Variant report

Variant	nsv972786
Chromosome Location	chr9:97308737-97320211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:467)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:467 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:97315560-97315747	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:97316828-97317415	HepG2	liver:	n/a	n/a
3	ATF2	chr9:97316593-97317233	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr9:97316673-97317135	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr9:97316667-97316977	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr9:97316492-97317057	K562	blood:	n/a	n/a
7	BRCA1	chr9:97316794-97316973	HepG2	liver:	n/a	n/a
8	BRCA1	chr9:97316748-97317370	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr9:97316650-97317300	H1-hESC	embryonic stem cell:	n/a	n/a
10	CBX3	chr9:97316658-97317103	K562	blood:	n/a	n/a
11	CCNT2	chr9:97316782-97316973	K562	blood:	n/a	n/a
12	CEBPB	chr9:97316653-97317274	MCF-7	breast:	n/a	chr9:97316884-97316895
13	CEBPB	chr9:97315429-97315642	HepG2	liver:	n/a	n/a
14	CEBPB	chr9:97316700-97317276	ECC-1	luminal epithelium:	n/a	chr9:97316884-97316895
15	CEBPB	chr9:97316733-97317111	Hela-S3	cervix:	n/a	chr9:97316884-97316895
16	CEBPB	chr9:97316697-97317044	H1-hESC	embryonic stem cell:	n/a	chr9:97316884-97316895
17	CEBPB	chr9:97315504-97315656	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:97315349-97315821	MCF-7	breast:	n/a	n/a
19	CEBPB	chr9:97315576-97315645	K562	blood:	n/a	n/a
20	CEBPB	chr9:97316685-97317057	K562	blood:	n/a	chr9:97316884-97316895
21	CEBPB	chr9:97316689-97317077	K562	blood:	n/a	chr9:97316884-97316895
22	CEBPB	chr9:97316730-97317018	K562	blood:	n/a	chr9:97316884-97316895
23	CEBPB	chr9:97316739-97317051	HepG2	liver:	n/a	chr9:97316884-97316895
24	CEBPB	chr9:97315445-97315761	HepG2	liver:	n/a	n/a
25	CEBPB	chr9:97316779-97316925	HepG2	liver:	n/a	chr9:97316884-97316895
26	CEBPD	chr9:97317000-97317220	HepG2	liver:	n/a	n/a
27	CEBPD	chr9:97316984-97317225	HepG2	liver:	n/a	n/a
28	CHD1	chr9:97316774-97317575	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr9:97315483-97315610	HepG2	liver:	n/a	n/a
30	CHD2	chr9:97316757-97317614	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr9:97316491-97317373	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr9:97316691-97317240	HepG2	liver:	n/a	n/a
33	CREB1	chr9:97316994-97317206	A549	lung:	n/a	n/a
34	CREB1	chr9:97316620-97317234	A549	lung:	n/a	n/a
35	CREB1	chr9:97316575-97317433	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr9:97316541-97317412	HepG2	liver:	n/a	n/a
37	CREB1	chr9:97316576-97317390	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr9:97315320-97315470	RPTEC	kidney:	n/a	n/a
39	CTCF	chr9:97316658-97316958	Medullo	brain:	n/a	n/a
40	CTCF	chr9:97317469-97317628	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr9:97316686-97316923	A549	lung:	n/a	n/a
42	CTCF	chr9:97315484-97315634	LNCaP	prostate:	n/a	n/a
43	CTCF	chr9:97315380-97315673	GM12878	blood:	n/a	n/a
44	CTCF	chr9:97316715-97316870	GM13976	blood:	n/a	n/a
45	CTCF	chr9:97315421-97315747	MCF-7	breast:	n/a	n/a
46	CTCF	chr9:97315469-97315657	LNCaP	prostate:	n/a	n/a
47	CTCF	chr9:97316740-97316862	GM10248	blood:	n/a	n/a
48	CTCF	chr9:97315459-97315683	K562	blood:	n/a	n/a
49	CTCF	chr9:97316602-97317182	K562	blood:	n/a	n/a
50	CTCF	chr9:97315465-97315642	GM12892	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:97317179-97317229	NT2-D1	testis:	n/a
2	chr9:97317179-97317229	ProgFib	skin:	n/a
3	chr9:97317179-97317229	BE2_C	brain:	n/a
4	chr9:97317179-97317229	GM12892	blood:	n/a
5	chr9:97317179-97317229	SK-N-SH_RA	brain:	n/a
6	chr9:97317179-97317229	HCPEpiC	choroid plexus:	n/a
7	chr9:97317179-97317229	LNCaP	prostate:	n/a
8	chr9:97317179-97317229	GM12878	blood:	n/a
9	chr9:97317179-97317229	HIPEpiC	eye:	n/a
10	chr9:97317179-97317229	HAEpiC	amniotic membrane:	n/a
11	chr9:97317179-97317229	HRPEpiC	eye:	n/a
12	chr9:97317179-97317229	HepG2	liver:	n/a
13	chr9:97317179-97317229	MCF10A-Er-Src	breast:	n/a
14	chr9:97317179-97317229	HNPCEpiC	eye:	n/a
15	chr9:97317179-97317229	HRCEpiC	kidney:	n/a
16	chr9:97317179-97317229	GM06990	blood:	n/a
17	chr9:97317179-97317229	SK-N-MC	brain:	n/a
18	chr9:97317179-97317229	ovcar-3	ovarian:	n/a
19	chr9:97317179-97317229	T-47D	breast:	n/a
20	chr9:97317179-97317229	NB4	blood:	n/a
21	chr9:97317179-97317229	HRE	kidney:	n/a
22	chr9:97317179-97317229	Jurkat	blood:	n/a
23	chr9:97317179-97317229	HMEC	breast:	n/a
24	chr9:97317179-97317229	HCF	heart:	n/a
25	chr9:97317179-97317229	AG04450	lung:	fetal
26	chr9:97317179-97317229	RPTEC	kidney:	n/a
27	chr9:97317179-97317229	GM19239	blood:	n/a
28	chr9:97317179-97317229	HL-60	blood:	n/a
29	chr9:97317179-97317229	GM12891	blood:	n/a
30	chr9:97317179-97317229	NHDF-neo	bronchial:	n/a
31	chr9:97317179-97317229	NHBE	bronchial:	n/a
32	chr9:97317179-97317229	HEK293	kidney:	embryo
33	chr9:97317179-97317229	A549	lung:	n/a
34	chr9:97317179-97317229	MCF-7	breast:	n/a
35	chr9:97317179-97317229	HUVEC	blood vessel:	n/a
