| Tag | Content |
|---|
EnhancerAtlas ID | HS116-22067 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr22:26338000-26339430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr22:26338797-26338810 | AGCAGCTGTCTCC | + | 6.21 | | Myog | MA0500.1 | chr22:26338796-26338807 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr22:26338796-26338807 | CAGCAGCTGTC | - | 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 |
| GH22I025941 | chr22 | 26337259 | 26339725 |
|
Enhancer Sequence | TAATGTTTTC TCACTGCCAG ACACTGTGTA AGCACTTTGC ATGTTTTCAT CCATGTATCC 60
TGCAGACATC CTGTGATGGA ACCATCCCTA TTTTATAGAG GAGGAAAACT GAGGCATAGC 120
AAGACGGTGC TGCTGGCAGA AGCAGACTGC CTCAGGTCTG GCTCCAGTGC CCAAGCTCTG 180
AACCACACAC ACAGTGAAAT CTGGCACTTA GTGTTGGTAA CGTTGGTTTC CTTCCTCTGT 240
CCTTCGGAAT GAATGTGTTC ATCCCTGGCA GGTTCCAGGA ATGATGCATA TTTCCACCAC 300
ATTTGCTCAA ACTCCGAGTT CTGTCATTTT ACAGACTCCC AACTTAGTCC AGGCTCTCCT 360
GATGCTGCCT AAGAGGTTTC CGTTATAGCA CGAAACCACT GAGCTGTTTT CTCTGCAACA 420
GAGCTCTCTC TTTATTTTGA TCCATTCCGT CTGTGTGGTC AGACCTCCCA GTGAGTGGCT 480
TTCTATGAGG GGCAGTGAAG CTCAGTAGTT AAGAGCTTGG GCTCTGGCGT TGGAGCAAGC 540
AGGCTCTCCA CAGACCAGCT CTGTGATGGT GAACAAGTCA CTTCCCCTCT GTGTGTCTCA 600
GAGTCCGCCT TTATCAAAAG GTCCTAATGG TGGCACCTTT CTCCTAGAGG TGCTGTGGGG 660
CTGTCATGAA GCAAGGCAGA GAAAGCACAG TGCCTTGAAC ATGGTCCCCA AGCAACAGTA 720
GCAGGTGGGA CTGCTAATGC CAAAACCATC AGGGCCAAGA TAATCCTATC TCCAGCCCAG 780
TATGAGCTAA GAAGGCCAGC AGCTGTCTCC ATTGACTGCT GTCTGTGTTC ATCTCTCTCT 840
GGGGATAAGT CGTCCCTCTC TCTGCTTGCT CCAAGGAAAG AAGGGAAAGG AAAGAGCATT 900
TCTGGATCAT GCACCATTAT GCCATCTATA AAATGGGGAT AAAAATAGAG TCTCCTTTCT 960
CCAGGGGCTC CGAGGACTGG CGGGATCATG CTGCTGAAAC CCTCTGCTGA AGTAGGGGCT 1020
GGGCAGATGG GAACTGTGTC ATCGTGTTCT GCTTTGCCCT GTTGCTTTAT TTACAATGAC 1080
TCTCTCTTGC CTCCTGGCTC CCAGCCCAGC TCCTTGGCCT GGCAGAGGGG CCCTGCGTGA 1140
GGCCTCCTCT TCCACCATTA GTTATCTGAC ATCATCTCCC TTGATGGCCC ATCTGCTCCT 1200
GCCGCCCAGA CCTTTTGTTG TTTGCATGCC CTGCTGTGCC GATTCTTCCA TTTCTTTCCA 1260
CTTCCACCCC TTCCACCCCG GCTGGAGCAC CTCCACCGCC TCCTTCCTGC AGGACCATGG 1320
CGATCCCCTC ACTGGCTGCC CTATTTGCAA TCTGGTCCCA CCCTCCCCAC AGCAGCCAGA 1380
GGGAGATTAG GCCACCTACC TCCTTAGAAA CCATCCATGG CTTCCTGGCA 1430
|
