| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00810 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:35936560-35937420 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr1:35937131-35937142 | TTAATTAAAAT | - | 6.62 | | MAFF | MA0495.3 | chr1:35936734-35936749 | CTGCTGACTCAGCTA | + | 6.43 | | MAFF | MA0495.3 | chr1:35936734-35936749 | CTGCTGACTCAGCTA | - | 6.55 | | MAFK | MA0496.2 | chr1:35936732-35936751 | TGCTGCTGACTCAGCTACA | + | 6.18 | | MAFK | MA0496.2 | chr1:35936732-35936751 | TGCTGCTGACTCAGCTACA | - | 6.46 |
|
| | 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 |
| GH01I035471 | chr1 | 35936941 | 35936950 |
|
Enhancer Sequence | CCTATAGAAG GGCAGTTACA AAAATCATGA AAACACACAC CAACACACAA AGAGGACAGC 60
CACATAGCCT GCCAATAACA AATCTCTTCT GATCTTGACA AGGCTTTAGT TTTTAAGATT 120
TCACCCCAAA GCCTGTAGGG AAACCAAACC ATCTGCTGAA AGAAAGAGCG AATGCTGCTG 180
ACTCAGCTAC AGTTAGGGCT TCTTCCAACT CTCTCCCAAC AATGCTTATT CCTGCCCTAT 240
ACCGACCCTC TCAGGGCCAA TCCTCCCTAA AAAATACCAG GTTGCTCATG GTGTGGCATA 300
CCACTGAAAA TACATGTCCG ACCAACCATT ATAGATGAAC TCATTGGGAA CAAAGGCCAT 360
TTTCTTGCAA AACTTCTTTT GCAACAAAGA ACAGCAATGA CTTCTAAATA ACATGGTTCA 420
AAAATAGCTT TTTACAGAGT GCTAACAATG CTCGTCTCAC TGAGGTCATC ACACCCTGGT 480
GAGTTAAAAG AGCTACTTCA TTCCTGCTGA GCTAAATAAC ACACTGCAGA AGATGGTAGG 540
AGATGGCCCA TTTAAAACAG GCCCAGTGAA ATTAATTAAA ATCAAATGAA GCATTAAATG 600
GTACCCACTT GCAGGTCAGA CTATATCACT AGGTAAGGCA ATGGTAGGAT CCTATCTAAA 660
TGGCATCCCT CCCCAGAAAA AGTAGTCTTA AATTTTTTTG GATCAAAATG CATTTCTGAT 720
TAGGGAAGGG AGGACTTTGG TAGGAAGGTT TAGTTTAAGT TACTAACCAA AAGTAAAAAA 780
GAAAAAGGGG GAAAAAAAAA CCTGAAACAC TTAGCAGAGA GTGGTCATCT TTTTCTTATT 840
TCATGAGTTC AAATGTTAAA 860
|
