Tag | Content |
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EnhancerAtlas ID | HS048-00799 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:28431050-28431930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:28431909-28431920 | CATGAGTCACC | - | 6.62 | JUND | MA0491.1 | chr1:28431909-28431920 | CATGAGTCACC | - | 6.02 | ZNF263 | MA0528.1 | chr1:28431385-28431406 | GGAGGAGAAGGAAGCGGAAAG | + | 6.77 |
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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 |
GH01I028104 | chr1 | 28431218 | 28432370 |
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Enhancer Sequence | ATCTTTCCAA TAAAATATTT TTGTTGTTGT TGTTATTAAG ACCAGAATTG GTCACTGATG 60 TTTTCAATCA ATGAACCATG GCTGATCCAA TGTCTTATCT ATAAAAGACA TAGAAAATCG 120 GCATAGTGAA AATTCCTAGC ATAAAAAAAC TATTGCTTTT ATGTAACAGT TTAATATTCT 180 CCAGGCAAGA GGCAAATTAC AACTTTGTGA AATGGGCTGT GAGCTACAAA ACTAATAAAA 240 ATCATTCAGA GGTGAAAAGA ATGAAAGGTG AGAGAGGCAT TACATGTACT CTGCCTCTGG 300 AATACAATTC CACTTCCCTA CCAAAGAAGG CAATGGGAGG AGAAGGAAGC GGAAAGTAGA 360 AAAAGCTTCT CCGGCTCCCC TGAATAGGAA TCTGGCAATA ATCTGGCTGC TATTTACTAG 420 CATGCAGCAT CCGAGGCACT GTGTTAGTCC TTCATATGCA GCGCCTCACT GACTTCTCCC 480 AAGGGCACAA TTATTATCTA TCATTTGGCT ATATATATTC TGATTCTCTC CACTTTACAG 540 AAAACTGGGG CTCAAGGTTG TTAAATCATT AAGTCGAAGT CCCAGAGGTG GGAAGGGCGG 600 GATCCAAACA CAAGTGTGTG ACTCCAGCGC TGGGGTAGGA GCACCTTGAA GGTGAAGGAG 660 CCCAGCGAGC TGCAGCTTCC TAGTCCAGCC TCACGTCATC ATCCCTGAGA CCTAAGCTCC 720 TCCCACTCAG ATTCCTGAGC CAATCCGGAG AGAGGCCAAT GGATATTGAT AGACTCTGCA 780 TCTCTCCACC CTCTCTGAAC CCAAGAGCTT TGTTTGCAAA CTTGGTACAA AGCACTCAAC 840 TGCTAGCTTC CGAGGTTCCC ATGAGTCACC TCTGCTGCCT 880
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