| Tag | Content |
|---|
EnhancerAtlas ID | HS040-28663 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr5:137837060-137838690 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr5:137838076-137838088 | GGCCACGTGCTC | + | 6.92 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27104 | chr5:137836968-137838665 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I138501 | chr5 | 137836969 | 137838665 |
|
Enhancer Sequence | CTCTCCAAAC TCACCCTCTC ATCTCTCCAG CTAACCCAGG TCCCCACATA GACCTAGCAC 60
CCCCAGAGGA GGAAGGAGCC ACCCTGCACT CCCCTTGTCC TTTAACACTC ATTGTCATTC 120
CTTGTTCAGA GTCTCCACTG CTGGACCTTC AACACCGAAG GGCAGGGTGT GCACCTGCAC 180
TGTTTGCCAC TGAATCTTGC ACGGGACCTA GTACACGGGA CATGTCTAAA TGCTTGCTGA 240
GTCAAGGAAT GAGACTGGCT TAACCCAAGT CTCATTTAAG GAATAGAGGT GGCCGTGGAG 300
TGCGTCTGTG GAGAAGGCTG GAGGAGACTG GGGTAGAACT CCTTCCATGT TACCTTTCAG 360
AATCAGAGCC CGACAGGGGT GCAAGGGAGG GCCTCTAGCC CTGAGCACAG AAATTCGTCT 420
TTATCTGGAG GAGCAACTCT CTCCCAGGCA ACATCCTGCC TTATTACAAA GAGTCCCCCT 480
CTGCAGGCCC TCCAGGCCCA CCCCAGCTGG CTCATGTTGC CTTTCCCCAC CAGAGAGCCT 540
AGGCTGGGCA TGTCTTTGGG TCTGGACAGT AATACAACAT GGGGCAGAGG GTCCTGGCAT 600
CATCAAGCCC TGATTTCTCC TCATGCCTTC TCCCAGGAAT CGGAATATCT CTGCATCTTT 660
GCCTCTCAGA AGATCCTTGC CATTCCTGCT CGGAGCCTTT CTCTCAAGTT TCCACCCTCC 720
TTCCTTATTC TCCTGGCTTC CTTGGAAATG GGTTTGCCCT CTAGCTTTGA GTGGGGATGG 780
ACAGGCAAGC AGAAGGGGCT AAGCCTAGGT ATAGTATCTC AGCAGAGTGG GAGGAGCTGG 840
AAGTCTGTGG CAGTCAGGGA GAGCTAGATG GGGCTAATTT GGAAGGCCGG GGGCTGAAGA 900
AGCAAGTTGA TCCACACACC CAAGCCAACC TTGACTCACA GGGAAGTGAC TTCAAACAGC 960
TTTCATAACT CCATCTGGAT GTTGGCCACC TTTCCTCTCC TAGCTCTTTG GTTTCAGGCC 1020
ACGTGCTCCC TCCAATTGTC CCTTCTCTCA TTTATAACAT TAGAGAGAAC AGGGCCTGGA 1080
TGAAGAATAA CAAGATCATC CGGCTGTTAA GAGCACCGAA TCTGGAGTTG GAGCAAGTGT 1140
TCATGTTGGC TCTGCTAATT TGCTGCATGA GCCTGACAGG TCACTATATT CCTCTCTGGC 1200
CTCAGCTTTC TTCTGTCTTT AGTGAGGGGA TTGGAATAGG TAAGGTGCAA GACCCTTTCT 1260
AGTGCTAAAA TTAAGGGGCC CGGCACAGTG GCACACACCT GGAATTCCAA CACTTTGGGA 1320
GACAGAGGCG GGCCAATCAC TTGAGCTCAG GAATTCAAGA CCAGCCTGGG GAGGCTGGGC 1380
ACAGTGGCTC ACGCTTGTAA TCCCAGCACT TTGGGAGGCT GAGGCGGGCG GATCACAAGG 1440
TCGGGAGATC AACACCATCC TGGCTAACAC GGCGAAACCC TGCCTCTACT AAAAAAACAA 1500
AAACAAAAAA TTAGCCGGGC GTGGTGGCTG GCGTCTGTGG TCCCAGCTAC TCAGGAGGCT 1560
GAGGCAGGAG AATGGCATGA ACCTGGGAGG CAGAGCTTGC AGTGAGCCGA GATCGCACCC 1620
CTGCACTCCA 1630
|
