| Tag | Content |
|---|
EnhancerAtlas ID | HS146-10033 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr22:44946370-44947480 |
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 | GCCACCGCGC CTGGCCCACG TCCAGCTAAT TTTTGTATTT TTAGTAGAGA CGGGGTTTCA 60
CCATGTTGGC CAGGATGGTC TTGATCTCTT GACCTCGTGA TCTGCCTGCC TTGGCCTCCG 120
AAAGTGCTGG GATTACGGGT GTGCGCCACC GTGCCCAGCC TCGAAATATC TTTATTCTAC 180
TCTCCTAGCT GATCAGTGGC TTGAGTGGTT ATCCTAGGCC CAGTTCAGTC CAGGAAGAGA 240
AGCCACAATG AGCATTGTGG GAGGAGGGGC CCATCATAGG AATGAGACCT TGCACAATCC 300
TAGGAAGAGC AGGGGAGCGG AGCTGGGGAG GAGGGGAGCG GGAGAGTCAG GAAAGACTCA 360
GCAGCCAGCC CTCCTGAAGC CTGGGGCAGG AGGCCAGCTC GGAGCTTGCA GGAAAGTCAT 420
GAGAAAGTCA CGCACATCCA GCTGCACGGG TCAGGGCGCC GGGGGAGGTC TGGCCAAGAG 480
GCTGCAGGAG CTGCTGCCTC TGCAGCTGCC ACCTCTGTGG GGAAGCCCAG GGCCACTGTC 540
GGGGCAGCAG GGTCAACGGT GGGGAGCATG AGCAGGACCC AGGGTGAGGA AGAGTGCGGA 600
CACCCTGGAA CTCACGGAGC ACCTGTGCAG CGGTCTCTCC CCATCTCCGA TCACAAAGTC 660
GCTCAGAGGA GCGCAGCCTG CTTGCTTTTG CCTGCCAACA GCCCGCGAGT TGTCAGCCTG 720
CCATCTAAAC AAACCCCTTC TCACTATATT TAACTTCCTA ATAAAGACAG CAATGAAATC 780
AGGCTGCTTC CTCACACGAT GCAACTGTTC CTTATTAAAA TCGAAAGTGC ACTAACCTTC 840
TACCCTCCCA GCCTCAAAAA GAGACTTTCT CCATCTGCGA AGGGGGCAAT CCCCCTTCTG 900
GCTGAGTCAC TCCCTCTTTG ACATCCTGTG ACTTAAGTAT CAAGACGTAA GGCCAGTCAC 960
GATGAACACA GCTTATGTGA GATAGCAGGG GAATGGAAGA AGGAAATGAT AATTGGTTAA 1020
TATGGGGGCC GGGCGTGGTG GCTCATGCCT GTAATCCCAG CACTTTGAGA GGCTGAGACA 1080
GGTGGATCAT CTGAGGTTAG GGGTTCAAGA 1110
|
