Variant report

Variant	nsv982639
Chromosome Location	chr9:95671744-95685131
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:68)
CpG islands
(count:184)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:68 , 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	chr9:95675989-95676120	HepG2	liver:	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	chr9:95673745-95674076	HepG2	liver:	n/a	chr9:95673917-95673928
8	CEBPB	chr9:95673759-95674088	A549	lung:	n/a	chr9:95673917-95673928
9	CEBPB	chr9:95675967-95676048	K562	blood:	n/a	chr9:95676020-95676031 chr9:95676018-95676031 chr9:95676018-95676029
10	CEBPB	chr9:95673734-95674174	MCF-7	breast:	n/a	chr9:95674160-95674171 chr9:95673917-95673928 chr9:95674160-95674171
11	CTCF	chr9:95675500-95675650	K562	blood:	n/a	n/a
12	CTCF	chr9:95675505-95675763	K562	blood:	n/a	n/a
13	CTCF	chr9:95675597-95675664	K562	blood:	n/a	n/a
14	CTCF	chr9:95675546-95675752	K562	blood:	n/a	n/a
15	CTCF	chr9:95675535-95675726	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr9:95675613-95675677	MCF-7	breast:	n/a	n/a
17	CTCF	chr9:95675560-95675710	HepG2	liver:	n/a	n/a
18	CTCF	chr9:95675520-95675670	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr9:95675624-95675649	HepG2	liver:	n/a	n/a
20	CTCF	chr9:95675489-95675720	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr9:95675539-95675658	HepG2	liver:	n/a	n/a
22	CTCF	chr9:95675450-95675858	K562	blood:	n/a	n/a
23	E2F6	chr9:95679882-95680269	H1-hESC	embryonic stem cell:	n/a	n/a
24	E2F6	chr9:95679789-95680340	H1-hESC	embryonic stem cell:	n/a	n/a
25	ELF1	chr9:95679681-95679947	K562	blood:	n/a	n/a
26	FOXA1	chr9:95674075-95674491	T-47D	breast:	n/a	chr9:95674266-95674281
27	FOXA1	chr9:95674123-95674482	T-47D	breast:	n/a	chr9:95674266-95674281
28	FOXA1	chr9:95673967-95674562	HepG2	liver:	n/a	chr9:95674266-95674281
29	FOXA1	chr9:95673980-95674536	HepG2	liver:	n/a	chr9:95674266-95674281
30	FOXA1	chr9:95674129-95674500	HepG2	liver:	n/a	chr9:95674266-95674281
31	FOXA1	chr9:95673998-95674497	HepG2	liver:	n/a	chr9:95674266-95674281
32	FOXA2	chr9:95673997-95674644	A549	lung:	n/a	n/a
33	FOXA2	chr9:95674143-95674436	HepG2	liver:	n/a	n/a
34	FOXA2	chr9:95673925-95674695	HepG2	liver:	n/a	n/a
35	FOXA2	chr9:95673962-95674963	A549	lung:	n/a	n/a
36	HEY1	chr9:95679528-95679969	K562	blood:	n/a	n/a
37	JUND	chr9:95683019-95683118	H1-hESC	embryonic stem cell:	n/a	n/a
38	MAFF	chr9:95672805-95672821	K562	blood:	n/a	n/a
39	MAFK	chr9:95672679-95672949	HepG2	liver:	n/a	chr9:95672811-95672825 chr9:95672736-95672747
40	NFATC1	chr9:95682688-95683078	GM12878	blood:	n/a	n/a
41	NFIC	chr9:95679746-95680171	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr9:95679495-95680139	HL-60	blood:	n/a	n/a
43	POLR2A	chr9:95683399-95683424	K562	blood:	n/a	n/a
44	POLR2A	chr9:95679580-95679990	K562	blood:	n/a	n/a
45	RAD21	chr9:95675517-95675667	HepG2	liver:	n/a	n/a
46	RAD21	chr9:95675429-95675781	H1-hESC	embryonic stem cell:	n/a	n/a
47	RAD21	chr9:95675449-95675806	H1-hESC	embryonic stem cell:	n/a	n/a
48	RAD21	chr9:95675273-95675903	H1-hESC	embryonic stem cell:	n/a	chr9:95675408-95675422
49	REST	chr9:95673991-95674539	A549	lung:	n/a	n/a
50	SP1	chr9:95673833-95674521	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	chr9:95675274-95675324	Jurkat	blood:	n/a
2	chr9:95675274-95675324	Jurkat	blood:	n/a
3	chr9:95675274-95675324	HIPEpiC	eye:	n/a
4	chr9:95675274-95675324	ProgFib	skin:	n/a
5	chr9:95678583-95678633	Hepatocyte	liver:	n/a
6	chr9:95678583-95678633	Jurkat	blood:	n/a
7	chr9:95678583-95678633	CMK	blood:	n/a
8	chr9:95675274-95675324	HCM	heart:	n/a
9	chr9:95675546-95675596	GM19239	blood:	n/a
10	chr9:95678583-95678633	HRPEpiC	eye:	n/a
11	chr9:95678583-95678633	AG04449	skin:	fetal
12	chr9:95675546-95675596	AG09309	skin:	n/a
13	chr9:95675274-95675324	NH-A	brain:	n/a
14	chr9:95675274-95675324	SK-N-SH_RA	brain:	n/a
15	chr9:95675274-95675324	ovcar-3	ovarian:	n/a
16	chr9:95675546-95675596	HEK293	kidney:	embryo
17	chr9:95675546-95675596	AG10803	skin:	n/a
18	chr9:95678583-95678633	RPTEC	kidney:	n/a
19	chr9:95678583-95678633	NHDF-neo	bronchial:	n/a
20	chr9:95675546-95675596	NH-A	brain:	n/a
21	chr9:95678583-95678633	NT2-D1	testis:	n/a
22	chr9:95678583-95678633	Caco-2	colon:	n/a
23	chr9:95675546-95675596	H1-hESC	embryonic stem cell:	embryo
24	chr9:95678583-95678633	HCPEpiC	choroid plexus:	n/a
25	chr9:95675546-95675596	GM06990	blood:	n/a
26	chr9:95675274-95675324	HMEC	breast:	n/a
27	chr9:95675546-95675596	HMEC	breast:	n/a
28	chr9:95678583-95678633	H1-hESC	embryonic stem cell:	embryo
29	chr9:95678583-95678633	BJ	skin:	n/a
30	chr9:95678583-95678633	PANC-1	pancreas:	n/a
31	chr9:95675274-95675324	AG04450	lung:	fetal
32	chr9:95675546-95675596	BJ	skin:	n/a
33	chr9:95678583-95678633	GM12891	blood:	n/a
34	chr9:95675546-95675596	AG04450	lung:	fetal
35	chr9:95675546-95675596	AoSMC	blood vessel:	n/a
