Variant report

Variant	esv2755868
Chromosome Location	chr8:113282795-113634842
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	chr8:113350397-113350810	HepG2	liver:	n/a	chr8:113350726-113350742
2	ARID3A	chr8:113477312-113477622	HepG2	liver:	n/a	n/a
3	ATF1	chr8:113500282-113500373	K562	blood:	n/a	n/a
4	ATF2	chr8:113407709-113408069	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr8:113407778-113408009	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr8:113407703-113408043	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr8:113472001-113472616	A549	lung:	n/a	n/a
8	BCL3	chr8:113472029-113472628	A549	lung:	n/a	n/a
9	BCL3	chr8:113623801-113624046	GM12878	blood:	n/a	n/a
10	CEBPB	chr8:113322419-113322604	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr8:113447659-113448026	HepG2	liver:	n/a	chr8:113447842-113447853
12	CEBPB	chr8:113482875-113483091	K562	blood:	n/a	chr8:113483052-113483065
13	CEBPB	chr8:113584277-113584402	H1-hESC	embryonic stem cell:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
14	CEBPB	chr8:113584175-113584533	IMR90	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
15	CEBPB	chr8:113584252-113584508	A549	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
16	CEBPB	chr8:113447678-113447992	H1-hESC	embryonic stem cell:	n/a	chr8:113447842-113447853
17	CEBPB	chr8:113482822-113483178	Hela-S3	cervix:	n/a	chr8:113483052-113483065
18	CEBPB	chr8:113347479-113347753	HepG2	liver:	n/a	chr8:113347586-113347597
19	CEBPB	chr8:113392132-113392452	HepG2	liver:	n/a	chr8:113392419-113392430 chr8:113392276-113392287 chr8:113392419-113392432 chr8:113392419-113392430
20	CEBPB	chr8:113482858-113483155	A549	lung:	n/a	chr8:113483052-113483065
21	CEBPB	chr8:113584173-113584544	HepG2	liver:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
22	CEBPB	chr8:113447657-113448038	Hela-S3	cervix:	n/a	chr8:113447842-113447853
23	CEBPB	chr8:113447683-113448031	K562	blood:	n/a	chr8:113447842-113447853
24	CEBPB	chr8:113574808-113574989	A549	lung:	n/a	chr8:113574860-113574871 chr8:113574860-113574873 chr8:113574860-113574873
25	CEBPB	chr8:113584151-113584545	Hela-S3	cervix:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
26	CEBPB	chr8:113311107-113311386	HepG2	liver:	n/a	chr8:113311249-113311260
27	CEBPB	chr8:113304728-113304928	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:113447665-113448035	A549	lung:	n/a	chr8:113447842-113447853
29	CEBPB	chr8:113574810-113574943	H1-hESC	embryonic stem cell:	n/a	chr8:113574860-113574871 chr8:113574860-113574873 chr8:113574860-113574873
30	CEBPB	chr8:113543052-113543379	HepG2	liver:	n/a	chr8:113543224-113543235
31	CEBPB	chr8:113584242-113584491	K562	blood:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
32	CEBPB	chr8:113458738-113458836	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr8:113447661-113448018	IMR90	lung:	n/a	chr8:113447842-113447853
34	CEBPB	chr8:113482886-113483126	H1-hESC	embryonic stem cell:	n/a	chr8:113483052-113483065
35	CEBPB	chr8:113358419-113359052	Hela-S3	cervix:	n/a	chr8:113358680-113358693
36	CEBPB	chr8:113347546-113347746	A549	lung:	n/a	chr8:113347586-113347597
37	CEBPB	chr8:113482783-113483181	HepG2	liver:	n/a	chr8:113483052-113483065
38	CEBPB	chr8:113628682-113629030	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr8:113584132-113584520	A549	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
40	CEBPB	chr8:113482832-113483200	IMR90	lung:	n/a	chr8:113483052-113483065
41	CEBPB	chr8:113341220-113341397	HepG2	liver:	n/a	chr8:113341236-113341247
42	CEBPB	chr8:113513141-113513369	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr8:113358923-113359044	A549	lung:	n/a	n/a
44	CEBPB	chr8:113513135-113513454	MCF-7	breast:	n/a	n/a
45	CTCF	chr8:113475600-113475750	NHEK	skin:	n/a	n/a
46	CTCF	chr8:113477360-113477510	HVMF	connective:	n/a	n/a
47	CTCF	chr8:113477380-113477530	HCM	heart:	n/a	n/a
48	CTCF	chr8:113477380-113477530	K562	blood:	n/a	n/a
49	CTCF	chr8:113477385-113477482	GM13976	blood:	n/a	n/a
50	CTCF	chr8:113477340-113477490	HCPEpiC	choroid plexus:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:113351420-113351470	NH-A	brain:	n/a
2	chr8:113351420-113351470	LNCaP	prostate:	n/a
3	chr8:113351420-113351470	A549	lung:	n/a
4	chr8:113351420-113351470	SK-N-MC	brain:	n/a
5	chr8:113351420-113351470	AG10803	skin:	n/a
6	chr8:113351420-113351470	T-47D	breast:	n/a
