Tag | Content |
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EnhancerAtlas ID | HS050-35899 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr2:30733930-30734820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr2:30734734-30734745 | CTAATCCTCTT | - | 6.62 | FOSL1 | MA0477.1 | chr2:30734159-30734170 | CATGAGTCACC | - | 6.62 | HNF4G | MA0484.1 | chr2:30734025-30734040 | TGAACTTTGGGCTTT | - | 6.09 | JUND | MA0491.1 | chr2:30734159-30734170 | CATGAGTCACC | - | 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 |
GH02I030511 | chr2 | 30733965 | 30734547 |
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Enhancer Sequence | TGTTAGAGTG TTTGCTCAGA AGTCTCATTA TCTGTTCCTA ATAAAAAATG GGTGATTTAG 60 AAAGCCAGTA GAGGCTTGCA CGTAGGTGAG GCTTGTGAAC TTTGGGCTTT ACTGAGGGGT 120 GATTTATGTG GGCTGTTTAT TAGGGAATCC CTCAATGTTT CTGTATTTTC GAACTCCTGA 180 CCTCAAGTGA TCTGACCGCC TCGGCCTCCC AAAGTGCTAG GATTACAGGC ATGAGTCACC 240 GCGCCTGGCC TGTTTCTGTA TTTTTGTCTT TCCTCATAGC CTGGTCAGAC ATCCCAGAGA 300 GTACACTCCT GTCTTCTGCC TAGGACTGTG CTGTTCAATA CTGTGGCCAC TACCCACATG 360 TAGCTATTTA AATTGAAATA TAATTAAGTT AAAAATTCAT TTCTTCAATG GCACTAGCCA 420 CATTTCAGAT GCTCAATAGC TACATGTAGC TAATGGCTGC AGTTTTGGAC AGCATAACTA 480 GGGAACATTT CCATCATTGC AGAATATTCT ATAGGACAAC TGGCATAGGA CCAAAGATCT 540 TGTTGCCAGC CATCTGAGAG CTCATCCAGG GAAGATGGTC TGAGGTTTTA GCATTCAGGA 600 TTCAGCATGT ATATGGTCAC TTAATCCCAC TGTTCTTAGA GTGGTGACCA TGCCCTAAAC 660 TGTGCATTTC CTAATTGGGA AACTCTGTTT TACCTTCTCT AGAGAATAGA CATGCAAGTT 720 TATGCTGCGG TAGGAGAGGG ACAGTTACCC AGAGGTGCAG AGAGAGAAGG GAATCTAGGA 780 ATCCACCTGC CCCTCACTCA TTACCTAATC CTCTTTATTT TGGCAAACTG CCATTCATCT 840 CCATTTGCAT CCAGCAGTAC CTGATGCTTC CGCCTCCTAG GCCTTAGGAG 890
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