| Tag | Content |
|---|
EnhancerAtlas ID | HS053-19122 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr19:10137800-10138840 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:10138559-10138578 | TTGCGCCCTCTGGTGTCCA | - | 6.9 | | Foxd3 | MA0041.1 | chr19:10137802-10137814 | AAACAAATAATC | - | 6.07 |
|
| | 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 | AAAAACAAAT AATCATAGAA ACGGGGGTCT TGCTTTATTG AGCAGGCTGC TTTTGAATTC 60
CTGGGCTCAA GTGATCCTCC CACCTCGGCC TCTCAAAGTG CTGGGATTAC AGACATGAGC 120
CACCACGCCC GGCAGGCATA TACCACTGTT TCTTGCTTGT CTCCACCCAC TAAAATGTCA 180
GCTCCATGGG CAGGGGACTG TTGTCTATTT GCTCTACCCA CATCACCAGC ACCGTGGAAA 240
CCAAAAAATG ACTCAAGGAG TTAACCAAGC TGGCACATCC TGGCAGTACA GTCCACCCTG 300
AGAAGCTCCT GACACCTCCT ACCTGGACAA GACAGGGTAC TTCTCTGACC CTCAGTTTCT 360
TCATCTGTGA AATGGAACTT GCCAGGGAGA AAGTTATATT AAGGGCTGGA ATGTAGTCGG 420
GGTCTAATAA ATTAGAGCCC TTAATAGTTA TGTTGATGGT AGCCTTATTC CTTGGTCTCC 480
TGGGTCCTGC CCGGCCTTCC CTGGGAAGCT CTGAGCTCAA AGCCCTGGAG GAGGGAGTAA 540
AACCAGAGGC TGCATCTCTG CAAGGACACA TCCCTGCAAG TCCACCCCTC CCGCCCGCGC 600
CTTCTCGGTG CAAACTCCCG ATCCCAGGGA GGGGAAGGCG GGCGGAATCT GAGCGGCAGG 660
CGCAGCTGCT CCGGGCGGGC GGCCAAGGTT CCCTCCCTCG AGCACTGGCA TTCCTGAGGG 720
AGGGGCCGAG CGCAGCTGCC CGCCTGGCCG GAGGCTCGCT TGCGCCCTCT GGTGTCCAAG 780
TACGAGAGGC CACGTGGACT TGCGCACCAG CAGCCGGTCT GTTCTAGGCC ACTGTCTGCA 840
GCTCAGGTGG ACCTGGGTGG AGCTAGGTCT ACCCCCTACC TTTCTTGGGC TCCCTTTTCT 900
TATCCGGGTT CACGAACTCA GCTTCCATCA CTAAACTTGC TGTGTGACCC TGAGCAAGAC 960
ACTCAACCTC CCTGTACCAC AGTTTCTTAG CTGTGCAATT TGGGACAGGA TCCTTTACCT 1020
TTTTAGTGCC ACTTTTTCTT 1040
|
