| Tag | Content |
|---|
EnhancerAtlas ID | HS187-02319 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr1:211868380-211869360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr1:211868658-211868669 | TCAAGGTCATT | + | 6.32 | | Esrrg | MA0643.1 | chr1:211868658-211868668 | TCAAGGTCAT | + | 6.02 | | NKX2-3 | MA0672.1 | chr1:211868971-211868981 | TTCAAGTGGT | - | 6.02 | | RORA | MA0071.1 | chr1:211868657-211868667 | ATCAAGGTCA | + | 6.02 |
|
| | 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 |
| GH01I211695 | chr1 | 211868601 | 211868750 | | GH01I211696 | chr1 | 211868753 | 211869196 |
|
Enhancer Sequence | AGAACACCCA AATGTGCCCA CCCACCCTAC AGATTCTTGG AGGTCTGGCT CACTTATCTC 60
CAAGAAAGCC CCCTCTGGAC CATCCAGAAG CCACGAGATG GTAACAGTGC TTCCTCTGCA 120
GGGGCTCTGA TCGACCTTGG GTCTGCAAGG GGTAGCAGTC AGGGGTCACC TGAGCCTAGC 180
TCAGTGGGTG TGCTCCTCAC ACTGCATGAC CGCATGCTGT GGGTGGGCCT GTGCACATGT 240
GTGTTTGTGC ACACAGAGGA AACGAGTGTA GGCGGGGATC AAGGTCATTT TTACAAACAG 300
AAAAGCTGCA GCATCTCCAT AACTCAGCTT GTGGGCTAGA CAGTCACCAC AGAAAAAAGG 360
AAGCCAGACC AAAACTGAAC CACTGGACTA CTGCAAGCCC GCCCCAGCAG GGAGCCAGTG 420
CAGGACCCCT GTGAGAAATG GGAACTCTGT ACTATCTTTA TAGCTTTTCT ATAAATCTAA 480
AACTCTTCAA AAATAAAGCA TTTATTAACA ACAATGACAA CAAAAGCATT GACTAAGCTC 540
TGTGAACTGA GAATTTTGTT CTTTACCAAA TGGGGATTTC TAACACATCT TTTCAAGTGG 600
TTTGGCAGCA TCTTGGAGCT TCCCATTGCT AACAGCGTGC TAATGACAAC TGCCCTTAAA 660
GGAGGCCTCC TGCAGAGCGC CCGCTGCCCC CGTGACCCTC CTCCAGCTGT CTGTGAGATA 720
AGAGTAGTGA TAACATAGCT GCTCTTGGAG GAGCATTGTG TGACGGCCAA GGCCCAGAGG 780
CCCCGAAGAG GAGGCACTGT TACCATCTCT ATTTTACAGA TGAGGAAACC CAGGCTCTAG 840
AGGGTGAGAA AATGCCAGAG CTGGACCTAC AGTTCTGCCT GATTCCAAAG TTCAAATCTT 900
AACCACTGCT AAAGAAATAA AGCGGTATAT ATACATATAT ACATATACAC ACACACACAT 960
ACATACATAC ATACATATGT 980
|
