| Tag | Content |
|---|
EnhancerAtlas ID | HS141-15216 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr5:159720700-159722060 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr5:159721672-159721683 | CCACACCCTCC | + | 6.32 | | RREB1 | MA0073.1 | chr5:159721625-159721645 | CCTCCAAACACCCCCATACA | + | 6.59 |
|
| | 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 |
| GH05I160293 | chr5 | 159720530 | 159722098 |
|
Enhancer Sequence | CTCCGAGGTG GAACCAGCAC TAGCCCTAGT AGCCAGGAAA CTGAGGCACA GAAGTATAAC 60
TGCCAAGGCC ACACTGCAGG TGAGTGGTAA ATCTTGGGCT TGGACATCAG AGGAGCGGGC 120
CAGGGCTTGG GGTATGACAA TACTTGGAGG GCGACAACCA CTTCGTAAAC AGCTCAAGGT 180
GCAGTAAAGC AGGGCTGAGC TGCTCTCAAA CACCAGCCAC CAAGAGAAAC CACTCTGCTT 240
TCCTCCTCCA ATCTCCCTAC CATGCCTATC CCTACTGCTG CCAACAAGAG CCCGGGAATC 300
CACGCCCTGG GTTGAGACAA CAGCTAGAGG GGTCTTGTCT AAGAACAAAG AACCGCAGAG 360
AGGTGAAGAA ACACCATGTG TAACCAAGGT GACCAACAGG AAGTGGAGAC TTGCAAATGT 420
AAAGTGGCAA AGAAAGGGGG AGAAAGGCTG GCTCTTCAGA GGCCTCAGTA CACAGCACGA 480
CCTGGGAGGC CCAGCAAGGC AGGAGGCTCA CCCTCCTTCC TCTCTCTGCC CCGATTGCTT 540
CATAAGGCCC AAGGAAGCAT TTTCCGTAAA GCATCAACAC CTCTGTGGGA ACACTATTTC 600
AACATTCTTG AGAGGGTGGC CCGTGTCACA TAAGGCCAAC AATGCCCGTA ACGTCCCCTC 660
CTGCTGAAGT CCAGCCTGTA GCTTCCTTCC AGCAGAGTGA AAGGTAACCC AGGCACCACA 720
TCCGCAGCCG GCGTCTGTAC TACTCCTGGG CAGATGGCAG GCAGGCCAGC TCCAAGCACA 780
CCTCCTCATT CCCGGAAGCC AGAGCCACTG CCCTTCTGGG CAAACTCTGT ACCAGGCCCA 840
GCCACAGCTG CCAGGGCATC CACAGTGACC ACACACATGC GTGCACAACC CTCACTGGTC 900
CCCCATCCAA CCCATGGCTC TGGGGCCTCC AAACACCCCC ATACACAACA TTCATGGCCT 960
TTTTAAAAGA CGCCACACCC TCCAACTGAA TTCTTTACTT CTGCCAGCTT CCTACAGGAC 1020
CGCATCCCCC ATACCTTCTG GAGTGGAGGA CTGGGGTGCC CCTCATCCTC CCACGCCCTC 1080
TGTTATCCAG GGGAAGAGGT CCCGATGTCC CCCTCCATGC TGGTTCTCTG TCACAGGTCC 1140
AATTCTTGGA TCTCTCCGCT TTCCTCCTGG ATCACTCTGT GGAGTGGCTC CAAAGCTCTT 1200
CCCTCCACAC CTCCAGCTCC TGCCCCCGAT TTCCAGATTC CTTTTGTGGA TTCTCCTGGG 1260
AGCTTCGACC CTAATGAGAA GCCCAAAATG GGACAGTAGG GTGACTGCAC CACTACCCCC 1320
TCGCTGCGAC TCTACTTCCC TACCCATCTA CAGTCCAAAG 1360
|
