Variant report

Variant	nsv893481
Chromosome Location	chr9:79304043-79348193
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:526)
CpG islands
(count:244)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:526 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:79344928-79345129	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:79303783-79304126	HepG2	liver:	n/a	n/a
3	ATF2	chr9:79322288-79322922	GM12878	blood:	n/a	n/a
4	ATF2	chr9:79322453-79322794	GM12878	blood:	n/a	n/a
5	ATF3	chr9:79333094-79333353	K562	blood:	n/a	n/a
6	ATF3	chr9:79333086-79333341	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:79323931-79324316	GM12878	blood:	n/a	n/a
8	BATF	chr9:79322377-79322785	GM12878	blood:	n/a	chr9:79322530-79322541
9	BCL11A	chr9:79322459-79322843	GM12878	blood:	n/a	n/a
10	BHLHE40	chr9:79307626-79307916	K562	blood:	n/a	n/a
11	BHLHE40	chr9:79332728-79332903	K562	blood:	n/a	n/a
12	BRCA1	chr9:79319550-79319818	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr9:79303787-79304073	Hela-S3	cervix:	n/a	chr9:79303968-79303979
14	CEBPB	chr9:79323791-79324054	K562	blood:	n/a	chr9:79323929-79323940
15	CEBPB	chr9:79303773-79304164	HepG2	liver:	n/a	chr9:79303968-79303979
16	CEBPB	chr9:79303459-79304123	HepG2	liver:	n/a	chr9:79303968-79303979
17	CEBPB	chr9:79344871-79345127	HepG2	liver:	n/a	n/a
18	CEBPB	chr9:79333074-79333449	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr9:79315069-79315303	IMR90	lung:	n/a	n/a
20	CEBPB	chr9:79333098-79333349	K562	blood:	n/a	n/a
21	CEBPB	chr9:79333091-79333418	K562	blood:	n/a	n/a
22	CEBPB	chr9:79307718-79307984	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr9:79333132-79333374	A549	lung:	n/a	n/a
24	CEBPB	chr9:79303801-79304071	HepG2	liver:	n/a	chr9:79303968-79303979
25	CEBPB	chr9:79302822-79304106	IMR90	lung:	n/a	chr9:79303968-79303979
26	CEBPB	chr9:79344910-79345144	A549	lung:	n/a	n/a
27	CEBPB	chr9:79303488-79304100	A549	lung:	n/a	chr9:79303968-79303979
28	CEBPB	chr9:79323812-79323968	HepG2	liver:	n/a	chr9:79323929-79323940
29	CEBPB	chr9:79303455-79304150	HepG2	liver:	n/a	chr9:79303968-79303979
30	CEBPD	chr9:79303806-79304084	HepG2	liver:	n/a	n/a
31	CREB1	chr9:79322355-79322925	GM12878	blood:	n/a	n/a
32	CREB1	chr9:79322427-79322941	GM12878	blood:	n/a	n/a
33	CTCF	chr9:79319620-79319770	HUVEC	blood vessel:	n/a	n/a
34	CTCF	chr9:79319540-79319690	HAc	cerebellar:	n/a	n/a
35	CTCF	chr9:79319620-79319770	HMEC	breast:	n/a	n/a
36	CTCF	chr9:79319960-79320110	WI-38	lung:	n/a	n/a
37	CTCF	chr9:79319760-79319910	WI-38	lung:	n/a	n/a
38	CTCF	chr9:79319563-79319832	Medullo	brain:	n/a	n/a
39	CTCF	chr9:79319620-79319770	HEK293	kidney:	n/a	n/a
40	CTCF	chr9:79314780-79314930	AG04450	lung:	n/a	chr9:79314883-79314892
41	CTCF	chr9:79319601-79319792	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr9:79333200-79333350	GM12875	blood:	n/a	n/a
43	CTCF	chr9:79320020-79320170	GM12868	blood:	n/a	n/a
44	CTCF	chr9:79314920-79315070	AG10803	skin:	n/a	chr9:79315033-79315049
45	CTCF	chr9:79319580-79319730	GM12872	blood:	n/a	n/a
46	CTCF	chr9:79311667-79311759	GM19239	blood:	n/a	n/a
47	CTCF	chr9:79333200-79333350	HRE	kidney:	n/a	n/a
48	CTCF	chr9:79319680-79319830	GM12865	blood:	n/a	n/a
49	CTCF	chr9:79319580-79319730	RPTEC	kidney:	n/a	n/a
50	CTCF	chr9:79319640-79319790	HCPEpiC	choroid plexus:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:79328522-79328572	SKMC	muscle:	n/a
2	chr9:79320026-79320076	HCM	heart:	n/a
3	chr9:79328644-79328694	HCT-116	colon:	n/a
4	chr9:79306054-79306104	HRE	kidney:	n/a
5	chr9:79306054-79306104	MCF10A-Er-Src	breast:	n/a
6	chr9:79320026-79320076	Jurkat	blood:	n/a
7	chr9:79306054-79306104	SK-N-SH_RA	brain:	n/a
8	chr9:79306054-79306104	GM06990	blood:	n/a
9	chr9:79328644-79328694	SK-N-SH	brain:	n/a
10	chr9:79320026-79320076	H1-hESC	embryonic stem cell:	embryo
11	chr9:79306054-79306104	HCM	heart:	n/a
