Variant report

Variant	nsv914981
Chromosome Location	chr22:32912277-32940660
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:858)
CpG islands
(count:0)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr22:32927917-32928729	HepG2	liver:	n/a	n/a
2	ARID3A	chr22:32925026-32925394	HepG2	liver:	n/a	n/a
3	ARID3A	chr22:32935839-32935972	K562	blood:	n/a	n/a
4	ATF1	chr22:32928229-32928869	K562	blood:	n/a	n/a
5	ATF1	chr22:32935674-32936110	K562	blood:	n/a	n/a
6	ATF2	chr22:32927973-32928621	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF3	chr22:32928709-32928855	K562	blood:	n/a	n/a
8	BHLHE40	chr22:32929724-32929924	HepG2	liver:	n/a	n/a
9	BHLHE40	chr22:32928708-32928975	HepG2	liver:	n/a	chr22:32928807-32928820
10	BHLHE40	chr22:32935800-32935819	HepG2	liver:	n/a	n/a
11	BHLHE40	chr22:32927937-32929019	HepG2	liver:	n/a	chr22:32928807-32928820
12	BHLHE40	chr22:32927917-32929366	K562	blood:	n/a	chr22:32928807-32928820
13	BHLHE40	chr22:32935518-32936146	K562	blood:	n/a	n/a
14	BRCA1	chr22:32925141-32925319	HepG2	liver:	n/a	n/a
15	BRCA1	chr22:32935365-32936055	Hela-S3	cervix:	n/a	n/a
16	BRCA1	chr22:32927916-32928309	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr22:32925043-32925163	H1-hESC	embryonic stem cell:	n/a	n/a
18	BRCA1	chr22:32928577-32928898	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr22:32928356-32928557	HepG2	liver:	n/a	n/a
20	BRCA1	chr22:32925012-32925318	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr22:32914791-32915192	HCT-116	colon:	n/a	n/a
22	CCNT2	chr22:32935850-32936010	K562	blood:	n/a	n/a
23	CCNT2	chr22:32928240-32928931	K562	blood:	n/a	n/a
24	CEBPB	chr22:32928076-32928873	HepG2	liver:	n/a	n/a
25	CEBPB	chr22:32929657-32929924	A549	lung:	n/a	n/a
26	CEBPB	chr22:32928305-32928688	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr22:32925753-32925798	HepG2	liver:	n/a	n/a
28	CEBPB	chr22:32928492-32928898	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr22:32925049-32925244	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr22:32935956-32936271	HepG2	liver:	n/a	n/a
31	CEBPB	chr22:32935754-32936210	K562	blood:	n/a	n/a
32	CEBPB	chr22:32929620-32929962	HepG2	liver:	n/a	n/a
33	CEBPB	chr22:32928364-32928693	K562	blood:	n/a	n/a
34	CEBPB	chr22:32929668-32929955	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr22:32928027-32928207	HepG2	liver:	n/a	n/a
36	CEBPB	chr22:32930401-32930731	HepG2	liver:	n/a	n/a
37	CEBPB	chr22:32930426-32930588	HepG2	liver:	n/a	n/a
38	CEBPB	chr22:32924961-32925331	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr22:32935561-32936337	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr22:32929635-32929980	IMR90	lung:	n/a	n/a
41	CEBPB	chr22:32930445-32930706	HepG2	liver:	n/a	n/a
42	CEBPD	chr22:32930368-32930649	HepG2	liver:	n/a	n/a
43	CEBPD	chr22:32925163-32925532	HepG2	liver:	n/a	n/a
44	CEBPD	chr22:32927955-32928396	HepG2	liver:	n/a	n/a
45	CEBPD	chr22:32928312-32928628	K562	blood:	n/a	n/a
46	CHD1	chr22:32928156-32928356	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD1	chr22:32924862-32925416	IMR90	lung:	n/a	n/a
48	CHD1	chr22:32925012-32925174	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr22:32928429-32928969	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr22:32935876-32936034	K562	blood:	n/a	n/a

