Tag | Content |
---|
EnhancerAtlas ID | HS184-31162 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:100908350-100909270 |
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 | AAAGCCACGG TGTCCATTAG GCCCTCAGGC CCATGTCCCC TCTGGCCTGT CTACTCCCAG 60 CAGGGTTCCA GGGCTGACCC CCAGGGGCTC TGCCTGCCCT TGCTTTCATT CCTCCCCACC 120 CTCCACACCT CACAGCAAAG TCCACCTTCT TCACCCCCTC CCTGGAGTGA CTCTGTGGCA 180 GGCTGGGCCC CAGGCTCAGG AGCACAGTCC TGGCCTCTCC CCAGCCTTCC CCTGCTGCCT 240 TTGTTCCCTG AGTACAGTCC CTGGTTGCCA AGGCTGCAGG TTGCGAAACT CACCTCCAGC 300 CTCCCTCTAA CCAGCTCACC CTGGGTCACA ACAGGCAAGA GGGAGGGACC CTGCCTGCAG 360 TGTCACTCCC TTTGGGACAT CTGAAACTGC CTGGGGCAGC CCGGCCCCTC TGAGAAGGAC 420 TTCCTGCACG CTGTGGCAAG GCCAGACATC TCCCAATCTC AATGCAATTT ATGTACTTAA 480 TTAAATCATT AGCTAGCTTG TCCCTTCCTT GTTCTCACAT CACTCACCTA CTGATACATC 540 TCTGTGCCTG GCACAGAACG TAATCCTGGT AACAAGTAGG AGCTGATGCA AATCAGTGCC 600 AAACCTCAGG GGCCTCATGT CAGTGAAGTG AGAGCAAGGC CCGAGGCCAC ACCCAGGTCT 660 GGGCTCCCAT TCGGGTCCTG GACACACTGC ACAGGGTCCT CTGGGAAGTC ATCTTCCTGA 720 GCCTCAGCGA CCTCATCTGT GCAATGGGGC AAGATCCCCT ATAAATGGGG CTAATGTTCA 780 TAAGGTATCA GCATAATCAC TCCAACCCTG GTTACAACAT AATAAAGAGC CTCTAAGGCC 840 TGTCTGTGCA GGTAAGTGCT ATGGCATGGT GCCTGCACAG TAGTAATGGA TGTGGTTACT 900 TAATAAGAAA CATATTGGCC 920
|