Variant report

Variant	nsv831330
Chromosome Location	chr8:60270398-60514078
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:520)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:520 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:60468004-60468241	K562	blood:	n/a	n/a
2	ATF2	chr8:60489320-60489706	GM12878	blood:	n/a	n/a
3	ATF3	chr8:60467971-60468280	K562	blood:	n/a	n/a
4	BACH1	chr8:60359423-60359566	K562	blood:	n/a	n/a
5	BACH1	chr8:60359389-60359727	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr8:60489407-60489752	GM12878	blood:	n/a	chr8:60489577-60489588
7	BCL3	chr8:60489407-60489652	GM12878	blood:	n/a	n/a
8	CCNT2	chr8:60468005-60468205	K562	blood:	n/a	chr8:60468068-60468088
9	CEBPB	chr8:60494668-60495053	IMR90	lung:	n/a	n/a
10	CEBPB	chr8:60467934-60468304	K562	blood:	n/a	chr8:60468135-60468146
11	CEBPB	chr8:60307275-60307548	ECC-1	luminal epithelium:	n/a	chr8:60307369-60307380
12	CEBPB	chr8:60494671-60495036	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr8:60307304-60307513	MCF-7	breast:	n/a	chr8:60307369-60307380
14	CEBPB	chr8:60508755-60509399	A549	lung:	n/a	n/a
15	CEBPB	chr8:60326032-60326232	A549	lung:	n/a	chr8:60326188-60326199
16	CEBPB	chr8:60496324-60496661	A549	lung:	n/a	chr8:60496476-60496487
17	CEBPB	chr8:60494684-60495035	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:60494709-60495016	K562	blood:	n/a	n/a
19	CEBPB	chr8:60307261-60307512	Hela-S3	cervix:	n/a	chr8:60307369-60307380
20	CEBPB	chr8:60494688-60495029	A549	lung:	n/a	n/a
21	CEBPB	chr8:60496387-60496610	K562	blood:	n/a	chr8:60496476-60496487
22	CEBPB	chr8:60307206-60307544	HepG2	liver:	n/a	chr8:60307369-60307380
23	CEBPB	chr8:60494730-60494930	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr8:60307321-60307464	A549	lung:	n/a	chr8:60307369-60307380
25	CEBPB	chr8:60508681-60509309	IMR90	lung:	n/a	n/a
26	CEBPB	chr8:60496316-60496661	IMR90	lung:	n/a	chr8:60496476-60496487
27	CEBPB	chr8:60337868-60338028	A549	lung:	n/a	n/a
28	CEBPB	chr8:60467943-60468336	K562	blood:	n/a	chr8:60468135-60468146
29	CEBPB	chr8:60496328-60496627	HepG2	liver:	n/a	chr8:60496476-60496487
30	CEBPB	chr8:60375074-60375574	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr8:60278396-60278596	HepG2	liver:	n/a	chr8:60278500-60278513 chr8:60278501-60278512
32	CEBPB	chr8:60505957-60506245	K562	blood:	n/a	n/a
33	CEBPB	chr8:60468043-60468284	IMR90	lung:	n/a	chr8:60468135-60468146
34	CEBPB	chr8:60326057-60326333	HepG2	liver:	n/a	chr8:60326188-60326199
35	CHD1	chr8:60302619-60302948	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr8:60374982-60375495	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr8:60438040-60438190	BE2_C	brain:	n/a	n/a
38	CTCF	chr8:60438121-60438155	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr8:60375240-60375390	SAEC	small airway:	n/a	n/a
40	CTCF	chr8:60332973-60332990	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr8:60347099-60347371	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr8:60346860-60347010	HCT-116	colon:	n/a	n/a
43	CTCF	chr8:60347260-60347410	HMEC	breast:	n/a	n/a
44	CTCF	chr8:60489460-60489610	GM12869	blood:	n/a	n/a
45	CTCF	chr8:60347180-60347330	GM12866	blood:	n/a	n/a
46	CTCF	chr8:60491426-60491461	MCF-7	breast:	n/a	n/a
47	CTCF	chr8:60347180-60347330	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr8:60438740-60438890	BE2_C	brain:	n/a	n/a
49	CTCF	chr8:60438040-60438190	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr8:60438073-60438174	GM12892	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:60444511-60444561	SK-N-MC	brain:	n/a
2	chr8:60444511-60444561	BE2_C	brain:	n/a
3	chr8:60444511-60444561	HCM	heart:	n/a
4	chr8:60444511-60444561	AG04450	lung:	fetal
