| Tag | Content |
|---|
EnhancerAtlas ID | HS003-05032 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr10:30872280-30873760 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr10:30872766-30872787 | TTTTCCTTTCAGTTTCACTGT | + | 7.32 |
| | | 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 |
| GH10I030583 | chr10 | 30871931 | 30873642 |
| Enhancer Sequence | TGCAGTGGTG CAATCTTGGC TCACTGCAGC CTCCACCTCC CGGGTTCAAG CAATTCTCAT 60
GCCTCAGCCT CCCAAGTAGC TGAGGTTACA GGTGCAAACT GCCATGCCAA GCTAATTTTT 120
GTATTATTAG TAGAGATGGG GTTTTACCAT GTTGACCACG CTGGTCTCAT GGTCTCCACC 180
CGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCACATCC AGCCACTATT 240
TATTTTTTGT CCTTCTAATC CTTGGAACCT GTGAATTGTT TTTCCTTATT TATTTAATTA 300
CGTATTTATT GTTATGCTGC TAATCTCAAA GGACGCTTTC TTCTAGAAAG CAGAAACAAT 360
TGATTCTGCA AATGTGTGGT TTCCCATTGA CATCTAAGGA AAAATGAAAC AGGGCCTGGG 420
AGACAGTTTA CACCGTATTC ATCCAGGACA TTCTCACTGA TGGACTTTCC ACGAAAGCTC 480
TGCAAGTTTT CCTTTCAGTT TCACTGTCCG TTGGCCGGTA CTGGTTGCTT GACTAAGCCC 540
TGTTGGCGTG GGTTACTGCT CACCCTGACA GGTCTTTGTG AAACATGAAA CAATACAAAC 600
ATTCTTCTCA TTTCCCCTCC GTTCTTCCTC TTGGAGCTGT TCCCAGTCCC GGTGGCCCTT 660
CTGAAGCCGA GTGGGAAGCT CAGAAGGAAC CTCTGGATTT GTTTACCGGT GTCAGGAATG 720
GAAACTGCTG GGGCACCTGT GTACTCTTGC TGGTTTCTTA AACTCTGTCT GAATCCCACA 780
CACCCTTGCT TTTCGGGGAG TTGTGGCTGG CTGGGACAGG AGCAAGGAGT CTCTCCTTTG 840
AGTCAAAGGA GGCACAGTAG CCAGAAGGAG GGCTTAGATA TGAGAATGTT ACAGGCCAAG 900
AAGCTAGACG GACCATCTGG AGAGTGACCA AAATGAAAAG CGCAGCGGCA GTTGTGCAGC 960
TGTGGTCTGG AGCGAGGTGT CCAGGGTCTT GGGCAATGGA AGACATAGAG GAGGCCAGAG 1020
ATGATTGCTT CCAATGGAGT CTGTAGCTCG CACTTGCTTT TGTGGCCAGT GATGTGAGCA 1080
GATGGGTTTA CCAGGCTATA AGCTTTTGGT GGCTGTGTGC AAAGACTTCC ACTGAGATGA 1140
TCGTGTCTCC TCAGGCACAT CTGGGTGTTG GTCCTGACAG CTGGAGTATT GGGGTTTGAG 1200
TTTTGCCTGA AGGACTCACT GGTGAGGCTG AACCAAGTGT GTTTCTTTGG CCATCACAAG 1260
GACCCAGGCA GGATGTCATA CTCAGCAGTA CAGCAAGAAC TGGTCCAATG CTTCAGATCT 1320
GTGATTCTCA ATGGGCAGAG GGCAATAAGT AATGTCTGAA GACTTTTTAA AAAAAAATTA 1380
ATTAGAGAGA GGGTCTTGGC TCACTGCAGC CTCCAACTCC TGGGTTCAAG TGATCCTTCT 1440
GCCTCAGCCT CCCAAGTAGC TAGGACTACA GAGGTGTCCC 1480
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