Variant report

Variant	esv1818795
Chromosome Location	chr9:95656340-95689158
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:88)
CpG islands
(count:183)
Chromatin interactive
region (count:17)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:88 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:95674149-95674446	HepG2	liver:	n/a	n/a
2	BACH1	chr9:95682915-95683006	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr9:95682685-95683040	GM12878	blood:	n/a	n/a
4	BCL3	chr9:95682617-95683152	GM12878	blood:	n/a	n/a
5	CEBPB	chr9:95675967-95676048	K562	blood:	n/a	chr9:95676020-95676031 chr9:95676018-95676031 chr9:95676018-95676029
6	CEBPB	chr9:95673895-95673966	Hela-S3	cervix:	n/a	chr9:95673917-95673928
7	CEBPB	chr9:95673734-95674174	MCF-7	breast:	n/a	chr9:95674160-95674171 chr9:95673917-95673928 chr9:95674160-95674171
8	CEBPB	chr9:95673745-95674076	HepG2	liver:	n/a	chr9:95673917-95673928
9	CEBPB	chr9:95675989-95676120	HepG2	liver:	n/a	chr9:95676020-95676031 chr9:95676018-95676031 chr9:95676018-95676029
10	CEBPB	chr9:95673759-95674088	A549	lung:	n/a	chr9:95673917-95673928
11	CTCF	chr9:95667560-95667710	HepG2	liver:	n/a	n/a
12	CTCF	chr9:95675505-95675763	K562	blood:	n/a	n/a
13	CTCF	chr9:95675450-95675858	K562	blood:	n/a	n/a
14	CTCF	chr9:95675613-95675677	MCF-7	breast:	n/a	n/a
15	CTCF	chr9:95659039-95659102	Pancreas_OC	pancreas:	n/a	n/a
16	CTCF	chr9:95667500-95667650	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr9:95675560-95675710	HepG2	liver:	n/a	n/a
18	CTCF	chr9:95670224-95670305	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr9:95675539-95675658	HepG2	liver:	n/a	n/a
20	CTCF	chr9:95658836-95658887	Lung_OC	lung:	n/a	n/a
21	CTCF	chr9:95660616-95660691	GM10248	blood:	n/a	n/a
22	CTCF	chr9:95685628-95685670	Medullo	brain:	n/a	n/a
23	CTCF	chr9:95657599-95657671	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr9:95675546-95675752	K562	blood:	n/a	n/a
25	CTCF	chr9:95675597-95675664	K562	blood:	n/a	n/a
26	CTCF	chr9:95675535-95675726	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr9:95667540-95667657	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr9:95675500-95675650	K562	blood:	n/a	n/a
29	CTCF	chr9:95675489-95675720	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr9:95675520-95675670	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr9:95675624-95675649	HepG2	liver:	n/a	n/a
32	E2F6	chr9:95679882-95680269	H1-hESC	embryonic stem cell:	n/a	n/a
33	E2F6	chr9:95679789-95680340	H1-hESC	embryonic stem cell:	n/a	n/a
34	EGR1	chr9:95688532-95688739	K562	blood:	n/a	n/a
35	EGR1	chr9:95688455-95688707	K562	blood:	n/a	n/a
36	ELF1	chr9:95679681-95679947	K562	blood:	n/a	n/a
37	FOS	chr9:95688648-95688786	MCF10A-Er-Src	breast:	n/a	n/a
38	FOXA1	chr9:95673998-95674497	HepG2	liver:	n/a	chr9:95674266-95674281
39	FOXA1	chr9:95674129-95674500	HepG2	liver:	n/a	chr9:95674266-95674281
40	FOXA1	chr9:95667781-95668019	HepG2	liver:	n/a	n/a
41	FOXA1	chr9:95673967-95674562	HepG2	liver:	n/a	chr9:95674266-95674281
42	FOXA1	chr9:95673980-95674536	HepG2	liver:	n/a	chr9:95674266-95674281
43	FOXA1	chr9:95674123-95674482	T-47D	breast:	n/a	chr9:95674266-95674281
44	FOXA1	chr9:95674075-95674491	T-47D	breast:	n/a	chr9:95674266-95674281
45	FOXA2	chr9:95673962-95674963	A549	lung:	n/a	n/a
46	FOXA2	chr9:95674143-95674436	HepG2	liver:	n/a	n/a
47	FOXA2	chr9:95673997-95674644	A549	lung:	n/a	n/a
48	FOXA2	chr9:95667676-95668135	A549	lung:	n/a	n/a
49	FOXA2	chr9:95667668-95668170	A549	lung:	n/a	n/a
50	FOXA2	chr9:95673925-95674695	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:95675274-95675324	PANC-1	pancreas:	n/a
