| Tag | Content |
|---|
EnhancerAtlas ID | HS062-10058 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr20:23422270-23423250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr20:23422636-23422655 | CTACCACAAGATGGCGATG | + | 6.01 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH20I023441 | chr20 | 23422561 | 23422730 |
| Enhancer Sequence | AGATAATTAT TATACTGTAC TGTTTAGGGA ATAATTACAA GAAAAAATGT TCAGTATACA 60
GGCAACCATA CATTTTTTTT TCCTGAATAT TTTGATGCAC GGTTGTTTGC ATCCACAGAT 120
ATGGAGCTCG TAAGTACAGA GGGCTGACTG TAGAAGTTGG GGCAGCAACA ATGCTACGTC 180
CTAGTTCAAT TAGCTAGATT TGGGAAAACA CAACTGGCTA TGGGAAAGCT CTCTCGCCAG 240
AGAGTAAGGC AGCTGGAACA GAGAGAACCG GCAAGGCGGG AGGGCAGCGT GGGGAGGACC 300
AGTCAGCATA GGTCAAATCC TCATCCCAAT GCAGACTGTC CCACAGGCTG GCTCAGTGAG 360
GCACTTCTAC CACAAGATGG CGATGTTGCC CATTTGGTTC TTGGTTCTTC CACAATTGGT 420
TAAGACCCCA AGGAGGCTTG CCTTGTGAAA TCAATCCATC ACCATTAAGT TAGCTGTTAA 480
GGAATAATGA TGAGCATTTG ATGTCATTCA CATTGATAAG CAGACAGAGC AGGCGTGCCT 540
CCTGGTAGCT GGGTGATCTT GGCATGGGCC TCTGGGCACC CCCACACCCA TATGACCATT 600
GTGTCTGTCC TTACACCTCA CAGAGGGGAC AAGAGCAGGC GTGGAGGGCT GCCAGGTGCC 660
TCTGGGGGCT TCACGCCCAG CTCCTCCCAA CTGAGGCTCC TGGTCAAGTG ACATCCAGAC 720
TCTCCAGACC TCAGTTTCTT CACCTGCAAA GTGCCTCAGA ATAGGAGGGA AGCACTTAGC 780
ACAGTGCCAA CATCTGGTAG CACTTATAAA AAATCTTTGC TGTTATTATG ACTACTCCTG 840
TCATTATCGA ACAAATAAGT CTAATAACGA ATAACACTTT GCACACTGGA ATGTCAGTTA 900
CAGTGATGAC GGGTGGTTTA GTTTTTTCTT ACATTCTGAG CATGCTGAAA GTCAGTGTGA 960
CCGTGCCTGG GGCAGCCCTG 980
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