| Tag | Content |
|---|
EnhancerAtlas ID | HS060-17812 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:39123320-39124750 |
Target genes | | Number: 22 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr19:39124329-39124350 | AAAAAAAAAAAGAAACTAAGG | - | 6.57 | | Nr2f6(var.2) | MA0728.1 | chr19:39124635-39124650 | TGAACTCCTGACCTC | - | 6.22 | | POU4F2 | MA0683.1 | chr19:39123504-39123520 | CTCATTTATTTTGCAT | - | 6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26525 | chr19:39123042-39123902 | Esophagus | | SE_34299 | chr19:39123228-39123958 | HCT-116 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I038632 | chr19 | 39123043 | 39123958 |
|
Enhancer Sequence | AACGCCCTCT GGGTCCTGGT GCACATCTGG GAGGTTGGGG GTGGCTAGGG CAGTGGACCT 60
CAGTCAGCTC CTCCAACAGG CCTGTCTGGG TCTCATCAGG TCAGCATGGA AGGCCCAGCC 120
CAAGGAGGAA ATAAGAACTT GGTATAAGAC AGTCTCTGCC TTGAGGGAGA TCCTATGCCA 180
TTTGCTCATT TATTTTGCAT TAATTGAGTG CCTACCGTGT GTCAGTGTGC TAAACTGGGC 240
GTGCAGCAGT AAACAAAGTG GGATGGCTCC AATTCATTCT CATGGAGGTA GCAAAGCACA 300
TGGCGACATG GAGGTGTCCA GTGGTGATTC CTGTCATGAA GGAAAGCAAG ACAGCTCACA 360
GACCAGCGGC ATCTGAGCCC TTACCTCCGT AGAGAGAGGC CCGTGGCCTG AGGTAGTGCA 420
GAGGAGGATA GTAGAGCAGG GCCCTGACTT GTAACGTTCA TGGGTAGCCA GGGTGTATGT 480
GGCCAGAGCA GAGTAAGCAT GGGCGAAAGT AGAGAGCTGG GGGTTGGAGG GGCATTTCCA 540
GGTCATGTGG GGCCTCGGGA GGACCTTGTC CTTTCCCCTG ACTGAGAAGG AGCCACCGGA 600
GGGCTCTGAG CAGGGTAGGG CTCTGATCAG ATGGATATTT TTTAAAGATC CCCCCAAGAA 660
CAAAAAAAGA AAAAATAACT TATTTGCTTA CTTTTGTAAA AAGAAACGTA GAAAAGGAAG 720
TCAAGAAACT AAGGAAGGCC GGGTGCGGTG GCTCCCGCCT GTAATCCAGC ACTTTGGGAG 780
GCCGAGGTGG GCGGATCATC TGTGGTCAGG AGTTCGAGAC CAGCCTGCCC AACATGGTAA 840
AACCCCCTCT CTACTAAAAA TACAAAAAAT TGCTGGGTGT GGTGGCGTGC ACCTGTAATC 900
CCAGCTACTT GGGAGGCTGA GGCAGGAGAA TTGCTTCAAC GCAGGAGGCG GAGGTTGCAG 960
TGAGCTGAGA TCGCACCATT GCACTAGTGA TAAGATCGAA ACTCCATCTA AAAAAAAAAA 1020
GAAACTAAGG AAGGCCACGT GTGATGGCTC ATACCAGTGA GGGAGGCAGA TCACGTGAGG 1080
TCAGGAGTTC GAGACCAGCC TGGCCAACAT GGGGAAACCC CGTCTCTACT AAAAATACAA 1140
AAATTAGCTG GACGTGTTGG CATGTGCCTG TAATCCCAGC TATTCGGGAG GCTGAGGCAG 1200
GAGAACCGCT TGAGCCCAGG AGCAGAGGTT GCAGTGAGCC AAGATCACAC CACTGCATTC 1260
CACTCTGGGC ACTTTTAGTA GAGAAGGAGT TTGACCATGT TGGCCAGGCT GGTCTTGAAC 1320
TCCTGACCTC AAGTGATCTG CCCACCTTGG CCTCCCAAAG TACTGGGATT ACAGGCGTGA 1380
GCCGCTGCAT CCAGCCAAGT AAAAGCTAAC TTTTTTTTTT TTTTTTTTTT 1430
|
