| Tag | Content |
|---|
EnhancerAtlas ID | HS044-03274 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr12:53994810-53995940 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr12:53994998-53995008 | TTTAATTAGA | - | 6.02 | | Lhx3 | MA0135.1 | chr12:53995194-53995207 | ATTTAATTAATTA | - | 6 | | MEF2C | MA0497.1 | chr12:53995797-53995812 | GGAATAAAAATAGAA | + | 6 | | SOX10 | MA0442.2 | chr12:53995315-53995326 | AAAACAAAGCA | + | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_05715 | chr12:53993209-53999082 | Brain_Cingulate_Gyrus | | SE_08304 | chr12:53993595-53998576 | Brain_Inferior_Temporal_Lobe | | SE_09913 | chr12:53994789-53998314 | CD14 | | SE_60234 | chr12:53994293-54021784 | Ly4 |
|
| | 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 |
| GH12I053601 | chr12 | 53994985 | 53996384 |
|
Enhancer Sequence | GAGGGGGAGG TGAGGGAAAA AGTTATGTTA AATATGCTGG AGCAAAAAAA AAAAAAAAGT 60
GCTTCAAAAA TATCAACCCT AGAAACAGGT GTTCCACGAA TGCCATCTAT CAAAGTTGTA 120
AACACAGGCT ACTTTGGGGA GACCCATTAG ACAGGTGGCA TATGATCTAC TGTGTCTCAA 180
CTGAAACTTT TAATTAGAAA GAATGAGATC TAAATAGTCA AGGAATTTCA AACCTTTGCT 240
AGATTTTCCC TCTTTCTACT ACAGTATATA ACACACTTCT CCAGTCTGTT GAATTACAAC 300
TAGTGCAGTT CCTTATGTCA ATAAATTCAC TGAACGCTCG ATGCGGAAGC CATATTTCTG 360
AACGAGAGAA GACCAAAATT TGTCATTTAA TTAATTAAGG GATTATAGGA GGGGTGCTCC 420
ATTTTACAGG GCCATAATCT GGCTCCCTGG TGTATAAACT ACGAGACTGT TGGCAAGGGC 480
TGTTTATCCC ATATTATTGC CAAAGAAAAC AAAGCACCCA TCCTATTGGG CTACATGGGA 540
AATGGCTTTC ATTAATAAAA AAATAAAAAT AAAAACCGGG AGCCTCCTCC TCCCCCCACC 600
AATCGTCTGT GGCAAATGGA GAAGTATCGA TGCCCTTCCC CCTTCTGATT CTATTTACGG 660
CTAGGTTTTT AAAAGCAGCA ATAAAACAAA TGTCGACTCT TTGGGGGTTT ACTGGGTGAA 720
CATGTTCCGG CTGTTTGTGC TGCTTTCGGC CAGTGTTCTT GGGCTGCTCT GTTGCAGCCA 780
ACAGATGTGT GCTGCTGCAG GGGATGAAAG AAATGGCACT AAAAGGCATC ACCATCTATC 840
CCTTCTATTT CTCTGAAGAC TTTAACAGGG TTTATACCGT TTTATAAATT ATTGAAGCTA 900
AACTCTCAAA GTGTTTATTG AAATTCTTTG TTGAAGAACA ATAATTCCAA TCTGAATGTG 960
TGGGAGAAAT TTCTCATATT CCAACTAGGA ATAAAAATAG AAGTGGAGAT GGATAAAGAT 1020
TAGAAATGCA AATCATAGTA AAAAACAATT CCTAAAAGAT AAACTGTATT TTGGAAGGTG 1080
GAAGAGAAAA ATGGAGTGGG GGGTAAAATA GTCTTATAAA CTCCTAAAGG 1130
|
