| Tag | Content |
|---|
EnhancerAtlas ID | HS187-16246 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr22:35705540-35706320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr22:35705823-35705833 | ACCAACTGTC | + | 6.02 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_26916 | chr22:35705608-35714280 | Esophagus | | SE_29512 | chr22:35705714-35710610 | Fetal_Intestine_Large | | SE_35740 | chr22:35706215-35710142 | HepG2 | | SE_40932 | chr22:35705597-35713399 | Left_Ventricle | | SE_45844 | chr22:35700652-35712469 | Osteoblasts |
|
| | 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 |
| GH22I035309 | chr22 | 35705933 | 35712670 |
|
Enhancer Sequence | ACAGGAGAAT CGCTTGAACC GGTGAGGCGG AAGTTGCAGT GAGCCAAGAT CGTGCCACAG 60
CACTCCAGCC TGGGCAACAG AGTGAGACTC CATCTCAAAA AAAAAAAAAA AAAGAGAGAG 120
AACTGAGAGA CCTGCTGGGT TTCCCTTTGA GTGACAACAT CTGTGTCCAT CTAGAATGAA 180
TTCGTTCAGT AGTGGCTTCT TCTGTATTTC TGCCTAACCT TCTTGACCAC ATTGGTTTCA 240
TCCTCGTGCT TGCATTCTCA CGGTAGGAAG CACAGGTGAA AGTACCAACT GTCTGTGTCT 300
CTGTTACCAA GAAAGCAAAA CCTTCCCCAG GAGCCGCCCA AGAGACACCC GCTTCCATCT 360
CTGTGGCCAG AAGTCCCAGG GCTACTTCTG GCTGCAAGGG GGTCTAGAAA AGCTAAATGC 420
TGTGAGCCCA GGGGGAGCAT CTTCCACAAC TATTGGAGTC AGCTCCACAT GGTAGGGTTA 480
ATAAAAATTT CACATAGTCA CTGAGTACAG TAATAGAAAT ACAGTATCTA GCAAGGACAG 540
GTAAATGTGG CGTGTGGGTT CCCACACTGC ATTTCCAGAT GGACAGCATG GCTGGCCTAT 600
ATCCAGAGGG GTCGGTCAGA ATAGGGTGAA GGCTCTGGAG ATCATTATCA GAGTGGAGTG 660
GTCACAGGTC CTGAGGATGT TGGAGGACAG ATTAAGGAGG GACGTGGTAC TTTTTAAAAG 720
TATTCAAAGG GTCACGGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCCAAGACGG 780
|
