| Tag | Content |
|---|
EnhancerAtlas ID | HS108-11586 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr13:109421400-109422500 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYB | MA0100.3 | chr13:109422032-109422042 | GACAGTTGGT | - | 6.02 | | Rhox11 | MA0629.1 | chr13:109421578-109421595 | AAGAAGCTGTAAAGGAA | + | 6.23 | | TEAD1 | MA0090.2 | chr13:109422393-109422403 | ATGGAATGTG | - | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I108769 | chr13 | 109421455 | 109422500 |
|
Enhancer Sequence | CAGCACCCAA AGGATATTCT CTCACAGATC TTGCAATCCA GGAGGGTATA CTATCAGTTA 60
GTAAACATAT GTGTGTTTAA AACATTGAAT AGTAACCATC GCTGGGAGGA AATGAGAACG 120
GTAAGGGAAT ATGAAGTGAG GTGTGAGGGA AAGAAGCCCT TGGACGAGTG GCTCTAGGAA 180
GAAGCTGTAA AGGAACAAGC AATTCCAAGA CACCCTTGGT GGCACCAGGA TGGGCCAGAG 240
AGGTTGGGGC AGAAGGGACA AAGTCAGTGG GAGCCACGTG TGTGAGGGAC AGGAGAAGAT 300
CTGTGTGGCC AGAATGGAGC ACGCTAGAGG CTGGTGGAAG TGTGAAGTTC AGAGAGAGGG 360
TTGGGAGCAG AAGGCTGAAT CCACAGAGAC ACTTGAAAAC CAAGGGAAAG GGGAGCTTTC 420
ATTCTGGGGA TCATGGTGGA TTTTGACTGA GAGGGGGAGG CAATGAAAAG TGTCTTTTAA 480
ACATCCCTCT GGCTATTCTG TGAAAAATTA ACTCTGCAAA AGGTTTTGAG GTGGGGCTGT 540
GGTTTTGATA AACTAGAAGC AAGTAAACCT GTTAAGCAAC CGCTAGAGCA ATCTGAGCAA 600
GACCGGGTGG TTCTGGAATA ACAGATTAGA AAGACAGTTG GTGAGAATGG TCAGGTATGA 660
TTCATCAGGA AGGAAAGAGG AGGCCAAACT CGCCGATTGA TTTGACAAGT ATGGCAAGAG 720
AGAGAAATCA AGAATTTCCT TATCTGGGGC TAAGTAACTA GGTGGTTAAA AAGTCAGTGA 780
GGCGGAGGCA CTGAGCACTT AAGCAGAATG TATTAAGCAC CCTAATAATT TTATATGATT 840
TGGTATAATA GTAATTCTAG TGATGGAAAC GCTTTAAATG TGGTAAAGGG AAATGTTGCC 900
TAGATATATG TATAATAATG TTATTTATAG TAATGATGTA TAAAAATCAA TGTGTAAAAA 960
TAAAATGGCT AAGTGAATTG GTATATAAAT GTAATGGAAT GTGGCGTAGT AATTTAGGTA 1020
CTGCCTAGTG ACACGGGAAA GAAAATTTTG ATGATAAACT ACTAAAAAAT GATTATATAA 1080
AACTATAGGC ATGTAATATT 1100
|
