chr22:29075860-29075946	GM12891	blood:	n/a	n/a
43	CTCF	chr22:29075938-29075985	LNCaP	prostate:	n/a	n/a
44	CTCF	chr22:29075941-29076035	GM10266	blood:	n/a	n/a
45	CTCF	chr22:29075840-29075990	GM12864	blood:	n/a	n/a
46	CTCF	chr22:29080765-29080844	Lung_OC	lung:	n/a	n/a
47	CTCF	chr22:29075841-29075970	LNCaP	prostate:	n/a	n/a
48	CTCF	chr22:29075836-29076027	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr22:29094104-29094212	LNCaP	prostate:	n/a	n/a
50	CTCF	chr22:29078468-29078509	GM13976	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr22:29074955-29075005	CMK	blood:	n/a
2	chr22:29074955-29075005	CMK	blood:	n/a
3	chr22:29076383-29076433	A549	lung:	n/a
4	chr22:29075159-29075209	SK-N-SH	brain:	n/a
5	chr22:29076383-29076433	HNPCEpiC	eye:	n/a
6	chr22:29075247-29075297	HCT-116	colon:	n/a
7	chr22:29076175-29076225	MCF10A-Er-Src	breast:	n/a
8	chr22:29076113-29076163	BE2_C	brain:	n/a
9	chr22:29076383-29076433	AG04449	skin:	fetal
10	chr22:29076113-29076163	AG04449	skin:	fetal
11	chr22:29075159-29075209	AG09309	skin:	n/a
12	chr22:29073496-29073546	HMEC	breast:	n/a
13	chr22:29078644-29078694	HNPCEpiC	eye:	n/a
14	chr22:29076383-29076433	GM12891	blood:	n/a
15	chr22:29073496-29073546	NB4	blood:	n/a
16	chr22:29076113-29076163	HCT-116	colon:	n/a
17	chr22:29076175-29076225	Hepatocyte	liver:	n/a
18	chr22:29076113-29076163	SK-N-MC	brain:	n/a
19	chr22:29075247-29075297	Caco-2	colon:	n/a
20	chr22:29076113-29076163	GM12892	blood:	n/a
21	chr22:29075159-29075209	SK-N-MC	brain:	n/a
22	chr22:29078644-29078694	ECC-1	luminal epithelium:	n/a
23	chr22:29076383-29076433	U87	brain:	n/a
24	chr22:29075159-29075209	SAEC	small airway:	n/a
25	chr22:29074955-29075005	NT2-D1	testis:	n/a
26	chr22:29076113-29076163	HRCEpiC	kidney:	n/a
27	chr22:29076383-29076433	AG09319	gingival:	n/a
28	chr22:29076113-29076163	HAEpiC	amniotic membrane:	n/a
29	chr22:29074955-29075005	HUVEC	blood vessel:	n/a
30	chr22:29075159-29075209	HCT-116	colon:	n/a
31	chr22:29076113-29076163	HRE	kidney:	n/a
32	chr22:29073496-29073546	BJ	skin:	n/a
33	chr22:29076383-29076433	LNCaP	prostate:	n/a
34	chr22:29075159-29075209	HAEpiC	amniotic membrane:	n/a
35	chr22:29076383-29076433	AG10803	skin:	n/a
36	chr22:29076383-29076433	Hepatocyte	liver:	n/a
37	chr22:29074955-29075005	PrEC	prostate:	n/a
38	chr22:29075159-29075209	NB4	blood:	n/a
39	chr22:29075247-29075297	HNPCEpiC	eye:	n/a
40	chr22:29075247-29075297	LNCaP	prostate:	n/a
41	chr22:29076383-29076433	IMR90	lung:	fetal
42	chr22:29074955-29075005	IMR90	lung:	fetal
43	chr22:29075159-29075209	GM06990	blood:	n/a
44	chr22:29075159-29075209	AG04450	lung:	fetal
45	chr22:29078644-29078694	HPAEpiC	pulmonary alveolar:	n/a
46	chr22:29076175-29076225	HUVEC	blood vessel:	n/a
47	chr22:29078644-29078694	MCF-7	breast:	n/a
48	chr22:29073496-29073546	CMK	blood:	n/a
49	chr22:29073496-29073546	AG04449	skin:	fetal
50	chr22:29075247-29075297	SAEC	small airway:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:29074345..29076106-chr22:29137826..29140000,2	K562	blood:
2	chr22:29071306..29073725-chr22:29073922..29075807,2	K562	blood:
3	chr22:29094612..29096688-chr22:29136318..29138280,2	K562	blood:
4	chr22:29090716..29093047-chr22:29154418..29156765,2	K562	blood:
5	chr22:29069948..29071525-chr22:29073386..29075260,2	K562	blood:
6	chr22:29093925..29096043-chr22:29097734..29099299,2	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
CHEK2	TF binding region
TTC28	TF binding region
CHEK2	CpG island
TTC28	CpG island
ENSG00000100154	chromatin interactions
ENSG00000100209	chromatin interactions
ENSG00000183765	chromatin interactions

Extended variants
information (count: 1008 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1008 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3896159	chr22:29072435-29072436	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs535328434	chr22:29072438-29072439	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs4035560	chr22:29072447-29072448	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs9613663	chr22:29072468-29072469	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs4035561	chr22:29072481-29072482	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs4080335	chr22:29072497-29072498	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs537209764	chr22:29072499-29072500	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550770012	chr22:29072542-29072543	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs4035562	chr22:29072581-29072582	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs4035563	chr22:29072588-29072589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs3896160	chr22:29072600-29072601	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs568932629	chr22:29072608-29072609	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537581646	chr22:29072626-29072627	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs2346868	chr22:29072666-29072667	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs2346869	chr22:29072689-29072690	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs201383902	chr22:29072707-29072708	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs202103995	chr22:29072711-29072712	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs34102970	chr22:29072744-29072745	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs558768286	chr22:29072771-29072772	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs577351883	chr22:29072791-29072792	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs72617288	chr22:29072864-29072865	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs5762741	chr22:29072917-29072918	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs575219500	chr22:29072933-29072934	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541248468	chr22:29072938-29072939	