| Tag | Content |
|---|
EnhancerAtlas ID | HS105-08396 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr10:5655710-5656940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr10:5655752-5655766 | GGGGCCAGAGGGGG | + | 6.18 | | RUNX1 | MA0002.2 | chr10:5656397-5656408 | AAACCACAGAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_01811 | chr10:5655318-5656721 | Aorta | | SE_23669 | chr10:5655526-5656582 | Colon_Crypt_1 | | SE_24448 | chr10:5655562-5656509 | Colon_Crypt_2 | | SE_26546 | chr10:5655379-5656709 | Esophagus | | SE_30703 | chr10:5655305-5656961 | Fetal_Muscle | | SE_33798 | chr10:5655451-5656860 | HCC1954 | | SE_35816 | chr10:5655438-5656955 | HMEC | | SE_55779 | chr10:5655688-5656873 | u87 | | SE_58135 | chr10:5655600-5656059 | VACO_9m |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I005613 | chr10 | 5655442 | 5658170 |
|
Enhancer Sequence | CTACCCCCTG CTCCCCAGCC TAAGCGCCTG GATGGGGGAC TAGGGGCCAG AGGGGGACGC 60
AGGTCCCAGC TCCCATCTGT GCCAGGGCAC AAGGCACTCC TTCCCCTAGG CAGGAAGCAT 120
TTGCTCCCCT AAGCAGGTCT TTCTTCCAGA AGCCTTGCTT ATCACAGGCA AATTCACCCA 180
CCCTGAAGCT GCAGGCCATA GTGGGGGCAG GGAGGAGATT TATATGGCCT TCTAGCTAAA 240
GCTTGGGACC ACTCTGTGGA AGGTTTTTCA GGAAATCAAG GTCTGCCAGG AACCAGGAAC 300
CTGGTTGCGT TTAGCTGTGC ACACTGGCCT TGACGGTCAT GGAACAGTCC AGAAATGCAC 360
CACCCTGATC CACCCTAGGG CCAGTATTTT GGTTAGGTGT GTTTTGCACC ATCTCATCAG 420
TAACCCTGTG GTTTCCAAAT GCCTCCTCCC TGCCCCTGTT CCACTAGGGC CCTCTGCCTG 480
GGGCCAAAAT AAACACTGGG AATTGGAACA GAGGAGGACT TTTCCAAGGG AGCGGCCACT 540
GCCTCTTTTT CTCCACAGAG CCACCACCTG CATTTTAGCT GCTCACGCCA GCTGAGCTAA 600
GGGCCAGCTC CAGCTCCTGG CTGCTAAGAT TCCTCCAGTT TCCTTAGATT GTCAGCCTGG 660
GACATGCCAA TGTGTTTCAT CTATCTCAAA CCACAGAGCG CCATAATGAA CAGACACATG 720
GAGAAACTGG TGTCTTTCCC CCACCATCCC AAATGTGGGT CTCTCCGCCC ACCAGCCTGG 780
GAAACAAGGG AAAATGATTA ACAGACACTC TAATTAGGGC ATGGTTGAGC CTGTGGGGAT 840
CAAGGATGGG CTTTGGTTTC CTTGGGGAAG AATGTTGCTT TCACTATGCT GGATAAAGTG 900
CTGGAATTTC ACAGATCTCA GATTTCATAA CCAAAGCTGG GATTCATTCC ATGCTTTCCT 960
GAAGTAACCA AACTCAAGCT ATAGAATCTT AACCAAGTTA ACAGATACAT CCCATCCTTA 1020
CCAATATTTG GAAGGGACCC TAATTAGCAA TTCATTGTCA TTCTTCTTGG TTGTGGTGTT 1080
TTAGCCATTT CTTCTTTTCT TTTTTTTCTC TTTTTTTCTT TTTTTTTTTT TTGTGATGGA 1140
GTCTTGCTCT GTCGCCCAGG CTGGAGTGCA GTGATGCAAT CTCGGCTCAC TGCAACCTCT 1200
GCCTCCCGCT TCAAGCAATT CTCCTGCCTC 1230
|
