| Tag | Content |
|---|
EnhancerAtlas ID | HS133-21365 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr22:37598870-37600140 |
Target genes | | Number: 25 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr22:37599151-37599172 | TCACTCCTCCCTCCCTGCTCC | - | 6.04 | | ZNF263 | MA0528.1 | chr22:37599117-37599138 | GGAGGAGGAGAGGAGTGGGCA | + | 6.42 | | ZNF263 | MA0528.1 | chr22:37599114-37599135 | GGAGGAGGAGGAGAGGAGTGG | + | 7.34 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65579 | chr22:37599397-37600060 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 37599009 | 37599125 | | chr22 | 37599802 | 37600083 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I037203 | chr22 | 37599398 | 37600060 |
|
Enhancer Sequence | TCAACTCCCA TGGGTCAGTG GCCTCACCTG CCCCATCGCT TCTAGGTAAA GAGGATCCCA 60
AAGATCTGGG GGCCGTGGTC TTTCCTGCCC CAGGCCCTGC GGGTTCCCAG CTCCCCTCTG 120
ATAATGCTGA TGCTGATGCA GGAAGTCCTG GTCCAGAGCC TGGTGGCCAA GGGCTGTTGC 180
CTGGCAACCG CCTCGGAGAG ACAAGTTCAA GGTAAAGCCT CTGGTCTGAG CAACTTCAAT 240
GGCTGGAGGA GGAGGAGAGG AGTGGGCAAG GTGCGTTATC ATCACTCCTC CCTCCCTGCT 300
CCTGCTCACA ACTGCAGAGC CTCCCCTCAC CCTACAGCCC CAATGGCTCC CCTAACCCAC 360
AGATTCTAGC CCCAACCCCA TACAAGCTCC TTCAGTACCC CTGCCCCTTA TCACTCATTT 420
ATTCAGAGGC ACCATGCTGT AGCTTCACAG GAGGTTACAG GAACAGCGTG TACAGTACCC 480
CCTGCAGTTG TGACATGCAG TGGCCCCCTT TGTTCATTCA TTCCAGATAC TCCTAAGAAA 540
GGCCACGGCA GCACTGCCAG GCCCGGGGAA CGCAAGGCTG CCAGACACAC GTGTGTGGGG 600
GGACAAGCAC ATGCACACAC AGGCTGCACG TGAGCATGCA CAGGCGGGGA CACCCAGTGT 660
GGTGGGGAAG CAAGGGCTGC CGGGGCTAGG TGAGGGACCC TACCCAGGCA GCCACTCCCA 720
CCCAACGCTG GGGCCCCAGC AGTTCCTCCA CTCCCACCAC TTGCACACCG GCCGCATGTC 780
ACACCTCAGT GCCCATTCAC TCACGGACGC AGCTAAGATG TCCCGACCAC CTACTGTGCA 840
CCCTGCACTG GGCTCACACA AACCTGGACA CACAATATCA CACCCAGCAA AGGCAGCCAC 900
ACACAGCAAA CCCCACACAC ACCCAGACCC GCATGTTGTT GGTTGCTGGT GCCTGGCCCA 960
CCTCCCCTAG CCATTAGTAG GCTGTCCCTG ACCCACCCCT GCCCCACAGG CCAGGCCAGA 1020
GTGTCCATCA CAGTGCCCTA CCTTCTCTCT GGCTGGAAAT GTAGGCACAT GACCCGCACC 1080
TGGCCAACCA TGGCACCCTA TCACCACGTC TTTGGTGATT GGCCCAAGGG ACCATCATGT 1140
GACCTAGTTG GAGCCAATCC ACTTTCTTCC CTGAAATCTG CTATTTGGAT AATAGGGAGA 1200
AAGGACATCT ACTGCTTTTG GATCAAGGTC TATAAGGATG TGGGCTCAGC CCCATCAAGG 1260
GTATCTTCCA 1270
|
