| Tag | Content |
|---|
EnhancerAtlas ID | HS187-19863 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr5:114969670-114970650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr5:114970181-114970202 | TACCAGTTTCAGTTTCAGCTG | + | 6.34 | | IRF8 | MA0652.1 | chr5:114970185-114970199 | AGTTTCAGTTTCAG | - | 6.86 | | Nr2f6(var.2) | MA0728.1 | chr5:114969724-114969739 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 114970000 | 114970132 | | chr5 | 114970134 | 114970432 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I115634 | chr5 | 114969844 | 114971130 |
|
Enhancer Sequence | AATTTTTGTA TTTTTAGTAA AGATGGGGTT TCACCATGTT GGTCAGGCTG GTCTTGAACT 60
CCTGACCTCA TGATCCGCCC ACCTCGGCCT CCCAAAGTTA GCAATTTTGG GAATTACAGG 120
CATGAGCCAC TGTGCCCAGC CTATCCCTGA TATTTAAGAG AAAGCCAAAT AGACACATCA 180
ATGCATTATA TTTCACAGTT CCTTAATCTG TTTGAAGAGA TGGACACAAA AATATACACA 240
AAGGACACAT TTTCAGACCT TTGTGAATTC CCAAATCTAT GAGTACTTCT GCAGCATATG 300
ATTTTTCTAC AGCAGGCAAT GCATTTGAAG TTTAAAAATT AATGTGAAAT TTTCAGAGCC 360
TTACTAAGAG TGATTGCCAA CTTGATAGTG TATTGAATAG AAAGCAAAAC CACAAGGAAA 420
CCCTGATGTT GGCCAGTAAC GCAAATCATA TTTGTGTCTC AAGAAAAGAA CAAATTCAGA 480
AGCCACTAGT CCTCAAAAGC CACTTACCAC TTACCAGTTT CAGTTTCAGC TGAAACTGAA 540
AACGCGAAAT CTCTGGAAAC CAGGAATCCA GGCTACTAGA TTGTCAGCTC CTCAGAAACC 600
TCTGTAGTTG GACCATGTTG CTCACCTTCC TGCAGAAATT CCTCAACATT ATAAAGATTT 660
CAGATTATAA ACATAATATT ACGGGGCAAT ATTTTAAATC CTCATTTAAA ATGGAAGTTG 720
AAGACAGTAA CAAACACACC ACCTTCCTTA AGAAAACCAG TTTTGCATTC TCCAAAATGT 780
AGGGAGCAAC AGAGAAAGAA GTTTCTCTTG TAAATGACCA GTGAACCGGA AACCACGCTG 840
TGGCTTTCAT ATTCATCGGC TCCCTTTCAA CTCTCCCTCC TACCCCACCA ACACCAAGCT 900
GGCCACTAGG CGGTGCTGCT CCCATTCTAA TATTACTGCC CAGGCACCAA TAATGGATTG 960
TTCCTTTTTC ATCTGAGATT 980
|
