| Tag | Content |
|---|
EnhancerAtlas ID | HS150-00598 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr1:78702200-78703660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:78702598-78702609 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr1:78702598-78702609 | GGGTGACTCAG | + | 6.02 | | PRDM1 | MA0508.2 | chr1:78703081-78703091 | GTGAAAGTGA | - | 6.02 | | RUNX1 | MA0002.2 | chr1:78703110-78703121 | CTCTGTGGTTT | + | 6.14 |
|
| | 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 |
| GH01I078237 | chr1 | 78703441 | 78703590 |
|
Enhancer Sequence | TCTGGTTGTA CTGAAGAAAA ATCTGGAGAC AGGTCTTTTG TCCTGGTAGT GAGATTGCAA 60
GATTTGTCTG AAAAGAAAGT TGGAGTTTCT GAAACAGGAA TCAAGGCAAA AAGAATCCCA 120
AGAACAAGAA ATGGAGCAGA GAGACTGCGA ATTGAACAAG ATATGATAAA GGATTTGCAA 180
CAGAGTTGTT GTTCACCTCT TACCTTCCTC AACTAGACTG TGGGCTCCCT GAGGGCAGGG 240
CTCTTAACTT CCTTATCCTT ATTTCTTTTG CGCCTGATAT AGGGTCTGGT GCAAAGTAGG 300
CTTTCAGATG TTTTTTAAAT AAGTTAATAA GTAAATGTGA GATTGGCAAG GGTGACTTGA 360
TGCTGAGCTC TGGAATGTGG GCTGGAATTA CTTGGTCTGG GTGACTCAGT TCATACTGGG 420
TCCTGGGATT TGGATCTGGA GCTGCACTTG TAGATTTGGA GTTAAGAGAG GGAGGAATCA 480
GACTGATTGA AGACATTGGC TGAGGCTACA GTTAGGATAG TTTAGGGTGA CTTCTGAAAG 540
AAGGTGTGAT TTGAATCTGG CTTGAAGCAA GACAGATATT AAATAATTCA ATCCAACTTA 600
ATGGACATTA GTTGGGCATC TGGTCTGCAC AATGGCTTGC AACCCAATGG TGGGTAAAAT 660
ACAGTTCTTG CCTTGTAGGA AACCAAAAGG AAAGAAATGA CTGAAACATA ATGTTATATT 720
TGGATGGGGA GGTATGGGAT GTGAAAAGGA AAACTATGGA GGAAAATTGA GAGGAGGGAT 780
AATGTTTACC TGGGCCTTAA AAATTGGTCA AGCTTTGTTC TACAGTTAAG GCAGGGAAGG 840
ACTCTCAGTG GAGAAAACAG CCAGAATAAG AGTAGGTAGG CGTGAAAGTG AAGGTGACCT 900
GGGAGGTAGC CTCTGTGGTT TGGTGGATGA GAGCACAGCA TGAATTATGG GTAGGGGGTC 960
TGGACCTCAA ACAAAGGTTA ATGGGTTAAC AAGGGGGGGT TTATTGGGTG TTAATGGGTG 1020
TTAACAAGGG CGGATTTATT CTACAAACAT TTAAATTTGT CAAAGTGTTT GTTTTAAGCA 1080
GAAGAATCAC ACAATTCAAC TTATATTAGG AAGAGAATTT GGGCCAGAGG GTAAAAGAAG 1140
GCCTGCAGGA GAGGAAGGCC AGAGGGAGGA ATCTGGGCAG GGCAGCAAGG CGAGCCACAC 1200
TTCACCTAAA CTAATTCCTG CTGAGATACT AAAGTAAATA ATGGCTTAAG ACAAACTCCC 1260
TCTGAGTGAG CTGTTTGCCT TTGAACTGGC CCCTCCTCAC CTGGAGGAGG TGTGACTTCT 1320
AGTGGATAGA CTTGCCAGGC CACTGGGAAG ATTTGCCAAT TTTTGATTCA TTCTTCTCAC 1380
GCCCATAACT GGCTCTTACT AGCTGTTCGG CCCTGAATAT GAAATGCAGT TTTGTGACCT 1440
GGCTGAGAGT TCACAGGCCC 1460
|
