Variant report

Variant	nsv1052872
Chromosome Location	chr9:72040184-72081554
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:183)
Chromatin interactive
region (count:9)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 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	BACH1	chr9:72044969-72045003	H1-hESC	embryonic stem cell:	n/a	n/a
2	CBX3	chr9:72046604-72047163	K562	blood:	n/a	n/a
3	CBX3	chr9:72046628-72046987	K562	blood:	n/a	n/a
4	CEBPB	chr9:72062154-72062778	HepG2	liver:	n/a	n/a
5	CEBPB	chr9:72078852-72078856	K562	blood:	n/a	n/a
6	CEBPB	chr9:72062134-72062154	IMR90	lung:	n/a	n/a
7	CEBPB	chr9:72062496-72062722	IMR90	lung:	n/a	n/a
8	CEBPB	chr9:72067054-72067658	ECC-1	luminal epithelium:	n/a	n/a
9	CEBPB	chr9:72078749-72078894	H1-hESC	embryonic stem cell:	n/a	chr9:72078782-72078793 chr9:72078780-72078793 chr9:72078782-72078793 chr9:72078768-72078781 chr9:72078777-72078794
10	CEBPB	chr9:72066922-72067693	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPD	chr9:72046554-72047083	K562	blood:	n/a	n/a
12	CEBPD	chr9:72046517-72047194	K562	blood:	n/a	n/a
13	CHD2	chr9:72078593-72078773	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr9:72058200-72058350	GM12871	blood:	n/a	n/a
15	CTCF	chr9:72043412-72043545	MCF-7	breast:	n/a	n/a
16	CTCF	chr9:72058348-72058380	Hela-S3	cervix:	n/a	chr9:72058355-72058376 chr9:72058360-72058378
17	CTCF	chr9:72040369-72040615	MCF-7	breast:	n/a	n/a
18	CTCF	chr9:72058180-72058330	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr9:72056860-72057010	NHEK	skin:	n/a	n/a
20	CTCF	chr9:72058300-72058450	GM12865	blood:	n/a	chr9:72058355-72058376 chr9:72058360-72058378
21	CTCF	chr9:72065780-72065930	HEK293	kidney:	n/a	n/a
22	CTCF	chr9:72057820-72057970	HRE	kidney:	n/a	n/a
23	CTCF	chr9:72043428-72043517	GM19238	blood:	n/a	n/a
24	CTCF	chr9:72043380-72043530	GM12875	blood:	n/a	n/a
25	CTCF	chr9:72057980-72058130	RPTEC	kidney:	n/a	chr9:72058013-72058021
26	CTCF	chr9:72056760-72056910	NHEK	skin:	n/a	n/a
27	CTCF	chr9:72056946-72057005	MCF-7	breast:	n/a	n/a
28	CTCF	chr9:72044680-72044830	GM12872	blood:	n/a	n/a
29	CTCF	chr9:72080640-72080790	HRE	kidney:	n/a	n/a
30	CTCF	chr9:72058350-72058388	MCF-7	breast:	n/a	chr9:72058355-72058376 chr9:72058360-72058378
31	CTCF	chr9:72040239-72040740	MCF-7	breast:	n/a	n/a
32	CTCF	chr9:72078880-72079030	GM12864	blood:	n/a	chr9:72078991-72079004
33	CTCF	chr9:72057920-72058070	HBMEC	blood vessel:	n/a	chr9:72058013-72058021
34	CTCF	chr9:72040380-72040530	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:72040440-72040548	LNCaP	prostate:	n/a	n/a
36	CTCF	chr9:72057960-72058110	HAc	cerebellar:	n/a	chr9:72058013-72058021
37	CTCF	chr9:72067340-72067490	HRE	kidney:	n/a	n/a
38	CTCF	chr9:72056930-72056998	MCF-7	breast:	n/a	n/a
39	CTCF	chr9:72043403-72043515	GM19239	blood:	n/a	n/a
40	CTCF	chr9:72043378-72043557	MCF-7	breast:	n/a	n/a
41	CTCF	chr9:72043426-72043504	A549	lung:	n/a	n/a
42	CTCF	chr9:72056920-72057070	HepG2	liver:	n/a	chr9:72057008-72057021
43	CTCF	chr9:72040377-72040593	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:72056948-72056970	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:72043360-72043510	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr9:72058000-72058150	HEEpiC	esophagus:	n/a	chr9:72058013-72058021
47	CTCF	chr9:72040460-72040610	MCF-7	breast:	n/a	n/a
48	CTCF	chr9:72058330-72058404	MCF-7	breast:	n/a	chr9:72058355-72058376 chr9:72058360-72058378
49	CTCF	chr9:72043423-72043514	GM12891	blood:	n/a	n/a
50	CTCF	chr9:72058326-72058420	GM12892	blood:	n/a	chr9:72058355-72058376 chr9:72058360-72058378

