| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01198 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:38330290-38331430 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:38330642-38330657 | GAGGTCAGTAGTTCA | + | 6.07 | | RARA | MA0729.1 | chr1:38330642-38330660 | GAGGTCAGTAGTTCAAGA | + | 6.1 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27392 | chr1:38329969-38332738 | Esophagus | | SE_64990 | chr1:38329749-38333393 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I037864 | chr1 | 38330043 | 38332562 |
|
Enhancer Sequence | TTAACTACAT GTTCCTATAA GACTGAAAGA AATAAGACAT TTTAGTTGGG TCTTGAATGT 60
AAGACAAAAT GGGACTTACA GAGGTTAATA ACTGGGGTGA GAGCAAAGAA AGTATAAAAA 120
AAGGGCAGGA GAAGGGAAAT AGTGAAGTAA GTAGAGAGAA CACTTTATGA GAAGTCAATT 180
TTGGCAGGAG CATAATTAGA AGGGTTGATC AGGCCCTGAT CAATGAGTAC TCCAGCTATC 240
TGCATATCAG AATCAGTTTG GAAGTTTGAA TAGATTCCAA AAGTGATTAT GGGCTCAGTG 300
GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCGAAGAG GGTGGATCAC CTGAGGTCAG 360
TAGTTCAAGA CCAACCTGGC CAACATGGTG AAACCCCATC TCTACTAAAA ATACAAAAAT 420
TAGCCAGGCA TGGTGGTGCA CGCCTGTAAT CCCAGCTACT CAGGAGGCTG GGGCAGGAGA 480
ATCGCTTGAA CCTGGGAGGC ATTACAGTGA GCTGAGATCG CGCCAATGCA CTCCAGCCTG 540
GGTGACACAG CAAGACTCCA TCTCAAAAAA AAAAAAAGTG TGATTCAGTA GATTTGGGGT 600
GTGGCTTTAG AATCTCTATT ATTGGCAAGT TTTCTAGATT ATTCTGCCAA GGCCTGTTGT 660
ATGTGTGAAC CACCAAGCTA GATCATAGAA CGTCTTCAAT ATTTAAGAAA ATCAGTAATT 720
GGCAATAGAG AGCCAAGTAT AGTTTTTGAC CAACAGTCAC ATGACAATAG CTTTAGAATA 780
CACAATCTGA TGGCAGCATG CAAAACAAAT CAGCAGAAGG AGATCGTGAA TGCAGGGCAC 840
TGAACCAAGC TAAGTGCAAT GAGAATGGAA GAGAGAGGAT GGGTGATAGA TCAACGAGAC 900
TGGGCACATG GGAGGCAAGG AGAGGGTGGA GTCAGAAATG ACTCAGGTTT CGGGGTTGAC 960
TCACTGGAAT TAAGGGTGAT GCCATTAAAA GAAACAAAGA CATAAGAGAA AGAGCAGGTT 1020
TGAGAAGGAA AGATAAGGTG TTCAGTTTCT GAGATGCTGC ACTTGAGGAA CTGTGTCCAC 1080
TCTGTTCCCT TAGCCCCATG GGGTCTGGGG CTAACCACAT GCTGCTCAAT GCTTCCTCTC 1140
|
