Tag | Content |
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EnhancerAtlas ID | HS048-03838 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:244509860-244510930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr1:244510824-244510835 | AAGTAAACAAA | + | 6.62 | LMX1B | MA0703.2 | chr1:244510138-244510149 | GATTTAATTAA | + | 6.02 |
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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 |
GH01I244346 | chr1 | 244509866 | 244514858 |
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Enhancer Sequence | GCCGACTGCA ACCTGAACAA AATTGTGGTT GTGTTGGCCA GGAAGAAATG AGGGCTGCTC 60 GGTGGAGAGG GGACCTACAG GCTCAGCTCA CAGTCTTTCA AACAGGTCCA AACAAGAAGT 120 GATAAGGAAC AGAACTAGCA GATGAGTTGA GAACAGCATG GTGAGACTAT CAGGAAGCAG 180 AAGTGAAAGT ACTTAGTGAG CTACCAGAAG TGAGGGCTGA GGGAGAAGGA TTCTTAGGCG 240 ATTCCCAAAT GTATGACTTG GGTGACTGAG ATGTCGGTGA TTTAATTAAT TGGGGGCGGA 300 GGGTGAGGAC TGGGGAAGGC AGGCTAATGA GATGCACAAA ATGATCTTAT GACTTAGGAG 360 ACAATCTTTT GCTTGGGGGA TCCTTCAGAG ACTTTCCTGT CTCTTGATCT GTTGGGCAAA 420 TCAAATAAAG AAAGCAAGTA AAAGCCTTTT CGTATAAGCC TCATATAATG GTAAATGTCT 480 TCATCTCTTA AATAGAAAGC AGCTGGGGTG GCTGCCTGAT CTTATTTCCC CAGTGGCTGT 540 GTCTATGTGA CCTGACCCCA ACAGACAGGG TGTCATGGAA GCCGCGTCAT ATCAATGGCA 600 GTGCCCAAGG GACCATGAAC CCCTGCTTCT GGGATCCCAA GACCTGACCT GGTACTGCCT 660 CCTTGAGGCA TGGTGAGTCC CGTCCTTCCT TCAATTCTAT AGTCCACTCC AATAAACTGC 720 CTTCCAAGAA GTTAATTTTT TTATCAAGTT AATAGTGATT ATTTTTGTAA CTTAAAACCA 780 AAAGAACTCT ATTTAAGTCC TTGATAAGGT CTTTAAAGGT ATACAGTATG CCACAAATTC 840 CCACATGGGG TACTCATGCC AACAGTGTTT CCTTAGAATC TTATCATGAG CAAATGAGAA 900 AAAAATTGAC TGTGAGACAT TCTACAACTG GCACACACTC TTTAAACCAA GTTATTATCA 960 TGAAAAGTAA ACAAAAGAAT GAGGGGAAAT AGATTAGAAG AGGCCAGAGA CATAATAACC 1020 GAATAGAATG TGATTCGATC ATGGGTCACT GAAAATAAGA GAGGAAGAAA 1070
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