| Tag | Content |
|---|
EnhancerAtlas ID | HS040-02084 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:109370510-109373180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:109370909-109370928 | TGGCCACCAGGTGGCGTCA | + | 7.66 | | FOSL2 | MA0478.1 | chr1:109372116-109372127 | GGATGACTCAG | + | 6.32 | | Foxd3 | MA0041.1 | chr1:109370709-109370721 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370713-109370725 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370717-109370729 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370721-109370733 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370725-109370737 | AAACAAACAAAC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:109370729-109370741 | AAACAAACAAAC | - | 6.32 | | JUNB | MA0490.1 | chr1:109372116-109372127 | GGATGACTCAG | + | 6.14 | | Nkx2-5(var.2) | MA0503.1 | chr1:109372001-109372012 | CTTGAGTGCTT | - | 6.02 | | Nr5a2 | MA0505.1 | chr1:109370665-109370680 | GAGTTCAAGGTCAGC | + | 8.73 | | SOX10 | MA0442.2 | chr1:109372564-109372575 | AAAACAAAGGA | + | 6.32 | | Sox3 | MA0514.1 | chr1:109372564-109372574 | AAAACAAAGG | - | 6.02 | | TCF3 | MA0522.2 | chr1:109372398-109372408 | AACACCTGCT | + | 6.02 | | ZNF143 | MA0088.2 | chr1:109372298-109372314 | TTCCCACAATGGAATG | + | 6.01 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_30391 | chr1:109370337-109374495 | Fetal_Muscle | | SE_36681 | chr1:109370360-109373490 | HMEC | | SE_37339 | chr1:109370071-109375258 | HSMMtube | | SE_44724 | chr1:109370379-109375021 | NHDF-Ad | | SE_44981 | chr1:109370319-109374859 | NHLF | | SE_46396 | chr1:109370357-109374983 | Osteoblasts | | SE_52099 | chr1:109370333-109374370 | Skeletal_Muscle_Myoblast | | SE_63886 | chr1:109370319-109374573 | HSMM | | SE_65077 | chr1:109370440-109375164 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 109371058 | 109371477 | | chr1 | 109370643 | 109372061 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I108827 | chr1 | 109370415 | 109375263 |
|
Enhancer Sequence | TCACATACAC ATTCACAAAA CACATTTGAA GTATGGAATT ATAAAATTTG GAGTTTTCCT 60
CATGCATCAA AATCCATTCC AGGCTGGGTA TGGTGGCTCA TGCCTGTAAT CCCAGCACTT 120
TGGGAGGCCA AGGAGGGTGG ATGGCTTGAG ACTAGGAGTT CAAGGTCAGC CAGGGCAACA 180
TGGCAAAACC TCATCTCAAA AACAAACAAA CAAACAAACA AACAAACAAA CAGTTCCTAC 240
CAGGGGAAGA AACTATGCTA TACGTCAGTA ATGGGTCACG TAGCTTTGGT CCTGGAAGTA 300
CAAGCTGATT ACATCCAACA ACTCCAGCAA AGTGGGCTTT GCCGGGTGTC TGTGGGACTA 360
AAGGCTGAGG GAGCACGTGA AGGTGATTTT AGTTGCACAT GGCCACCAGG TGGCGTCAGA 420
AAGAAGCAAC TGCAATGGAC ATTGTTCAGG AGCCTTCCTG TGGCCCACCT GCAGCTTCCT 480
CCCTCCTCCT CAGAAATCCC AACTCCTCCA AAGGAATTCG AATTAATAAC AGTTCTGAAC 540
