Variant report

Variant	nsv482531
Chromosome Location	chr9:92907692-93096360
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1165)
CpG islands
(count:184)
Chromatin interactive
region (count:35)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1165 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:92931825-92932207	HepG2	liver:	n/a	n/a
2	ATF2	chr9:93049726-93050109	GM12878	blood:	n/a	n/a
3	ATF2	chr9:92951642-92951847	GM12878	blood:	n/a	n/a
4	BACH1	chr9:93088544-93088830	K562	blood:	n/a	n/a
5	BACH1	chr9:93088508-93088797	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr9:92989234-92989338	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr9:92965282-92965468	GM12878	blood:	n/a	n/a
8	BATF	chr9:93038458-93038777	GM12878	blood:	n/a	n/a
9	BATF	chr9:92999499-92999649	GM12878	blood:	n/a	n/a
10	BATF	chr9:92989140-92989405	GM12878	blood:	n/a	n/a
11	BATF	chr9:92989064-92989394	GM12878	blood:	n/a	n/a
12	BATF	chr9:93049762-93050054	GM12878	blood:	n/a	n/a
13	BATF	chr9:93049789-93050096	GM12878	blood:	n/a	n/a
14	BATF	chr9:93038508-93038817	GM12878	blood:	n/a	n/a
15	BCL11A	chr9:92951650-92951969	GM12878	blood:	n/a	n/a
16	BCL11A	chr9:92951613-92951890	GM12878	blood:	n/a	n/a
17	BCL3	chr9:93063601-93063866	GM12878	blood:	n/a	n/a
18	BCL3	chr9:92989044-92989494	A549	lung:	n/a	n/a
19	BCL3	chr9:92988991-92989508	A549	lung:	n/a	n/a
20	BHLHE40	chr9:92951617-92952004	GM12878	blood:	n/a	n/a
21	BHLHE40	chr9:92989171-92989351	GM12878	blood:	n/a	n/a
22	BHLHE40	chr9:93049743-93050128	GM12878	blood:	n/a	n/a
23	CCNT2	chr9:93013376-93013527	K562	blood:	n/a	n/a
24	CEBPB	chr9:93050591-93050923	MCF-7	breast:	n/a	n/a
25	CEBPB	chr9:93000337-93000525	K562	blood:	n/a	n/a
26	CEBPB	chr9:93016538-93016930	H1-hESC	embryonic stem cell:	n/a	chr9:93016688-93016699
27	CEBPB	chr9:92960940-92961231	HepG2	liver:	n/a	chr9:92961075-92961086 chr9:92961211-92961224 chr9:92961211-92961222 chr9:92961077-92961088 chr9:92961075-92961088
28	CEBPB	chr9:93016581-93016902	IMR90	lung:	n/a	chr9:93016688-93016699
29	CEBPB	chr9:92980940-92981132	A549	lung:	n/a	n/a
30	CEBPB	chr9:93050622-93050837	HepG2	liver:	n/a	n/a
31	CEBPB	chr9:93069270-93069439	A549	lung:	n/a	chr9:93069351-93069362
32	CEBPB	chr9:93011313-93011854	MCF-7	breast:	n/a	chr9:93011567-93011578 chr9:93011531-93011542
33	CEBPB	chr9:93063626-93063880	IMR90	lung:	n/a	n/a
34	CEBPB	chr9:93011425-93011709	Hela-S3	cervix:	n/a	chr9:93011567-93011578 chr9:93011531-93011542
35	CEBPB	chr9:93011414-93011691	MCF-7	breast:	n/a	chr9:93011567-93011578 chr9:93011531-93011542
36	CEBPB	chr9:93013800-93013912	Hela-S3	cervix:	n/a	chr9:93013876-93013887
37	CEBPB	chr9:93000303-93000594	K562	blood:	n/a	n/a
38	CEBPB	chr9:93063609-93063862	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr9:93050594-93050828	IMR90	lung:	n/a	n/a
40	CEBPB	chr9:93069304-93069454	HepG2	liver:	n/a	chr9:93069351-93069362
41	CEBPB	chr9:92989382-92989579	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr9:93094451-93094892	A549	lung:	n/a	n/a
43	CEBPB	chr9:93016544-93016967	HepG2	liver:	n/a	chr9:93016688-93016699
44	CEBPB	chr9:93094507-93094784	HepG2	liver:	n/a	n/a
45	CEBPB	chr9:93000387-93000543	A549	lung:	n/a	n/a
46	CEBPB	chr9:93011423-93011691	A549	lung:	n/a	chr9:93011567-93011578 chr9:93011531-93011542
47	CEBPB	chr9:93094442-93094853	A549	lung:	n/a	n/a
48	CEBPB	chr9:93000257-93000471	K562	blood:	n/a	n/a
49	CEBPB	chr9:93094378-93094918	A549	lung:	n/a	n/a
50	CEBPB	chr9:93050566-93050865	A549	lung:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:92981825-92981875	HEEpiC	esophagus:	n/a
2	chr9:92981825-92981875	HEEpiC	esophagus:	n/a
3	chr9:92983726-92983776	ECC-1	luminal epithelium:	n/a
4	chr9:92982316-92982366	ovcar-3	ovarian:	n/a
5	chr9:92981825-92981875	AoSMC	blood vessel:	n/a
6	chr9:92981825-92981875	Hepatocyte	liver:	n/a
7	chr9:92982316-92982366	SK-N-SH	brain:	n/a
8	chr9:92981825-92981875	GM06990	blood:	n/a
9	chr9:92981825-92981875	T-47D	breast:	n/a
10	chr9:92982316-92982366	GM12892	blood:	n/a
11	chr9:92982316-92982366	HNPCEpiC	eye:	n/a
12	chr9:92983726-92983776	NH-A	brain:	n/a
13	chr9:92982316-92982366	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:92982316-92982366	HepG2	liver:	n/a
15	chr9:92983726-92983776	PFSK-1	brain:	n/a
16	chr9:92982316-92982366	HCPEpiC	choroid plexus:	n/a
17	chr9:92982316-92982366	SKMC	muscle:	n/a
18	chr9:92981825-92981875	HUVEC	blood vessel:	n/a
19	chr9:92981825-92981875	SK-N-MC	brain:	n/a
20	chr9:92982316-92982366	HCT-116	colon:	n/a
