Variant report

Variant	nsv892597
Chromosome Location	chr9:14163383-14233159
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:14179625-14179721	HepG2	liver:	n/a	n/a
2	ARID3A	chr9:14213525-14213725	HepG2	liver:	n/a	n/a
3	BRCA1	chr9:14178829-14178846	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr9:14221572-14221947	ECC-1	luminal epithelium:	n/a	chr9:14221755-14221768
5	CEBPB	chr9:14165805-14166100	IMR90	lung:	n/a	chr9:14165924-14165935
6	CEBPB	chr9:14222198-14222504	H1-hESC	embryonic stem cell:	n/a	chr9:14222335-14222352
7	CEBPB	chr9:14221536-14221962	MCF-7	breast:	n/a	chr9:14221755-14221768
8	CEBPB	chr9:14215550-14216153	A549	lung:	n/a	n/a
9	CEBPB	chr9:14175873-14176095	HepG2	liver:	n/a	chr9:14175990-14176001 chr9:14175989-14176002
10	CEBPB	chr9:14221397-14222104	A549	lung:	n/a	chr9:14221755-14221768
11	CEBPB	chr9:14165927-14165989	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr9:14165711-14166096	ECC-1	luminal epithelium:	n/a	chr9:14165924-14165935
13	CEBPB	chr9:14221529-14222062	MCF-7	breast:	n/a	chr9:14221755-14221768
14	CEBPB	chr9:14198428-14198626	HepG2	liver:	n/a	chr9:14198556-14198567 chr9:14198554-14198565
15	CEBPB	chr9:14205407-14205944	A549	lung:	n/a	chr9:14205641-14205653
16	CEBPB	chr9:14221406-14222505	Hela-S3	cervix:	n/a	chr9:14222335-14222352 chr9:14221755-14221768
17	CEBPB	chr9:14215842-14216031	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr9:14205523-14205859	A549	lung:	n/a	chr9:14205641-14205653
19	CEBPB	chr9:14165742-14166077	Hela-S3	cervix:	n/a	chr9:14165924-14165935
20	CEBPB	chr9:14179824-14179864	H1-hESC	embryonic stem cell:	n/a	chr9:14179829-14179840
21	CEBPB	chr9:14215703-14216037	MCF-7	breast:	n/a	n/a
22	CEBPB	chr9:14188183-14188210	K562	blood:	n/a	chr9:14188196-14188207 chr9:14188196-14188209 chr9:14188198-14188209 chr9:14188196-14188209
23	CEBPB	chr9:14215661-14216040	A549	lung:	n/a	n/a
24	CEBPB	chr9:14212117-14212457	IMR90	lung:	n/a	n/a
25	CEBPB	chr9:14164243-14164443	HepG2	liver:	n/a	n/a
26	CEBPB	chr9:14222175-14222547	ECC-1	luminal epithelium:	n/a	chr9:14222335-14222352 chr9:14222497-14222510
27	CEBPB	chr9:14215666-14216071	IMR90	lung:	n/a	n/a
28	CEBPB	chr9:14184102-14184384	K562	blood:	n/a	chr9:14184256-14184267
29	CEBPB	chr9:14165760-14166100	HepG2	liver:	n/a	chr9:14165924-14165935
30	CEBPB	chr9:14173264-14173475	HepG2	liver:	n/a	chr9:14173346-14173357
31	CEBPB	chr9:14179672-14179995	IMR90	lung:	n/a	chr9:14179829-14179840
32	CEBPB	chr9:14170904-14171247	A549	lung:	n/a	n/a
33	CEBPB	chr9:14184145-14184422	Hela-S3	cervix:	n/a	chr9:14184256-14184267
34	CEBPB	chr9:14221242-14221954	A549	lung:	n/a	chr9:14221755-14221768
35	CEBPB	chr9:14215698-14216032	A549	lung:	n/a	n/a
36	CEBPB	chr9:14221226-14221960	IMR90	lung:	n/a	chr9:14221755-14221768
37	CEBPB	chr9:14213511-14213868	A549	lung:	n/a	n/a
38	CEBPB	chr9:14165758-14166093	A549	lung:	n/a	chr9:14165924-14165935
39	CEBPB	chr9:14221517-14222018	A549	lung:	n/a	chr9:14221755-14221768
40	CEBPB	chr9:14184083-14184433	IMR90	lung:	n/a	chr9:14184256-14184267
41	CEBPB	chr9:14184163-14184357	H1-hESC	embryonic stem cell:	n/a	chr9:14184256-14184267
42	CEBPB	chr9:14216850-14217153	A549	lung:	n/a	n/a
43	CEBPB	chr9:14215700-14216044	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr9:14221522-14222575	ECC-1	luminal epithelium:	n/a	chr9:14222335-14222352 chr9:14221755-14221768 chr9:14222497-14222510
45	CEBPB	chr9:14170942-14171250	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:14213584-14213839	HepG2	liver:	n/a	n/a
47	CEBPB	chr9:14216742-14217223	A549	lung:	n/a	chr9:14216768-14216779
48	CEBPB	chr9:14179755-14179917	K562	blood:	n/a	chr9:14179829-14179840
49	CEBPB	chr9:14188121-14188244	HepG2	liver:	n/a	chr9:14188196-14188207 chr9:14188196-14188209 chr9:14188198-14188209 chr9:14188196-14188209
50	CEBPB	chr9:14205499-14205786	A549	lung:	n/a	chr9:14205641-14205653

