| Tag | Content |
|---|
EnhancerAtlas ID | HS183-11080 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr8:41467470-41468250 |
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 | TCAGGTGAGG CAGGGCCTGC GGGAGTGGGG CTCGCTGCTG CCACCCCACG TGGTGCACAG 60
CCCACCTGCC TGCTCTGCTG TGTATTCCCG TTTTAGAAAG GAGGAGGGAA TGACTGTCGT 120
TAGCCAGGCC ACGTGACTCT TTGGAGGGAT ACACTGGTGA TTCTCCTTTA GAGGCCCTTG 180
GATTCTCTGC ATATCAGACA GAAATAGTTG GATTTCTTAA AGACAGCTTG CTTCTCTAGA 240
TGACAGCAAA CACAGGGACA GGGAACATTG TGTGCTTTCT GCCACTCCTT CCTGGACATG 300
GCTCATTCTT TCCTGAAGCT TGCCTCTCAG GTACAGGGGC AGTATTGATC TTTCAGCTTC 360
TCTGCACCAT GTGCTGCTCT GAGTGTGCCT TGCCAGATGC TAATACCTTC AAGCTCCACC 420
TCCTGTTGCT TCAGAGGGAA GCTGTGCTTC CACCGGGGTT TCCAGCCAAA GGGAAGGGGA 480
GGGCAGCAGG GAGCAGCCCT GTGGCAGAAT GGCCAGCTTA GGGTTTTCCA GCCTTCCAGC 540
TGCCTGAGGC CTCAGGAGAT GCAGGCAGCT GAGAGCCAGA CCCATGGCTC ACTGTCAGCT 600
GGAATCAAAA GGATCTCTGG TTCTGATAGG CCTGCTTACA TTTCTAGGTG AACTCTGGTC 660
CAGGTCCCAG GTGAGCAGGT CTTGGGGGTG GTTTTTGTGA TGCCCCCTTT GATTTTCACA 720
CCTTCAGTTC TGTACTTGGT AGAATGATTT GCTGGCTGTG CTCTAACTTT TCTTCTTCTT 780
|
