| Tag | Content |
|---|
EnhancerAtlas ID | HS023-16863 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr22:18324780-18325790 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr22:18325238-18325248 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr22:18325238-18325248 | GGCACGTGCC | - | 6.02 | | IRF8 | MA0652.1 | chr22:18325326-18325340 | ACTTTCGGTTTCAT | - | 6.72 | | MYCN | MA0104.4 | chr22:18325342-18325354 | GGCCACGTGGGC | + | 6.27 | | MYCN | MA0104.4 | chr22:18325342-18325354 | GGCCACGTGGGC | - | 6.27 | | Nr2f6 | MA0677.1 | chr22:18324887-18324901 | CAGGACAAAGGTCA | + | 6.08 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_05876 | chr22:18323949-18325741 | Brain_Hippocampus_Middle | | SE_23167 | chr22:18324737-18325691 | Colon_Crypt_1 | | SE_24250 | chr22:18324867-18325658 | Colon_Crypt_2 | | SE_27268 | chr22:18324050-18325699 | Esophagus | | SE_40598 | chr22:18324155-18325748 | Left_Ventricle | | SE_52809 | chr22:18324750-18325684 | Small_Intestine | | SE_54633 | chr22:18323752-18339434 | Stomach_Smooth_Muscle |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I017841 | chr22 | 18324638 | 18325606 |
|
Enhancer Sequence | AACCTGCGGG ACAAGCACAG AAGCACTGCA CTGAGGTCCA ACCACAGACG GGGCGTGGGG 60
GTGGGGGCTG ACACCCAGGC TGCAGGCCCT CCTGCCAGAA TGTGGGGCAG GACAAAGGTC 120
AGAGCATTTG CAGAGTTGCC AGAGGCCAGA GAAGGACCCT GGCATGTGAG AGGGAATTTC 180
ACTCTGCAGG AGAAAGGAAG GTGGCCCTGT CTGCCCTCCA GGTCAGAGCG TTCTCTCTCC 240
TTCATCACCC TGAACCCGGC CCCCAGAGGG GAGACGCAGT CTCCCCACAA GAGTGACTGG 300
TGGTGAGGGG TGTGGGCCAG ACCGCAGGCA GCCAGGAGCC AGGTGCCCCT GAAGCAGCCT 360
TGCCTGAGAA GGGCATCCCC GGTGCAGTCT GCCCCAGGGA TCCAGGCCCC CACCAGGTGC 420
CTCCCCCAAT GCCTGCCCCG GGATCCAAGT CCCCACCAGG CACGTGCCCC ACCACTGAGG 480
GGGCCTGGCC AGCTGCCTGA AGAACGTCTC ATGCTGCGGA TCTGTCTCCT CACAGTTAGA 540
TAAGGCACTT TCGGTTTCAT AAGGCCACGT GGGCGATGCT GCCCCTACCG CAGCACCGCT 600
GCTCAGAGGA AGGACACCAG GCCCGACCGC TCACAGAGGT GGCACCCAGG CCTCTCTGCG 660
ATGCACAGGC ACACTTCCCC ATCAGTCCTC CGTGGGCTTC TGAAGCCACG GGGTGCCCTG 720
CCTGCGTCCT TTCACCCTGT GGTTTCAGCA TCGTCGGCGA TCTTGGCCGG AGTCCTTTGT 780
GTGCACAGGG CGTCACACCA GGTGATTTTA AAATCCCATC ACTCTGGCTG GGTGCGGTGG 840
CTCACGCCTG TAATCCCAGC ACTTGGGGAG GCCGATGCAG GTGGATCACG AGGTCAGCAG 900
ATCAAGGCCA TCCTGGCTAA CACAGTGAGA CCCCATCTCT ACTAAAAATA CAAAAAATTA 960
ACCAGGCACG GTGGCGGGCG CCTGTAGTCC CAGCTACTCG GGAGGCTGAA 1010
|