36	chr9:97317179-97317229	H1-hESC	embryonic stem cell:	embryo
37	chr9:97317179-97317229	U87	brain:	n/a
38	chr9:97317179-97317229	NH-A	brain:	n/a
39	chr9:97317179-97317229	ECC-1	luminal epithelium:	n/a
40	chr9:97317179-97317229	AG09319	gingival:	n/a
41	chr9:97317179-97317229	HCT-116	colon:	n/a
42	chr9:97317179-97317229	K562	blood:	n/a
43	chr9:97317179-97317229	IMR90	lung:	fetal
44	chr9:97317179-97317229	PrEC	prostate:	n/a
45	chr9:97317179-97317229	Hepatocyte	liver:	n/a
46	chr9:97317179-97317229	HCM	heart:	n/a
47	chr9:97317179-97317229	PANC-1	pancreas:	n/a
48	chr9:97317179-97317229	Caco-2	colon:	n/a
49	chr9:97317179-97317229	Hela-S3	cervix:	n/a
50	chr9:97317179-97317229	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr9:97316005..97317970-chr9:97766242..97767931,2	MCF-7	breast:
2	chr9:97308118..97310790-chr9:97312751..97314524,2	MCF-7	breast:
3	chr9:97309308..97311468-chr9:97313942..97316861,2	MCF-7	breast:
4	chr9:97309308..97311468-chr9:97313942..97316861,2	MCF-7	breast:
5	chr9:97308189..97309860-chr9:97315997..97318299,2	K562	blood:
6	chr9:97315606..97318346-chr9:97888439..97891401,2	MCF-7	breast:
7	chr9:97311721..97313513-chr9:97315633..97318443,2	MCF-7	breast:
8	chr9:97308189..97310804-chr9:97316799..97318658,2	K562	blood:
9	chr9:97316754..97318987-chr9:97400777..97403144,3	MCF-7	breast:
10	chr9:97316090..97317268-chr9:97365275..97366675,11	MCF-7	breast:
11	chr9:97316341..97317245-chr9:97365199..97365958,5	K562	blood:
12	chr9:97314619..97316650-chr9:97365797..97368541,2	K562	blood:
13	chr9:97316436..97317261-chr9:97893369..97894207,2	K562	blood:
14	chr9:97308118..97310790-chr9:97312751..97314524,2	MCF-7	breast:

No data

Variant related genes	Relation type
PCAT7	TF binding region
PCAT7	CpG island
ENSG00000165140	chromatin interactions
ENSG00000158169	chromatin interactions
ENSG00000231806	chromatin interactions
ENSG00000148120	chromatin interactions

Extended variants
information (count: 532 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7853756	chr9:97308794-97308795	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546875735	chr9:97308829-97308830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189431073	chr9:97308841-97308842	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs568344846	chr9:97308869-97308870	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150658176	chr9:97308888-97308889	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs557248618	chr9:97308890-97308891	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs568484275	chr9:97308936-97308937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs539048404	chr9:97308990-97308991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs537512500	chr9:97309011-97309012	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs61010937	chr9:97309014-97309015	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113153907	chr9:97309064-97309065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140009373	chr9:97309109-97309110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149420120	chr9:97309113-97309114	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540367169	chr9:97309121-97309122	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs10993239	chr9:97309159-97309160	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs181710800	chr9:97309200-97309201	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs117285943	chr9:97309236-97309237	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs200293877	chr9:97309287-97309288	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562776373	chr9:97309314-97309315	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530888185	chr9:97309339-97309340	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs545870254	chr9:97309341-97309342	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564554294	chr9:97309365-97309366	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs184456160	chr9:97309371-97309372	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs35238481	chr9:97309386-97309387	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541110378	chr9:97309394-97309395	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs561913752	chr9:97309406-97309407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs529467741	chr9:97309436-97309437	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs139514455	chr9:97309480-97309481	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569217032	chr9:97309494-97309495	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559454558	chr9:97309519-97309520	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112261423	chr9:97309526-97309527	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