7	chr8:113351420-113351470	HCT-116	colon:	n/a
8	chr8:113351420-113351470	Hela-S3	cervix:	n/a
9	chr8:113351420-113351470	ProgFib	skin:	n/a
10	chr8:113351420-113351470	GM12891	blood:	n/a
11	chr8:113351420-113351470	AG09319	gingival:	n/a
12	chr8:113351420-113351470	Caco-2	colon:	n/a
13	chr8:113351420-113351470	GM12892	blood:	n/a
14	chr8:113351420-113351470	MCF-7	breast:	n/a
15	chr8:113351420-113351470	GM06990	blood:	n/a
16	chr8:113351420-113351470	HUVEC	blood vessel:	n/a
17	chr8:113351420-113351470	HNPCEpiC	eye:	n/a
18	chr8:113351420-113351470	GM12878	blood:	n/a
19	chr8:113351420-113351470	NB4	blood:	n/a
20	chr8:113351420-113351470	SK-N-SH	brain:	n/a
21	chr8:113351420-113351470	ovcar-3	ovarian:	n/a
22	chr8:113351420-113351470	SAEC	small airway:	n/a
23	chr8:113351420-113351470	H1-hESC	embryonic stem cell:	embryo
24	chr8:113351420-113351470	HepG2	liver:	n/a
25	chr8:113351420-113351470	AG09309	skin:	n/a
26	chr8:113351420-113351470	HCPEpiC	choroid plexus:	n/a
27	chr8:113351420-113351470	HAEpiC	amniotic membrane:	n/a
28	chr8:113351420-113351470	NT2-D1	testis:	n/a
29	chr8:113351420-113351470	NHDF-neo	bronchial:	n/a
30	chr8:113351420-113351470	K562	blood:	n/a
31	chr8:113351420-113351470	HRE	kidney:	n/a
32	chr8:113351420-113351470	AoSMC	blood vessel:	n/a
33	chr8:113351420-113351470	PFSK-1	brain:	n/a
34	chr8:113351420-113351470	MCF10A-Er-Src	breast:	n/a
35	chr8:113351420-113351470	U87	brain:	n/a
36	chr8:113351420-113351470	HMEC	breast:	n/a
37	chr8:113351420-113351470	AG04449	skin:	fetal
38	chr8:113351420-113351470	ECC-1	luminal epithelium:	n/a
39	chr8:113351420-113351470	HL-60	blood:	n/a
40	chr8:113351420-113351470	PrEC	prostate:	n/a
41	chr8:113351420-113351470	NHBE	bronchial:	n/a
42	chr8:113351420-113351470	HRPEpiC	eye:	n/a
43	chr8:113351420-113351470	CMK	blood:	n/a
44	chr8:113351420-113351470	GM19239	blood:	n/a
45	chr8:113351420-113351470	BE2_C	brain:	n/a
46	chr8:113351420-113351470	PANC-1	pancreas:	n/a
47	chr8:113351420-113351470	RPTEC	kidney:	n/a
48	chr8:113351420-113351470	SK-N-SH_RA	brain:	n/a
49	chr8:113351420-113351470	HEEpiC	esophagus:	n/a
50	chr8:113351420-113351470	HCF	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:113396804..113398846-chr8:113404177..113405971,2	MCF-7	breast:
2	chr8:112878252..112879995-chr8:113601916..113604196,2	MCF-7	breast:
3	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
4	chr8:113476778..113477604-chr8:114449777..114450474,2	MCF-7	breast:
5	chr8:113334749..113337746-chr8:113352582..113354421,2	MCF-7	breast:
6	chr8:112976314..112977253-chr8:113408305..113409151,3	MCF-7	breast:
7	chr8:113396804..113398846-chr8:113404177..113405971,2	MCF-7	breast:
8	chr8:113495952..113497684-chr8:113532113..113534940,2	MCF-7	breast:
9	chr8:113352984..113355457-chr8:113360171..113363116,2	MCF-7	breast:
10	chr8:112946524..112947507-chr8:113386902..113387446,2	MCF-7	breast:
11	chr8:112946347..112947268-chr8:113386770..113387527,2	MCF-7	breast:
12	chr8:113536029..113539003-chr8:113540588..113542968,2	MCF-7	breast:
13	chr8:102371552..102373757-chr8:113387253..113389057,2	MCF-7	breast:
14	chr8:112976391..112977811-chr8:113408288..113409205,6	MCF-7	breast:
15	chr8:113461648..113464072-chr8:113471155..113472872,2	MCF-7	breast:
16	chr8:113282212..113283944-chr8:113285167..113287640,2	MCF-7	breast:
17	chr8:113352984..113355457-chr8:113360171..113363116,2	MCF-7	breast:
18	chr8:113408283..113409229-chr8:113477372..113477931,2	MCF-7	breast:
19	chr8:113408283..113409229-chr8:113477372..113477931,2	MCF-7	breast:
20	chr8:113334749..113337746-chr8:113352582..113354421,2	MCF-7	breast:
21	chr8:112946373..112947269-chr8:113476964..113477520,2	MCF-7	breast:
22	chr8:112976151..112977081-chr8:113386595..113387462,4	MCF-7	breast:
23	chr8:113411416..113413911-chr8:113414434..113416216,2	MCF-7	breast:
24	chr8:112976579..112977386-chr8:113471922..113472710,2	MCF-7	breast:
25	chr8:112976187..112977006-chr8:113476921..113477813,7	MCF-7	breast:
26	chr20:18661388..18664062-chr8:113586254..113588798,2	MCF-7	breast:
27	chr8:113461648..113464072-chr8:113471155..113472872,2	MCF-7	breast:
28	chr8:113411416..113413911-chr8:113414434..113416216,2	MCF-7	breast:
29	chr8:113282212..113283944-chr8:113285167..113287640,2	MCF-7	breast:
30	chr8:112947101..112947938-chr8:113477362..113477935,2	MCF-7	breast:
31	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
