| Tag | Content |
|---|
EnhancerAtlas ID | HS026-26243 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr5:24547060-24548450 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr5:24547434-24547450 | TGCTATGTAAACAAGA | + | 6.03 | | Foxa2 | MA0047.2 | chr5:24547435-24547447 | GCTATGTAAACA | - | 6.32 | | Foxo1 | MA0480.1 | chr5:24547439-24547450 | TGTAAACAAGA | - | 6.02 | | Stat6 | MA0520.1 | chr5:24547763-24547778 | CATTTCCAGAGAATT | + | 6.87 |
|
| | 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 |
| GH05I024547 | chr5 | 24547381 | 24547530 |
|
Enhancer Sequence | AGTTCATAAT GAAACATGGG GTCAACAATT ACTCTATGTT AAAAGTATAA ATCTGCACAA 60
AGAAAATTTT AGCCTTCAAA CTGAAAAAGA TTGGGCTGTA AGATATACAG GACTTCCAGT 120
TAACTATGAA ATTAGATCAG TGGACTATGT ATACATGGAT TACCAGAGGA CGATTTAAAA 180
TTTTTAGTGA ACTGCTAATA ATATAAATGC TAATCCAAAT TTGCCTTTGA AACTGTAAGT 240
TAGATCATTG TAAACATCTG TAATTTATCT TAAGTGTAGG ATGAGGTAGG TAAGCAACAG 300
CAGGCCAACG TTCCCACTGT CATCATGTAG AACAGCTAAA TAAATCACAG AAAATCATAT 360
TGCCAGGGCC AAATTGCTAT GTAAACAAGA ACTGAATAAA CTGAAACCTG AGAGAAGAGA 420
ATTGTACAGA TGTGAGCTGA TTACTGGCAG CTGCTTTTTC CCGAGGGAAT TTGCCAATTC 480
TTGGCCAGGG GCTTGAAGGT GAGTATCTGT AACTGGCCAA GGAAAGGGCA CTTCTAGGAG 540
AAAAAAAAAT AAGAGTTTTT ATGGTACTGG AGTAAAAATA TTGGTAAACT GAAGGTCTTC 600
AAGCACATTG CCAGTCTTCC CCAAAAGACT TTTGTTGAAT AGAGTCTGTA GGAGGCTAAA 660
GGGCAAGGCT GAAAGCTTCT GAAAGCTGTA ATATAATTAC CCACATTTCC AGAGAATTGT 720
GGTTCTTAGA TTCAATTTTG TTTTTTAAGT AAAGAGGTGA AAGTTGGAAG TCCTCCAGAG 780
ATTATGGAAT TGAACTTGAG GATTTACAGA GACTTATTTT TTAACCTAAG GGCATTCAAC 840
AATTCTCAGT GCCTCTAGAA ACTAAACATA CACACTGGTC CCTTGACAAA TGGCCATCGC 900
TCAGGAGAAG AGAAAGTAGA AGATACACTG CTCTTCATGT CAAGCTTAAG TGGCAAAACA 960
CACAGACAAA TTCCTCCTGG TGACTTCTGT CAATTGTTGA AGAAGCGTAA AGCAAACAAA 1020
TGTTAAGAAA TTGGGTCATG CAATTGTCAG GGTTGGCAAG TCCAAAATCT ACAGGGAAGG 1080
GCAGCAGATT CAAAATTCAT GTAAGCGTTG ATATTCCAGT CTTGAATCAG AAATCCACAG 1140
ACTAGGCCAC CACATGGGAA CCTCAGCAGG GTTTCTTTTC TCTTTTTTTT TTCTGAGACT 1200
GAAGCTTGCC CTGTCACCTA GGCTGGAGTG CAGTGGCGTG ATTTCAGCTC ACTGCAACCT 1260
CCACCTCCCA GCTTCAAGCG ATTCTCCTGC TTCAGCCTCC TGAGTAGCTG GGATTACAGG 1320
CACCTGCCAC CATGCCCCAT GTATTTTTAG TAGAGATGGG GGTTCACCAT GTTGGCCAGG 1380
CTGGTCTTCA 1390
|
