| Tag | Content |
|---|
EnhancerAtlas ID | HS078-07992 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chr17:80287700-80288710 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr17:80288312-80288323 | CCCACCTGCCC | + | 6.14 |
| | | 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 |
| GH17I082328 | chr17 | 80285936 | 80289111 |
| Enhancer Sequence | TCATCTCCCT GACTCCCCCT CCTCTCTCCC TCTCCTGGAG ACCCTGTGAT GGCATCAAGG 60
GCCCCCCTGG GTGACCCAGG ACACATGCCC CAGCTCAGCA CCCGAGGCTT CATCCCATCT 120
GCATAGTCTC TTTGCCATGT CAGGTTCTGG GATGAGGACG TGACATCTTT GGGGACTGGT 180
AGCCGACCAC AGAACCCCCA CCCCCAGTGC GGTGGGAGAC CCAGGCCACC TGCAGACCCC 240
TGCATGGAGG TGAGGTTCAC ACAAGGAGAC CCCAGGGGGC CTGGGTCCGG CTCCCTCACC 300
CCACGCTCCA CGATGCCAGC TCAGCCACCC ACCTTGGAAC CGTGCAGATG GACAGCAGGG 360
AGGGTCGGGG CTGCTGGGGG CTCCCCCACT GCTCTCCGCA CCACCCCGCC GACCGTGTCC 420
GGGAGGGGAT GCCCTGCTGC TCTCCCCAGG CTGCTCTGGG GAGTCCTGCC CTCACCTGGA 480
GCCTGGAGGC CATCTGAGTC TGTTTCACAA ATGCTTCCAG GGACTGCCCC TGCCATGTGT 540
TAGGGGTGGG AATTCTGGGC ACACAGCCAA AGGTCACAGA TCCCCAGAGA GCCCCGACAG 600
CGCTGCGTCC ACCCCACCTG CCCACCCAGG TGCTGGCTCT GCCACCCGTC TGTGTCCTGA 660
GTCAGCCCTG ACTCGGCAGA GAGCTGCACC CTGAGCCAGA CCTCAGCAGC TGGGTCCTGG 720
AGGCCCCCAA GGGCCAGCTG CACGCACCTG GCTTCATGCC AAGCTCCTCC CGCCTGGCAG 780
TGGCTGCATC TGCCTCCCCT CCACCCTGAG TGTCCCAAGT CTGCCCGCTG TGCATTCCAT 840
GGGGCCAGCA GCTCGGTGGA GCCTCTGCTC TCGGGGGCTA CAGCTGCTCC TAGATGCCTC 900
TGCCACCGAG GGTGGACCCT GCAGTGCTGG CTCCTAGCCT CCCTGCCGAT TGCTTCCTGA 960
AGACCTGGGG CCCTGGGCTG CAGTGGTTGG GGAGAGGGGG GTGGGAGTGA 1010
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