| Tag | Content |
|---|
EnhancerAtlas ID | HS064-07307 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr19:9896000-9897080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr19:9896387-9896402 | CAGACCCCGCCCCCA | + | 6.25 | | SP4 | MA0685.1 | chr19:9896387-9896404 | CAGACCCCGCCCCCATC | + | 6.43 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_28527 | chr19:9894046-9897642 | Fetal_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTAGCTGGGA CTACAGGCGC CTGCCAGCAT GCCCAGCTAA TTTTTGTATT TTTAGTAGAG 60
ATGGGGTTTC ACCATGTTGG CCAGTATGGT CTTAATCGAT TGCCCTCGTG ATCCGCCTGC 120
GTCAGCCTCC CAGTCTGTCC CCTCACCACT ACTCTCTTTC ACGGAGACCC CACCCCCATC 180
TCTCCCTTCA CCGACTCCCC GCCCCCGTCT CTCGCTCACG GAGTCCCCGC CCCTGTCTCA 240
ACCAAGACCG AGTCCCCGCC CCCATCTCTC CCTCGCCGAG TCGCCGCCCG CGTCTCTCCC 300
TCACCCAGAC CCCGCCCCAT CTCTCCCTCA CCGAGACCCC GCCCCATCTC CCCCTCACCG 360
AGACTCCGCC CCCGTCTCTC CCTCACCCAG ACCCCGCCCC CATCTCCCTC TCACCGAGTC 420
CCCGCCCCCA TCTCTCCCTC ACCAAGACCT TGCCCCCATC TCCCCCTCAC CGAGGCTCCG 480
CCCCCGTCTC ACCCTCACCG AGACCCCACC CCCATCTCGC CCTTCACCCA GTCCCCGCTC 540
CCATCTCTCC CTCACCGAGA CCCCGCCCCC GTCTGCCTCC CTCCGGGTGG CTAAGCCGCA 600
CCTGAAGCCG CACCTGGTCG CAGAGGCTAC TGCTGGGGAA ACCGTTGGGC CAGCGGCGGC 660
TAAAGGGCAG GAGGCGCCGC TGTGGCCACG CGCACTTCTG ATTCCGCTCC AGGGTTTCAG 720
AAGGAACTGA GGGCTCTGGA CCCGGCCTCG GAGGCCTGAG GAGTTGGGAG GGGCGGCGGC 780
CGCGTCCTCC GCAACTCTGG GGAGAAGTCT TAGTTTCCGC GCAGCCAAAC GCGATTGGAC 840
CCCGCCCTCC GGCTTCACTG GGGACCGTGG GGGCGGAACC CGGCGGGAGG ACGTATGGGG 900
GGCTGGACCA TGATGGAGGG AGTCGGTTGG GCTGGACCTC GAAATGCCTC TGCTCGCTTT 960
CCTCTGCGCT TATGCCGCCA TGTACGAGTA TGCGCTGTTT CCAGGTGGTT TGTTATACAG 1020
CAGTAGATAA CTGATACATC CCTTTTCACT AATATTTTTA TTTCCTAATA CAATTTTTAA 1080
|
