| Tag | Content |
|---|
EnhancerAtlas ID | HS051-17008 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr20:4065440-4066620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr20:4066064-4066083 | AGCTGCCCCCTGGTGGTCA | - | 7.51 | | NKX2-5 | MA0063.2 | chr20:4065533-4065543 | ACCACTTGAG | + | 6.02 | | RARA(var.2) | MA0730.1 | chr20:4065810-4065827 | GGGTCACACCAAGGTCA | + | 7.26 |
|
| | 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 |
|
| | 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 |
|
Enhancer Sequence | TCCTAGACTC AGATGTCCTC AGTCTTCATC ACTCTCTCTG GGTCTGATGG TCAGGAGGCC 60
TAATGCTCAA GCTGTAAGGC GAGGCTCCTT AGAACCACTT GAGTCACCTG TCCGAAGCTG 120
AATTGCATGA TGGCTTCATT CAGAGCCACC CAAATCATTC TGGCCAATCA CGGGCAACTG 180
TGGATGGTTC AATGGCACCT TCCTTTCAGA GAATAGAAGT CCCAGGAGGG CAGGGGTCTT 240
TGTCTGATTT GTTCACTGAA GAATCCCAGG TGTCTAATAG GCTGCTGGTA TATAGTAGAT 300
GCTAAATAAA TACTGGTTAA ATAAATGAAG GATTGCAATG GGTTTGGGGG AAGTCTGAGG 360
CCAGGGTTAG GGGTCACACC AAGGTCAGGT TTTTAAAGTA TAGGATCCCA TTTTTGGTAC 420
TGAAACGTGG TTGGGGTATT TAGGGGTCTG CCTATTGGGA CAAAGGTTTC TTGGAGGACA 480
TCGCACACCT CTCAACCTGA GGACTCCTTA TGGGCTCAGG GGAGCAGCTA CTGGCTGAGA 540
TTTTTAAAGC AGGGTCTCAG TCAGTGAAAG CCTGGCTTGC TTTCCCTGAA GAGAGCTATG 600
CGCGTGCCTG GCCATGGGGC TCACAGCTGC CCCCTGGTGG TCAGCCACAG CCCCCTGCCA 660
ACCCTTGGGC GTGGTATTTT TCCAGCCTTA AGTCAGGCAG CAACGGCACA TCCTAACGCA 720
GGGTCCGTCT GGTTCCCGGG CCCCAGGTGG CGAGGGAACA GGAATGAGGG CTCTCCGGCA 780
CTCTCCGCTT TGCCCTTGGC CTCCTTTTTT CATCAGGGAA GACTCAGGGG AGGGCCTGCG 840
CTGTGCCTCT CTTCAGCATC TGTGAAGATT CTGCCAGCTC CCCAGCCCCG TGCTCTCCGA 900
GGGCATTTTT GTGCACGCAG GGCAGATTCC GGATTCCAAG AACATCAGTC ATGGAATGAC 960
CTCTCTCCGG CCCCTTGGTG TGACCTCACT GTCTTGCCTC CTCCACCTGC ACGTTCTTTG 1020
CCAGCCTGTA GGTCCTATCG TGGGGACTCC TCCCTGACCT CTGCCAATTT GAAGTGGGAA 1080
CTCAGATGAG TGCCTCTGAC TTTTTTTTTT TTTTTTTTTG AGACGGAGTC TCGCTCTGTC 1140
GCCCAGGCTG GAGTGCAGTG GCGCGATCTC GGCTCACTGC 1180
|
