Variant report

Variant	esv3330012
Chromosome Location	chr8:95917076-95920874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:95918596-95918902	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:95917530-95917787	HepG2	liver:	n/a	n/a
3	ATF1	chr8:95917539-95917811	K562	blood:	n/a	n/a
4	ATF2	chr8:95917510-95917745	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCLAF1	chr8:95917492-95917859	GM12878	blood:	n/a	n/a
6	BHLHE40	chr8:95917587-95918243	GM12878	blood:	n/a	n/a
7	BHLHE40	chr8:95917571-95917898	K562	blood:	n/a	n/a
8	BHLHE40	chr8:95918552-95918996	HepG2	liver:	n/a	n/a
9	BRCA1	chr8:95917774-95917779	GM12878	blood:	n/a	n/a
10	CBX3	chr8:95917470-95917842	K562	blood:	n/a	n/a
11	CEBPB	chr8:95917289-95917798	K562	blood:	n/a	n/a
12	CEBPB	chr8:95917485-95917771	IMR90	lung:	n/a	n/a
13	CEBPB	chr8:95917409-95917776	A549	lung:	n/a	n/a
14	CEBPB	chr8:95917452-95917695	HepG2	liver:	n/a	n/a
15	CEBPB	chr8:95920174-95920215	IMR90	lung:	n/a	n/a
16	CEBPB	chr8:95917496-95917746	K562	blood:	n/a	n/a
17	CEBPB	chr8:95917319-95917797	K562	blood:	n/a	n/a
18	CHD2	chr8:95918509-95918775	HepG2	liver:	n/a	n/a
19	CHD2	chr8:95917608-95918225	GM12878	blood:	n/a	n/a
20	CTCF	chr8:95917600-95917750	GM12865	blood:	n/a	n/a
21	CTCF	chr8:95917539-95917843	T-47D	breast:	n/a	n/a
22	CTCF	chr8:95917560-95917710	NHDF-neo	bronchial:	n/a	n/a
23	CTCF	chr8:95917560-95917710	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr8:95917541-95917831	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:95918620-95918770	GM12875	blood:	n/a	n/a
26	CTCF	chr8:95917620-95917770	HAc	cerebellar:	n/a	n/a
27	CTCF	chr8:95917640-95917790	RPTEC	kidney:	n/a	n/a
28	CTCF	chr8:95917920-95918070	GM12874	blood:	n/a	n/a
29	CTCF	chr8:95917560-95917710	HCT-116	colon:	n/a	n/a
30	CTCF	chr8:95917620-95917770	GM12867	blood:	n/a	n/a
31	CTCF	chr8:95917555-95917835	Fibrobl	skin:	n/a	n/a
32	CTCF	chr8:95917600-95917750	HRE	kidney:	n/a	n/a
33	CTCF	chr8:95917560-95917710	GM12878	blood:	n/a	n/a
34	CTCF	chr8:95917538-95918024	GM12878	blood:	n/a	n/a
35	CTCF	chr8:95917580-95917730	HCM	heart:	n/a	n/a
36	CTCF	chr8:95917580-95917730	BJ	skin:	n/a	n/a
37	CTCF	chr8:95917600-95917750	SAEC	small airway:	n/a	n/a
38	CTCF	chr8:95917960-95918110	GM12874	blood:	n/a	n/a
39	CTCF	chr8:95917560-95917710	HAc	cerebellar:	n/a	n/a
40	CTCF	chr8:95917600-95917750	GM12864	blood:	n/a	n/a
41	CTCF	chr8:95917560-95917710	WI-38	lung:	n/a	n/a
42	CTCF	chr8:95917600-95917750	AG04449	skin:	n/a	n/a
43	CTCF	chr8:95917640-95917790	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr8:95917590-95917798	A549	lung:	n/a	n/a
45	CTCF	chr8:95917587-95917769	LNCaP	prostate:	n/a	n/a
46	CTCF	chr8:95917600-95917750	GM06990	blood:	n/a	n/a
47	CTCF	chr8:95917640-95917790	HVMF	connective:	n/a	n/a
48	CTCF	chr8:95917580-95917730	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr8:95917600-95917750	NHEK	skin:	n/a	n/a
50	CTCF	chr8:95917640-95917790	GM12867	blood:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:95624726..95625394-chr8:95917214..95918137,2	K562	blood:
2	chr8:95915511..95918504-chr8:96036526..96038312,2	MCF-7	breast:
3	chr8:95907392..95910679-chr8:95917896..95921327,5	K562	blood:
4	chr8:95913634..95919106-chr8:95960002..95963177,4	MCF-7	breast:
5	chr8:95825413..95826534-chr8:95917013..95918128,4	MCF-7	breast:
6	chr8:95918169..95919782-chr8:95960752..95962481,2	MCF-7	breast:
7	chr8:95908439..95909385-chr8:95917472..95918058,2	MCF-7	breast:
8	chr8:95911771..95913789-chr8:95918971..95920628,2	MCF-7	breast:
9	chr8:95907473..95909813-chr8:95916100..95917629,3	K562	blood:
10	chr8:95910895..95913798-chr8:95915630..95917632,3	K562	blood:
11	chr8:95905635..95908338-chr8:95917636..95919532,2	MCF-7	breast:
12	chr8:95825385..95826868-chr8:95917211..95918138,5	K562	blood:
13	chr8:95919394..95921112-chr8:95924687..95926221,2	K562	blood:
14	chr8:95907089..95909246-chr8:95918351..95920995,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-INTS8-3	chr8:95918723-95919169	NONHSAT127805

