Variant report

Variant	esv2754232
Chromosome Location	chr8:113294967-113634842
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	chr8:113477312-113477622	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:113350397-113350810	HepG2	liver:	n/a	chr8:113350726-113350742
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	chr8:113407703-113408043	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr8:113407778-113408009	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr8:113472029-113472628	A549	lung:	n/a	n/a
8	BCL3	chr8:113472001-113472616	A549	lung:	n/a	n/a
9	BCL3	chr8:113623801-113624046	GM12878	blood:	n/a	n/a
10	CEBPB	chr8:113584277-113584402	H1-hESC	embryonic stem cell:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
11	CEBPB	chr8:113304728-113304928	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:113584132-113584520	A549	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
13	CEBPB	chr8:113574810-113574943	H1-hESC	embryonic stem cell:	n/a	chr8:113574860-113574871 chr8:113574860-113574873 chr8:113574860-113574873
14	CEBPB	chr8:113513141-113513369	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr8:113584175-113584533	IMR90	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
16	CEBPB	chr8:113513135-113513454	MCF-7	breast:	n/a	n/a
17	CEBPB	chr8:113482875-113483091	K562	blood:	n/a	chr8:113483052-113483065
18	CEBPB	chr8:113447678-113447992	H1-hESC	embryonic stem cell:	n/a	chr8:113447842-113447853
19	CEBPB	chr8:113482858-113483155	A549	lung:	n/a	chr8:113483052-113483065
20	CEBPB	chr8:113628682-113629030	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr8:113584173-113584544	HepG2	liver:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
22	CEBPB	chr8:113358419-113359052	Hela-S3	cervix:	n/a	chr8:113358680-113358693
23	CEBPB	chr8:113584242-113584491	K562	blood:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
24	CEBPB	chr8:113482822-113483178	Hela-S3	cervix:	n/a	chr8:113483052-113483065
25	CEBPB	chr8:113392132-113392452	HepG2	liver:	n/a	chr8:113392419-113392430 chr8:113392276-113392287 chr8:113392419-113392432 chr8:113392419-113392430
26	CEBPB	chr8:113322419-113322604	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr8:113447683-113448031	K562	blood:	n/a	chr8:113447842-113447853
28	CEBPB	chr8:113543052-113543379	HepG2	liver:	n/a	chr8:113543224-113543235
29	CEBPB	chr8:113447665-113448035	A549	lung:	n/a	chr8:113447842-113447853
30	CEBPB	chr8:113482783-113483181	HepG2	liver:	n/a	chr8:113483052-113483065
31	CEBPB	chr8:113447661-113448018	IMR90	lung:	n/a	chr8:113447842-113447853
32	CEBPB	chr8:113482832-113483200	IMR90	lung:	n/a	chr8:113483052-113483065
33	CEBPB	chr8:113584252-113584508	A549	lung:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
34	CEBPB	chr8:113447659-113448026	HepG2	liver:	n/a	chr8:113447842-113447853
35	CEBPB	chr8:113358923-113359044	A549	lung:	n/a	n/a
36	CEBPB	chr8:113574808-113574989	A549	lung:	n/a	chr8:113574860-113574871 chr8:113574860-113574873 chr8:113574860-113574873
37	CEBPB	chr8:113341220-113341397	HepG2	liver:	n/a	chr8:113341236-113341247
38	CEBPB	chr8:113447657-113448038	Hela-S3	cervix:	n/a	chr8:113447842-113447853
39	CEBPB	chr8:113347546-113347746	A549	lung:	n/a	chr8:113347586-113347597
40	CEBPB	chr8:113347479-113347753	HepG2	liver:	n/a	chr8:113347586-113347597
41	CEBPB	chr8:113458738-113458836	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr8:113482886-113483126	H1-hESC	embryonic stem cell:	n/a	chr8:113483052-113483065
43	CEBPB	chr8:113584151-113584545	Hela-S3	cervix:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
44	CEBPB	chr8:113311107-113311386	HepG2	liver:	n/a	chr8:113311249-113311260
45	CTCF	chr8:113334695-113334721	Lung_OC	lung:	n/a	n/a
46	CTCF	chr8:113475635-113475716	GM10248	blood:	n/a	n/a
47	CTCF	chr8:113475540-113475690	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr8:113477280-113477430	AG10803	skin:	n/a	n/a
49	CTCF	chr8:113477382-113477512	GM10266	blood:	n/a	n/a
50	CTCF	chr8:113467224-113467274	GM13976	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:113351420-113351470	MCF-7	breast:	n/a
2	chr8:113351420-113351470	AG09309	skin:	n/a
3	chr8:113351420-113351470	SKMC	muscle:	n/a
