Tag | Content |
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EnhancerAtlas ID | HS101-29682 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr3:46464010-46465430 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr3:46465091-46465111 | GGGGAGTTGGTGGGTGGGTG | - | 6.51 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I046422 | chr3 | 46463773 | 46465176 |
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Enhancer Sequence | GGAGCCAAAG GGGCTCAGGA GCATCAAACC CAACATGAGA TCCCTCATGT GGGAGGTGAA 60 ACATTTATCA TCTGGCCCTC AGGTATTCAG GACAAACATA GCCTGCCGCA TACCCATCTC 120 CCGAATGACT TACACCAAAT TGGCATATGA CTGCCATTTA CTCACAGTTT TGGGCATTTC 180 ACCAGCATTA TTCCACACAG TTCATATGGC TGCCTGTAGC CACTCAGTCA GGGTGTGGTC 240 TCCTTGCGCT GCCACTAACC ACCTGCTCAC TTGCAGCCGC TGACAGAGAG AGGGGTGAGT 300 CATGGTGGAG GCCAGCTTGT CCATCTCAGA GGTGGAATGG GAGATACCAT CTGCTCCCTT 360 GTTCCACAGA CGAAGCATCC AGGCAGGCAG GGGTTCCCCT GGACACTGGC AACACTGCTT 420 GCCTAATTCC TGCAACTCAG TTGGGGTACA GGCAATATAC GAAATGTGTT GCATTATGGT 480 GGGGAGTCCC TGAGTCCACC CTTGGAGCCC CAGTGGCTGT TCATGATCTA CCTTCTGTCA 540 GACCACCGGG TGAGCCCGCA ACAGGGGTTC TTCCTCCTTG GTATGAAACT GAGTGGGGAT 600 CTCCAGACAA GATGATGGAC CCAGGCCTGC ATTCATGGTA GCCTCTAATT CCTTTTCCAA 660 GCTCTGAAGC CACACCTCCA GGCATCCTGC CTGCACCTGG AGGTCCCCAT TCATGGCAGC 720 CTCTAATTAT TTTCCAGATC GGTGTAGCCA GACCTCCAGT CTGCATCCCT CAGGGACTGG 780 GTGTGTACTT TTCTTAGCAC AGTTAAAAAT GCCCATCCAA CTCTGCCAGC AAAGGCTCTC 840 TCCTTCTTGG TGCTCTGCAC TTCCAGCTGC TTCAGCGCCT TCTCCATGCT CATGGGGGAC 900 CCATCTACTG CCACCCAGGT TTCCACTCAG GCCCACCCTC ACAGCACGGC TACCACCGGG 960 TACCACAACC CATGTTGTGG TCACATGGCC AACCTGGAAT CAGCAGGGAC CGAAGGCTCA 1020 CTTACCTTAG GATCCTGTTC GTGATGCCAA TTGTCAGGTT CTAGCCCAAA CTAAAGTCCA 1080 AGGGGAGTTG GTGGGTGGGT GGCAGGTAAC TGGAAAAACA CTCGAGTAGG CGGTTTCGAC 1140 ATGGCTTTAT TCTCTCTCTG GGTGCAAGCC ATATGTAGTG TCAGCAGGGT AATTTTACCT 1200 TTTACAGACA ATAGTGGCTT TGAGCCAAGC ACGTGCTCAT ATGAGTGGTC ACCTAATGCA 1260 CCTCACATGG CATGGTTACA TAATGTGTGG AGTTGTGTGC CTGCCTCCAA ACCCACTGAG 1320 TCATGCTGCA CCAGAAGGCT GCCTCGGCCT ACTCCTGACT AAAGCACAAC CATCTCCCTT 1380 AGAGTGGGCT AAATCTACTG CTATTTATAC TATTAGAAAT 1420
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