| Tag | Content |
|---|
EnhancerAtlas ID | HS048-01118 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:42930810-42932300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:42931627-42931648 | TTTGCCTTTCTTTTTCACTTT | + | 6.54 | | KLF4 | MA0039.3 | chr1:42931188-42931199 | CCACACCCTGC | + | 6.62 |
|
| | 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 |
| GH01I042465 | chr1 | 42930990 | 42932295 |
|
Enhancer Sequence | GACTCTACAA AAAATGCAAA AAATTAGCCA GGCATGGTGG AGCACTCCTG TAGCCTGGCT 60
ACTCTGGAGG CTGAGGTGGG AGGATCACTT GATCCTGGGA GATCGAGGCT GCAGTGAGCT 120
ATGATCGCAC CACTGCGCTC CAACCTGGGC TACAGAGTGA GACCCTGTCT CAAAAAAAAT 180
AAATTCCTGT CATTCTAGGA CAGTTTTTTT TGTTTTTGTT TTTGTTTTGT TTTGTTTTGT 240
TTGAGACGGA ATTTCACTCT TGTTGCCCAG GCTGTATTGC AATGGCGCGA TCTTGGCCCA 300
CTGCAACCTC CGCCTCCCGG GTTCAAGTGA TTCTCCTGCT TCAGCCTCCT GAGTAGCTGG 360
GATTATAGGC ATGTGCCACC ACACCCTGCT AATTTTGTAT TTTTAGTAGA GACGGGGTTT 420
CTCCACGTTG GTCAGGCTGA GTCTTGAACT CCTGACCCCA GGTGATCCGC CCACCTCAGC 480
CTCCCAAAGT GCTGGGATTA CAAGTGTGAG CCACGGTACC CGACCTCTAG CACAGTTTTA 540
AACCTGGGGA GTGGGGTGGG GTTTTGCCCC CTGTGAGACA TTTGGCAATG TACGTAAGCA 600
TTTTTAGTTG TCACAACTAG GGATATGCTA CTGACATATA GTTGGTAGAG ATCAGGGATG 660
CTGCTCCATA TCTTAATATG CACAGAACTG CCTCCACAAC AGCTCAGAAT GTCAGTAGTG 720
CCAGGGTTGA GAAACTCTGT CTTAACACAT CAACAGTTCA TTTTTTTGTT CTGTCACTCT 780
TGCTTAGCTG TGTACATTTT TACATAGTTA TGTACATTTT GCCTTTCTTT TTCACTTTAT 840
ATTTTAAACA TTTTTTACAT TGCTACAGTG TTTTCAACTT TTGAAAAAAG TATACTAATT 900
TTATTTGGGA ATTGAAAAAC TGTGCATAAT ATGTATTTTA TTTAAGATGT GTGTGAGTTT 960
TAAATTATAT TTGTGTGAAA GGAGTGGAAA ATAGAAGAAA GAAAGGTTAC AGTGAAAAGT 1020
CACCTGACAG CATATTTCAG TTTTTGTGGC TGTGCTATGT ACTTTGTTCC CTAGAGTCAC 1080
TCAAAGACTT TGGAATCCAA AGCTCAGCCT TTGCTCAGAG GCAGGAGATG TGCTATGGCG 1140
TAAGATAGGG TCCTGGCCCC TGCAATGCAG TTGGAGAGTA CCTACCAGGA GAAAAAACAA 1200
GGAGACTGCA CCCATTCTCC TTGTCCTCTT CTCGTTTAAA ATTCTTTGTC TCAGTTTGCT 1260
TTACCACCTT ATTCTTTACA TCTAGAAGTT TTTGGAGGCC TAAACCTACT TCAGGATGCA 1320
CTTCTTTCCA GAGATTGGAT TTTTAAGAGA TTTAATGAGC ATTTACTTAG TATCTACTTT 1380
GGACAGAATA GTTTTTTTGT TGTTGTTGTT TTGTTTTGTT TTTTTTTTTT GAGATGGAGC 1440
CTTGCTCTGT CGCCCAGGCT GGAGTGCAGT GTTGAGATCT CGGCTCACTG 1490
|
