Variant report

Variant	nsv1047465
Chromosome Location	chr9:98217524-98228225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:395)
CpG islands
(count:122)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:395 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:98224854-98225426	K562	blood:	n/a	n/a
2	ATF1	chr9:98224654-98225251	K562	blood:	n/a	n/a
3	ATF2	chr9:98224649-98225239	GM12878	blood:	n/a	n/a
4	ATF2	chr9:98224457-98225273	GM12878	blood:	n/a	n/a
5	ATF3	chr9:98224774-98225257	K562	blood:	n/a	n/a
6	BACH1	chr9:98227166-98227236	K562	blood:	n/a	n/a
7	BACH1	chr9:98224894-98225069	K562	blood:	n/a	n/a
8	BATF	chr9:98224831-98225171	GM12878	blood:	n/a	n/a
9	BATF	chr9:98224780-98225220	GM12878	blood:	n/a	n/a
10	BCL11A	chr9:98224740-98225225	GM12878	blood:	n/a	chr9:98225195-98225204
11	BCL11A	chr9:98224728-98225264	GM12878	blood:	n/a	chr9:98225195-98225204
12	BCL3	chr9:98224832-98225231	GM12878	blood:	n/a	chr9:98225195-98225204
13	BCL3	chr9:98224804-98225467	K562	blood:	n/a	chr9:98225195-98225204
14	BCLAF1	chr9:98224502-98225248	GM12878	blood:	n/a	chr9:98225195-98225204
15	BCLAF1	chr9:98224534-98225309	GM12878	blood:	n/a	chr9:98225195-98225204
16	BHLHE40	chr9:98223976-98224105	K562	blood:	n/a	n/a
17	BHLHE40	chr9:98224564-98225398	K562	blood:	n/a	n/a
18	BHLHE40	chr9:98224478-98225574	GM12878	blood:	n/a	n/a
19	CBX3	chr9:98224396-98225508	K562	blood:	n/a	n/a
20	CBX3	chr9:98224692-98225259	K562	blood:	n/a	n/a
21	CCNT2	chr9:98224778-98225492	K562	blood:	n/a	chr9:98225171-98225191 chr9:98225271-98225280
22	CEBPB	chr9:98221567-98221811	IMR90	lung:	n/a	n/a
23	CEBPB	chr9:98224804-98225223	GM12878	blood:	n/a	n/a
24	CEBPB	chr9:98224783-98225209	K562	blood:	n/a	n/a
25	CEBPB	chr9:98219991-98220380	IMR90	lung:	n/a	chr9:98220176-98220193 chr9:98220177-98220190
26	CEBPB	chr9:98224660-98225226	GM12878	blood:	n/a	n/a
27	CEBPB	chr9:98224798-98225320	K562	blood:	n/a	n/a
28	CEBPD	chr9:98224818-98225434	K562	blood:	n/a	n/a
29	CEBPD	chr9:98224641-98225442	K562	blood:	n/a	n/a
30	CHD1	chr9:98224386-98225214	GM12878	blood:	n/a	n/a
31	CHD1	chr9:98225475-98225550	GM12878	blood:	n/a	n/a
32	CHD2	chr9:98224930-98225160	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr9:98224440-98225583	GM12878	blood:	n/a	chr9:98225271-98225281
34	CHD2	chr9:98224863-98225284	K562	blood:	n/a	chr9:98225271-98225281
35	CREB1	chr9:98224682-98225302	GM12878	blood:	n/a	n/a
36	CREB1	chr9:98224680-98225316	K562	blood:	n/a	n/a
37	CTCF	chr9:98224820-98224970	AG10803	skin:	n/a	n/a
38	CTCF	chr9:98223060-98223210	AG09319	gingival:	n/a	n/a
39	CTCF	chr9:98222820-98222970	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr9:98223886-98223985	K562	blood:	n/a	n/a
41	CTCF	chr9:98221860-98222010	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr9:98224774-98225209	K562	blood:	n/a	n/a