No data

Variant related genes	Relation type
ENSG00000238791	TF binding region
ENSG00000164938	chromatin interactions
ENSG00000156170	chromatin interactions
ENSG00000253878	chromatin interactions
ENSG00000175305	chromatin interactions
ENSG00000164941	chromatin interactions

Extended variants
information (count: 141 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:141 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4570121	chr8:95917088-95917089	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553287	chr8:95917099-95917100	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs571626203	chr8:95917100-95917101	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs568104649	chr8:95917114-95917115	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs142416945	chr8:95917122-95917123	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs554383229	chr8:95917166-95917167	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs556911662	chr8:95917202-95917203	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs185006180	chr8:95917208-95917209	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs539331230	chr8:95917249-95917250	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs552775471	chr8:95917259-95917260	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs9643350	chr8:95917276-95917277	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9643351	chr8:95917290-95917291	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs562044332	chr8:95917294-95917295	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs191177505	chr8:95917302-95917303	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs183843278	chr8:95917307-95917308	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs564488093	chr8:95917343-95917344	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs10101601	chr8:95917351-95917352	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs188859867	chr8:95917411-95917412	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs537000535	chr8:95917427-95917428	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs146834042	chr8:95917433-95917434	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs140723445	chr8:95917436-95917437	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs191989300	chr8:95917471-95917472	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs529523362	chr8:95917513-95917514	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs34379696	chr8:95917517-95917518	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs549511377	chr8:95917536-95917537	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs528390	chr8:95917541-95917542	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs537142336	chr8:95917542-95917543	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs550340884	chr8:95917564-95917565	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs536700163	chr8:95917620-95917621	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs115271320	chr8:95917657-95917658	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs556747566	chr8:95917727-95917728	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs539019566	chr8:95917759-95917760	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs4735330	chr8:95917770-95917771	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs117408367	chr8:95917778-95917779	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs182905429	chr8:95917811-95917812	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs682510	chr8:95917871-95917872	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs575682303	chr8:95917929-95917930	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs4735331	chr8:95917958-95917959	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs564541538	chr8:95917959-95917960	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs145891908	chr8:95918035-95918036	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs78140437	chr8:95918108-95918109	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs140075856	chr8:95918115-95918116	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs187590605	chr8:95918122-95918123	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs2459962	chr8:95918156-95918157	Weak transcription Enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs9643352	chr8:95918288-95918289	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs563084121	chr8:95918302-95918303	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs560283949	chr8:95918303-95918304	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs530549355	chr8:95918339-95918340	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs34803559	chr8:95918340-95918341	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs77493131	chr8:95918378-95918379	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

