Tag | Content |
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EnhancerAtlas ID | HS053-32394 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr5:130945540-130946980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr5:130945799-130945810 | AAACCACAGAC | - | 6.62 | Stat6 | MA0520.1 | chr5:130946453-130946468 | TCTTCTCAGGAAAAG | - | 6.31 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I131609 | chr5 | 130944721 | 130947124 |
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Enhancer Sequence | AATCCAGGGG CTTCCAGAAT GCCTGAACCA CAGGACTAGA ATCCCACATA CCAGAGTCCA 60 ACCAGTGGAC CCAATTCAAA GCAAACACAG GAGTATGATC ACAACCTTGG GACCACTAGT 120 CATATCACAT ACCACACAAT CCAGAAGCAA CTGGCCTCAC AGAACGCTGT AATAACCTTA 180 TAAAGGCATA GCTGAACTTT CAGCTTAAAG GCAATAATGT GAAATAATGG AATGACACCT 240 TTTAATATGA AGATACATCA AACCACAGAC CTCTATATGG AGCAGTGTAT ACAGCAGGAA 300 GAACAGATGG GCCTAGAAAC AAATGAGTAG AAGCAAGAGT CACCCATTTA TCATTATTCC 360 CAATGAGCCA CAAAGGGATT TTGTACTTCC CATTCCTACA GCTATGGACT CTGCATGTTT 420 GCAGGTCCTG GTTCCAAAGG CCTATACTCT TGCCAGGCAA CAGTACAAGA GTCTCAGTGA 480 ACAAGTTTAC AGCTGCCACC AGGGCACTTT AAACACCAGG GCCCAAGAAT CAGCAGGTAA 540 GAAGAGTTGC CATTTTGGCA GGGATAACTG ATCCTGAGCA GTAGGTGGAC GCAGGGCTGC 600 TTTTATGTAA TGTGAACAGA GAGGAATGTG TGGAATCCAC ATGACTCGCT TGGTTATTCC 660 TTTACCTCAC TGTAACTGTA AACGGATATA TATCCCAGCA TTAGCCTGAG AAGAATGATT 720 ACCAAGGGTT CAGACATTTC AGGAAAGAAG GCTTGAGTCA TACCAACATA TAAGCCACTG 780 AGACCTGCAG AGCTGATTAT GTGAGGAGAA AACAAAATGC ATAGTGGAGG AGAGAGGATA 840 AGTACCAGTT GCAACCCCGA GATCAACCAT ACAGGGGCTA TAATTCTTCC CACCACCATC 900 TCTTGTCTAA GTTTCTTCTC AGGAAAAGAA GCTCATTGAG AGCCATGGAG GAGCTGCTCC 960 CTGAACTTCA AACCTATGTG AAGAAGTAGA TTTGTGTGGT GCAAAGTGTA AGCTCAGGTG 1020 GCCTTGAAAA TATGCCTCTC AGATTCCAAA CTACAGGGAG TGTATTTGAA CAAAATCCCT 1080 ATTACGGGGC TCTGTAATTT ATCAACATGT TTGAACTGGG GCCCAGCTTC CCATGCGATA 1140 CTCCCAATCA ATAACTGAGC CTGGTAAAAA TACTAAGGAA TGCCTGTTCT GGGAGACTCA 1200 GGAATACTCT GATGGGTTCA AGGATTCTCC TTCCACCTTG CTAAACCACT GTTACAGTGC 1260 AGTCTAAGGC TCTTCCACTC AAACTTCCTT TCGTCTCTCC TTCACAAATG TCACATGAGC 1320 ATTCTGGTGT GAATGCTCTA CCAACTCTCT CCATTTTTGC TCAGAGGCAT TTTCCCTAAT 1380 AAATTCCTTG CATGTCTAAT ATTGTTGTGA CAACTGCTTC TAACAGAACC CAGACTAACA 1440
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