5	chr8:60444511-60444561	HUVEC	blood vessel:	n/a
6	chr8:60444511-60444561	HEK293	kidney:	embryo
7	chr8:60444511-60444561	MCF-7	breast:	n/a
8	chr8:60444511-60444561	HEEpiC	esophagus:	n/a
9	chr8:60444511-60444561	RPTEC	kidney:	n/a
10	chr8:60444511-60444561	HNPCEpiC	eye:	n/a
11	chr8:60444511-60444561	BJ	skin:	n/a
12	chr8:60444511-60444561	AoSMC	blood vessel:	n/a
13	chr8:60444511-60444561	HAEpiC	amniotic membrane:	n/a
14	chr8:60444511-60444561	GM19239	blood:	n/a
15	chr8:60444511-60444561	SK-N-SH_RA	brain:	n/a
16	chr8:60444511-60444561	PANC-1	pancreas:	n/a
17	chr8:60444511-60444561	Caco-2	colon:	n/a
18	chr8:60444511-60444561	AG09309	skin:	n/a
19	chr8:60444511-60444561	Hepatocyte	liver:	n/a
20	chr8:60444511-60444561	Hela-S3	cervix:	n/a
21	chr8:60444511-60444561	AG09319	gingival:	n/a
22	chr8:60444511-60444561	NT2-D1	testis:	n/a
23	chr8:60444511-60444561	GM12891	blood:	n/a
24	chr8:60444511-60444561	Jurkat	blood:	n/a
25	chr8:60444511-60444561	HPAEpiC	pulmonary alveolar:	n/a
26	chr8:60444511-60444561	GM06990	blood:	n/a
27	chr8:60444511-60444561	NHDF-neo	bronchial:	n/a
28	chr8:60444511-60444561	U87	brain:	n/a
29	chr8:60444511-60444561	LNCaP	prostate:	n/a
30	chr8:60444511-60444561	HCT-116	colon:	n/a
31	chr8:60444511-60444561	HCPEpiC	choroid plexus:	n/a
32	chr8:60444511-60444561	NHBE	bronchial:	n/a
33	chr8:60444511-60444561	IMR90	lung:	fetal
34	chr8:60444511-60444561	A549	lung:	n/a
35	chr8:60444511-60444561	ovcar-3	ovarian:	n/a
36	chr8:60444511-60444561	HIPEpiC	eye:	n/a
37	chr8:60444511-60444561	MCF10A-Er-Src	breast:	n/a
38	chr8:60444511-60444561	K562	blood:	n/a
39	chr8:60444511-60444561	PFSK-1	brain:	n/a
40	chr8:60444511-60444561	HepG2	liver:	n/a
41	chr8:60444511-60444561	H1-hESC	embryonic stem cell:	embryo
42	chr8:60444511-60444561	AG04449	skin:	fetal
43	chr8:60444511-60444561	HRE	kidney:	n/a
44	chr8:60444511-60444561	HCF	heart:	n/a
45	chr8:60444511-60444561	SKMC	muscle:	n/a
46	chr8:60444511-60444561	SAEC	small airway:	n/a
47	chr8:60444511-60444561	GM12892	blood:	n/a
48	chr8:60444511-60444561	ProgFib	skin:	n/a
49	chr8:60444511-60444561	AG10803	skin:	n/a
50	chr8:60444511-60444561	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:60353422..60355080-chr8:60359821..60362576,2	K562	blood:
2	chr8:60353422..60355080-chr8:60359821..60362576,2	K562	blood:
3	chr8:60307556..60310133-chr8:60318318..60320436,2	K562	blood:
4	chr8:60505094..60507330-chr8:60508230..60511083,3	K562	blood:
5	chr8:60270318..60271875-chr8:60274683..60276592,2	K562	blood:
6	chr17:56735699..56736532-chr8:60431326..60431826,2	Hela-S3	cervix:
7	chr8:60491495..60494237-chr8:60524811..60527779,2	K562	blood:
8	chr8:60485014..60486699-chr8:60491744..60493871,2	K562	blood:
9	chr8:60270318..60271875-chr8:60274683..60276592,2	K562	blood:
10	chr8:60352662..60355420-chr8:60364405..60366691,2	K562	blood:
11	chr8:60303688..60306205-chr8:60408820..60411087,2	K562	blood:
12	chr8:60303688..60306205-chr8:60408820..60411087,2	K562	blood:
13	chr8:60349625..60352522-chr8:60358997..60361385,2	K562	blood:
14	chr8:60485014..60486699-chr8:60491744..60493871,2	K562	blood:
15	chr8:60432149..60433929-chr8:60440083..60443026,2	K562	blood:
16	chr8:60307556..60310133-chr8:60318318..60320436,2	K562	blood:
17	chr8:60352662..60355420-chr8:60364405..60366691,2	K562	blood:
18	chr8:60432149..60433929-chr8:60440083..60443026,2	K562	blood:
19	chr8:60349625..60352522-chr8:60358997..60361385,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOX-1	chr8:60473892-60474119	XLOC_007091
2	lnc-RAB2A-3	chr8:60513937-60514011	ENSG00000253879
3	lnc-RAB2A-3	chr8:60513963-60514011	ENSG00000253879
4	lnc-TOX-1	chr8:60506137-60506377	XLOC_007091
5	lnc-TOX-4	chr8:60470087-60470414	NONHSAT126805

