Variant report

Variant	nsv540148
Chromosome Location	chr9:71405224-71450033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:0)
Chromatin interactive
region (count:40)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 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	ARID3A	chr9:71432365-71432517	K562	blood:	n/a	n/a
2	ARID3A	chr9:71431767-71432536	HepG2	liver:	n/a	n/a
3	ATF1	chr9:71408890-71409217	K562	blood:	n/a	n/a
4	ATF1	chr9:71413396-71413615	K562	blood:	n/a	n/a
5	ATF1	chr9:71434023-71434218	K562	blood:	n/a	n/a
6	ATF1	chr9:71420516-71420729	K562	blood:	n/a	n/a
7	ATF2	chr9:71417493-71418032	GM12878	blood:	n/a	n/a
8	ATF2	chr9:71417409-71418026	GM12878	blood:	n/a	n/a
9	ATF2	chr9:71408787-71409342	GM12878	blood:	n/a	n/a
10	BACH1	chr9:71424797-71424814	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:71440605-71440702	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr9:71417492-71417937	GM12878	blood:	n/a	n/a
13	BCL11A	chr9:71417486-71418006	GM12878	blood:	n/a	n/a
14	BCL11A	chr9:71417582-71418030	GM12878	blood:	n/a	n/a
15	BCL3	chr9:71434026-71434318	GM12878	blood:	n/a	n/a
16	BCL3	chr9:71417549-71417857	GM12878	blood:	n/a	n/a
17	BHLHE40	chr9:71437438-71437970	K562	blood:	n/a	chr9:71437641-71437662 chr9:71437646-71437655
18	BHLHE40	chr9:71432034-71432370	HepG2	liver:	n/a	n/a
19	BHLHE40	chr9:71413322-71413818	K562	blood:	n/a	n/a
20	BHLHE40	chr9:71442911-71443570	K562	blood:	n/a	n/a
21	BHLHE40	chr9:71417260-71418013	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:71408968-71409340	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:71420912-71421142	K562	blood:	n/a	n/a
24	CBX3	chr9:71442943-71443333	K562	blood:	n/a	n/a
25	CCNT2	chr9:71420614-71421142	K562	blood:	n/a	n/a
26	CEBPB	chr9:71410074-71410294	K562	blood:	n/a	n/a
27	CEBPB	chr9:71443364-71443491	K562	blood:	n/a	n/a
28	CEBPB	chr9:71432047-71432318	HepG2	liver:	n/a	chr9:71432226-71432237
29	CEBPB	chr9:71432135-71432282	K562	blood:	n/a	chr9:71432226-71432237
30	CEBPB	chr9:71448178-71448491	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr9:71433861-71434223	K562	blood:	n/a	n/a
32	CEBPB	chr9:71442858-71443604	K562	blood:	n/a	n/a
33	CEBPB	chr9:71432050-71432324	HepG2	liver:	n/a	chr9:71432226-71432237
34	CEBPB	chr9:71432025-71432394	HepG2	liver:	n/a	chr9:71432226-71432237
35	CEBPB	chr9:71420396-71420738	K562	blood:	n/a	n/a
36	CEBPB	chr9:71405010-71405242	K562	blood:	n/a	chr9:71405134-71405145 chr9:71405134-71405147
37	CEBPB	chr9:71410017-71410303	MCF-7	breast:	n/a	n/a
38	CEBPB	chr9:71442846-71443159	HepG2	liver:	n/a	n/a
39	CEBPB	chr9:71448147-71448455	K562	blood:	n/a	n/a
40	CEBPB	chr9:71432022-71432406	HepG2	liver:	n/a	chr9:71432226-71432237
41	CEBPB	chr9:71443319-71443495	K562	blood:	n/a	n/a
42	CEBPB	chr9:71409986-71410268	MCF-7	breast:	n/a	n/a
43	CEBPB	chr9:71433882-71434131	K562	blood:	n/a	n/a
44	CEBPB	chr9:71410046-71410340	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPD	chr9:71447958-71448286	K562	blood:	n/a	n/a
46	CEBPD	chr9:71408810-71409328	K562	blood:	n/a	n/a
47	CTCF	chr9:71448220-71448370	GM12875	blood:	n/a	n/a
48	CTCF	chr9:71417660-71417810	GM12864	blood:	n/a	n/a
49	CTCF	chr9:71413499-71413525	Fibrobl	skin:	n/a	n/a
50	CTCF	chr9:71440247-71440309	ProgFib	skin:	n/a	n/a

