| Tag | Content |
|---|
EnhancerAtlas ID | HS098-11118 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:102308910-102309690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr11:102309252-102309262 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr11:102309252-102309262 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr11:102309252-102309262 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr11:102309252-102309262 | AACAGCTGTT | - | 6.02 | | NFKB1 | MA0105.4 | chr11:102309548-102309561 | TGGGGAATCCCCT | + | 6.71 | | NFKB1 | MA0105.4 | chr11:102309548-102309561 | TGGGGAATCCCCT | - | 6.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTAGCTGGGA TCACATGCAC ACATCACCAC ACCCAGCTAA TTTTTGTATT TTCAGTAGAG 60
AGGGGGTTTC ACCATGTTGG CCAGGTGGTC TCGCATTCCT GACCTCAAGT GATCTGCTCC 120
CCTCAGCCTC CCAGAGTGCT GGGATTACAG CCATGAGCCA CCGTGCCCAG TTTATTTATT 180
TTTAATCACA ACCCAAAATC ATCTTTTTAG TTGTTTACTT CCTTATAGTC TACGTCTCTC 240
CACCTGGATA TTATCTTCAT GAGAGCAGGA ACTTATTCAT CTTATTTACC ACTTCATGCC 300
TTGTGCCTAA AACAGTGACT AACGGAGTGG GCAGTCCAAA CTAACAGCTG TTCACTGAGT 360
AAGTGAGCAT AATATTGCAT TATTTTCCTA CATTTCATTC CTTTAAACAA AATTGGATGA 420
TGTTAAAAAT TACCAGCAAC GGGTTCCAAG ATGGCCGAAT AGGAACAGCT CCAGTCTACA 480
GCTTCCAGTG TGAGCAATGC AGAAGATAGG TGGATTTCTG CATTTCCAAC TGAGGTACCA 540
GGTTCATCTC ACTGGGGCTT GTCGGACAGT GGCTGCAGCC CACAGAGCGT AAGCCGAAGC 600
AGGGCAGGGC ACTGCATCAC CCGGGAAGCA CAAGGGGTTG GGGAATCCCC TTTCCTAGCA 660
AAGGGAAGCC GTGACAGACA GTACCTAGAA AATCGGGACA CTCCCACCCT AATACTGCGC 720
TTTTCCAATG GTCTTAGCAA ATGGCACACC AGGAGACTGT ATCCTGCACG TGGCTCAGAG 780
|
