| Tag | Content |
|---|
EnhancerAtlas ID | HS187-25223 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr9:117246860-117248010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr9:117247393-117247404 | GATGAGTCACC | - | 6.32 | | FOSL2 | MA0478.1 | chr9:117247394-117247405 | ATGAGTCACCC | - | 6.14 | | JUNB | MA0490.1 | chr9:117247394-117247405 | ATGAGTCACCC | - | 6.32 | | JUND | MA0491.1 | chr9:117247393-117247404 | GATGAGTCACC | - | 6.62 | | Nr5a2 | MA0505.1 | chr9:117247762-117247777 | GAGTTCAAGGCCAGC | + | 8.25 | | Zfx | MA0146.2 | chr9:117247730-117247744 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_00989 | chr9:117243175-117248201 | Adrenal_Gland |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 117247262 | 117247587 | | chr9 | 117247067 | 117247705 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I114483 | chr9 | 117245441 | 117247950 |
|
Enhancer Sequence | TTAGAGTGCT GTGTTCCCAT ACCTGTTATC ACGTGTTTAC TGGTGAAACT TGACCCTGGG 60
GCATTCCACC AACTCAAATC ATAGAGAAAT CTCGATCTGA CCCAGCAGAT GGCACGACTA 120
AGATACTATC CATCACCAGA TGACTATTCT GGCAGCACGT TATGATTATG GAAATGTAAA 180
TTATATGTGT ATGTCTTCAA ACTTAATAAC TTGCTACTTG GATTAATGCT CTCAGGAGGC 240
AAATTTGCCT CACTCAGCTC TTTGGAGCCA ACTCTGAAAC CCCAAAATCA TAGACCAGGC 300
TGACATGATT CTCTGCTTAG CAGAGGAGTG AGAAATAGAC TGGAGAGGGT CACAGTGTAG 360
GGGGCTAATG GGATGTGTTA ACATGGCAGA CGCACACATG CTTCTGTGTT CAAAACCATA 420
CACCAAAGGC AAGCATGGGG TGGACCTCAA GGTCACAAGA CTATCAGATC ACTGTGCTGA 480
GGAGCACGTG CAACAGAGGT ATTCCAAAAA AGTCTCAAGC AAGGACACGT AATGATGAGT 540
CACCCAGCTT ATTTCAGGGT GCAGACCTCA AAGGGCAAGG TTTTCTCTTT TCGGAAACAG 600
AGACTCAACA ACAGGAAGGA GAACTGGTCT AAGACCCATC TTAGTGACCC AGAAGGGAGG 660
AAAAAATTAT GCATGCCTGC TCTTCGCAGC CGCACCTTGC CTAGCTGGGG CTTTGTGTGT 720
TCAGACACAC CGGACAATGG TGTTGGCTCT GTAGATGACT TGCTGTGTGA CACTGAGCCA 780
ATTGCCTAAA CTCTCTGTGC CTGTTTCTAT ATTTAAAAAG CAATTGCTGG TCAGGCGCAG 840
TGGCTCAGGC CTGCAATCCC AGCACTTTGG GAGGCCGAGG CGGGTGGATC ACCTGAAGTC 900
AGGAGTTCAA GGCCAGCCTG GCCAACATGG TGAAACCACG TCTCTACTAA AAATACAAAA 960
AATTAGCCAG GCATGGTGGC GGGTGGCTGT AATCCCAGCT ACTCAGGAGG CTGAGGCAGA 1020
AGAATTGCTT GACCCCAGGA GGCGGAGGTT ACCATGAGCC AAGATTGCAC CACTGCACTA 1080
CAGCCTGAGC TACAGAGCGA GACTCCGTCT CTAAATAAAT AAGTATATAA ATATCAATTG 1140
TTGCCTGGGC 1150
|