4	chr8:113351420-113351470	Caco-2	colon:	n/a
5	chr8:113351420-113351470	Hela-S3	cervix:	n/a
6	chr8:113351420-113351470	ovcar-3	ovarian:	n/a
7	chr8:113351420-113351470	HIPEpiC	eye:	n/a
8	chr8:113351420-113351470	SK-N-MC	brain:	n/a
9	chr8:113351420-113351470	GM12878	blood:	n/a
10	chr8:113351420-113351470	HCT-116	colon:	n/a
11	chr8:113351420-113351470	LNCaP	prostate:	n/a
12	chr8:113351420-113351470	PFSK-1	brain:	n/a
13	chr8:113351420-113351470	HCPEpiC	choroid plexus:	n/a
14	chr8:113351420-113351470	HEK293	kidney:	embryo
15	chr8:113351420-113351470	GM12892	blood:	n/a
16	chr8:113351420-113351470	CMK	blood:	n/a
17	chr8:113351420-113351470	AG04450	lung:	fetal
18	chr8:113351420-113351470	T-47D	breast:	n/a
19	chr8:113351420-113351470	IMR90	lung:	fetal
20	chr8:113351420-113351470	HCM	heart:	n/a
21	chr8:113351420-113351470	GM12891	blood:	n/a
22	chr8:113351420-113351470	NH-A	brain:	n/a
23	chr8:113351420-113351470	AoSMC	blood vessel:	n/a
24	chr8:113351420-113351470	NB4	blood:	n/a
25	chr8:113351420-113351470	K562	blood:	n/a
26	chr8:113351420-113351470	HRPEpiC	eye:	n/a
27	chr8:113351420-113351470	GM06990	blood:	n/a
28	chr8:113351420-113351470	HMEC	breast:	n/a
29	chr8:113351420-113351470	HNPCEpiC	eye:	n/a
30	chr8:113351420-113351470	NHBE	bronchial:	n/a
31	chr8:113351420-113351470	SK-N-SH_RA	brain:	n/a
32	chr8:113351420-113351470	PrEC	prostate:	n/a
33	chr8:113351420-113351470	BJ	skin:	n/a
34	chr8:113351420-113351470	NT2-D1	testis:	n/a
35	chr8:113351420-113351470	A549	lung:	n/a
36	chr8:113351420-113351470	RPTEC	kidney:	n/a
37	chr8:113351420-113351470	PANC-1	pancreas:	n/a
38	chr8:113351420-113351470	AG09319	gingival:	n/a
39	chr8:113351420-113351470	AG10803	skin:	n/a
40	chr8:113351420-113351470	HCF	heart:	n/a
41	chr8:113351420-113351470	HL-60	blood:	n/a
42	chr8:113351420-113351470	MCF10A-Er-Src	breast:	n/a
43	chr8:113351420-113351470	HepG2	liver:	n/a
44	chr8:113351420-113351470	AG04449	skin:	fetal
45	chr8:113351420-113351470	SAEC	small airway:	n/a
46	chr8:113351420-113351470	NHDF-neo	bronchial:	n/a
47	chr8:113351420-113351470	HUVEC	blood vessel:	n/a
48	chr8:113351420-113351470	BE2_C	brain:	n/a
49	chr8:113351420-113351470	ProgFib	skin:	n/a
50	chr8:113351420-113351470	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:112976314..112977253-chr8:113408305..113409151,3	MCF-7	breast:
2	chr8:112946373..112947269-chr8:113476964..113477520,2	MCF-7	breast:
3	chr8:112976391..112977811-chr8:113408288..113409205,6	MCF-7	breast:
4	chr8:113495952..113497684-chr8:113532113..113534940,2	MCF-7	breast:
5	chr8:112976579..112977386-chr8:113471922..113472710,2	MCF-7	breast:
6	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
7	chr8:113334749..113337746-chr8:113352582..113354421,2	MCF-7	breast:
8	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
9	chr8:113411416..113413911-chr8:113414434..113416216,2	MCF-7	breast:
10	chr8:112946347..112947268-chr8:113386770..113387527,2	MCF-7	breast:
11	chr8:113352984..113355457-chr8:113360171..113363116,2	MCF-7	breast:
12	chr8:113396804..113398846-chr8:113404177..113405971,2	MCF-7	breast:
13	chr8:113396804..113398846-chr8:113404177..113405971,2	MCF-7	breast:
14	chr8:113408283..113409229-chr8:113477372..113477931,2	MCF-7	breast:
15	chr8:113536029..113539003-chr8:113540588..113542968,2	MCF-7	breast:
16	chr8:112947101..112947938-chr8:113477362..113477935,2	MCF-7	breast:
17	chr8:113536029..113539003-chr8:113540588..113542968,2	MCF-7	breast:
18	chr8:102371552..102373757-chr8:113387253..113389057,2	MCF-7	breast:
19	chr8:112946524..112947507-chr8:113386902..113387446,2	MCF-7	breast:
20	chr8:113408283..113409229-chr8:113477372..113477931,2	MCF-7	breast:
21	chr8:113334749..113337746-chr8:113352582..113354421,2	MCF-7	breast:
22	chr8:112976187..112977006-chr8:113476921..113477813,7	MCF-7	breast:
23	chr20:18661388..18664062-chr8:113586254..113588798,2	MCF-7	breast:
24	chr8:113411416..113413911-chr8:113414434..113416216,2	MCF-7	breast:
25	chr8:112976151..112977081-chr8:113386595..113387462,4	MCF-7	breast:
26	chr8:113352984..113355457-chr8:113360171..113363116,2	MCF-7	breast:
27	chr8:113476778..113477604-chr8:114449777..114450474,2	MCF-7	breast:
28	chr8:113461648..113464072-chr8:113471155..113472872,2	MCF-7	breast:
29	chr8:113495952..113497684-chr8:113532113..113534940,2	MCF-7	breast:
30	chr8:112878252..112879995-chr8:113601916..113604196,2	MCF-7	breast:
31	chr8:113461648..113464072-chr8:113471155..113472872,2	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: 11261 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:11261 , 50 per page) page: 1 2 3 4 5 6 7 ... 226

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16883360	chr8:113294967-113294968	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370771288	chr8:113294978-113294979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147559384	chr8:113295031-113295032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs16883361	chr8:113295050-113295051	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs560163816	chr8:113295087-113295088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557273467	chr8:113295089-113295090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183158875	chr8:113295122-113295123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552110822	chr8:113295146-113295147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs199969964	chr8:113295189-113295190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114161194	chr8:113295293-113295294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs186808206	chr8:113295300-113295301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs570708494	chr8:113295340-113295341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191235045	chr8:113295366-113295367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs75159867	chr8:113295404-113295405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568243380	chr8:113295413-113295414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183484489	chr8:113295484-113295485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs373699152	chr8:113295490-113295491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs553209467	chr8:113295504-113295505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549351524	chr8:113295562-113295563	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs558525474	chr8:113295579-113295580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572501995	chr8:113295583-113295584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544489756	chr8:113295622-113295623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs367846696	chr8:113295661-113295662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs571119510	chr8:113295753-113295754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554768825	chr8:113295777-113295778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142667177	chr8:113295808-113295809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540786196	chr8:113295837-113295838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs560000691	chr8:113295859-113295860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188270418	chr8:113295875-113295876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561258673	chr8:113295915-113295916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545858555	chr8:113295964-113295965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372159223	chr8:113296009-113296010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs16883363	chr8:113296013-113296014	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs192606623	chr8:113296026-113296027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568143055	chr8:113296028-113296029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs574724418	chr8:113296065-113296066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571423714	chr8:113296122-113296123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs532452110	chr8:113296135-113296136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs536780247	chr8:113296145-113296146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185351391	chr8:113296191-113296192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527506270	chr8:113296210-113296211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563636424	chr8:113296234-113296235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs35796784	chr8:113296247-113296248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs398086917	