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:72046240-72046290	AG10803	skin:	n/a
2	chr9:72081155-72081205	MCF10A-Er-Src	breast:	n/a
3	chr9:72078829-72078879	Caco-2	colon:	n/a
4	chr9:72046240-72046290	CMK	blood:	n/a
5	chr9:72081155-72081205	H1-hESC	embryonic stem cell:	embryo
6	chr9:72081155-72081205	IMR90	lung:	fetal
7	chr9:72081155-72081205	T-47D	breast:	n/a
8	chr9:72078829-72078879	NHBE	bronchial:	n/a
9	chr9:72078829-72078879	LNCaP	prostate:	n/a
10	chr9:72081155-72081205	HUVEC	blood vessel:	n/a
11	chr9:72046240-72046290	SK-N-MC	brain:	n/a
12	chr9:72078829-72078879	Jurkat	blood:	n/a
13	chr9:72081155-72081205	HCM	heart:	n/a
14	chr9:72081155-72081205	Hepatocyte	liver:	n/a
15	chr9:72081155-72081205	AG10803	skin:	n/a
16	chr9:72046240-72046290	PrEC	prostate:	n/a
17	chr9:72081155-72081205	HRPEpiC	eye:	n/a
18	chr9:72081155-72081205	HCF	heart:	n/a
19	chr9:72046240-72046290	HAEpiC	amniotic membrane:	n/a
20	chr9:72046240-72046290	U87	brain:	n/a
21	chr9:72078829-72078879	SK-N-MC	brain:	n/a
22	chr9:72046240-72046290	HCF	heart:	n/a
23	chr9:72081155-72081205	HEEpiC	esophagus:	n/a
24	chr9:72046240-72046290	MCF10A-Er-Src	breast:	n/a
25	chr9:72078829-72078879	BE2_C	brain:	n/a
26	chr9:72081155-72081205	GM19239	blood:	n/a
27	chr9:72078829-72078879	GM12891	blood:	n/a
28	chr9:72078829-72078879	SAEC	small airway:	n/a
29	chr9:72081155-72081205	MCF-7	breast:	n/a
30	chr9:72046240-72046290	MCF-7	breast:	n/a
31	chr9:72081155-72081205	PrEC	prostate:	n/a
32	chr9:72046240-72046290	LNCaP	prostate:	n/a
33	chr9:72046240-72046290	Hepatocyte	liver:	n/a
34	chr9:72046240-72046290	GM12878	blood:	n/a
35	chr9:72081155-72081205	U87	brain:	n/a
36	chr9:72046240-72046290	A549	lung:	n/a
37	chr9:72081155-72081205	ovcar-3	ovarian:	n/a
38	chr9:72078829-72078879	GM06990	blood:	n/a
39	chr9:72046240-72046290	IMR90	lung:	fetal
40	chr9:72081155-72081205	BE2_C	brain:	n/a
41	chr9:72046240-72046290	NT2-D1	testis:	n/a
42	chr9:72046240-72046290	HRCEpiC	kidney:	n/a
43	chr9:72081155-72081205	HepG2	liver:	n/a
44	chr9:72078829-72078879	GM19239	blood:	n/a
45	chr9:72078829-72078879	IMR90	lung:	fetal
46	chr9:72046240-72046290	Jurkat	blood:	n/a
47	chr9:72078829-72078879	AG04450	lung:	fetal
48	chr9:72081155-72081205	GM06990	blood:	n/a
49	chr9:72046240-72046290	GM12891	blood:	n/a
50	chr9:72081155-72081205	NHBE	bronchial:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:72068242..72070671-chr9:72077608..72079150,2	MCF-7	breast:
2	chr9:72044312..72045985-chr9:72046714..72048470,2	MCF-7	breast:
3	chr9:72036807..72037778-chr9:72056686..72057333,2	MCF-7	breast:
4	chr9:72038579..72040872-chr9:72161729..72164338,3	MCF-7	breast:
5	chr9:72059861..72061593-chr9:72066565..72068301,2	MCF-7	breast:
6	chr9:72039845..72040903-chr9:72160889..72161458,4	MCF-7	breast:
7	chr9:72059861..72061593-chr9:72066565..72068301,2	MCF-7	breast:
8	chr9:72068242..72070671-chr9:72077608..72079150,2	MCF-7	breast:
9	chr9:72044312..72045985-chr9:72046714..72048470,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-APBA1-1	chr9:72043544-72043637	ENSG00000243888
2	lnc-APBA1-1	chr9:72043164-72043467	ENSG00000243888
3	lnc-APBA1-1	chr9:72042449-72044751	NONHSAT131778

No data

Variant related genes	Relation type
ENSG00000243888	TF binding region
ENSG00000243888	CpG island

