Variant report

Variant	esv2754389
Chromosome Location	chr9:79318677-79333056
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:281)
CpG islands
(count:184)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:281 , 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	ATF2	chr9:79322288-79322922	GM12878	blood:	n/a	n/a
2	ATF2	chr9:79322453-79322794	GM12878	blood:	n/a	n/a
3	BATF	chr9:79323931-79324316	GM12878	blood:	n/a	n/a
4	BATF	chr9:79322377-79322785	GM12878	blood:	n/a	chr9:79322530-79322541
5	BCL11A	chr9:79322459-79322843	GM12878	blood:	n/a	n/a
6	BHLHE40	chr9:79332728-79332903	K562	blood:	n/a	n/a
7	BRCA1	chr9:79319550-79319818	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr9:79323812-79323968	HepG2	liver:	n/a	chr9:79323929-79323940
9	CEBPB	chr9:79323791-79324054	K562	blood:	n/a	chr9:79323929-79323940
10	CREB1	chr9:79322427-79322941	GM12878	blood:	n/a	n/a
11	CREB1	chr9:79322355-79322925	GM12878	blood:	n/a	n/a
12	CTCF	chr9:79319620-79319770	BE2_C	brain:	n/a	n/a
13	CTCF	chr9:79319640-79319790	BE2_C	brain:	n/a	n/a
14	CTCF	chr9:79319580-79319730	GM12872	blood:	n/a	n/a
15	CTCF	chr9:79319680-79319830	GM12866	blood:	n/a	n/a
16	CTCF	chr9:79319780-79319930	HFF-Myc	foreskin:	n/a	n/a
17	CTCF	chr9:79319967-79320064	GM19240	blood:	n/a	n/a
18	CTCF	chr9:79319660-79319810	GM12866	blood:	n/a	n/a
19	CTCF	chr9:79319496-79319890	ECC-1	luminal epithelium:	n/a	n/a
20	CTCF	chr9:79319620-79319770	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr9:79319600-79319750	HepG2	liver:	n/a	n/a
22	CTCF	chr9:79319960-79320110	GM12865	blood:	n/a	n/a
23	CTCF	chr9:79319434-79319916	IMR90	lung:	n/a	n/a
24	CTCF	chr9:79319620-79319770	NHEK	skin:	n/a	n/a
25	CTCF	chr9:79319620-79319770	HCT-116	colon:	n/a	n/a
26	CTCF	chr9:79319640-79319790	AG09309	skin:	n/a	n/a
27	CTCF	chr9:79319600-79319750	GM12878	blood:	n/a	n/a
28	CTCF	chr9:79319448-79319897	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr9:79319600-79319750	GM12875	blood:	n/a	n/a
30	CTCF	chr9:79319640-79319790	HUVEC	blood vessel:	n/a	n/a
31	CTCF	chr9:79319407-79320050	HCT-116	colon:	n/a	n/a
32	CTCF	chr9:79319620-79319770	HRPEpiC	eye:	n/a	n/a
33	CTCF	chr9:79319660-79319810	GM12865	blood:	n/a	n/a
34	CTCF	chr9:79319629-79319798	LNCaP	prostate:	n/a	n/a
35	CTCF	chr9:79319620-79319770	NB4	blood:	n/a	n/a
36	CTCF	chr9:79319631-79319806	NHEK	skin:	n/a	n/a
37	CTCF	chr9:79319640-79319790	HMF	breast:	n/a	n/a
38	CTCF	chr9:79319840-79319990	GM12869	blood:	n/a	n/a
39	CTCF	chr9:79319620-79319770	AG09319	gingival:	n/a	n/a
40	CTCF	chr9:79319660-79319810	SAEC	small airway:	n/a	n/a
41	CTCF	chr9:79319639-79319801	GM13976	blood:	n/a	n/a
42	CTCF	chr9:79319652-79319782	GM19239	blood:	n/a	n/a
43	CTCF	chr9:79319600-79319750	HL-60	blood:	n/a	n/a
44	CTCF	chr9:79319640-79319790	HCM	heart:	n/a	n/a
45	CTCF	chr9:79319640-79319790	GM06990	blood:	n/a	n/a
46	CTCF	chr9:79319601-79319792	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr9:79319563-79319832	Medullo	brain:	n/a	n/a
48	CTCF	chr9:79319580-79319730	BJ	skin:	n/a	n/a
49	CTCF	chr9:79319620-79319770	HAc	cerebellar:	n/a	n/a
50	CTCF	chr9:79319620-79319770	GM12869	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:79320026-79320076	GM19239	blood:	n/a