12	chr9:79306054-79306104	Caco-2	colon:	n/a
13	chr9:79328522-79328572	HCM	heart:	n/a
14	chr9:79328644-79328694	PFSK-1	brain:	n/a
15	chr9:79306054-79306104	HIPEpiC	eye:	n/a
16	chr9:79320026-79320076	HCPEpiC	choroid plexus:	n/a
17	chr9:79328522-79328572	CMK	blood:	n/a
18	chr9:79328644-79328694	GM12878	blood:	n/a
19	chr9:79328522-79328572	BE2_C	brain:	n/a
20	chr9:79320026-79320076	BE2_C	brain:	n/a
21	chr9:79328644-79328694	BJ	skin:	n/a
22	chr9:79328522-79328572	K562	blood:	n/a
23	chr9:79328644-79328694	AG04449	skin:	fetal
24	chr9:79328522-79328572	HAEpiC	amniotic membrane:	n/a
25	chr9:79320026-79320076	PrEC	prostate:	n/a
26	chr9:79328522-79328572	AG09319	gingival:	n/a
27	chr9:79328522-79328572	GM12891	blood:	n/a
28	chr9:79320026-79320076	AG09319	gingival:	n/a
29	chr9:79320026-79320076	T-47D	breast:	n/a
30	chr9:79328644-79328694	A549	lung:	n/a
31	chr9:79320026-79320076	HCF	heart:	n/a
32	chr9:79320026-79320076	ECC-1	luminal epithelium:	n/a
33	chr9:79320026-79320076	GM12891	blood:	n/a
34	chr9:79306054-79306104	HCPEpiC	choroid plexus:	n/a
35	chr9:79320026-79320076	RPTEC	kidney:	n/a
36	chr9:79320026-79320076	HL-60	blood:	n/a
37	chr9:79328522-79328572	Jurkat	blood:	n/a
38	chr9:79306054-79306104	AG10803	skin:	n/a
39	chr9:79328522-79328572	NHBE	bronchial:	n/a
40	chr9:79320026-79320076	HCT-116	colon:	n/a
41	chr9:79306054-79306104	SK-N-MC	brain:	n/a
42	chr9:79306054-79306104	NHDF-neo	bronchial:	n/a
43	chr9:79328522-79328572	PANC-1	pancreas:	n/a
44	chr9:79328644-79328694	SAEC	small airway:	n/a
45	chr9:79320026-79320076	HRE	kidney:	n/a
46	chr9:79328522-79328572	HUVEC	blood vessel:	n/a
47	chr9:79328522-79328572	MCF-7	breast:	n/a
48	chr9:79306054-79306104	HEK293	kidney:	embryo
49	chr9:79306054-79306104	HPAEpiC	pulmonary alveolar:	n/a
50	chr9:79320026-79320076	AoSMC	blood vessel:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:128943460..128943995-chr9:79320014..79320514,2	MCF-7	breast:
2	chr9:79281569..79282479-chr9:79319831..79320484,2	MCF-7	breast:
3	chr9:79074075..79075836-chr9:79309039..79310925,2	MCF-7	breast:
4	chr9:79300396..79301994-chr9:79302706..79305324,2	K562	blood:
5	chr9:79280331..79281278-chr9:79319093..79320181,5	MCF-7	breast:
6	chr9:79306577..79308697-chr9:79313991..79316581,2	MCF-7	breast:
7	chr9:79307128..79309630-chr9:79312231..79313981,2	MCF-7	breast:
8	chr9:79213561..79216371-chr9:79320656..79323527,2	MCF-7	breast:
9	chr9:79017921..79018920-chr9:79318594..79320251,5	K562	blood:
10	chr9:79347384..79348921-chr9:79351965..79353979,2	MCF-7	breast:
11	chr9:77880081..77881018-chr9:79319218..79320052,2	K562	blood:
12	chr9:79277119..79278141-chr9:79318359..79319673,4	MCF-7	breast:
13	chr9:79280437..79281078-chr9:79317445..79318438,2	MCF-7	breast:
14	chr9:79323952..79326747-chr9:79342430..79344889,2	MCF-7	breast:
15	chr9:79073827..79075700-chr9:79322081..79324440,2	MCF-7	breast:
16	chr9:79321119..79322904-chr9:79325137..79328012,2	MCF-7	breast:
17	chr9:79305411..79307396-chr9:79308812..79311308,2	MCF-7	breast:
18	chr9:79062552..79063515-chr9:79319220..79320201,4	K562	blood:
19	chr9:79296367..79298472-chr9:79320957..79323696,2	MCF-7	breast:
20	chr9:79280496..79281467-chr9:79318110..79319001,3	MCF-7	breast:
21	chr9:79307128..79309630-chr9:79312231..79313981,2	MCF-7	breast:
22	chr9:79280654..79281415-chr9:79319254..79320174,3	K562	blood:
23	chr9:79077933..79079433-chr9:79321608..79323340,2	K562	blood:

No data

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

Extended variants
