Tag | Content |
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EnhancerAtlas ID | HS180-27665 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr2:160953760-160954790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr2:160954458-160954469 | TTCTTATCTCT | + | 6.32 | Gata1 | MA0035.3 | chr2:160954458-160954469 | TTCTTATCTCT | + | 6.32 | IRF2 | MA0051.1 | chr2:160954040-160954058 | CTTTTGGATTCACTTTCC | - | 6.26 | STAT3 | MA0144.2 | chr2:160954053-160954064 | TTTCCCAGAAG | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I160097 | chr2 | 160953691 | 160954754 |
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Enhancer Sequence | CTGGAAATTG CAAAGGTCAG ATTAAAATTT CAAACTGAAC TAGATCCTCC ATGGGATTTG 60 TGAAGTCTTG CCAAGTCAAT GACACCAAAG AGTGGGGGGT GGGGTAATGG TGGTCAAATC 120 TGTGTCTTTG ACTGTCAGGC CTCTCCCAGG ACCTAGCTCC AGGAGAGCTC ATGGGATGCA 180 AAACTTCTGG GGTGCCATGT TGCTCCCTTG CTGGTTGTGT AACCAAATGA AAAGACAGAA 240 GATCAAGTTT TCCACCCTTT GCCCTGTCTA GAGCAATTCA CTTTTGGATT CACTTTCCCA 300 GAAGGCGGAA ATTGCAGTGA GCTGAGATCA TGCCACTGCA CTCCATTCTG GGTGACAGAG 360 TGAGACTCTG TCTCAAAAAA ATAAACAAAT AAAAATAAAA GAAATTACAA CTCTTTCTAA 420 GGGTGCACTC TCACAGGGCA TTGTGTAGCT TTTTGTCCTG CTTTATTTTC TGCATAGTTC 480 TTAGGACGGT TAGACAGTCT TAGTCCAGTC TTCTTATATA ATAAGAACCC GAGCAAGGTT 540 ATGTGCTAAT GTTTTATTGA GGGGTGCTAG CCCAGTGAAA AAGGGCAGGG AGGCAGCTAA 600 TGAGGGAACG CAGGTACAAG GTGAGGCATT TGGAAGCTGG CCACTGCTTC CCCAGAAGAC 660 ATCGCTGGTG GCTCATCTCC TGTTCATCTG CTGGTTCCTT CTTATCTCTG TCTCTTATGG 720 ATCTACATTC ATTCTTCAGA GTGTTGACTC CCCTGAACCT CCCTGTTGTC TTATGTGGTC 780 CCTTGGGGCA GCAGCTAGGG AAGCCATTCT GGACTTGGGC ACAGGAATTG CAGCAGCTCC 840 TTAACCTGTT AGGAGTTAGG AAGAAGCTGG GGTTTTACTA CCAAGGAGAC TGTGCAGGTT 900 GGTGCTGGGG TAACTCCTGG CATAGGCCTG GAAGGCAGGT GGGACCAAGT GGATCTGGGG 960 TCTGCACAAA CTGGGTCCAG GACCCTGATA ATGTATATTT ACTTGTTTAT TATTTTCTCT 1020 CTCATTTGGA 1030
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