| Tag | Content |
|---|
EnhancerAtlas ID | HS040-20139 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr2:85481990-85483890 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXC1 | MA0032.2 | chr2:85483818-85483829 | ATATTTACATA | - | 6.62 | | TFAP2C | MA0524.2 | chr2:85482641-85482653 | AGCCCCAGGGCA | + | 6.11 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_30140 | chr2:85481584-85483979 | Fetal_Muscle | | SE_32959 | chr2:85481675-85483962 | H1 | | SE_37756 | chr2:85482637-85487486 | HSMMtube | | SE_68755 | chr2:85480692-85483989 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I085254 | chr2 | 85481196 | 85487497 |
|
Enhancer Sequence | CTTCTGAGGG TCTGGAACTA CCAGGTCAAG AGAAGAAAGA CTTCAGATTG TCACTGTTGG 60
ATGTCTTAAT ATGAGGAAGG ACTCAAACAG AGCTGTCCGC AGCTGCAACT GGCTGTCTTG 120
AGAGGTGGTG ACCTTTCTCG AGAAGGGTGG AAACTGTAGC CAGACAACTA CTTGGTGAAG 180
CAGCATACAG AGAGATCGCC CTTCTGATGA TGCGCCCAGT CTGAGGCCTC ACTGAGATGG 240
CCTCAAGAGT GTGTCTTGAG CTGGTTAGAA ACTTACCATC CTGGGCCCCA CGACACACCT 300
CTTGACCCAG ACTGCATCTT AACAGGATCC TCAGCTAATG CATGCGATTG TTCACTTCCA 360
GGGCCTCTGG TTCAGGACCA GGGTGCATGA GCATCACCTG GAGGAGATTT TTAATACAAA 420
TGCAGGGGCT GAGCTGCTGG CCTAGGACAT AGAAGGACCA TTCCCATACC TCACAGTCCA 480
GCTGTCTCCC CATTCCCTCC CCCCTACATG CTGTTGTGTT TCCAAGTTCA TGCCTGTGTG 540
CACACCTGCA CACAAGGGAA TAGGAAAATG GCTTTGATGT ATGGAATCAT GTCTACAAGC 600
TGCTTCAGTC AGGGGCCCTT CTTGCTGAGA GACCAGGCAG CTTTCCCAGG GAGCCCCAGG 660
GCAGGGGCCT GAGGCACCTG CTTCCTGTTC TGTCCCCTGA GAGCTCCGCT TTGCCGGGAG 720
AAAGGAGAAG CCTAAACAGG GTGGGCTGGG TCTGCGAGGC CTGCCTAAGG CTGCCCTCTG 780
CCTTCCCAGC CCTTCAGTCC CTGATCCTTT CGGGCCCCTC CTAGGCCAGA ATGTCCCAGA 840
TTAGATGGGG TGGGGAGGAT GTCTTCTGGT TGCTGTAGGC CTGCATTAGG GGAGTATCCT 900
CTCTGGTCCC ACGTGGGGCA GGTGCCCAGA GCCAGGAATG AGCCGCCTGT GGTGATTCCT 960
GTGTGTCTGG AGTCCAGGAG TCCCTTGCAC TGTTGGCCAG TGGTCACTGT GCGGTGATTG 1020
ACTGGGCTCA GTGTCTGTAG CTTTTGTCTG AGCCCCTTGC ACCCCTCCCC GGGGATGATT 1080
GTCTGAGTTG GTGGATGTTA ATCTGCAGCC CCTGAGAAGC TGCCTGGCAA ATGGGAGGTT 1140
AATGTGCAAA CAGCGGGGAG CATTGTCCAT GTGTGAGGCT GGACAGCAAG TGGGAGGGAA 1200
ATAGTTAAAA ATCCTATTCA TGGCTCAGGA GGGGAGGAGG GGTGGGCGCA GGAGCAGGCC 1260
CGGCCTTGTG CTAATCTTGC TGGAATGTAA CTAGTTCGGG CAGTTTCTGG CTTCGATGTG 1320
CTTTGGGGCC GGTTGGCGTC CCCCCCGCCC CAACCCAGTA CATCGATGGT GCGTCCGCGC 1380
GCCGAAGGCT GCTCTTTGTG TTCTCTGCAG CCACAGCTTA GAAGCGTCCG AGTCAGACCG 1440
CTTTCAGTTG TAAGGATGGG GAGGGAGGAA GCTCAGCGAG GCAGTTGTGT TATCCAAATC 1500
CACAGGCTCT TTCTCTGTTG GAGGATTTGG GTGGGGGAAG GGAATGGGCA GAAGAGAATG 1560
TTCAAGGAGA AAGACCCTAA ACCTGTTGGG TCAGGCTGCT CAGCTGCCTA GAGGCCTGGG 1620
AATGCCTAGG GGGAAGCCCC TGCTTCCGGA CACACAATCA ATTACATATA ACAGTGGGGC 1680
CTTGTGTGTG TAGGCGGGAC ACTGGGAGGG GTCGGCTCAC AGCTCATGTT TTAATGCTTT 1740
ACAAGGAGAG TGTGTTCATG CATTGCTTCT GCAACTTATA ATCAATTTAA AACATTCTAC 1800
ATCTTGATCT AGGCTGGTGG TTACATTGAT ATTTACATAT TGGGCCAGGT TTGGTGGCTC 1860
ATGCCTGTAA TTTGGGAGGC CGAGGTGGGT GGATCACCTG 1900
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