Variant report

Variant	nsv539349
Chromosome Location	chr8:3015881-3159246
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:683)
CpG islands
(count:610)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:683 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:3141618-3141628	K562	blood:	n/a	n/a
2	ARID3A	chr8:3040106-3041476	K562	blood:	n/a	n/a
3	ARID3A	chr8:3086380-3086594	K562	blood:	n/a	n/a
4	ARID3A	chr8:3038551-3038716	K562	blood:	n/a	n/a
5	ATF1	chr8:3040555-3041348	K562	blood:	n/a	n/a
6	ATF2	chr8:3102629-3103169	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr8:3102725-3103166	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr8:3029134-3029226	K562	blood:	n/a	n/a
9	BACH1	chr8:3053456-3053567	K562	blood:	n/a	n/a
10	BCL11A	chr8:3102751-3103131	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr8:3041030-3041434	K562	blood:	n/a	n/a
12	BHLHE40	chr8:3038381-3038540	K562	blood:	n/a	n/a
13	BHLHE40	chr8:3016188-3016208	K562	blood:	n/a	n/a
14	BHLHE40	chr8:3142129-3142341	GM12878	blood:	n/a	n/a
15	BHLHE40	chr8:3021027-3021615	K562	blood:	n/a	n/a
16	BHLHE40	chr8:3086290-3086714	K562	blood:	n/a	n/a
17	BHLHE40	chr8:3040394-3040793	K562	blood:	n/a	n/a
18	BRCA1	chr8:3142211-3142538	Hela-S3	cervix:	n/a	chr8:3142419-3142426
19	CBX3	chr8:3040352-3041356	K562	blood:	n/a	n/a
20	CBX3	chr8:3040455-3041321	K562	blood:	n/a	n/a
21	CCNT2	chr8:3086362-3086710	K562	blood:	n/a	n/a
22	CEBPB	chr8:3087872-3088071	HepG2	liver:	n/a	chr8:3087984-3087995
23	CEBPB	chr8:3086425-3086769	K562	blood:	n/a	n/a
24	CEBPB	chr8:3030493-3030781	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr8:3120563-3120733	HepG2	liver:	n/a	chr8:3120612-3120623
26	CEBPB	chr8:3119754-3120007	A549	lung:	n/a	n/a
27	CEBPB	chr8:3030465-3030844	K562	blood:	n/a	n/a
28	CEBPB	chr8:3119734-3120051	HepG2	liver:	n/a	n/a
29	CEBPB	chr8:3030503-3030805	A549	lung:	n/a	n/a
30	CEBPB	chr8:3120608-3120683	A549	lung:	n/a	chr8:3120612-3120623
31	CEBPB	chr8:3044874-3045155	K562	blood:	n/a	chr8:3045029-3045042 chr8:3045029-3045042
32	CEBPB	chr8:3028339-3028476	HepG2	liver:	n/a	n/a
33	CEBPB	chr8:3030536-3030806	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr8:3061961-3062119	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr8:3119761-3119974	K562	blood:	n/a	n/a
36	CEBPB	chr8:3030500-3030827	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:3041073-3041386	K562	blood:	n/a	n/a
38	CEBPB	chr8:3101750-3102364	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:3102686-3103382	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr8:3025337-3025339	K562	blood:	n/a	n/a
41	CEBPB	chr8:3078974-3079006	K562	blood:	n/a	n/a
42	CEBPB	chr8:3040459-3041408	K562	blood:	n/a	n/a
43	CEBPD	chr8:3086293-3086755	K562	blood:	n/a	n/a
44	CEBPD	chr8:3086261-3086786	K562	blood:	n/a	n/a
45	CEBPD	chr8:3040404-3041424	K562	blood:	n/a	n/a
46	CHD2	chr8:3051238-3051369	HepG2	liver:	n/a	n/a
47	CHD2	chr8:3142082-3142314	GM12878	blood:	n/a	n/a
48	CHD2	chr8:3102747-3103223	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chr8:3074271-3074891	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr8:3074300-3074852	H1-hESC	embryonic stem cell:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:3016640-3016690	HPAEpiC	pulmonary alveolar:	n/a
2	chr8:3047756-3047806	AG04450	lung:	fetal
3	chr8:3102222-3102272	GM06990	blood:	n/a
