| Tag | Content |
|---|
EnhancerAtlas ID | HS105-20889 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:122072300-122073030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:122072641-122072662 | GGGAGAGGGAGAGGGAGAGGG | + | 6.44 | | ZNF263 | MA0528.1 | chr12:122072632-122072653 | GGAGGGGGAGGGAGAGGGAGA | + | 6.53 | | ZNF263 | MA0528.1 | chr12:122072639-122072660 | GAGGGAGAGGGAGAGGGAGAG | + | 6.5 | | ZNF263 | MA0528.1 | chr12:122072623-122072644 | TGGGGAGAGGGAGGGGGAGGG | + | 6.77 | | ZNF263 | MA0528.1 | chr12:122072629-122072650 | GAGGGAGGGGGAGGGAGAGGG | + | 8.08 | | ZNF263 | MA0528.1 | chr12:122072635-122072656 | GGGGGAGGGAGAGGGAGAGGG | + | 8.44 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_22457 | chr12:122072473-122073347 | CD8_primiary |
|
| | 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 |
| GH12I121634 | chr12 | 122072474 | 122073347 |
|
Enhancer Sequence | TGCACTCCAG CCTGGGCACC ATTGAGCACT GAGTGAAGGA GACTCCGTCT GCAATCCCGG 60
CACCTCGGGA GGCCGAGGCT GGCGGATCAC TCGCGGTTAG GAGCTGGAGA CCAGCCCGGC 120
CAACACAGCG AAACCCCGTC TCCACCCAAA AGATACGAAA ACCAGTCAGG CGTGGCGGCG 180
CACGCCTGCA ATCGCAGGCA CTCGGCAGGC TGAGGCAGGA GAATCAGGCA GGGAGGCTGC 240
AGTGAGCTGA GATGGCAGCA GTACAGTCCA GCTTCGGCTC GGCATCAGAG GGAGACTGTG 300
GAAAGAGAGG GAGAGGGAGA CTGTGGGGAG AGGGAGGGGG AGGGAGAGGG AGAGGGAGAG 360
GGCCTTTCTT CTCACTTTGA ATCATTCTTT TACACGGCCC CCTGAACCCT GTGGCATTGA 420
ACTTGGTTCC AAGTGTGGGC ACATACAGCC TGCCTAAGTG GACGGAGTTC CAGGAATCGT 480
AGGGTCTGGT GAGGGTAATG GGCTTTCTTC CGGAGCAGGG CAGCAGGCCC TTTCCTCTTC 540
CTCGGAGAGC CCAGCCTCTC CCCTCTCCCC AGCCCAAAAC CTCAGGGCTG GCGAGTGTGG 600
GTGTCCCCGG GCCGTGTGCG TCCCAACAGC TGCACTGCTT TCTGGCCCTG GAGCCTGTGG 660
GTGTGACAAA TGGTGTGGAA TGTGGTGGTC TCTGTCCTGT GGAGGTGGCC ATCAGGCCAG 720
GTGTGGCGTG 730
|
