Tag | Content |
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EnhancerAtlas ID | HS048-20929 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:102856850-102857520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:102857456-102857475 | TTGCGCCCTCTAGTGGCTG | - | 7.46 | RUNX1 | MA0002.2 | chr2:102857249-102857260 | GTTTGTGGTTT | + | 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 |
GH02I102238 | chr2 | 102854507 | 102858977 |
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Enhancer Sequence | GACAGAGTTT CGCTTTTGTC ACCGAGGCTG GGATTACAAG CATGAGCCAC CGAGCCCGGT 60 CAAGGCTTTC ATATTTTTAA AACTTTGAAG TACAGTGAGA AACATAATTT AGTAAGCAAC 120 TCAGTATGCA CACACGGAAT GGAAAAAGCT CTGTTCTATG TTATTTGTTC TATTTTGTTC 180 AAGTCTAGCT CAATTTTTCA AAATGCTGGT CACAGCTCGC CAACTTGTTT TAATAACCAA 240 CTTATGCCTT TCCACTGCAA TCTGGAGAGC TCAGCCTCTC AGGCTGCTGG TCCCCCTGTC 300 AATCACGATA CTTTGGCTAC TTTGCTTTCT TCAATCAACA AGGCTTTATC AAGAACTTAT 360 GGCTCTTTTA ATTATCTGAC TTCCTGGTCA ATCAGCTTTG TTTGTGGTTT TAAATGACCA 420 CAGGATAGTA GAAGTGAACA TAATTTCCTG CCTGTGTAAA AGGATGACAT CAAGAGGAAA 480 AGAAAGCAGC TCACTGGGTG AAGGACCTTG AGAAAGAGAT GAACATTTCC TCTCTTGAGA 540 CACAGGACAA ACAAGGTCAC GCCTGAGCTC GGCAAACAAG GACTTCGGTG CCTGCCTACG 600 GCGCCATTGC GCCCTCTAGT GGCTGCTGAG GAACCGCTGT CCAGCCCGAA GCTCACAGAG 660 CCCCGTTCAG 670
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