4	chr8:3102222-3102272	HAEpiC	amniotic membrane:	n/a
5	chr8:3016640-3016690	BJ	skin:	n/a
6	chr8:3016640-3016690	RPTEC	kidney:	n/a
7	chr8:3047536-3047586	T-47D	breast:	n/a
8	chr8:3046483-3046533	ovcar-3	ovarian:	n/a
9	chr8:3100524-3100574	A549	lung:	n/a
10	chr8:3141844-3141894	HNPCEpiC	eye:	n/a
11	chr8:3102222-3102272	HCF	heart:	n/a
12	chr8:3016640-3016690	SAEC	small airway:	n/a
13	chr8:3100413-3100463	AG04449	skin:	fetal
14	chr8:3016640-3016690	BE2_C	brain:	n/a
15	chr8:3086479-3086529	Hepatocyte	liver:	n/a
16	chr8:3100413-3100463	ProgFib	skin:	n/a
17	chr8:3141844-3141894	HIPEpiC	eye:	n/a
18	chr8:3016640-3016690	AG10803	skin:	n/a
19	chr8:3141907-3141957	BE2_C	brain:	n/a
20	chr8:3047536-3047586	ECC-1	luminal epithelium:	n/a
21	chr8:3016640-3016690	HNPCEpiC	eye:	n/a
22	chr8:3102222-3102272	U87	brain:	n/a
23	chr8:3141844-3141894	ovcar-3	ovarian:	n/a
24	chr8:3141844-3141894	SK-N-SH	brain:	n/a
25	chr8:3016640-3016690	PANC-1	pancreas:	n/a
26	chr8:3102222-3102272	NT2-D1	testis:	n/a
27	chr8:3086479-3086529	ECC-1	luminal epithelium:	n/a
28	chr8:3016640-3016690	HCM	heart:	n/a
29	chr8:3046483-3046533	HCF	heart:	n/a
30	chr8:3100413-3100463	ECC-1	luminal epithelium:	n/a
31	chr8:3102222-3102272	GM12878	blood:	n/a
32	chr8:3141907-3141957	GM12891	blood:	n/a
33	chr8:3047536-3047586	NT2-D1	testis:	n/a
34	chr8:3047536-3047586	Hepatocyte	liver:	n/a
35	chr8:3141907-3141957	H1-hESC	embryonic stem cell:	embryo
36	chr8:3086479-3086529	IMR90	lung:	fetal
37	chr8:3046483-3046533	U87	brain:	n/a
38	chr8:3047536-3047586	AG04449	skin:	fetal
39	chr8:3016640-3016690	A549	lung:	n/a
40	chr8:3100524-3100574	SAEC	small airway:	n/a
41	chr8:3102222-3102272	HPAEpiC	pulmonary alveolar:	n/a
42	chr8:3047536-3047586	RPTEC	kidney:	n/a
43	chr8:3141844-3141894	SK-N-SH_RA	brain:	n/a
44	chr8:3047756-3047806	AG09309	skin:	n/a
45	chr8:3100413-3100463	HCT-116	colon:	n/a
46	chr8:3141844-3141894	ECC-1	luminal epithelium:	n/a
47	chr8:3141844-3141894	LNCaP	prostate:	n/a
48	chr8:3047756-3047806	SKMC	muscle:	n/a
49	chr8:3102222-3102272	HCPEpiC	choroid plexus:	n/a
50	chr8:3100413-3100463	LNCaP	prostate:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:3024774..3027498-chr8:3038626..3041696,3	K562	blood:
2	chr8:3029280..3032071-chr8:3037936..3040025,3	K562	blood:
3	chr8:3121428..3123841-chr8:3126010..3128450,2	K562	blood:
4	chr8:3030633..3032243-chr8:3035809..3037381,2	K562	blood:
5	chr8:3028449..3030172-chr8:3031870..3033947,2	K562	blood:
6	chr8:3038911..3040740-chr8:3044152..3047075,2	K562	blood:
7	chr8:3121428..3123841-chr8:3126010..3128450,2	K562	blood:
8	chr8:3028449..3030172-chr8:3031870..3033947,2	K562	blood:
9	chr8:3066725..3070066-chr8:3071271..3074010,3	K562	blood:
10	chr8:3029280..3032071-chr8:3037936..3040025,3	K562	blood:
11	chr8:3039240..3042725-chr8:3044731..3047075,3	K562	blood:
12	chr8:3024715..3026622-chr8:3029423..3032227,2	K562	blood:
13	chr8:3142221..3142747-chr8:3393835..3394631,2	MCF-7	breast:
14	chr8:3012415..3014148-chr8:3015659..3017279,2	K562	blood:
15	chr1:32879411..32879983-chr8:3091793..3092520,2	MCF-7	breast:
16	chr8:3004483..3006837-chr8:3020468..3022186,2	K562	blood:
17	chr8:3066725..3070066-chr8:3071271..3074010,3	K562	blood:
18	chr8:3030633..3032243-chr8:3035809..3037381,2	K562	blood:
19	chr8:3024715..3026622-chr8:3029423..3032227,2	K562	blood:

