| Tag | Content |
|---|
EnhancerAtlas ID | HS095-06159 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:113448090-113449160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arid3b | MA0601.1 | chr11:113448805-113448816 | CTAATTAATAT | - | 6.02 | | ZNF263 | MA0528.1 | chr11:113448943-113448964 | AAGGGAGTGGGAGGGGGAGGA | + | 6.33 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I113578 | chr11 | 113448921 | 113448990 |
|
Enhancer Sequence | CAAGGCAGCT GTAATCCAGC ATAACCAATG TGCTGTTAGG GATCAGCCCA CGCTGCTGTG 60
AGAACACAGA AGGCTCACCC AGCCCAGTCC GGCAGGTCAG AGAAGGCTTC CTGGAGAAGC 120
AGAGGTCCAA GAAACAAGAC AGGGAGCAGG AGCTCAGCAG GTGACAAGGG GGCAGGGACT 180
GTACCCAGAA GATGTGCATG GGATGGATGC ATGGTGCCCA CTCTGGATGG GTGCTCAAAA 240
GAAACAGCAA GTGCTGCATC TGCTTGTAGG GTAGAGACAG GATCTGACGA GGGCAAGGCT 300
GGGCACAGAG AGCCCATTCA GAAGCCACCA CAATCACCTA GGTGGGAGCC GATGGTGGTG 360
TGGACTCAGG CAATGATCAT ATGGAGGGAG AGCTGGGGAA GAAGTTGACA CATAATCAGG 420
AGGTTAATTT ATGAGACTTG GTGACTGACA TGCTGAAAAG GTGAGGGAGC AAGTGGAGCT 480
GAACCACAGT GGGGTGGCAG GGCACATTTC TCCTTGAGCA TCTGGCCGTC AGCCAGGCAC 540
CTCTGCGGGC AGCCTGTAGG GACCCAGGGA TGCTCCACCC CTCAGCCACT ACCTGTTTCT 600
GGCTTGAGTC TGCTCTTCCT GTTCTGGCTG GGGCTGAGAA GGGAAAAGGG GGGAGAGAGG 660
AGGGTGCAGC ACCCTGATAC TGAAGGTGCA TTTTTATTAC CTCACTAATG CTCTCCTAAT 720
TAATATACCT AGAGGCTGCG CCTGCCACTT CACTACTTTC ACTGCTGATT TGCCCCTTGA 780
GACAAAAGGA AATTGGAATT AAGAGGAGAC AATGGAATTG CCAGCAGGAC TATTAGCTTC 840
AATGAAGCTA ATGAAGGGAG TGGGAGGGGG AGGAGAGGAG AGCCTGGGGG GCACTATGAC 900
TCACTCTAGG AGCTGCCAGA TGGACAGATG GAGACTAGGG GAGGGCTGTG ACTGGAAGGA 960
CTCTGCCTTT CTGGGCTCCA GAAGTCCTGG GGGTACCCCA AGGTCAGGGG TTCCCAAGGT 1020
CAGGAAGTGT GATCCGATGG GAAGAAAACA GGAATTAGAA GTTGGACGGG 1070
|