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs560885000	chr22:29072959-29072960	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs182424971	chr22:29073000-29073001	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs147027991	chr22:29073034-29073035	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564013882	chr22:29073056-29073057	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs376138654	chr22:29073082-29073083	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs35292146	chr22:29073146-29073147	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs147048243	chr22:29073147-29073148	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs538860596	chr22:29073163-29073164	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs143954002	chr22:29073164-29073165	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs375445264	chr22:29073165-29073166	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200368283	chr22:29073167-29073168	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs201195363	chr22:29073169-29073170	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371416180	chr22:29073171-29073172	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs375501570	chr22:29073173-29073174	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs369487207	chr22:29073186-29073187	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34541193	chr22:29073188-29073189	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201903787	chr22:29073190-29073191	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs9620814	chr22:29073191-29073192	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs58904905	chr22:29073195-29073196	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs9625527	chr22:29073209-29073210	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs184415738	chr22:29073231-29073232	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs188971981	chr22:29073296-29073297	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2346870	chr22:29073372-29073373	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs3963401	chr22:29073397-29073398	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4035564	chr22:29073401-29073402	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529175102	chr22:29073404-29073405	Strong transcription Weak transcription	Chromatin interactive region	1 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:646 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

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	chr22:29064600-29074800	Weak transcription	Left Ventricle	heart
5	chr22:29067000-29074400	Weak transcription	Fetal Lung	lung
6	chr22:29067200-29073800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr22:29067200-29074400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr22:29067600-29074400	Weak transcription	Fetal Brain Female	brain
9	chr22:29067800-29074400	Weak transcription	HepG2	liver
10	chr22:29069800-29072600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr22:29070600-29074400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr22:29070600-29074400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr22:29070600-29074400	Weak transcription	HUVEC	blood vessel
14	chr22:29070600-29074600	Weak transcription	K562	blood
15	chr22:29070600-29074600	Weak transcription	NHLF	lung
16	chr22:29070600-29074600	Weak transcription	Osteobl	bone
17	chr22:29071400-29074400	Weak transcription	NHDF-Ad	bronchial
18	chr22:29071400-29074800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr22:29071800-29074200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr22:29071800-29074600	Weak transcription	A549	lung
21	chr22:29072600-29073800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr22:29073200-29074600	Weak transcription	Fetal Muscle Leg	muscle
23	chr22:29073800-29074200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr22:29073800-29074400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr22:29073800-29074400	Enhancers	Ovary	ovary
26	chr22:29074000-29074200	Weak transcription	Fetal Stomach	stomach
27	chr22:29074000-29074600	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr22:29074200-29074400	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr22:29074200-29075000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr22:29074200-29076400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr22:29074400-29074600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr22:29074400-29074600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr22:29074400-29074600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr22:29074400-29074600	Flanking Active TSS	Fetal Lung	lung
35	chr22:29074400-29074600	Enhancers	Fetal Stomach	stomach
36	chr22:29074400-29074600	Flanking Active TSS	Ovary	ovary
37	chr22:29074400-29074600	Flanking Active TSS	HepG2	liver
38	chr22:29074400-29074600	Flanking Active TSS	HUVEC	blood vessel
39	chr22:29074400-29074800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr22:29074400-29074800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
41	chr22:29074400-29074800	Enhancers	Fetal Brain Male	brain
42	chr22:29074400-29074800	Enhancers	Fetal Muscle Trunk	muscle
43	chr22:29074400-29074800	Enhancers	Placenta	Placenta
44	chr22:29074400-29074800	Enhancers	Right Ventricle	heart
45	chr22:29074400-29074800	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr22:29074400-29075000	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr22:29074400-29075000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr22:29074400-29075000	Active TSS	Brain Germinal Matrix	brain
49	chr22:29074400-29075200	Bivalent Enhancer	Primary T helper naive cells from peripheral blood	blood
50	chr22:29074400-29076400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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