| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00255 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr11:70413810-70415170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr11:70414894-70414905 | GGAGGGTGTGG | - | 6.32 | | Klf1 | MA0493.1 | chr11:70414896-70414907 | AGGGTGTGGCT | - | 6.02 |
|
| | 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 |
| GH11I070567 | chr11 | 70413715 | 70415541 |
|
Enhancer Sequence | GAAGGCAGCG CCTACAAGCC ATGGAAGGAA GACCCAGACC CTGAGACACC TTGATCTTGG 60
ACTTCTGGAC TCCAGAACTG TGAGAGTCAA CGTCTACTGT CCCAGCCACC CTGTCTGTGG 120
TGCTTTGCTG GGGCAGCCCG AACTAAGACA GATGCCACAC CCTGGAATAG CTGCAGGGCT 180
GGGAGGGAAG CTGCAGACAC CCTATGTATT TGTCCAACCC AAACACGTCA AATGGACTGA 240
GCTATTCAAA CCAAAACTCA GCGAGGAGAC GGGCAACAAA AGAGTTAATG GGGAGACAGG 300
ATGTGAAATG GGTCTGGGCC ATCAGCTGAT GGCCAGTACT GGAGGCTGGG TGCAAAACTG 360
CCGTGAGGCC AGCAGCGGGG TGGTGGAGTC TGGCTCCGAT CCTGCCTGCA ATGGATCCAG 420
TGAAAGGGTC AGGGCAAAGC TTCCAACAAG GATAACCTAG AAAGCAGGCC CGCAGGCAGC 480
TGTAGCTGCA GCCTCTTCCG CGAGACTTAA GCTGAGGAGG CTGGAGCCAG GGATCCTTCG 540
AGGGGCGGCG CCGTCTCCAG CACCAGGAAG AATCTTCACT TCCTCTTCGA AACCGCCCTG 600
GAAGTGAGCT TAGGGACAGA GCTCAGGCAA GGCAGTGCCT CACTCGGTGG GTGAAGCCTC 660
CTTGCCTCTC TCACAGCTCC CTGAAAGCTC CTTGCAGAGA ACTTCTCTGT TTAATAACCT 720
CGGAAAAGCA TTAAAAGCGA GTCTGAAGAA CTCATTTAAT GGATTCTTGG AGGCGGCTGC 780
AATCCTCGGA GCTCCGTGAA GCTGGGGAAC TTATTCTTGG TGGAGCCTCC AGCTGGAGAG 840
AAACTGTTTG AATTTCCCCA AAGCCAATTC GAGTTGTTGT TCCTTCTGGG AGGATACATC 900
TCCCAGCACC TCCCCTCTCC CATGTGGGCA GCGGATTCCT GCCCCCCCCG CCCACTTCCT 960
CCCGGCCGGG AGCTGTTCTT TTCAGCAAAG CCACGAGTAG CAGGCAGGGG CGCCCCAGGC 1020
CAGGCATGGT CCGTCTGGAA GAAGCCAGGT TCAGGGAGCA ATTCTGCAAG ATAAACCACC 1080
CTCTGGAGGG TGTGGCTCCA AGACTTTGAT TCTTTGAGCC ACCATGGCTA GACAGCCCCC 1140
TCCTTCCTTT CTGACAGAGG ACTTGAGCCC TTGGCACCGC AACCCAGCTG TTTATAGATG 1200
GCTGAGAAGC CTGCCTGTGT CCAGCAAGAG TGCAGCTGTG TGGCCAGTGG ACTCAGCATC 1260
CACGTCCGAG GGACTGCTCA CGTTCTCTGA AGATGTTCAA GGCTGCCCAT GTGCCCTTTC 1320
CCCGTTTTCA GGCATGCAGC ATGCAGGCCC CACTCCTGCC 1360
|
