| Tag | Content |
|---|
EnhancerAtlas ID | HS116-29588 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr6:44168420-44170160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:44169429-44169447 | GGGTGGAAGGAAGGAAAC | + | 6.33 | | FOXH1 | MA0479.1 | chr6:44168703-44168714 | TGTGGATTGGG | - | 6.14 | | MSC | MA0665.1 | chr6:44168614-44168624 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr6:44168614-44168624 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr6:44168614-44168624 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr6:44168614-44168624 | AACAGCTGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29878 | chr6:44168112-44171585 | Fetal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 44168422 | 44169635 | | chr6 | 44169696 | 44169875 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I044200 | chr6 | 44168324 | 44171755 |
|
Enhancer Sequence | TATGCTAGGC ATGTCCTTCC TTACCTTCTC CTCAAGCTCC TCTGTCCACC CTCATCCCTC 60
TCACTGTCCA GGAAACAGCT GTCTCCTGCC CCAACAACTG ACTGTTCCCT CTGAGGCATT 120
GCCAGAGAGG GTAGGGCCCC CACCTCCCAC CCTCAGGGTC CTGTCAGCTG AGTGGGGGGT 180
GGGGGGCAGT GGGCAACAGC TGTTGCAGTG GGGACAATGG CTGTATTCTA TACAAGCTCC 240
TTTCCTGGGC CACCTCCTCC TCCCTGGCTA GAACAACTGT TCTTGTGGAT TGGGGAGTCC 300
CATCTGTCTG TGCTAGCTAC TCTTTCAGGC AACCTCCAAC TCCCTGGCCC ATTTTGCTCA 360
TGTCTTACAG GCATATCCAG TGTGTGTCCC ACTGCCCGGT CGCCTGTGCA TGGGTCTATC 420
ATTGCCTGGA ATTGGTGGGC AGAGGAATGA TGGTCATGGA TAAGGGACCA TCCCTCCAAA 480
GCGCATCACC TCTTCTTTCA GTGGTCACAT TCAGGCCCTA GCTCCTCACT CAGGTAGGTG 540
GTTTCTGGCC TGTTGTCCCA GGCAGAAAGG CACTGTGATT ATGACAGGGC TGAGCTCCCA 600
GTTCCTGGGC TAGAACTCCG CCCATTCCCC ACCCACACTG CCTATACCTG GCTGGCTCTG 660
GTTCCTGGCC CCAAGGTCTC CCCACCTGCT CCTTGGTAAC ATCACCCCTT GACACACCCT 720
GCCCTTGATG AGGCCTCCCT GGCTCCTTGT CAGAACTCCT TGTTTAGGGG TCAGAGCTGT 780
CCTCAACCTC CCACAAACAG GAAGGGCCCC ACACCAATGC TGATTTCCCA GAGGACAACA 840
GGCCAGTGAA ACATGACAGA GCGAGGGGCC ACAGCCTCCG CAGGCCTCCC TTGATTCTTC 900
AAGCATTAAC AGAGCCCCAG CCTCTGATCT AAGTGCTGCC CATGAGCAGC AGGGTGCCTT 960
GCATCAGGCC TCCAAGGAGC AGCAAGTTCT CTGCTGGCCT CTGACATAAG GGTGGAAGGA 1020
AGGAAACTAA TATTTATGAG ACACCTACCT GGTAGCCAAA CTCTGAGCCT CACATTCTCC 1080
TCATCTCTTT ATCTGGTCAG CTGTAGGTAT TATTATAATT CCCATTTTAG GGAGGGGGAC 1140
CACCCCATAG CACAGCTCCG GAAGGTGCCA CTCTCAACTC CCGCTGTGCA ATATACAGCC 1200
TGCTCTGGCA TCCAGAGGGG CCCTGAGAGA GGGTCCCAGA GCCAGCATGT GGTTCCAGAG 1260
CGACCAACTC AGAAGCACCT CCAGCCAACT TCACGAGCTG GGACCCAGAC ACATGTTTTT 1320
AATGCAAGTC ATGCGGAGGC AGTGGCCTGT CGCAGCATGC TCTTGAGCGC CTGGGTGGAG 1380
ACATGCAGAA GGGGTGGGAA GAGCAGGACT CTCGGTGCCC GTGGGTCTGG CAAGAACCCA 1440
TTAGCTCTAG TGCAACTCTT GCTATCATTC CTGCTTTCCC CATCTGCTGT CTGTCACTCT 1500
GGTGGCTCTT GGTGTGTCTG TCCTCTTCAC CATTGACCCA GAGCCTTGCA CGGGCTTTCA 1560
CACAGTTGGC ACACAATGTA TGTTGTCATG TCTGGCCCGA TTAACTGATG CCTGTGTATG 1620
GGCATCATCC AGAATGTTTC TGGATGGCCC TGGGCATCTG GGGAGTGGAC CACAAAGGCA 1680
GATCCCAGGG GCCACTTAGT GCCAGCCCAC AGTCCTCACC TTCACAGGTT GGTATCCAGA 1740
|
