| Tag | Content |
|---|
EnhancerAtlas ID | HS003-26163 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr2:75373420-75374760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr2:75373527-75373538 | AATGAGTCACC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 75373675 | 75373831 | | chr2 | 75373915 | 75374243 |
| Enhancer Sequence | GTATTTTTAG TATACACAGT GTTTCACCAT GTTGACCAGG CTGGTCTCGA ACTCCTGACC 60
TCAGGCGATC TGCCAGCCTT GGCCCCCCAA AGTGCTGGAA TTACAGGAAT GAGTCACCAT 120
GCCCGGCCAG CAGCATCTTA GAAACCAAAG AAGACAGCCT CAAAAGGTAG GGAGTAGCCC 180
ATGTGGTCAT TTGTTACAGA GGAATCAGGC AAGATAAGGA TGAAGAAGAG TCCGCTGTAT 240
TTGGCTTCTA GGAGATTACT GGTCACAATG GCAAGAATAG CTTTAATTCA TTGCAGCTGT 300
GGGGGTACCA AAGTGGAGAT GAGGATTATT GCGTTACTTG TGATGCTAAT AACCATAGAG 360
GAGCCAGCAC ATGTGGAATC TACTAGTTAC TGAGTGAAGT CACCAAACCC TAATGAGTCT 420
CAATTTCCTC ATCTATAAAA TAGAGTTGCA GTTGCAGTAA AAAAGTGTGA TAATGACTGT 480
AAAATGCTTT TTAAACTATA AACCACTATA CAAACAGATG GCATTATTTT TGGTTCTGGT 540
GATCTTCCAG GCAATATTTT AACATGAAAT GTGCTAATGA TGATGGCACT GAAATAATGG 600
CCTTGAACAA TTTCCCCATC ACTTCTTCTG TGGTCCCAGT GTTTCATTCC AGGATGGGTT 660
CTGTAACCCT TTTAACACAG AAACACAATC TGCTGTGTGC ATTTACACTG ATGCAAACTA 720
AGCTGCTGGG GGAAGTCAAC TGATCTGAAA TGTTTTGCAA TACTGTGCAT TGTTTCAGCC 780
ATCAGACGGT GAGTAGGATT CCTGTTCCAG TCAAGTTAGG TGGCAGAATA TTTTCCTGTT 840
TGTCTAAGCA GATGCCAGCA CTTAAATAAA CACCATGTTC CTTCCCAGAA TTTAGCTGGA 900
AAATGCCCCC ACCAAAGAGA ACCCTGAGAT GCTTGGCACA TGGCCAAAAC CAGCTAACAT 960
TTCAATTTTC CTTTACTCCT ATTGTGTGGC CATAGGGCTG ATATTTCCCC AGAACCTCAG 1020
TGGGAACATT CCAGTGACAA CTACCAAGTG GTCATAACAT AATGGGTTTA TCCCCACATT 1080
CCTTTCATCC TTTATCCATC CCTATAAAGT GTATTTTTAA AAATTTTTAT TTTACTTTAA 1140
GTTCTGGGAT ACACGTGCAG AATGTGCAGG TTCATATATG CGTGCCATGG TGGTTTGCTG 1200
CACCTATCAA CCTGCCATCT AGGTTTTAAG ACCCGCATGT ATCAGCTATT CGTTTTAATG 1260
CTCTTGCTCC CCTCCTGCTC CACAGGCCCC AGCATGTGTT GTTCCCCTCC CTGTGTCCAT 1320
GTGTTTTCAT TGTTCAACTC 1340
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