| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06181 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:115493020-115494260 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr11:115493296-115493311 | TGGGGGCAAAGGGCA | + | 6.09 | | STAT3 | MA0144.2 | chr11:115493977-115493988 | CTTCCCAGAAG | - | 6.14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I115621 | chr11 | 115492691 | 115494507 |
|
Enhancer Sequence | TACAAGACAA ATTTCTCACC CAACCTCCTT GCCCTTGGCT GAATCATCCA ATCCTGAACT 60
TCCATGGAGA AGAGAGAAGT CCATGGACAG GGATTTTCCT CATCAGCTGC TCCTGACCAC 120
AGTATTGGGG TTTGAGTGCT CAAGGTGCCC CTAAGGAACC ATCCCAAGGG TATTTTCCCT 180
AGAGGTCTCT TAAGAGTTGG GTGAAATTTA AGAAGAGCAA GCTGCCTTCC ATCTGCTATC 240
CCCGGGGTCA TGTGCCCCCA GATGGTGCAG GATGAGTGGG GGCAAAGGGC AAGGGGGAAG 300
TATGTCAACT GGAACATCAC AGAAGTCTAA ATAAGGACTG TTCTGTTTGC CATCCATCTC 360
TTAATTTTTT GATCTCACTA AAGGAATACA ACCCTATAAT AAACACTCCA GCCTTACATA 420
AATAAGCACC AGCTTGCAAC TGCCTCTGTA GCCAGCTCAC TGGATTCCTG AGATTAAGAA 480
CACAGGTATA CCTCTTAGAA GGTGTCACAG CTAGGAACTA TAAAAGTCAT CCACAATGAA 540
AGTGATGAGA CACTTGGGTG GGTAGCCAAA TGGTGTTGGG GTGGGGTCGG AAATGGGGTA 600
AATGCTACAG AAACAGCTTC CCTGGGGATA AGAAAGCCTA GGAGAAATGC TGGTGTCTGA 660
ACAGTCCAGA TGTAGGAACA GTTGAAACAA TCTTATTTGG GCTTGAGCAG CCAAAAGACT 720
CTGGAAATCC AGGTCTGAGC CTCTGGAGCT TTCTTTTCAG CTGCCCCAGC TGCACATTCC 780
TGAAAAGCCA GCACTTGCAC GAGGCATCTC CCAACTCAGA CATGAGTCAC GCCAGCTTAT 840
TTTAAGTCCT GACCTCTTCC CGGGAAGGGA CTCTGACATG GAAAGCCACG TGCTGTGAAG 900
CAACCATGGA CCCCGGCCAA GGGAAACAGA GGCCCCCAAC AGCTTCCTGA CAGTGTCCTT 960
CCCAGAAGCC CAGTGTGAGC AAGGGCCAGG AGCAGCTGTG GGCACTCATG CCCCCTCCCT 1020
TGCCAGGGCG GAACAGTGGG CCGCACCACA CCAGCAGCTC TTGTACCCAC CGTGATGCTG 1080
CTGACGGCTG GGGCAGGGGG TGCCAGGCAG TGAGGGAAGC CCTGTGTGCT CCTCTTTCCA 1140
GGACTCTGGC CTTGGTTTTC CAGTCCACAC CAGATTGTCC TGAAAGGCTA CTGCAGTCCT 1200
TTGGGGATAA ATGGACAGAG GGAGTATGAA GCCCATGCTC 1240
|