32	rs10761331	chr9:97309562-97309563	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs188930626	chr9:97309563-97309564	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs533633296	chr9:97309588-97309589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181309406	chr9:97309602-97309603	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558789910	chr9:97309605-97309606	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140059232	chr9:97309630-97309631	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs10993240	chr9:97309654-97309655	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs556440551	chr9:97309671-97309672	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs142629810	chr9:97309697-97309698	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545314331	chr9:97309736-97309737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564308502	chr9:97309774-97309775	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368082993	chr9:97309782-97309783	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs10821364	chr9:97309796-97309797	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs200268884	chr9:97309807-97309808	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs79613668	chr9:97309815-97309816	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs561848081	chr9:97309887-97309888	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs529404761	chr9:97309914-97309915	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs550751382	chr9:97309917-97309918	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs562788442	chr9:97309925-97309926	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Breast cancer	17133270	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
Acute lymphoblastic leukemia	21339820	CNVD
Microcephaly	18830227	CNVD
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:97296400-97314200	Weak transcription	Liver	Liver
2	chr9:97297200-97315000	Weak transcription	HepG2	liver
3	chr9:97302600-97315000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr9:97304800-97315200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr9:97308400-97312000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr9:97310600-97312600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr9:97311600-97315200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr9:97312000-97313600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr9:97312000-97315600	Weak transcription	A549	lung
10	chr9:97312400-97313800	ZNF genes & repeats	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr9:97312600-97313200	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:97312600-97313200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
13	chr9:97313000-97313400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
14	chr9:97313000-97316800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr9:97313200-97315000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr9:97313200-97316600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr9:97313400-97315600	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr9:97313600-97316000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr9:97313800-97315400	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr9:97313800-97315800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr9:97314200-97315200	Enhancers	Liver	Liver
22	chr9:97314200-97315400	Weak transcription	H1 Cell Line	embryonic stem cell
23	chr9:97314800-97315400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr9:97314800-97315800	Enhancers	Stomach Mucosa	stomach
25	chr9:97315000-97315200	Enhancers	Duodenum Mucosa	Duodenum
26	chr9:97315000-97315200	Enhancers	HepG2	liver
27	chr9:97315000-97315400	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr9:97315000-97315400	Enhancers	Hela-S3	cervix
29	chr9:97315000-97316000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr9:97315200-97315400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr9:97315200-97315400	Enhancers	Rectal Mucosa Donor 29	rectum
32	chr9:97315200-97315600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr9:97315200-97315600	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr9:97315200-97315600	Flanking Active TSS	HepG2	liver
35	chr9:97315200-97315800	Enhancers	Gastric	stomach
36	chr9:97315200-97315800	Enhancers	Pancreas	Pancrea
37	chr9:97315200-97316400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr9:97315200-97316400	Flanking Active TSS	Liver	Liver
39	chr9:97315200-97319200	Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr9:97315400-97315600	Enhancers	HUES64 Cell Line	embryonic stem cell
41	chr9:97315400-97315600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
42	chr9:97315400-97315600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
43	chr9:97315400-97315800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
44	chr9:97315400-97315800	Flanking Active TSS	Hela-S3	cervix
45	chr9:97315400-97316200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr9:97315400-97316400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr9:97315400-97318800	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr9:97315600-97315800	Active TSS	HepG2	liver
49	chr9:97315600-97316000	Enhancers	A549	lung
50	chr9:97315600-97316400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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