chr8:113296249-113296250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs397892150	chr8:113296250-113296251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs547526644	chr8:113296263-113296264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11782443	chr8:113296272-113296273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146904468	chr8:113296309-113296310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs368881697	chr8:113296354-113296355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs558564131	chr8:113296355-113296356	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:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113288800-113331400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:113298000-113298200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr8:113313600-113314400	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr8:113313800-113314200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr8:113313800-113314400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:113314000-113314400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:113322400-113324600	Enhancers	Dnd41	blood
8	chr8:113338600-113339000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:113338800-113339000	Enhancers	Brain Hippocampus Middle	brain
10	chr8:113338800-113339000	Enhancers	Brain Substantia Nigra	brain
11	chr8:113338800-113339000	Enhancers	Pancreas	Pancrea
12	chr8:113338800-113339200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr8:113347200-113347400	Enhancers	Stomach Mucosa	stomach
14	chr8:113347400-113349400	Weak transcription	Stomach Mucosa	stomach
15	chr8:113347600-113348400	Enhancers	Duodenum Mucosa	Duodenum
16	chr8:113347600-113348600	Enhancers	Fetal Intestine Small	intestine
17	chr8:113348400-113350000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr8:113348600-113349400	Weak transcription	Fetal Intestine Small	intestine
19	chr8:113349400-113349800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr8:113349400-113350000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr8:113349400-113350200	Enhancers	Fetal Intestine Small	intestine
22	chr8:113349400-113350400	Enhancers	Stomach Mucosa	stomach
23	chr8:113349600-113350000	Enhancers	Dnd41	blood
24	chr8:113349600-113350200	Enhancers	Rectal Mucosa Donor 29	rectum
25	chr8:113349800-113350000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr8:113349800-113350400	Enhancers	Fetal Intestine Large	intestine
27	chr8:113350000-113350400	Enhancers	Duodenum Mucosa	Duodenum
28	chr8:113350000-113355600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr8:113350000-113378600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr8:113350200-113351200	Weak transcription	Fetal Intestine Small	intestine
31	chr8:113351200-113351600	Enhancers	Fetal Intestine Small	intestine
32	chr8:113355600-113355800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr8:113358400-113358600	Active TSS	A549	lung
34	chr8:113358600-113358800	Flanking Active TSS	A549	lung
35	chr8:113362000-113362600	Enhancers	Dnd41	blood
36	chr8:113368200-113368800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:113382000-113383200	Weak transcription	Pancreas	Pancrea
38	chr8:113383200-113383400	ZNF genes & repeats	Pancreas	Pancrea
39	chr8:113383400-113386000	Weak transcription	Pancreas	Pancrea
40	chr8:113385400-113385800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:113386000-113386200	Enhancers	Pancreas	Pancrea
42	chr8:113393400-113394600	Enhancers	Fetal Intestine Large	intestine
43	chr8:113393400-113396400	Enhancers	Fetal Intestine Small	intestine
44	chr8:113396400-113400000	Weak transcription	Fetal Intestine Small	intestine
45	chr8:113399400-113410600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr8:113402200-113403200	Enhancers	Fetal Intestine Large	intestine
47	chr8:113405400-113405600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr8:113405600-113405800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
49	chr8:113406400-113408000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
50	chr8:113406600-113408200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell

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