| Tag | Content |
|---|
EnhancerAtlas ID | HS129-00545 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:23709970-23710830 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Arntl | MA0603.1 | chr1:23710211-23710221 | GCACGTGACC | - | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27061 | chr1:23710018-23711255 | Esophagus | | SE_50618 | chr1:23709942-23711264 | Sigmoid_Colon | | SE_53272 | chr1:23709967-23711232 | Small_Intestine | | SE_65133 | chr1:23709934-23711086 | 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 |
| GH01I023383 | chr1 | 23710092 | 23712491 |
|
Enhancer Sequence | AAAATGATCC TCACATCATC AAACCTGGGA GAAAGGCATT ATTATTACTC TTTTGCTCAA 60
TGAGGTGAGT AACATGCTCA GCATGAGTAG GGCAGAATGG GACCTGAAAC CAGGGATCCT 120
GACTTATCTT GTACTTCTTG CTAAGTACCT TAGAACTTTT GGAGCACCTG CAGCCTGCCT 180
GGTGGCCCAG ACATCACATG GTGCACATGC AAGTCAGAGA GCAGTTGGAA ACTGACAATA 240
GGCACGTGAC CACACTCTGT TCCTTCAGGA GACTTGGCAG GAAGGAGCAC TCTGGGAGGA 300
GTCTTTGTTT GGCTCCCATG CGTGAAAACA AAACTTCTGC CTTTGCAGGA GCTGGGGCAG 360
TCTGAGTTAC AGACTTGGGT AAGACTTTCA GAGCTTCCTT AGGAGGGAAG GATGGCCTGG 420
TGGCATTTAG GTTCAACTCC TTTCTGACAG GGCTCAGCCT TCCTGTTTCC CATCCTTGGC 480
TGTGGCCAGG TTCAAAGGAA ATACCATCTG TGGAAGCACT TTCCAAAGAG GCGTGGTCCA 540
AGTGCAGAAT GTTTTTCCTC TCCTCTGTGG ATCTCAGGAA GCCGATTCCA TCTGTGCTCA 600
AATGACAGAC TTGCTCATCC TGTGATAAAA TGTGGGCTGC TGCCCCCACC CCAGCTTGGT 660
GCCCTTCTAA AATGAAAACA TGCATGTGTG TTCTCTCCCC ACCTCCCCAA CAGCAATCCG 720
CCACTATCTC TGGCTCTGCA GACCTACTCT GTGCAGGCTG GCAAGTGCTG CCATGCACAA 780
GGCCCCTTCT GGGTTGTGGG TACACTACGC CTTATGCGGG CGAGGTATGT GGATAACAGG 840
GAAGGGGGAA ATACATAAAC 860
|
