| Tag | Content |
|---|
EnhancerAtlas ID | HS059-14824 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr14:100402980-100404150 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr14:100403929-100403940 | AAAACAAAGAA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGATGTGGCC GAAGTGGGTG GGTCCGGAGC TGTCCAGGCA GGAGGAGGGC CTGTAAAGGT 60
GTTATCCTCA CAGGAGGGAC CATGAAGTCC ATCCCCGCTG GGTGGACGGC AGCCCTGGGA 120
CCCCTCCTCC TCCCCTCCCA ACCTGACCCT GGCCAGTCTC TGGGCCCAGG CAGTGCTTGG 180
GAACAGCGAG GATGATCGTG GCGGGCACTT ACAAGCACAT CCTCATGCCA CGCACTGGTT 240
CCTTAGACAC CCACCAGGCA CCTGCCACGT GCCCCACTCT GGGCCACGCA GGGCGGCGCG 300
TGGGCACAAG GAAGGCCTCG CTGCTCCCCT GCTGGAAGTT ACTGGAAAGC GCAGCGCTCC 360
TCCTCTGCGT CTTCTCAGAT GACCTACAGC ACTTTCTGGC TTGGCCGCAT GATGCAGGGA 420
AGGGCTCAGA GCCCAAAACA CAGGCCCCAA GAGCCCACGG GGGTGGGCGG GTCACACTCA 480
CTTGAGCGTC CCCACTTGTT GAGGACCAGG ACAGGCAGGA CCACTGGCGG CAGGGAAAGC 540
AGGGCAGTGT GTACCGAGAC TGAGCTCGCT CCAGTGCGGA GGGCGGCCGC ACCGTCTCAC 600
CTCCTCCCTG TCCAGCTCCT GCCTGACACA GGCACAGGAA CGGTATGATT TTCAGGGACA 660
AGCCCTGGGT CTAGAGCCTT CTCAGATGTG GTCTCGTACT CTGCTGGTGA GAGCTCATTT 720
GGGGAACACA CAAGTCCCCT GGGAGGCCCT TGGTTTGACT GGTTTCAATA ACCTCCATTC 780
CTGACACTGA TCTGAAGGGA CTGAGGGGTA TAGGGAGGCG AGGGGGCCTG ACCGCAGAGG 840
CAGAGCTGTG TTCAGGGGCT CGGGTGGGGG TGGGCAGCAG GCGGAGACCC AGGAACCAGA 900
GGCTAGAGAA GCCAGACTGT GGGAAACAGA CTTGGACGGA GATGGGAAAA AAACAAAGAA 960
GAGGGCACCT CCACCCAGGC CCATGGGCTC GGGCTCAGTT CCAGGGGAAC TCACATCTGT 1020
GCACACGTGG TTCCTGCCCG ACTGGGAAGT GGAAGGTCTC CCTCTCCAGG AAGGGCTCTG 1080
TACCCAACGG GGCACAGCTC TGGGGGCTCA GCCTTGCTTA GGGGAGGGGT GGGGCCTTGG 1140
CTTAGATGTT GCCAGACTGT TTGCTTTTTG 1170
|
