| Tag | Content |
|---|
EnhancerAtlas ID | HS092-04961 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:226291900-226293050 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr1:226292430-226292443 | TCCAGCTGTCCCT | + | 6.16 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTAAGTGAT GCATGACTGT ACTCAACACT GCTAGAAAGG CGAGTCCAGA GCAGGACTCA 60
TCAGAATGCA GCTGTCTTAG CTGAGAGAAC TCAGTAACCT GCACAGCCCC ACAAACCATG 120
GATAAGAGGG AGGCTAGGGC CCGAGTTCAC CTGTGTCCCA AGGAGAGACA GACTCTGTGG 180
GGGTTGGCAA GAAGAGGAAC TGGTCCTGGA TGTGGGAAGG AAAGGGAGCC AGTGCTGCCC 240
AGGCCCTGGA GCATACAAGA AGCAAAGGAG ATGGCATATG CCTTCACTGG GAGCTGTTTT 300
CCTTCAGTCT TATAATAAAA AGAAGAGTTC TGATGGTGGG ATAGGTAAGG GGATAACTGC 360
AAATGGGGAA CACCGATTCA GAGGCAAATC CAAAGTACCA AATTGAAGCA ATCAGAAGAG 420
AACTTCCACA AGTTCCCACC ACTGCCTCAC GCACCGCCCT GCATCTGGGC CCAAGAATTC 480
TGCTCTCCCT GTTGTACCTA TGAGTGAACC CTCAACCCCC CGGCCAAGAC TCCAGCTGTC 540
CCTGTGCATG CCACCCAGCT CCCTCCCACT CAGGACTTCC GCTCCAGCCA CTCTGGCCTC 600
TCCGAGTCAT CCCCATCAGC AGGACGCATG CTGCTATTCC TCCCAGCTAT ACAAGAGCCC 660
TTCCTGTCAC ACCTCCTACT CCAGTCACCC CTCCCTTCTT CCTTTACAGC AAAACTCTGC 720
TGATGAGTCC ATTCCTGCGG ATGAGTCCAT TTCTGCTCTC TCCTGGACCT ATTCCCATCA 780
GGCTTGGCCC TCGCTGTTCC TCCAAAACTG CTCTTGCCAG CGTCACCATT GCTGAACTTG 840
GTGTTCATCC CTTGTCCTCA TTACTTGATC TTGCAGCAAC ATCCATCTGA CCAGATGGCT 900
CCCTTCATCC TGGTAACGCC CTCTTCCAGG AGCTTCCAGG ACAACACACG TACCTGGTTT 960
TCCTCCTACC TCTCAGACTG TTCCATCCCA GGCTTTTCTG CTGGTTCTTC CCCATATCAC 1020
TGGCTTCTGC GTAAAGCAGT GCCCCAGAGT GCAATCTGTG AACTCCTCTT CTCTAGCCAT 1080
ACTCCCTCCC AAGATTGACG CTATCTAACA GAAATTTAAT GTGAACCACA TGTGTAATGC 1140
AAAATCATCT 1150
|
