| Tag | Content |
|---|
EnhancerAtlas ID | HS017-33463 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr9:100904360-100905850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr9:100905624-100905637 | AGCAGCTGTTCCT | + | 7.22 | | TFAP2C | MA0524.2 | chr9:100905474-100905486 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr9:100905474-100905486 | TGCCCTGGGGCA | - | 7.22 | | ZNF263 | MA0528.1 | chr9:100905096-100905117 | CCTCCCCTCCGCCCCACCTCC | - | 6.07 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09950 | chr9:100904103-100905141 | CD14 | | SE_24386 | chr9:100904263-100906392 | Colon_Crypt_2 | | SE_26852 | chr9:100904207-100909935 | Esophagus | | SE_27659 | chr9:100903802-100910551 | Fetal_Intestine | | SE_28584 | chr9:100903818-100910565 | Fetal_Intestine_Large | | SE_42027 | chr9:100904412-100905212 | LNCaP | | SE_53152 | chr9:100904184-100910435 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I098141 | chr9 | 100904020 | 100910418 |
|
Enhancer Sequence | ATACAGATTT TCTGAAAAAA TGGGTCCATC CAGGATTAGC CAAAAACTTC TGTTATAAAA 60
CTGTAGCTCT TGAAGGGCTC TAGAGACCAG GAATGGAGCC CACAGCTGCA CTGTCTTATC 120
CTGCACCTGT GGCAGGCATT GCGAATGGAT CCCAGCACCC TCTCTCGGAC CTCAGACTTG 180
GGGAAATCCA GCATGGAGTA GGGACTTGCC CAGGGTCACT GCAAAGGTGA GGGGCAGAGC 240
TGGGCTTGAG CCCAGGCCTC TGGTTCCCCA AGTGTGAGCC TGGTGCTGTA CTTCCTGTGC 300
TCTGAGGGAG CACCAGTGAG TGCTCTGTGA GTCCCTGCCC TGGCCTCCTT CCTGCACACA 360
GCCTTTCCTT TCTCTGGGAT CATTTCCTGG GTCAAAGGCC ATGAGCAGTA CTGTGTCTTT 420
GGCTGTGGGG CACTGATTGC TCTCCGGGCC TTTAGACTCT GGCCCAGGGC CATGCCCCAA 480
TTTCCGCAGT GCGGTTTCCC AAGAAAAGCC AGATGAGCCA ATAGTCAGGC TGCCCTCGGG 540
CTGACGGGAG GCAAAGTGCC CAGGAGCCCC ATTCAGACAC ACACCTCCCA CCTCCCACAG 600
ACTCAGGGAA GGCGCCTTAG GGTTGGGCGT GGCTCAGAAG GGCCTAGCCC TAGACAGCTT 660
CTCTTCCTTC TCAGCCTTCT CTTCCTTCTC AGCTGATGAG GGAAGGCTGC CCACTCACAC 720
CCCAGCCCAC CCCAGCCCTC CCCTCCGCCC CACCTCCCCT GCCCTGCCCT GCCCTGCGCT 780
GCCCTGCGCT GCCCTGCGCT GCCCTGCCCT GGGCTGGCAG ATTGCTCTGC TTCTAAAAGG 840
TTTTACGCTG AGGACCACAG GCAGGAGCGG ACATTAGCCA GCCTGGTGGG CTATTGACTG 900
AGCTGCTAAA AGCCTGTCAG GGACATTTAT CATCAGGAGG CCATTTCCAC CTTCTGCCCA 960
TTAGGCCAGC ACTCAGCCAG AAACAGGCTT CTGATGGATG TGGTGTACAA GCTCTAAATC 1020
AGGGGAGACA CGCCTGCTCC CCTCGCAGAC CCCACAGAAC CCTGGCTTGG GCCGCCCTGC 1080
CTGGAGAGGC ATCACCTCCA AGTCTCCAAG GGGCTGCCCT GGGGCAGAGG GGGAAGACAG 1140
GACAGAAGGA CCCAGGAGGA GTCAGGCGGG TGGGGGACCA GACTGGGGAC TCTCTACGGC 1200
TGACCTCCAT TGCCAGAAAG GGAGAGGTTG TGAGGCCACT GTCACGACCC TCAGCAGTCA 1260
AGGGAGCAGC TGTTCCTACA ACAGCATCAT AGTCATGGCC TCAAATGAGC ATCCCAACAG 1320
CTCAGGGTGG AGACTGGGAG GCAGGGGTGG CAGGACGGGC AGAGGGAGGA CACACAGTGT 1380
AGCAGAGGTG AAGTGGGCAG GCAGACTCTG GCTTCCAGGG GTGGAATCCC TGCCACATCC 1440
CTTACCATGG TGCAGCCTTG GGCAAGTGAC CTCAGTTCTC TATGCCTCAG 1490
|
