Tag | Content |
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EnhancerAtlas ID | HS049-04888 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr20:4065800-4066690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr20:4066064-4066083 | AGCTGCCCCCTGGTGGTCA | - | 7.51 | RARA(var.2) | MA0730.1 | chr20:4065810-4065827 | GGGTCACACCAAGGTCA | + | 7.26 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_02096 | chr20:4062805-4066636 | Aorta | SE_44675 | chr20:4065364-4066652 | NHDF-Ad | SE_45422 | chr20:4065808-4066698 | NHLF | SE_46211 | chr20:4061994-4066607 | Osteoblasts | SE_50015 | chr20:4062987-4066550 | RPMI-8402 | SE_56592 | chr20:4062109-4066596 | u87 |
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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 |
GH20I004081 | chr20 | 4062025 | 4066999 |
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Enhancer Sequence | CCAGGGTTAG GGGTCACACC AAGGTCAGGT TTTTAAAGTA TAGGATCCCA TTTTTGGTAC 60 TGAAACGTGG TTGGGGTATT TAGGGGTCTG CCTATTGGGA CAAAGGTTTC TTGGAGGACA 120 TCGCACACCT CTCAACCTGA GGACTCCTTA TGGGCTCAGG GGAGCAGCTA CTGGCTGAGA 180 TTTTTAAAGC AGGGTCTCAG TCAGTGAAAG CCTGGCTTGC TTTCCCTGAA GAGAGCTATG 240 CGCGTGCCTG GCCATGGGGC TCACAGCTGC CCCCTGGTGG TCAGCCACAG CCCCCTGCCA 300 ACCCTTGGGC GTGGTATTTT TCCAGCCTTA AGTCAGGCAG CAACGGCACA TCCTAACGCA 360 GGGTCCGTCT GGTTCCCGGG CCCCAGGTGG CGAGGGAACA GGAATGAGGG CTCTCCGGCA 420 CTCTCCGCTT TGCCCTTGGC CTCCTTTTTT CATCAGGGAA GACTCAGGGG AGGGCCTGCG 480 CTGTGCCTCT CTTCAGCATC TGTGAAGATT CTGCCAGCTC CCCAGCCCCG TGCTCTCCGA 540 GGGCATTTTT GTGCACGCAG GGCAGATTCC GGATTCCAAG AACATCAGTC ATGGAATGAC 600 CTCTCTCCGG CCCCTTGGTG TGACCTCACT GTCTTGCCTC CTCCACCTGC ACGTTCTTTG 660 CCAGCCTGTA GGTCCTATCG TGGGGACTCC TCCCTGACCT CTGCCAATTT GAAGTGGGAA 720 CTCAGATGAG TGCCTCTGAC TTTTTTTTTT TTTTTTTTTG AGACGGAGTC TCGCTCTGTC 780 GCCCAGGCTG GAGTGCAGTG GCGCGATCTC GGCTCACTGC AAGCTCCGCC TCCTGGGTTC 840 ACGCCATTCT CCTGCCTCAG TCTCCCGAGT AGCTGGGACT ACAGGCGCCC 890
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