| Tag | Content |
|---|
EnhancerAtlas ID | HS078-02056 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:229980230-229980860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | + | 8.23 | | Ar | MA0007.3 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | - | 8.58 | | Foxq1 | MA0040.1 | chr1:229980815-229980826 | TATTGTTTATT | + | 6.62 | | NR3C1 | MA0113.3 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | - | 7.22 | | NR3C1 | MA0113.3 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | + | 8.14 | | NR3C2 | MA0727.1 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | - | 7.35 | | NR3C2 | MA0727.1 | chr1:229980718-229980735 | AGGTACACAGTGTTCCC | + | 7.67 |
|
| | 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 |
| GH01I229843 | chr1 | 229979382 | 229980770 |
|
Enhancer Sequence | CCCCTCTTGC CTGCAATTCT CAGAGAGAAG GTACTGAGAA TGCAACACCC TGAGATAAGC 60
AGGAACCATC TGAAACAGGC TGGGATTTAT CCATCCAGGA CATCTTCCTA GAACAGGATA 120
TCCTGCAAAG CTTGGGCTCA GCAAACCATG TTGCCCCTGG GGTATAAAAA CCAAAACACA 180
GCCCTTTCAG GGTCTCTCGG CTGGGATGCG AAGTGAGGCA CGTGTAGACA AGACTCCATC 240
TGCCCTGGGC AGCTTTCCTG AACCCGAGGG ACTGGTTTGC CATGGATCCT CGGCTTCTGT 300
TTATCTTTGC TGCTCACCTG TGAGTTGTAA ATCTGCTTTG CCTGACTTGT GTGACAGTTC 360
CATCTCACCA GACTCACTGG GACAGCCGGG CTAGTGCAAA ACCTCCTGCT AGACCTGGAA 420
GCCTGCCATA TCTAGGAACC TTAGCAGAAA ATGCAAGGAC TTTTGAGTGT TCCTCTAGGA 480
TTAGCAACAG GTACACAGTG TTCCCCTCAC AGGGATTGAT ACTGATGTAT GTTATTCTGC 540
TTCACAGGCA CTGTTTAGAG TTTTGCAGAC TGAGTGTTCA TTTCTTATTG TTTATTGTTC 600
TTGAGATTCC TTGGTGTTGC TGAATCTAAG 630
|
