| Tag | Content |
|---|
EnhancerAtlas ID | HS091-01556 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:45258430-45259790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:45258644-45258656 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:45258648-45258660 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:45258652-45258664 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:45258656-45258668 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:45258660-45258672 | AAACAAACAAAC | - | 6.32 | | Mecom | MA0029.1 | chr1:45258693-45258707 | AAGACAAGATAATA | + | 7.58 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 45258684 | 45259000 | | chr1 | 45258862 | 45259675 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I044792 | chr1 | 45258601 | 45259872 |
|
Enhancer Sequence | TGTCCAGGAA TTCGAGACCA GCCTGGACAA CATGGCAAAA CCCCATCTCT ACAAAAAATA 60
CAAAAAACTA GCCGGGTGTG GTGGCGCATG CCTCTAGTCC CAGCTACTTG GAGGCTGAGG 120
TTGGAGGATC GCTTGAGCCA GGAAGTCGAG GCTGTAGTGA GCTGTGATTG CACCACCTGC 180
ACTCCAGCCT GGGTGACAGA GCAAGACGCC ATCTAAACAA ACAAACAAAC AAACAAACAA 240
ACAACAACAA AAGACAGAAG AGGAAGACAA GATAATAAGC TCACAGCCCC AGCCTGGGTG 300
TGGGCCCACC CAGCCAGTTG AGGAAGCCAC AAGACAACAG CAAGAAAGGC CAGATGGGAT 360
TTCATTTTGT GCCTGAGTAG TGGCCCCTGG CTAGGGTCCT GTGTGGCAGA GATTAGAGAG 420
GTAACATGGC CATGGATCAG ACAGCCTGAG CTCAACCTTA AATCCCAGCC TGGGAAGAGA 480
AGGGAACCCA GTCTTAGGCT CAGCACCTAC GTGCTTGGCA GGAGCTCCTC AGCTTTGCGG 540
AGGAGGCTCT AGGGAACCAG GCCAGGAGGG CAAATCAGCT TTCTCTTGCA AGGAGCCTGT 600
CCTGGCCCCT CCTTCCCACT AACTTTCCAG ACCCACTCCC TGGCTATATT GTCAGACTTC 660
ACCTGAACTC ACCAAATTCA AAACTTAGGT CAGCTTGGGA ACTTGGCAAA TTGGGGAAGG 720
GGCAAGTAGA CCTTCACTCC TCCACACACA TTGCAAAGCC TTTGGAGTTC TGGCCCCTGG 780
ACTGTTCCAG TCACCCTTCC CCTTTCCTCC AGCTACTCTG AACTTTCAGC TTTTTCAAGG 840
ACCAACAGCT CTCACTCCAT GCCTTAAGGA GCACAGGGTT CCTCTTATGG AATACTTTCT 900
CCTCCTGTCC ATTACTGTTC CTGGCTAACT CCTCCTCAGC TCTCAGGTTT CAACTTAGAA 960
ATCTCAGCCT ACGTACATTC CCCAAACTGG GTGTGATCCC ACCTCTGGGC TCCCATAGGC 1020
CACCTCTATA CCCTGTCTGT CTTCACCACT TAGCACTAAT TACAGTCCAG TGTCCTTGTC 1080
CTACCGACAG GTCACGCCAG GGTGCAGCAC AGGACCTGAC ACATAGAGGC TGCTCAAGAA 1140
AACGTTTGTT GAAAAAATGA ACAACTGGCC TGGCTCAGTG GCTCATGCCT GTAATCCCAG 1200
CACATTGGGA AGCCGAGGCA GGCGGATCCC TTGAGGTCAG TAGTTTAAGA CCAGCCTGAC 1260
CAACATGGTG AAACCCATCT CTACTAAAAA TACAAAAATT AGCCAGGCGT GGTGGCGGGG 1320
GCCTGTAACC CCAGCTACTC AGGAGGCTGA GGCACAAGAA 1360
|