43	CTCF	chr9:98224873-98224943	GM12892	blood:	n/a	n/a
44	CTCF	chr9:98224780-98224930	BE2_C	brain:	n/a	n/a
45	CTCF	chr9:98223160-98223310	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr9:98223000-98223150	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr9:98224533-98225121	GM12878	blood:	n/a	n/a
48	CTCF	chr9:98224520-98224670	GM12871	blood:	n/a	n/a
49	CTCF	chr9:98222860-98223010	AG09319	gingival:	n/a	n/a
50	CTCF	chr9:98224760-98224910	HCPEpiC	choroid plexus:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:98221975-98222025	HUVEC	blood vessel:	n/a
2	chr9:98221619-98221669	HEEpiC	esophagus:	n/a
3	chr9:98221619-98221669	NH-A	brain:	n/a
4	chr9:98221975-98222025	HPAEpiC	pulmonary alveolar:	n/a
5	chr9:98221975-98222025	Hela-S3	cervix:	n/a
6	chr9:98221619-98221669	SK-N-SH_RA	brain:	n/a
7	chr9:98221975-98222025	ProgFib	skin:	n/a
8	chr9:98221619-98221669	PFSK-1	brain:	n/a
9	chr9:98221619-98221669	ECC-1	luminal epithelium:	n/a
10	chr9:98221975-98222025	U87	brain:	n/a
11	chr9:98221975-98222025	SK-N-MC	brain:	n/a
12	chr9:98221975-98222025	RPTEC	kidney:	n/a
13	chr9:98221975-98222025	SAEC	small airway:	n/a
14	chr9:98221975-98222025	CMK	blood:	n/a
15	chr9:98221619-98221669	ProgFib	skin:	n/a
16	chr9:98221975-98222025	SKMC	muscle:	n/a
17	chr9:98221975-98222025	H1-hESC	embryonic stem cell:	embryo
18	chr9:98221619-98221669	HL-60	blood:	n/a
19	chr9:98221619-98221669	HCT-116	colon:	n/a
20	chr9:98221975-98222025	MCF-7	breast:	n/a
21	chr9:98221975-98222025	GM19239	blood:	n/a
22	chr9:98221975-98222025	SK-N-SH	brain:	n/a
23	chr9:98221975-98222025	Hepatocyte	liver:	n/a
24	chr9:98221619-98221669	SK-N-MC	brain:	n/a
25	chr9:98221619-98221669	GM12878	blood:	n/a
26	chr9:98221619-98221669	T-47D	breast:	n/a
27	chr9:98221619-98221669	U87	brain:	n/a
28	chr9:98221619-98221669	Hepatocyte	liver:	n/a
29	chr9:98221619-98221669	HepG2	liver:	n/a
30	chr9:98221975-98222025	MCF10A-Er-Src	breast:	n/a
31	chr9:98221975-98222025	AG04449	skin:	fetal
32	chr9:98221975-98222025	NHBE	bronchial:	n/a
33	chr9:98221619-98221669	Jurkat	blood:	n/a
34	chr9:98221619-98221669	CMK	blood:	n/a
35	chr9:98221975-98222025	GM12891	blood:	n/a
36	chr9:98221619-98221669	A549	lung:	n/a
37	chr9:98221975-98222025	AG04450	lung:	fetal
38	chr9:98221975-98222025	NH-A	brain:	n/a
39	chr9:98221975-98222025	HCT-116	colon:	n/a
40	chr9:98221975-98222025	PrEC	prostate:	n/a
41	chr9:98221619-98221669	NHDF-neo	bronchial:	n/a
42	chr9:98221619-98221669	GM12892	blood:	n/a
43	chr9:98221619-98221669	AG04450	lung:	fetal
44	chr9:98221619-98221669	AoSMC	blood vessel:	n/a
45	chr9:98221619-98221669	HCPEpiC	choroid plexus:	n/a
46	chr9:98221619-98221669	HPAEpiC	pulmonary alveolar:	n/a
47	chr9:98221975-98222025	NT2-D1	testis:	n/a
48	chr9:98221975-98222025	NHDF-neo	bronchial:	n/a
49	chr9:98221975-98222025	AG09309	skin:	n/a
50	chr9:98221975-98222025	IMR90	lung:	fetal

