| Tag | Content |
|---|
EnhancerAtlas ID | HS141-00805 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:95200450-95201780 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:95200685-95200703 | GAAAGGAAGGGAGGAGTG | + | 6.42 | | EWSR1-FLI1 | MA0149.1 | chr1:95201108-95201126 | GGGAGGAAGGGAGGCAAG | + | 6.44 | | Mecom | MA0029.1 | chr1:95201458-95201472 | TCTTATCTTCTCTT | - | 6.13 | | Stat6 | MA0520.1 | chr1:95201576-95201591 | ATTTCTCTGGAAAAG | - | 7.58 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_50020 | chr1:95199951-95203706 | RPMI-8402 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 95200679 | 95201609 | | chr1 | 95200535 | 95201697 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I094734 | chr1 | 95200319 | 95201910 |
|
Enhancer Sequence | TTTCAGAATT CCTGGGCAAT TTCAACATAG AGCGAAGGTG AAGAATCTCC AGTTTGGCAC 60
GGCTCAGGGT CTTGGAGGCG CCATTTCCAC GTTTGCAGGA GAGAGGATGT GATTGGCCCA 120
GCCTGGGTCA GGTGTCCACG CTGGTCCAAT CAACTGTGGC TGTAGACAGG GGCACCGGGA 180
CAGGATGGGA ATAAGCAGGG GTTTTTTTTA GCTCAGCCTC TCCTGCTAAG GAGTGGAAAG 240
GAAGGGAGGA GTGGCCCGGA CAACATCAAG GTTCTGTAGT TCCACATGGC ACAGGCAAAT 300
CAGGTTTCGT GTTTACCTCT TGCTCCTTCT TCCCAGGACA AAGCCCTGGC CTTAGTGGAA 360
AATGAGTACT TTATATCACT GGCACGGGTC CCATTACTCC CTCCCTGCCC GAAAGGACAA 420
AGGGAGTGGC CTCGTCCCTG GGCTGCAGTC CCCAGGCTTC CCTCCTCCAC CAGGAGCCCG 480
AGCTGCCTGA AGGTGCCTCT CTCAGAGCCA TTTAACCAAG TCCCTCGGCA AAGAGCATGT 540
CTGCTGGGAA GTGGAAGCAA ACAGCTGTGA AATGATAGGC TGGAATCAAC TTCTTTTTTG 600
TCATCAGAAT GAGTGACGGG GGAGTGAACT GTGGCTTCAT ATTTCCACCC AGATTTGGGG 660
GAGGAAGGGA GGCAAGAAAT TGCTGACCGG AGGAATTTGA ATGCTAGAGA AGCTGGCCAT 720
TTGCTGTGTC TTCCCTCATA TTTACTTCAA CTGTTGTTAG GCAGTTCCTC CCACTCGCCT 780
AAGACCCGTC TTCCTAAATG GAGAATTCCT CACACCCGGC CTCAACGGGA GGTGAAACCT 840
GGGCTGCATT TGAAGGGACT TAGCCTAACC GCAAGAGATT CATGTTTCCT GTGCCTCCAA 900
CTCAAAGTCA GATTGCTATG GGGGCGTGGA TCTTAACATA ACTATCCAAA CCCAAGAACA 960
GCCCGAGGGT GGGTTGGAAG AGGCCTCTTT GTCTTCCTGT CTGCCAGGTC TTATCTTCTC 1020
TTTTCATATC CTGGTCTTGA TCACCGCTTC CACAGTGTTT TTATACTTGG CCCACTTGGC 1080
AATTTATGCA TGTGTTTTTG AGTGAATATT TTTCAGTTTT GTTTTTATTT CTCTGGAAAA 1140
GCTAAGAGGG TTATATTGCT GTGCCAAGAC AGAGGACTTA CTCTAGATTC AGAAGACCCA 1200
GATCTCAAGT CCCAGATCTT CCAATTGCTA GTTTTGTACC TTAGGCAAAT GACTTCGGTC 1260
CCCCCACCCC CATTCTCCTG TGGCTGTGTT TATACTTCTC TTATTATAGC TATCCTATGT 1320
CTGTGTTTCC 1330
|