Disease	PMID	Source
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
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	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
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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute myeloid leukemia	19651601	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Mental retardation	17847001	CNVD
Neuropsychiatric disorder	20069037	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Colorectal cancer	21645411	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:95909400-95917200	Weak transcription	Fetal Intestine Small	intestine
2	chr8:95909400-95917600	Weak transcription	Pancreas	Pancrea
3	chr8:95909400-95918000	Weak transcription	Gastric	stomach
4	chr8:95909400-95920800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr8:95909400-95932600	Weak transcription	Esophagus	oesophagus
6	chr8:95909400-95939000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
7	chr8:95909400-95941000	Weak transcription	Ovary	ovary
8	chr8:95909400-95941200	Weak transcription	Fetal Stomach	stomach
9	chr8:95909600-95917800	Weak transcription	Stomach Mucosa	stomach
10	chr8:95909600-95920600	Weak transcription	Brain Angular Gyrus	brain
11	chr8:95909600-95937000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr8:95909600-95938400	Weak transcription	Primary T cells from cord blood	blood
13	chr8:95909600-95941800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr8:95909800-95930400	Weak transcription	Fetal Brain Female	brain
15	chr8:95909800-95940600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr8:95910000-95940200	Weak transcription	Thymus	Thymus
17	chr8:95910400-95917200	Weak transcription	Fetal Thymus	thymus
18	chr8:95910400-95918200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:95910800-95931600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr8:95910800-95940200	Weak transcription	Hela-S3	cervix
21	chr8:95913600-95930200	Weak transcription	Brain Germinal Matrix	brain
22	chr8:95913600-95932600	Weak transcription	Fetal Brain Male	brain
23	chr8:95914000-95917800	Weak transcription	Brain Cingulate Gyrus	brain
24	chr8:95915400-95917800	Enhancers	Primary hematopoietic stem cells	blood
25	chr8:95916000-95918400	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr8:95916200-95917800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr8:95916600-95918400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr8:95916800-95917400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr8:95916800-95917400	Enhancers	Dnd41	blood
30	chr8:95916800-95917400	Enhancers	K562	blood
31	chr8:95916800-95917600	Enhancers	HUVEC	blood vessel
32	chr8:95916800-95917800	Enhancers	Monocytes-CD14+_RO01746	blood
33	chr8:95916800-95918000	Enhancers	A549	lung
34	chr8:95916800-95918400	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr8:95916800-95918600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr8:95917000-95918800	Enhancers	Primary B cells from cord blood	blood
37	chr8:95917000-95919600	Weak transcription	HSMM	muscle
38	chr8:95917200-95917400	Enhancers	Fetal Thymus	thymus
39	chr8:95917200-95920600	Enhancers	Fetal Intestine Small	intestine
40	chr8:95917400-95917800	Weak transcription	Dnd41	blood
41	chr8:95917400-95918000	Weak transcription	Fetal Thymus	thymus
42	chr8:95917400-95918600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
43	chr8:95917400-95919400	Enhancers	HepG2	liver
44	chr8:95917400-95920400	Enhancers	Fetal Intestine Large	intestine
45	chr8:95917400-95921400	Weak transcription	K562	blood
46	chr8:95917600-95917800	Enhancers	Duodenum Mucosa	Duodenum
47	chr8:95917600-95917800	Enhancers	Rectal Mucosa Donor 29	rectum
48	chr8:95917600-95918000	Enhancers	Sigmoid Colon	Sigmoid Colon
49	chr8:95917600-95918400	Enhancers	Primary B cells from peripheral blood	blood
50	chr8:95917600-95918400	Enhancers	Rectal Mucosa Donor 31	rectum

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