2	chr9:79320026-79320076	GM19239	blood:	n/a
3	chr9:79320026-79320076	AG09319	gingival:	n/a
4	chr9:79328644-79328694	GM06990	blood:	n/a
5	chr9:79328522-79328572	U87	brain:	n/a
6	chr9:79320026-79320076	HRPEpiC	eye:	n/a
7	chr9:79328644-79328694	HPAEpiC	pulmonary alveolar:	n/a
8	chr9:79320026-79320076	HCT-116	colon:	n/a
9	chr9:79328522-79328572	GM12891	blood:	n/a
10	chr9:79328522-79328572	HMEC	breast:	n/a
11	chr9:79328644-79328694	HUVEC	blood vessel:	n/a
12	chr9:79328644-79328694	ProgFib	skin:	n/a
13	chr9:79328522-79328572	BJ	skin:	n/a
14	chr9:79328522-79328572	ProgFib	skin:	n/a
15	chr9:79328644-79328694	HCPEpiC	choroid plexus:	n/a
16	chr9:79328522-79328572	NHBE	bronchial:	n/a
17	chr9:79328644-79328694	Hela-S3	cervix:	n/a
18	chr9:79328522-79328572	HRE	kidney:	n/a
19	chr9:79328522-79328572	A549	lung:	n/a
20	chr9:79328522-79328572	HRCEpiC	kidney:	n/a
21	chr9:79328644-79328694	HRE	kidney:	n/a
22	chr9:79328522-79328572	GM12892	blood:	n/a
23	chr9:79328644-79328694	IMR90	lung:	fetal
24	chr9:79328644-79328694	AG09319	gingival:	n/a
25	chr9:79328522-79328572	AG09309	skin:	n/a
26	chr9:79328644-79328694	GM12878	blood:	n/a
27	chr9:79328522-79328572	IMR90	lung:	fetal
28	chr9:79320026-79320076	SAEC	small airway:	n/a
29	chr9:79328522-79328572	BE2_C	brain:	n/a
30	chr9:79328644-79328694	HEEpiC	esophagus:	n/a
31	chr9:79328522-79328572	SK-N-SH_RA	brain:	n/a
32	chr9:79328522-79328572	K562	blood:	n/a
33	chr9:79328522-79328572	NT2-D1	testis:	n/a
34	chr9:79328522-79328572	PFSK-1	brain:	n/a
35	chr9:79320026-79320076	PFSK-1	brain:	n/a
36	chr9:79320026-79320076	NH-A	brain:	n/a
37	chr9:79320026-79320076	HMEC	breast:	n/a
38	chr9:79328644-79328694	LNCaP	prostate:	n/a
39	chr9:79328522-79328572	Jurkat	blood:	n/a
40	chr9:79328644-79328694	H1-hESC	embryonic stem cell:	embryo
41	chr9:79328644-79328694	ovcar-3	ovarian:	n/a
42	chr9:79328644-79328694	PrEC	prostate:	n/a
43	chr9:79328644-79328694	NB4	blood:	n/a
44	chr9:79320026-79320076	Hepatocyte	liver:	n/a
45	chr9:79328522-79328572	HCM	heart:	n/a
46	chr9:79320026-79320076	ECC-1	luminal epithelium:	n/a
47	chr9:79328644-79328694	GM19239	blood:	n/a
48	chr9:79328522-79328572	PrEC	prostate:	n/a
49	chr9:79320026-79320076	NT2-D1	testis:	n/a
50	chr9:79320026-79320076	Jurkat	blood:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:128943460..128943995-chr9:79320014..79320514,2	MCF-7	breast:
2	chr9:79277119..79278141-chr9:79318359..79319673,4	MCF-7	breast:
3	chr9:79017921..79018920-chr9:79318594..79320251,5	K562	blood:
4	chr9:79062552..79063515-chr9:79319220..79320201,4	K562	blood:
5	chr9:79280654..79281415-chr9:79319254..79320174,3	K562	blood:
6	chr9:79077933..79079433-chr9:79321608..79323340,2	K562	blood:
7	chr9:79213561..79216371-chr9:79320656..79323527,2	MCF-7	breast:
8	chr9:79281569..79282479-chr9:79319831..79320484,2	MCF-7	breast:
9	chr9:79280331..79281278-chr9:79319093..79320181,5	MCF-7	breast:
10	chr9:77880081..77881018-chr9:79319218..79320052,2	K562	blood:
11	chr9:79296367..79298472-chr9:79320957..79323696,2	MCF-7	breast:
12	chr9:79321119..79322904-chr9:79325137..79328012,2	MCF-7	breast:
13	chr9:79073827..79075700-chr9:79322081..79324440,2	MCF-7	breast:
14	chr9:79280496..79281467-chr9:79318110..79319001,3	MCF-7	breast:

No data

Variant related genes	Relation type
PRUNE2	TF binding region
PRUNE2	CpG island
ENSG00000106772	chromatin interactions
ENSG00000265488	chromatin interactions
ENSG00000187210	chromatin interactions

Extended variants
information (count: 773 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:773 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561970	chr9:79318677-79318678	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs151140026	chr9:79318695-79318696	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371803635	chr9:79318702-79318703	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs375292576	chr9:79318725-79318726	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs368767936	chr9:79318738-79318739	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs371921844	chr9:79318755-79318756	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551462975	chr9:79318771-79318772	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs374790626	chr9:79318776-79318777	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs114286793	chr9:79318795-79318796	Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs56261747	chr9:79318812-79318813	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs140137838	chr9:79318820-79318821	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs41288767	chr9:79318824-79318825	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs562742243	chr9:79318855-79318856	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs147789214	chr9:79318858-79318859	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs149845863	chr9:79318865-79318866	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs7868609	chr9:79318866-79318867	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs183450874	chr9:79318872-79318873	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs373284279	chr9:79318874-79318875	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs377719959	chr9:79318887-79318888	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs371356883	chr9:79318897-79318898	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs374100873	chr9:79318898-79318899	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs376665436	chr9:79318901-79318902	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs371268210	chr9:79318909-79318910	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs620985	chr9:79318921-79318922	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs368031833	chr9:79318922-79318923	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs201127294	chr9:79318926-79318927	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs73650279	chr9:79318971-79318972	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs187947807	chr9:79318982-79318983	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs190606277	chr9:79318983-79318984	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs11145014	chr9:79318995-79318996	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs620552	chr9:79318998-79318999	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs145883751	chr9:79319006-79319007	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571795113	chr9:79319044-79319045	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs620476	chr9:79319050-79319051	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs554426254	chr9:79319060-79319061	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs144378754	chr9:79319129-79319130	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs59728338	chr9:79319131-79319132	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs74447479	chr9:79319134-79319135	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76071203	chr9:79319135-79319136	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs67865932	chr9:79319143-79319144	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs566455	chr9:79319146-79319147	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs565112728	chr9:79319154-79319155	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs141714232	chr9:79319172-79319173	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs566584	chr9:79319195-79319196	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs182779936	chr9:79319297-79319298	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs187818507	chr9:79319298-79319299	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565271642	chr9:79319308-79319309	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs192335397	chr9:79319328-79319329	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540799587	chr9:79319386-79319387	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs138356928	chr9:79319389-79319390	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
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
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
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
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intellectual disability	22102821	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	22522925	CNVD
Neurodevelopmental disorder	22521361	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:79300400-79332200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr9:79314200-79320000	Enhancers	Fetal Brain Male	brain
3	chr9:79314400-79318800	Enhancers	Fetal Muscle Leg	muscle
4	chr9:79314800-79318800	Enhancers	Fetal Stomach	stomach
5	chr9:79315200-79319400	Weak transcription	Stomach Mucosa	stomach
6	chr9:79315200-79319600	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr9:79315200-79327600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr9:79315400-79319400	Weak transcription	Fetal Kidney	kidney
9	chr9:79316200-79330800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr9:79316400-79319800	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr9:79316400-79332000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr9:79316600-79319000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:79316600-79319400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr9:79316600-79324600	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr9:79316800-79319400	Weak transcription	Brain Angular Gyrus	brain
16	chr9:79316800-79319800	Weak transcription	Brain Anterior Caudate	brain
17	chr9:79316800-79322800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr9:79316800-79325400	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr9:79316800-79331000	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr9:79316800-79331200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr9:79317200-79319600	Weak transcription	Brain Hippocampus Middle	brain
22	chr9:79317400-79319800	Enhancers	Primary neutrophils fromperipheralblood	blood
23	chr9:79317400-79327800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr9:79317400-79328600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr9:79317600-79318800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:79317600-79319200	Strong transcription	Stomach Smooth Muscle	stomach
27	chr9:79317600-79319400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr9:79317600-79319400	Weak transcription	NHDF-Ad	bronchial
29	chr9:79317600-79320000	Weak transcription	Aorta	Aorta
30	chr9:79317600-79330800	Strong transcription	HSMM	muscle
31	chr9:79317800-79318800	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr9:79317800-79328600	Strong transcription	HSMMtube	muscle
33	chr9:79318000-79318800	Active TSS	Fetal Lung	lung
34	chr9:79318000-79330400	Weak transcription	Rectal Smooth Muscle	rectum
35	chr9:79318200-79319000	Strong transcription	Brain Substantia Nigra	brain
36	chr9:79318200-79319400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr9:79318200-79319400	Weak transcription	Colon Smooth Muscle	Colon
38	chr9:79318400-79318800	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
39	chr9:79318400-79318800	Enhancers	Fetal Thymus	thymus
40	chr9:79318400-79319800	Enhancers	HUVEC	blood vessel
41	chr9:79318400-79330000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr9:79318800-79319800	Weak transcription	Fetal Muscle Leg	muscle
43	chr9:79318800-79319800	Weak transcription	Fetal Stomach	stomach
44	chr9:79318800-79319800	Weak transcription	Fetal Thymus	thymus
45	chr9:79318800-79320000	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr9:79318800-79323200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr9:79319000-79319800	Weak transcription	Brain Substantia Nigra	brain
48	chr9:79319200-79319800	Weak transcription	Stomach Smooth Muscle	stomach
49	chr9:79319400-79319600	Enhancers	Stomach Mucosa	stomach
50	chr9:79319400-79319600	Enhancers	NHDF-Ad	bronchial

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