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:98227321..98228997-chr9:98229888..98232177,2	K562	blood:
2	chr9:98077820..98081322-chr9:98214829..98218712,4	K562	blood:
3	chr12:53297243..53298949-chr9:98222802..98225552,2	MCF-7	breast:
4	chr9:98222888..98225027-chr9:98277335..98280257,3	K562	blood:
5	chr9:98211125..98213950-chr9:98219693..98221314,2	MCF-7	breast:
6	chr9:98218910..98222494-chr9:98224731..98227835,5	K562	blood:
7	chr9:98187259..98193172-chr9:98208629..98217669,12	MCF-7	breast:
8	chr9:98222216..98224760-chr9:98225950..98227870,2	MCF-7	breast:
9	chr9:98218003..98222058-chr9:98271885..98274474,3	K562	blood:
10	chr9:98223555..98229775-chr9:98269693..98275962,10	K562	blood:
11	chr9:98187807..98190501-chr9:98217714..98219257,2	MCF-7	breast:
12	chr9:98209521..98214013-chr9:98214744..98218073,4	K562	blood:
13	chr9:98228127..98229820-chr9:98239088..98240889,2	K562	blood:
14	chr9:98218196..98221051-chr9:98231021..98232882,2	K562	blood:
15	chr9:98195732..98198631-chr9:98215123..98217873,2	K562	blood:
16	chr9:98223181..98225027-chr9:98277335..98280257,2	K562	blood:
17	chr9:98199109..98200665-chr9:98217953..98219861,2	K562	blood:
18	chr9:98227014..98229023-chr9:98271434..98274318,2	MCF-7	breast:
19	chr9:98223864..98226761-chr9:98228381..98231062,3	K562	blood:
20	chr9:98222977..98229750-chr9:98267050..98274823,12	K562	blood:
21	chr9:98223412..98227347-chr9:98253313..98257210,3	K562	blood:
22	chr9:98214310..98216415-chr9:98227721..98230889,3	MCF-7	breast:

No data

Variant related genes	Relation type
PTCH1	TF binding region
PTCH1	CpG island
ENSG00000158169	chromatin interactions
ENSG00000185920	chromatin interactions
ENSG00000237857	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000271155	chromatin interactions
ENSG00000271314	chromatin interactions

Extended variants
information (count: 469 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:469 , 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	rs28701981	chr9:98217581-98217582	Enhancers Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79036813	chr9:98217610-98217611	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs374162800	chr9:98217635-98217636	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs146408848	chr9:98217651-98217652	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs188389505	chr9:98217658-98217659	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs551852440	chr9:98217675-98217676	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs368443462	chr9:98217689-98217690	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs139811231	chr9:98217700-98217701	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs28390100	chr9:98217724-98217725	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs79867865	chr9:98217744-98217745	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs538183457	chr9:98217757-98217758	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs371690127	chr9:98217771-98217772	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs556305667	chr9:98217772-98217773	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs578140958	chr9:98217777-98217778	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs116837586	chr9:98217789-98217790	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs374868827	chr9:98217798-98217799	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs572088966	chr9:98217801-98217802	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs542643294	chr9:98217858-98217859	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs180923140	chr9:98217899-98217900	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs564105830	chr9:98217913-98217914	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs185971006	chr9:98218010-98218011	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs543758795	chr9:98218040-98218041	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs73542167	chr9:98218041-98218042	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs532345763	chr9:98218042-98218043	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs547316505	chr9:98218052-98218053	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs143207512	chr9:98218076-98218077	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs527808531	chr9:98218152-98218153	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs548952211	chr9:98218181-98218182	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs567339257	chr9:98218206-98218207	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs192051313	chr9:98218219-98218220	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs550065677	chr9:98218234-98218235	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs73654562	chr9:98218242-98218243	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs539216692	chr9:98218251-98218252	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs554120129	chr9:98218312-98218313	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs572087404	chr9:98218314-98218315	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs536366657	chr9:98218391-98218392	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs554575416	chr9:98218442-98218443	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs576107587	chr9:98218446-98218447	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs531236471	chr9:98218474-98218475	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs5899258	chr9:98218475-98218476	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs201186714	chr9:98218476-98218477	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs151321835	chr9:98218486-98218487	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs550035984	chr9:98218504-98218505	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs568281763	chr9:98218529-98218530	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs565175725	chr9:98218548-98218549	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs577110118	chr9:98218566-98218567	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs141016655	chr9:98218573-98218574	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs150217389	chr9:98218602-98218603	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs201094264	chr9:98218612-98218613	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs202052415	chr9:98218617-98218618	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	Chromatin interactive region	3 gene(s)	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
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
overgrowth syndrome	16570072	CNVD
Effusion lymphoma	18079361	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Neurodevelopmental disorder	22521361	CNVD
Basal cell carcinoma	21518781	CNVD

