Tag | Content |
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EnhancerAtlas ID | HS133-21083 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:24164100-24165100 |
Target genes | Number: 23 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:24164666-24164684 | GCTCCCTTCCTCCCTCCC | - | 6.09 | ZNF263 | MA0528.1 | chr22:24165038-24165059 | CTTTCTCCCCCTCCCTCCCTT | - | 6.24 | ZNF263 | MA0528.1 | chr22:24165044-24165065 | CCCCCTCCCTCCCTTTCCTCC | - | 6.84 | ZNF263 | MA0528.1 | chr22:24164670-24164691 | CCTTCCTCCCTCCCCGCCTTC | - | 6.88 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_11313 | chr22:24158927-24165716 | CD20 | SE_37327 | chr22:24163740-24170163 | HSMMtube | SE_40795 | chr22:24162712-24172446 | Left_Ventricle | SE_43086 | chr22:24163881-24168612 | Lung | SE_49124 | chr22:24164228-24167883 | Right_Atrium | SE_49502 | chr22:24164203-24165203 | Right_Ventricle | SE_58708 | chr22:24131220-24192441 | Ly1 |
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| 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 |
GH22I023821 | chr22 | 24164075 | 24170194 |
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Enhancer Sequence | GCTGGTCTCG AACTCCTGGG CTCAAGCAAC TCTTCCACCT TGGCCTCCCA AACTGCTGGG 60 ATTACAGACA TGAACCACTG TGCCTGGCCA GAGCTGGGTG TTTCTGTAAG GACGTCCTTT 120 GTCTTGATCC TGGAACATGA CTGAAGGAAA ACAAGAATCT TTGGAGCCAT GGCACATGAG 180 GACCATCTCT CTCCTCAGAA AGAGTGCCTT AGGTTAGAGC AGCATCTTCC AGATATTCTT 240 GGCAATGCTG GGACCAAAGC CCAGGCCTGG CTGCCCTTGC CAGGGCACCT GGCCCAAGTC 300 GGCTTTGCCC AGTTCCAGCA GGGGTTGGGG GGCAGGGGAG GAAGCTGGGG ACATGGTGCT 360 GCTGCAGTTT GAGCCATCAG ACCCTGTGGC ACTGTCCAGG CCCCGTCCAG AGAGTGCATG 420 GGGTGAGATG TGAGTCAGGG CTGGGGAGGT GGGCAGGGGC CTGGCCCTGC TGTGCACCTG 480 CTTGGGAGTC CTGGCCCCGT CTTAGCTCTG TGAGTCCACC TGGAGTCCAG CACTCCTCAC 540 TACCCCACCA AGGCCACTGC CAGATGGCTC CCTTCCTCCC TCCCCGCCTT CCAGTAGAGG 600 TCTCAGCATG GCAGCTCAGC CCATGTCTCT TGTCTGCCCA AAATACCGCA GAAGCTTCCC 660 ACATCCCTCT GTGGAAGCCA AGCCTGTCCA AAGGCCTCAG GGCCCTAACT GCTCTCTGCT 720 ACAGTCCCTC GCCACCCTCA TCTCCTCCCT TTTCCCCTCA CTGGGCAGAT CCGGGTACCA 780 GACCTTGGCT CCTCAGTCTT TTACATCTCT GTGTCCCCCA CCTGGGACTG TTCTCCCCCA 840 GGGAGCCACA TTCCTGCTCC CTGGGCACAT TCACTTCTTC CTAAAGGCCA CCTTCCTAGA 900 AGCCTTCCTG GCCTCCTGAC TTCTGAGGCC AGCCTGGACT TTCTCCCCCT CCCTCCCTTT 960 CCTCCCTGGC ACTCCCGTGC TTTCTGGTAC ACCACATGCT 1000
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