| Tag | Content |
|---|
EnhancerAtlas ID | HS145-05247 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr12:6381430-6383660 |
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 | TGAGACTCGG TCTTAAATAA ATAAATAAAT AAATAAATGT CATTCTGACT CGTGTTGAGC 60
ATAGACTGTG GGAGGTGGGG AAGGTGGGAG TTAGGAAACT AGTGAGGAGG GAGGAGGTCA 120
AGCAGGATTC CAGGTGGGAG AGCCAGCTGG CAGCCGTGGA CGGGGTGAGG AGTGGCTGGG 180
TTCGGATCTG CCTTGCAGGA TTTCCTAATG GATTGAGTGT TGGTGTGAGA CAGAGTCAAA 240
GGTAGCTGCA AGGGGTTTGG CTCTGTGCAC CTGGAAAGGT GCAGTGTTGA GACATGCAGC 300
AACAGCTCCC CACCCAACTC CATATTCCCC AGCAACCTCA GCAGAGTGAA AAATCCTGCT 360
TCCCAATGAC TCCAGCTGGA ACATAGGGGA ACACAGTAGG CACTCACCAC TCATTGTTGA 420
GTGGTAAATA AGTTTATTCA ACAGATGTTT ATTTCAACCT ACTTGGCACC AGGCCCCATG 480
TCTACACAGT GAAGACAGAC ACAGTCTTTG CATTTCTGAA GTTTGCAGTC AAGCTTCTTA 540
TCTGACGAAA CTAAGGCAGG TAGAGAAATG AATGATTGGC TATGACGCCC CCCTTCCTGG 600
GGAATGTGGA ATCTTTCCCG AAAGTTTTTA GACCACAAGA ATGGCCCTCT AAACTTCAGG 660
TTTCAGCCTG GCTATTTCCA GGCAGGGCAG CCTTCTGGGT GCATCTCAGA TTACACCTGG 720
GAGGCCACCC CACCCACACA TTCAGCCTGC CAGAGCCCTG ACCACAAAAA AAGGTGTCCT 780
GAGACAGCCG CCCGCCTTCC TTTTTTTTTT GAGACAAACT CCATCGCCCA AGCTGGAGTG 840
CAGTGACGTG ACCTCAGCTC ACTGCTCAGC TCAGCACTGC TCAGCTCGGC TTGGCTTCCA 900
GGGCTCAGGT GATTTTCCAC CTCAGCCTTC TGAGTAGCTG GGACTACAGG CATGCATCAT 960
CACGCCCGGC TAAATTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTGTGT AGTTTTTGTA 1020
GAGACAGGGT CTCGCCATGT GGTCTCAAAC TCCTGGGCTC AGGCAATCTG CCCACCTTGC 1080
CCACCCCAAG TGCTGGAATT ACAGGCATAA GCCACCGCAT CCAGCCTCCC CCTTCATTGT 1140
TGAGACATTC TCAGTAGCAG TCAGGGTCTC AGCAGCAAAC AGAATGTATC CAAAAGGGGT 1200
GACCAAGGAG AATTCAACAG AAGAGCTTAT TGTGGAGAGG TGGGCAGGGT TGAGGGAAGT 1260
CCACAAGGAA CAAGGGACAG TGAGGCCCAC TGCAGCCAGC AAGAGCCGAG GCCCCTCCCC 1320
TCCAGGGCTG GGGAGCAGGG GAAGGAGCAG GGAACCCGAG CCAGGAGACC TGGAGCTTCA 1380
GTGGGAGCTG CTGACAGGAG CTATGGCCTT CAGGAGAGGG AGGTAGCCAC TGCCCACCAG 1440
CAGCCCAGCA GGGAGTGGGT GTCCCATCTA CTCCCCTCTC ACCCTCCGAT TCCTGCTGGT 1500
GCCTCCTGCT GGCTGACTGG AACCCAGAGG GCAAGGGAGC CCGTCAGAAG CAGCGGAGAA 1560
GTCAGCCTGG TGGGCCCTGG GGCATGGGGA GTGGGGTGGA GTGTGTGTCT GCGGGGCACA 1620
CAGGGAAGGG CCAGCACACG CTCTTTATCC CAGAGGCCCC ACCTGCTTCC TTTGGTCAGG 1680
CTGGGAAACT GAGGCAAGAG CAGCTCAGCC TGAGGAATCT GAACTTCACA CCAGGCAGAA 1740
GCCTGAGGGG TTCGAGCTGG GAAAAGGCAC AACCACCATT ATGCAGTTTG GGGCTGGTGG 1800
GGAGGGGTGT GGGTGTTTGT CTGGCTATCA CCATGGCAAC CACGCTAAGC TGCCATCTAG 1860
GTCAGGCCAG GGAATGGCTG GAAGTCACTT TTTCCATCAC CTACCCATTC AGTCCCATCC 1920
CTCTTTCCTT CCTCCTTGGC CCCAAACAGA GTGACTTCCC CTGTTGCTCC ATTCCCAAGC 1980
ATGAGAACAA TGGATGCTGC TGGCTCAGGG TAGGGTGATA AGCTCGGGCT GGCATACCAT 2040
GTTGTGGGGG GAGGAAAATA GAGGGGAAGA AGTTACAGAG GGAGATGGCA CAGGGGGTAC 2100
CAGATAACCC AGAGCGAAGG AGGGAGGATT GCGGCAGATG GCCGCTGTCC AGGAGGGGTG 2160
ACCTGCCACC TAGAACATTC AGCCTGTGGT CAGCAAGCAG CTTTCATTGG TGTGGTGACA 2220
CCACAGCATA 2230
|
