| Tag | Content |
|---|
EnhancerAtlas ID | HS076-52854 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr7:158587150-158588620 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PHOX2A | MA0713.1 | chr7:158588072-158588083 | TAATTAAATTA | - | 6.62 | | PROP1 | MA0715.1 | chr7:158588072-158588083 | TAATTAAATTA | + | 6.32 | | PROP1 | MA0715.1 | chr7:158588072-158588083 | TAATTAAATTA | - | 6.62 | | Phox2b | MA0681.1 | chr7:158588072-158588083 | TAATTAAATTA | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26837 | chr7:158588218-158588914 | Esophagus |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I158795 | chr7 | 158588219 | 158588914 |
|
Enhancer Sequence | CTCCTGACTA GGCAACAGAG TGAACCCCCA TCTCTTAAAA ACAAAACAAA ACTGGGCACA 60
ATGGCTCAAA GCTGTAATCC CCGCACTTTG GCAGGTGGAG GCGGAAGAAA CACTTGAGCC 120
TAAGAGTTTG AGACCAGCCT GAGTGGAGAC CCCCATCTCT ACAAAAACTC CCCAGGCGTG 180
GTGGCGTGCA CCTGTAGTCC CAGCTACTCG GGAGGCTGTG GTAGGGGGAA TCCACTGAGC 240
CCGGGGGGGT AAGGTTGCAG TCGGTGGTGA TCACGCCACT GTACTCCAGC CTGGGTGACA 300
GAGTAAGACC CTGTCTCAAA AATGAAAGAA GCACTTTACC TTTAGAGTAC TACTGCTTAC 360
TTTGACAAGC ATGAGTGTAT TAAAATCACA CCTCTCAACG AGCTGTCAAA TCAAACTCTA 420
AGCCTTTACT TGAAAGTCTA GCCACCTCCT ATGCTCCCAA GTTCCCAGGC TTTTTCTTTA 480
TGGTACTAGC TAAGCCATGT ACAGACTGCA CTAAAAAACA CAATCAACAC ACTATTCTAA 540
TAAGTGAAAA TGGGGCAGGC ATGATGTGCA TCAGATAACA TACTCCCCAA ATGACGTGGA 600
GATGAGGGGA CCAACCCCAC TCCAGATGAC TGGGCATTAC CTAATGAAGG ACAAACACCA 660
GAAGGCAACA TTGCCCAGCT GCCGGGAGTC TTGGTCAGCA CACAGTCTGG CCAAGGACCC 720
TGCACAGGAC TCCACATGCC ATTCTATCCA TCCCTTCATC AGAAAGCCTG GGTTTGACAC 780
TTGTAAGACA TTGGTACAGT AGATGAAAAT GCCAAAGCTA TCTTTATTGA ATCAGCACTC 840
CTCTTAATAC TCTTGCTATT CTCCAAGGAT TTCCTTATTC AGCTGGTATC AAACTTAAAG 900
TGTGTGTGAT GGAACTCAAA CATAATTAAA TTATTCCTAA AATAAACCCA GCTGAGATGG 960
AATTTTAAAT ATCCACAAAC ACGAACATGC TGTAACTTAG GGCATAACAG GCTAAATGTG 1020
CCTTTGGCCT GACTCTACAG CCCTGGAGCT AGTATGGTTT TCACCTGGCT AAAGGGCTGT 1080
AGAAGAAGGG AGGGAGAGAC AGCAGGACAA TGCAGCCCCT GCGGCCACGT ACAGACAGAG 1140
CATGCAGCCC CTGCGGCCAT GTACAGACAG AGCATGCAGC CCCTGCTTTA CAGCATTTAA 1200
CTTGTCACTG GGACTTTAAC CTGCACTCAC ATGGCACTTT AACTTGTAAT TGTGTTTTTT 1260
CCCATCTGTG GTTACCATTT TAGGTGTTGA AGGTAAAGTC AACACTGAAA GTGTCCTACA 1320
GGCGTCCCGT GTAGAGACAT GGGCTCGTCC TACGGGCGTC CTGTGTAGAG ACATGGACTC 1380
TTGCACAGGA TGGCCACACC TCAGGCATGT CACAGGAAAA GCAGCAGCAC ATACAGGCAG 1440
GTGTCACACG TAAGGCTGCA CAGGAGGCAC 1470
|