Extended variants
information (count: 1730 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:1730 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550641143	chr9:72040194-72040195	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
2	rs184204510	chr9:72040195-72040196	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs368886302	chr9:72040214-72040215	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs554786188	chr9:72040295-72040296	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs372155513	chr9:72040313-72040314	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs57405094	chr9:72040332-72040333	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs112254755	chr9:72040350-72040351	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs560274475	chr9:72040394-72040395	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs58538285	chr9:72040395-72040396	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs11138585	chr9:72040435-72040436	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs189375112	chr9:72040438-72040439	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs576779689	chr9:72040498-72040499	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs181014778	chr9:72040507-72040508	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs541370640	chr9:72040532-72040533	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs559963511	chr9:72040541-72040542	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs530254426	chr9:72040543-72040544	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs542390086	chr9:72040546-72040547	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs570742996	chr9:72040562-72040563	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs543556164	chr9:72040563-72040564	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs530616149	chr9:72040574-72040575	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs552252357	chr9:72040575-72040576	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs570463011	chr9:72040607-72040608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs528048817	chr9:72040629-72040630	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2309480	chr9:72040633-72040634	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568315059	chr9:72040647-72040648	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs186427611	chr9:72040650-72040651	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535317800	chr9:72040658-72040659	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs532942262	chr9:72040694-72040695	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs557102632	chr9:72040734-72040735	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs368308529	chr9:72040735-72040736	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs189476637	chr9:72040791-72040792	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537145101	chr9:72040852-72040853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs547038654	chr9:72040899-72040900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558586527	chr9:72040908-72040909	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs80297719	chr9:72040932-72040933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541388829	chr9:72040969-72040970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs553418791	chr9:72041013-72041014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs575063989	chr9:72041035-72041036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs542100086	chr9:72041039-72041040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181468598	chr9:72041084-72041085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs563872158	chr9:72041112-72041113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531083151	chr9:72041113-72041114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs79197111	chr9:72041133-72041134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566832337	chr9:72041164-72041165	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371796391	chr9:72041195-72041196	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142203297	chr9:72041199-72041200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs187020351	chr9:72041236-72041237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs546553211	chr9:72041256-72041257	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs191059862	chr9:72041283-72041284	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529177889	chr9:72041389-72041390	Weak transcription Enhancers	n/a	n/a	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
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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:72036200-72043000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr9:72036600-72082600	Weak transcription	Rectal Smooth Muscle	rectum
3	chr9:72036800-72045200	Weak transcription	Fetal Brain Female	brain
4	chr9:72037200-72040200	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr9:72037200-72046600	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr9:72037200-72048600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr9:72037200-72055600	Weak transcription	Fetal Lung	lung
8	chr9:72037200-72056200	Weak transcription	Fetal Muscle Leg	muscle
9	chr9:72037400-72045200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr9:72037600-72044800	Weak transcription	Fetal Stomach	stomach
11	chr9:72037600-72046600	Weak transcription	Fetal Kidney	kidney
12	chr9:72039600-72040200	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr9:72039600-72040400	Enhancers	Brain Substantia Nigra	brain
14	chr9:72039600-72043200	Enhancers	Brain Hippocampus Middle	brain
15	chr9:72039800-72040200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr9:72039800-72040200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:72039800-72041600	Weak transcription	Liver	Liver
18	chr9:72039800-72043000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr9:72039800-72043400	Enhancers	Brain Angular Gyrus	brain
20	chr9:72039800-72043400	Enhancers	Brain Cingulate Gyrus	brain
21	chr9:72040000-72040200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr9:72040000-72040200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr9:72040000-72040200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr9:72040000-72040400	Enhancers	Brain Anterior Caudate	brain
25	chr9:72040000-72042000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr9:72040200-72040400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr9:72040200-72040600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr9:72040200-72040600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
29	chr9:72040200-72040800	Enhancers	Skeletal Muscle Male	skeletal muscle
30	chr9:72040400-72041400	Weak transcription	Brain Anterior Caudate	brain
31	chr9:72040400-72041400	Weak transcription	Brain Substantia Nigra	brain
32	chr9:72040400-72045200	Weak transcription	Brain Germinal Matrix	brain
33	chr9:72040400-72046600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr9:72040600-72043600	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr9:72040600-72045000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr9:72040800-72041000	Weak transcription	Gastric	stomach
37	chr9:72040800-72042200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr9:72040800-72046800	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr9:72040800-72057400	Weak transcription	Fetal Heart	heart
40	chr9:72041000-72041200	Enhancers	Gastric	stomach
41	chr9:72041000-72043400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr9:72041000-72045400	Weak transcription	Ovary	ovary
43	chr9:72041200-72069600	Weak transcription	Gastric	stomach
44	chr9:72041400-72042400	Enhancers	Brain Anterior Caudate	brain
45	chr9:72041400-72043200	Enhancers	Brain Substantia Nigra	brain
46	chr9:72041600-72049400	Strong transcription	Liver	Liver
47	chr9:72041800-72045600	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr9:72041800-72046600	Weak transcription	Adipose Nuclei	Adipose
49	chr9:72042000-72045400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr9:72042000-72070400	Weak transcription	Spleen	Spleen

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