36	chr9:95675274-95675324	GM19239	blood:	n/a
37	chr9:95675546-95675596	ovcar-3	ovarian:	n/a
38	chr9:95678583-95678633	NHBE	bronchial:	n/a
39	chr9:95675546-95675596	NHBE	bronchial:	n/a
40	chr9:95675274-95675324	H1-hESC	embryonic stem cell:	embryo
41	chr9:95675274-95675324	BE2_C	brain:	n/a
42	chr9:95678583-95678633	T-47D	breast:	n/a
43	chr9:95675274-95675324	HCPEpiC	choroid plexus:	n/a
44	chr9:95678583-95678633	GM12892	blood:	n/a
45	chr9:95678583-95678633	MCF-7	breast:	n/a
46	chr9:95675546-95675596	ECC-1	luminal epithelium:	n/a
47	chr9:95678583-95678633	ovcar-3	ovarian:	n/a
48	chr9:95675274-95675324	T-47D	breast:	n/a
49	chr9:95675274-95675324	AG09319	gingival:	n/a
50	chr9:95675274-95675324	U87	brain:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:95684419..95686072-chr9:95691628..95694362,2	MCF-7	breast:
2	chr9:95677020..95680081-chr9:95681150..95683718,3	MCF-7	breast:
3	chr9:95675676..95677800-chr9:95688606..95691210,2	MCF-7	breast:
4	chr9:95677020..95680081-chr9:95681150..95683718,3	MCF-7	breast:
5	chr9:95672518..95675002-chr9:95676684..95678735,2	MCF-7	breast:
6	chr9:95672518..95675002-chr9:95676684..95678735,2	MCF-7	breast:
7	chr9:95668983..95671268-chr9:95672944..95675033,2	K562	blood:
8	chr9:95680681..95683680-chr9:95689468..95691855,3	MCF-7	breast:
9	chr9:95680955..95683491-chr9:95687222..95689030,2	K562	blood:
10	chr9:95675136..95677184-chr9:95685005..95687595,2	MCF-7	breast:
11	chr9:95526781..95528975-chr9:95672458..95674391,2	MCF-7	breast:

No data

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

Extended variants
information (count: 458 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:458 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529630246	chr9:95672464-95672465	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs548171795	chr9:95672525-95672526	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs574614746	chr9:95672555-95672556	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs535754735	chr9:95672576-95672577	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs79660423	chr9:95672626-95672627	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs554166571	chr9:95672699-95672700	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs527597273	chr9:95672703-95672704	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs184509517	chr9:95672741-95672742	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs375445608	chr9:95672752-95672753	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs188895002	chr9:95672769-95672770	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548271965	chr9:95672791-95672792	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs569850841	chr9:95672840-95672841	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs80262263	chr9:95672855-95672856	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs535233235	chr9:95672879-95672880	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs191816237	chr9:95672881-95672882	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs575078494	chr9:95672901-95672902	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs541815811	chr9:95672923-95672924	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs138373206	chr9:95672950-95672951	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs552312126	chr9:95672951-95672952	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs565047266	chr9:95672980-95672981	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs546296926	chr9:95673031-95673032	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183893588	chr9:95673086-95673087	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532174161	chr9:95673089-95673090	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541243074	chr9:95673150-95673151	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs142472794	chr9:95673158-95673159	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs146981827	chr9:95673239-95673240	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs548230293	chr9:95673251-95673252	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs189532531	chr9:95673275-95673276	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530453414	chr9:95673315-95673316	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551843541	chr9:95673346-95673347	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs200612998	chr9:95673362-95673363	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs547330742	chr9:95673370-95673371	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs564609981	chr9:95673372-95673373	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs60023125	chr9:95673390-95673391	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs576562927	chr9:95673420-95673421	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs57248419	chr9:95673493-95673494	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs547178845	