information (count: 1987 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:1987 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs520365	chr9:79304043-79304044	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs537890438	chr9:79304052-79304053	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs569713245	chr9:79304072-79304073	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs111329572	chr9:79304086-79304087	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs564288533	chr9:79304099-79304100	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs577977432	chr9:79304129-79304130	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs7869922	chr9:79304173-79304174	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs554740966	chr9:79304204-79304205	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs7869945	chr9:79304218-79304219	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs7851781	chr9:79304261-79304262	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs375795649	chr9:79304292-79304293	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs528921002	chr9:79304321-79304322	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs370226087	chr9:79304324-79304325	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs207470278	chr9:79304327-79304328	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs7851884	chr9:79304332-79304333	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs7870110	chr9:79304348-79304349	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs549057595	chr9:79304400-79304401	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs562469844	chr9:79304429-79304430	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571833013	chr9:79304454-79304455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs115221940	chr9:79304489-79304490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34637475	chr9:79304518-79304519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs550730626	chr9:79304549-79304550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373449719	chr9:79304561-79304562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs570736218	chr9:79304565-79304566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs116742566	chr9:79304572-79304573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs77404410	chr9:79304580-79304581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs555439072	chr9:79304617-79304618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs534517991	chr9:79304623-79304624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs566849431	chr9:79304662-79304663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs535527526	chr9:79304724-79304725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555808744	chr9:79304750-79304751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs77439825	chr9:79304812-79304813	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75359145	chr9:79304813-79304814	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs11145008	chr9:79304835-79304836	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs140066640	chr9:79304932-79304933	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs557936905	chr9:79304947-79304948	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs114425220	chr9:79304951-79304952	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs540523261	chr9:79305011-79305012	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs116492555	chr9:79305038-79305039	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs576871785	chr9:79305107-79305108	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs145247198	chr9:79305225-79305226	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs117846579	chr9:79305257-79305258	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs143627392	chr9:79305265-79305266	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs549611818	chr9:79305299-79305300	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs677061	chr9:79305305-79305306	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs7027319	chr9:79305336-79305337	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs111567416	chr9:79305364-79305365	Weak transcription Enhancers Bivalent Enhancer Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs376981539	chr9:79305405-79305406	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs12684415	chr9:79305410-79305411	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs677913	chr9:79305452-79305453	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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:785 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:79266400-79306800	Weak transcription	Fetal Stomach	stomach
