| Tag | Content |
|---|
EnhancerAtlas ID | HS098-14116 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:95496370-95497400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr12:95496592-95496603 | AAATCACAGCT | + | 6.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_36502 | chr12:95496115-95498227 | HMEC | | SE_65110 | chr12:95496509-95498232 | NHEK |
|
| | 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 |
| GH12I095102 | chr12 | 95496201 | 95498305 |
|
Enhancer Sequence | ACTGCTAGCT GCGAAGCATT TGACAAACCC TAGACACAGG TATTTGTCTT CTCCTGTCAT 60
CCTGTATGTC AGGCAGCAGT AGCCATTGCA TTTCAGAGGA GTAGCACACC CCAGGATGAC 120
TCTTGTGGTC CTCTGATTTT GGGAAGTCAG ACATTTGGTT TGAGTCCTTG ACATTCATGG 180
ACGTAAGCAA AATTATAAAG GTTGTCAGAA ACACCTAGGT TCAAATCACA GCTCCACTGC 240
TTACTACTCG TGTAACCTTA GATGTGTTAT TGAACCTCTC TGAGCCTCCA TTTTTCTAAT 300
CTGGAAGATC AAGATAATAT CCACCCCACA AAGTTATCAT AGAACTTAAA AGAGAAAATA 360
AATATAAAAC GAAACATGAG CACTGTGACT GATGCAGAGT AATAAATGAT TCTGGCCACT 420
ACTCCACCTG CTCCTAAGAT CCTAGTTGAT TTCAGTGGTA TGGACAATTG GAAACAGACT 480
GCCTGGTTTC AAATCCTGGC TCTGCTAGTA TAGCTGAGTG GCTTTTCTCA GCATAGAATG 540
GGTATAATAA CGACAACTTG CCTTACAGGT TGCTGTGAAG ATGAAACGAA GTACTACACA 600
TAAAGTCTTT ATGATGGTGC CTGGCATACA GTAAGTGTTA CAAAAGCGTT TGCTTCTATT 660
TTTATTAGAT CAAAGGTTAG GTCTGAGAAG ACAGTGTCTC ATTATTTAGA TTGTGCAGTG 720
GAGCATGCTA TGACTATTGG CATCTCTCCC TTCACCAGTC AAACCTTCCC AAATACCCAC 780
TTCCGCCACT CAGTCAGTAA CTCAGTAATG TATTTTTATG AGTCATAGAG TTTCAGGTTT 840
CCTCAGCACT TGAATTACAT TATGGCAACA TATTAAGTCA CTGCAGGTTC CGGTCTGGGG 900
CAAGGTGGTA TCATAAATAA TAATGGATTT CTTTTCCCGC CCTCCCTCCA TTCTTTCTGA 960
GATGGAGTCT TGCTCTATCA CCCAGGCTGG AGTGCAGTGG AGTGATCTCG GTTCACTGCA 1020
ACCTCCACCA 1030
|
