| Tag | Content |
|---|
EnhancerAtlas ID | HS091-24058 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:39993700-39994710 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP1 | MA0079.4 | chr19:39993887-39993902 | CAAACCCCGCCCACC | + | 6.44 | | SP2 | MA0516.2 | chr19:39993886-39993903 | CCAAACCCCGCCCACCA | + | 6.31 | | SP4 | MA0685.1 | chr19:39993887-39993904 | CAAACCCCGCCCACCAT | + | 6.07 |
|
| | 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 |
| GH19I039502 | chr19 | 39993481 | 39993710 |
|
Enhancer Sequence | AGTCCTGCGT TCGACCCCAC CCCGTCCCAG CCGGGGACCC CGGCCCCTCC TGAGCGTCAC 60
TCGCGGCCCC CAGTCCCCTC TCACAACCCA CTCACCCTCT TCAGGGTACT CTAGAGTCCC 120
CCACCATGTA CCCCAGGCAC CCCTCTTCAG GGAGCTGGGG AACGCGCTGA CTGCTGCGGA 180
TGTATCCCAA ACCCCGCCCA CCATCCAGCT GCCACCTTCG GAGAAACTGA GGACCCTGGA 240
CCTCTCTCCA GCCCTGCCTT GCTACTCGAG CCCCCTTCCC TCTCCCAGCC CTCTTGTTGC 300
CCCAAATCGG AAGCCCACGT CCATTTTCTA TGCTGGCACC CTCCAGTTCC TTCCCTAACC 360
CACATTCACA CCCTGTCCTG ATGCTAGGAC TCCAAAGCTC TTCTAATTCT GCGGCCCTCC 420
CGACTCCCAC TCGGAAGCTT TGGAATCTCC TCCCAGTCCA CTCTGGCCAA GGGGCCCTCC 480
ATCCTCCCTC CCTAGGGTTG CAGGCCAGAA CCCATGGCTT CTTAAAGCTT GGAATTCTTC 540
AGACTTCTCC CCAAATTTCA GAGCCCCACC AAGGCCCCTA GGACTCCCAG GCTAATCCAG 600
ATCTTCTCAG AGCCACCCTA ATTCAATACA CTCCCATCTT CCCTGAAAGG CCAGGGGTCC 660
CCCCACCAAT CCCAAATCCC CTCACTGTCT CCTATCCTCA CGATCTCACC TGGGTGCCCC 720
TGTCCCATCC TCTTTCCAAG AGCACAGACT CCAGCCCGAT GGCCTGGGTT CACATCATCA 780
CTCCTCCACT TCCTAGGTGG GCTGGTCACC TCGTCTCTGT GGGCCTCAGT TTCCCTATCT 840
GTAAACTGGG GGGGCGGTCA CAGTACCATC TAGTCCCGAT GATTATCTGT CACAAAGATG 900
AAGCAAGGTG GCTCAGGGAA CGTGCTCAGA AACCTCCCTG CTTTCCATCT TGTCCCTGGC 960
CCTCCCCGAC GTTGGTGTTC CCTTTCTCTC TGCCTCTCTG TCCCCCATAG 1010
|
