| Tag | Content |
|---|
EnhancerAtlas ID | HS101-22892 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:9878860-9880180 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr2:9879625-9879639 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_19759 | chr2:9878016-9880316 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_27173 | chr2:9878709-9880168 | Esophagus |
|
| | 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 |
| GH02I009738 | chr2 | 9878146 | 9880198 |
|
Enhancer Sequence | AATCACTGGG TCACCGTGAC TGGCTTAGAC CAATCAAGAC ACTGTGCTAG GCTCCCAGGG 60
AGTCCTGCTT CTCCTGAAGC ATGTGGCTGC CAGAAACCCT GAATAAAACA GGCCTCTGGC 120
TTGCTGGTGA GGGAGAGGAA CTGGAAGGGT TGCGGGCCTG TCACACAGCA TCGCTATTTC 180
TGGCTCCCAC ATCAGCCTTG TGAGATCAGG ACTTTTATCG TTTTATGAAT AAGGAAACCA 240
AGACTCAGAG ACAATGAGGT GCTTGGCCAA GGTCAGCGGC TGGTGAGTGA CAGAGTCTGC 300
ATGCTCAGCC CATCCCTAGG AGTCTGGCAA GGCTGGAAAT TGGTCTTTCT TTTCCCATCC 360
TAGATGGATT GCGTTGGAAA GATTCAGGCT CCTGTCAGCT GGCTCTTGCT GTCCCTTCCT 420
GACAGCTGCG ACTCTGAGAA CAGTTTAATT TCAGAAACCC TCACACGGTG GCTCCTCTCC 480
CTGCCAGGCA TCAGGAGGCC CCAGAGGAGC AGCAGAGGCA AGACTCGCTG TCCAGACTCC 540
CTTCTGAGGA GACTGCGGTC AGGGAGCCCA GGCTGACCCT CGTGTTCTCA TGCCTCGGTC 600
CTGTTGATAA GAGGGAAGTC TGTGCTGGGT TCCTATCCAC AAAGCCCTTG CGGGGAATGG 660
GTCCCACACG CCGCTTCTGC AGACCCAGCT CATCCTGTTT CCGGTTTCTA TTTTGTTTTT 720
TCTTTTTTTT TTTTTTGATA CGGAGTCTCG CTCTGTCGTG ATCCGCCCGC CTCGGCCTCC 780
CAAAGTGCTG GGATTACAGG CGTGCGCTAC CGCGCCCGGC CCTGTTTCTG GTTTCCAATT 840
CTCTTAGGAT GTCAGTGCCT TTGATCCTCT GAGCCCCCGG AAGGGCTCAG CCCTCTCACA 900
TCTGCCTTCC TCCTAGAGGT GTGACGCCTG CCCTTCCGCC AGGGCGAGGC AGGGGAGTGA 960
CTTGGCGCCC GAGTCCCGTT TCCCGTCCCC TCTCCGTTGC CTGTGCTCAG AGCCAGGGAC 1020
TCTGCTATTT GTAGGCCCCG CGGGCTCTGT CTGGGGTCTT TCCCCAGGGG AGGGTGTGCG 1080
TCCGGGAAGG AGAGGCAGCC TGGAGTTCCT TCTGGATACC GGCCAGGCCT GCGCTATTTG 1140
CCTGGAGAGG CCATCGGCAT CACTGAGAAG GTCCCTGGAA CTCGCTGCTC AGACACATAT 1200
GTGGCAGCCA GTCAGGAGCT ACGTTCTTCT TTGCTGGAAA CAAGCAAGGA TAGACTGTGA 1260
TTTTCCTCTC CCTCTGTTGT GTATTTTTCA CTCCTGTCTC TCCATCAACC CACCCACCCA 1320
|
