| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13087 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr17:13085750-13086650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr17:13086397-13086412 | TGACCTCTCACCCTG | - | 6.51 |
| | | 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 |
| GH17I013182 | chr17 | 13085837 | 13086583 |
| Enhancer Sequence | ATTATGTCAA TTAAAAAAAG ACAAAAGGAG AAAAGAAAAG AATAAAGTAT ATGTCCCAAG 60
CTTATAGAGC ACCTGCAAGA CCTTGGGTTT ATACTGAGTT CTCTTTGGCT TCAGCCCTTT 120
TCCCTTCCTG TTAGAACACA AAGCTTTCCA GGGGTCACCT GGTTTGTCCC TGGCACTGCT 180
GCTGGGTGTC ACCTCATCAT AAATCCATCC AATGTTGCTG CACATCACTG CTTCCTGGTC 240
CTCAGGAGGC TAATGCTCCT GACAGGTGCC ATCTGACCAT GTCACTACCT GAAGAGCTGA 300
CCTGCTTCAC AGGCAGGGGG ACAGAGTGGC ACATCAGAAA GCCACTGCTA TGCATTTCAC 360
CTACAATTAA GTGCTAAGGA ATAATAGTGG GGCTTTTATG CTACATGCAT GTTTTCCTTT 420
CCATTAAATC TCAGATATGC TGTTTGCATA TCTTAGTTCA GGCTGCTCTG AAATCCATAG 480
GGGGAAAGAA ACCCTTCATT AAGTTCAGCA GCACTGTCCG GCAATGCAGC AGCACTCCTA 540
TTTATTTTTC CTTCTGTAAA TATTTGTGCT CTCTCAGGCT AAGGAGTGGC CTGTGCTAGA 600
GACTAAAATA TCCCCATTTA TATCCTCCAG GTGCAGCAGG AAACGCCTGA CCTCTCACCC 660
TGCCCCTGCA ATGACCTCAA CCTCACTTAT GGGGACCACC CTCTGGGCTG CCCTAATGCA 720
GACCCATGAT CACCTCTCCA GGTTGACTGC TGAATAGCAG GAGAAGATGA ACCTGAAATT 780
GAATGGTTAT TGCAACCCAG TTTTTTCGGT CGAAAGGTGA AGGTTACTTA GCTTTTGTTG 840
CTGCCTTCAA GCTTGTTAAT GAAAAGATGG AAAAACAATA TTGACATCAG TGAAGTCCAA 900
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