2	chr9:95675274-95675324	PFSK-1	brain:	n/a
3	chr9:95675274-95675324	HL-60	blood:	n/a
4	chr9:95675546-95675596	LNCaP	prostate:	n/a
5	chr9:95675274-95675324	HCM	heart:	n/a
6	chr9:95675546-95675596	GM12878	blood:	n/a
7	chr9:95675546-95675596	MCF-7	breast:	n/a
8	chr9:95678583-95678633	IMR90	lung:	fetal
9	chr9:95675546-95675596	PANC-1	pancreas:	n/a
10	chr9:95678583-95678633	SAEC	small airway:	n/a
11	chr9:95675274-95675324	NHDF-neo	bronchial:	n/a
12	chr9:95675274-95675324	K562	blood:	n/a
13	chr9:95678583-95678633	ProgFib	skin:	n/a
14	chr9:95675546-95675596	HL-60	blood:	n/a
15	chr9:95675274-95675324	GM12878	blood:	n/a
16	chr9:95675546-95675596	AG04449	skin:	fetal
17	chr9:95675274-95675324	HPAEpiC	pulmonary alveolar:	n/a
18	chr9:95675546-95675596	ovcar-3	ovarian:	n/a
19	chr9:95675274-95675324	U87	brain:	n/a
20	chr9:95675274-95675324	HIPEpiC	eye:	n/a
21	chr9:95678583-95678633	HMEC	breast:	n/a
22	chr9:95675274-95675324	AG10803	skin:	n/a
23	chr9:95675546-95675596	Caco-2	colon:	n/a
24	chr9:95678583-95678633	HUVEC	blood vessel:	n/a
25	chr9:95678583-95678633	HCT-116	colon:	n/a
26	chr9:95675274-95675324	GM19239	blood:	n/a
27	chr9:95675546-95675596	HUVEC	blood vessel:	n/a
28	chr9:95678583-95678633	HepG2	liver:	n/a
29	chr9:95675274-95675324	Hepatocyte	liver:	n/a
30	chr9:95675274-95675324	AG04449	skin:	fetal
31	chr9:95678583-95678633	NHBE	bronchial:	n/a
32	chr9:95675274-95675324	CMK	blood:	n/a
33	chr9:95678583-95678633	NHDF-neo	bronchial:	n/a
34	chr9:95678583-95678633	HCM	heart:	n/a
35	chr9:95678583-95678633	AG04450	lung:	fetal
36	chr9:95678583-95678633	Jurkat	blood:	n/a
37	chr9:95675274-95675324	NHBE	bronchial:	n/a
38	chr9:95678583-95678633	ovcar-3	ovarian:	n/a
39	chr9:95675274-95675324	SK-N-SH_RA	brain:	n/a
40	chr9:95678583-95678633	BJ	skin:	n/a
41	chr9:95675274-95675324	BJ	skin:	n/a
42	chr9:95675274-95675324	GM12892	blood:	n/a
43	chr9:95675546-95675596	AoSMC	blood vessel:	n/a
44	chr9:95678583-95678633	AG09309	skin:	n/a
45	chr9:95678583-95678633	PFSK-1	brain:	n/a
46	chr9:95675546-95675596	HIPEpiC	eye:	n/a
47	chr9:95678583-95678633	SK-N-SH	brain:	n/a
48	chr9:95678583-95678633	HNPCEpiC	eye:	n/a
49	chr9:95675546-95675596	HCT-116	colon:	n/a
50	chr9:95675546-95675596	HNPCEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95675676..95677800-chr9:95688606..95691210,2	MCF-7	breast:
2	chr9:95680955..95683491-chr9:95687222..95689030,2	K562	blood:
3	chr9:95675136..95677184-chr9:95685005..95687595,2	MCF-7	breast:
4	chr9:95675676..95677800-chr9:95688606..95691210,2	MCF-7	breast:
5	chr9:95680955..95683491-chr9:95687222..95689030,2	K562	blood:
6	chr9:95526781..95528975-chr9:95672458..95674391,2	MCF-7	breast:
7	chr9:95680681..95683680-chr9:95689468..95691855,3	MCF-7	breast:
8	chr9:95684419..95686072-chr9:95691628..95694362,2	MCF-7	breast:
9	chr9:95686470..95688704-chr9:95692364..95694888,3	K562	blood:
10	chr9:95668983..95671268-chr9:95672944..95675033,2	K562	blood:
11	chr9:95685909..95687885-chr9:95716846..95719770,2	K562	blood:
12	chr9:95687513..95689669-chr9:95700476..95703248,2	K562	blood:
13	chr9:95668983..95671268-chr9:95672944..95675033,2	K562	blood:
14	chr9:95677020..95680081-chr9:95681150..95683718,3	MCF-7	breast:
15	chr9:95672518..95675002-chr9:95676684..95678735,2	MCF-7	breast:
16	chr9:95672518..95675002-chr9:95676684..95678735,2	MCF-7	breast:
17	chr9:95677020..95680081-chr9:95681150..95683718,3	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FGD3-2	chr9:95659186-95659353	NONHSAT133223
2	lnc-FGD3-3	chr9:95661581-95661890	NONHSAT133212
3	lnc-FGD3-2	chr9:95660214-95660436	NONHSAT133223
4	lnc-FGD3-3	chr9:95660664-95660887	NONHSAT133210

