| Tag | Content |
|---|
EnhancerAtlas ID | HS012-01869 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr10:118453650-118454820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU6F1 | MA0628.1 | chr10:118453684-118453694 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr10:118453684-118453694 | ATTAATTAAT | - | 6.02 | | ZNF263 | MA0528.1 | chr10:118454040-118454061 | GTTCCCTCCACCTCCTCCCTC | - | 6.16 | | ZNF263 | MA0528.1 | chr10:118454044-118454065 | CCTCCACCTCCTCCCTCCCCT | - | 6.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr10 | 118453652 | 118454170 | | chr10 | 118454426 | 118454501 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I116694 | chr10 | 118453631 | 118454697 |
|
Enhancer Sequence | GGTAGGGAAC AGCTTGGAAG GGAAAGGCGC CAGCATTAAT TAATTGACCA TCTCATGTGT 60
CAGGCACTGT CACGGGCTTT CCTTCATGAC CCACTGGGTG GCTTCATTTC TGTGACTCTT 120
GGACGTCCCA CTTGAGTAGG TATCCTGCCT TTGCTTATTC CAGCCAAGCA AGCCATAACC 180
CCCTCCCTCC AACTCCAGCC AGCCCCTGGC AAGGTCTAGC TCCTCCTATA CATCAAACAG 240
CTTTTTCTCC TGGAATTTAT TCACGGCATA TTCCCTGCTG GGAGGAGCTA CCTTTGAAAG 300
AAAGGTGCCA GCAAGTTCCC TGGAGTCTCT CTGGCTGAGC TGAGGAATTC ACAAACAACC 360
ACCCACATGG CCACTTGACC TTCTGGGGCC GTTCCCTCCA CCTCCTCCCT CCCCTTCTGA 420
GATGGGCTGC TCACTCCTTT CCTGTTGGCA AATTTGAAAC GCACCAACAT CCTGGGCTTT 480
CTGAGTCCTA AATTTTGCCC CCGAGCCCCT ACGGCTCCTC CTCCTAACTC AGGAGCCCCT 540
GTGCGCTCTG CACTCTCTGC TCCTTCACCT GCCTCGGTGC CCACAGACAC ATCCTCACGT 600
GGCCTCCTGG GCCACCAGGC GCTGAGCCTG TCCCTCTGCA ACCTTTGCTC TTCCAGCAGA 660
CCTGGGTCCA CCTCGTTGTG CCCCTCCCCT TCTGCCCTTT TGCCGCCTGG AACAAAGGGG 720
CTGACCCCTT CTCCAGTTCC AAGCAGGCTT CACAACGCTT GTCTCTGACT GTGGTCACCT 780
TCCCGAACAC CACCCAGTCC CCTCCCTTCC CTCTCCCATG CCTCAACCCC CACCCCACAG 840
TGACCTTGCT GCCAGGCCTC CCCTGTCCCC TTGTCCCCTT ACTGGTGGAA TACTGTTTGC 900
CCAGAACCCA CTCCTTCCCA GCCCACGGGC CCTCTTTCTT CTTGGTTGTC AGATCCTCCT 960
TCTTGCTCCC CAAATGACCC TGTGGCTCTC AGTCTCAGAG CCTCCCTCTC TCCCTGCAGA 1020
CAAACCTGCA GAATCTGAGT CAACTGCCTC CACACCACCG ACCTCCACCC TGCAGGCTCT 1080
CGGGATTACT GGGGTCTCTC ACTCTATGCT GTGTTCTGAA TGTGTCCCCG AAAACTCATG 1140
TGTTGGAAAT GTACTCCCCA GTGCAACTGT 1170
|
