| Tag | Content |
|---|
EnhancerAtlas ID | HS136-18555 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chr7:106597890-106599040 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr7:106598345-106598356 | TGCCTGAGGCT | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATGTGCCTGT AATCCCAGCT ATTCAGGAGG CTGAGGCAGA AGAATCACTT GAACCTGGGA 60
GGCAGAGGTT GCAGTGGGCC AAGAACACGC CACTGCACTC CAGCCTGGGT GACAGAGTGA 120
GACTCCATCT AAAAAACAAA AGAACTACTG CTCCAGGTGC TCAAACAAGA AAGGCAGACC 180
TGTGATGATA AGAGGGGTGG ATCACAGTAC AGAGGTACCC CCAAAATCAA ACCAGTGTGC 240
TGTTACTTCT TTTCTCCAGT CTTTCCCAAA CCATTCCCTT TTTGCCTGAA TTTCTGGATC 300
TTTCCAGGGT TCTTCCTAAA TGTCCTAAGA AAGGCGTTTT CCTTCTGGTG TTTTCAAGGC 360
CTCACCTTTC TACCCTACCC CACTGCCCAG CCAGGATTCT CAGTGCCAAG AAGTCTCCCT 420
CTGCAGCTCA GATTAGAGCT ACAGAGCCTG CAAGTTGCCT GAGGCTATGT GAAAAACACT 480
CCTCCTCTTC TGGAGCGTCA CTCACTGATG GTGAGTAGTG GCAAGGAGAA GTGGTGACTG 540
GCTAGGCCAG AGAAGTGAGG CAATAAGATG AGGAACTGGC TGTGCTGGGA CACAAGCTAA 600
GACTTAACAC TTTTGGCTGG AGACCAAGGG GTCTCATCAT GTCAGTTATA GTCACTTATC 660
AGCTTTCCTT TCAGGCCTTT ATCTAAAAAC ACTATCCAAG CTTCCCCCAG ACACCCACTG 720
CATATTGTTC ACCTGCTCAG CAGGTGAAGC AAGTAGGCAC CTTACACAGC ATCCCAGCCA 780
CAGGCACCCC CAGGAACTCA ATCAAAACTC CTGCCACCCC AGAAAGCCCT GCTCCCAGCC 840
ATATCACAGG AACAAGGAGA CTAGAAACAT TCTTCCAGAG TGGCTGGAGA GCAAGGTATT 900
TCATGAACTA ATGGAGTCCT CTATGAAGCA TATACAGTGC AAAGGGGGAG GGTAGATGCT 960
TTTATAAGCT GTTTCATTTG CCCTTACCAC AACACGTAAG ACAGCAATTA GTATGTCTCC 1020
TTTACAGCTA GACAACGGCC CAACGGGGAT ACATACCCAG GATCTAGAAG GCAATAAAAG 1080
TAAAAGCATT TGTATACAGG CATCAAGCTT AGGGGATGGA GGTATAGACT GCTAATGGAT 1140
GGCAAATCTG 1150
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