| Tag | Content |
|---|
EnhancerAtlas ID | HS105-75436 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr7:129464600-129466420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr7:129465750-129465769 | GTACGCCCCCTGGTGGCCG | - | 6.61 | | KLF5 | MA0599.1 | chr7:129465797-129465807 | GCCCCGCCCC | + | 6.02 | | Klf12 | MA0742.1 | chr7:129465270-129465285 | GGCCACGCCCTACCC | + | 6.28 | | MYC | MA0147.3 | chr7:129465189-129465201 | GGCCACGTGCCC | + | 7.22 | | RREB1 | MA0073.1 | chr7:129465141-129465161 | CCCCAAGCCAGCACCCCACC | + | 6.04 | | ZNF263 | MA0528.1 | chr7:129465077-129465098 | CTCTCCCTTTCTCCCTTCCCC | - | 6.14 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_02142 | chr7:129465064-129465784 | Aorta | | SE_02142 | chr7:129465803-129466453 | Aorta | | SE_34395 | chr7:129464092-129474199 | HCT-116 | | SE_56604 | chr7:129464314-129466546 | u87 | | SE_65233 | chr7:129464974-129465773 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I129824 | chr7 | 129464291 | 129466543 |
|
Enhancer Sequence | TCCCAGTTTC CAAGGGTCAG GAGCCCGGGA AGCTGCTCTC AGGCTGCTGC GGCTCAGGAT 60
CGCTGATGAG GCCTGCCGCA GCCATTCTCA GCTGCACCGG GTCCGGGCAT CCACAGCCGG 120
CTCACGCGCT GGTGGTCGCC AAGCCTCAGC TCTTGCTGGC TGTTGGTTCA GGGCTTCGGT 180
TCCCAGCCAG GTGGGGCTCT CCAAAGGAGA GGGCAGCTCA AAACAACCCG CTGGCTTCCC 240
CCAGAGCAAG TGATAGGAGA CAGGAAGAGG GAGCTAGAGA GAGCCCTGAA GGTGGACGTC 300
GCAGTCTTCA CTCAATCAAT CTCCGCAGGG AACGCCCTGC AGGCCCAGGT ATCCTTCCGG 360
TCCCTTCCTC CTGCCCCTGT GCTCCAGATC CCCCAGGCTC CAGCCCTGCA GCCCGAGCCC 420
CACCCACTAT CCTCGCCTCC CGCCCTGCCG CTCGGCCCTC CCGCTTCAGG TCTCTGTCTC 480
TCCCTTTCTC CCTTCCCCTC TCTCTGTATC CTTTACTTTG TGCCTCTGAT GCCTGACCTG 540
GCCCCAAGCC AGCACCCCAC CATCCCACCC TCTTCCCACC CTGCCCCCCG GCCACGTGCC 600
CCCGGGCCAG CCAGAACGCT GACCCCTCCC CCTGAGTCCA CTCCCCGCTC CCCGCTCCCC 660
GCACAGCCCG GGCCACGCCC TACCCGGGTG CCCTCCCTTT ACCCAGCTCC TTCCCATCCA 720
GCCGGGTCCT GATCCAGCCC CCTGCTCCAG GATGCCCCCT CCTAGCGGTG TGTGAGGCTT 780
TCATGACCCT TCTTCCTCCT TTCCCGACAG ATCAGCGGGG GAGGTGGGCT GAGCCGCCCC 840
TCTCGTCGTC ACCCCTGCCT TGGCCGCCCA GCCGTGCTGG GAGAGTTTGG TGGCCGTGGC 900
TGGCACTGCG GCAGTGCCCA TGTCAGCTCT GGCGCCTCTA CCGAACTCCC TGTTTTGGGG 960
GCTCTTTCCC TACCAGGGTC ACGTCGATGA GGAATCTACG TCCCTCCCAG CCCGGTTCCC 1020
ACCTCTCAGG TGGGGCAGAT GCCAGAGGCC TCCCGGGTCC ACGCCCGCGG GCCACTTGGA 1080
CCGCCCTGCC CCGGCCAACC CCGCCCCACC CAGACTCCCG CCCGCGAGCG GGTGCCGAAG 1140
CACGAAGCAC GTACGCCCCC TGGTGGCCGT GGCGGGGACT GCCGCGCGGA CTCCGCAGCC 1200
CCGCCCCACC CCGCCCGCCC AGCCCAATCC CACCCGCTCC GCCCTGCTCG CCCCTGCCTG 1260
CTCACCTACT GGGCTGCGCT GTCCACGCCT GGAGCCCGGG CAGCTTCAGT TCCGCGGAGG 1320
ACAGGTGTAA CCCACAGAGT GATTCCTTTA CCGGGGCCTG CTAGGCTCCG GCCCACGAGG 1380
CAGGACTGGC GGCGTTCTCA CGTCCTGGAA GTCAAGGCCC CAAGGGGACC GAGGCGCTGC 1440
CCAGGCTCCC CTGACTGCCA GCTCCGGCCT GGCCACCCAG TCCGCCCCCA GGGACCGGAC 1500
TGGGTGCGCC GTCCACCCTT CCAGTACCTG GAACATTCTC CGCGGATTGG GAGGTTCTGG 1560
GTTCTGCCCT AGATTCCCAA GCAAAGTTGC TCCTTTGCTC TTGTCACTTG CCAGCTTCGT 1620
GGTTTTTGTT TTTTGTTTTT GAGACGGAGT CTCGCTTTGT CGCCCAGCCT GGAGTGCTGT 1680
GGCGCAATCT CGGCTCACTG CAACCTCTAC CTCCCCAGGT TCAGGCGATT CTCCTGACTC 1740
AGCCTAGCTG GGATTACAGA TGTGTGCAAC CATGCCCGCA TAATTTTTGT ATTTTTAGTA 1800
GAGACGAGGT TTCACCATGT 1820
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