| Tag | Content |
|---|
EnhancerAtlas ID | HS081-00929 | Organism | Homo sapiens | Tissue/cell | HACAT | Coordinate | chr1:112490670-112491870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:112491131-112491152 | TTCTACTTTCTCTTTCTTCTT | + | 7.57 |
| | | 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 |
| GH01I111947 | chr1 | 112490499 | 112492188 |
| Enhancer Sequence | TGAATACCTA GTGAGTTCCT AGTGTACCCT GGGGTACAAG GATGGCCAAG GAAAGTCCTA 60
TCTGTGTGCT TTGGGGAGGC TGCCCCATCA TGCCCACAGG GCAAATGGGC CCCACCATGC 120
CCCTATCCTG TGCGTGGCCT CCCTCTCTGC TCTGCCTCTA CAGAAAGATC TATTTCAAGC 180
CACGGGGCTG GTGCTGGCCA TGGGCTCCCC TGCCAGAGAT GAGTGCTGTT CCCATCTGTA 240
AATGACTCCA GCTCCTGGAA AAGCAGCCAC AGACAAGTGC TTAGCAGCAA ATAGATCACT 300
CCCCACAGAG CCTGTGATTC ACAGGGCAGA AAGCCAGCCT CCTGAGGTGG CGTAGGGAGG 360
CGGCAGCCCT GGGAGGTGCC AGGGAGGTGC TCAGGACTCT GGCCCACACT TAAGGATAGA 420
ATTTATCTCT TCCCTTCCCC ACAGCATAGG GCTGTTCTGC CTTCTACTTT CTCTTTCTTC 480
TTTCTTCTGT TCTCCCACTT TTTTCCCCCT GGGTTGGAGA GAGTTCCTAT CCCATCTGCA 540
CAGGTCACTT CCCCAGAGAG GCTTAAAAAC CCTCGGACCA ATTAGCTGGA AGCCTGTGGC 600
CAGGGTCTTT TCCCTCTGCT GCAAGCAGAC CTGCTGCTCC CCTCTGGGGA GCTGGCCCAG 660
TCTAGCCCTC CTCACTGCCA GGAGGGCTGG GCAAGATCCT CTTATCACAG CTGTGAGCAG 720
ACAACCATGC ACAGCAGGAG AGGGAGGGAC AGGGAAGTGG GGAAGATGAG GGAGGGATAG 780
GCGAGAAGGG AAGGGCTTCT GGAAGGTGAG AGAAGGAGGA GCAGCAAGCA GCAGGCAGAG 840
AAGAGAGGGC AAGTCCAAAC AAAGAAGAAC ACAAACAATA GAAGGGCTGG CTATCAAGAA 900
GATCTTTTCT TTGGGGGCCA ATGCCATATT CCAGCATGGG CAGGAAACCA CAACAAGCCT 960
TTCTGAGCCT CACTCTGAGT GTCTAGGCTT GTGGGAGGTG TAGAAGCATG ACACGCAGCC 1020
TTTGTCCCAC AGGGGCTTGC AACTGGGCTG AAGGGCTGGT GTGAGTATCA CATGTGCAAG 1080
TCCAACTAAA TGGAAATAAA ATGCTTTTGT CTGGGAATAG AAAGTAGGAT GATAGTTCTG 1140
ACTGTGTCAC TCACAGCAAA GTGAGCCTGG GCCTTTGGTG GATCTCCGGG TGCCTTGGTT 1200
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