No data

(count:40 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:71398863..71402159-chr9:71407140..71410574,3	K562	blood:
2	chr11:62608627..62609154-chr9:71420682..71421202,3	MCF-7	breast:
3	chr3:73159932..73161523-chr9:71419682..71421202,3	K562	blood:
4	chr9:71424350..71426384-chr9:71436426..71438854,2	K562	blood:
5	chr9:71424350..71426384-chr9:71436426..71438854,2	K562	blood:
6	chr9:71438576..71440423-chr9:71455612..71458592,2	K562	blood:
7	chr11:62607625..62610617-chr9:71419682..71421202,4	K562	blood:
8	chr9:71392481..71394675-chr9:71428955..71431546,2	K562	blood:
9	chr9:71400597..71404451-chr9:71406708..71409668,4	MCF-7	breast:
10	chr1:160081967..160082488-chr9:71420682..71421202,3	HCT-116	colon:
11	chr17:41465178..41465698-chr9:71420682..71421202,2	NB4	blood:
12	chr10:103124108..103124632-chr9:71420682..71421202,2	Hela-S3	cervix:
13	chr9:71394580..71396149-chr9:71409083..71412062,2	K562	blood:
14	chr11:62608622..62609223-chr9:71420682..71421202,6	Hela-S3	cervix:
15	chr17:41464327..41464854-chr9:71420702..71421202,2	Hela-S3	cervix:
16	chr9:71408861..71411177-chr9:71411346..71415020,3	K562	blood:
17	chr3:73160073..73160620-chr9:71420702..71421682,2	NB4	blood:
18	chr3:73160048..73160628-chr9:71420682..71421702,10	HCT-116	colon:
19	chr9:71420662..71423189-chr9:71425741..71428511,3	K562	blood:
20	chr9:71394942..71397004-chr9:71406786..71409059,2	K562	blood:
21	chr11:62608645..62609222-chr9:71420682..71421202,5	MCF-7	breast:
22	chr9:71403930..71406409-chr9:71407791..71410873,3	MCF-7	breast:
23	chr13:90584707..90585217-chr9:71420682..71421182,2	HCT-116	colon:
24	chr9:71437717..71440700-chr9:71443079..71445018,2	K562	blood:
25	chr17:41463871..41465691-chr9:71419702..71421202,3	K562	blood:
26	chr3:73159867..73160571-chr9:71420682..71421682,2	Hela-S3	cervix:
27	chr11:62608617..62609218-chr9:71420682..71421202,9	HCT-116	colon:
28	chr9:71420662..71423189-chr9:71425741..71428511,3	K562	blood:
29	chr17:41464187..41466151-chr9:71419682..71421202,4	K562	blood:
30	chr3:73158387..73161479-chr9:71419682..71422682,3	K562	blood:
31	chr9:71392687..71396802-chr9:71403243..71407898,5	MCF-7	breast:
32	chr9:71437717..71440700-chr9:71443079..71445018,2	K562	blood:
33	chr9:71390215..71393175-chr9:71408433..71409952,2	K562	blood:
34	chr9:71398048..71400496-chr9:71420484..71423422,2	K562	blood:
35	chr17:41398972..41401127-chr9:71419682..71422702,5	K562	blood:
36	chr9:71408861..71411177-chr9:71411346..71415020,3	K562	blood:
37	chr9:71392572..71394227-chr9:71414871..71416644,2	K562	blood:
38	chr9:71397068..71400120-chr9:71405362..71406999,3	MCF-7	breast:
39	chr11:62608599..62609145-chr9:71420682..71421202,3	NB4	blood:
40	chr3:73160110..73160620-chr9:71420682..71421202,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRKACG-3	chr9:71439046-71439206	ENSG00000236733.1
2	lnc-PRKACG-3	chr9:71437319-71437564	ENSG00000236733.1

No data

Variant related genes	Relation type
ENSG00000236998	TF binding region
ENSG00000133316	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000236733	chromatin interactions
ENSG00000236998	chromatin interactions
ENSG00000187866	chromatin interactions

