Tag | Content |
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EnhancerAtlas ID | HS158-30613 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr2:73258750-73259860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr2:73259468-73259482 | GATCCCTTGGGACT | - | 6.02 | HNF4G | MA0484.1 | chr2:73258917-73258932 | TGGACTTTGGCCCTC | - | 6.69 | Hnf4a | MA0114.3 | chr2:73258915-73258931 | CATGGACTTTGGCCCT | - | 6.21 | Klf12 | MA0742.1 | chr2:73259073-73259088 | GGCCACGCCCAGCTT | + | 6.41 | ZNF263 | MA0528.1 | chr2:73259800-73259821 | CTCCCCTTCCCCTCTGCCTCC | - | 6.31 | ZNF263 | MA0528.1 | chr2:73259803-73259824 | CCCTTCCCCTCTGCCTCCTTC | - | 7.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 73258875 | 73258976 | chr2 | 73259404 | 73259789 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I073030 | chr2 | 73258057 | 73262529 |
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Enhancer Sequence | AAGTGGTGCT TGAAGCTCTT CTTGAGGCAT CTGACAACAC ACCAGACTCA GAGGTTTTGG 60 GGTGAGTTGG GAGGAACATC TCCATTTTCA ACAAAAATTC CTAGTCATGA TCTGATCTTG 120 TTTGGGCTGA TCCCATCACC AGGCTGCAGT GACAACAGTC AGGATCATGG ACTTTGGCCC 180 TCTCTCAGTC ACTAACTTAC ATAGCCTGCC TGTGCAAGTT ACCTCACAGC TTGGACTTGT 240 ATTATTTTTA AAATTAGGCA GAAGCAGGGA CAGGAGGTAG AAGCAAGTCT CTCCAGGGCC 300 CCTTCCTGTC CTACGGTGTA TGAGGCCACG CCCAGCTTAG AGGGAGAACA GGACAAGGAC 360 TCAGGTCTGA CTCCTTGGGT CTAGGCTTTT CCCTAGGACC TGCTGGATTA AATGTTGACT 420 TTAAGGGGTT AAATGTCAGA TGCAAAAATG GCAGCAGGTA ATGTACCACC CACAAGCCAA 480 GAGCTGGTTG CTAGTTTGAA GTTTCACAAG CCAGTCCTGC AAACAGGTGA TGGGGGAGGA 540 TCATCCTAGG GTGTCAAGAG TTCGACGGGA CATCCTAGGA TATCAAGAGT TCAACGTCTT 600 CTCACTAGAC CACTGAAGCA TCTCCACTTT AAACTACAAT TCCTGCTTAA GACCTCATCT 660 TGTGTGGGCT CAGCCCATCT CCTCTGTGCC TCTGCTGAGC ATAAAAATAT GCAGCTTTGA 720 TCCCTTGGGA CTTACTGGCT CCAACAACAA ATCAGTGTGG ATATGAGACT TTGAACCTTG 780 CTTGATTTCT CAACTTGGTA AATAAGAACA TGGAGCAGGT GTGGAGAAGC AATCCGGGTG 840 AGAGGTGGCT GGAAGATCCC AGAAGTTGGC TAATTTCAAA AACAGCCAGC ATCTCAGCTG 900 AAGTGCCATC TGAACCTACC TGAAGTTCGG TGTAGAGTCC AAGGGAGGGG CAGAGGACAC 960 TCACCAACTG GCCTTCTCGG GCAGAGCGGG GCACACCCCC AACACCCAGA GGGAGGAGGA 1020 ACAGCCCAGC CCCACCCCCA ATCTGGCTCG CTCCCCTTCC CCTCTGCCTC CTTCCAAGCT 1080 GCTTCTCCAA ACCTCCCAAG GCAGCAAAGA 1110
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