| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00731 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:28015520-28016970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:28016166-28016187 | ACTCTCTTTCAATTTCATTTT | + | 6.47 | | REL | MA0101.1 | chr1:28016893-28016903 | GGGGATTTCC | + | 6.02 | | STAT1 | MA0137.3 | chr1:28016877-28016888 | TTTCTGGGAAA | + | 6.02 | | STAT3 | MA0144.2 | chr1:28016877-28016888 | TTTCTGGGAAA | + | 6.32 | | Stat4 | MA0518.1 | chr1:28016877-28016891 | TTTCTGGGAAAGGG | + | 6.56 |
|
| | 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 |
| GH01I027685 | chr1 | 28011638 | 28017588 |
|
Enhancer Sequence | AATAACAGGG AGCGGAAGGA AAAACAATTG TTCTTGGAGA GTCCATCCAG TCTTTATATA 60
GATAGTGGGA GAAGTCTCTT CTAGTGGCTG TGGATCTCGA AAGGCCTTTA ATTAAAAATT 120
TAAAATACTC ATTATACCAA AGGGAGCCAT ATTTTTGGGT GAAGTTCTTT GAGCTCCTTC 180
AGGAGAGTCT CCCTTCTCAG GGTAAACAAA TTTTACAGTG GCTTTTATCC AATCTACTGG 240
GCTGGCTGTT CCCTCAGGAA TAACCTCCTG TTTGTGTGTG GGTCATGTAT AGCTACCTGC 300
AATTGTTCTG TAGTGTGCTG TGGATCCTGC ATCAACCTCA ACATGCTCTT CCATTCTGCA 360
GCACTTGAAA TCTAGTTACT CTTGCAATCC ATCTTAGTAA TGATTCCTCA GGAAGCTGAA 420
GATAGTAATC TACAAAATGG AATAATTCCT TCACATCGTA CCCTCTAGTC TATAGTGACT 480
TGGTTTTGCC CTTCCCCTAC ATTGACTGTC CTCTTGGTAA CCCAGTTCTC AGTTATTTTC 540
TGTTTCCCTG CGTAAGTTTT CCCTTGGGGA TCAGTTTGGA GGCTAGTGGC TGAAGCTCAG 600
ACTCACTGAA ATCTGAACTT GGTTTAGCAC CAAGGTCTGA CACAGCACTC TCTTTCAATT 660
TCATTTTAGC TATTATAGTT AACAGTAAAC AAGAATGTTT TTCTTTTTGC TTATTAGTTT 720
GCATTTCCTT ATGCATCCAG TGAATCAACT CTCCAGGAGT TGGTTCTGTC TCTAAATTCC 780
ATTCATAACT TTTATCTTCA GTAACTGAGC ACAGCACAGC TGCGGCTCTA AACCATGGGT 840
GACCACATGG CTACTCAGGG ATCAAAAGTT CCTCACCCAG CACTCTTTCA TCCTTTCTCT 900
TCCCAAACCA CAACTTTCCA TCAGCCCAGG CCATTCTAGC AAATCTCACT TCCGTGACAC 960
CAACTCTGCC AGGGTGGGGG GAAACAACAC TCAGTGTGCC TGTTCTATTA TCTCACTTAA 1020
CAACAACAAT CAACACAGAA GACTTTTGTG ACCAAATTTG TATGTGAGGA TTTCCCCACA 1080
CACCAAGCAG CAGTCACCAG TTGAGTGTCC TCTGATTCAA TTCAGACACT ACCTACTCTG 1140
AGATAGTGTT ATCAGAAAGG GGTCCCGATC CAGACCCTGA GAGGGTTCTT GTTGGATCTT 1200
ATGCAAGAAA GAATTTGGGG CAAGTCCACA GAGTAAAGTG AAAGCAAGTT TGTTAAGAAG 1260
AAACAAAAGA ATGGCTACTC CCTGAGGGCC ACTGGGTGGC TATTTTTATG GTTATTTCTT 1320
GATGATATGC TAAACAAGGG GTGAGGTATT CATTCGTTTT CTGGGAAAGG GGTGGGGATT 1380
TCCCAGAACT AAGGGTTCCT CTTCCTTTTA GACCATAGAG GGTAACTTCC AGATGCTGAC 1440
AAGGCATTTG 1450
|