No data

Variant related genes	Relation type
CSMD1	TF binding region
CSMD1	CpG island
ENSG00000183117	chromatin interactions

Extended variants
information (count: 5712 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:5712 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563558334	chr8:3015902-3015903	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs141083983	chr8:3015918-3015919	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs77202669	chr8:3015929-3015930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs559639384	chr8:3015948-3015949	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145555655	chr8:3015955-3015956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs528577000	chr8:3015956-3015957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182267715	chr8:3015993-3015994	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75719636	chr8:3016001-3016002	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs116636757	chr8:3016004-3016005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186887977	chr8:3016126-3016127	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191691381	chr8:3016159-3016160	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148534474	chr8:3016161-3016162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200668917	chr8:3016169-3016170	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs398047045	chr8:3016171-3016172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369780987	chr8:3016174-3016175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183133979	chr8:3016176-3016177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553126933	chr8:3016178-3016179	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs572890594	chr8:3016180-3016181	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs535490501	chr8:3016212-3016213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs147634293	chr8:3016241-3016242	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574862150	chr8:3016243-3016244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543791969	chr8:3016260-3016261	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79529095	chr8:3016274-3016275	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577118423	chr8:3016299-3016300	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs546122093	chr8:3016311-3016312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs559857395	chr8:3016339-3016340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs372899973	chr8:3016349-3016350	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs548635604	chr8:3016355-3016356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76201267	chr8:3016357-3016358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530962492	chr8:3016360-3016361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550970497	chr8:3016371-3016372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185741468	chr8:3016411-3016412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs140872002	chr8:3016414-3016415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150149780	chr8:3016459-3016460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566611702	chr8:3016470-3016471	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs375522750	chr8:3016494-3016495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561783557	chr8:3016505-3016506	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs189667927	chr8:3016521-3016522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138583428	chr8:3016523-3016524	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs564126599	chr8:3016538-3016539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149177326	chr8:3016561-3016562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs182290086	chr8:3016564-3016565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530624693	chr8:3016599-3016600	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs186944472	chr8:3016608-3016609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs145029252	chr8:3016636-3016637	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs553313611	chr8:3016641-3016642	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573350844	chr8:3016692-3016693	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs193237154	chr8:3016710-3016711	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs9886387	chr8:3016719-3016720	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562191317	chr8:3016727-3016728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:301 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:2999800-3016400	Weak transcription	Brain Cingulate Gyrus	brain
2	chr8:3014400-3016800	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr8:3014800-3020000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr8:3015200-3016000	Enhancers	H9 Cell Line	embryonic stem cell
5	chr8:3015200-3016600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr8:3015200-3037600	Weak transcription	K562	blood
7	chr8:3015800-3016000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr8:3015800-3016800	Enhancers	Brain Germinal Matrix	brain
9	chr8:3015800-3017400	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr8:3015800-3017400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr8:3015800-3017400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr8:3016000-3017000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr8:3016000-3017200	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:3016000-3017600	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr8:3016600-3026600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:3016800-3017200	Weak transcription	Brain Germinal Matrix	brain
17	chr8:3016800-3017600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr8:3016800-3018200	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr8:3017000-3017400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr8:3017000-3017600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:3017000-3018000	Enhancers	H1 Cell Line	embryonic stem cell
22	chr8:3017200-3018400	Enhancers	Brain Germinal Matrix	brain
23	chr8:3017400-3018000	Enhancers	Brain Hippocampus Middle	brain
24	chr8:3017600-3021200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:3018000-3020600	Weak transcription	Brain Hippocampus Middle	brain
26	chr8:3020600-3021600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr8:3020800-3021200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr8:3021000-3021200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr8:3021200-3021400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr8:3021200-3021400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr8:3021200-3021600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr8:3021200-3032000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr8:3021400-3021800	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr8:3026600-3026800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr8:3026600-3027200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:3026600-3027600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:3026600-3027600	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr8:3027000-3027400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr8:3027000-3027600	Enhancers	H9 Cell Line	embryonic stem cell
40	chr8:3027000-3027600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:3027400-3027600	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr8:3027600-3028800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr8:3028400-3029000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chr8:3028800-3029000	Enhancers	H9 Cell Line	embryonic stem cell
45	chr8:3034400-3034800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr8:3037600-3038000	Strong transcription	K562	blood
47	chr8:3038000-3038600	Weak transcription	K562	blood
48	chr8:3038600-3038800	Genic enhancers	K562	blood
49	chr8:3038600-3039400	Enhancers	Placenta Amnion	Placenta Amnion
50	chr8:3038800-3039400	Flanking Active TSS	K562	blood

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