| Tag | Content |
|---|
EnhancerAtlas ID | HS054-00718 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr1:225878830-225880350 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr1:225879781-225879792 | TGTGGATTGGG | - | 6.14 | | MEF2A | MA0052.3 | chr1:225879217-225879229 | GCTAAAAATAAA | + | 6.04 | | MEF2A | MA0052.3 | chr1:225880289-225880301 | TTTATTTTTAGA | - | 6.07 | | Mafb | MA0117.2 | chr1:225880032-225880044 | AAAATGCTGACT | + | 7.22 |
|
| | 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 |
| GH01I225690 | chr1 | 225878701 | 225880319 |
|
Enhancer Sequence | TTTCAGTGAG CCAAGATGGC GCCACTGCAC TCTAACCTGG GCTACAGAGA GAGATTTTAT 60
CTCAAAAAAT AAATAAAATA AAAAAGAAGC CCAGGGACAA ATGAGCCCAC CTCCACTGTA 120
GACACTGGGA GCCACATTCT CAAAATGAGT AACTGCAGGG AAGAGACAGA ATTCTCACAA 180
GAGGGCATAT CCTCCGCCCT TCATACATTT CTCCTGTAAC ACCCTTCTGG TTGAAAAGAA 240
ATAAGAAAGC TGTGCTTGAC TTTTGCTCTA GTGCTTTTTA AGATCAAGCA GGAATCTTAC 300
ATTCTTTCAT TGCCTTTCAC ATTTCTTTTC CTTCTTCCGT GTCCTCTTTC TTTTTAAATT 360
CAGATCATTT AACAGACAAG GGTCATAGCT AAAAATAAAT CTTCATTGAC CTGAGCTACC 420
TATGATGTCA TTTACTGTAT TCATAGGTCT CCAGAGTCAA CACTCCAGGC ATGTAGACAC 480
ACACAGGAGA ATAAAACCTC AGTTCCCAGG CAGCTTCCAG AAGCTGTGGC ATTGCTGTGG 540
CCTGAGGCCT GGACTTTCCC AGGGGATAGG TATCCAGATC GTTTGTGCCC TTCCATATCA 600
CCTTTCATTC AGAGGCCTTA CCTGGATTGG TAGCCAAGCA TTGATACTCA TGCCTCCCCA 660
AAGAGGTAAG TTTTAGTAGG AAACTGAAAG AAACCAAGGC CCAACAAAAT GAGGCAACTA 720
GACGGAGTGA CTGGGGAAGT TTCCAGCCAA GTCAGATATA AAATTTGTAC TGTGAAAAAC 780
TGTTATCTGT ATTTTGGTAT TTACCAAAAA ACAGTGAGCC ATGATCACTC CATGCAGTGG 840
GTTAAACTTG TGGGAGAAGT AAATTCTGTG GTGTCAGCTC AGAACAGAAC ATATTGGGAA 900
TGCATAATAG AAAAGCAGTA CTCTCACTCA GCTTCATAAC TCCAGCAAAT TTGTGGATTG 960
GGGTTAACCA CGTCTGGAAT TCCAGAACTC AAGTTACCCA AGTGTGGCAG GCCAGGGGAA 1020
TTTCTGCGGG CTGGATGGGA AATCTTCAAA GTCAGCATTT ATTTTCATCT GCACTCAATA 1080
TTTTGGCCCA ATATGTAAGT AACTTGATGT CCATTCTTGT GTTGATAAGG AGCCTAAAAG 1140
CCTGGAACAG AGAAAGGAAA AGTTGGTCTC CACTTGGATC TCAATGTGGT CATCAGTCAT 1200
GGAAAATGCT GACTATGACC ATTCCCAATC AGCTCCTCAT GCCTGGCACT AAGAGACACT 1260
AGACACCTTG GGCTGCAATG ACTGCATTGT GCGTTTGTCA CTTTACCATA AGCTACATGA 1320
GTCCCCAGCT GGCTGTGTTA AAGTGCTCCA TCTTCCCAAT AGCCATGTGT CCCTTGACGG 1380
CAGGAACACT TTCATGTTTC TTCTGCAGCT CTCATGGTGC ACCATGTTGC TTATTCTTTT 1440
TTTTCCCTTT TTAAATTTAT TTATTTTTAG AGATGGGGTC CTGCTATGTT GCCCAGGCTG 1500
GTCTAGAACT CCTGGCCTTA 1520
|