No.	Distal block	Cell Line	Cell type
1	chr9:14213715..14216528-chr9:14218687..14222056,3	K562	blood:
2	chr9:14180541..14184155-chr9:14313790..14316409,3	MCF-7	breast:
3	chr9:14163618..14165126-chr9:14226393..14229305,2	K562	blood:
4	chr9:14228943..14231168-chr9:14236666..14238906,2	MCF-7	breast:
5	chr9:14185623..14188206-chr9:14197745..14200671,2	MCF-7	breast:
6	chr9:14211963..14213596-chr9:14216891..14219507,2	K562	blood:
7	chr9:14203657..14206657-chr9:14311874..14315004,3	MCF-7	breast:
8	chr9:14197932..14199524-chr9:14315702..14317595,2	MCF-7	breast:
9	chr9:14215028..14217662-chr9:14219597..14221108,2	K562	blood:
10	chr9:14162427..14164558-chr9:14167650..14169724,2	MCF-7	breast:
11	chr9:14183906..14185833-chr9:14191618..14193505,2	K562	blood:
12	chr9:14200461..14204358-chr9:14312033..14315867,4	MCF-7	breast:
13	chr9:14207480..14210173-chr9:14216530..14218374,2	MCF-7	breast:
14	chr9:14157830..14160337-chr9:14162200..14164831,2	MCF-7	breast:
15	chr9:14198108..14200232-chr9:14207218..14209041,2	MCF-7	breast:
16	chr9:14207480..14210173-chr9:14216530..14218374,2	MCF-7	breast:
17	chr9:14207609..14210437-chr9:14312286..14315152,2	MCF-7	breast:
18	chr9:14198598..14200536-chr9:14204416..14206854,2	MCF-7	breast:
19	chr9:14231753..14233744-chr9:14314125..14316304,2	MCF-7	breast:
20	chr9:14198598..14200536-chr9:14204416..14206854,2	MCF-7	breast:
21	chr9:14179037..14181363-chr9:14186626..14189533,2	K562	blood:
22	chr9:14211963..14213596-chr9:14216891..14219507,2	K562	blood:
23	chr9:14213715..14216528-chr9:14218687..14222056,3	K562	blood:
24	chr9:14171238..14174758-chr9:14313381..14316374,3	MCF-7	breast:
25	chr9:14215028..14217662-chr9:14219597..14221108,2	K562	blood:
26	chr9:14220500..14222113-chr9:14225343..14228147,2	MCF-7	breast:
27	chr9:14218690..14221524-chr9:14235018..14237230,2	MCF-7	breast:
28	chr9:14220500..14222113-chr9:14225343..14228147,2	MCF-7	breast:
29	chr9:14163618..14165126-chr9:14226393..14229305,2	K562	blood:
30	chr9:14198108..14200232-chr9:14207218..14209041,2	MCF-7	breast:
31	chr9:14231565..14234116-chr9:14237847..14240047,2	MCF-7	breast:
32	chr9:14180288..14182933-chr9:14314004..14316162,2	MCF-7	breast:
33	chr9:14185623..14188206-chr9:14197745..14200671,2	MCF-7	breast:
34	chr9:14223793..14226601-chr9:14227808..14230396,2	MCF-7	breast:
35	chr9:14228061..14230332-chr9:14313117..14314724,2	MCF-7	breast:
36	chr9:14214360..14220386-chr9:14311987..14316578,6	MCF-7	breast:
37	chr9:14182648..14184578-chr9:14311573..14313374,2	K562	blood:
38	chr9:14183906..14185833-chr9:14191618..14193505,2	K562	blood:
39	chr9:14223793..14226601-chr9:14227808..14230396,2	MCF-7	breast:
40	chr9:14162427..14164558-chr9:14167650..14169724,2	MCF-7	breast:

Variant related genes	Relation type
NFIB	TF binding region
ENSG00000234982	TF binding region
ENSG00000147862	chromatin interactions
ENSG00000225472	chromatin interactions

Extended variants
information (count: 3178 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:3178 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12156582	chr9:14163383-14163384	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546012948	chr9:14163460-14163461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs12156460	chr9:14163477-14163478	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs567431085	chr9:14163502-14163503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs542064028	chr9:14163503-14163504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535218191	chr9:14163504-14163505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192739614	chr9:14163509-14163510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs563845973	chr9:14163527-14163528	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs527622090	chr9:14163552-14163553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7047737	chr9:14163594-14163595	