| Tag | Content |
|---|
EnhancerAtlas ID | HS138-00338 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr1:19838960-19839860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr1:19839581-19839591 | CTCAAGTGGT | - | 6.02 |
|
| | 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 |
| GH01I019512 | chr1 | 19839147 | 19839427 |
|
Enhancer Sequence | TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATTGCTTGA ACCGAGGAGG CGGAGGTTGC 60
AGTGAGTCGA GATCGCGCCA TTGCACTCCA GCCTGGGTGA CAGAGCAAGG CTCTGTCTCA 120
AAAACAAAAC AAAACAAAAC AAAACAAAAC AAAAAACCAC CTAAGATCAG AGAAAGGCAA 180
TCACCAAGTA AAAGGATAGG ACAGACAGAA ACTACTATTA ACTGCTTTAA TTCTGTCAGT 240
ATAATTCCCA CTGGGCCTAC CCACATGCCA ATTTCATTAG TTGATATGAT TTGGCTCTGT 300
GTCCTCCCCC ACATCTCATG TCGAATTGTA ATCCCCACGT GTCAGGGGAG GGACCTGGTG 360
GGAGGTGATT GGATCATGGG GGTGGAATTC CCCCTTGCTG TTCTTGTGAT AGTGGGTGAA 420
TTCTTATGAG ATCTGATTTT TAAAAGTGTG TGGCCTTTTC CCCTTTGTTC TCTCTCTTCT 480
GCCAGCATGC GAAGAGGGTC TTTGCTTACC CTTCACCTTC CACCATGATT GTAAGTTTCC 540
TGAGGCCTCC AAGCCATGAT TCCTGTTAAG CCTGCAGAAC TGTGAGTCAA TTAAACCCCT 600
TTTCTTCAAA AATTACCCAG TCTCAAGTGG TTCTTCACAG CAGTGTGAAA ATGGACTAAT 660
ACATTAATTT TCCAAGTTAT CTCAACGAGA ACAATAATAA CGATTACTAC TACATTTTAT 720
TCAGAGCCTA GGTACTGTGG CATGTGCTTT TTTTTTTTTT TTTTTTCTTG TGAAATAGGG 780
TCTTGCTCTG TCACCCAGGC TGGAGTGAAG TGGTGCAATT ATGGCTCACT ACAGCCTTGA 840
CCTACGAGGC ACAAACAATC TTCCCTCCTG AGTAGCTGGC ACTACAGGAT CACGCCACCA 900
|
