| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23940 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:36421520-36423020 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HLTF | MA0109.1 | chr19:36421966-36421976 | AACCTTATAT | + | 6.02 | | Klf1 | MA0493.1 | chr19:36422531-36422542 | TGGGTGTGGCC | - | 6.62 | | NRF1 | MA0506.1 | chr19:36422443-36422454 | GCGCCTGCGCA | + | 6.62 | | STAT3 | MA0144.2 | chr19:36422588-36422599 | CTTCTGGGAAA | + | 6.62 |
|
| | 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 |
| GH19I035927 | chr19 | 36418745 | 36423925 |
|
Enhancer Sequence | AGACCAGCCT GGCCAACATG GTGAAACCCT GGTGCAGTGG CCCATGCCTG TAATCCCAGC 60
TACTCAGGAG GCTGAGGCAG GGGAATCGCT TGAACCTGGG AGGTGGAGGT TGCAGTGAGT 120
TGAGATCGTG CTATTGCACT CCAGCCTGGG TGACAAAAGA GAGATTCCAT CTTAAAAAAA 180
AAAAAAAGTA TAAAATTAAA AAATTAGACT GAGATGAATG AGAGGGAGAG GGAACAGTTA 240
TAAAATAGAA GACTTAAAGA GGTAACAAAC AAATACAATG TACAATGCAG GCACCCTGGT 300
CGGATTCTAA TTTGAACAAG CCAACAGTTT AAAGACATTT CTATGACATT TAGGGAAATT 360
TGGAGACAGG ATGAATGTTA AGACACTACT AAGGATTTGT TGGTTTTTTA GGTGCGATAA 420
AAATGTTATA GTAATGTTTT TTTAAGAACC TTATATTTTA GAGATACATA ATGGATGAAA 480
TCATGTGATG TCTGGGATTT GCTTTAAACT AACTTTGGGG GAGGTGGAAT AAATAAAACA 540
AGATTGGCCA TATGTTGATA ATTGTTGAAG CTGGGTGATG GGTACTTAGA GGATCATTAC 600
ATTATTCTAT TTCTGTGTAC GACTGAACAT TAATAAGGCT TTAAAAGGGG GACTGCTGTG 660
AAAAAGAGAA AAAAGTAGGG AAATTGTGTG TTTTTTCCCC CCAGGATCGA AGCGCCTTTA 720
ACAGGCTCCA CAGCTGACAA GGACGTTGGG ATGCAAGAGA GTGAGAAGGC GCCAGGGTGG 780
CTGCAGGGCA CATTCAATAG TCGGTCTAGC TCTTGCTCCC GCGGCTGCCT TCTCTGCAGC 840
TCTGGAGGCT GCAGCTTCTG GTCCTGGACC GGGACTTAGG TCCACACCCA CGTGCTGACG 900
TCGGGCAGGC TCAGCGGCCT CCCGCGCCTG CGCAGCACCG CCCTTTTCGG GCGCGGCGCC 960
CAGTCCCTAC ACCCCACAAT CCCCCGCGCC GTTCCGGAGG CGCGCTAGGA GTGGGTGTGG 1020
CCTCTGCCTC CACATTGGAA CAAGGTGAGG CAGAGGGTGT CGCGTGGTCT TCTGGGAAAT 1080
GTAGTTCGTC TGCCAGGCCG GAACCACCGC TCAACCGGCT CGCGAGACTA TGCACCCCAC 1140
AATGCGCCGC GCGCGCAGCG GCTAAGCGAT GCGTTGCTGC CTCCACGTGG TGGCTGAGTG 1200
ATCATGCTCC GGTTTGGGAA TGGGGCCCAG AAGGGTAGGG TTAGGGGCGG GGACGGTGCT 1260
GGGGATGCTG AGGGTCGCCC TGGAAACCTC TGGGAAGATT TTCCAGAGGG TAAGTCCCCT 1320
GAACCTGGCC CACGAAAGGG TAGTAGTAAT GAAGAAATTG GAGGTGGGGC CCGCTATGAG 1380
GACCGAATGA CAGAGCAGCA CCTGTTGGCT GCATATGATA ATCAGGCTAC TGTTACACCT 1440
AAGACTCACA CAGTAGGCAC TTCCTAGGCC ACTTACCGCT CCCTGCGCTT CAGGTATCTT 1500
|
