Tag | Content |
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EnhancerAtlas ID | HS105-02121 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:36574040-36575180 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HOXA13 | MA0650.2 | chr1:36574193-36574204 | CCCCATAAAAC | + | 6.02 | Mafb | MA0117.2 | chr1:36574217-36574229 | AGTCAGCATTTT | - | 7.22 | REL | MA0101.1 | chr1:36574167-36574177 | GGGGATTTCC | + | 6.02 | ZNF263 | MA0528.1 | chr1:36574915-36574936 | GACTCCTCTCTCCCCTCCTCC | - | 6.52 | ZNF263 | MA0528.1 | chr1:36574918-36574939 | TCCTCTCTCCCCTCCTCCTTC | - | 8.9 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_45971 | chr1:36574036-36575529 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I036108 | chr1 | 36573751 | 36575310 |
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Enhancer Sequence | GAAAGACGGC AGGGCTGGCA GGGGCACGGA GCCCGAGGTG GGACGCACAC AGGAGACGCT 60 GATTCAGAGG ACGGCGCAGT GGCGGCCTCG GGTAGATGCA GTGTTTGGAC AGCTGCAAGT 120 CCTTAACGGG GATTTCCCCC CTTTTCAGCA AATCCCCATA AAACAGCATT CTGTCCAAGT 180 CAGCATTTTG TGGCAGCCCG GGCCTCCTCC CAGGGAGGCC AAGGAGACCG GCTGGGAGTG 240 GGGAGTGCTC TGGGATCTTT CAGACCAGTG GTGGCAGAGT GGCGGTGGTG TGCAGCAAAT 300 GGGCCCCAGC AGAAATAATT GGCAAGAAGC AGACCCCTTC ACTGCTCCCA GAAATGCCTG 360 AAGAGGGGAA AGGACATTAG CTAGCAGGGA CCCTTCCCAG CAGTCCTGGT CTCCGAAAGA 420 GTCCTTTCCT AGAGGCGACC AGCAGAGGAG GGCTATGTGG TAGCATGGAA TTGAAAGACC 480 TGCCCACTCT CCCATCCCAT TTCACAGGTG AGCGATCAGA GGTCTCAATA AAAAAGGGGG 540 GCCTGAGAGT TGGTGCCTCA GGACCCCAGG CACCCGCTAG GTTCCCAACG GACCGGCAGA 600 CCCCCACAGG GTGGGTGGAT GAAACGCAGC CCTGCGCAGG CCCCTACTGC TCCAAGCCCC 660 CCACCCACCC CAGACAGAGC AACTGCAGCT GAGGGAGCGG TGGGGGCACT CAGGCAGCCC 720 CAGGGCCTGG CCAAACCACA GGTATGTTAT GAGACGCTTC CTGTTGTGGA GACATTGCTG 780 TGGGATCCGG CTGCCCTGCT TGCTCACCCG CCCCGCGCTG CTCTCTCCTT GCTCCCCAGC 840 CTTGCTCTCT GCGCTCTTGC TGGGTCTCTA CTCCTGACTC CTCTCTCCCC TCCTCCTTCT 900 GGCTCTGTCT CTGTCATCAC AACAGGTGAA CAGCACTTCT GGCTCAGGCC CTCCCTATCA 960 GGGACCCATC CCTGAGACCT CTAAGGCCCT CCTAGTTCCA GGCAGCCCCT GGACTCCTGT 1020 TTCAGCACAG CTACTTACCA GCTGGGTGAT CTTGGATGGG TCACTTAAAC ACTCTGAACC 1080 TCAGTGTCCT CATCTGCAAA AGGATTAACT CAGGGGCTGC TCTGCCTATG GAGTAACCAC 1140
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