Tag | Content |
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EnhancerAtlas ID | HS098-57867 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:97696470-97697900 |
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) |
MYB | MA0100.3 | chr9:97697473-97697483 | ACCAACTGTC | + | 6.02 | ZNF263 | MA0528.1 | chr9:97696536-97696557 | CCTCCCTCCCTTCCCTCTCCC | - | 6.18 | ZNF263 | MA0528.1 | chr9:97696538-97696559 | TCCCTCCCTTCCCTCTCCCTC | - | 6.23 | ZNF263 | MA0528.1 | chr9:97696544-97696565 | CCTTCCCTCTCCCTCTCCCTC | - | 6.68 | ZNF263 | MA0528.1 | chr9:97697694-97697715 | GGAGGTGGAAAGGGAAGGGAA | + | 6.73 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01684 | chr9:97696233-97699876 | Aorta | SE_37024 | chr9:97694730-97697400 | HSMMtube | SE_45593 | chr9:97694893-97696761 | Osteoblasts |
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Enhancer Sequence | AGCTACCTGA GGCCCTCCTC CACCAGGACC TGGCTCTGTC GTCACCCACG GTCCTCTGTC 60 CTCCACCCTC CCTCCCTTCC CTCTCCCTCT CCCTCTAACT GCTGACTATG CTCACACTTC 120 TCCCATCTTT TTTTTTTTTT TTTTTTGAGA CAGAGTCTGG CTCTATTGCC CAGGCTGGAG 180 TTCAGTGGCG CGATTTCGGC TCACTGCAAC CTCTGACTCT GGAGCTCAGG TGATCCTGCC 240 GCCTCAGCCT CCCAAGTAGC TGGGACCACA GGCACGAGCC ACCACACCCA GCCTCTCCTA 300 TCCTTAATAA TCTCTCCTTT AAACTGCTGC ACCCTCATCT AATTATCAAA ACACTTCTTG 360 TCTCCATTCC CACAGCTCTT AAGAACTTCC AGTCCTCTGG AATCTGCTTT CTGCTCTCAC 420 CAGTACAGGA AAACTGTTTT TTCCTTGGCT CATTGTGCCC TGACAGTCAC CAGATTATGG 480 AAGCAAATTT TATTTTTAAT CTTTTGAGAC TCTTCTGCTT TGTTTGGTAC TGTTGACAGC 540 TCTTCTGGAA GTTTTTGTCA CTGGCTTTTG TGGCAGTCCC TCACCTGATT CTTCTTGCCC 600 TCTGTCATTC CTCCTCCATC TCCTTCGAGG TCTGCCCTTT GCCTGCCTGT GTCTTCAGAG 660 CTGATCTTCC TCGGGGCCTC CACACTCGGC TGCGTGTCCT CCCAGAGTGG TCTCATCTAA 720 ACCCCCATCT TAGGTGGGAG TCTCCAGGTG CAGACCCTGA TGCAAGGGGT ATGGGAAAGA 780 GATTTATTAG GAATTGTTCT GATACGGGTT GGCTGTGTGT CCCCGCCCAA ATCTCATGTT 840 GAATTGTAAT CCCCAGTGTT GGAGGTGGGG CCTGGCGGGA GGTGACTGGA TCACAGAGGT 900 GGTTTGTCAT GGTTTAACAC CATCCCCCCT TGGTGCTGTG GTCACAATAG TGAGTGAGTT 960 CTCATGAGCT CTGGTTATTT AAAAGTGTGT GGCACCTTCC TCCACCAACT GTCTCCCTCC 1020 CGCCCCAGCC ATGTAAGATG TCCTGCTTCC CCTTTGCCTT CTGCCATAAT TGTAAGTTTC 1080 CTGAGGCCTC CGAGCAGGTG ACAGCATCAT GCTTCCTGTA CAACCTGCAG AACCGTGAGC 1140 CAATTAAACC TCTTTTATTT ATAAATTACC CAGTCTTGTG TATTTCTTTA TGGCAATTCA 1200 GGAACAGACT AATATATGTT CCCAGGAGGT GGAAAGGGAA GGGAAATGGA AGTGAGGAGG 1260 CCAAGCCAGG GTGCCGTGAC ATCAGGCCAG GTCATGCAGG GTTACTCTGG AAGAAGCATG 1320 GGTCACCCTC AGTTGTTCGC ATCAGGCAGT GGACCCCCAG GGTGCATGTA CCCCTGCACT 1380 TGTCTCATTG GTTGGAAAAA TGTACAGTCC CAGGTGCTTC CAGCTCCATG 1430
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