chr9:95673545-95673546	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs138060038	chr9:95673735-95673736	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs75544512	chr9:95673746-95673747	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs536142472	chr9:95673803-95673804	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs4744153	chr9:95673804-95673805	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs77651851	chr9:95673805-95673806	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs547326694	chr9:95673871-95673872	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs149511398	chr9:95673897-95673898	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs558256164	chr9:95673911-95673912	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs547695732	chr9:95673919-95673920	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs371576144	chr9:95673924-95673925	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs573291402	chr9:95673931-95673932	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs144105606	chr9:95673969-95673970	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs35159409	chr9:95673982-95673983	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS	TF binding region Chromatin interactive region	2 gene(s)	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:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:95673000-95673200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr9:95673000-95675000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr9:95673400-95673800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr9:95673400-95674400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr9:95673600-95674000	Enhancers	A549	lung
6	chr9:95673600-95674200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
7	chr9:95673600-95674600	Enhancers	Fetal Lung	lung
8	chr9:95673600-95675000	Enhancers	Fetal Stomach	stomach
9	chr9:95673800-95674000	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr9:95673800-95674000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
11	chr9:95673800-95674000	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
12	chr9:95673800-95674000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
13	chr9:95673800-95674000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr9:95673800-95674000	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
15	chr9:95673800-95674000	Enhancers	Brain Germinal Matrix	brain
16	chr9:95673800-95674000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
17	chr9:95673800-95674000	Bivalent Enhancer	NH-A	brain
18	chr9:95673800-95674200	Enhancers	Brain Hippocampus Middle	brain
19	chr9:95673800-95674200	Enhancers	Fetal Kidney	kidney
20	chr9:95673800-95674200	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
21	chr9:95673800-95674400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
22	chr9:95673800-95674400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr9:95673800-95674400	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr9:95673800-95674400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr9:95673800-95674400	Enhancers	Hela-S3	cervix
26	chr9:95673800-95674600	Enhancers	Adipose Nuclei	Adipose
27	chr9:95673800-95674600	Enhancers	Brain Anterior Caudate	brain
28	chr9:95673800-95674600	Bivalent Enhancer	Stomach Mucosa	stomach
29	chr9:95673800-95674800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr9:95673800-95674800	Enhancers	Liver	Liver
31	chr9:95673800-95674800	Enhancers	Colonic Mucosa	Colon
32	chr9:95673800-95674800	Enhancers	HepG2	liver
33	chr9:95673800-95675000	Enhancers	Gastric	stomach
34	chr9:95673800-95675200	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr9:95674000-95674200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
36	chr9:95674000-95674400	Bivalent Enhancer	Brain Cingulate Gyrus	brain
37	chr9:95674000-95674400	Active TSS	Brain Substantia Nigra	brain
38	chr9:95674000-95674400	Flanking Active TSS	A549	lung
39	chr9:95674000-95674600	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr9:95674000-95674600	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
41	chr9:95674000-95674800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr9:95674000-95674800	Enhancers	Ovary	ovary
43	chr9:95674000-95674800	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr9:95674000-95675000	Enhancers	Pancreas	Pancrea
45	chr9:95674000-95675200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr9:95674200-95674400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
47	chr9:95674200-95674600	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr9:95674200-95674600	Enhancers	Fetal Brain Female	brain
49	chr9:95674200-95674600	Bivalent Enhancer	Fetal Muscle Leg	muscle
50	chr9:95674400-95674600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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