32	chr8:113495952..113497684-chr8:113532113..113534940,2	MCF-7	breast:
33	chr8:113536029..113539003-chr8:113540588..113542968,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-67H2.1.1-6	chr8:113551118-113551546	NONHSAT128340

Variant related genes	Relation type
RPL30P16	TF binding region
ENSG00000264794	TF binding region
CSMD3	TF binding region
ENSG00000238656	TF binding region
RPL30P16	CpG island
ENSG00000264794	CpG island
CSMD3	CpG island
ENSG00000238656	CpG island

Extended variants
information (count: 11642 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:11642 , 50 per page) page: 1 2 3 4 5 6 7 ... 233

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16883344	chr8:113282795-113282796	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558473669	chr8:113286075-113286076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147293002	chr8:113286080-113286081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs192624362	chr8:113286096-113286097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs11784683	chr8:113286111-113286112	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs554301312	chr8:113286138-113286139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs559152161	chr8:113286139-113286140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145186368	chr8:113286164-113286165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs76420606	chr8:113286166-113286167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs76030401	chr8:113286178-113286179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148333356	chr8:113286225-113286226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs551129196	chr8:113286277-113286278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545727495	chr8:113286281-113286282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs552865637	chr8:113286300-113286301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs78684171	chr8:113286304-113286305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533419149	chr8:113286311-113286312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs573658695	chr8:113286312-113286313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549954584	chr8:113286331-113286332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs112620899	chr8:113286370-113286371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs536189027	chr8:113286380-113286381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs150836301	chr8:113286387-113286388	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs199655002	chr8:113286428-113286429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs201565352	chr8:113286444-113286445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs143639057	chr8:113286445-113286446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542682725	chr8:113286452-113286453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370495711	chr8:113286467-113286468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376305322	chr8:113286485-113286486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566348222	chr8:113286537-113286538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555904759	chr8:113286544-113286545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs535246708	chr8:113286577-113286578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575619307	chr8:113286602-113286603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558288583	chr8:113286607-113286608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1113603	chr8:113286608-113286609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573861530	chr8:113286615-113286616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537144269	chr8:113286619-113286620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185601158	chr8:113286627-113286628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1114081	chr8:113286650-113286651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112271026	chr8:113286705-113286706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189369595	chr8:113286758-113286759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs544932835	chr8:113286816-113286817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs538012603	chr8:113286875-113286876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192700831	