| Tag | Content |
|---|
EnhancerAtlas ID | HS050-03656 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:110672510-110673470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:110673128-110673149 | AGAGCAGGAGCAGCAGGGGGA | + | 6.13 | | ZNF263 | MA0528.1 | chr1:110672990-110673011 | GGATGAGGGAGGAGGGGAGGT | + | 6.66 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 110672728 | 110673048 | | chr1 | 110672711 | 110672989 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I110130 | chr1 | 110672728 | 110673048 |
|
Enhancer Sequence | CCGGACCAGC TGTGAGAAAT TTCCCCACGT CCCCTCTTGG AGTCCCTTCC TTCTCTAGGT 60
GCTGGCCACT CTCAGGAGTG TGTGCATGGT GGGAGCATAT GGGGAAGGTG GCGGGGGGCG 120
GTGTTTGCAG ATGTTCTGGC CAAGGGAGCC TCTGAATGGG GCATTGGGGA CCCCGAGACC 180
TCTCAGCAGG CATTCTAGAG GCTCGTCGGC TGCCCTGCTG TTTGGATACT CTACAGAGCC 240
GGGATTTATG TCCCTTCCCG GCTCCCACGC CTCTTGCTGG GGAGGGTGGC TCATTTTTCA 300
CGGGTGCCGC GTGACTTTCC AGACTGTATT TTCAGCCTCG GTTTGACGTC AGGCTCTCAC 360
GGTCCCAAAG GATGGGCTTT GTACATTTCC AGGCCGCAGA CCGGAGCCTC CCATCCCTTT 420
GGGCCTCTTG GGCGGTCCCT ACGGCCACCT CCCGCAGCTC CCTGGGGGCG GGGGACCGCT 480
GGATGAGGGA GGAGGGGAGG TACTGGGGGG AAAGGGCGGT TGGCGGGAAG GAAGTCCAGG 540
TGAGACAGGC CCGCGTTGGG ACTATCGTGC GCGGTATGTC GGCCGGCAGG TGGGGCTGGT 600
CCGGGCGCAG GAGGCGGTAG AGCAGGAGCA GCAGGGGGAG CCAGGCTGGC CGAGCTGGGG 660
GGTGAGCACG TTTGTCTCAG GCAGCTCATC GCCTGACACC CCCGGGAACG GGCTCTGCCC 720
CAAGGCCTAA AATGAGGGAA GATGAGGAAA TGGGGGTGGG GACGATGGAG AGGATGGAAG 780
GGGCGGCGGG GGGGTGCGGT GGTCTGCGCG GTACAGCAGC GTCCCTGCGG GTTCCCCTCA 840
TTTAGTCCTC AAAACAACCT TGCCGCGGGT TGTGGTTGTC TCTTTTCACA GACGGAGAAA 900
AATTGTTGCG GGGAGACTGC TCTTGGCCTC CCCTCAGCTT TTGTTCAGCA TTGAAGGGGC 960
|
