| Tag | Content |
|---|
EnhancerAtlas ID | HS118-18269 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr8:41467480-41468250 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr8:41467730-41467747 | GGGAACATTGTGTGCTT | - | 6.35 | | Ar | MA0007.3 | chr8:41467730-41467747 | GGGAACATTGTGTGCTT | + | 6.55 | | NR3C1 | MA0113.3 | chr8:41467730-41467747 | GGGAACATTGTGTGCTT | - | 6.23 | | NR3C2 | MA0727.1 | chr8:41467730-41467747 | GGGAACATTGTGTGCTT | - | 6.21 | | TBX21 | MA0690.1 | chr8:41468184-41468194 | TTCACACCTT | - | 6.02 | | TBX2 | MA0688.1 | chr8:41468183-41468194 | TTTCACACCTT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 41467500 | 41467975 | | chr8 | 41467768 | 41467860 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I041609 | chr8 | 41466536 | 41468482 |
|
Enhancer Sequence | CAGGGCCTGC GGGAGTGGGG CTCGCTGCTG CCACCCCACG TGGTGCACAG CCCACCTGCC 60
TGCTCTGCTG TGTATTCCCG TTTTAGAAAG GAGGAGGGAA TGACTGTCGT TAGCCAGGCC 120
ACGTGACTCT TTGGAGGGAT ACACTGGTGA TTCTCCTTTA GAGGCCCTTG GATTCTCTGC 180
ATATCAGACA GAAATAGTTG GATTTCTTAA AGACAGCTTG CTTCTCTAGA TGACAGCAAA 240
CACAGGGACA GGGAACATTG TGTGCTTTCT GCCACTCCTT CCTGGACATG GCTCATTCTT 300
TCCTGAAGCT TGCCTCTCAG GTACAGGGGC AGTATTGATC TTTCAGCTTC TCTGCACCAT 360
GTGCTGCTCT GAGTGTGCCT TGCCAGATGC TAATACCTTC AAGCTCCACC TCCTGTTGCT 420
TCAGAGGGAA GCTGTGCTTC CACCGGGGTT TCCAGCCAAA GGGAAGGGGA GGGCAGCAGG 480
GAGCAGCCCT GTGGCAGAAT GGCCAGCTTA GGGTTTTCCA GCCTTCCAGC TGCCTGAGGC 540
CTCAGGAGAT GCAGGCAGCT GAGAGCCAGA CCCATGGCTC ACTGTCAGCT GGAATCAAAA 600
GGATCTCTGG TTCTGATAGG CCTGCTTACA TTTCTAGGTG AACTCTGGTC CAGGTCCCAG 660
GTGAGCAGGT CTTGGGGGTG GTTTTTGTGA TGCCCCCTTT GATTTTCACA CCTTCAGTTC 720
TGTACTTGGT AGAATGATTT GCTGGCTGTG CTCTAACTTT TCTTCTTCTT 770
|
