| Tag | Content |
|---|
EnhancerAtlas ID | HS101-04141 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:228286910-228288420 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:228287200-228287218 | GCCTCCGTCCTTCCCTCC | - | 6.05 | | IRF1 | MA0050.2 | chr1:228288303-228288324 | GCAACAAAAGTGAAACTCAAA | - | 6.29 | | IRF2 | MA0051.1 | chr1:228288307-228288325 | CAAAAGTGAAACTCAAAA | + | 6.38 | | IRF9 | MA0653.1 | chr1:228288305-228288320 | AACAAAAGTGAAACT | + | 6.15 | | KLF4 | MA0039.3 | chr1:228287023-228287034 | CCACACCCTCC | + | 6.32 | | NR2C2 | MA0504.1 | chr1:228287540-228287555 | TGAGGGCAGAGGTCA | + | 6.76 | | Nr2f6(var.2) | MA0728.1 | chr1:228288112-228288127 | GAGGTCAGGAGTTCA | + | 6.22 | | RORA | MA0071.1 | chr1:228287108-228287118 | TGACCTTGAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 228288168 | 228288296 | | chr1 | 228287420 | 228287910 |
|
Enhancer Sequence | TCACCGGCTC TCCAGTGCTT CCACACAGGC ATGCTGCCCC CAGGAGATGG TGGGTGCATC 60
AGCCAGCTTT ACTCTAGGAA GTACAGGTGA CTGCCTAGGG CCGCCACCTC AGTCCACACC 120
CTCCCCATGT TCCCTCCTGA GTGTGCAGGC ACTTCTCTGT GTCTGTGTGA GAGGCTCTTC 180
CAGCATGGTT GCCCACAGTG ACCTTGATCT CGTTTGCAGT CCTGTCGGGC CCAGCCAATG 240
AGACCTGGGC CATACAGGGC AGGGGTCAGC AGGCACCATG GAAGACCTCA GCCTCCGTCC 300
TTCCCTCCAT CGGCCTGCTG CTGAACCCCA CTTTGTATAG CTGGCTATGG GGCAGGGCCA 360
CTGCTAGCAT ACATAGGGCT TTGTGCCAAC CAGGGAATGG TCCCTGCCTG AGTGGGCACA 420
GCCCCCACCT CTCCTCAAGA TGCCATGCAG CAGGGGGCTG CCAGTCTGGG GGTACCTGTT 480
TCTGGGATGG GGCCATCAGC AGGTCTAAGG TCTGCCTTCT GTTGGGCAGA GTCCCAAAAG 540
AGAGGGCTGC CCTGGCTAGG TGGCCCAACC TTCATCCCCC TTGACAGCAC CCAAGACAGC 600
ACAGTCTCTA CTCCAGTAGC CACCCGAGGG TGAGGGCAGA GGTCAAAGCC ACAAGCTACA 660
CCTTGGCCAG GGCCCTGAGG AAGGTCTGCA TAACTTCCCT TGAAATCAGA AACAGGCCAG 720
GTGAGGGAGC TCATGCCTCT GATCCCAACA CTGCAACGCT GCATTGAACT GTGATGCAGC 780
CCAGGTGCCA TCTGTCTTTA TGCCATGCAG CCTGGTGGCC GCACACATCC TGAACAGCCC 840
TGATCCTTCT TAGGGTCAGG CAGAAGGGAC ACCCAGCCCA CTGCCTCTGG AGAAGCGGAG 900
CTGAGGGTTG GGGTAGCAGG CAGTTGGAGG AGCTCCCCAA CCCCCACACC CAATTGAGGC 960
TGTGCCTCCA CAGACTGCAG TCTTTGACCT CACCTGTCGC AGGGATAGGG CTCCCTGCCC 1020
CAGGTTCCCA CATTGCCAGC TGAGCACCTG CTTCCAGGGC CTCAGCCCTC CCTGGGTTTT 1080
GGTGGGGGCT CTGGGCACAC ATGGGAGGAC TACATTCCCC CAGGACATTA AGAATCAGAT 1140
GGGCACCGGG GCTCACACCT GTAATCCCAG CACTTTGGGA GGCCAAGGCG GGCGAATCAC 1200
CTGAGGTCAG GAGTTCAAGA CCAGCCTGGC CAACACGGTG AGACCTCGTC TCTACTAAGA 1260
AATAACAAAA ATTAGCCTGG CGTAGTGGCA GCGCCTGTAA TCCCAGCAAC TCAGGTTGAG 1320
ACAGGAAAAT CGCTTGAACC CGCGAGGCGG AGGTTGCAGT GAACTGAGAT CACACCATTG 1380
CACTCCGGCC TGGGCAACAA AAGTGAAACT CAAAAAAAAA AAAAATCACC AGGTCTCAGA 1440
CTCCTGGGAG ACAGACCCCA GCTCCGACGT TCCAGTGGGA TCTCATTAAC CCCTGATACT 1500
GACCTTCCAA 1510
|
