| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01729 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:62587500-62588350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:62588075-62588086 | ATGAGTCATCC | - | 6.62 | | JUN(var.2) | MA0489.1 | chr1:62588075-62588089 | ATGAGTCATCCTCC | - | 6.43 | | JUNB | MA0490.1 | chr1:62588075-62588086 | ATGAGTCATCC | - | 6.62 |
|
| | 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 |
| GH01I062121 | chr1 | 62587265 | 62588599 |
|
Enhancer Sequence | GAAAAGCAGA AAGCTGGAGT GCATGGTAAA ATAAAATTAC TTACAAAGAG AAAATTAATA 60
AATTACAGGT CACTGGAGAA AGGTCAGAAG TGTGTATACC TTCTATGGGA AAATTGGGCC 120
AGTTAAAAGA AAAAAAAAAG TGTGTATATC CTTGGGGGCA GGGTGGGACA AGGGGTCCTT 180
TTAAGTCTTT TGTTGAATGG AGGGTTATCT TTGATTAAGG TAGAAAAAAA TGTACAATGA 240
AACACAAATG ACTCAGCCGG GCCCGGTGGC TCATGCCTGT AATCTTAGCA CTTTGGGAGG 300
CCAAGGCAGG CGGATCACCT GAGGTCAGGA GTTTGAGAGC AGCCTGGCCA ACATGGAGAA 360
ACCTCGCCTG TACTAAAAAT ACAAAAATTA GCCGGGCATG GTGGCACATG CCTATAATCC 420
CAGCTACTTG GGAGGCTGAG GCAGGAGAAT CGCTTGAACC CAAGAGGCAG AGATGGCAGT 480
GAGCTAAGAT CGGACCACTG CACTCCAGCC TGGGCGACAG AGTGAGACTC CATCTAAAAA 540
AAAAAAAAAA AAAAAAACCA CACACACACA CAAAAATGAG TCATCCTCCA AGCATTTACT 600
CACCATGTTC CAGGCAGCTG CTGCTATATA GCCCATCCAC TTTTGTCAGA CCAAATGGTT 660
ATGGCCACAT TGATCTCAAA CAGAGAGCAC TTCTTTAAAA TAGAGGACAC AGCAGGCCGG 720
GCACGGTGGC TCACGCCTGT AATCCCAACA CTTTGGGAGG CCGAGGCAGG TGGATCACTT 780
GAGGTCGAGA GTTTGAGACC AGCCTGGCCA ACATGGTGAA ACCCCGTCTC TACTAAAAAT 840
ACAAAAATTA 850
|