21	chr9:92983726-92983776	MCF-7	breast:	n/a
22	chr9:92982316-92982366	PFSK-1	brain:	n/a
23	chr9:92982316-92982366	MCF-7	breast:	n/a
24	chr9:92983726-92983776	HMEC	breast:	n/a
25	chr9:92982316-92982366	K562	blood:	n/a
26	chr9:92982316-92982366	NT2-D1	testis:	n/a
27	chr9:92982316-92982366	AG10803	skin:	n/a
28	chr9:92983726-92983776	T-47D	breast:	n/a
29	chr9:92983726-92983776	LNCaP	prostate:	n/a
30	chr9:92981825-92981875	HRE	kidney:	n/a
31	chr9:92981825-92981875	HPAEpiC	pulmonary alveolar:	n/a
32	chr9:92983726-92983776	U87	brain:	n/a
33	chr9:92981825-92981875	PANC-1	pancreas:	n/a
34	chr9:92981825-92981875	HCT-116	colon:	n/a
35	chr9:92982316-92982366	GM06990	blood:	n/a
36	chr9:92981825-92981875	HepG2	liver:	n/a
37	chr9:92981825-92981875	MCF-7	breast:	n/a
38	chr9:92982316-92982366	NB4	blood:	n/a
39	chr9:92983726-92983776	HUVEC	blood vessel:	n/a
40	chr9:92981825-92981875	NH-A	brain:	n/a
41	chr9:92982316-92982366	HL-60	blood:	n/a
42	chr9:92982316-92982366	HAEpiC	amniotic membrane:	n/a
43	chr9:92981825-92981875	ProgFib	skin:	n/a
44	chr9:92981825-92981875	Jurkat	blood:	n/a
45	chr9:92982316-92982366	AG09319	gingival:	n/a
46	chr9:92983726-92983776	HIPEpiC	eye:	n/a
47	chr9:92982316-92982366	AoSMC	blood vessel:	n/a
48	chr9:92983726-92983776	HCM	heart:	n/a
49	chr9:92983726-92983776	SAEC	small airway:	n/a
50	chr9:92982316-92982366	HRE	kidney:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:93080669..93081254-chr9:93407694..93408434,5	MCF-7	breast:
2	chr9:92889944..92891846-chr9:92907899..92909483,2	MCF-7	breast:
3	chr9:92936090..92938700-chr9:92964176..92966160,2	MCF-7	breast:
4	chr9:92989065..92989678-chr9:93404924..93405630,3	MCF-7	breast:
5	chr9:92919520..92922138-chr9:92936094..92937963,2	MCF-7	breast:
6	chr9:92904573..92905325-chr9:92981766..92982487,4	MCF-7	breast:
7	chr9:93011380..93015382-chr9:93016799..93018434,3	MCF-7	breast:
8	chr9:93080522..93081160-chr9:93309889..93310591,3	MCF-7	breast:
9	chr9:92921559..92924018-chr9:92927054..92929355,2	MCF-7	breast:
10	chr8:105501678..105502178-chr9:92935952..92936785,2	MCF-7	breast:
11	chr9:93005901..93009302-chr9:93010303..93013281,3	MCF-7	breast:
12	chr9:93067169..93069123-chr9:93074585..93076643,2	MCF-7	breast:
13	chr9:93080690..93081223-chr9:93404884..93405881,2	MCF-7	breast:
14	chr9:93011546..93013972-chr9:93052355..93054328,2	MCF-7	breast:
15	chr9:92931518..92933376-chr9:92938266..92940376,2	MCF-7	breast:
16	chr9:92903793..92904418-chr9:92981541..92982063,2	MCF-7	breast:
17	chr9:93011459..93013580-chr9:93031679..93033930,2	MCF-7	breast:
18	chr9:92931518..92933376-chr9:92938266..92940376,2	MCF-7	breast:
19	chr9:92918798..92921681-chr9:92947393..92950211,2	MCF-7	breast:
20	chr9:92921559..92924018-chr9:92927054..92929355,2	MCF-7	breast:
21	chr9:92919520..92922138-chr9:92936094..92937963,2	MCF-7	breast:
22	chr6:3000005..3000535-chr9:93027281..93027801,2	MCF-7	breast:
23	chr9:93080247..93081211-chr9:93633166..93633778,2	MCF-7	breast:
24	chr9:93011459..93013580-chr9:93031679..93033930,2	MCF-7	breast:
25	chr9:92906459..92907062-chr9:92981976..92982746,2	MCF-7	breast:
26	chr9:93051393..93052284-chr9:93404958..93405482,2	MCF-7	breast:
27	chr9:93080535..93081683-chr9:93405150..93405933,3	MCF-7	breast:
28	chr9:92936090..92938700-chr9:92964176..92966160,2	MCF-7	breast:
29	chr9:92918798..92921681-chr9:92947393..92950211,2	MCF-7	breast:
30	chr9:93011380..93015382-chr9:93016799..93018434,3	MCF-7	breast:
31	chr9:93011546..93013972-chr9:93052355..93054328,2	MCF-7	breast:
32	chr9:92904585..92905563-chr9:92981517..92982470,9	MCF-7	breast:
33	chr9:92905785..92906382-chr9:92981694..92982360,2	MCF-7	breast:
34	chr9:93005901..93009302-chr9:93010303..93013281,3	MCF-7	breast:
35	chr9:93067169..93069123-chr9:93074585..93076643,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DIRAS2-11	chr9:92965108-92965190	NONHSAT132995
2	lnc-SYK-11	chr9:92961872-92961910	NONHSAT132996
3	lnc-DIRAS2-13	chr9:92908568-92908774	NONHSAT132993
4	lnc-SYK-11	chr9:92964974-92967679	NONHSAT132996
5	lnc-DIRAS2-13	chr9:92909226-92909407	NONHSAT132993
6	lnc-DIRAS2-13	chr9:92908568-92908622	l_3807_chr9:92907194-92908622_whiteBloodCell
7	lnc-DIRAS2-2	chr9:93063178-93063935	NR_109795
8	lnc-SYK-9	chr9:93093837-93093904	NONHSAT133000
9	lnc-DIRAS2-10	chr9:93034039-93034046	NONHSAT132997
10	lnc-SYK-9	chr9:93087618-93087758	NONHSAT133000
11	lnc-DIRAS2-11	chr9:92921241-92921663	NONHSAT132995
12	lnc-DIRAS2-10	chr9:93028093-93029379	NONHSAT132997
