Tag | Content |
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EnhancerAtlas ID | HS139-34809 | Organism | Homo sapiens | Tissue/cell | Myotube | Coordinate | chr22:19767240-19768380 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr22:19767359-19767369 | GGGGATTAGC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH22I019779 | chr22 | 19767227 | 19767350 | GH22I019780 | chr22 | 19767440 | 19768630 |
| Enhancer Sequence | TCAGTACAGA CACCCACACA CTATGAGGAT GATTCCCTCA AACTGGTTCT GAAAGCAGTA 60 GCTGTGCTTT TCTCTATCGC GTTCTTATTC TTTCTCCGAC GTGCTCTTAG CACCCTCCTG 120 GGGATTAGCA TCCGACCCAC ATCACTCGGG AAAAGCCCTG GCTGGCGGCT CCCAGGCGGA 180 GGCACCACGG TGAGGCCAAG TGCTGCTGTC CAGTAAGCCT GACTGCCCCC TCAGGCTCTT 240 TCCCTTCACA TTTACTTATT TATTTTTTAA ATCGACATAT AAAATTGACG TATTTATTGT 300 GTAAACTTCT TACCACAAAA ATGAGAACTA TGTCAGGTGA TGTATTTGCT AGTTAGCTAG 360 ACTTAAGCAG GCCTTTAGTT TTCAGTTTTT AACATTGAGG GAAAATACAC GTAAATCAAA 420 TTTACCATCG TAGCCCTTTG TAAGTGTACA TTTCAGTGGC ATGAAGTCCA TCCACATGAC 480 TGTGCAGCCA TCACCACCAG CCATCTCAGA ACTCTTCATC TCAGAAAACT GAAACTCTGT 540 CCCCATTAAA CAAGAACTCC TCATTCCCCT CCCCTGGCAG CCAGCATTCT ACTCTCTGTC 600 TCTGTGAATC TGACTACTCT AGGCGCCTCA TGTAAGTGGA ATCACACAGC ATTTGTCTTT 660 TTGTGGCTGG CTTAGTTCAC TGAGTGTAAG GACCTCAAGG TTCATCCGTG TTCTAGCCTG 720 TGTCGGAACT CCCTGCCTTT ATAAGGCTGA ACACTATTCT GTTGTATGTC TGTACCACGT 780 TTTGTTGATT CATTCTTCTG TCAATGGACA CTTGGGTTGC TCCCACCTGT TGGCTGCTGT 840 GAGTAATGCC GCTATGAACG TGGGTATAGA AATATCTTTG CAGCCCTGCT TTCAGTTCTC 900 TTGGGTATTC TGCCACAAGA GGAACTGCTG GCTCATATGG TAATTCTATG TCCAGGATTT 960 TGAGAAATGA CCACACTGTT TTCCATAGCT GCTACTCCAT TTTTACATTC CCACCAATAG 1020 CGCACAAGGG TTCAGATTTC TCCACACACT TGTTTTCTGT TTTTTTTTTT GTTTTTTTTT 1080 TTTGAGATGG AGTCTCGCTC CGTCGCCCAG GCTGGAGTGC AGTGGCGCGA TCTCGGCTCA 1140
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