| Tag | Content |
|---|
EnhancerAtlas ID | HS158-29902 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr2:46187320-46188260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr2:46187398-46187409 | GATGAGTCACT | - | 6.02 | | JUND | MA0491.1 | chr2:46187398-46187409 | GATGAGTCACT | - | 6.32 | | RREB1 | MA0073.1 | chr2:46187586-46187606 | GGGCAGGGAGTGGTGTGGGG | - | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I045961 | chr2 | 46187321 | 46187490 | | GH02I045960 | chr2 | 46187957 | 46193089 |
|
Enhancer Sequence | GGAAAAGACA TGAACTTTGG AACCGGTCTG GCCTTGGGAC CAAATCGAAC TCCACCACTT 60
AATAACTATG TACACCTAGA TGAGTCACTT GGATTTTCTT AGTGCCGGTT TCCTCATTGT 120
GTGGTGGAGG TAGTGATACT AATCGTGTAG AATCCTTTCG AGAAATAGAG AAAATATGTT 180
TTAATCACCT GCTATACCAT AAATCAGTGT TCCCCAACCT TTTGGTACCA GGGACTGGTT 240
TCATGGAAGA CAGTTTTTCC ACTGATGGGC AGGGAGTGGT GTGGGGGGCA GAAGGGGAAG 300
GGCATTAGAT TCTCATAAGA AGCCCCCAAC CTAGATCCCT CACGTGTGCA GTTTACAATA 360
GGGTTCCCGC TCCTATGAGA ATCTAATGCT GCTGCTGGTC TGACAGGAGG TGGAGCTCAG 420
GCAATAATGC TTGCCCACCC ACCAATCACC TCCTGCTGTG CAGCCAGGTT CCTAACAGGC 480
CACAGACCAG TACTGTGGTC CCCTGGGGAT TGGGGGCCCC TGCTGTAAAT GGTGCCTATT 540
ATTTCTAACA TCCCGTTTTC AGTGGATTTT ATCTTTTGCT TTAGAGATGC CAAGCACCCA 600
TCAGCCTTTG ACTGAAAAAT TCCCCAAATT TAGCTCCTGC CTCACTCTCC TTGCAGTTCC 660
TACAATCCTT TCTGCCCCCC AGTTTTCCTA CCTGCCCAGC ACAACCTCTC CAAAAAGGAT 720
CTGAGATTCA CCTATGTTGA ACTTATAATG GCCCTCGCAG AGGCTTTCTG TTTCAACAGG 780
GTTGAAAGCC TGGCACTAAG GAGTAAAGCA AACACAGAGG GGCTGGAAGC AAGAGGGATC 840
ACTTTATTTT TTAGAATACC AGGACTTTAG CGTCTCTGAA TTCCCAGCTC TCAGGAGCTA 900
AGTCAGCCTT ACTCACTTAT ACACAGGCCC TGGTTTCCAT 940
|