Extended variants
information (count: 1526 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1526 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191633944	chr9:71405284-71405285	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs562542376	chr9:71405334-71405335	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs111558748	chr9:71405386-71405387	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113204500	chr9:71405479-71405480	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs566839826	chr9:71405499-71405500	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs143405792	chr9:71405500-71405501	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs556737462	chr9:71405510-71405511	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs62552130	chr9:71405511-71405512	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs537540679	chr9:71405512-71405513	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs368321432	chr9:71405513-71405514	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs146501554	chr9:71405516-71405517	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs4745268	chr9:71405525-71405526	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs397954571	chr9:71405526-71405527	Weak transcription Strong transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577670447	chr9:71405649-71405650	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs546715237	chr9:71405664-71405665	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs538651194	chr9:71405687-71405688	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs148367893	chr9:71405688-71405689	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572227874	chr9:71405754-71405755	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs114008735	chr9:71405854-71405855	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs554459633	chr9:71405873-71405874	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs146348725	chr9:71405882-71405883	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs544253712	chr9:71405897-71405898	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs562653709	chr9:71405998-71405999	Weak transcription Strong transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs189770718	chr9:71406008-71406009	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs138411573	chr9:71406048-71406049	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs560568503	chr9:71406065-71406066	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs527968467	chr9:71406074-71406075	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192632369	chr9:71406075-71406076	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567705820	chr9:71406088-71406089	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184481100	chr9:71406090-71406091	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs549865693	chr9:71406113-71406114	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs571383439	chr9:71406120-71406121	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs545328610	chr9:71406136-71406137	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553789198	chr9:71406184-71406185	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs78666219	chr9:71406235-71406236	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536155312	chr9:71406256-71406257	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs565021088	chr9:71406290-71406291	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs554853180	chr9:71406477-71406478	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs189184975	chr9:71406517-71406518	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs543230022	chr9:71406529-71406530	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs142491756	chr9:71406592-71406593	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs145962152	chr9:71406635-71406636	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs139474051	chr9:71406639-71406640	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs181949288	chr9:71406641-71406642	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs527688064	chr9:71406643-71406644	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs542910132	chr9:71406646-71406647	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs185677524	chr9:71406669-71406670	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368920753	chr9:71406726-71406727	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs527715005	chr9:71406731-71406732	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs149656803	chr9:71406746-71406747	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Melanoma	22183965	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	17899364	CNVD
Mantle cell lymphoma	19029149	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	20729466	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Oral cancer	21386901	CNVD
Epilepsy	22083797	CNVD
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:600 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71396000-71408200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:71396200-71409800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr9:71397200-71409600	Weak transcription	Colonic Mucosa	Colon
4	chr9:71397200-71417400	Weak transcription	Lung	lung
5	chr9:71397800-71408000	Weak transcription	Gastric	stomach
6	chr9:71398600-71405400	Strong transcription	Primary B cells from cord blood	blood
7	chr9:71398800-71406000	Weak transcription	Spleen	Spleen
8	chr9:71398800-71408000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr9:71398800-71409800	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr9:71399000-71405600	Weak transcription	Stomach Smooth Muscle	stomach
11	chr9:71399000-71406200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr9:71399000-71408400	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr9:71399000-71408400	Weak transcription	Stomach Mucosa	stomach
14	chr9:71399000-71420200	Weak transcription	Fetal Stomach	stomach
15	chr9:71399200-71407800	Weak transcription	GM12878-XiMat	blood
16	chr9:71399600-71407200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr9:71399800-71413200	Weak transcription	Dnd41	blood
18	chr9:71400200-71405800	Weak transcription	Brain Angular Gyrus	brain
19	chr9:71400200-71406000	Weak transcription	Colon Smooth Muscle	Colon
20	chr9:71400400-71408000	Weak transcription	K562	blood
21	chr9:71400400-71408600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr9:71400600-71409200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr9:71400800-71409000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
24	chr9:71400800-71409000	Weak transcription	Adipose Nuclei	Adipose
25	chr9:71400800-71409000	Weak transcription	Small Intestine	intestine
26	chr9:71401000-71407000	Weak transcription	Brain Germinal Matrix	brain
27	chr9:71402000-71405400	Weak transcription	Aorta	Aorta
28	chr9:71402400-71405600	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr9:71402600-71405800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr9:71402600-71413400	Weak transcription	Primary hematopoietic stem cells	blood
31	chr9:71402600-71413600	Weak transcription	Primary T cells from cord blood	blood
32	chr9:71403000-71405600	Enhancers	Left Ventricle	heart
33	chr9:71403200-71406400	Weak transcription	Psoas Muscle	Psoas
34	chr9:71403200-71407200	Weak transcription	Placenta	Placenta
35	chr9:71403200-71419800	Weak transcription	Pancreas	Pancrea
36	chr9:71404200-71405400	Weak transcription	Fetal Heart	heart
37	chr9:71404200-71408400	Weak transcription	Duodenum Mucosa	Duodenum
38	chr9:71404400-71409800	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr9:71404600-71405400	Weak transcription	Right Atrium	heart
40	chr9:71404600-71408600	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr9:71404600-71408800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr9:71404600-71408800	Weak transcription	Monocytes-CD14+_RO01746	blood
43	chr9:71404600-71431400	Weak transcription	HepG2	liver
44	chr9:71404800-71408200	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr9:71404800-71408600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr9:71404800-71408800	Weak transcription	Fetal Intestine Large	intestine
47	chr9:71404800-71413200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr9:71405000-71405400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr9:71405000-71405400	Weak transcription	Right Ventricle	heart
50	chr9:71405000-71408200	Weak transcription	Primary B cells from peripheral blood	blood

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