| Tag | Content |
|---|
EnhancerAtlas ID | HS076-11130 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr11:75161520-75162900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:75162690-75162709 | CAGCTCCCCCTTGTGGCCA | - | 7.25 | | E2F6 | MA0471.1 | chr11:75162353-75162364 | GGGCGGGAAGA | + | 6.14 | | RREB1 | MA0073.1 | chr11:75161827-75161847 | ACTCCACCCACCCCCCTCCA | + | 6.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 75161998 | 75162079 | | chr11 | 75162200 | 75162563 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I075451 | chr11 | 75162621 | 75162750 |
|
Enhancer Sequence | GCACCCTGGG CTGGGCTCAC AGTGGCACTT CAGGCGGGAG TGGGTGGTGA AACACATCGC 60
CACCTGCCCC ATCTCCACGG CCTGCCCTCT CCCGGACTCC CAGCATCTAG GTCCGCCGTG 120
ATGGGGGCCA TCCTCCTTGC AGCCTCCAGA AGAAAGCAAA GCACAGCTCT CATGGAGGAT 180
GAGGTGGCAC CTCTACGGGA CAGAGATCTC TGGTGACAGG TAAGACCTGA AATCTTTAAC 240
CACGTGAAGC TCGGCAGAGG TTTTCGGCTC CTCGGCCCCC AGCCCCTCGC CCCTAGCCGT 300
GGATCTCACT CCACCCACCC CCCTCCACAC CCCCAGGCGT GCCTCCCCGA AGCCCAGGTT 360
GTGGCTCTCC TCCAAAGCCT CCCGCAGATC CCAGTCTCTG GAAGGGTCAG TCAAAGCCGC 420
CACCTCCGTC CCCCTAGTTT CTCCAGACTC GTCTCCCATC TCCCTCCAAA GGCCTGTCCT 480
TCTCCCACAG CACTGCCGGC CGCCCTGCCT CCCTGGAGCC GTTCTAGCTG CTGGCAGGGC 540
CTTCACCCCC TTTCTCCCGA GGCAACCTTT CCCAGAGGCA GCAGCGGCCA GGGCCCTCTG 600
ATGCCGAGCA GGGACAGTGG CATTTCTAGA CGATGAGGGT GGGGCGGTGG CCAGCATCTC 660
CGCTCCCTAC CCAGGGACCT TCACTCGCCG GCGGGGAATG CTGAGTCTCG CCTGGGATGA 720
AGTTTCCCTT TGGAGGCTTT TCATTCCAGC CCATCAGCCT GGAAACAAAT GTTCCCCCAA 780
GAGACCTGAG CGAGGCAGGT GAGGAGCTGG AAGGGCTGTG ACATGGGGGC TCGGGGCGGG 840
AAGAGGCATG GGCGTGCCTG GGCCTGTGGG GGCGCTTCGC GTGGTCCCCA GGTTGGTTCC 900
GCGGAGGCAC GAGCATCCTC ATCTCACACA CGGGAAGCGA GGTTCGGGGA GAGGAACAGC 960
TGGCTGGGTC ACGGAGCTTT GAAGGGGCAG AACCAGAAAC GAACACCTTC TGCCCATCTC 1020
AGGGGGTAAG GGGGTGTGCG CTTTCTCGGA CAGACAGCAC GCTGGTGTCA GAGAGGCTGC 1080
GCAGTCTCTG GGAGGCCCAG CTGCGCCTCC GAACCCCTGA GAACCCCGCC CTCGGCACTC 1140
AGGCCCCTTC TCCCGGCTGC CCCCGGCGCG CAGCTCCCCC TTGTGGCCAT CGTGGGAGGT 1200
GGCCCTGCAC ACAGTGAGTT AAGGATGGTT TCCAGGAGCA TCTCATCACA ATACCTATTA 1260
ATGGAAACGA CTTGCAATAA AACTGATTCC CCAAACCCTA ATACAATTAA AAATGTTATT 1320
ATCTCTGAGT TCCACAGTTG CTTTGGTGCT AATCAACACA CTCAGCAGCA TCACTGCATG 1380
|
