Tag | Content |
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EnhancerAtlas ID | HS046-00485 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr1:23710000-23710830 |
Target genes | Number: 12 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chr1:23710211-23710221 | GCACGTGACC | - | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27061 | chr1:23710018-23711255 | Esophagus | SE_50618 | chr1:23709942-23711264 | Sigmoid_Colon | SE_53272 | chr1:23709967-23711232 | Small_Intestine | SE_65133 | chr1:23709934-23711086 | NHEK |
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| 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 |
GH01I023383 | chr1 | 23710092 | 23712491 |
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Enhancer Sequence | GAAAGGCATT ATTATTACTC TTTTGCTCAA TGAGGTGAGT AACATGCTCA GCATGAGTAG 60 GGCAGAATGG GACCTGAAAC CAGGGATCCT GACTTATCTT GTACTTCTTG CTAAGTACCT 120 TAGAACTTTT GGAGCACCTG CAGCCTGCCT GGTGGCCCAG ACATCACATG GTGCACATGC 180 AAGTCAGAGA GCAGTTGGAA ACTGACAATA GGCACGTGAC CACACTCTGT TCCTTCAGGA 240 GACTTGGCAG GAAGGAGCAC TCTGGGAGGA GTCTTTGTTT GGCTCCCATG CGTGAAAACA 300 AAACTTCTGC CTTTGCAGGA GCTGGGGCAG TCTGAGTTAC AGACTTGGGT AAGACTTTCA 360 GAGCTTCCTT AGGAGGGAAG GATGGCCTGG TGGCATTTAG GTTCAACTCC TTTCTGACAG 420 GGCTCAGCCT TCCTGTTTCC CATCCTTGGC TGTGGCCAGG TTCAAAGGAA ATACCATCTG 480 TGGAAGCACT TTCCAAAGAG GCGTGGTCCA AGTGCAGAAT GTTTTTCCTC TCCTCTGTGG 540 ATCTCAGGAA GCCGATTCCA TCTGTGCTCA AATGACAGAC TTGCTCATCC TGTGATAAAA 600 TGTGGGCTGC TGCCCCCACC CCAGCTTGGT GCCCTTCTAA AATGAAAACA TGCATGTGTG 660 TTCTCTCCCC ACCTCCCCAA CAGCAATCCG CCACTATCTC TGGCTCTGCA GACCTACTCT 720 GTGCAGGCTG GCAAGTGCTG CCATGCACAA GGCCCCTTCT GGGTTGTGGG TACACTACGC 780 CTTATGCGGG CGAGGTATGT GGATAACAGG GAAGGGGGAA ATACATAAAC 830
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