Tag | Content |
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EnhancerAtlas ID | HS180-25651 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr2:30733760-30734940 |
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 | TCF7L2 | MA0523.1 | chr2:30733846-30733860 | TTTCTTTGAAGTTT | - | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 30734376 | 30734545 | chr2 | 30734733 | 30734838 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I030511 | chr2 | 30733965 | 30734547 |
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Enhancer Sequence | CTTTCTTCAT TTTATTTTCC CACAAGAACA TGTTATTGTT TCCTGATTGC AGTATTTATT 60 GTCTTTTTGA AAATGTTAAA GATAGTTTTC TTTGAAGTTT TCTTTTCCCC TGAATAGTTT 120 ATTTCCTTCA AGTATACTTT TTTTTCTGTT TAATTTAGTC TCTAATGTCA TGTTAGAGTG 180 TTTGCTCAGA AGTCTCATTA TCTGTTCCTA ATAAAAAATG GGTGATTTAG AAAGCCAGTA 240 GAGGCTTGCA CGTAGGTGAG GCTTGTGAAC TTTGGGCTTT ACTGAGGGGT GATTTATGTG 300 GGCTGTTTAT TAGGGAATCC CTCAATGTTT CTGTATTTTC GAACTCCTGA CCTCAAGTGA 360 TCTGACCGCC TCGGCCTCCC AAAGTGCTAG GATTACAGGC ATGAGTCACC GCGCCTGGCC 420 TGTTTCTGTA TTTTTGTCTT TCCTCATAGC CTGGTCAGAC ATCCCAGAGA GTACACTCCT 480 GTCTTCTGCC TAGGACTGTG CTGTTCAATA CTGTGGCCAC TACCCACATG TAGCTATTTA 540 AATTGAAATA TAATTAAGTT AAAAATTCAT TTCTTCAATG GCACTAGCCA CATTTCAGAT 600 GCTCAATAGC TACATGTAGC TAATGGCTGC AGTTTTGGAC AGCATAACTA GGGAACATTT 660 CCATCATTGC AGAATATTCT ATAGGACAAC TGGCATAGGA CCAAAGATCT TGTTGCCAGC 720 CATCTGAGAG CTCATCCAGG GAAGATGGTC TGAGGTTTTA GCATTCAGGA TTCAGCATGT 780 ATATGGTCAC TTAATCCCAC TGTTCTTAGA GTGGTGACCA TGCCCTAAAC TGTGCATTTC 840 CTAATTGGGA AACTCTGTTT TACCTTCTCT AGAGAATAGA CATGCAAGTT TATGCTGCGG 900 TAGGAGAGGG ACAGTTACCC AGAGGTGCAG AGAGAGAAGG GAATCTAGGA ATCCACCTGC 960 CCCTCACTCA TTACCTAATC CTCTTTATTT TGGCAAACTG CCATTCATCT CCATTTGCAT 1020 CCAGCAGTAC CTGATGCTTC CGCCTCCTAG GCCTTAGGAG GATTCTGTGG GTTTGTTTTC 1080 AACTTTTTCC TCTGCTGGCT TACACTTTGT CTTTGCAGGT CAGCCAGGAT AGTCAACATT 1140 TGGCTTTCTG CTTTCCAGCT TTTAAAATGT TGTTCTTTTT 1180
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