| Tag | Content |
|---|
EnhancerAtlas ID | HS093-31569 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr9:100908210-100909090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr9:100908994-100909005 | GGCCACACCCA | + | 6.62 | | LMX1B | MA0703.2 | chr9:100908826-100908837 | TTAATTAAATC | - | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09950 | chr9:100906687-100909717 | CD14 | | SE_24386 | chr9:100908125-100909316 | 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 | chr9:100908189-100909398 | LNCaP | | SE_53152 | chr9:100904184-100910435 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I098141 | chr9 | 100904020 | 100910418 |
|
Enhancer Sequence | CTCGAATGCC TGACCTCAAG TGATCTCCTG CCTTGGCCTC CCAAAGTGCC AGGATTACAG 60
GTGTGAGCCA CCATGCTGGC TAAGGCTGGC CTTTAAGATC ATGGCAGTGA AATGCTCCTC 120
TCCACTCTCC CAGGCACCTG AAAGCCACGG TGTCCATTAG GCCCTCAGGC CCATGTCCCC 180
TCTGGCCTGT CTACTCCCAG CAGGGTTCCA GGGCTGACCC CCAGGGGCTC TGCCTGCCCT 240
TGCTTTCATT CCTCCCCACC CTCCACACCT CACAGCAAAG TCCACCTTCT TCACCCCCTC 300
CCTGGAGTGA CTCTGTGGCA GGCTGGGCCC CAGGCTCAGG AGCACAGTCC TGGCCTCTCC 360
CCAGCCTTCC CCTGCTGCCT TTGTTCCCTG AGTACAGTCC CTGGTTGCCA AGGCTGCAGG 420
TTGCGAAACT CACCTCCAGC CTCCCTCTAA CCAGCTCACC CTGGGTCACA ACAGGCAAGA 480
GGGAGGGACC CTGCCTGCAG TGTCACTCCC TTTGGGACAT CTGAAACTGC CTGGGGCAGC 540
CCGGCCCCTC TGAGAAGGAC TTCCTGCACG CTGTGGCAAG GCCAGACATC TCCCAATCTC 600
AATGCAATTT ATGTACTTAA TTAAATCATT AGCTAGCTTG TCCCTTCCTT GTTCTCACAT 660
CACTCACCTA CTGATACATC TCTGTGCCTG GCACAGAACG TAATCCTGGT AACAAGTAGG 720
AGCTGATGCA AATCAGTGCC AAACCTCAGG GGCCTCATGT CAGTGAAGTG AGAGCAAGGC 780
CCGAGGCCAC ACCCAGGTCT GGGCTCCCAT TCGGGTCCTG GACACACTGC ACAGGGTCCT 840
CTGGGAAGTC ATCTTCCTGA GCCTCAGCGA CCTCATCTGT 880
|
