| Tag | Content |
|---|
EnhancerAtlas ID | HS182-20990 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:101511200-101512400 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr8:101511907-101511928 | CCCACCTTGCCTTCCTGCTCC | - | 6.03 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_10674 | chr8:101510902-101515105 | CD19_Primary | | SE_18643 | chr8:101511307-101518472 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19354 | chr8:101511461-101517986 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_32509 | chr8:101503517-101515892 | GM12878 | | SE_43976 | chr8:101510817-101513392 | MM1S | | SE_62291 | chr8:101421434-101542088 | Tonsil | | SE_65844 | chr8:101511567-101512474 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I100487 | chr8 | 101499294 | 101515906 |
|
Enhancer Sequence | GACAGCAGAC AATGCAGAGC AAGCCCTTCC CTCCTAGACC CTCCCCAAAT TCACCTAACC 60
AAAGCCCAAA GCCTAAAAGT CCCTTTGAAC ACCTTTTTAG TGAAATGGTG CCCCCATGAT 120
ATCTTCCTCA TTGCAACCAG TAATAAAGCC AACTTGTTCA AATGCCGGTT TGCAAATAAA 180
TCACTTGGGG ATTTGTTAAA ATGCAGACTG TGGTTCAGTA GGTCTGAAGT AGAGCTTATT 240
CTGTGTTTGC CACAAGCACC CAGTGAGGCA CTTGCTGCTG GACCATGGTC CCACTTTGGG 300
TAGCAAGGCA GTTAAGGGTG GCAGATTAGA ACACTGGACA TGCTTAACCT TGACCATGGG 360
ACCACTGTAT GCATCCTGTT GTTTCTCAGT GAAAATATGC CTGTATTTCA TGTAAGCCCC 420
CGCTATATAT GTTGGCTACT AGCAACTTAA CCAACACGTT GTCCTTGTCC TTAGAAAATG 480
TGTGGTTACA GCCAGGTGTG AGCAGGCCTA GACCAGGCTT GGGGATTTAT TGACCAAATG 540
TGGTGCCTTT GAGGTGAAAC CACAAGTAAT CAGAGAAGCT GAGTCACTCC ACTTAGTGGA 600
CTGGTGGAAA ATTCTCAAAT GGTCTTAAGC TGGCCCCATG TTGGGCTGAG GACTAGAGAT 660
CTCAGAGGCT CCACCTGCCC ATCCAATTGC AGGTGTCTGG GCCTGGCCCC ACCTTGCCTT 720
CCTGCTCCAT TGCTCACCAT TCCACACCCA AAGGCACCAT GATGTTTTGT ACCTCCTTGC 780
CTTTGCTCTT CCCTTTGCCA GGGATGCCCT TCCCACCTTC CTCCACGTGG CTAACCCTCC 840
CTCAGCTCTG CTTCCAGGGT GTCTCCCCTG GTCGCCAAGG GCTGGCTAGT GCCTCTTCTT 900
TGCTCCCAGG GCACCCTGTG CCTTTCTGTG CCCCAACTAT TTCCCAGTTT GTAGCAGTTA 960
TTTATTTTGT GGTCATCTTC CCACTGGTCG TCAGCTCCTA GAGGGCAGGG ATCATGTTTT 1020
GGGTTATTCA TCACTGCATC CCCTGACATA GTCCCCAAAC CTCGAGAACT ATGAAACTGC 1080
ACCAAAGGTT CCAGCTCCCC CACAGCCTGC CCTTAACCTT GAGCCATTTG AAGGGAGAGT 1140
ATGAGACAAT AGTGAAAGAA ACCCTTCTCT AATGTTTTCC CCATTTAGGT TATGTGAAGT 1200
|
