| Tag | Content |
|---|
EnhancerAtlas ID | HS052-38927 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr9:100908250-100909020 |
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 | CCAAAGTGCC AGGATTACAG GTGTGAGCCA CCATGCTGGC TAAGGCTGGC CTTTAAGATC 60
ATGGCAGTGA AATGCTCCTC TCCACTCTCC CAGGCACCTG AAAGCCACGG TGTCCATTAG 120
GCCCTCAGGC CCATGTCCCC TCTGGCCTGT CTACTCCCAG CAGGGTTCCA GGGCTGACCC 180
CCAGGGGCTC TGCCTGCCCT TGCTTTCATT CCTCCCCACC CTCCACACCT CACAGCAAAG 240
TCCACCTTCT TCACCCCCTC CCTGGAGTGA CTCTGTGGCA GGCTGGGCCC CAGGCTCAGG 300
AGCACAGTCC TGGCCTCTCC CCAGCCTTCC CCTGCTGCCT TTGTTCCCTG AGTACAGTCC 360
CTGGTTGCCA AGGCTGCAGG TTGCGAAACT CACCTCCAGC CTCCCTCTAA CCAGCTCACC 420
CTGGGTCACA ACAGGCAAGA GGGAGGGACC CTGCCTGCAG TGTCACTCCC TTTGGGACAT 480
CTGAAACTGC CTGGGGCAGC CCGGCCCCTC TGAGAAGGAC TTCCTGCACG CTGTGGCAAG 540
GCCAGACATC TCCCAATCTC AATGCAATTT ATGTACTTAA TTAAATCATT AGCTAGCTTG 600
TCCCTTCCTT GTTCTCACAT CACTCACCTA CTGATACATC TCTGTGCCTG GCACAGAACG 660
TAATCCTGGT AACAAGTAGG AGCTGATGCA AATCAGTGCC AAACCTCAGG GGCCTCATGT 720
CAGTGAAGTG AGAGCAAGGC CCGAGGCCAC ACCCAGGTCT GGGCTCCCAT 770
|
