| Tag | Content |
|---|
EnhancerAtlas ID | HS193-31238 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr7:2915340-2916380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr7:2916059-2916072 | GGGGGCAGCTGCT | - | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 2915365 | 2915542 | | chr7 | 2915575 | 2916141 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I002875 | chr7 | 2915376 | 2916288 |
|
Enhancer Sequence | CAAAGTGCTG GGATTACAGG CGTGAGCCAC TGTGCCCGGT CAAGTTCCTT CTTCTGATAA 60
GGACTCCATT CACCGGGCTA GGGCCCTTCC TACTCCAGTG TATCCTCATC TAACTAATTA 120
CATCTGCAAT GATGCTATTT CCAAATAAAG TGATGTTTGC AGTTACCAAT GGTTAGGACT 180
TGCGCATATC TTTTGGGGAA TATAATTCAA CTCACAAGAG AAGGTTGTAG CTGCAGGCAC 240
TTGGGGCTCA GTCTTGGTGG CACCCCTCCC TCCAAGAGGC TGTGTGGAAT GTGCTTGAGA 300
ATTGCCCCCG TGAGGCGTGA GGAGCTGCGG CATTGACCCG CCCCCTCCTG CCTGGAGGTG 360
TCTCGGAGCC CTGGGATTTT CCTCCCAATG TGGCATTCAC AGGCATCACA TCACTATCTG 420
GCCATCAGCC ACGGTGGGAG TATTGACACC ACAGACATCA GCGGATGTTA CAAATCAGGC 480
TTCTTTTTCC CCGTGAATCA GCCTCCTGTA CCACTCCGGC CCCTCCCTGG TGCAGGAGCA 540
GTGCAGTGAG CTGATTCATG CGGAGAAAGA TTGGTCTGGC CTGCCCCGTG AACGGTCTGT 600
GTGTGGTCCT GGCCTGAGGA CACCCCAGCG GGCTCATGTG GGGACTGCCT GCAGGTAACC 660
TCTAGACTTG GCTGAGCACC AAGAGTGTTG GCCATAGGGG ACCAGGCAGG TGGACGCCTG 720
GGGGCAGCTG CTGGCTTCCC AGCGGGGCGC TGCCTGAGGC CCGGTTTGCC CAGAGAAGTG 780
AGCAGCCAGC TGTGGCCCGG CAGAGTCCCA GGCCGTGCTG ACAGGTGTGG CCAAAGGGCA 840
AAGGGTGTTA TTATAAAAGA GAATTTACGG CAGCGGCAGC TTGGGCTGGC TGAGCCCACG 900
GGCAGCAGGA GGATGGAGTG GGGCTGGCAG GATGCTGGCA GGATGAAGGA TCTGCATTTC 960
ATTGAGACAG TGGGTTGGAG TCCACGCGGC TGAGATTAAA TAGCCCGTCC CCGGAATGCA 1020
GAGAGCCAGA GATAAATCAG 1040
|
