| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02211 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:144593600-144594730 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Rhox11 | MA0629.1 | chr1:144593901-144593918 | ACGGTTTACAGCGAAGT | - | 6.29 |
| | | 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 |
| GH01I120414 | chr1 | 144592862 | 144595660 |
| Enhancer Sequence | CTTTTCCTGG CCCGCGCGAA CCCGCTGTGC TGCAGAGGCG GCCATGTACC TTTAAGGCCC 60
CGCTGCGCCT GCGCCTTGGG CTCTCCTGAC GCGCTGAGCG GGACCCTGAG GAGCCAGCTG 120
GCGCAGGCTA TGGGCTGGGC GGCGGTTGAG ACAGCGGCGG TATTGGGAGG GGTAGGTGAG 180
GGTCGCGAGG CTGCGTGAGC ATCTGAGTGA ACGCGGTGCT TTTGGGAACG CGGGACGGGC 240
GACCTGTGGC GCCAGGAGCG GGCCGAGGCG CGGCGCACGG ATGCCGTCTG GATGGGAAGT 300
TACGGTTTAC AGCGAAGTCC ACCCAGCGTT TCCGAGGTGA AGGCGCCGCG CCAGGCCGGG 360
GGGCGGTGAG TCCGGGACCC GCGGGTACAC AGCTGGGTCG AGCTGCGGCT GTCGCAAGTT 420
TTGTTGCGAG CGACGGAGGG CGAGGCGGGG TGGGGGGTTG GGAGGGCATG TGTTCCGGCC 480
CCGCCGAGGC TTAAGTTCCA TGCGTTCGAT TCCTCGCTTG CCGCTGCCGC CCGCAGCCCT 540
CATCTCTTGG GCGCTGGGGA AGAAACTCGC TGGCGGGTGT TCTGTGGCAT CCCAGGGGGT 600
GGAGGGACGA GCAGCTTCGG GGGCACGTCC TCGTGTATCC TGTGGAGGAC CCTGACCCCG 660
CACCCCACCC TCGAGGCCAG AAATCAGTTG CCTCTGGGGA CCTGAGAGGC GAGACCACTC 720
GCGCCCCTGA CTTGCAAAGT TGGGGTCTTT ATTGGCCTCC GGGATTCTGC TCCTGGCGGT 780
TTCTCCAGGC TGGTGATGGG CAACACATGA GGCGCGTTTG TAGCCATCAC TGAATCACCT 840
CATGACTAGC GGGGCAGGCC TCTAATTCAC CGCAGGATTT CCAGTAGGTT GGATTGTGGG 900
GTTGGTGTTT GCACTCCAAA GAGTTGGCGT GATTTCCCTG TATCTGTCTT TCTGGCTTGT 960
TAGATCTTCT CATTTGGCGT CCTTTCTCCG AAGAGTTAAC CAAGACGTTT GGCGTGGTTT 1020
TCTTGCTTTC CTCCTATCTT TTGCTGCTAG AGCTGCTTTC AAAAAGAAGT CTTTTCTTGC 1080
AGTGATACCT TTTCTTTGGG TTACAGTGTT GTTCATCCTT TCTTTGCCGA 1130
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