| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01979 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:226291990-226293140 | 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 | TCAGTAACCT GCACAGCCCC ACAAACCATG GATAAGAGGG AGGCTAGGGC CCGAGTTCAC 60
CTGTGTCCCA AGGAGAGACA GACTCTGTGG GGGTTGGCAA GAAGAGGAAC TGGTCCTGGA 120
TGTGGGAAGG AAAGGGAGCC AGTGCTGCCC AGGCCCTGGA GCATACAAGA AGCAAAGGAG 180
ATGGCATATG CCTTCACTGG GAGCTGTTTT CCTTCAGTCT TATAATAAAA AGAAGAGTTC 240
TGATGGTGGG ATAGGTAAGG GGATAACTGC AAATGGGGAA CACCGATTCA GAGGCAAATC 300
CAAAGTACCA AATTGAAGCA ATCAGAAGAG AACTTCCACA AGTTCCCACC ACTGCCTCAC 360
GCACCGCCCT GCATCTGGGC CCAAGAATTC TGCTCTCCCT GTTGTACCTA TGAGTGAACC 420
CTCAACCCCC CGGCCAAGAC TCCAGCTGTC CCTGTGCATG CCACCCAGCT CCCTCCCACT 480
CAGGACTTCC GCTCCAGCCA CTCTGGCCTC TCCGAGTCAT CCCCATCAGC AGGACGCATG 540
CTGCTATTCC TCCCAGCTAT ACAAGAGCCC TTCCTGTCAC ACCTCCTACT CCAGTCACCC 600
CTCCCTTCTT CCTTTACAGC AAAACTCTGC TGATGAGTCC ATTCCTGCGG ATGAGTCCAT 660
TTCTGCTCTC TCCTGGACCT ATTCCCATCA GGCTTGGCCC TCGCTGTTCC TCCAAAACTG 720
CTCTTGCCAG CGTCACCATT GCTGAACTTG GTGTTCATCC CTTGTCCTCA TTACTTGATC 780
TTGCAGCAAC ATCCATCTGA CCAGATGGCT CCCTTCATCC TGGTAACGCC CTCTTCCAGG 840
AGCTTCCAGG ACAACACACG TACCTGGTTT TCCTCCTACC TCTCAGACTG TTCCATCCCA 900
GGCTTTTCTG CTGGTTCTTC CCCATATCAC TGGCTTCTGC GTAAAGCAGT GCCCCAGAGT 960
GCAATCTGTG AACTCCTCTT CTCTAGCCAT ACTCCCTCCC AAGATTGACG CTATCTAACA 1020
GAAATTTAAT GTGAACCACA TGTGTAATGC AAAATCATCT AGTAGCCACT TTTTTTTTTT 1080
TTTTTTTTTG AGATGGGGTC CCACTCTGTT GCCCAAGCTG GAGTACAGTG GCATGATCTT 1140
GGCTTGTTGC 1150
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