2	chr9:79290400-79306000	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr9:79296800-79304800	Weak transcription	Fetal Thymus	thymus
4	chr9:79300400-79332200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr9:79300800-79304200	Enhancers	NHDF-Ad	bronchial
6	chr9:79301600-79305000	Enhancers	Stomach Mucosa	stomach
7	chr9:79302000-79304200	Enhancers	HMEC	breast
8	chr9:79302000-79304200	Enhancers	HSMM	muscle
9	chr9:79302200-79304200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr9:79302200-79304200	Enhancers	HUVEC	blood vessel
11	chr9:79302400-79304200	Enhancers	HSMMtube	muscle
12	chr9:79302600-79304200	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr9:79302600-79304400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr9:79302600-79305600	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr9:79302600-79306600	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr9:79302600-79306800	Enhancers	Fetal Intestine Large	intestine
17	chr9:79302600-79306800	Enhancers	Fetal Intestine Small	intestine
18	chr9:79302800-79306600	Weak transcription	Adipose Nuclei	Adipose
19	chr9:79303000-79304200	Enhancers	Brain Angular Gyrus	brain
20	chr9:79303000-79304200	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr9:79303000-79305800	Weak transcription	Brain Germinal Matrix	brain
22	chr9:79303000-79306600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr9:79303200-79306000	Weak transcription	Brain Cingulate Gyrus	brain
24	chr9:79303200-79306000	Weak transcription	Rectal Smooth Muscle	rectum
25	chr9:79303200-79306200	Enhancers	HepG2	liver
26	chr9:79303400-79304200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr9:79303400-79304200	Enhancers	Brain Substantia Nigra	brain
28	chr9:79303400-79304200	Enhancers	Stomach Smooth Muscle	stomach
29	chr9:79303400-79305200	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr9:79303400-79306800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr9:79303600-79304600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr9:79303600-79304600	Weak transcription	Aorta	Aorta
33	chr9:79303600-79305600	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr9:79303600-79306000	Weak transcription	Brain Hippocampus Middle	brain
35	chr9:79303600-79306000	Weak transcription	Gastric	stomach
36	chr9:79303800-79304200	Enhancers	Osteobl	bone
37	chr9:79303800-79304400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr9:79303800-79304400	Enhancers	Muscle Satellite Cultured Cells	--
39	chr9:79303800-79304800	Weak transcription	Duodenum Mucosa	Duodenum
40	chr9:79303800-79305000	Weak transcription	Brain Anterior Caudate	brain
41	chr9:79303800-79305200	Weak transcription	Colon Smooth Muscle	Colon
42	chr9:79303800-79305200	Weak transcription	Rectal Mucosa Donor 29	rectum
43	chr9:79303800-79305400	Weak transcription	Small Intestine	intestine
44	chr9:79303800-79305800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr9:79303800-79306800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:79304000-79304400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr9:79304000-79306400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr9:79304000-79306800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr9:79304200-79305000	Weak transcription	Brain Angular Gyrus	brain
50	chr9:79304200-79305000	Weak transcription	HSMM	muscle

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