| Tag | Content |
|---|
EnhancerAtlas ID | HS180-01166 | Organism | Homo sapiens | Tissue/cell | Small_intestine | Coordinate | chr1:32296920-32297580 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr1:32297152-32297167 | TGAACTTTGAACCTT | - | 7.37 | | Hnf4a | MA0114.3 | chr1:32297150-32297166 | ATTGAACTTTGAACCT | - | 7.05 | | Rxra | MA0512.2 | chr1:32297152-32297166 | TGAACTTTGAACCT | - | 6.55 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTTGGCTGTT GGGGGCTCTG GGTCTCTTTA ACATTTTGTT GTACCCCCAT TATTGTGGGG 60
TGGGATATAT CTCCTACCTC CTTGAAGACT TTCCACTCCC CTGATGACAA ACATCAAATG 120
CCGTTGAGAC TCCAATTCAC CCCTCCCTCA CTCACCCCTG CCACTTGCTA CTCCGGACCC 180
TGAGCCCTGG CTGGGCCTCT GGTCCTGGGG ATCTCAGAGC TGCTGGACAC ATTGAACTTT 240
GAACCTTGCC CTTCCCTTCC CTCTGCCCAG CCACTATCAC GCACAAACAA TGCCCTTTCC 300
CCTGGTTGAG TCTGTCTGTC CTCCAGTTCC AGCCTCCAAA AAGCTTTATC ACTTTAGTGC 360
CAAAGCTGCC AACTTCAGTG TATATGAACA AACGTACTTA AAGGACAAAA CAAAACAAAA 420
AGACCTGCCT CTCTATTGCC TTTGAAACCT ACCTTATCTT CTTCACTCCC ACACTTTAGA 480
TAAATGTCCA TTTGCCTGCA ACTGTTTTTA TCACACACCC TCTCATTGGC CAGGGTAGTG 540
TCATGGTCTC TGGAATCCTC CAGACTCTGA TTCCAATCCC GGTGACCCTA GGCAGTGAGT 600
TGATCCCTCA AAGCCTCACT TTTAGTCATC TGTAAAAGAG AGTCAGTAAT AGCCTCCAAA 660
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