| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21386 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:37937730-37938940 |
Target genes | | Number: 29 | Name | Ensembl ID |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_26741 | chr22:37937341-37939334 | Esophagus | | SE_34331 | chr22:37937672-37938670 | HCT-116 | | SE_36256 | chr22:37937471-37939501 | HMEC | | SE_37242 | chr22:37937593-37938751 | HSMMtube | | SE_42365 | chr22:37937450-37938594 | Lung | | SE_47469 | chr22:37937583-37937860 | Pancreas | | SE_47469 | chr22:37937924-37938602 | Pancreas | | SE_56081 | chr22:37936055-37939489 | u87 | | SE_64898 | chr22:37937222-37939009 | NHEK |
|
| | 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 |
| GH22I037541 | chr22 | 37937467 | 37939222 |
|
Enhancer Sequence | CTCACTGTGC TGTGCAAGGG TTACCCCGAT TACACGGTGG TCTTCCCCTC CCAGAAGCCC 60
CCGGAAAACT TCACTGTTCT TGTCTAGGTC CCTGGTAACT GGCACAGTGC AGGAGTTTAA 120
TAAACGAGAA TGAATGAGCT CATGAGCAAA TGGTTTCCAG GGAAATTGGG CCCTGGGGAT 180
TTCTCACCCT CCTCAAAGAA CAAATTATGC AAATTCTCTG GGACCAGGCC CTCTGCTTTC 240
CTCCTCCCCA CTAGGTTTCT GGGAGGGTGT CTGGGCTCAC CAGAAAGTGC CCCGGGCTCT 300
CTAGTGGCCC GTTTCCTGAT TACAAATGAA ACTAGGGCTT AAAGCTGGTG AATCACTAGC 360
AACTGCCAGC CAGGGCGTGC TGGGTGTCAG GTGGGGTGGA TGGGAGAAGG CAGGCTCACA 420
ACCAGACTTC CCTACTACTC CTGCCACCCC CAACTTTGCC ATCGTGGCAT GACCTCCCCA 480
GCCACTGATG ACACTAGCTA GGAAAGAGCC TAGCTCTGGG GGCTAGACAA GCTTGAGCAA 540
CTCCTGGACT GTCCACACTC CTATCCCTGA GCCTACCACC CCTGGGTCCC AGGAACCCAC 600
AGCCTGAACC ATTCGCAAAC CTCTTTCCCA AGCCCAGTCT CAGGTAACTC AGGGATGGTA 660
TCCAGGGAGG TACTGTATCC CCATTTTAGA AATACAGAAA CCAAAGTTCA GGGTGAGGGA 720
ACTACCCAAG ACCACCCCAA AGAAAGTAAG TAGGGCCTAG GAAGTTGAAC CCCAGTCTTC 780
TGCCTCTCCA GTGGGGTTTA AAGCAGAACT GGCCTTTTTT TTTTTTTTTT TTTTTTTTTT 840
TTTGAGACTA GGAATTGCCC TGTGGCCCAG GCTGGAGCGC AGTGGTGCAA TCATGGCTCA 900
CTGCAGCCTG CTCAAACTCC TGGGCTCAGG CGATCCTCCT GCCTCAGCCT CCTGAGTAGC 960
ACCACCATGC CCAGCTCATT TTCTTTTCTT TTCTTTTCTT TTTCTTTTTG AGATGGAGTC 1020
TCGCTCTGTC ACCCAGGCTG GAGTGCAATG GCATGATCTC AGCTCACTGC AACATCCGCT 1080
TCCCAGCTTC AAGCAATTCT CCTGCCTCAG CCTCCCAAGG AGCTGGGATT ACAGGCATGT 1140
GCCACCACAC CCTAGAGATG GAGTCTCACT GTGTTCATTA GGCTGGTCTC AAACTCTGGG 1200
CCTCAAGCAT 1210
|
