| Tag | Content |
|---|
EnhancerAtlas ID | HS116-27882 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr5:137229100-137229990 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR3C1 | MA0113.3 | chr5:137229261-137229278 | AGGAACAATATGTTCTA | - | 6.26 | | NR3C1 | MA0113.3 | chr5:137229261-137229278 | AGGAACAATATGTTCTA | + | 6.47 | | NR3C2 | MA0727.1 | chr5:137229261-137229278 | AGGAACAATATGTTCTA | - | 6.37 | | NR3C2 | MA0727.1 | chr5:137229261-137229278 | AGGAACAATATGTTCTA | + | 6.46 | | Stat4 | MA0518.1 | chr5:137229416-137229430 | TCATTTCCTGGAAG | - | 7.38 | | ZNF263 | MA0528.1 | chr5:137229675-137229696 | GGAGGAGGGTTGGGAGGAGGG | + | 8.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAAAGAACAG TTAAGGGGAC AGCAGTTTCA GCTATCCCAG GTCACAAAAC CTGGCATATG 60
CACATTGGGG CATATAAGGA CAAGGCAGAG AACGCTTCCA GTGGTGATGA CAATTTAGTT 120
GCATTTTGAA GCATGAATCA GGGATGGGTA TTTTAGGAAG AAGGAACAAT ATGTTCTATA 180
AGTAATTCTA CATGTGGAGC TATGTTTGGT ATTGTGAGCA TATGGAAGAT GAGGTGGAAA 240
AGACCAAATT ATGAATTGGA CAGAGTTCAT ATCATGAATG CTGTGCAGGA ATTTGAAACT 300
TATCAAGGAG ACACGGTCAT TTCCTGGAAG AGGGCAAGTG TGAGATGAGG GCTAAATGAT 360
CCTAGACGGT TGGTTTAGGC TAGGTGAAAT AGGAAACAAT AATAAAAGAG GTGGAGGTCA 420
CCTTGCCACT TTGTTATTGT GTTTTCTGAA GCATGTATGT GGCCAATGGC AGAGAAGACA 480
AAGGGAGGAA GTAAATGAAC CCTGGGCTTG GGTTCATCTT AGAACGATCA GCAAGGGCCA 540
GAGCCAGGAG TAGCAGGCAC CATGGCCAGA GTCGGGGAGG AGGGTTGGGA GGAGGGGTAC 600
AGACAACTTT GGAGTGAAAT CATGATGTGT GGCTATGACC AGCTCTGATA CTCATGTATT 660
GGAAGAAAAT TTTCGATTTA CTCATATAAG GAGAGAAGAA GGGCTATGGG ATTCCATAAG 720
TTAATGCTTG TAAAGTGCTT AGAGCAGTGC CTAGTACACA GTACGTGCTT AATGAGTGTT 780
AACCATCCAC AGTAGCTTCA TTAGCATTAC CATTACCATT AATGGTAGCT TGGTCAATAG 840
TTTGATTTTC ATACTCAAAA TCTCTTATGC ATAATGTTAT GAATGTAGAT 890
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