| Tag | Content |
|---|
EnhancerAtlas ID | HS184-25592 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr6:3139460-3140140 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MLX | MA0663.1 | chr6:3139622-3139632 | ATCACGTGAT | + | 6.02 | | MLX | MA0663.1 | chr6:3139622-3139632 | ATCACGTGAT | - | 6.02 | | MLXIPL | MA0664.1 | chr6:3139622-3139632 | ATCACGTGAT | + | 6.02 | | MLXIPL | MA0664.1 | chr6:3139622-3139632 | ATCACGTGAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29199 | chr6:3138405-3141085 | Fetal_Intestine_Large |
|
| | 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 |
| GH06I003137 | chr6 | 3137709 | 3140515 |
|
Enhancer Sequence | CTAGTGAAAG GTTGGTATTA CTGTTATTAC AGAAGTCCTT AATGAACAAA CATTTTTATA 60
TGCTGAATGA GTTAAAACAT GTAACTACTG TGTTTAACAG ATGTGAAATT GTTTAAACAG 120
TTGCTGGCAC CAAGTGAGCA CTCAGGCATG TTGACTTTGA TCATCACGTG ATGATGCAGC 180
TGGCCGGTGT GTGTCATCTC GGGACAGGAG AGGGAAGTGT CAGAGACCTG GAGAAGTATT 240
TCCCTAGTCA GCAGGTCCGC TTCTCACTTA GCAGGCAGTG ACTTCCCACT GAAGAGGAGG 300
GAAAGGCCTG GGGCCCGTGC AGGGCGGGGG AGCACTGCCC CGTCGGGGCA GCTCCCAGCC 360
TTCTCAGAGC TGCAGTGCCT TCCTCTTGAC ACACACGGAG AGGGAATGGA GAAGGAAAGA 420
GCTAGCTTAG GGATGCCAGG AACCGCAGAC GCAACTCTCT TTTTAGCCCC ACAACAGCCC 480
CGGGGAACTG TGATTGTTCC TGTTTGTGGC TGAAGCTCCC AGTGGTTAAG GAGCCACCAC 540
AGCCTCACAG AGGCAGGAAA CTGCAGTACA GGGACTAGGG CCCAGGCTGT CCATCATTGC 600
CTCAGGAAAG TTCTCATAAA TGGGGGTAAG TCCTTACAGT CTCTCCAAAG TATGTTAGTC 660
AGGAGTGTCA CAGATGCATC 680
|
