| Tag | Content |
|---|
EnhancerAtlas ID | HS069-06883 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr5:156575330-156576780 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr5:156576051-156576070 | TTACCAGCAGGGGGAGCAG | + | 6.43 | | ONECUT2 | MA0756.1 | chr5:156576648-156576662 | TTTATTGATTTATT | - | 6.29 | | ONECUT3 | MA0757.1 | chr5:156576648-156576662 | TTTATTGATTTATT | - | 6.71 |
|
| | 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 |
| GH05I157148 | chr5 | 156575687 | 156576394 |
|
Enhancer Sequence | CACCGGATTA AAGAAGGAAG AGGTTATTTA TTCAGCCAGG AGCGTCGGCA GACTTGTGTC 60
TTAGGAGCCA AGCTCCCCGA AAAAGAAATT CTCGGCCTTT TTAAAGACTT ACAACTTTAA 120
GGGGTCCATG TGAAAGAGTC GTAATACATC AAGCAAGCGT GGGAAACGTG ACTGGGGGCT 180
ACATGCATCA GCTAACAGAA CAAAAAGTTT TACAATGCTT TTTTCATGCA GTGTCTGGAA 240
TTTACAGATA ACACAAGTAG TTTAGGTCAG GGGTTGATGT TATTGTTACT TTTTTTAACT 300
CCTAGGGCTG GGTGGTGTTG CCAAGGTTGT CTGGCTATTT ATCTTACTTT TGTTTTTTTC 360
CAACTTTTTG CTTTTTCTCT CTTTCCTCCT GTCTTGTGAA CTAGGCAAGG TGAGGGGAGG 420
AAGGCAGCAG GAGTAGTAGT GGTCTCCTGC CTTATACCCA CCTTGACCTC CCGAAGTGTT 480
GGGATTACAG GCATGAGCCA CCGTCCCCGG CCTTAATGAT GCACTTTGGA TGAGAGTCAT 540
TGCTAATGTA TTTTTTTTCT GCAGTCTGCA GTATAGTTTC AATTCCTAAT CACTATTTTT 600
TTGTTGTTGT TACTTCATGG CTGCTAATGA CCTTATCACT AAAACGTCAA CAATCCAGAT 660
CTGTGTGCAG CACATGGGTG GGGAGAGTGC TTGTGGTTTG CTTTGCCTAC AGCATTTTTT 720
CTTACCAGCA GGGGGAGCAG CAACCTTGGC ATTTGGAAAT AATCCCCAGC TTAAACTTTT 780
CTATGGGAAA GATTTGTGTC TTGCATATTG GGTCCTCCTG AGTTGTTACT TGCAGGCTGA 840
AGAACCTAAA ATGAATTTGT AATCCTACAA AAAGGCAGGT AAGCCCTTTT GAATTTGTTG 900
TAGCTGTTAC TATTAAAATC TACATTTACC TTATGTGGAA TTTCACCAGA GGAAAAAAAT 960
AGCCATGCCA TCATCATACC TGTTCTTTGA ATTATCACAA AATATACCCA TTACGGCCGG 1020
GCACGGTGGC TCACGCTTGT AATCCCAGCA GTTTGGGAGG CTGAGGTAAG TGGATCACCT 1080
AAGATCAGGA GTTGGAGACC AGCCTGGCCA ACATGGCGAA ACCCTGTCTC TACTAAAAGT 1140
ACAAAAATTA GCCAGGCGTG GCTGTGTGTG CCTGTAATCC CAGCTACTCG GGAGCCCGAG 1200
GCAGGAGAAT CGCTTGAACC CAGGAGGCAG AAGTTGCAGT GAGCTGAGAT TGCAGCATTG 1260
CACTCCAGCC TGGGCAACAG AGCAAGACTC CGTCTCAACA ACAACAAAAA ATAACTGTTT 1320
TATTGATTTA TTGATTGATT GATTTTCTAT ACACTCCCTA AAGGATCTGG GCTCTGTCCG 1380
ATCCATTTAA GTTCCCGCTT TAAGATCCAT CTCAAAGATG GTCTTCTCCA AAAGGTTTCT 1440
CTCAGTTCAC 1450
|
