| Tag | Content |
|---|
EnhancerAtlas ID | HS043-02321 | Organism | Homo sapiens | Tissue/cell | Fetal_heart | Coordinate | chr1:112490440-112491900 | 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 | CCTGGGCTGG GATGATAATT GTTGTTCGAT TAGTTTTTTG TTTATTTGCT TGTATTACTG 60
TGTTTGGCTT TCTAACCCTT GTCTTGGGTA CGATGACACT TCTCCAGTGG GGACTATGTG 120
TGTATATATG TGAGGAGGGT CAGGTAAGCA GTCAGGGGGA AGTGAGGAGG GACAGGTTGT 180
ACAGGCCTCA CCTCCGAGGA GCCCTGTTCA GCCACCACTC ATTCCTTCCA TGAATACCTA 240
GTGAGTTCCT AGTGTACCCT GGGGTACAAG GATGGCCAAG GAAAGTCCTA TCTGTGTGCT 300
TTGGGGAGGC TGCCCCATCA TGCCCACAGG GCAAATGGGC CCCACCATGC CCCTATCCTG 360
TGCGTGGCCT CCCTCTCTGC TCTGCCTCTA CAGAAAGATC TATTTCAAGC CACGGGGCTG 420
GTGCTGGCCA TGGGCTCCCC TGCCAGAGAT GAGTGCTGTT CCCATCTGTA AATGACTCCA 480
GCTCCTGGAA AAGCAGCCAC AGACAAGTGC TTAGCAGCAA ATAGATCACT CCCCACAGAG 540
CCTGTGATTC ACAGGGCAGA AAGCCAGCCT CCTGAGGTGG CGTAGGGAGG CGGCAGCCCT 600
GGGAGGTGCC AGGGAGGTGC TCAGGACTCT GGCCCACACT TAAGGATAGA ATTTATCTCT 660
TCCCTTCCCC ACAGCATAGG GCTGTTCTGC CTTCTACTTT CTCTTTCTTC TTTCTTCTGT 720
TCTCCCACTT TTTTCCCCCT GGGTTGGAGA GAGTTCCTAT CCCATCTGCA CAGGTCACTT 780
CCCCAGAGAG GCTTAAAAAC CCTCGGACCA ATTAGCTGGA AGCCTGTGGC CAGGGTCTTT 840
TCCCTCTGCT GCAAGCAGAC CTGCTGCTCC CCTCTGGGGA GCTGGCCCAG TCTAGCCCTC 900
CTCACTGCCA GGAGGGCTGG GCAAGATCCT CTTATCACAG CTGTGAGCAG ACAACCATGC 960
ACAGCAGGAG AGGGAGGGAC AGGGAAGTGG GGAAGATGAG GGAGGGATAG GCGAGAAGGG 1020
AAGGGCTTCT GGAAGGTGAG AGAAGGAGGA GCAGCAAGCA GCAGGCAGAG AAGAGAGGGC 1080
AAGTCCAAAC AAAGAAGAAC ACAAACAATA GAAGGGCTGG CTATCAAGAA GATCTTTTCT 1140
TTGGGGGCCA ATGCCATATT CCAGCATGGG CAGGAAACCA CAACAAGCCT TTCTGAGCCT 1200
CACTCTGAGT GTCTAGGCTT GTGGGAGGTG TAGAAGCATG ACACGCAGCC TTTGTCCCAC 1260
AGGGGCTTGC AACTGGGCTG AAGGGCTGGT GTGAGTATCA CATGTGCAAG TCCAACTAAA 1320
TGGAAATAAA ATGCTTTTGT CTGGGAATAG AAAGTAGGAT GATAGTTCTG ACTGTGTCAC 1380
TCACAGCAAA GTGAGCCTGG GCCTTTGGTG GATCTCCGGG TGCCTTGGTT TCTCTTTTGT 1440
AAAGTGGAGA TAATACGGTA 1460
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