| Tag | Content |
|---|
EnhancerAtlas ID | HS044-08613 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr22:39682650-39684010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr22:39683958-39683969 | TCAAGGTCATT | + | 6.32 | | Esrra | MA0592.2 | chr22:39683957-39683968 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr22:39683958-39683968 | TCAAGGTCAT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_30056 | chr22:39683241-39683968 | Fetal_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 39683110 | 39683318 | | chr22 | 39682922 | 39683753 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I039286 | chr22 | 39682108 | 39684201 |
|
Enhancer Sequence | CTTCTCTTTT TCTTATTTAT TTATTTATTT TGAGATAGGG TCTCACTGTG TCACCAAGGC 60
TGAATAGCAG TGGTGCAACC ATGGCTCACT GCAGCTGTGA ACTCCTGAGC TCAAGTGATC 120
TTCCCACCTC GGCCTCCCAA GTAGCTGGGA CTACAGGCAT GCGCCACCAC ACCTGGCTAA 180
CTTTTGTATT TTTTATAGAG ACGAGGTCTC CCTGTGTTGC CCAGACTGGC CTTAAACTCC 240
TGGGCTCAAG CGATCCTTGC ACCTTGGCCT CCCGAAGTGC AAGGATTACA GGCATGAGCC 300
ACTGCACCAA ACCTTCTCTC CTTCTTAAGA TTCTGAGTTT CTGTTTTGAC TCTATTTGAC 360
AGCATCAGTC AAATTGCAAA CGGGCTTACC CTTTGACCCA GCAATTCTCC TTCTAAGGAA 420
TCTTCCAGCC TCCAGAAGTC ATCAAGCATG TGCAGAAGAG ACAAGGCAAA AGTGTTCACA 480
GTGGCTTCTT GTGTAACCAA GGAAAACTGG GAGCTGCCCC CATCTGCACC AATGGCCAGA 540
GCAATTTATG GAACGTTTAC GGAACACCGC GTCTGGTATG TGCCTATGAA ACTTCTGCAT 600
TCAACAGACA AAACTTCTGC ATTCAAAACA CCACATTTCA AAACAAAACT TCTGCATTCA 660
GCATGCCACA GTCATGTGTG GAGAGCAGAG AGGAACCCTG GAGGGAGGAG CTGCAGACGG 720
AGCAGGGCCG TGGGGCAGGT GTCTACTGGT TTCCTGTAAT AAATTACCAT ACACTTGGTG 780
GTGGAAATAA CAGGCATTTA TTCTCATAGC TCTGGAGGCT AGAAGTCCAA AATCAAGGTG 840
TCTACAGGGC CATGCTGCCT CCACAGCTCC AGGGGGCAAT CTTTCAGCTT CTGGGGACTC 900
CCGGGTTCCT TGGCCTGTGA CCGCACTGTT CAATCCCTGC CTCTGACTTC ACAGGGCCCT 960
TTCCTCTCCT GAGTCTCTGT TTGCAAATCT CCCATCCCTT TCTCTTGTAA GAACACTCTA 1020
ACTGGATTTA GGATCCACCC CAACCCAGGG TGACCTCATT CTGAGATCCA TACTCTAATT 1080
ACATCTGCAA AAATCCTTAT TCCAAATAAG GTCACGTTCT GAGGTGCAGA ATAGACATGA 1140
ATTTTGGGGA GATCCTTTTC AACCCACAAC AATGTGGAAG GCCAATGTGT CTTCTCCATC 1200
ATTTGGTCCT GCTGCAAGGA GGGTGTGTTT CTGGACCTGT GTATTATTTG TGTATCATTT 1260
CATTTATGCC TAGTGTTCCA TTATTGGGAA TTATTTCTGT CCTCCTTCTC AAGGTCATTG 1320
CCAAGGTCTG ATTGCAAAAG TTTTAAAAAT TGCAACTTAA 1360
|
