| Tag | Content |
|---|
EnhancerAtlas ID | HS003-06120 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr10:93057640-93058840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr10:93058176-93058195 | CGGCCTCCAGAGGGCGCCA | + | 7.52 |
| | | 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 |
| GH10I091297 | chr10 | 93057661 | 93059062 |
| Enhancer Sequence | CCCACTGCCA CAGTTTTAAT GGGAGTGTCC CGGTTTTAGC ACTTAATAAT CTCATGACCC 60
GGGAGCTCCA CTAGTCTTCT GCAAACTGCG ATGGTGGTTT CCTCTACCTG GGAGCCTGGC 120
AGCCCCACCA GGCCCTACAG GATTACATCT GTTGACTGCA CTCAGTTTTA CTTCATTGCA 180
GGTGGTGTTT CTTTCCCTTG GTAGAGTTCT TTCACTAACA CCCCTGTGAG TCTTGTCAGA 240
TGTGATTAAA CTCTGGGCAA CACAAATGGA ATGAAAAGAG GGAGGTGGAA TTGTTTTTTT 300
TTTTTTTTTT TAACGTGAGA TAACTGACAG GTAAGACTTG AGATGAACCG GGGGGTTAAA 360
GAAGGGTATG CGTGCCTCTG GGTGCTTTGC TATCTATGTG CTCACACATA AGAAGGAGTA 420
TGTGTAATGT ACTGAGGAAG AGACCTTGGG AAGCCCGACC TGGGCAGGAG CCCCTGGAAA 480
GTGGGGGAGG GGAAGGCAGC CGTGGCTGCA AAATTGAGGC ACACAGTTTC CCATCACGGC 540
CTCCAGAGGG CGCCATCAGC CCGCAGTGGT TCTTTGCCTT TTGAGGGCGG GCAGAAGGAA 600
GAGGATCCAC CTGGAGGATG GGTAACGAGA GCTGCAACCC ACTTCCTTCA GGGCTGGGGC 660
ATGCAAGAAC GAGGAGTGGA CCGCTCGCAG TGCTTGAATG TCCTCCTTGT TAACCCCAGC 720
TGGGATAAGC ACCTCCGCCT CATAAGATCA AAGCTCTTTC ATTCCTGCTT TAACTTTGCC 780
AGTTCCCTTT ACTTCGGAAA GAATGAGAAA CCTCATCCTA GCAATCCCAG GGATCTGTGC 840
CCTCCAGAGG AAGATCTCTG CAAAGCTGTT TACAGCGGGT TGTTTGGAGG CCAGCTTCTC 900
TGGCACGGCG CGGTGTCCCC GTGGAGCGTT TCCAGGGCGC GGAGGCCCTG GGTCACCAAC 960
TCGAATGAAT AGTGAGTGAG CTGATTGCCG CTCCACGCTG ATGGATGTAT ATTTGTTACA 1020
TTTGAAGTGT TCTGAGAAAA GAACTGCTTC TGAAAAGAAG AGCTTTGTGT GAGCACAGTG 1080
AACATGAAGG GCGAGATTCC AAAACCTTTA GGAGGGTTTT CTTTCTATGC AAGAATGAGC 1140
CACAGAAAGC TGTTCCCAGC ATCCTCTGCT AATCTAGGAA CACCTATGGA AAAGCGTTGT 1200
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