13	lnc-DIRAS2-12	chr9:92920310-92920928	NONHSAT132994

No data

Variant related genes	Relation type
OR7E116P	TF binding region
OR7E31P	TF binding region
OR7E116P	CpG island
OR7E31P	CpG island
ENSG00000165023	chromatin interactions
ENSG00000124588	chromatin interactions

Extended variants
information (count: 5359 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:5359 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112784547	chr9:92908583-92908584	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs531537068	chr9:92908608-92908609	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs563395368	chr9:92908615-92908616	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs386736175	chr9:92908623-92908624	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs114066725	chr9:92908624-92908625	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs12341265	chr9:92908637-92908638	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs567827483	chr9:92908662-92908663	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs10992274	chr9:92908682-92908683	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs539509930	chr9:92908745-92908746	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs549224070	chr9:92908754-92908755	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs149336104	chr9:92909234-92909235	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs532912636	chr9:92909240-92909241	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs188177787	chr9:92909245-92909246	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs569733405	chr9:92909254-92909255	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs534577252	chr9:92909295-92909296	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs538452680	chr9:92909301-92909302	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs548753822	chr9:92909338-92909339	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs116192458	chr9:92909339-92909340	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs77604360	chr9:92909369-92909370	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs144598541	chr9:92909391-92909392	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs549061352	chr9:92911601-92911602	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs371365682	chr9:92911639-92911640	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs114079059	chr9:92911640-92911641	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs34989448	chr9:92911677-92911678	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs557968831	chr9:92911688-92911689	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs571447233	chr9:92911711-92911712	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs138307574	chr9:92911763-92911764	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs537217714	chr9:92911839-92911840	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs114697313	chr9:92911848-92911849	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs7859452	chr9:92911851-92911852	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs143077127	chr9:92911885-92911886	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs556833249	chr9:92911890-92911891	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs552682351	chr9:92911907-92911908	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs28495955	chr9:92911915-92911916	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs544755387	chr9:92911916-92911917	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs185549076	chr9:92911920-92911921	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs377446468	chr9:92911922-92911923	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs539129109	chr9:92911923-92911924	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs371724360	chr9:92911939-92911940	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs376432571	chr9:92911945-92911946	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs190886853	chr9:92911946-92911947	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs531731417	chr9:92911948-92911949	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs28741023	chr9:92911958-92911959	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs372652615	chr9:92911966-92911967	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs549399268	chr9:92911975-92911976	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs182604462	chr9:92911977-92911978	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs150284770	chr9:92911978-92911979	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs138218076	chr9:92911989-92911990	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs143696562	chr9:92912024-92912025	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs373806689	chr9:92912039-92912040	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Bipolar disorder	18458673	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Biliary cancer	19435499	CNVD
