| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21177 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:29913360-29914040 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr22:29913373-29913385 | GATGACGTCACA | + | 6.02 | | CREB1 | MA0018.3 | chr22:29913373-29913385 | GATGACGTCACA | - | 6.02 | | ESR1 | MA0112.3 | chr22:29913521-29913538 | CATGTCAACCTGACCTT | + | 6.17 | | JDP2(var.2) | MA0656.1 | chr22:29913373-29913385 | GATGACGTCACA | + | 6.32 | | MIXL1 | MA0662.1 | chr22:29913671-29913681 | GTTAATTAGA | - | 6.02 | | RORA | MA0071.1 | chr22:29913713-29913723 | TGACCTTGAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH22I029517 | chr22 | 29913661 | 29913690 | | GH22I029518 | chr22 | 29913701 | 29913810 |
|
Enhancer Sequence | AGAGAACAAG ACAGATGACG TCACAGGTAG AAATCAGGTG CCACAGATGG GTAACTAGCA 60
TCCTCCTGGG GCTCTCTGAA GGGCTCAGAT GGCCCGGCCA GCTATCCTGG TATACCTGGT 120
ACTCAGGAAG TACCCAGGTC AACACGTGCC AGGAATGCAA GCATGTCAAC CTGACCTTCA 180
CCCAGTGCTA TGTGCTTGTG GCCAGATCCA GTGCCAGCAC TTATGGTGCT TTCTCTTTAA 240
TGCAAATGAT AGCCTGCCAA AGAAAAACCC TTACAGTCAG AACTAGGGAG GGTGCCCCTG 300
CAGCAGTGAC TGTTAATTAG ATCAAATAGC ATAGAGGCCT GTGTTTTCAT AGCTGACCTT 360
GATGGAGGAA ACAACTGAAG TGTTGTGTGT CAGGGAGAAG AGCCAGATAA CTGCTCCAGG 420
GTAAATTCCT GCTGGCATTT AAATAAGCAA ATATGCCAAC ACAGTAAGTA CTGTCCAGAA 480
TGACAAGTTC CCTACCTTGG GACAAAACAA ACTCAGCAGT GCTGATGGGG AGCACGGCCC 540
GATGGACAAA CATCAGTGCT CTGGAGAGAT CGGCAGCCAT GTGGAGTCTA AGAACTGGTG 600
GGGAGTGGTC TCCAGATGTG TCCTGGAAAC CCAATGCCTT TCCTGACAGA GACTCTTTTT 660
TATTTTTTAC TTTTTATTTT 680
|
