| Tag | Content |
|---|
EnhancerAtlas ID | HS044-03015 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr12:6381310-6383580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:6382926-6382945 | TGGTGCCTCCTGCTGGCTG | - | 6.82 | | EWSR1-FLI1 | MA0149.1 | chr12:6383344-6383362 | CCATCCCTCTTTCCTTCC | - | 6.57 | | NFIA | MA0670.1 | chr12:6381890-6381900 | ACTTGGCACC | - | 6.02 | | ZNF263 | MA0528.1 | chr12:6383347-6383368 | TCCCTCTTTCCTTCCTCCTTG | - | 6.05 | | ZNF263 | MA0528.1 | chr12:6383344-6383365 | CCATCCCTCTTTCCTTCCTCC | - | 6.19 | | ZNF263 | MA0528.1 | chr12:6383476-6383497 | GGGGGAGGAAAATAGAGGGGA | + | 6.41 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27184 | chr12:6381289-6384356 | Esophagus | | SE_34915 | chr12:6381456-6383182 | HeLa | | SE_36152 | chr12:6380476-6383785 | HMEC | | SE_64776 | chr12:6381105-6383327 | NHEK |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I006271 | chr12 | 6380636 | 6384166 |
|
Enhancer Sequence | GGCAGGTGCC TGTAATCCCA CCTACTCTGG AGGCTGAGGC AGGAGAATCA CTTGAACCCG 60
GGAGGGGAAG GTTGCAGTGA TCCAGGATCA CGCCACTGCA CTCCAGCCTG GGCGACAGAG 120
TGAGACTCGG TCTTAAATAA ATAAATAAAT AAATAAATGT CATTCTGACT CGTGTTGAGC 180
ATAGACTGTG GGAGGTGGGG AAGGTGGGAG TTAGGAAACT AGTGAGGAGG GAGGAGGTCA 240
AGCAGGATTC CAGGTGGGAG AGCCAGCTGG CAGCCGTGGA CGGGGTGAGG AGTGGCTGGG 300
TTCGGATCTG CCTTGCAGGA TTTCCTAATG GATTGAGTGT TGGTGTGAGA CAGAGTCAAA 360
GGTAGCTGCA AGGGGTTTGG CTCTGTGCAC CTGGAAAGGT GCAGTGTTGA GACATGCAGC 420
AACAGCTCCC CACCCAACTC CATATTCCCC AGCAACCTCA GCAGAGTGAA AAATCCTGCT 480
TCCCAATGAC TCCAGCTGGA ACATAGGGGA ACACAGTAGG CACTCACCAC TCATTGTTGA 540
GTGGTAAATA AGTTTATTCA ACAGATGTTT ATTTCAACCT ACTTGGCACC AGGCCCCATG 600
TCTACACAGT GAAGACAGAC ACAGTCTTTG CATTTCTGAA GTTTGCAGTC AAGCTTCTTA 660
TCTGACGAAA CTAAGGCAGG TAGAGAAATG AATGATTGGC TATGACGCCC CCCTTCCTGG 720
GGAATGTGGA ATCTTTCCCG AAAGTTTTTA GACCACAAGA ATGGCCCTCT AAACTTCAGG 780
TTTCAGCCTG GCTATTTCCA GGCAGGGCAG CCTTCTGGGT GCATCTCAGA TTACACCTGG 840
GAGGCCACCC CACCCACACA TTCAGCCTGC CAGAGCCCTG ACCACAAAAA AAGGTGTCCT 900
GAGACAGCCG CCCGCCTTCC TTTTTTTTTT GAGACAAACT CCATCGCCCA AGCTGGAGTG 960
CAGTGACGTG ACCTCAGCTC ACTGCTCAGC TCAGCACTGC TCAGCTCGGC TTGGCTTCCA 1020
GGGCTCAGGT GATTTTCCAC CTCAGCCTTC TGAGTAGCTG GGACTACAGG CATGCATCAT 1080
CACGCCCGGC TAAATTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT AGTTTTTGTA 1140
GAGACAGGGT CTCGCCATGT GGTCTCAAAC TCCTGGGCTC AGGCAATCTG CCCACCTTGC 1200
CCACCCCAAG TGCTGGAATT ACAGGCATAA GCCACCGCAT CCAGCCTCCC CCTTCATTGT 1260
TGAGACATTC TCAGTAGCAG TCAGGGTCTC AGCAGCAAAC AGAATGTATC CAAAAGGGGT 1320
GACCAAGGAG AATTCAACAG AAGAGCTTAT TGTGGAGAGG TGGGCAGGGT TGAGGGAAGT 1380
CCACAAGGAA CAAGGGACAG TGAGGCCCAC TGCAGCCAGC AAGAGCCGAG GCCCCTCCCC 1440
TCCAGGGCTG GGGAGCAGGG GAAGGAGCAG GGAACCCGAG CCAGGAGACC TGGAGCTTCA 1500
GTGGGAGCTG CTGACAGGAG CTATGGCCTT CAGGAGAGGG AGGTAGCCAC TGCCCACCAG 1560
CAGCCCAGCA GGGAGTGGGT GTCCCATCTA CTCCCCTCTC ACCCTCCGAT TCCTGCTGGT 1620
GCCTCCTGCT GGCTGACTGG AACCCAGAGG GCAAGGGAGC CCGTCAGAAG CAGCGGAGAA 1680
GTCAGCCTGG TGGGCCCTGG GGCATGGGGA GTGGGGTGGA GTGTGTGTCT GCGGGGCACA 1740
CAGGGAAGGG CCAGCACACG CTCTTTATCC CAGAGGCCCC ACCTGCTTCC TTTGGTCAGG 1800
CTGGGAAACT GAGGCAAGAG CAGCTCAGCC TGAGGAATCT GAACTTCACA CCAGGCAGAA 1860
GCCTGAGGGG TTCGAGCTGG GAAAAGGCAC AACCACCATT ATGCAGTTTG GGGCTGGTGG 1920
GGAGGGGTGT GGGTGTTTGT CTGGCTATCA CCATGGCAAC CACGCTAAGC TGCCATCTAG 1980
GTCAGGCCAG GGAATGGCTG GAAGTCACTT TTTCCATCAC CTACCCATTC AGTCCCATCC 2040
CTCTTTCCTT CCTCCTTGGC CCCAAACAGA GTGACTTCCC CTGTTGCTCC ATTCCCAAGC 2100
ATGAGAACAA TGGATGCTGC TGGCTCAGGG TAGGGTGATA AGCTCGGGCT GGCATACCAT 2160
GTTGTGGGGG GAGGAAAATA GAGGGGAAGA AGTTACAGAG GGAGATGGCA CAGGGGGTAC 2220
CAGATAACCC AGAGCGAAGG AGGGAGGATT GCGGCAGATG GCCGCTGTCC 2270
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