| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00915 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:26002350-26003570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:26002631-26002644 | AGAAACAGCTGCA | - | 6.29 | | Myog | MA0500.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.02 | | Tcf12 | MA0521.1 | chr1:26002634-26002645 | AACAGCTGCAG | + | 6.62 | | Znf423 | MA0116.1 | chr1:26002536-26002551 | TGCCCCCTGGGTGGC | - | 6.13 |
|
| | 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 |
| GH01I025675 | chr1 | 26002283 | 26003398 |
|
Enhancer Sequence | GATGAGGAAA CTGAGACTTA CAGGGGTTAA GTCACTCACT CAAGGCCACA CAGCCAGTAA 60
GGTGGCAGAG CCCTAGAGCA GCCTCTCAAG CTTCAATGTG CGTTTGAATC ACCTGGGGCT 120
CTTGTTAAAC TGCTGCTACA GATTCAGCAG GTGGGAGAGT GGAACTGAGG TACTCTGTTT 180
CTGACGTGCC CCCTGGGTGG CCCTACTCCT GGTCCCTGGA GCACTTTGAG CAGCGAGAGT 240
TTCTCTGCCT GTATGGCCCA CACTCTCGAC CCTGATGCCT TAGAAACAGC TGCAGACAGG 300
ATGCGATTCC TGAGACTGCT CAAACCTGAA ACCCCATGGG CAGGATGTGG GTGAGCTGTC 360
TGGACCTCAG GTGGGTGGGA GTTGTATCAT ATGCTCATTT CCCACATTGG CCTTTCAATA 420
GCTTGAGTAA ACCCGAAACT GAGAGGGTTG GAGGCAGCAT CTCCCCTTCT ACTCCCCCGC 480
TTCACCTCCC CGGGCAACCA AACCCCACCC GTGCCCAGCT TCTGAGCGAT AGACCTGGGC 540
TGTGTATTTG CAGGAGCCTC ACTGGGGTCA CCAACCAGGT CATGTTGTGT TGCCCCAATA 600
AATGGAACTG GATCAGAAAA TCCAACGTGG ATAGTTTTTA GGTGCCAAGC TGTCAGCTCT 660
TCCCTTGGAC TGTGCTGAAA GTGGAAGAGG AGAAAAAAAT CAACCCAATG TTCTAAGCTC 720
TCTGTCTACA TAGTCATTAG ATCCCAGGAT CGTTAGAGAC CAAATCCCTT CCCACTTGGC 780
CCCTGCAAAT GGGGCCAGGT GTCACTGCTG GGAGACGCCA GTAAGGCTGC ACGTCATGGT 840
GTGAGCACTT GTCTTTAATG ACTGGGAAAA TCCATTTCCT TCCTTGGCAG CTTTGAATGT 900
AGCAACTGTG GTTCTGGGTC ACTGCCAGAG CCAGCCTTGT GTGTATGTGT GTGATTTTTT 960
AAAGTGGGGG AGAATGTCTC AATATTCAAT GCTCACCCCC TTCCTTCCAA GTTGTACCCC 1020
CAGAGAACTG TCCAACACAA ACTTTGGAGT TTTCCACTCT GGGAGTGGTC TGCTGGCACC 1080
CACGTGTCCT CCCCTCCTCT AATGCATCCT TTCTCTCTTG ATCTCATTGT TCTGGGGTCC 1140
TCAGCTGAGT GGGCATCTGT GCCTGGGTGA TCGATTCTAG TCTCTTTTCT GCAGGAGAGA 1200
ACTCTTGAGC TCTGAGACAG 1220
|
