Tag | Content |
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EnhancerAtlas ID | HS111-01008 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr11:75247940-75249010 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr11:75248639-75248657 | TATTCGTTGCTTCCTTCC | - | 6.31 | EWSR1-FLI1 | MA0149.1 | chr11:75248651-75248669 | CCTTCCTTTCTTCCTGCT | - | 6.47 | EWSR1-FLI1 | MA0149.1 | chr11:75248643-75248661 | CGTTGCTTCCTTCCTTTC | - | 7.07 | EWSR1-FLI1 | MA0149.1 | chr11:75248647-75248665 | GCTTCCTTCCTTTCTTCC | - | 8.78 | NFE2L1 | MA0089.2 | chr11:75247982-75247997 | TGAGCTGAGTCATTG | - | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_40143 | chr11:75244525-75250142 | K562 | SE_56776 | chr11:75248261-75248733 | VACO_400 | SE_59711 | chr11:75184251-75249346 | Ly4 |
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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 |
GH11I075536 | chr11 | 75247240 | 75249656 |
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Enhancer Sequence | AGACATCTGC TGGGCAGAAA CGGCCAGACC TCCTTCTCCC ACTGAGCTGA GTCATTGGCT 60 AGGGCTGCCC AAGGAGAAAG TGGCCTTGTC AGGAACACAG CAGTAGATCC CAGGGTGTTG 120 CTGCTGGGAT CTGTTGCTAA CGACACTCCT GCTCTACACT CTCTTAAAGG AAGATCTGAG 180 TGGCAAACCT CCATGGCTTG ATGGATGTTA AAGTTGGAAG GAATTTAAGA GATGCTCTAG 240 GCCAGCCGCT GTCACATTTT ACAGATGAGA AAACTGAGGT TGGCCAGAGG AAGTGACTTG 300 CCCAAAGCCA CCCAGCATGT AAACCAATAT GCAAACCCAG GTTCTGACAC CCAAGTCTGC 360 GCTCTTCTGA ATCATTGCTG ACTCAGAGTC ACAGTGGGGC TAGAGGGCAG TGGGAGGAGA 420 GTGGCAAGGT ATGACTTCAG GACGCGGCTC AGGTGTCACT TCCTCACAGA AGCCCTGCCT 480 GGACCCAAGC TCTTCTCTGG GCTCCCCGAG GCCTCTATCC ACTCATTTAC CAGTCAGTTC 540 TGTGAATGTC AGCTTGTGTG TCTGCTTCCA TGAGGCCATG TCCCCAGCAC CCAGCATGGG 600 ACCCGGAACA TCGTGCTACA TGTGAAGGTA CACGCCTCTG GTTTCTACTG CCCTCTCTGG 660 CAGCTCAACC CTCCAGGACA GAAGAGCAAT CGGTTCCGCT ATTCGTTGCT TCCTTCCTTT 720 CTTCCTGCTT TAAATAAATG TATACTGAGT GATTACTTCA TACAGTCCTG GGGACACAGC 780 GGTGAAAAAT TTTGCCTTCA TGAAATTTAC TTTCTAGTAG AGGGAGGTAG ACAATAAGCA 840 AAACAAATAC AAGGAGTGGT GTATTAGATG GGATACATGC TATGGGCAAA AGAAAGAGCC 900 TCAGAGACAG AGGAGACCAG GAGGTGTCAG CGAGGACACT TGCCACTTAG AGGAGTCAAG 960 GAAGCTGACG TTTGAGTAAA AGCCTGAAGC AGATGACAGG TGTGAAGGCC CCTGGTGTGT 1020 TCACACTAGG AGGCCAATGT GGCTGGAATG GAGGCAGTGA TTGATGGGGT 1070
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