| Tag | Content |
|---|
EnhancerAtlas ID | HS040-16505 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr17:79680350-79681520 |
Target genes | | Number: 32 | Name | Ensembl ID |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_24622 | chr17:79678798-79681606 | Colon_Crypt_2 | | SE_24986 | chr17:79678720-79682705 | Colon_Crypt_3 | | SE_35549 | chr17:79677340-79681743 | HepG2 | | SE_41699 | chr17:79678768-79683021 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 79680800 | 79681393 | | chr17 | 79681398 | 79681490 |
|
Enhancer Sequence | GGCCTGAGGC TTTGCACAGT CTGCCCAGCA GGCCCTGCCC TGTGAACCTG GCTGTGGTCA 60
CTGGGCAGCC GCCTGTCTAG GGGACCTTTA TTTTAGCAGC CTGTCCAGGG GACTTGTATT 120
CCAGCAGCCT TTGAGGGGAC TGGCTTTACT AATGAGCAAC AATGCTGGTC GCTGCGTGAA 180
GGCCAGGTGA GCAGATGTGG GCGTCTTGGG GCACCTGAGA CCTCACTGGT CCTGGGAGAG 240
GCCTTCAGAG CTCCCAGGCC ACAGGCAGCC ACGGCCAGTG AGATGCAGCC ACAGCGACAG 300
GAAGGCGCTG GCATGGGCAG AAGAAGCGAG CCCCTCCTTG GCATCGGGCT CTTCCTTTCC 360
TCCTGGGCGC CGCACAGGTG CCCCTCCCCC AGGGCCTCTC CCACGTTCAT CTGGGTGTTG 420
AAGGCGGGAC CTGCGTGCTG CTGTCCCTTG TCCGGGGTCT GAGCCCCACT GCCCCTTGGC 480
CCTCCCCAAC CAGGCGCTCT CTGGCTGCAG AACACCGCCT GGGGGAGGCG GGACTGCCCT 540
CTGGCCTGGG AGGGCGGGAG GAGCCAGCTG CTGGCAGCAT ATGGCGCTGT GGTCAGGGTG 600
TGCTCCTGAG GACTGCTCAC CAGGCCTCTC TGCCTGGCCG TCGGAAAGAT CTTTTAAAGC 660
TTCTTGAGCA CTTTGTCCCA TGTCCCTACA GTCCCTACCG TCGCATCTGG CCGGGACGGG 720
GGCTGCTACC TGTGTGGCCC AGTCCCTCTG TTCTGCTGGG CTCGCACAAT GGGAGGCCCC 780
TCTCTGTCCC CACCCATCTT TGCCGACCCC TGGGCGTGCG TTACGGGGCC GCGCACGTGC 840
AGGTCACACT GAGCGGCGGA AGGACTTCTT TGGGGTCAGT GCTGGGGGTG GGACCCAGGA 900
GCTGGGATCC TGGGCCAGGT GCTGGCCTTC CTGTCTGGCC CTGGCCAATC CCCCTACTGC 960
CGGGAGCTCT CAGCTGGCCA GGCGAGGAGG CAGAGGTCCT GTGAGTGGTG GAGGCCAACA 1020
GAATGGGAGG TTGTCGGGCT GACAGCCCCC GAGTGCCTGC CCACAGCTCC TAGGTGCTTT 1080
GCAGAGGAGG CCGCTATGCC CTGCCGCCAG CCACACCGTC CCCTTGTCTG CTGCTGAGCT 1140
CCTGCTGCCT TTCAAGGCCT TCTATGGCTA 1170
|
