| Tag | Content |
|---|
EnhancerAtlas ID | HS133-17465 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:112292410-112293960 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr2:112293257-112293270 | CAGAGGTCACGTG | + | 6.04 | | Nr2f6(var.2) | MA0728.1 | chr2:112293757-112293772 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_38958 | chr2:112288701-112293901 | IMR90 | | SE_45056 | chr2:112288758-112293525 | NHLF | | SE_59305 | chr2:112276470-112293872 | Ly3 | | SE_64190 | chr2:112292352-112293282 | HSMM | | SE_64420 | chr2:112289234-112292941 | 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 |
| GH02I111532 | chr2 | 112289579 | 112293509 |
|
Enhancer Sequence | ATCTTGCAAA AAAGAAACCA CAGCTTTAAA CCCGGGCTTC TCTTCTCGGT TCTGCTTTCT 60
TCCAGGGATT CCAAGCGACA GGGCACATGG TACAATGCCT CCCATTCAGT AGATGCACCC 120
CAGAAACATT GTTATGTTGC CCTCACCATG AAAACCACTC TTCACTGAGC ACTGGCCGTT 180
TAATGGGCCT GACGTCATAT TGCCACGTGA AGCAGCCAGC CCTCTACTTT TGAAAACACC 240
CTTTAAGGAA ATGATTGCAA AGCTTGACTA TAAAATATTT TCAGATATTT GAATGAGAAA 300
ACAAAAAGCC ATGGTTCCCC ACTGAGAGAC ACAGAAAGAA CTCCTACAGC TCTGCCCCCT 360
CCCCACACAG ACCAGCCCTC CTTCCTTGAG GACAGGACTG ACTAGGTCTG AACACAGCAG 420
GTGCCCCACG CATGAGCTGA ACTCCACTGA ACTACAGCCA GTCACACAGA CTGGAGGGTC 480
TTTCTGTGGG ATTCTCCCAT TCCCACTGAA TCCTTCCCAT AGGCAAAAGG TAGTTCCCTA 540
AAACAAATGA GAACAGCTGG AAGGGATCTG TTTACTGAAT CAAGAAAACA CTTAAATCTA 600
TTAACTGAAT GAAGACAACT GAAAAACAAA ACATTCCTGA AGGATTAAAC TCTGCAGAAA 660
GAAGCTGGCA TTTGCCCAGG ACAAGGACAG GCATCCTTTA CAATGCTTAT CTCAGTTAGA 720
ACAGCCTTGT AGGTAGACAG GGCAGAAGGA TCTCTGCTGG GTCAGCCTAA CAGGAGCAGG 780
AAGGGTCACC TGGTGCAAAA ACAGGGGAGG AAAGTTTCTG ACCAGCTGAT GTGAAAGCAA 840
AGTTGGCCAG AGGTCACGTG AGGGAAGTCT GCTAGGATGC CTGTCTCAGT CTGTGTAGTT 900
TTGCTATGAA GAAATATCTG AGGCTGGGTA TTTACTTTTA AAAGAGGTGT ATCTGGCTCA 960
TGGGTCTGCA GACTGTACAA GCAGGGTGTC AGCATCTGCT TCCAAAGAGG GCTTCAGGCT 1020
GCATCTGCTT ACGGTGGAAG GTGAAGGGGA GCCCTGTGCA GAGATCACAT CATGAGAGGA 1080
GAAGCAAGAA AGAGGACACG AAGGTGCCAA GCTCTTTTTT TTTTTTTTTT TTTTTGAGAT 1140
GGAGTCTCGC TCTGACGTCC AGATTGGAGT GCAATGGTGT GATCTCGGCT CACTGCAACC 1200
TCCACATTCC AGGTTCAAGC GATTCTCCTG CCTCAGTCTC CTGAGTAGCT GTGATTACAG 1260
GTGCACGCCA CCACACCCGG CTAATTTTTT TTATTTTTTT GTATTTTTAG TAGAGATGTG 1320
GTTTCGCCAT GTTGGCCAGG CTGGTCTTGA ACTCCTGACC TCAAGTGATC CACTCTTTTT 1380
AACAACCAGC TCTCACAAAC TAACAGAGTG AGAACTCATT CTCCCTCACC CTACCCAGGG 1440
AGGACATTCA TCTATCATGA AGGATTCACC CTCATGACCC AAACACCTCC CATTAGGCCC 1500
CACTTCTTAA CACTGGGGAT CAAATTTCAA CATGAGATTT GGTGGAGACA 1550
|