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs185532644	chr9:14163596-14163597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111335987	chr9:14163614-14163615	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529584286	chr9:14163663-14163664	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552759249	chr9:14163667-14163668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs549447019	chr9:14163678-14163679	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs190734725	chr9:14163685-14163686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs62532513	chr9:14163689-14163690	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs535113441	chr9:14163701-14163702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181670685	chr9:14163713-14163714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568764540	chr9:14163744-14163745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs7033653	chr9:14163754-14163755	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs142464967	chr9:14163766-14163767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs548597946	chr9:14163859-14163860	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577526534	chr9:14163880-14163881	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs13299433	chr9:14163888-14163889	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs111884374	chr9:14163896-14163897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs28379954	chr9:14163907-14163908	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs576347123	chr9:14163944-14163945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs28546939	chr9:14163950-14163951	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs149095980	chr9:14163999-14164000	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs561794334	chr9:14164003-14164004	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs571988390	chr9:14164019-14164020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540961074	chr9:14164048-14164049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs563905683	chr9:14164050-14164051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs79401929	chr9:14164076-14164077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs10810100	chr9:14164100-14164101	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs10961398	chr9:14164148-14164149	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs10738354	chr9:14164151-14164152	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs548974649	chr9:14164153-14164154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs184391637	chr9:14164167-14164168	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs118079438	chr9:14164187-14164188	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs576150920	chr9:14164218-14164219	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10810101	chr9:14164224-14164225	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs35559875	chr9:14164225-14164226	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs10961399	chr9:14164250-14164251	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs570981011	chr9:14164279-14164280	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189154280	chr9:14164285-14164286	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs181082283	chr9:14164296-14164297	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576458205	chr9:14164321-14164322	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs535973739	chr9:14164328-14164329	Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

Disease	PMID	Source
Lung cancer	16740712	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Breast cancer	21364760	CNVD
Glioblastoma	19074898	CNVD
Malignant melanoma	19074898	CNVD
Prostate cancer	16573809	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Glioma	17123091	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Gastric cancer	16891809	CNVD