AAAGCTCTTG CTAAGCTCCT GGGATACAGT CATAGCCCCC AGGGAAAGTT GTTCATTCTT 600
AGTATGGAAG GCACTGTGCC CGAGATATCC TGGCATAAAT GAGGCAGATT GCCCAGGGCT 660
AGGGTTTGAG CCCAAGGCAT TGCTGGGCAA ACACATGCTC GCCGCGCTGT GCCCTGGCCT 720
GCTGTTGGCG GAGAAGGGAT GGGGCTGCGG GTTTGTGGGG CTGGGGCTGA GAAGCCAGGC 780
TCTTTCCCTC CTCTTGGAAA AACATGCTGT CCTCTTGAGT CACATATTTT CTCACACCTC 840
ATTTTCTGTC TCCACCCTTC TCCTCTGGGG CATTTGAACA TCTGCTCTCC AAAGTGGGAA 900
ACTTGGATCT CACTCAAGTG CATGCAGTCC AACACAGGAC TTTTTCTGCT TTTAAACTCC 960
TTTGTGTACT CAAATCTTCT GGCCAAACAT AATTCCTCTG GAGAAGACAG TTTTTCAACA 1020
AGACAAAGCA GCTAAAGTAC ACACTTAAAT CCAAAGTTTT GCATCAGAAA TAACATAAAG 1080
GGATAAGCAT ATTTTACATT TTATACATAT GTAATTTATC CACTTATATA TAAACAATTT 1140
ACAAATATCC TGAAAACAGT ATGTACCTCA GCAAGCTTCA TAAAGGACAA GTCCCATCAG 1200
AGAGAGATTT AATCTTCTAA CAGAAAGAAT ATATAGTCCT CCCTTCAATC AATAATTCCT 1260
CAGGGATTAT GTAAGTTACA AGATTTTAAT TCATAAGTCA TGTGTATCTT CTCATCACTC 1320
CCCAGCAGTG GATTCACTGT GAGATTTGAT TTTACACTTG GTTGTGCTTG TCTTTCCAGC 1380
TTGTCTATCA TAAAAAAGTA TTATTTAGTC TGGAACATTG GTCCCTGTCT TGGTACTTAA 1440
TGTACTTCTG TAGGGTCTAG ACTAGGAATT TAGAAGAGAG AAATTTAGTA CCTTGAGTGC 1500
TTAATAAAAA TGGTTCTTTA ATGTCAAAAT ACTTTCATTA TACTTAGTAA AACCTTTAAA 1560
AATCCAAAAT TAGACTTTAA TTCAATAAAT AAAAATAGTA GGCCTGGGAT GACTCAGTGA 1620
GTAAGCTTCA TGAGTGCCCC TTGGATTAAA GGGCAGCTCA AAGCTGATGA CTGACATGGT 1680
GGTTTAATGA CCCACACACA ATGACACATG ACCATTTTTA GCACGAGCTT CATGCAGTTT 1740
CTTTTTTCAG GGGTGGACAC TCATTAGAAC TCTTAAGGCA GGTGCCCATT CCCACAATGG 1800
AATGCTTTCT AACAGGAAGC CTCAGTCTTT CAGACCCTGT CATCTGCTTC TATTAGAATC 1860
CATTACGTAC ATATAACAGT GGTTGCTAAA CACCTGCTGC CTCCCTGACT CTTGACCTTC 1920
CAAAGGTCAA TGAGCCGAGC TTTGGCCGGA GTCCACAGTG AGCTTAGAGG TAACATCTCT 1980
CGCTACCTGA AAGAAGCTTC AAATAAATGA TACTGAATCG ACACAGATTA ATAGTTGCAC 2040
CAATGGGTGT TTCAAAAACA AAGGATTTCT CCTGAGGATT TTACATGATT TACAGCTTGT 2100
TAGCTCTGGA AGATTTCGTC CTTAGGAATG GGAAGAAATC AGCCCTGAGA AGAGGGATGA 2160
GGCTTGTTCC TGGGACTGGG GGGCTCAGGT GAAACCCAAC AGAGAAGACT TTTGCTCATC 2220
ATAAGGAGAG AGTAGGGATG GTGGGAGCTG TTTGTTATAC AGGATAAGAA TCCCCCATGT 2280
GGGCAATGAT CAAAAGCCTA CAGGACCACC CTCCGTGGGC TGTAACCATG ATTCTTAACC 2340
AAGGGGGCTT ATCGGAATCA CCTGGGGAGA TTTAAAAGCA ATATTCCTAC CAGAGCCCCA 2400
CCGCTGGCGA TGCTGAGACA GTAGGTGGGA TGGAGGCATG TGCATGATTG TAAAATCTCC 2460
CATGGTGATT TTGATGGTCT CCCCAGTTGA GGACCACTGC TAGAGGATCT GTAGGGTGCG 2520
AGGGAGGCTG GGCTCTGTGC CCAGGCCTGA GATCTGTGAC TCTATAACTC AGCCAGTGGC 2580
CTCAGTTAGT TGCCGCCCAC TCTCACTGGA GTTACTATGC CAGGACTGAC TCCAATCCAC 2640
CCTGGGAATG TAGCCACAAG AAGCCCTCAC 2670
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