| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14607 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:114287920-114288960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr12:114288185-114288196 | AAATCACAGCT | + | 6.14 | | Myog | MA0500.1 | chr12:114288306-114288317 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr12:114288306-114288317 | GACAGCTGCAG | + | 6.14 |
|
| | 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 |
| GH12I113850 | chr12 | 114288009 | 114288811 |
|
Enhancer Sequence | CTTAGCCCTA CCTATGCCTC CATAAATACC TCTTCATTCA CACCACCTGG GGGTGGGGAT 60
AGATTCTGTT TCTTGCCAGA TCCCTGGCAG GATCTGGAGT CCCTTTGCCT TGACCGGGGG 120
ACAGGTGGAT TTCCTACTTC AGATGGGGTG TCTCGCATGC CTTGGCCCTA CTCAGAATTT 180
GAGGCCTACC CAGGAAAGCT CTGAGCAGGT CTAGCCAGAC TCCAGGGCTG CCCTCATGAT 240
CCAGCTCTCT GGCTCTGCTG TCCTGAAATC ACAGCTCTTT GAGCTCCTCT GACTCAAGCC 300
ATGGACTCCA GGCATCAAGA GGCCTGGCCT CCTGCCGCCT TTTCTGAATT CCCTTAGAAG 360
GCAATCTGCT AAGGTGGTGT GGGGTTGACA GCTGCAGGCT AGACTGTGGC CCAGCCTGGT 420
GGCCTCTTTC AAGAACTGGG AAGGCATTGG AAGGCTGCCA TTGCAGCACT GGGCCTGACC 480
TTTCTGCAGC TTCCCTGGAG ACAGACCTCC TCTCAGCAAC AAAAGGCATT GCATGCCCTT 540
GGCAGGACTT CCATCCCAAG GGGCTGCGAA GAACTGCCCA GGGCCACGGC TTCTGGGCAG 600
AGCTGAGGAC AGTATTCCTG TCTTTAGAAC TCTAAGGCAT TCTCCTGGCC CCTTCTGCTC 660
CTCAGGGAGC TGTCCCTGGC AAAGCCAGAG GGCTGCATCT CTCAGCAGAC GATAAATCTG 720
TCCTAACAAG GACGACATCA ACCCCTCCGA AACCTGCTGT GCCCCCAACA CCTAGAGTAA 780
GTGGCTGGCA CTGTTGGGGG CTCTCTGCAG AGGTGGTCAA AAAATTGAGG CCAAGGACTT 840
CTGGGAGGAG GGTCTGCCTC CCTGGGGTGT TTTAACGCCA TCACCCTGAG AGAGAGATAG 900
ATCCTTTCCT TCGGTCCCAA GGCTCCCACT GTCCTGTGAG TAAGCTCTCA GCAAACCTCA 960
CTAGCTGCTT CCATCCTCAC AGGGTAGCTG TCTGCTAGGC AGGAGTTTGC CCAGAATAAG 1020
TTAAGCTCCC TGCACAATCT 1040
|
