| Tag | Content |
|---|
EnhancerAtlas ID | HS098-46046 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:131653880-131654860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr5:131654642-131654653 | AGGCCATAAAA | + | 6.02 | | NFE2L1 | MA0089.2 | chr5:131654592-131654607 | ACTGCTGTGTCATCT | - | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr5:131654778-131654793 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09625 | chr5:131653988-131654910 | CD14 | | SE_27887 | chr5:131653835-131654911 | Fetal_Intestine | | SE_28847 | chr5:131653891-131655264 | Fetal_Intestine_Large | | SE_40097 | chr5:131653490-131654882 | K562 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I132317 | chr5 | 131653665 | 131655210 |
|
Enhancer Sequence | TTCCACTGGG CCTTTTTGGA TCAAAAGCAT TGTACTTTCC ATCACTCCCC TGACATGTAG 60
CACATTTCAA CTGCTTGATC AGGATAAAGA ATAACTATTA CTGAGCACCT GCCACATGCC 120
AGACACCCTC CTAGGCACTT TGCATACATG ATCTCAGTCT TCATAATAAT ATCTCCATGA 180
AAGACGGCTT ATCACAGTCA CTCTAGTAGC AACTCAGCAT CAAGGAACCC AGGTTCTCCC 240
CGTGCCAGAT GGAGGACACT CCTAGCCCAT GGTTCCTGGG TCTCGCCTCA TATCCTGGCA 300
GCTGCACTAC AGTCTTGTTT CTTGAGCTGG GGTCTACTGA GAGCCTATGT TGGTCATTTA 360
TGAAGGTGCA TGTCCTGCCT CTGTGTGGAA TGGGCCCAGC GGTTCCTGGG GCAGGTACTG 420
CTCTACATGG AAGGCAGCCT GGCCCTCTCT GAGTCACTCC CTCTTGGAGA GAGTGCTCAG 480
ATTCAGAGGG GTGTGACAGG TGGTGGGCAA TACTCCTAGG GCTATGCTGG CCCTCATCCT 540
AGCCAGGTCA TGTCCCTTTG GCTTAGATGT CAAAGTTTCA CTCCCAGGAG AAACTCAGAA 600
GCCCAGCCAG ACCAAGACCA ACCAGGCTTT GCCCTAGAAG CAAAGCAGGC AGAAGAGGCA 660
GATAGAGCAT AGGGGGCCAG GACAGGGATC CCCCGTCAGC ACAGCAGGAG TCACTGCTGT 720
GTCATCTGTT TCACTGCCAC ATGGAAAGCT CATGGCAGCT GCAGGCCATA AAAGATCTGT 780
GTAATCAGGG TTCTCTCCTA GCATTACTCA GAGGGGTCTG GCTGGCTTCC AGTGACAAGC 840
CAAGGAAGGG AAAATGTAAA TCCACTTCTG AAAGGGGGAT AAGGTGGGTG GATCACCTGA 900
GGTCAGGAGT TCAAGACCAG CCTGGCCAAC ATGGCAAAAC CCCGTCTCTA CTAAAAATAC 960
AAAAATTAGC CGGGCATGGT 980
|
