| Tag | Content |
|---|
EnhancerAtlas ID | HS012-00581 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr1:120264380-120265000 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESX1 | MA0644.1 | chr1:120264709-120264719 | GTTAATTGGT | - | 6.02 | | IRF1 | MA0050.2 | chr1:120264460-120264481 | CACTAGTTTCTCTTTCAGTGC | + | 6.09 | | NR2C2 | MA0504.1 | chr1:120264531-120264546 | CAGGGGCAGAGGTCA | + | 6.72 | | Nr2f6(var.2) | MA0728.1 | chr1:120264706-120264721 | GAGGTTAATTGGTCA | + | 6.02 | | RARA | MA0729.1 | chr1:120264652-120264670 | CATTGTCCTTAAGACCTT | - | 6.32 |
|
| | 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 |
| GH01I119720 | chr1 | 120263376 | 120266116 |
|
Enhancer Sequence | CAGAGGCACA ACCTTTGCTA GCAGACTAAT GACTAGAATC CTTGCCCTCC CCACTTCCCT 60
GCCACCTTCT GGAACTAAGA CACTAGTTTC TCTTTCAGTG CTCTAGGGCA AGAGGAGAAG 120
GGTCCCATTT AAAGCTGTTT CTGCAGAAAC ACAGGGGCAG AGGTCATCAG CACGCCAGTG 180
CTGTACTGTA CCCGTTCTGT CACTTAGATG GTATGGCAAG GCCATCCCCA GGCCTCTTTG 240
TTCTTAAGAC TTTTCTCTTC CCTTGGGGAC TTCATTGTCC TTAAGACCTT TCCCCTCCCC 300
TGCACTGCAC TTCCCCCTGT AGGGTAGAGG TTAATTGGTC ACCTGACTGA AGTCAATATT 360
CAACAGCAGA AATGTTAAAC GATAACCCAT CCCACATTCT TGCCTTGGAC CCAGAGGCAG 420
CCAGGCCCCA ATCTCTGCAC CTCTACTTGC GCCCCCATAC AGCCTGTTTG CTGTGGGAGG 480
ATGAGAAGCC AGGTGGTTTT GCAGGCAGAC AGACTCTGAG AGTCCGTTTA TCTTATACAG 540
GATCTCTTGA CTTTTTCTTC TTGTAACCTT ATTAACCTTC ATTCCAGAGA TGAAAAAGAC 600
AGACCCAGTA GGGGAATAAT 620
|
