| Tag | Content |
|---|
EnhancerAtlas ID | HS052-22857 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr2:242524140-242525200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr2:242524354-242524366 | GATTGTTTATTT | + | 6.62 | | Myod1 | MA0499.1 | chr2:242524648-242524661 | AGCAGCTGTTTCC | + | 6.14 |
|
| | 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 |
| GH02I241584 | chr2 | 242523777 | 242524642 |
|
Enhancer Sequence | CTGAGCAGGA GAATGGAACA AAGATAGCTT AGTTTTATCT TCAAAAGATT CAATCAATGC 60
CTGTGCGCCC ACTGCATGCC ACACACTCAT CACGGGCTGT GAGCCAGGCA GTGGCCCTGC 120
CAGAGGAGGG TAGACACACA GCCCAGGGCC CCTGGGCATG TCACAATCCA GGTGCCCTTC 180
AGCTGCCTCC AGAAGACCAC CAGGGGAACA CAGGGATTGT TTATTTAGAA GTCACCTTTT 240
TTGTCGACGG CCATACCACC CTGAACGCAC CTGATCTCGT CTGACCTCGG AAGCTAAGGA 300
GGGTCGGGCC TGGTTAGTAC TTGGATGGGA GAAGTCACCT TTTTTTGGTC TCTACAAATC 360
ATATACCTGA TCAGACAAGC GCTGAGCTTC CAGTGCTTCC CTTCTCCACT GCCTCCCACT 420
TTCACTGTAA CTAGAACTGA TGTCCAGTGT GTTCTTGGAA AGCTCAGAAA TACCATCTTT 480
GGAACAGTAA TTCATCAGAA TAAATTATAG CAGCTGTTTC CAACAAGAAT CCAAGCCTAT 540
GGCAGCTAAG TCCCGAATGA GTCAGCCCTA TATGCCCAGA ATGTTTGCCG GCAAATTGTG 600
AGAGTGACCA CTGTCAAAAG ACAATTCTCT GATGGGCACT ATCTCTCTAG TGCCCCAGAT 660
GTGTGGGGGG TCATGTGGGG TGGGGGGCAC CAGAAGTGGA TGAAACGGAG TTCTGCTTAT 720
GGCCATGGCT GACTACTCTG TAACTGACCA ACCCTCCTGC AGATAACAAC CCAGGTTTTA 780
AGAAGTTTCT TTAAAGGTGT CAGAGAACCA CCAAGTCAGC GAGGACCAGC ACCCCAAAGA 840
GAAGGAAGTG TGGAGGTGAG ACCCAATTTG GAGCAACTGG CCCCGATGCT TTTGCTGCCC 900
GGAAGTCAAG GGGTTCAAGG GGTGGAGGCT GAGAGGGATG TGGTAGCTAA GAGGCTGAGA 960
AGCTAAGTGG GGCCTTCTCA GACTCATGGA GCTGGAGGGA CAAACACTGG AATTCAGTGT 1020
CCATCTAGGA GGAGAGGCGC AGCCGGGCAT GGTGGTATGC 1060
|