small cell lung cancer	20016488	CNVD
Intracranial aneurysm	16715129	CNVD
Cardiac fibroma	18329553	CNVD
Mental retardation	21693067	CNVD
Glioma	17123091	CNVD
Mantle cell lymphoma	19029149	CNVD
Breast cancer	17133270	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Basal cell nevus syndrome	21572526	CNVD
Mental retardation	19951919	CNVD
Retinoblastoma	22278416	CNVD
9q22.3 microdeletion syndrome	22283845	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:92911600-92912200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
2	chr9:92911800-92912200	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr9:92918000-92921000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr9:92919000-92924600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr9:92920200-92920600	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr9:92920200-92920600	Active TSS	Spleen	Spleen
7	chr9:92920600-92920800	Flanking Active TSS	Spleen	Spleen
8	chr9:92920800-92924000	Weak transcription	Spleen	Spleen
9	chr9:92921000-92921200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr9:92921000-92921200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr9:92921000-92921200	ZNF genes & repeats	Pancreas	Pancrea
12	chr9:92921200-92924600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr9:92921200-92924600	Weak transcription	Pancreas	Pancrea
14	chr9:92923600-92923800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
15	chr9:92923800-92924400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
16	chr9:92923800-92924600	Enhancers	Primary hematopoietic stem cells	blood
17	chr9:92923800-92925200	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr9:92923800-92925600	Enhancers	Primary B cells from peripheral blood	blood
19	chr9:92924000-92924400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr9:92924000-92924800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr9:92924000-92925200	Enhancers	Spleen	Spleen
22	chr9:92924200-92924400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr9:92924600-92924800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr9:92924600-92924800	Enhancers	Duodenum Mucosa	Duodenum
25	chr9:92924600-92925000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr9:92924600-92925000	Active TSS	Fetal Heart	heart
27	chr9:92924600-92925200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr9:92924600-92925200	Enhancers	Esophagus	oesophagus
29	chr9:92924600-92925200	ZNF genes & repeats	Fetal Kidney	kidney
30	chr9:92924600-92925200	Enhancers	Pancreas	Pancrea
31	chr9:92924800-92925000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr9:92924800-92925000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr9:92924800-92925000	Enhancers	Colonic Mucosa	Colon
34	chr9:92924800-92925400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
35	chr9:92924800-92925600	Flanking Active TSS	Duodenum Mucosa	Duodenum
36	chr9:92924800-92925600	Enhancers	Stomach Mucosa	stomach
37	chr9:92924800-92925800	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr9:92925000-92925400	Enhancers	Primary B cells from cord blood	blood
39	chr9:92925000-92925400	Enhancers	Sigmoid Colon	Sigmoid Colon
40	chr9:92925000-92925600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr9:92925000-92925600	ZNF genes & repeats	Fetal Intestine Large	intestine
42	chr9:92925000-92928800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
43	chr9:92925000-92929000	Weak transcription	Colonic Mucosa	Colon
44	chr9:92925200-92925400	Enhancers	Primary hematopoietic stem cells	blood
45	chr9:92925200-92927600	Weak transcription	Pancreas	Pancrea
46	chr9:92925200-92928800	Weak transcription	Fetal Kidney	kidney
47	chr9:92925200-92933200	Weak transcription	Esophagus	oesophagus
48	chr9:92925400-92930000	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr9:92925600-92926000	Enhancers	Duodenum Mucosa	Duodenum
50	chr9:92925600-92927600	Weak transcription	Fetal Intestine Large	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links