| Tag | Content |
|---|
EnhancerAtlas ID | HS153-00121 |
Organism | Homo sapiens |
Tissue/cell | Osteobl |
Coordinate | chr1:12111830-12112900 |
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 | | ZNF263 | MA0528.1 | chr1:12112822-12112843 | CTCTCCCCTCTCTCGTCCTCC | - | 7.02 | | ZNF263 | MA0528.1 | chr1:12112825-12112846 | TCCCCTCTCTCGTCCTCCCCC | - | 7.31 |
|
| | 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 | ATCCTAGCTC ACTGCAGCCT CGATTTCCTG GGTTTAAGCA ATTCTCCCGC CTCAGCCTCC 60
CAGGCAGCTG GGACCGCAGG TGAGCACTGT ATTAGTCCTA CATACCTGGC TAATTAATAC 120
TAGGATTTAA AAAAAAAAGT TTGAAGCAAT GATCACATAA AAAATGTTTT CTGTGTGCTG 180
CTTATTTTGA CCTGAGTTCT GAGGAAGGCG ATGGGACCAG CTGCCACAAG GCGAAGCTGC 240
CTTGCCACCT GGGGCCTTGC AGGGTTGAGC CCCGAGCACA GGGGCCCTGG TAGTTGAGCT 300
CTGCCTGACC TGGTCATTCT GAAATCAGGG GCCCCTCCCA GGAAGGCTGC GGGCCCAGGA 360
GAGCAGCGAG GCAGGCTCAG AATTGGGGCT TGAGATGACT CATCTGTGGC TATTTATTAC 420
CCGTCTCCAT TTCTCGGTCT GATTGGGCTG CTCATGGCCA AGCCTCCCTC CCTGTTGGTG 480
CTGAGTAAGC AGCCTGGACC CGTCCTGCCC CTCTGGCCTC ATCTGGAGCT CTCTCCTTTC 540
CCTGTCAGTA ACCCTCGGGC CCCCCTGGGG CCACTGAAAG TTCCCCCAGC CACCCTCAGC 600
GAGCTCTTCC CAGCAGTCCC ACTCTTTGCT GTTCTCACCC CTTTCTCCCC AGCCTGCTCC 660
TTCTTTCAGG TCTCAGCTTG AGCCTCACCT CTGCCAGGAA GCCCTCACTG ACCACTGCAT 720
CCACCCCACC ACAGTCTGGG TAGGTGGCCG CTGACAGGTG CTCCTAAAGC CCCTGCCCTC 780
CCTCAGTAGT CCCTCCTCAC CCCAGCTGAA GGCAACGTCA CTCTTCCAGT TTCCCAGGCC 840
AAACCTTTGC CTCATTCTCG CACACATCCA ATCCTTCAGT AAATCCCATC CCCAAAGTTC 900
ACCCCTAATC CGGCCCCTTC CCTCTCCCAC AGCTCCCTCC TGGCCCCAGC CTCCACCCCC 960
TCCACCCTGG ATGCTTCAGT TGCCCCTGCC TGCTCTCCCC TCTCTCGTCC TCCCCCTCTT 1020
TTCCTGGGCC ATCTATTTCC CACGCAACAG CCGGAGTGAC CCGGACAACC 1070
|
