| Tag | Content |
|---|
EnhancerAtlas ID | HS187-06665 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr13:31348020-31349130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK4 | MA0076.2 | chr13:31348675-31348686 | GCCGGAAGTGC | - | 6.14 | | IRF2 | MA0051.1 | chr13:31348567-31348585 | GGAAAATGAAAGTTAAAG | + | 6.22 |
|
| | 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 |
| GH13I030773 | chr13 | 31347638 | 31349586 |
|
Enhancer Sequence | CAGAGAGAGG GGAAGATAAC TTGTGCAAAG CAGGGTTTTA ATAGAAATAA TTTGGCAGTT 60
TCCTAGAGGA TAGTTTGATG ATAAAAACCA GCCAGGCTAG AAACAGGAAA CCAGCTGGAG 120
ACAATTGGTA GGGGACAATT TCAACGGTCT AAATGCAAGA TGGCACCCAG ACAAAGATGG 180
CAGCTGACAG AATGGAAAAA TAAAATGGAA GGTGTAACAT TATGAATGAC AGCAAACAGG 240
AAGCAGGATT GGTTGGTAGG GATCAGGAAA AGGAGAGAGA ATAAGAGAGA ATGCTTGGTT 300
TTGAGCCTGG GTGCTGAGGA GACTCAGTAC AGATAAATCC CAATTGCACT CCCACCATAT 360
ACCAGGCATA TGGATAGGTC CTGGGCATCA GTGGTGATGA CAGAGACAAT GTCGCTATCT 420
TTGCAGAACT TTCATTGTGC TGGAGGACAG GAAGCAGTCA GAGAGGCAGC AGAAACACCA 480
CAGCAAAGTA GGTCACAGAA ACCCAAGAGT GAACAGTTTC GATTTATAGT TCTAAATAAA 540
TCATCATGGA AAATGAAAGT TAAAGGACAT TGGAAAGCTG TTTATAATAA GAAAGAAGAA 600
TACCTAAACT CATAATAATA ACCGTGACCA TGCATTTGTT ACTTTCTTAC CGTAAGCCGG 660
AAGTGCACTG TGTGCTTTGC ACGCTGTATT AGTCAGGGTT CTTTGGTGAA ACAGCACTGA 720
TAGAATTGAT TGATTGCTTG ATTAATTGGT TATGAGAATT GGCTCACACA ATTACGGAGG 780
CTGAGAAGGC TCAAGATCTG CTGCCTGCAA CCTGGAGAAC CAAGAAAGCG GTGGTGTAGA 840
TCAGTGTAAG TCTGAAGGCC TGAGAACCTG TGTGGGAGGG GACATCGGCA TGGTATAAGT 900
ACTAGACAGG GTCTGGAGGC CCAAGAGCCA GTAGTGCTGA TGTCCAAAGG CAGAAGAAGA 960
TGGACGTCCC AGCTCAAACA GAGAAGGAGA GAACTTACCC TTCTTCTTCC TTTTTTTTCC 1020
TCAACGAATT GGAGGATGCC TGCCCACATT GGTGAGGGCA GAGCTTCTAT ATTCAGTCTA 1080
CTGATTAAAA TGCTGAATCT TCTGAAAACA 1110
|
