Tag | Content |
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EnhancerAtlas ID | HS048-02607 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:162391140-162392220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ONECUT2 | MA0756.1 | chr1:162391436-162391450 | TTTATTGATTTTGT | - | 6.08 | ONECUT3 | MA0757.1 | chr1:162391436-162391450 | TTTATTGATTTTGT | - | 6.51 |
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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 |
GH01I162421 | chr1 | 162390971 | 162392330 |
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Enhancer Sequence | GAAGGAGATT GTAATCAACT GGCCACTTCT AGCTCCAGCC ACAGCACAAC TGTGGTTATT 60 GTTTATGTCC AGCATATCTG ATAACACCAG CATTAGGGCT CTCTGATCTA CTGCCAGAGT 120 GAGCGGGGGT GTCAACAAGA GATGCTTTTG TACACGTTTT CCTTCCGGAC TTACAAGAAA 180 CATAATTTCA CACACTAAAC CTGTTTTATC CTCTTATCAT GAACAGTTGT CTGGAGGAGT 240 TGTTGGCTCT CTCCCTGAAA GCTCTTAGAA GAAAGCAGAT TAATATCACT ACCTAGTTTA 300 TTGATTTTGT ATCTCTTGCC CTCATAATAC CAAAAGAAAG AAAGCCAGAA AGCATCAGGG 360 TAAATGAAAC CAAAAGTGTA ACTGACCTTT ACCTACTTTT TGCTGCAGCT CAGTATCTTG 420 ACCATGTTAA AGGGCCCAGA GTATGTTATT GTCCTCCAGA GCATTCTTCC ATTTCTCTGT 480 TAGGGGCTTC AGAGTGTAAG GATGCAAGTG ACATCACTGA TGGCAAGGTG GGGACGTTTC 540 TCACAAGACC TTGGGGACTG GATATCTCTT ATTAGAGGTG ATCACTGACA TGGACATTGG 600 CCCAGAATGC TTTCTGGAAA GACTTCTTGT TCCCTCCTTG TATTCGTTTC CTGGGGCAGA 660 GTCCCAGAAG CCAGGAGGTT TATTGTCTTA CAGAGGCTTG AAGTCTGCAA CCAAGGTACC 720 AGCAGGATAG TGCCCTCCAG AAATTCATGT CCTACCCCAA ACCTCAGAAT GTGATCTTAT 780 GTAGAACTGT GGTCATGGCA AATGAACTTA ATTAGGCTCT AAGATTTAGA AGAGGAAGAA 840 AGAGGTGGAA GAAGGGGACT AGGTTGCTAG ATTCTTGAGA AGAGCCCGTC TAAACAAGAA 900 CTGTAGAAAT GAACCCTACC CCTCAGAGCA ATGCCAGAGC AGAGAAATAA TGTACCTTGA 960 TGACCAGAAC TCACCAACAG ATCCCAGCTG ATGTAATTAG TTATAATTGG CTGAACAAAC 1020 TCAGATGATC TGTTTCTTTT TCCAGAGGCT AAGATTTCTC AGAGTCTGGG ATTAGAAGAG 1080
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