| Tag | Content |
|---|
EnhancerAtlas ID | HS101-26865 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr20:23610100-23611360 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr20:23611063-23611073 | GGTAATTAAA | + | 6.02 | | ZNF740 | MA0753.2 | chr20:23610369-23610382 | GTGGGGGGGGGAG | - | 6.52 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35782 | chr20:23609017-23611658 | HepG2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 23610288 | 23610365 | | chr20 | 23610367 | 23610915 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I023628 | chr20 | 23609090 | 23611363 |
|
Enhancer Sequence | TCCTGGATTT GGGTAAAATA AATAGATAAA TAAATAACTG TTGCTATTAG TGATCTCAAG 60
TCCCTCACAA AGAAGGTGGT CCTGTTCACT AGGAAGGCCT TTGGTTTATA AGCACCTTGA 120
TGGGTGTGGG GAAGTCTACA AAGAGCTGAG TGGTTCTACC CCACAAAGGA GCCTTTGGAC 180
TTGCTGAGGG ACTCAGTGGA GAGGATGCGT GGACAGATGG GGAATGCCAC GGCGAAGAGC 240
AGGCAGGGGA ACAATCAGGC CAGTGACTGG TGGGGGGGGG AGGGGGTGGA ATGTGAAGGT 300
CAAGTGGCAA CTACCTTTGG GAGGGAAGCC AAGGGCATTT CAAGGACAGA AATACCCAGT 360
GCTGGGTTTG AGGAAGTGGG GGTTACTGTT CCACAGGGCA GGAGGTGATT TCCTGAAATC 420
ACCGACAAAT TTCATTGCCC CAAACAAAGC TTTGGTGGAA GGAATTTCCG TTTGCTTTTG 480
CTTTGTTGAG TTTCATTTAC TGGAAATCAA GGGCTACACG TTTGCAGAGA TACCTGGCAC 540
GGAAAGTGTG TCCACAGGCA GATGTGACCA TGAGACTATC TTTACCTGCT GCAATTTGCA 600
GATGTTTTAG GAGCAACTGG ACTTTGACCA GGACTCTAAT TGAGTTATAG TCCAGTGGTT 660
CCTTGGGGAA GCAATGGGAG GAGTATTTAA ACATCCAATG TCCACGTCCC ATCCCAGAAC 720
ACGATCAACT TTTCCGACTG GGATCATGGG ATTGCCATGT GCAGCCAGGC TCCCCAGTGA 780
CGCCATGTAC AGCCAAGCTT GAGACTAGAG TTCAGATGAG CCTGACCTGG TCTCAAGGGA 840
GCCAGAGCCC CAGCTGATGT CACAGTGGCC TGAGCACATC TGACTCGACC CCATAAGCCT 900
CAGGTGACAG GATTTGGAAG TGACCCACTT GGCATCCCAG CACCAAGGGT GAGAGCAGGT 960
ATGGGTAATT AAAGGAATGT CTGTTCCCTA TTTTAGTCAC CATTGTGTTC ATGGCTTCTC 1020
AGTGTTGTGT CTTTGAGCAG TGAACTCAGA CAGCACAGCA GAGCATAAGG AGAGGAAGGG 1080
GTGACTAGCT GCTGTCTTCC TGGGCCTCGT CTCTCCAGCT TCGCCCTGGA GTTATGGGAC 1140
AGGGCTGGCG ATTTGCTCTC TCTACATCTT TTAGGGAGGC TTGTGGCCTA GTCCAAGGTC 1200
ACTCCCGTCA GCCAATCATA AGCCAGCTCT CCTCTGTCTC TCACAGCCAC ATGGGTGGCA 1260
|