Chromatin state (count:898 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:98202000-98224600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:98204400-98220400	Strong transcription	Fetal Intestine Large	intestine
3	chr9:98204800-98224400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr9:98205200-98218000	Weak transcription	Small Intestine	intestine
5	chr9:98206000-98224400	Weak transcription	HUVEC	blood vessel
6	chr9:98206000-98237600	Weak transcription	Psoas Muscle	Psoas
7	chr9:98206200-98221400	Strong transcription	Fetal Intestine Small	intestine
8	chr9:98206400-98217600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr9:98206400-98218400	Weak transcription	NHEK	skin
10	chr9:98206600-98220200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr9:98206600-98220200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr9:98206600-98220400	Strong transcription	Duodenum Mucosa	Duodenum
13	chr9:98206600-98221200	Strong transcription	Brain Hippocampus Middle	brain
14	chr9:98206600-98223000	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr9:98206600-98224000	Strong transcription	Adipose Nuclei	Adipose
16	chr9:98206600-98224600	Strong transcription	Aorta	Aorta
17	chr9:98206600-98225200	Strong transcription	Pancreas	Pancrea
18	chr9:98206800-98219200	Strong transcription	Gastric	stomach
19	chr9:98207000-98221000	Strong transcription	Rectal Mucosa Donor 31	rectum
20	chr9:98207000-98221800	Strong transcription	Ovary	ovary
21	chr9:98207000-98223000	Strong transcription	Primary T cells fromperipheralblood	blood
22	chr9:98207200-98219400	Strong transcription	Brain Substantia Nigra	brain
23	chr9:98207200-98223200	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr9:98207200-98224400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr9:98207400-98224200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
26	chr9:98207600-98224400	Strong transcription	Skeletal Muscle Male	skeletal muscle
27	chr9:98208000-98224400	Weak transcription	HSMM	muscle
28	chr9:98208400-98220000	Weak transcription	NH-A	brain
29	chr9:98208600-98224000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
30	chr9:98209200-98219000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:98209200-98220200	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr9:98209400-98218200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr9:98209400-98222600	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr9:98209600-98218000	Weak transcription	Pancreatic Islets	Pancreatic Islet
35	chr9:98209600-98224000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr9:98209600-98224400	Weak transcription	NHDF-Ad	bronchial
37	chr9:98209800-98219800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr9:98210000-98218400	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr9:98210400-98223800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr9:98210600-98221800	Strong transcription	Brain Cingulate Gyrus	brain
41	chr9:98210800-98221200	Strong transcription	Fetal Muscle Leg	muscle
42	chr9:98210800-98221800	Strong transcription	Fetal Muscle Trunk	muscle
43	chr9:98211200-98224200	Strong transcription	Left Ventricle	heart
44	chr9:98211400-98224600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
45	chr9:98211600-98218200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr9:98211800-98218200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr9:98211800-98222600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr9:98212000-98224600	Strong transcription	Skeletal Muscle Female	skeletal muscle
49	chr9:98212200-98217600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr9:98212400-98220400	Weak transcription	Hela-S3	cervix

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