| Tag | Content |
|---|
EnhancerAtlas ID | HS139-14065 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr12:124098430-124099730 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr12:124099314-124099324 | GCTAATTGGG | - | 6.02 | | FOSL2 | MA0478.1 | chr12:124099227-124099238 | GGATGACTCAG | + | 6.32 | | JUNB | MA0490.1 | chr12:124099227-124099238 | GGATGACTCAG | + | 6.14 | | Sox3 | MA0514.1 | chr12:124098661-124098671 | AAAACAAAGG | - | 6.02 |
|
| | 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 |
| GH12I123614 | chr12 | 124098960 | 124099844 |
|
Enhancer Sequence | GAAGGCAGCG TAGGGACAGA TGCATATGTT CTTTGGACTG GTTGGTTCTT TTCCCCTTTT 60
CTCCAGAGAT AAATGTGTTG ATCTTTAGTA GTACATAAAA AATAATTTTA TATTTATTTA 120
TATATTTATA TTTATAATTT CTTTTCTATC TGTTATCCTA CAAATAAAAT GCAATATTGA 180
CCATGACCCA CAGTAAGAAG TACAATTTGG TACACACCCA AACAAGACAA TAAAACAAAG 240
GTTTTCATGA AACTGCACCC TGCTAGGTGG GATGTTTTCT ATTCTGTTCT ACTCCAGCTG 300
TTAATTTTTT TAAAATGCTG GTCGAGACCC ACTAAATTGA TTTCAGAACC CACCAGGTCT 360
GTGGGTTGTG AGGCTTAGTG TGTGAAACAC CACTTCATTA CATACTATGT GACTCAAGGT 420
GGAAAAGAGC GGTCACAGCA CAGGTGGAGG GACTGAAGTA GACAAGAGTT AGCCCAAACT 480
GGAATGCAGT AGTGCAGTAG TCTGGTCTAG TGGGAGGAGC ATTAGACCTG GGTTCTGGTT 540
CTGCCACTTA CTCTGTGTCT CTGGTAAGTT TTAGTTCCCT CATCTGCAAA AGGATGGGAA 600
GTCACTTGGG AATGCTTCCA GTTAAGGAAA AGGGTCCAGG GTGAACTTTA TTAGAAGGGT 660
GCCGGGTAAG GAGCTCACAG ATTCAGAGAA TGTTGAGTGT CCAGCTCCCA GGGAAGGAGG 720
CTCCCTGGCA GGAGTTCATG GGCCATCTCT TTAGGGCATA TCTTTATTGG GATGACTGCC 780
AACCCCTTTT TGTCTTTGGA TGACTCAGCT CCAAGTCCCA AATATCTGGG AGAAGGGATC 840
TGACTGGCCT AGCTTGGGTT ATTTGCTGAG CCCTTGGGAA TCCTGCTAAT TGGGAAAGAA 900
GCAGTTCCCT AAACGGAAAG CAGAAATGTT TTTAAATCTT GTAACACTAT TTGTGGCTAA 960
GATGTCATTG CTTTTGTTCT GAATGACTGT TTCACTTTAA TTCCTTTCTC GGGGTCAGGG 1020
AGATTTCCCG TGAGAACATC TTTAGACAGT AAAATATGTC CTTGGGGGTT TTAATTCATG 1080
TTTAAGGGAT TTTGTCAAAA GATTGGCCTT TCATTGGCTG AGAGGATTAC AGATTGAGAA 1140
CTCAGTTGTG GATGATTTCC ACTGCCATTT TCCTTGTCAT TCCCCTAGGG AGGGCTTGTA 1200
GTTAGGTTGC GTCTGCTGCA GCTATTGCTC ACTGTTCCCC TCTCCCGGTT GTAGAAGGAC 1260
CAAAGTGGCC AATGACTCTA AGCCCTCTGT CCCTCTTGCA 1300
|
