| Tag | Content |
|---|
EnhancerAtlas ID | HS047-20356 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr2:219094660-219095790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr2:219095156-219095166 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr2:219095156-219095166 | GGCACGTGCC | - | 6.02 | | SP2 | MA0516.2 | chr2:219095725-219095742 | ACCAGCCCCACCCACTC | + | 6 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_13998 | chr2:219092733-219096279 | CD34_Primary_RO01536 | | SE_18808 | chr2:219092605-219096775 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20558 | chr2:219092995-219096679 | CD56 | | SE_22627 | chr2:219092425-219096844 | CD8_primiary | | SE_59378 | chr2:219081057-219096488 | Ly3 | | SE_62975 | chr2:219080664-219095830 | Tonsil |
|
| | 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 |
| GH02I218228 | chr2 | 219093103 | 219096788 |
|
Enhancer Sequence | TGAAAGAAAA CAAATGGCTA TTAAAGCAGC CCTGCCTCTT TTTTTTTTTT GAGGTGGAGT 60
CTCACTCTGT TGCCCCAGGC TGTACTGCAG TGGCGCCAGC TCAGCTCACT GCAACCTCCA 120
ACTCCTGGGT TCAAGCAGTT CATCTGCCTC AGCCTCCTGA GTAGCTGGGA TTACAGGCAT 180
GCACCGCTAC ACCTGGCTAA TTTTTTGTAC TTTTCATAGA GATGGCGTTT CACCACATTG 240
GCCAGGCTGC TCTCAAACTT CTGACCTCAG GTGATCTGCC TGCCTCGACC TCCCACAGTG 300
CTAAGATTGC AGGTGTGAGC CACCGTGCCC AGCCTTTTCT TTTTTTTTTC TTTTTTTTTT 360
TTTTTTTTTT TTTTGACAAG GTCTTGTTCT GTCACCTAGG CTGGAGTGCA GTGGCACAAT 420
CACAGCCACT GCACCCCTCA ACCTCCCAGG CTCAAGCAGT CCTCTCACCT CAGCCTCCTG 480
AGTGTCTGGG ACTACAGGCA CGTGCCACCA CACCTGGCTT ATTTTTTGTT TGTTTGTTCT 540
TTAGAGAGAG GAGGTTTCAC TATGTTGCCC AGGCTAGTTT CAAACTCCTG GGCTCAAGCA 600
GTCCTCCTTC CTGGGCCTCC CAAAGTGCTG GGATTATAGA TGTGAGCCAC CATGTCCAGC 660
TGCATCGCTG CTTTGGATCA GCTATAACTA CCTGAAAAGA AGTGTTAAAA TATTTGAATA 720
GACTTTTTTT AAATTGTGTA ATCATTCTCC CCTAGACAGT CTTCACTAGG TGCAAGCCTG 780
CACAGTGGCA CACACCTGTA GTGCCAACTG TGTGTTGGGA CTTCACACAG TTGGCTTGAG 840
GGGTTCAAGT GGGGAGAGTT GCTGGAGCCC AGGAGTTCAA GTCCAGCCTG GACGACATAG 900
TGAGATTCCA CCTCAAAAAA AGGAAAAGAT CTAAATGCAA TAATAATAAT CCTGGAAAGA 960
AAGAGTTAAG CTAGATTTCT TAAATCTCCT TTCCATTCTG TGCTTTTCTT ACGATGGAGC 1020
TCCAGAACAC ATTGCTATTC TTGTAGCTAC CACAAGGGTC AAAGAACCAG CCCCACCCAC 1080
TCAAGTGGGT GGAGTAAGTA ACATTCATAG TGTTGGAGCA GAGTGCACAG 1130
|