Mental retardation	17847001	CNVD
Cutaneous squamous cell carcinomas	17420988	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21611746	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Glycine encephalopathy	21572526	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Renal cell carcinoma	21215367	CNVD
Cancer	21215367	CNVD

Chromatin state (count:1816 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:14116600-14179200	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr9:14117000-14171200	Weak transcription	Hela-S3	cervix
3	chr9:14123800-14198600	Weak transcription	Gastric	stomach
4	chr9:14131800-14173200	Weak transcription	Pancreas	Pancrea
5	chr9:14134000-14181000	Weak transcription	Ovary	ovary
6	chr9:14156800-14175600	Weak transcription	Liver	Liver
7	chr9:14157400-14164400	Weak transcription	Fetal Brain Male	brain
8	chr9:14157600-14173600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr9:14159600-14164200	Weak transcription	Brain Anterior Caudate	brain
10	chr9:14159600-14164400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr9:14159800-14164200	Weak transcription	HMEC	breast
12	chr9:14159800-14164800	Weak transcription	Psoas Muscle	Psoas
13	chr9:14159800-14164800	Weak transcription	Right Ventricle	heart
14	chr9:14159800-14165000	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr9:14159800-14167200	Weak transcription	Left Ventricle	heart
16	chr9:14159800-14169200	Weak transcription	Aorta	Aorta
17	chr9:14159800-14176600	Weak transcription	Fetal Muscle Trunk	muscle
18	chr9:14159800-14180200	Weak transcription	Fetal Stomach	stomach
19	chr9:14160000-14164200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr9:14160000-14164200	Weak transcription	NHEK	skin
21	chr9:14160000-14164400	Weak transcription	Brain Substantia Nigra	brain
22	chr9:14160000-14164800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr9:14160000-14168200	Weak transcription	Fetal Muscle Leg	muscle
24	chr9:14160000-14169600	Weak transcription	Right Atrium	heart
25	chr9:14160200-14164200	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr9:14160200-14164400	Weak transcription	Brain Angular Gyrus	brain
27	chr9:14160200-14164800	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr9:14160200-14165200	Weak transcription	Fetal Brain Female	brain
29	chr9:14160400-14164200	Weak transcription	Brain Hippocampus Middle	brain
30	chr9:14160600-14164200	Weak transcription	Brain Inferior Temporal Lobe	brain
31	chr9:14160600-14164200	Weak transcription	Fetal Heart	heart
32	chr9:14160600-14164200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr9:14160600-14164400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr9:14160600-14164400	Weak transcription	Brain Cingulate Gyrus	brain
35	chr9:14160600-14165000	Weak transcription	Brain Germinal Matrix	brain
36	chr9:14160600-14165000	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr9:14160600-14181400	Weak transcription	HSMM	muscle
38	chr9:14160800-14165200	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr9:14161000-14164800	Weak transcription	A549	lung
40	chr9:14161000-14170600	Weak transcription	HUVEC	blood vessel
41	chr9:14162000-14164200	Weak transcription	Small Intestine	intestine
42	chr9:14162000-14170200	Weak transcription	Adipose Nuclei	Adipose
43	chr9:14162200-14164200	Weak transcription	Fetal Lung	lung
44	chr9:14162400-14175400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr9:14162600-14164200	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr9:14162600-14164200	Weak transcription	Colon Smooth Muscle	Colon
47	chr9:14163200-14164600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr9:14164200-14164600	Enhancers	Small Intestine	intestine
49	chr9:14164200-14164800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr9:14164200-14165000	Enhancers	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links