| Tag | Content |
|---|
EnhancerAtlas ID | HS139-09109 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr11:34227960-34229390 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr11:34228461-34228476 | GTGCTGACTTAGCAA | + | 6.31 | | MAFF | MA0495.3 | chr11:34228461-34228476 | GTGCTGACTTAGCAA | - | 6.33 | | MAFK | MA0496.2 | chr11:34228459-34228478 | CAGTGCTGACTTAGCAAAG | - | 6.06 | | RARA(var.2) | MA0730.1 | chr11:34228347-34228364 | TGACCTTCCCCTGACCC | - | 6.72 |
|
| | 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 |
| GH11I034206 | chr11 | 34228089 | 34230609 |
|
Enhancer Sequence | TGATGGGTAC TACTGACTTC CATTTGAGAT ACTGGGCTAC TGCCATTCAG AGACTTTGAG 60
TAACTTGCTC AGGTAAGTGG AAGAGCTAGG ATTCAAATCT GGGATGGACT GGTTCCACAA 120
TGCATATACT TAACTCCTCT GTGAGCTCAG AGTCCAGTGA ACACATCACC AAAGCTCACT 180
CATGGCTGTC CTTATGTGTG GCTGGTGCAT ATGACAATAT GGCTGTATTA TTACTGCCCA 240
TTTCACTCAT GGACACCCTG TGCTGAACCC CATGTGTTTT TCTTTGTTGA GGAAATGCAC 300
ACAGAGGTCT TCCTCCAGCC CAGGGCCTCA GTGTGTTCTC TGACCGTTCT GCAGGTTCAG 360
CTGATGGTCA GTCCTGCCCT CCTAGCTTGA CCTTCCCCTG ACCCAGGCCT CCCCGCTCTC 420
CTCCTGGCTG ATGTGGTGAA GGCCCCCTCT CCATCTCCCT TTGCCTCTCC TGGATGGCAG 480
CGACCCCTCT CATCACATCC AGTGCTGACT TAGCAAAGCA CTGCTTCAAA GCACTTCCTT 540
CAAGCTTTGT TTCTGTTGGA GGAGGAGGAA GAGTTCATGA TTGGGCTCTC CCCCGCAGCC 600
CCCTGCCAGG GCCCCAGTCC CTAAAGCAGA AACTCTCCCT GACAGCTGAG TAACCAAACA 660
CATTGGGAAG AGCTGGCCGT AAGCTTTAAA ACAAGTAAAA CAAAAGGGAA AACCACCCCA 720
ACTACAGGCT GAAACCCACG ACAGGCCAAA CAGCTGGGAG AGCCCAGTGC AGGCCTGACT 780
CCTCCTCCTT TCTCCATTAT TAATCTACAG AAACAACACT GGAGACATGT GGATCAAATT 840
TACAGAGCTT AGGGTAAGGG AATAGGAAAT TCAGCTGATT TGTCAAAGGA TTCCCAGAGA 900
GAAATATTAT GTCAATGGAG CTAGTAACAG GAGCTGTCAG CTCCATTAAT AATAGTTCCC 960
ATTTTCTCAG TCATCACCCA CCCAAAGAGG CCTTCACTTA ATACCGTGGC AAAAGTAATT 1020
AGGAACCTAT TATTAATAAT AGTAATTGAT AGCATCACAA CTTTTGCCTA GTACCTTTTG 1080
CTTTTAAATG ACTTTTTACA TCTAGTAATT TGTTCTTCCA GCAAGGGAGA CAGGACAGTC 1140
ATGATCAGTA ACAACCACAG CTGACTTTTA TTGAAGGCTT ACTATGTGCC AGGCACTTAC 1200
ATGCGTTATC TAACACCCCA GAACTGCAGG AGGTACTATT CCCACCCATC TTACAGCTGA 1260
GAAAACTGAG GCCTGAAAAG TTTAGTGGCT TGCCTAAGGT CACTGAGGGT CAGAAACGGA 1320
ACAGGGACTG GAGTTTCAAT TTCTTCTCAA GCTGCTGAAA TAAATGACAT TCTAACTTTG 1380
CCCACCTTGT CCTTTCTCGA GCTAGGCAGC GCCTAGGATA TTGGAGAGGA 1430
|