chr8:113286881-113286882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs139254297	chr8:113286884-113286885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556411805	chr8:113286886-113286887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544808575	chr8:113286894-113286895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs564833610	chr8:113286932-113286933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73709208	chr8:113286956-113286957	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs7011864	chr8:113286963-113286964	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs114710888	chr8:113286982-113286983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs144185814	chr8:113287043-113287044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Schizophrenia	20967226	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113282600-113282800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr8:113286000-113288400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:113288000-113288800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
4	chr8:113288400-113288800	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:113288400-113289000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr8:113288400-113289000	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:113288800-113289200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr8:113288800-113331400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr8:113289600-113290600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr8:113298000-113298200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:113313600-113314400	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr8:113313800-113314200	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr8:113313800-113314400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr8:113314000-113314400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
15	chr8:113322400-113324600	Enhancers	Dnd41	blood
16	chr8:113338600-113339000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:113338800-113339000	Enhancers	Brain Hippocampus Middle	brain
18	chr8:113338800-113339000	Enhancers	Brain Substantia Nigra	brain
19	chr8:113338800-113339000	Enhancers	Pancreas	Pancrea
20	chr8:113338800-113339200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:113347200-113347400	Enhancers	Stomach Mucosa	stomach
22	chr8:113347400-113349400	Weak transcription	Stomach Mucosa	stomach
23	chr8:113347600-113348400	Enhancers	Duodenum Mucosa	Duodenum
24	chr8:113347600-113348600	Enhancers	Fetal Intestine Small	intestine
25	chr8:113348400-113350000	Weak transcription	Duodenum Mucosa	Duodenum
26	chr8:113348600-113349400	Weak transcription	Fetal Intestine Small	intestine
27	chr8:113349400-113349800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr8:113349400-113350000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:113349400-113350200	Enhancers	Fetal Intestine Small	intestine
30	chr8:113349400-113350400	Enhancers	Stomach Mucosa	stomach
31	chr8:113349600-113350000	Enhancers	Dnd41	blood
32	chr8:113349600-113350200	Enhancers	Rectal Mucosa Donor 29	rectum
33	chr8:113349800-113350000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:113349800-113350400	Enhancers	Fetal Intestine Large	intestine
35	chr8:113350000-113350400	Enhancers	Duodenum Mucosa	Duodenum
36	chr8:113350000-113355600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr8:113350000-113378600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr8:113350200-113351200	Weak transcription	Fetal Intestine Small	intestine
39	chr8:113351200-113351600	Enhancers	Fetal Intestine Small	intestine
40	chr8:113355600-113355800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr8:113358400-113358600	Active TSS	A549	lung
42	chr8:113358600-113358800	Flanking Active TSS	A549	lung
43	chr8:113362000-113362600	Enhancers	Dnd41	blood
44	chr8:113368200-113368800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr8:113382000-113383200	Weak transcription	Pancreas	Pancrea
46	chr8:113383200-113383400	ZNF genes & repeats	Pancreas	Pancrea
47	chr8:113383400-113386000	Weak transcription	Pancreas	Pancrea
48	chr8:113385400-113385800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr8:113386000-113386200	Enhancers	Pancreas	Pancrea
50	chr8:113393400-113394600	Enhancers	Fetal Intestine Large	intestine

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