| Tag | Content |
|---|
EnhancerAtlas ID | HS101-18784 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr17:44356810-44357750 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr17:44356856-44356877 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 44357048 | 44357501 | | chr17 | 44356903 | 44357020 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I046279 | chr17 | 44356971 | 44357567 |
|
Enhancer Sequence | AAGTGCTGGG ATTACAGGCA TGAGCCACCG CACCTGGCCT TTTTTTTCTT TCTTTCTTTT 60
TTTTTTTTTT TTTTTGAGAT AGGGTCTTGT TGTGTCGTCC AGGCTGGAGT GTAGTTGCAT 120
GAACATGGCT CACTGCAGTA TCTGTCTCCT GGGCTTAATC CTCCCACCTC AGCCTCTGGA 180
GTAGCTGGGA TCATGGGTGC ACATCACCAT GCCTGGCTAA TTTTTGTATT TTGTAAAGAT 240
GGGGTTTCCT CATGTTGCCC GGGCTGGTCT AGAATTCCTG GGCTCAAGCA TCCTCCTGCC 300
TCAGCCTCTC AATGTGTTGG GATTACAGGC ATGAACCACC ATTCCCAGCC AACAGGCCCT 360
CCTACACAAC TTTTTGTTTT TAGTGGCGTT TCTAATTGCC TTTCATTTTT ATCCCTGACA 420
TTCTTTGGCT TAATCATAGC CTTATGTTTT TCTGTCTTAA ACAAATTATC TAATGCATGA 480
GTCATTGTCT TGCCCTACTG ACCCTCTGGG GAGTGCTCCA TTCTCCTGCT AGGATTTGGA 540
TTGCTTACCG CACAGCCTGC TGTACAAATG TCACCTTGAG TCAGAGTAAT TCTCATTGCT 600
TTCCCTGAAC CTCTTGTTTT CTGAACCCAA ATAAATAAAA ATGTCTGGCC AGGCGCGGTG 660
GCTCACATCT GTAATCCCAG CACTTTGGGA GGCCAGGGCA GGTGGATCAC TTGCCTTGAG 720
ACCAGCTTGG CCAACATGGC AAAACCCCAT CCCTACTAAA AACACAAAAA TTAGCCAGGT 780
GTGGTGGCAG GCGCCTGTAA TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATCGCTTGA 840
ACGCGGGAAG CGGAGGTTGC AGTGAGGTGA GATTGCACCA CTGCACTCCA GCCTGGGCAA 900
CAGAGTGAGA CTCTGTCTCA AAAACACAAA ACAACAGAAA 940
|
