| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00162 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:7668720-7669870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:7669072-7669083 | TGTGGATTGGA | - | 6.62 | | JUN(var.2) | MA0489.1 | chr1:7669132-7669146 | CTGAGTCACTTCCT | - | 6.23 | | NFE2L1 | MA0089.2 | chr1:7669128-7669143 | AGTGCTGAGTCACTT | - | 6.51 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 7668813 | 7669345 | | chr1 | 7669462 | 7669554 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I007608 | chr1 | 7668605 | 7669456 |
|
Enhancer Sequence | ATTGCTTGTA GCTTCCACAC TGGCCATCAG TTTGATCTGA GCTCAAGGGT GCAGCAGAGG 60
CTCACCTTGT TCTGCTTAAA TAATGCAGGT AGTGAAGTTA TTGACAATCT GTCATCTGCT 120
TGAAAGTGGC TTCGACAGAG CCAGAAGCGT GGGAGGGCCC CAGGGGCCTC AGCCGGCCAC 180
AGGTCCAGTC TCTGGCTGAA CAGGGGCTCT TCAAGAAGGG CCAGGCCCTT GGCATGGTCC 240
AAGATGAATG GATGGGAGCT TGAGCCCTAC CTGGCCTTTT CTAGAAGGAC ATTCTATGGG 300
GAAATTCTAA GCAGAAGTGA GGGCAGGAGC TGTCTGGCTA GGAGGCCTGC GTTGTGGATT 360
GGAAAGGAGT CTCCTGATGC AGGCTGGGCC CCCCGCAGGG GTGGGGGCAG TGCTGAGTCA 420
CTTCCTGCCA GAGGACAGGG TCTGAACTCC CAGGACATTC TGGCCCCTTC CCACTACCGG 480
CCTAGCCCTG CCGCCTGTGC CTTGCCTCCT GGCCTCCTAG CCACAGACAG GGGTTTATGA 540
TGAGCCGGCT TGCTCATCCT TGAGCCTGGG TTGGATTTTT TTTTAATGTT TAAAAATTCC 600
CCACAGCATG GCAGGTGCCC GGCTGCTGGG TCACCCCATC GGCTGTTCTG TCATCAGACA 660
TCATGTTTAC CCATCAGACG CTGTTTTCCT GACACTCAAC ACTCAAAATA ATGATCTCGC 720
TGGAGCACCT TCATGAATGA TTCATGAGGC TCTGCTCAAC TTTGGGTGTT AACAGCAAAT 780
CAAAGCCCCT CAGTGAGGGC AGCAGAGCAG CAGCCAGAAG GCAAGCCCTG GCCCCAGCCT 840
CCAGGCCCCC AGGGATGCTC AGGGCCTGCC ACCCCTCTCT CAGGCTCCAG TCCAGCCCTG 900
CAGGAGTGAG CCAGCCTCAG CCAGGCCATG GCACAAAAGG GGAGGGGAGC AGGGTCCTGG 960
CTGTCACCCA TGTCCTGGTG ACCTTGCTGA GGACATTGGA GCTCCAGCCT CAAGTCAGAT 1020
CCCCTGGACC CCAGATCTCT TCCACCCACA GGTGGTGTGA CCTTGAGCAG GTCACTTTGC 1080
TTCTCTGAGC CTCTCTTTCC TGTCTGCAAA GCCAGGTGGG AACTGCCCTC CCGCAGGGCA 1140
CCTGTGAACA 1150
|
