| Tag | Content |
|---|
EnhancerAtlas ID | HS105-33951 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr17:37641480-37642880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr17:37642797-37642808 | CATGAGTCACC | - | 6.62 | | IRF1 | MA0050.2 | chr17:37642198-37642219 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 | | JUND | MA0491.1 | chr17:37642797-37642808 | CATGAGTCACC | - | 6.02 | | NFKB1 | MA0105.4 | chr17:37641763-37641776 | AGGTGATTCCCCT | + | 6.22 | | NFKB1 | MA0105.4 | chr17:37641763-37641776 | AGGTGATTCCCCT | - | 6.5 | | SREBF1 | MA0595.1 | chr17:37642261-37642271 | GTGGGGTGAT | - | 6.02 |
|
| | 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 |
| GH17I039484 | chr17 | 37640956 | 37643546 |
|
Enhancer Sequence | TACCTAATCT GTATTAGTAC TTTATTTGAG CTCATAAAGT AAACATTGGA GAAAACAAAA 60
ATATGAAACA CAGATTGGCT GGGCATGGTG GCTGATGCCT GTGATCCCAG CACTTTAGGA 120
GGCCAAGCTG GAGGATTGCT TCAGGTGGGA GTTTGAGACC AGAGCTTAGG CATCCCCCCC 180
CTTTTTTTTT TTTTTTTTTT TTTGGGAAAC AGAGTCTCAC TCTGTCGCCA GGCTGGAGTG 240
CAGTGGCTCA ATCTCAGCTC ACTAATCTCC ACCTCCCGGG TTCAGGTGAT TCCCCTGCCT 300
CAGCCTCCTG AGTAGCTGGG ACTAACAGGC GGGTGCCACC ACGCCTGGCT AATTTTTTTT 360
GTATTTTGGT AGAGACAGGG TTTCACAATG TTTGCCAGGA TGGTCTTGAT CTCCTGACCT 420
CATGATCCCC GGCCTCGGCC CCCTAAAGTG CTGGGATTAT AGGCATGAGC CACTGTGCCT 480
GGCCCCTGTC TCTTAAAAAA AAAAAAAGCA GCTGTGGTGG TATGCACCTG TAGTCTCAGC 540
TGCTTGGAAT GTTGTAGTGG GTAGATCACT TGAGCCTCGA GGCTGCAGTC AGCTATGATT 600
GCACCACTAC AGTCCAGCTT GGGTGACACA GCAAGATCCT GTCTCCAAAC AGACAAAAAA 660
CCATAGACTG AATTTATTTG AAATGATGAT GACACAATTA AAATACCTTA ATTTTTCTTT 720
TTTCTTTTTC TTTTTTTTTT TTTGAGACAG AGTCTTGCTC TGTCGCCCAG GCTGGAGTGC 780
AGTGGGGTGA TCTTGGCTCA CTGCAACCTC TGCCTCCTGG GTTGAAGCGA TTCTCCTTCC 840
TCAGGTTCCC AAGTAGCTGG GATTTTGGGA GTGCACCACC ATGCCCAGCT AATTTTTGTA 900
CTTTTAGTAG AGATGCGGTT TCACCATGTT GGCTAGGCTG GTCTTGAACT CCTGACTTCA 960
GGTGATCCGC CCGCTTGGCC TCCCAAAGTG CTGGGATTAC AGACATGAGC CACTGCACCC 1020
TGCCTCTTTT TTTTTTTTTT TTTTTTTTCT GTGAAACAGA ATCTTGCTCT GTCACTTAGA 1080
CTGGAGTGCA GTGGCACAAT CATGGCTCAC TGCAACCTTG GCCTCCTTCC CTGGCTCAAG 1140
TGATCCTCTC GCTTCAGCCT CGATAGTAGC TGGGACCAGA AGTGCATGCC ACCACTCCCA 1200
GCTAACTTTG TTTATTTTTT TTAGAGATAA GGTCTCACTA TGTTGCTCAG GCTGGTCTTG 1260
AACTCCTGGG CTCAAGCAAT CTTCCTGCCT TGGCTCCCAA AGTAGTGGGA TTACAGGCAT 1320
GAGTCACCAT GCTCAGCCTG ATTTTTCTTG TTCTTCTAGT GAAGCCAAAC CAAGAAGAAA 1380
TCTGTTTTGA ATAATGAGGA 1400
|
