| Tag | Content |
|---|
EnhancerAtlas ID | HS042-25580 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr2:121932220-121933240 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr2:121932491-121932502 | TTTCTGGGAAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27526 | chr2:121932036-121933595 | Esophagus | | SE_36212 | chr2:121929305-121933590 | HMEC |
|
| | 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 |
| GH02I121171 | chr2 | 121929501 | 121933265 |
|
Enhancer Sequence | TATCTTGCAC TTGACCCTAA GTTCACTAAG TGTGGCAAAG TTGTTCCCTT TATAAGCACT 60
GTATTTCCAC CACAAGCACC ATGTCTGACA CATACTATGC ACTCAGTAAA TATTTTCGGG 120
GGTGGCTACA CAAGATGGAT GAGCAGCGGT GAGCTCCCCT GACTCACCCA CTATAAGCCC 180
ACCACCCCAA AAATGGTCTC CTGTCCCTTG GCACAAGTAT TCCTTCCTTC AGCACGTGAG 240
ACAGACATGC CCTAACCCCC ACCCGACCCG CTTTCTGGGA AGCCGACACA GGGGCTTGGC 300
CCCGGCCACG GTGCCTGAGG CCTCTGAGAG GCAGGTAATG GCTTGGGCTA AGCTGGTCTC 360
TTTGTTCCCA GCATCAAGGC AGGCTGAGCA GATGCTTGGC AGTTACCACC GCCAGACTGG 420
GCCTGCCAGA ACAGGGGGTG AGGCCCAGCC AGGGAATGTG TCAGGAGAGA TTCCAGGGCC 480
GGGGGAACAC AAAGAGGGCA CTCTCAGGGC TCCGGGGAGC CTGCCCGGCC TCCGGGTCTG 540
CCAGTGTCAG GCTGTGCTGC CCATTGAGGC AAGAGCTCCT ACCAAGGGCA GGGAAGTGAC 600
AGAAGGAGGC TAAGTTGGCC CCAGTGCAGC CCCAGAAATG AGCAAAGAGG TCATAAAAGC 660
AGACAGCACT TATACAAGGC TGGGTGGTGG AGTGGCGAGT GTGAAACTTG AGGCAAATGT 720
CTTCAGCTCT CTGAGACTCC GTCTCTTTGA TGCCAAAACC ATGTTGCGAA CCACGTTCCT 780
ACATTGCCAG CGGGCTCTAT AGTAGTCTTA GCCAATAGGG GATGCTAACG GGAAGCTCAG 840
TGCTGGGCCT GGAAGACGGG GTTTGGTCCT GCCAGTCTCC TTTCAGCTCA GGTGATTGTA 900
GCTCCAGCCA CACTCCTTCC CCTCGGCAGC AGCAGGTCCC TCCCGTAGCA GCAGCTGAAT 960
CTAGTCTGCA GTTTCCCAAC CTTCACAGAA CCAGCCTCAT GGTGCTGCAT CTCAGAGACA 1020
|
