| Tag | Content |
|---|
EnhancerAtlas ID | HS026-34442 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr9:110125250-110126750 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ONECUT1 | MA0679.1 | chr9:110126589-110126603 | AAAAAATCAATAAA | + | 6.89 | | ONECUT2 | MA0756.1 | chr9:110126589-110126603 | AAAAAATCAATAAA | + | 7.52 | | ONECUT3 | MA0757.1 | chr9:110126589-110126603 | AAAAAATCAATAAA | + | 8.12 |
|
| | 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 |
| GH09I107363 | chr9 | 110125860 | 110126233 |
|
Enhancer Sequence | CAGGCCAGGA TGAGCACAAT GGCTCACGAC TGTAACCCCA ACACTTTGGG AGGCCAAGGC 60
AGAAGGATCA CTTGACCCCA GGAGATTGAG ACCAGCCTGG GCTAACATAG CGAGACCCCG 120
TCTCTACAAA ATAAAAATGA TAGGCCGAGC ACAGTGGCTC ACACCTGTAA TCCCAGCATT 180
TTGGGAGGCT GAGGCAGGCG GATCACTTGA GGTCAGGAGT TTGAGACCAG CCTGGCCAAC 240
ATGCTAAAAC CCTGTCTCTA CTACAAATAT AAAAATTAGC CAGGCATGGT GGTGGGTGCC 300
TGTAATCCCA GCTACGCAGG AGGCTGAGGC ATGAGAATCG CTTGAACCCA AGAGGCAAAA 360
GTTACAGTGA GCTGAGATCA TGCCACTGCA CTCCAGCCTG GGTGACGAAG TGAGACTCTG 420
TCTCAAAAAA ATAAATAAAA ATAAAATAAA ATAGCCAGGC ATGGAGGCAG CCCCCGTTGT 480
CCTTAGCTAC TTGAGAGGCT GAGGTGGGAG AATTGCTTGA GCCCAGTAGG TCTGCAGTGA 540
GCCATAATTG CACCACCGCT CTCCAGCCTG AGTGACAGAG TGAGATAGTG TCTCAAAAAA 600
AAAAAAAAAA AAAATACAGA GAGAGAAAGA AAGAGATGCA GAAACAGATG GCCTCTGTCT 660
TATAGGCCCT GGGGGCAAGA CACTGGGCAG ACAGAGGGAA GCCACACAAA GAAGCCCAGC 720
TGCACAGGCT CCAGGAGTGC TCCCAGATGC TGCAAGAATG CAGGCAGGGA GGGGACTGAA 780
AAGTGGGATG GCCCTTGGCT TGGTCACTTC CTGCTGCTGA GGGAATCAGG TGTGTTCTAC 840
GGTAAGATTT AAAAAATAAA ATGAGCCTAG GGAGAAAAAT CCAGGCTTGC TGAACTAATA 900
AATCAGTGGG AGAGGTGAGC GCTTGCTCTA GTGAGGCATT TATGATTGGC TGCCTTTCAT 960
TGAGCCACAC GGCGAGCTCA TTCGGTGAGC AGAAAGCCCG GCAGAGCAGG CCTGCGATCT 1020
GGCAGACTGC GGGGTCCAGT CCAGGCTGTG CTAATCTCTT CATCTTTCTG AGTCTCGGCT 1080
TCCTTATTTG TAATACAGGG GTGCTATATG TTCTACCTAC TTTACTGTGG TAGGAAGAGT 1140
CACTGAAATA AAGAAAACAA AAATTGCCTA TAATTCACAA AGTTCCTACA CAAGAAACCA 1200
GTAATAGTAT TCTTTTATAG GGAGGGGAAC GGGGTGGCTG GGAGATAGGA ATGGGAGGGA 1260
GACTTTATGG TGTGTATCTT TTTACATGTT TTGCTATTTT GAACCACAAG AATAAACTAT 1320
TCATTGAAAA AAACTTAGAA AAAAATCAAT AAAGGCAATA ATAAGGTCAG AACTAATAAT 1380
GCAAGCAATC GTCATTATCA TCATTATCAT GGTCAAAATC ACCAATGTCA TCATTATTTT 1440
ATTTATTTAT TTATTTTTTT GAGACGGAGT TTTGCTCTGT TGCCCAGGCT GGAGTGCAGT 1500
|
