| Tag | Content |
|---|
EnhancerAtlas ID | HS098-16542 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:107569620-107570840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr13:107570558-107570577 | CACTGCCCCCTACTGGCCG | - | 8.13 | | Gfi1b | MA0483.1 | chr13:107569857-107569868 | AAATCTCAGCA | + | 6.32 | | HSF1 | MA0486.2 | chr13:107569846-107569859 | GAATGTTCTAGAA | - | 7.52 | | RREB1 | MA0073.1 | chr13:107569784-107569804 | TGCGGGGGGGTGGGGGGGGG | - | 6.73 | | ZNF740 | MA0753.2 | chr13:107569796-107569809 | GGGGGGGGGGCGG | - | 6.64 | | ZNF740 | MA0753.2 | chr13:107569793-107569806 | GTGGGGGGGGGGG | - | 6.92 |
|
| | 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 |
| GH13I106915 | chr13 | 107567809 | 107573470 |
|
Enhancer Sequence | CGGTCCAGGG GGTTTGAGGG GACCGGGAGA CAGTGGCCGC AGCGGCCATG GGGTCCCCGC 60
AGACCTGGCC CAGAGTGCGG AAGGAGTCGC CTGAGCCGCT GTTTTAATTC GTGAATTCAT 120
TGAAAGACGA GAGGGCCCCA GGGACTCCCT GGGAACGCTT GGATTGCGGG GGGGTGGGGG 180
GGGGGGCGGT CAGGGCTTTC CTACCCTCCC CGTTTCCCAT CCCTCAGAAT GTTCTAGAAA 240
TCTCAGCACA CAGGAAGATG CAGTGGCCGA GGCCCGTAGA AGGAAGCGGG CGAAGGGCGG 300
AGGAGGACGC GCGGGGCCGG GGCCGGGGCC GGGGCCGGGG CCGGGGCCGG GGCCGGGGCC 360
GGGGTCGGGG ACGCGGGGCA GGTTCGTGGC GCAGCCCGGG GAGACCTTGG GCGAGGCCTC 420
CAGGCGGGGA CGGGAAAGGG AACGGGAACG GGGACAGGGC GCAGGGCAGA GGGCCGGGAC 480
GGAAACGGGG ACAGGGCGCA GGGCAGAGCA CAGAGCGCAG GGGCGCAGAG AAGGGGACGA 540
AGACGGGGCC GGAGGCGCCT GAGGGGGGCT CCGTGCGGGA ATCGGCGGCG CCACCCAGCC 600
CCGCACATCG CCGAGAGAGG CCCGCGTGCT TCTGAGAGCG CCGCCCCTGA CGTTTCTGCT 660
GCGCGCTGGG ACCGAACCTA CAGGAAGCAA AACCCTAGAG GAAGAAGTCG GCGGCTTTTT 720
GGCTCGGAGA CAAAATGGAG CCCCGCGGAT GCAGCCTGGG CTCCCTCGGG CGCATCCCCA 780
GAAGCTGCGG GTGTCCCCGG AGGACTTGAA GTCCTCCCGT GCGTCTCGAT GCCACCAGTT 840
TTTGTTTCTT TGGTGAGGAA TCGGTTCACG GTGAAACTTC ATTCCTCAGC CGGTGGGGAG 900
CCGAGGCTGG GCCGGGCGGC GAGGGTTGCG CTGGGACGCA CTGCCCCCTA CTGGCCGCTG 960
CGCCGCGTTC CCAGCTGCTC GAGCGGGTGG TTCAGTGAAC TCGGATTAAT TTAAATACAG 1020
CCGTAGATTT GGCTTTTTTC CCTCCCGGGC GAATCTAAAT TTAAAAAAAA AACTAGGGAG 1080
AGTACCAAAC TTAAAATAAT AAACAGACTG AAGGATATTA TTTCTTAACC TTTATACAGC 1140
CTCCTAAAAG AGTGAAAATT TTATTGTGAG TAAAATCAGA GTTTGGCTCT CTGGTATCCC 1200
TTCTGCTTTA ATGTGCTTTG 1220
|
