| Tag | Content |
|---|
EnhancerAtlas ID | HS180-03499 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:167012770-167014200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr1:167013258-167013269 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH01I167043 | chr1 | 167012838 | 167014050 |
|
Enhancer Sequence | CTCAATCTCT TTCTGGGGAA AAAAAAAAAA TCTATAAGAC AGCCCAGAAC TAACATAGTT 60
AGACCTGAGT TTGGGCTCTA TCTTTGTCAC TAACCAGCTG CATGTTCCTT AACAAGTCAC 120
TTTAATATCC CGAGCGTTGG TTTCCTCATC TGTAAACTAA GATGAATAAT GCCTGGCTGA 180
TAATGTGGCT GTGAAGATTA AAATGGGTCA TGCCTTTGAA TATGCTTTAT AAAATTCAGT 240
TCTTCTTTCA TTTCCTCAGC CGATTGCTCA TGTTCCTCTA ATACACTGTC CCCACCCTGG 300
ACAACCTCTA GCAGGTATAT GCACACCTGA AGATACTGAG ACAGGGAGAC TGACTAGTTG 360
AGATTCACTG AGGCTGATGT GTCTAGAAAG TTGCTCACTA AGTATTCCCG CAGGGTGTTT 420
GAAGCCTCTT CCTGGATGCC TGGTGAGACG AGACACTTTG AATCCACCTT GCAAAGCTCC 480
TGCTCCAAGA CAGCTGCAGC TTGTGCTCTG TAGAGCGATA TGAAATAATT GCCCGTTGGC 540
ACAATAAGCC CATCTCCTCT CCGGGCAGCA CAAAAGAAAG CTCAAAAGCA TCTCCGGTTT 600
TGATTGCCAA GTGGGGGAGG CAGTGAAAGT ACACTAAATT ATGAGTCCAG GTGCCTCTCT 660
ACAGAAATCC ACTTCCGCCT CGCTGCCGCT CTGAAGGCGC GCAGTGGGTG TTGACGTCAC 720
CTTCGGCCAC AGGAGCTTGG AGAGGCTGGG GCCCTGACTC CCCGCGGGAT CCGCTGGTAG 780
ACCAGGGCGT GCTCTCAGAC TGGAAGTGCA GGAAGGCTCG CTTACTCTCG CCATAGACCA 840
GACTGACAGG GGTCTGCCAA GGCTGCTGGG AATGTGGGAA GTGAACTTTA GGTGGAAACA 900
GAAAAGCTTC TCTCTCCGTG GGTAGCCTTT TTTTTTTTTT TTTAGTTCAG GAGAGAAAAA 960
AAAAATCATA GAAGCCTGCC AAGCCAAATA AACTATGCTC AATTAAGTCT TTCAACTGTG 1020
CAATTCCTCT TGTTGATTTT ATGAGGAAAA GGGCAGAATA GAAACATGAT GGGCTTGTTT 1080
AAAATACTTC AAAAGGGAAG AACCTATATT CTCCTGCTTC CCAGACCGAC CTCTTTCGGG 1140
CTTTCCTTTC CTCCAGCCAT GCTGCAGGCC TTTCACTGTC ATCTCCTCCA TCTGTGATAA 1200
AGCTGTCCAC AGAACCCGTC CTCAGCTGCT TTCTCACCAC ACACCCTCAC TCAGGGCATG 1260
TCCTCCATGT CATGCCCCTC ATCCAGGCCT GTGACTCCCA AGGAGCTGAA TCAGCCAAAA 1320
CTCTCCCTCC CCAACCCCAA CTCCAGGCGC TTATACCTCA CTCCCCACAG CTGTTTTTAT 1380
TATTCGTATT CACTGCTACT CAATCCCATC TTGTTTTCAA GAGGACTTAA 1430
|