No data

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:32927446..32930330-chr22:32933647..32935342,2	MCF-7	breast:
2	chr22:32924838..32926991-chr22:32927023..32929946,3	MCF-7	breast:
3	22:32920308-32927723..22:33389304-33403028	K562	blood:
4	chr22:32930459..32932142-chr22:32971211..32972775,2	MCF-7	breast:
5	chr22:32926743..32929840-chr6:24682818..24685708,4	K562	blood:
6	chr22:32926204..32927722-chr22:32933778..32935343,2	MCF-7	breast:
7	chr22:32930315..32931946-chr22:32951753..32954343,3	MCF-7	breast:
8	chr22:32774466..32775412-chr22:32914589..32915237,2	K562	blood:
9	22:31998728-32011472..22:32937912-32941862	K562	blood:
10	22:32920308-32927723..22:33208968-33216036	H1-hESC	embryonic stem cell:	embryo
11	chr22:32928032..32930048-chr6:24682726..24684882,3	MCF-7	breast:
12	chr22:32928085..32929693-chr6:24687618..24690090,2	K562	blood:
13	22:32920308-32927723..22:33178968-33185617	Hela-S3	cervix:
14	chr22:32922025..32930472-chr22:33196157..33204507,15	MCF-7	breast:
15	chr22:32926204..32927722-chr22:32933778..32935343,2	MCF-7	breast:
16	chr22:32936212..32939434-chr22:32941471..32944860,3	MCF-7	breast:
17	22:32920308-32927723..22:33253287-33262063	Hela-S3	cervix:
18	22:32906321-32912852..22:33339333-33353583	Hela-S3	cervix:
19	22:32912852-32915608..22:33262063-33266567	Hela-S3	cervix:
20	22:32053085-32061138..22:32906321-32912852	Hela-S3	cervix:
21	chr22:32928103..32930722-chr22:32934980..32936586,2	MCF-7	breast:
22	22:32264718-32278135..22:32906321-32912852	GM12878	blood:
23	22:32906321-32912852..22:33262063-33266567	K562	blood:
24	chr22:32928149..32930709-chr22:33046752..33049031,2	MCF-7	breast:
25	chr22:32935341..32940851-chr22:32952313..32956913,8	MCF-7	breast:
26	chr22:32938120..32940218-chr22:32990047..32992298,2	MCF-7	breast:
27	chr22:32933708..32937841-chr22:33196276..33199119,4	MCF-7	breast:
28	chr22:32928261..32930206-chr22:32941848..32945247,3	MCF-7	breast:
29	22:32906321-32912852..22:33452523-33459358	Hela-S3	cervix:
30	chr22:32927008..32929585-chr6:24687196..24690090,2	K562	blood:
31	chr22:32934249..32936537-chr22:32956952..32958878,2	MCF-7	breast:
32	22:32150875-32154575..22:32915608-32918105	GM12878	blood:
33	chr22:32927446..32930330-chr22:32933647..32935342,2	MCF-7	breast:
34	chr22:32931137..32932947-chr22:33197348..33199600,2	MCF-7	breast:
35	chr22:32928792..32930842-chr22:32975300..32976843,2	MCF-7	breast:
36	chr22:32927409..32931156-chr22:32954969..32961432,7	MCF-7	breast:
37	chr22:32926848..32928451-chr22:32942229..32944126,2	MCF-7	breast:
38	chr22:32928103..32930722-chr22:32934980..32936586,2	MCF-7	breast:

No data

Variant related genes	Relation type
SYN3	TF binding region
ENSG00000185666	chromatin interactions
ENSG00000100150	chromatin interactions
ENSG00000241878	chromatin interactions
ENSG00000197047	chromatin interactions
ENSG00000198089	chromatin interactions
ENSG00000242251	chromatin interactions
ENSG00000229673	chromatin interactions
ENSG00000183531	chromatin interactions
ENSG00000100234	chromatin interactions
ENSG00000112304	chromatin interactions

