| Tag | Content |
|---|
EnhancerAtlas ID | HS148-00099 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr1:12111920-12112820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr1:12112307-12112322 | GTGCTGAGTAAGCAG | - | 6.33 | | MAFF | MA0495.3 | chr1:12112307-12112322 | GTGCTGAGTAAGCAG | + | 6.48 | | RARA(var.2) | MA0730.1 | chr1:12112124-12112141 | TGAGCTCTGCCTGACCT | - | 6.22 | | ZNF263 | MA0528.1 | chr1:12112469-12112490 | CCTTTCTCCCCAGCCTGCTCC | - | 6.2 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_32538 | chr1:12111224-12119174 | GM12878 |
|
| | 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 |
| GH01I012051 | chr1 | 12111817 | 12113781 |
|
Enhancer Sequence | ATTAGTCCTA CATACCTGGC TAATTAATAC TAGGATTTAA AAAAAAAAGT TTGAAGCAAT 60
GATCACATAA AAAATGTTTT CTGTGTGCTG CTTATTTTGA CCTGAGTTCT GAGGAAGGCG 120
ATGGGACCAG CTGCCACAAG GCGAAGCTGC CTTGCCACCT GGGGCCTTGC AGGGTTGAGC 180
CCCGAGCACA GGGGCCCTGG TAGTTGAGCT CTGCCTGACC TGGTCATTCT GAAATCAGGG 240
GCCCCTCCCA GGAAGGCTGC GGGCCCAGGA GAGCAGCGAG GCAGGCTCAG AATTGGGGCT 300
TGAGATGACT CATCTGTGGC TATTTATTAC CCGTCTCCAT TTCTCGGTCT GATTGGGCTG 360
CTCATGGCCA AGCCTCCCTC CCTGTTGGTG CTGAGTAAGC AGCCTGGACC CGTCCTGCCC 420
CTCTGGCCTC ATCTGGAGCT CTCTCCTTTC CCTGTCAGTA ACCCTCGGGC CCCCCTGGGG 480
CCACTGAAAG TTCCCCCAGC CACCCTCAGC GAGCTCTTCC CAGCAGTCCC ACTCTTTGCT 540
GTTCTCACCC CTTTCTCCCC AGCCTGCTCC TTCTTTCAGG TCTCAGCTTG AGCCTCACCT 600
CTGCCAGGAA GCCCTCACTG ACCACTGCAT CCACCCCACC ACAGTCTGGG TAGGTGGCCG 660
CTGACAGGTG CTCCTAAAGC CCCTGCCCTC CCTCAGTAGT CCCTCCTCAC CCCAGCTGAA 720
GGCAACGTCA CTCTTCCAGT TTCCCAGGCC AAACCTTTGC CTCATTCTCG CACACATCCA 780
ATCCTTCAGT AAATCCCATC CCCAAAGTTC ACCCCTAATC CGGCCCCTTC CCTCTCCCAC 840
AGCTCCCTCC TGGCCCCAGC CTCCACCCCC TCCACCCTGG ATGCTTCAGT TGCCCCTGCC 900
|
