| Tag | Content |
|---|
EnhancerAtlas ID | HS040-03255 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:211820940-211822120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr1:211821818-211821832 | AAGAAATGACTCAT | + | 7.82 | | RREB1 | MA0073.1 | chr1:211821532-211821552 | CCCCAAAACACACCCAAGGA | + | 6.32 | | Sox6 | MA0515.1 | chr1:211821580-211821590 | AAAACAATGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28267 | chr1:211819385-211824621 | Fetal_Intestine | | SE_29189 | chr1:211819363-211824564 | Fetal_Intestine_Large | | SE_34866 | chr1:211820487-211823612 | HeLa | | SE_54270 | chr1:211820880-211822806 | Spleen |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I211646 | chr1 | 211819618 | 211824332 |
|
Enhancer Sequence | GCTATTGTAA GTGGGAACTT TTTGCATTAT ATTTTGTGGC CAGTTCACCC TAGTGTATAG 60
AAAGCTATGA AATGGGTACT AGTGTTTCTC GTTTACAGAT GAAGGAGTAG AAATTAAGGG 120
CACAGTGCCA GGTGAGACTC TAGTTGAGGA CAGGGCTATT CAGAGGTGCG GCCGTGTCTG 180
AACCTGCCTC AGTCATAACC ACTCTCTTAG AAGGAAGCTG CCCGTGCTCT CCAAAGACAG 240
TGTCTGGTCA GACCCAGCTT GGTGTCTGCT GCCTGGCTTG GTGCTCCTGG CTTGGTGTCT 300
GCTGCCTGGA CAGTTCCAGA TTCAAGGGCA GCCAAACATT TCTGGGCAGC AAGCTCCCTG 360
GCCTGATCAA GCTCTGGGCC ATGGCTGTGC CCCGCAAACC CCAGAACCCA ATAAAAGGAG 420
TCCCCATTAG GTGGGCATGG CTGCAGGTGA CTGTTGCACA GTAGGACTTT GGACCACTTA 480
TTTGAAAGCT GCTGTTCTTA CTGTTCAGCA TCAGAGAGAA TTTGATGAAC TCTATGGACT 540
CTCAGACAAA TGCCCCAAAT GCTGTTGACA CTTTCAGAGG ATGTATGGAC AACCCCAAAA 600
CACACCCAAG GATCTTGGGT TAAATTAATA TTCCTGTGTT AAAACAATGG CCCAGACAGG 660
GATTCCTCCA GGTGGGAGGT GCCCAGGGAT GGGGTCACGT TCAGAGGACA GAAGTCCTTG 720
TGTCTGTGTG ACTTTGGATG GGTCACTTCC CTCTCTGAAT CGTTATTTTC TCCATGAGAA 780
CAATATCTAC CCAGTCTAGT TATGGTGTTG TTTGGGAATC GTCTGGTATC CTGTCTTGTG 840
ACAGTGCTTT GAAAACTGCA GTTAAGTAAC ACAAAGGTAA GAAATGACTC ATGCCAGGAA 900
AGGGAATAGC ATGAGGCCCA GCTCTGATAT GCAAAGGCCT CTCAGATTCT TAGAGAATAT 960
TATTGGCTCT CACACCACCA GCTGCTCCCA GTGAACTTGG CCTTCGCCCC CAGGAATGGC 1020
TGATAAAGGC CTTCACTGCT TTCCACTTCT GAGCTGATGG GACTGTTTTA GCTGACCCAG 1080
CTAAAACCAT GATTAAGTGG CTGGATTTGG AAAAGAAGTG TTGGGGCTCA TGGTTCACAG 1140
ATACGTTTCT GGGTTGTTAT AAAAATTAAT AATTAGGCTG 1180
|
