| Tag | Content |
|---|
EnhancerAtlas ID | HS060-09328 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr13:43122710-43124130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr13:43123558-43123569 | TCCTGTTTACT | + | 6.32 | | IRF1 | MA0050.2 | chr13:43122809-43122830 | GCTTCCTTTCTTTTTCTTTTC | + | 6.03 | | SPIB | MA0081.2 | chr13:43122973-43122985 | CACTTCCCCTTT | - | 6.07 |
|
| | 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 |
| GH13I042548 | chr13 | 43122159 | 43124335 |
|
Enhancer Sequence | GATGTTATTA TTTTAAAGTG ATCTCTTCAC TCAAAAAAGG AAATGGCAGA GAATTCTATT 60
GGCTTTGTTG TGAACTCTAC CTCTAATTCC TTTCCCTCTG CTTCCTTTCT TTTTCTTTTC 120
AGAACATGTT GGAAATTATA AGCAAACTTG TAAGTGATGT ATGTATATTT AGTTTCATAG 180
ACAACCTCAG TGTTACTTTC TGGCATTCTT CCAAAGTATC TTACAAGTTA TCAATCTTGC 240
CAGGACAGAG TGTGTTTTCT GACCACTTCC CCTTTGCAAT TAAGGACTGT GACCACTCGC 300
TTACGCACAG ACTGAGACCA GCAGCCTTAA CCCCAAAGGA GGTCAGAAAC TCCCAGCTCT 360
CCCCGCCAAG GGGGCTAGCT GAGAACCCGA TACTGTGTGT TTCAAGGCTG TGGCTAAGGC 420
TGTGACCATA GGAACTGGGA ACACCCACCA ACACCCTGTT TCCCCCAGCC CCACTTCCTT 480
CGCTTCAATG CCATTAAGCA TGGTTGCAGC GCCTTTGTGA ATGTTTTGAG TAGAGTTAGG 540
TTTCTGGTGT TTATTGTTGA ATTGCTAAAG ATTTGGAGAG AAGACAAACA GACAAACAGA 600
CATACAATGA AGCAGATGAC AAACACCCCT GGACAGACTA GCACTATGAG CAGACACGCT 660
CAGGACGACC CAGGGTCCTG CGGAGAGGTC CGGGAAGGTC TGGGCTCTCA TCAGAGCCCC 720
AGGATTTGGT CAGTTGCTCT GCAAATAAAA CCTGCCTTAG ACATCCAGCA AAGAGGCTTT 780
ATTTGCATAG GAGATTTGCC AGTCTGGCCT CCAAGATAGT AGGTCACAGT GAGGGTGGTG 840
GTGAGTTTTC CTGTTTACTG TCTACCTTTG TGGACACATT GAATGTGGGG GCTGAAAGGG 900
GTCAGCAAGG GCTGTCTCCT CTCCTGTTTT CAGATTTGGT GTCTCAGTGA AATCCAGTGC 960
TTTGCCTCTT TGATTGTGCT CTGTCTCAGT GCTTCTCAAT AGCATGTGAT GTGCAGAGAA 1020
GTAAAAGAAA TGAACAAAGA TTTCTCTTCT GAAGGTGTGG GAGGGCATGG GAGTGGGGCT 1080
GGTTGGGCTG ATGATGGAAA GGTCAGATTG CATTGTGTCG TCCACAGGCT TTCCAGCTGG 1140
GCAGGAAGGC TTCCCCCTCT GACTGCATCA TGGCACTTCT TGTACATACT CACTTACCCA 1200
CAGAAACTAA ACTCCGCATG GATAGAGGCT GTGCCTATGC GGTTGGCTAT TGCACACCCA 1260
GCATCACCAC AGTGCCTGGC ACTATCAGAC TCTTCGTGCC TATTTGTTGA AATGTCTACA 1320
AATAGACTAA ATACATATCA GTTGGGATGG CCTTGATTTA AAATATATTA AGCCCCATTG 1380
CCTTTGTATC TACATTTGTG TTTGCCAGAA CAATCATGCT 1420
|
