| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04228 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:204720840-204721840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr1:204721173-204721183 | GCCCCGCCCC | + | 6.02 | | MEF2A | MA0052.3 | chr1:204721065-204721077 | TTTATTTTTAGA | - | 6.07 |
|
| | 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 |
| GH01I204752 | chr1 | 204721141 | 204721290 |
|
Enhancer Sequence | CTTTCTTTCA GGAGAGCCCA AGCTACTACC TGAAAATGTG ACAAGAGAAG AGGAGTTAAA 60
GGACTAAGTG GGAGATGGGA GATGGGGGGT TGGCAGTAGC GTTGCTTCTT CCAGCACTGG 120
GAAGCTTAAG GAGAAAATGA AAAACTCAAA CTCATGAATT TCAGCCCAAG GCATAGGCAG 180
AAACCCAGGG ACTTTCTAAG ACCTACTGAA TGGGGTTCAT ATTTATTTAT TTTTAGAAAC 240
AAGGTCTTAT TATGATGGCA GTGGCTGTTG CCATCACGCT GGCTGCAGCA GGGAGGCGCA 300
GCTGGGGCCG CATACTCCAT GGAGCCAGTG GGAGCCCCGC CCCTTCTGAG TTGGGACGCG 360
AGCTCCCTGG GTGCTGCTGT AGCCGCCCAA CCCGCAGCTA CAGACCCACG CCTCCTGCTG 420
TATGGAGCGG GCAGGAACCC CAGCCTCCTG GGTGGGGCTG CAGGCGCCCA AACTGCAGCT 480
GTGAATGGGA GCCTCCCTGT GCCCTTCCGG GAGGGCCAGG AGCAGGCAGG ATCTGCCTTC 540
CCTGGTGCGG CTGCCACGCC CTCCCAGGCT CAGGAGCCGG GTGTCTCTGC AGCCTGCACC 600
CTCGGGGCCC CAGGAGGAAC CTCTGTCCCT GCAGGTTCCG GGGTGTCTTC TCCTGCTGCC 660
TGGCCCCTCT CCACTCCCGG CACCTGCTCT GATCTTGGAG CCGGGGTTGG GGCCGAGCCT 720
GGGGGCTATG AATGGCAGCA GAAGGCAGAT TGATTCCTGG GCGGGGAAGA GGGGGAGTCC 780
CCAGTAAGGC CCCACCTTTG GGTCAGGGAG GGCCTGAAGG CTGGGGGCTG GGCTGCCAGT 840
CCTGCTGACT GGAATGGGGA CTCGTGGTGC CTCTTCTGGG CTGCCATTGG CCACCCCTGG 900
ACCTATCAGC ATGGACGCAC TTCCTCCCCG CTGAGGTCCA TAAAAACCCT GGGCTCAGCC 960
AGAGCAGGGC AGAGGATGGC CAGAAGACGA AAAGGGCAGA 1000
|
