| Tag | Content |
|---|
EnhancerAtlas ID | HS146-07800 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr19:50506630-50507960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr19:50507361-50507376 | TGCTATTTTTATCAA | - | 6.33 | | ZNF263 | MA0528.1 | chr19:50507600-50507621 | CTTCTCCCTTTCTCCTCCCTC | - | 6.08 | | ZNF263 | MA0528.1 | chr19:50507514-50507535 | CCTTCTCCCTCTTCCTTCCCC | - | 6.82 | | ZNF263 | MA0528.1 | chr19:50507508-50507529 | TCCTCTCCTTCTCCCTCTTCC | - | 6.85 | | ZNF263 | MA0528.1 | chr19:50507511-50507532 | TCTCCTTCTCCCTCTTCCTTC | - | 7.37 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr19 | 50507616 | 50507886 | | chr19 | 50506822 | 50506896 | | chr19 | 50506970 | 50507586 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I050003 | chr19 | 50506683 | 50508541 |
|
Enhancer Sequence | TAACACAAGC CCCACCTTTC ATCTGCAAAG GCAGAAGCTG CAGAGGGCAG CGTGGGCCCG 60
ACCCTGAGCT GCTGCTCACG GGCAGCTCTC CCAAGTGCAC CGCAGTGAGC AGCCGCACGG 120
ATTCATGTGA CTGATGACGG ATGGTGGTTC TCCCCTATAG CTCAGCGAGG CCCGGGATAT 180
ATGACATTAT AGTTCAGTAC TGGACAGAGA CACAAGAGTT AATAAAATGC TTAGAGCATG 240
GCGCAGAGAG TGGGGTAAAG TGTCCACTGC TCGAATAACC ATAACGATTC AGCTTGTTCT 300
TGTTGTTTTA CTGTTATTGC TTTAAATTAC GGGACATACA ACTCCACCAT CTCTTCTTGA 360
CTGGTGCAAA CTGGCAGAAG AAAAGGGCGA TTTGCTCTGG GGCGATGTCA CCCAATGGTG 420
GTGTGTCCCC AAATGCAAGC TCCGCATCAG CAGGGCCTTC ACCAGCCCCG CTCTCCCTGC 480
ACTGTCTGTG CTGGCACCGC GGCCAGACAC ATGAAATGGT AGGTGCTGCT TAAGGATCCA 540
CTGAGCAACC GGGCACAGTG CTCACGCCTA TAATCCCAAC ACTTTGGGAG GCAGAGGCAG 600
GAGGATGGCT TGAGGCCAAG AGTTTGAGAC CAGCCTGGCC AACATAGTGA GATCGTCTCT 660
ACTTTAAAAA ATAAATAAAT AAAGGGACTG CTGAAGGAAT GGATGACTCA CACAGGCTGG 720
GCACTGGGGT TTGCTATTTT TATCAAACAA CCTGAGTCAT ATAAGGGAAA ACCAAAACCA 780
CATTGGCCCA GAGTAGCTCC TCCTGTGCTT CCACTGTGGG TTTCTGGGGG AGGTCAAGCG 840
TGGTTTCTTC TCTCAGGAGC TCCTGGCTCT GTGTGTTTTC CTCTCCTTCT CCCTCTTCCT 900
TCCCCGCCCT CCTGCCCTCT CCCCACCCTG CTCTCTCACC TCAATCTCTT TCTTACTGTT 960
GGTTTTCATC CTTCTCCCTT TCTCCTCCCT CTGTGCTCCT CGGCCCCTCA TTCCTTCTCA 1020
TCATGATCCC TTCTCGCTCT TTCTCCCTGC CCTCTCCTTC TCCTTTCTCT CCCTTTCTTG 1080
GGAGAAGCCA GAGTGCCTGC GTTCAAATCC CAGCTCTACT ACTTCCAGGC TGTGTGCCCT 1140
TGGGCAAGTA GCTTCCTCTC TCTGTACCCC AGTTGCAGGA TGGGGTAATA TGGGTGCCTA 1200
TCTCACAGTG TGGCTGGCAG CATTACATGG GTAAGACACA GAGAGTTCCC AAAGTGTCTG 1260
GCATGGGATC CTGCCTGTAA TCCCAGCACT TTAGGAGGCT GAGGCGGGAG GATCGCTTGA 1320
GCCCAGGAGT 1330
|
