| Tag | Content |
|---|
EnhancerAtlas ID | HS049-03867 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr19:10137900-10138780 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:10138559-10138578 | TTGCGCCCTCTGGTGTCCA | - | 6.9 |
| | | 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 |
| GH19I010027 | chr19 | 10137829 | 10138918 |
| Enhancer Sequence | CTGGGATTAC AGACATGAGC CACCACGCCC GGCAGGCATA TACCACTGTT TCTTGCTTGT 60
CTCCACCCAC TAAAATGTCA GCTCCATGGG CAGGGGACTG TTGTCTATTT GCTCTACCCA 120
CATCACCAGC ACCGTGGAAA CCAAAAAATG ACTCAAGGAG TTAACCAAGC TGGCACATCC 180
TGGCAGTACA GTCCACCCTG AGAAGCTCCT GACACCTCCT ACCTGGACAA GACAGGGTAC 240
TTCTCTGACC CTCAGTTTCT TCATCTGTGA AATGGAACTT GCCAGGGAGA AAGTTATATT 300
AAGGGCTGGA ATGTAGTCGG GGTCTAATAA ATTAGAGCCC TTAATAGTTA TGTTGATGGT 360
AGCCTTATTC CTTGGTCTCC TGGGTCCTGC CCGGCCTTCC CTGGGAAGCT CTGAGCTCAA 420
AGCCCTGGAG GAGGGAGTAA AACCAGAGGC TGCATCTCTG CAAGGACACA TCCCTGCAAG 480
TCCACCCCTC CCGCCCGCGC CTTCTCGGTG CAAACTCCCG ATCCCAGGGA GGGGAAGGCG 540
GGCGGAATCT GAGCGGCAGG CGCAGCTGCT CCGGGCGGGC GGCCAAGGTT CCCTCCCTCG 600
AGCACTGGCA TTCCTGAGGG AGGGGCCGAG CGCAGCTGCC CGCCTGGCCG GAGGCTCGCT 660
TGCGCCCTCT GGTGTCCAAG TACGAGAGGC CACGTGGACT TGCGCACCAG CAGCCGGTCT 720
GTTCTAGGCC ACTGTCTGCA GCTCAGGTGG ACCTGGGTGG AGCTAGGTCT ACCCCCTACC 780
TTTCTTGGGC TCCCTTTTCT TATCCGGGTT CACGAACTCA GCTTCCATCA CTAAACTTGC 840
TGTGTGACCC TGAGCAAGAC ACTCAACCTC CCTGTACCAC 880
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