| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00712 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:23803570-23804620 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr1:23803651-23803661 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:23803651-23803661 | GGCACGTGCC | - | 6.02 | | NR2C2 | MA0504.1 | chr1:23803923-23803938 | GGAGGTGAGAGGTCG | + | 6.27 |
|
| | 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 |
| GH01I023477 | chr1 | 23803921 | 23804110 |
|
Enhancer Sequence | GTGACCTGGG CTCACTGCAA CCTCCACCTC CCGGGTTCAA GCAATTCTCG TGCCTCAGCC 60
TCCCAAGTAG CTGGGATTAC AGGCACGTGC CACCATACCC AGCTAATTTT TGTATTTTTA 120
GGAGAGACAG GGTTTCGCCA CGTTGGCCAG GCTGGTCTCG AACTCCTGAC CTCCAGTGAT 180
CCATCTGCCT TGGGGAGGCT GAGGCAGGAG AATCACTTGA ACCCAGGAGA CAGAGGTTGC 240
AGTGAGCCGA GATCACGCCA CTGCACTCCA GCCTGAGCAA CAGAGTGAGA CTCCATCTCA 300
AAAAAAAAAA AAAAAAAAAA AGAAGATGTT CCTTGGTGAT GAGGGGCACA CGTGGAGGTG 360
AGAGGTCGCA CCACTCATTG TGAAAACAGC TCTGGAAGGG AGCCTGAGGG AAGTTAGGAG 420
TGTGGTCAAG TATGCACTGG GACATGAGGA TCTAGGCTAC AGGTACAAAT GTGTGAGTCA 480
CCTGGAGATG GGAGGTAACT AAGGCCACAC GTGTGGACAA GATTCCCTGA AGAGATGAGG 540
ACCCAGAACA AACCTCAAAG AAGGCCTTGA CGAGGAGGAT GAGTCTTCGT GCCACTTAGT 600
ACAATGAGCA ACTTCTGACT TATTTGTTCT TTCTGTTTGT TTTGTTTTGT TTTGGAGACA 660
GGGTCTTGCT CTATCACCTA GGCTAGCATG CAGTGGCACC ATCGGAGTTC ACTGCAGCCT 720
CAATCTCCTG GGCTCAAGTG ATCCTCTCAC CTCGGCCTCC CAAAGTGCTG GCATTCAGGC 780
ATAAGCCACT GCACCCGGCT GTGACTTATT TGTTTACCTG CTTACTGTTG GGCTTTGCCA 840
GAAGACTGTA AGGTCCACAG GGCAGGGACT GCATCTCTAA CTGAGCGATG CATCTGCCCA 900
GTGCCTCATA CAGGGCCTGG CATGGAGCAG TCCCCCAGGC ACTATGCTGG CAGGGCCAAC 960
CCCATCCATT CCTTGAGCAA CATGATTGGG TCCACTGGTC CACACCGCCC AACAAAAAGT 1020
CAGAATGCTC AATTGGCATT CAAAACCCTC 1050
|
