| Tag | Content |
|---|
EnhancerAtlas ID | HS176-00163 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:12111800-12112650 |
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 | CTGTCACCCA GCCTGGAGTG CAGTGGTGCA ATCCTAGCTC ACTGCAGCCT CGATTTCCTG 60
GGTTTAAGCA ATTCTCCCGC CTCAGCCTCC CAGGCAGCTG GGACCGCAGG TGAGCACTGT 120
ATTAGTCCTA CATACCTGGC TAATTAATAC TAGGATTTAA AAAAAAAAGT TTGAAGCAAT 180
GATCACATAA AAAATGTTTT CTGTGTGCTG CTTATTTTGA CCTGAGTTCT GAGGAAGGCG 240
ATGGGACCAG CTGCCACAAG GCGAAGCTGC CTTGCCACCT GGGGCCTTGC AGGGTTGAGC 300
CCCGAGCACA GGGGCCCTGG TAGTTGAGCT CTGCCTGACC TGGTCATTCT GAAATCAGGG 360
GCCCCTCCCA GGAAGGCTGC GGGCCCAGGA GAGCAGCGAG GCAGGCTCAG AATTGGGGCT 420
TGAGATGACT CATCTGTGGC TATTTATTAC CCGTCTCCAT TTCTCGGTCT GATTGGGCTG 480
CTCATGGCCA AGCCTCCCTC CCTGTTGGTG CTGAGTAAGC AGCCTGGACC CGTCCTGCCC 540
CTCTGGCCTC ATCTGGAGCT CTCTCCTTTC CCTGTCAGTA ACCCTCGGGC CCCCCTGGGG 600
CCACTGAAAG TTCCCCCAGC CACCCTCAGC GAGCTCTTCC CAGCAGTCCC ACTCTTTGCT 660
GTTCTCACCC CTTTCTCCCC AGCCTGCTCC TTCTTTCAGG TCTCAGCTTG AGCCTCACCT 720
CTGCCAGGAA GCCCTCACTG ACCACTGCAT CCACCCCACC ACAGTCTGGG TAGGTGGCCG 780
CTGACAGGTG CTCCTAAAGC CCCTGCCCTC CCTCAGTAGT CCCTCCTCAC CCCAGCTGAA 840
GGCAACGTCA 850
|
