Tag | Content |
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EnhancerAtlas ID | HS184-19467 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr22:39648040-39648910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr22:39648508-39648519 | ACCACGCCCCC | + | 6.14 | SP3 | MA0746.2 | chr22:39648507-39648520 | CACCACGCCCCCT | + | 6.29 | SP4 | MA0685.1 | chr22:39648505-39648522 | CTCACCACGCCCCCTCC | + | 6.1 | SP8 | MA0747.1 | chr22:39648508-39648520 | ACCACGCCCCCT | + | 6.52 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_32163 | chr22:39648085-39651584 | Gastric | SE_38289 | chr22:39647989-39652396 | HUVEC | SE_42330 | chr22:39647356-39652306 | Lung | SE_47425 | chr22:39647811-39652103 | Panc1 | SE_48326 | chr22:39647869-39652821 | Psoas_Muscle | SE_51377 | chr22:39647884-39653044 | Skeletal_Muscle | SE_65688 | chr22:39644257-39654624 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I039252 | chr22 | 39648201 | 39652492 |
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Enhancer Sequence | TCCAGACACG ATCTGATTGT GGGGAGTGTG TGCGGACGTG CATGGCACGC CTCCGGAGTT 60 ATCCTCGGGA AGAATTGGCC ATTCCACCAC CAGCTCACCT CTCTGGAGCC CCCTGCCCTA 120 GGGGGGGCTT ACAGGCCAAA GCAGGCAGGC AGGTAGACAG TCGGAAAGAC CCAGACGACT 180 GTATAAACAC CCTGGGGCCG TGGTTATATA AGTCAATAAG CAAACAGAGG GCAGCCGGCA 240 TGAGTGACTA AGAGTCTTAA TAGGAACCAC CGCAGCCATG GGCATAGTAC GTGCTCCCCG 300 GGCACAGATG TGCTCTGGCC ATGGGGCACG TCCCTGCTGA AGCCACAGAG TTATCATCGA 360 TGGTCCCAGG TGGAAGGGGT GTTCCATGGA GGATGGGCTT TCCTCTGCCC CTTCCCCCTT 420 GGGGCACCAG GGGACCTCCC TGTTCTTCCT TGGATAACGA CAGTGCTCAC CACGCCCCCT 480 CCCAGCTGTG GGACCCTGGG TGAGTGTGAT TCTGGAACCT GTCCCATTTG GTAATGGGGT 540 TAAGCTAGCA AATGAATGAA GGGGGTTGGC ACAAACGGAG CACTCCATAC ATGGGAGCTG 600 TGGTTACCTT CCTCCCACTT GGCTGAGGCA CCTGAGGCAC AAACCTCATT CAGTCGCACA 660 ATCTGCCTCA AAGGGAAGCA AGCGGCATGG GAAGGATCAT ACCCCTCTTA CAGATGGGAA 720 AACTGAGGCT CAGAGAGGGA AAGTGACTTC TCTAACATCA CCCTGTTGGT TAGAGGTGGA 780 GCTGGGTTTG AACTGAAGTC ACAGCACTCC CAGGAAAGTG CTCAAAGGGA GGGAAGAATG 840 AATTAAGCCA GAAAGACAGA TCCCCCCATC 870
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