No data

Variant related genes	Relation type
ENSG00000253879	TF binding region
ENSG00000254150	TF binding region
RNA5SP267	TF binding region
ENSG00000253260	TF binding region
ENSG00000253879	CpG island
ENSG00000254150	CpG island
RNA5SP267	CpG island
ENSG00000253260	CpG island
ENSG00000253260	chromatin interactions

Extended variants
information (count: 3593 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:3593 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549008509	chr8:60270414-60270415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567595430	chr8:60270562-60270563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs564948896	chr8:60278415-60278416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532454998	chr8:60278418-60278419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs547868234	chr8:60278463-60278464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72655510	chr8:60278543-60278544	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs573392619	chr8:60278548-60278549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs530298160	chr8:60278590-60278591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs75106976	chr8:60278599-60278600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79026599	chr8:60278612-60278613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73685708	chr8:60278619-60278620	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs549757562	chr8:60278645-60278646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571264420	chr8:60278702-60278703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs576069318	chr8:60278729-60278730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs538302470	chr8:60278730-60278731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553816975	chr8:60278731-60278732	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs572075346	chr8:60278733-60278734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs183789907	chr8:60278746-60278747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs554359764	chr8:60278777-60278778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs147837180	chr8:60278794-60278795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs373973262	chr8:60278878-60278879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs551180304	chr8:60278898-60278899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577162564	chr8:60278913-60278914	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76964918	chr8:60278914-60278915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188570618	chr8:60278917-60278918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139773616	chr8:60278944-60278945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192945573	chr8:60278983-60278984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563882129	chr8:60278992-60278993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531182670	chr8:60279000-60279001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558879065	chr8:60279044-60279045	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs528381579	chr8:60279066-60279067	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs552899608	chr8:60279078-60279079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544942237	chr8:60279100-60279101	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs571197679	chr8:60279107-60279108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144990574	chr8:60279190-60279191	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547098778	chr8:60279194-60279195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs4132140	chr8:60279199-60279200	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs535976221	chr8:60279203-60279204	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs5891727	chr8:60279291-60279292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs554298603	chr8:60279359-60279360	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575831687	chr8:60279382-60279383	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573763260	chr8:60279397-60279398	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs5891728	chr8:60279404-60279405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs144903678	chr8:60279463-60279464	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558412590	chr8:60279497-60279498	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577088573	chr8:60279528-60279529	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199792023	chr8:60279533-60279534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541386529	chr8:60279566-60279567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532271756	chr8:60279745-60279746	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs370308602	chr8:60279789-60279790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60269000-60270400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr8:60269400-60270600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:60278400-60279000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr8:60278400-60279000	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr8:60278800-60280200	Enhancers	NHDF-Ad	bronchial
6	chr8:60278800-60280800	Enhancers	Fetal Brain Male	brain
7	chr8:60279000-60282800	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr8:60280200-60281200	Enhancers	Dnd41	blood
9	chr8:60280800-60282600	Weak transcription	Fetal Brain Male	brain
10	chr8:60282600-60283800	Enhancers	Fetal Brain Male	brain
11	chr8:60282800-60283000	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr8:60282800-60283200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:60282800-60283200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:60283000-60283400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr8:60283200-60285800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr8:60283400-60283800	Enhancers	Pancreatic Islets	Pancreatic Islet
17	chr8:60285600-60285800	Enhancers	Fetal Lung	lung
18	chr8:60285600-60287000	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr8:60285800-60286600	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr8:60285800-60287000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr8:60286000-60287200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr8:60288800-60289200	Enhancers	NHDF-Ad	bronchial
23	chr8:60292600-60294200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
24	chr8:60292600-60294400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
25	chr8:60292800-60293400	Enhancers	Dnd41	blood
26	chr8:60293000-60294800	Enhancers	Primary B cells from peripheral blood	blood
27	chr8:60293200-60293400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:60293200-60294400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr8:60293200-60294600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr8:60293400-60293600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
31	chr8:60293400-60293800	Enhancers	Primary T helper cells fromperipheralblood	blood
32	chr8:60293400-60294000	Flanking Active TSS	Dnd41	blood
33	chr8:60293400-60294200	Enhancers	Stomach Mucosa	stomach
34	chr8:60293400-60294400	Enhancers	Primary T cells fromperipheralblood	blood
35	chr8:60293400-60294400	Enhancers	Primary hematopoietic stem cells	blood
36	chr8:60293400-60294400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:60293400-60294400	Enhancers	Fetal Thymus	thymus
38	chr8:60293600-60294000	Enhancers	Thymus	Thymus
39	chr8:60293600-60294200	Enhancers	Primary T cells from cord blood	blood
40	chr8:60293600-60294200	Enhancers	Rectal Mucosa Donor 29	rectum
41	chr8:60293600-60294200	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr8:60293600-60294400	Enhancers	Sigmoid Colon	Sigmoid Colon
43	chr8:60293800-60294200	Enhancers	Lung	lung
44	chr8:60293800-60294400	Enhancers	Colonic Mucosa	Colon
45	chr8:60294000-60294400	Enhancers	Dnd41	blood
46	chr8:60299800-60300000	ZNF genes & repeats	Fetal Intestine Large	intestine
47	chr8:60300000-60302000	Weak transcription	Fetal Intestine Large	intestine
48	chr8:60300400-60301600	Enhancers	Fetal Brain Male	brain
49	chr8:60301400-60301600	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr8:60301400-60301600	Enhancers	Dnd41	blood

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