| Tag | Content |
|---|
EnhancerAtlas ID | HS187-14997 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr20:2686910-2688320 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr20:2687585-2687603 | GGAAACTGAAACCTGAAC | + | 6.18 | | Nr2f6 | MA0677.1 | chr20:2688289-2688303 | TGACCTTTGTCCTG | - | 6.08 | | RELA | MA0107.1 | chr20:2687502-2687512 | GGGAATTTCC | + | 6.02 | | ZNF263 | MA0528.1 | chr20:2688218-2688239 | GGAGGATGCTGGGGGAGGGGA | + | 6.3 | | ZNF263 | MA0528.1 | chr20:2687210-2687231 | GGAGCAGGGGAGGGAGGTAAG | + | 6.43 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GTGAGTCAGC GCAGAGGGTG CTGAGGCCCA TCTCACTCTC TTCCCGGACC CTGCCTCCCC 60
CTGGTCTGAG TGAGCCTCCT TGTTCCTGCC CTCATCTCCC TATGCCCTCC GTCCCCATCA 120
GCCTAGCTCC CCCAGTTCCC ACCCCAGCCT GTGCCGGAGG GTGTGTGGCT TTTGCCCTCT 180
GTTCTAGAAA AGACAATATT TGTACAAAAA CCCTGGCTTG GGTCATGTTT CCTAGCAGCC 240
CAGCCTTAGA TGGGAACTCA GGTGCAGGTA GTTTATTTGG GGAGATGGGA GGGGCTCCTA 300
GGAGCAGGGG AGGGAGGTAA GCTGGACAGA AAACTGCACA GGGAGCTCTG GAGAAGGAAT 360
GGCACCAGAA GTGTCCCCCC TCGAAGCAAG TACCAGGATT TTGCACCCCG TATCAATTAG 420
TCATTGGCTG GGAACCACTC CTAAGGGTAG CACGTAACCT CTGAGACATT TTCAGACCAG 480
GCAGTTCCTG TCCACTGAGA GCAGTTCTCA GGAGGAAGCC CTCTGCAGCT GACATCAGCC 540
ACAGCCACGG GAAGGTGCAC ATTTCCAGTA AAGGGGATGT GGGCACAGCC CTGGGAATTT 600
CCACTGCAGA CCCTTGCACC TTGCTGATGT GACGGTTACG GGAAGGAGGC TCAGAGGCCA 660
GCACAAGGAG CTGGAGGAAA CTGAAACCTG AACAGGCTCT GATGGATTCT GCCAACACAG 720
GGCCCCAAAT CTCAGGGCTT TTCAGAGAAG CTGTGCATGC TGGCAAGGAG GGGGCTGAGT 780
CTCAAATGGG CCAGATTAGT GGGCTAGGAA TGCAAGCTGG AGATCTGGGC TTCCTACATA 840
GGCAGGGTCT TTTGGCAGCC TCCACCCAAT CCCAGGGCAG AGGGAAGAAT GGTTTGTTTC 900
TAGAATACCC ATGGCCACTG GGCTGGGGGA GGCAGGCCAG GCAGTGCCTA GTGGAACTGT 960
CAAGGGGACG GGTGTGGAAG GGGTTCGAGG AAGTCCACAG AGAGAGGGAT CCCACAAATG 1020
GGGGAAGGCA CAGAGGGTTA TAAACTAGGA AGGCAGATTT GCAGTTAGGA AGCTCACTTC 1080
TTGCTTCTGG GCAGAGGGAG GCTGGAAGAC TGGTGAGGAG GTGATGCAGC AGTCCCAGGG 1140
GAAGACCGAG CCTGGGCTAG GGATGGTATG GGGGAAGAGG CGATAGTTAT CTAGGGGGAA 1200
GAGGCAGCTG TGCAGCCCTC GGAGCTGACT GGGCTGGCAG GGATAGCTGA GAAGGACAAC 1260
ACTCATCAAC AGAAGCAGAG GTCCGTCAGG ACATGGAGGA TGCACACAGG AGGATGCTGG 1320
GGGAGGGGAG GGGCCTGGTG CTGGGTGGGC ACAGGAGTAT GTCTACCCCA CCAGCCACCT 1380
GACCTTTGTC CTGGCACCCT GAGGAACCCC 1410
|