Extended variants
information (count: 1293 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:1293 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2097312	chr22:32912277-32912278	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553485018	chr22:32912295-32912296	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs115365689	chr22:32912304-32912305	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs534013786	chr22:32912310-32912311	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs544986662	chr22:32912324-32912325	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs375708657	chr22:32912331-32912332	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs532281551	chr22:32912334-32912335	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs2097313	chr22:32912337-32912338	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs2413123	chr22:32912341-32912342	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs2413124	chr22:32912345-32912346	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs2413125	chr22:32912349-32912350	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs2413126	chr22:32912353-32912354	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs2413127	chr22:32912357-32912358	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs2097314	chr22:32912361-32912362	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs7290998	chr22:32912365-32912366	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs58972175	chr22:32912368-32912369	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs561829925	chr22:32912372-32912373	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs552514172	chr22:32912373-32912374	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs151087050	chr22:32912411-32912412	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs141019023	chr22:32912412-32912413	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs183769973	chr22:32912454-32912455	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs5749453	chr22:32912458-32912459	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs201495430	chr22:32912459-32912460	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs574882936	chr22:32912495-32912496	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs542889158	chr22:32912557-32912558	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs376954835	chr22:32912576-32912577	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs563128854	chr22:32912579-32912580	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs536414338	chr22:32912602-32912603	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs370414425	chr22:32912617-32912618	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs150244493	chr22:32912628-32912629	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs189478303	chr22:32912639-32912640	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs181797004	chr22:32912664-32912665	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs527505497	chr22:32912698-32912699	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs564880937	chr22:32912736-32912737	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs186151065	chr22:32912737-32912738	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs371301322	chr22:32912749-32912750	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs199612353	chr22:32912791-32912792	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs560774110	chr22:32912793-32912794	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs67850676	chr22:32912796-32912797	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs398036911	chr22:32912799-32912800	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs189871355	chr22:32912811-32912812	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs549925303	chr22:32912830-32912831	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs5998525	chr22:32912902-32912903	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs138975037	chr22:32912931-32912932	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576576392	chr22:32913019-32913020	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs76955313	chr22:32913021-32913022	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs149426611	chr22:32913109-32913110	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs9621475	chr22:32913125-32913126	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs181715550	chr22:32913139-32913140	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548576255	chr22:32913164-32913165	ZNF genes & repeats Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Cancer	20164919	CNVD

Chromatin state (count:651 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32894400-32913200	Weak transcription	Fetal Brain Female	brain
2	chr22:32894800-32914200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr22:32895200-32913600	Weak transcription	Brain Germinal Matrix	brain
4	chr22:32895200-32918400	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr22:32895400-32914000	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr22:32895800-32913200	Weak transcription	Placenta	Placenta
7	chr22:32896000-32913200	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr22:32897200-32914200	Weak transcription	Primary T cells from cord blood	blood
9	chr22:32898600-32913800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr22:32898600-32928000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr22:32898800-32927200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr22:32904000-32924400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr22:32905400-32918600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr22:32906800-32913000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr22:32907600-32912800	Weak transcription	Brain Anterior Caudate	brain
16	chr22:32907600-32913600	Weak transcription	Adipose Nuclei	Adipose
17	chr22:32907800-32912800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr22:32907800-32913200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr22:32907800-32913800	Weak transcription	Fetal Stomach	stomach
20	chr22:32908000-32912800	Weak transcription	Brain Hippocampus Middle	brain
21	chr22:32908000-32913000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr22:32908000-32913800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr22:32908000-32916600	Weak transcription	Brain Substantia Nigra	brain
24	chr22:32908800-32914400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr22:32910200-32912600	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr22:32910200-32925600	Weak transcription	Spleen	Spleen
27	chr22:32910400-32912800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr22:32910400-32912800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr22:32910600-32912800	Weak transcription	Brain Angular Gyrus	brain
30	chr22:32910600-32915000	Weak transcription	HepG2	liver
31	chr22:32910800-32913000	Weak transcription	Fetal Muscle Leg	muscle
32	chr22:32911600-32912600	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr22:32911600-32913000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr22:32911800-32913000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr22:32912000-32914600	Weak transcription	NHDF-Ad	bronchial
36	chr22:32912600-32914000	Strong transcription	HUES48 Cell Line	embryonic stem cell
37	chr22:32912600-32914200	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr22:32912800-32913200	Strong transcription	Brain Angular Gyrus	brain
39	chr22:32912800-32913800	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr22:32912800-32913800	Strong transcription	Brain Anterior Caudate	brain
41	chr22:32912800-32914000	Strong transcription	Brain Cingulate Gyrus	brain
42	chr22:32912800-32914000	Strong transcription	Brain Hippocampus Middle	brain
43	chr22:32912800-32914200	Strong transcription	Brain Inferior Temporal Lobe	brain
44	chr22:32913000-32913400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr22:32913000-32913600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
46	chr22:32913000-32913800	Strong transcription	HUES6 Cell Line	embryonic stem cell
47	chr22:32913000-32914000	ZNF genes & repeats	Fetal Muscle Leg	muscle
48	chr22:32913000-32914800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr22:32913200-32913800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
50	chr22:32913200-32914000	Strong transcription	Duodenum Smooth Muscle	Duodenum

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