| Tag | Content |
|---|
EnhancerAtlas ID | HS060-30986 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr7:936070-937530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr7:936225-936236 | GGCTGTGATTT | - | 6.02 | | REST | MA0138.2 | chr7:936356-936377 | GACCCTGTCCTAGGTGCTGAC | - | 8.06 | | RUNX1 | MA0002.2 | chr7:936737-936748 | TTCTGTGGTTT | + | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41630 | chr7:936595-937921 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr7 | 936682 | 936727 | | chr7 | 936295 | 936576 | | chr7 | 936738 | 936818 | | chr7 | 936844 | 937277 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I000897 | chr7 | 936961 | 937985 |
|
Enhancer Sequence | GGCTGTGCAA CGCTGGTCCT TTCTTGGGCG CTGGTGTGGG GGATCTCTCT CTGCTCTCAG 60
GGCTGTGCCT GGGAGCCCCC AGAGGAGGCG TACCCTGTGG CCAGACTGCC CGTGCGTGGA 120
CGGAGCAGAG GGCTATCAGG AAGTCACGTT CACTTGGCTG TGATTTTAGA AATAAGTTTT 180
GTGTAATTTC ATCAAAATTC ATAAAAATCA AATCCACCAG GTCTGGGTGT CACAGCCTCA 240
AAGAGCAGGC CCTTGGGCTG CAGGGGAGAC AGTGGCGCAG AGCCCTGACC CTGTCCTAGG 300
TGCTGACAGG ACACCCGTCC CTCCCGTGTG GCACTTGCTT TGAGCAGCGA GTTCGATCCG 360
GAGTGACCAA GGATTTTGTG TGCGGCGTCA CTCGGGCTTA CCGTGAGACG GCAGGAACAG 420
CCGGCCGGAG CCCCGCAGGC GGCCCCTCGT GGCCCGTGCT GAGCCTGCGC CGCGGCGTCT 480
GCCTCTGCCT GCCTCAGGAC TTCGCGGCGG AGTCACGGTC CGTCCCTGTG CCTGCTGCCA 540
GCAAGGGGAT GCCCTTCCCC ACAGCTGTGT CCACGCGGGG AGGTGTGGAC AGCGAGTGAG 600
CGACCACCTT CTGTGCCTGC GCCACCTCCC CTGGTTCAAA AAATTCTTTC CCCCCATTAG 660
AAAGTTGTTC TGTGGTTTTT AAAATGTGAC AGTCGTCAGT GTCCTCAGCA CACACGTGGA 720
CACGTGCACA TTCGGGGACA CGCACACACT GAGCACGTGC CCACACTTCC ACGCCATGGG 780
GAGGGCTGTG GGCACTGCTG GTTTCCCCCG GGGGTGTGTC CAGCACAGCC CAGGGCTCTC 840
CCTGACCCAG GCCCACTCCT CTCACCTCGG GTTAGGACCG TGGCACCTGG TGAGGTTGCG 900
GGGCACTTGC CTGGGGTTTC AGCTCCAAGT GGGGGTACCT CGCCCACATC CTCGTCACCA 960
GCACAGCTGC CTTGGGGACC CCTAGGCTGG GATTGGGAGA CCTCTACTCC GCCCTAGAGT 1020
CCCAGCTCCT CATTGGAGAA GTGGGATTCA GCATGTTCTG TGTGAGGGCT GAGGGGCCCA 1080
GCATTGGGGG GGTGGGCTGG CAGGCACAGG GGACCCCCGA CCCGGGATGC ATCCCCCACA 1140
CTGTCCTTCA TGCTGAGCTT GGCTTGGCTT TCAGGCTGTG GACTCTGCCC AGGAACTGCC 1200
TGGCGGGCCT CAGATGGAGG GGGCACCTGG GGAAGGGGGG CACCTGGGGA AGGGGTGCTG 1260
GGGGGCACCT CGGGTAGGGA CCGTCTCCCG TGTACAAGGA GCATGGCGCT GTGACTAGCT 1320
CAGACACCGT GTCCTCCCTC CAAACCTCAG GGAGCGAGGG CCCTGTCAGG TCCCTGGGAG 1380
CAGACGAAGA TTCTCCTGAA GCCAGGGAGG CAGGGCCACG TGTTCCCAGC CCAACTTCCT 1440
CCCCACTCCA TCCTCGGACA 1460
|
