| Tag | Content |
|---|
EnhancerAtlas ID | HS148-08786 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr19:44138830-44139840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr19:44139340-44139351 | TCAAGGTCATA | + | 6.62 | | Esrra | MA0592.2 | chr19:44139339-44139350 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr19:44139340-44139350 | TCAAGGTCAT | + | 6.02 | | RREB1 | MA0073.1 | chr19:44139051-44139071 | CCCCCAACCACCTCCTCTCT | + | 6.01 | | ZNF263 | MA0528.1 | chr19:44139625-44139646 | CCTCCAGCCCCTTCCTCCCTC | - | 6.3 | | ZNF263 | MA0528.1 | chr19:44139205-44139226 | CCTCCAGCCCCCTCCTCCTTC | - | 7.19 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_05765 | chr19:44137194-44143793 | Brain_Cingulate_Gyrus | | SE_08713 | chr19:44137287-44143884 | Brain_Inferior_Temporal_Lobe |
|
| | 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 |
| GH19I043634 | chr19 | 44138366 | 44141114 |
|
Enhancer Sequence | TGTGTTGACA GCCAGGAGTC GTCATGGGGA TGGTGCTTGG AAAAGGGGAC AGGGAGGGTT 60
TGGGAAAGAG TGGCGGAGCA GGTAATGCGT AAGACCCAGG AATCCAGCCC CCAACTACCT 120
CCTCTCCCAG GACCCAGGAG TCTAGGCTCC CAGCCCCTCC TCCATCAGGT TCCAGGAGTC 180
TGGAACCCCG GCTTCTTTCC GCCTTAGACC CAGGAATTCA GCCCCCAACC ACCTCCTCTC 240
TCAGGTTCCC GAAATCCAGA CCCCTAGCCC CCTTCTCGAT CAGGACCCAG GAGTCTGGGC 300
TGTCAGCAGC CCCTTCCTTC AAACCTAGGA GTCAGAGCCC CCAGCCCTCT CCTAGCTTAG 360
ACACAGGAGT CTGGGCCTCC AGCCCCCTCC TCCTTCAGGA CCCAGGAGCC AGGGGTCCAG 420
AGTACACAGC TGGTGGATGT TTCCACGGAG ACTAAGCAGG GTGGGGGGAG CGCTTCCTGG 480
GTCCTGAGTC AGCGAATACC CAAGGGAGTC TCAAGGTCAT AGTTCCGGGA AGGTCACCAC 540
CACCCCCTCT GTATCCGCTC CCCAGGGGGC TCCTGGCATC CTGCCTCCTT CCCCCTTCCT 600
CCCTTAGGGA GGTGGTACAT CCCTGCGTCC TGACTGAACC CCCCTCAGCC CCCCATCAAT 660
GGCGGAGTCC GAACATCCTC GCACAAAGCG TCAATTCTTC CCCAGCTCAG CCTTGTGAAG 720
GCGCCTGTAT TCGCAGGACC TAGGCGTCAG GGTCTCAGCC CCTCCTCCCT CAGAAACCTG 780
CAGTGGAATC CCCCGCCTCC AGCCCCTTCC TCCCTCAGGA CCCAGGAGTC TGTATCCTCA 840
TCCCTTCCTC CCTCAAGACC TAGGAGTGTG GACTCCCAGC CCCCTTTTCC TTCCGGACAC 900
AGGAGTTCCA GCCCTCGGCC CTCTCCTCTC TTAAACCCAG GGGTCTAAGA CCCCAGCCTC 960
CTCCTCCCTC AAACTCAGGA GTCTAAGATC CCAGGCCCCT CCTCCCTCAG 1010
|
