Tag | Content |
---|
EnhancerAtlas ID | HS138-25724 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr22:44946280-44947650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr22:44946569-44946580 | CTTGAGTGGTT | - | 6.32 | Nr2f6(var.2) | MA0728.1 | chr22:44946451-44946466 | TGATCTCTTGACCTC | - | 7.23 |
|
| 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 |
GH22I044550 | chr22 | 44946336 | 44948302 |
|
Enhancer Sequence | GACGGGGTTT CACCGTGTTA GCCAGGATGG TCTTGATCTC CTGACCTCGT GATCCACCTG 60 CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACCGCGC CTGGCCCACG TCCAGCTAAT 120 TTTTGTATTT TTAGTAGAGA CGGGGTTTCA CCATGTTGGC CAGGATGGTC TTGATCTCTT 180 GACCTCGTGA TCTGCCTGCC TTGGCCTCCG AAAGTGCTGG GATTACGGGT GTGCGCCACC 240 GTGCCCAGCC TCGAAATATC TTTATTCTAC TCTCCTAGCT GATCAGTGGC TTGAGTGGTT 300 ATCCTAGGCC CAGTTCAGTC CAGGAAGAGA AGCCACAATG AGCATTGTGG GAGGAGGGGC 360 CCATCATAGG AATGAGACCT TGCACAATCC TAGGAAGAGC AGGGGAGCGG AGCTGGGGAG 420 GAGGGGAGCG GGAGAGTCAG GAAAGACTCA GCAGCCAGCC CTCCTGAAGC CTGGGGCAGG 480 AGGCCAGCTC GGAGCTTGCA GGAAAGTCAT GAGAAAGTCA CGCACATCCA GCTGCACGGG 540 TCAGGGCGCC GGGGGAGGTC TGGCCAAGAG GCTGCAGGAG CTGCTGCCTC TGCAGCTGCC 600 ACCTCTGTGG GGAAGCCCAG GGCCACTGTC GGGGCAGCAG GGTCAACGGT GGGGAGCATG 660 AGCAGGACCC AGGGTGAGGA AGAGTGCGGA CACCCTGGAA CTCACGGAGC ACCTGTGCAG 720 CGGTCTCTCC CCATCTCCGA TCACAAAGTC GCTCAGAGGA GCGCAGCCTG CTTGCTTTTG 780 CCTGCCAACA GCCCGCGAGT TGTCAGCCTG CCATCTAAAC AAACCCCTTC TCACTATATT 840 TAACTTCCTA ATAAAGACAG CAATGAAATC AGGCTGCTTC CTCACACGAT GCAACTGTTC 900 CTTATTAAAA TCGAAAGTGC ACTAACCTTC TACCCTCCCA GCCTCAAAAA GAGACTTTCT 960 CCATCTGCGA AGGGGGCAAT CCCCCTTCTG GCTGAGTCAC TCCCTCTTTG ACATCCTGTG 1020 ACTTAAGTAT CAAGACGTAA GGCCAGTCAC GATGAACACA GCTTATGTGA GATAGCAGGG 1080 GAATGGAAGA AGGAAATGAT AATTGGTTAA TATGGGGGCC GGGCGTGGTG GCTCATGCCT 1140 GTAATCCCAG CACTTTGAGA GGCTGAGACA GGTGGATCAT CTGAGGTTAG GGGTTCAAGA 1200 CCAGCCTGGC CAACATGGTG AAACCCCATC TCTACTAAAA ATACAAAAAT TAGCTGGGCG 1260 TGGTGGCAGG TGCCTGTAAT CCCAGCTATT CGAGAGGCTG AGGCAGGAGA ATCACTTGAA 1320 CCTGGGAGGC GGAGGTTGCA GTGAGCCGAG ATCACACCAT TGCACTCCAG 1370
|