| Tag | Content |
|---|
EnhancerAtlas ID | HS190-08460 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr22:17761320-17762720 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr22:17761335-17761356 | ACTTGGTTTCATTTTCCATTA | + | 6.49 | | IRF2 | MA0051.1 | chr22:17761334-17761352 | AACTTGGTTTCATTTTCC | - | 6.45 | | NFAT5 | MA0606.1 | chr22:17761345-17761355 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr22:17761345-17761355 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr22:17761345-17761355 | ATTTTCCATT | + | 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 |
| GH22I017280 | chr22 | 17761414 | 17761972 | | GH22I017281 | chr22 | 17762222 | 17762859 |
|
Enhancer Sequence | TTTTTTTTTT AAGAAACTTG GTTTCATTTT CCATTAAGGT GAAAGCTAAC ATCTGGGTTC 60
AATTCAGTTC TTAACCTACA CATTCTTGCT TTCTTTCTGT CTTGCCTGCT GTTTTGAGGT 120
GTTTTAGACA TTGATGAGTT TAAGTGCAAG GTGCAATGTA GACACATGTT GGCTAAGTTT 180
GGGTTGCTTA TTACTAAAAA GATTTTCTTT TCATGTCTTA AAAGTTTTGC TTCTTCTCTA 240
CCCTCACTGT TATTTTTACA GCATGTATTC TAGCTCCTAA GCAATCAAAA CATGTAGTGC 300
TTCAGAAAGG AGGGAAAGTC ATGTGTGGTC TGAATCGTAA CACCAGAAGG AGAATTGGCA 360
TTTGTGCATC CTTCCCCATG GTGCCAGTCA GAGATGTTGG CTGAAAGCAA TACCATCAAC 420
TGTGGGTAAC TCGAGCAGAG AAGGAATTGA CAAAAAGGTA ATTTCCAGGA AGCCTGGAGA 480
ACCAGGCTTG GACAGAACCA GGCTTGGACA ACAGGCTAAA CACCAAGGCT GTCCAGGCAC 540
ACAGGACACC AGCCAGGACC AGTGTCAGGA ACAGCCTGGC TGATAAGCCC CTATGGGTAC 600
TGCCTCTAGG GACCCTTGCC TGTGTTTCTG TGCATCAGCT TTAACCATCT TTACCTTTGT 660
GGGTCTCCCT CCAGAACTGA AGGCTTGGGA GGAGTTTCCA ATGGGTAAAC TGGGCTATTT 720
GTCCATGCCC ATACTACCTG GGGGAAGAGG GAATGCGTTC AGCCTTTCGT GAAGATGCAG 780
CCCTTCCCCA CACCCGGGCG TCCTCACTGA GGAAGACTCA CAAATAGGAT GAGGGGTTGG 840
GGAGAGGGCA ACCAAAGCAA TGGCCCAAGT CCACTCTAGC CCACTTTTTC ATTCCCAGTA 900
CCCACGTGCA ACCCTCTTCC AGGAGGAGCT CCCAGAAGCC ATGCACCTCC CTGTCCATAT 960
TGCCTGTCAG AACTTTTGGT AATTGGGATC AGTTAATCAC CCGAGCCAAC ACTTCAGCTC 1020
TCCTCTTTCT GTTTGCCTGA TGGCACAAGG AGACAACATA CCAGGTGTCT CTATTCACTT 1080
CCCTTCACCA TGACTCCTTG CGCAAGCACT TCCCGCTTCG GTACTGAAGC CTCAAAACCA 1140
GCTGAGAACA GATTCGTGAA GACAGGAAGC AAAAAACTCG AATGGATCAT TCAGTATAAC 1200
TTTATCCACT TCCACCTCCC GCTTCTTAGC TCTGTGTATT CTGGCTATGG GAGGGGCCAA 1260
ACCTTGTGTT CTTTACTGAT TCAGAGCATA CACTACATCC TGCCACCTAG CACGCCAATC 1320
TCTGAAAGTG TTATCATTGT GTCTTTGGAA ACTCATGCCA TGTCACTGTT CTATGACTTC 1380
TGGATAATGG GGTATGTGAC 1400
|
