Tag | Content |
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EnhancerAtlas ID | HS048-26867 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr3:182902920-182904180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr3:182903973-182903983 | AATGGAAAAT | - | 6.02 | NFATC1 | MA0624.1 | chr3:182903973-182903983 | AATGGAAAAT | - | 6.02 | NFATC3 | MA0625.1 | chr3:182903973-182903983 | AATGGAAAAT | - | 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 |
GH03I183185 | chr3 | 182902881 | 182904031 |
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Enhancer Sequence | TGGTCTCGAT CTCCTGACCA CGTGATCCGC CCACCTTGGC CTTCCAAAGT GCTGGGATTA 60 CAGGCGTAAG CCACCGCGCT TGGCCAATTA TGCACAACTT TTTAAGGACC ATCTCTATCA 120 CATGAACTAA AGGATATCAT TTTCACTTGG GGGTGGGAAG TGGTGAGCTG CTTAAAAGCA 180 ATGCCTAAAC CCCCTGGGCT TTCCTTCCTT TCACTTGGAA GAACCAGGGG GTAACTAACT 240 GCTAACAATT CCATGCTTTC AGAGATCTAG GCGCAAGCCT AAGGGCTTCA TCTCATTTAA 300 TCCTCATGGC AAGACTGTAC AGTATTATCT CCATTTTGTA AAATGAATGA TAAAAAGAAC 360 TTAAGCACAG ACAGGCTATA GAATCCATCC AAAGAGATGG AGCTGCACTT GAGGCTGGGT 420 CTTTGAGACC TGAGTTTGAG CCCTTCATCA TTGTGTTGTG TGTGCTGCTA ACCAATTTCC 480 CCTCTCTGTC TTCTAGGATT TAATACATGG TGTCACATTC TGTCTGATCC ATCCCAGTAG 540 CTCTCCAGAG CTCCCAACAG GAGAGAGTTC CAAAATGTTT CCAGGGGTAC TAGGCTCGGT 600 TACAATATTT TGCTTGGTGG CCCAGAGTAT AAACGTGGAT ATCTTAGGCT GGTCTATAGC 660 TGAAACGTCT ATTTCATTTG CAAGCCTATC TTTGGCTAAG AGGAAGTGAA TCATTCTTGA 720 GAACATCTAA TTAATTGCTT TCAGATTCCA CATGTTGACA TTCTCAGGGC ACATTTTTTT 780 TTTCCCGTGC ATTTCTGTTG TCAAAGTCCC TGCCAGCTCC TAAGGCAGTC TGAGCTGGCT 840 GTCTTAGACT TTCAGAGCTG CTGGAAGCTT GGGGGAGGGA GGGGCTGTAG GTCAAAGAAA 900 CTTTATAACC TAGCTTTACC TCCCAGCTCA GCCACCAGCT GCCCTCAAAT GTTCTGGATT 960 GGAATAAGCC CAAAGATGAG TGGCAGGAGG GAAGGGCAAG CCAATACGTC TAGTTTGGTT 1020 CAGTCAAAGC CTTGCCCATT TCATCAGAAT TTTAATGGAA AATTTCCAAT AAGATTAAAA 1080 TATAAGGTCA CCCCAATTTT AGTATGGCTC CATTTAAAAA AAATCATGCA TATCTTTGTT 1140 TTGCAATGGG GCCTTACTCT TGCCCAGGAG AGGTGCGGTG GTACAATCAT GGCTTACGGC 1200 AGCCTCAACC TCCTGAGCTC AAGCAATCCT TTCACCTTGG CCTGCCAAAT AGCTAGGATT 1260
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