Tag | Content |
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EnhancerAtlas ID | HS105-49078 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr20:4775600-4776460 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr20:4776216-4776231 | GTATGACTCAGCAGC | + | 6.55 | Nfe2l2 | MA0150.2 | chr20:4776214-4776229 | TCGTATGACTCAGCA | + | 6.24 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_06375 | chr20:4775424-4777225 | Brain_Hippocampus_Middle | SE_09197 | chr20:4775153-4780650 | CD14 | SE_10934 | chr20:4775238-4780631 | CD20 | SE_18653 | chr20:4775054-4778727 | CD4p_CD25-_Il17-_PMAstim_Th | SE_58920 | chr20:4775227-4805209 | Ly3 |
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| 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 |
GH20I004794 | chr20 | 4775525 | 4776350 |
|
Enhancer Sequence | AACAGAGAGG GCTTGGTTTT CATTTAAACC AGAAAAAAAG GTCACTGTGG TTTTGGCTGA 60 GAGGCGAGCA CACTCCACCC AGGCTGGGGC CGAAGGCAGT CAGCATCAGC AGGTTTCAGG 120 ATGGAGACAG GCTAGTCACT TGATCCTAAA ACTCAAGTCC CAGAAAGACA ATAAAGAGGG 180 CATGCCTTGC TAGAGGCATT TGGCGGCGCA TTTGGCGGCT TATTCAGCCA TGGAGGATAA 240 GGAGGGATGG ACTAGGTCTT CCCAGCCCTT CTGGTGGGAA CTTAGACTAC CACCATCTCA 300 CCAAACCCTG GCTCCCCGTA TGGTCTGCAG GGAGCAGACC CCTGGCTGAT CTCGCTTGGC 360 TGACTCTGAC AGAGCCTGAC ATTCCTTTTC CTCTTCTAGG TTCCCCCAAG ATTCAGAGAG 420 CTTTGGTCAG AAGGTTCAAG TCATAAATGC TTTGGAGTGG GGCTATTCTA TGAGGAGTGG 480 TCCCAGTGGG GAGGGTGCTG GGGCATGGGG CGCCCTGTTA GAAATATACA GGCTGGGCCT 540 CACTAGCCAC TAGCAGCTCC ACTCAGAGAC TCCTGAGTTC TCCCTAAGGG AGGACTCTGA 600 CTCAGCAGCT CCCCTCGTAT GACTCAGCAG CTCCCCTCCT GTGACCTCAT CAGTGATTGC 660 AGTGACAGGA AGGGGGCTCA ATCACAACCA CATCTGCTGC TTGTTCCTCA TTCCAAGGCT 720 AAGGCAGGTG GGCAGTAGAG GTAGTAGGAG GAGGAGCCAG GGTCAGGGCT GGCTGGAAGA 780 AGGCAGCATT TATCTGCTTG AGAACACATA GAACACCCAA GCATCCCAGT CATCTCCCTG 840 CCCCGTCTCT CCTCACTCAC 860
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