| Tag | Content |
|---|
EnhancerAtlas ID | HS048-28941 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:600830-602280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF14 | MA0740.1 | chr5:601462-601476 | AAGGGGGCGTGTCG | - | 6.2 | | KLF16 | MA0741.1 | chr5:601464-601475 | GGGGGCGTGTC | - | 6.32 | | KLF4 | MA0039.3 | chr5:601331-601342 | GGAGGGTGTGG | - | 6.32 | | SP8 | MA0747.1 | chr5:601463-601475 | AGGGGGCGTGTC | - | 6.27 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 601191 | 601577 | | chr5 | 601445 | 601732 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I000601 | chr5 | 601191 | 602157 |
|
Enhancer Sequence | TTTCCCCGCG GCTTGTTTTC GTTGGTCTTG TCAAAGACCA GACGGGTGTA TGTGTGCAGC 60
TTCATGTCTG AGTTTTCTAT TCTGTTCTAT ATGATAATGA AACCAAATCA ATGTCTCTGC 120
TCAGACCCCT TCTGACAAGG TCTGTGGCGC CCACCATGGC GTTAGGGCCA CAGCCTCCTG 180
CCCCATGTGC CAGGCCCGGC TCTGCCCAGC TCCCTGCAGC TGCGCCAGTG TGTGCTGTGA 240
CTCGTGCTCC TGGTTTGTCA TCTGCCTCTC AGTAGACACC ACGGCCTTCA AGCTTTCTCC 300
GCTCCGTGAC CAGCAGCTGG GACGGGACCA GCAGTGCATG CGGCTCTGGA TTCATGTTTG 360
TTGAATGACT GACTGAACGG AGGCTCCCTT ACAGAAGTGA ACGGCGCGGC CCTCCCTGAG 420
TTCCGGCCTG GCTCTGGATA CCAAGGAGCA AGGTGGTCAG GGGTCAGGGG CTGGAGTGGG 480
GAGATTGCCT GGGAGGGGGC TGGAGGGTGT GGTGGAACTG CAGGTTCTCT CCTTGACATG 540
CCTGTGGGGG AGCCTTTCCC GGCCCTCTCT CCGCTGGTTT TCACCCTTTC TCCGGTGCAG 600
CCACACTGGG CATCCCACCC CAGGGATCCA GGAAGGGGGC GTGTCGGCCG AGTGCGAGCC 660
CGTTTCTGAA CACCCTGTGA AGTTGGTGAG AATTCAGGTG CCTATCGGCC GGGCTCCACC 720
TGTGCACCAG GTGTGGCCGC CTCACTGTGA CTTCAAAGGT CCCCGGGGAG GAAGGAGGCT 780
CCCAGCTGCA CACAGGTGAG TCAGTCCCAT TGTTCCGTGT GTCTGAAAAA TCAATCGGGT 840
CCAAAGTAAA AATATTTATT TAATGAGCAG AAATGTATGG CCGATCGGTT TTTAAAGGAT 900
ATTGCTTCCT GCTCCTTGAT ACTGAAAAGG GGCGTTAGAA GAAATTCATT TGCAGGGATT 960
GAGTTCTGGA AATGGCCATT CTAGGTGAAA TAAGGACAGA AAATAGCACA GCACCCGCCA 1020
AAGACAGCTC ATTCTCTTCC TTGGGGTGCT GGGGGACACG GGCGCCCCTC GGGGGCAGGA 1080
GGATCCCAGC GGGAGGACAC TGGGCACTGC GTGAAGTCTC CCCTGGGAGC CCCAGTGAGG 1140
GGCAGGTGAT GGCCCCGAGT GTCCCTGGGT CTCCCAAACG AACGTCTGGG CTTCTCTGGG 1200
AGGAGGACTC CACCCTGCAG AAGAGAAGGG TCTGGGTCAG AACCCAGTGA GTCCGGGGCT 1260
CCCTCCGCCT CCTTTGCTCC CTGTGAGATG GGCACGGAGA ATGAGTCCCT CCGTGGACGT 1320
GGACGCCTGG TGGTTCTCGG CCGAGATCGC ACCCTCGTGG CACCTGCCGG GGACCGCCCA 1380
GCTCCTGCAG CTGCGGTCTC TGGAGAGCAC CGCCGGGATC CCCACGGCTC GAGAACCCGC 1440
GGTGCGTTTT 1450
|