No data

Variant related genes	Relation type
ALOX15P2	TF binding region
SNX18P2	TF binding region
ALOX15P2	CpG island
SNX18P2	CpG island
ENSG00000185963	chromatin interactions
ENSG00000188101	chromatin interactions

Extended variants
information (count: 807 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:807 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79254605	chr9:95656349-95656350	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs149183116	chr9:95656372-95656373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116047871	chr9:95656373-95656374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs184682843	chr9:95656399-95656400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143353508	chr9:95656434-95656435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186903799	chr9:95656501-95656502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564879826	chr9:95656593-95656594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs532717657	chr9:95656675-95656676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191304440	chr9:95656700-95656701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559586199	chr9:95656704-95656705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530349117	chr9:95656799-95656800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7044372	chr9:95656819-95656820	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569703801	chr9:95656848-95656849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530856491	chr9:95656851-95656852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142283872	chr9:95656892-95656893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570888624	chr9:95656895-95656896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368504562	chr9:95656917-95656918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375164254	chr9:95656956-95656957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554030038	chr9:95656984-95656985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565932522	chr9:95657009-95657010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs117570280	chr9:95657010-95657011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554946876	chr9:95657013-95657014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs575988861	chr9:95657021-95657022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs114699210	chr9:95657022-95657023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs16905839	chr9:95657053-95657054	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs541199598	chr9:95657146-95657147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559529178	chr9:95657152-95657153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530269358	chr9:95657176-95657177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542114575	chr9:95657183-95657184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184965305	chr9:95657184-95657185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs573547875	chr9:95657233-95657234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs117550505	chr9:95657243-95657244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146299560	chr9:95657289-95657290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs12346689	chr9:95657299-95657300	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs12352388	chr9:95657305-95657306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs545142822	chr9:95657317-95657318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547575510	chr9:95657321-95657322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs10821036	chr9:95657330-95657331	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs138171520	chr9:95657394-95657395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554884668	chr9:95657396-95657397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530737970	chr9:95657425-95657426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569886575	chr9:95657490-95657491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs189299542	chr9:95657541-95657542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558291913	chr9:95657553-95657554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576826120	chr9:95657618-95657619	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs534403684	chr9:95657620-95657621	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs552696010	chr9:95657642-95657643	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs534267128	chr9:95657654-95657655	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs538178263	chr9:95657687-95657688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527265695	chr9:95657699-95657700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95653400-95660600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr9:95658400-95658800	Enhancers	Primary T cells fromperipheralblood	blood
3	chr9:95661000-95661200	Bivalent Enhancer	Small Intestine	intestine
4	chr9:95667600-95667800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:95667800-95668400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr9:95668200-95668400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr9:95673000-95673200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr9:95673000-95675000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr9:95673400-95673800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr9:95673400-95674400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr9:95673600-95674000	Enhancers	A549	lung
12	chr9:95673600-95674200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
13	chr9:95673600-95674600	Enhancers	Fetal Lung	lung
14	chr9:95673600-95675000	Enhancers	Fetal Stomach	stomach
15	chr9:95673800-95674000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr9:95673800-95674000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
17	chr9:95673800-95674000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
18	chr9:95673800-95674000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
19	chr9:95673800-95674000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr9:95673800-95674000	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
21	chr9:95673800-95674000	Enhancers	Brain Germinal Matrix	brain
22	chr9:95673800-95674000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
23	chr9:95673800-95674000	Bivalent Enhancer	NH-A	brain
24	chr9:95673800-95674200	Enhancers	Brain Hippocampus Middle	brain
25	chr9:95673800-95674200	Enhancers	Fetal Kidney	kidney
26	chr9:95673800-95674200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
27	chr9:95673800-95674400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
28	chr9:95673800-95674400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr9:95673800-95674400	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr9:95673800-95674400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
31	chr9:95673800-95674400	Enhancers	Hela-S3	cervix
32	chr9:95673800-95674600	Enhancers	Adipose Nuclei	Adipose
33	chr9:95673800-95674600	Enhancers	Brain Anterior Caudate	brain
34	chr9:95673800-95674600	Bivalent Enhancer	Stomach Mucosa	stomach
35	chr9:95673800-95674800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr9:95673800-95674800	Enhancers	Liver	Liver
37	chr9:95673800-95674800	Enhancers	Colonic Mucosa	Colon
38	chr9:95673800-95674800	Enhancers	HepG2	liver
39	chr9:95673800-95675000	Enhancers	Gastric	stomach
40	chr9:95673800-95675200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr9:95674000-95674200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
42	chr9:95674000-95674400	Bivalent Enhancer	Brain Cingulate Gyrus	brain
43	chr9:95674000-95674400	Active TSS	Brain Substantia Nigra	brain
44	chr9:95674000-95674400	Flanking Active TSS	A549	lung
45	chr9:95674000-95674600	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr9:95674000-95674600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
47	chr9:95674000-95674800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr9:95674000-95674800	Enhancers	Ovary	ovary
49	chr9:95674000-95674800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr9:95674000-95675000	Enhancers	Pancreas	Pancrea

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