| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01133 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:23710020-23710800 |
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 | TTTTGCTCAA TGAGGTGAGT AACATGCTCA GCATGAGTAG GGCAGAATGG GACCTGAAAC 60
CAGGGATCCT GACTTATCTT GTACTTCTTG CTAAGTACCT TAGAACTTTT GGAGCACCTG 120
CAGCCTGCCT GGTGGCCCAG ACATCACATG GTGCACATGC AAGTCAGAGA GCAGTTGGAA 180
ACTGACAATA GGCACGTGAC CACACTCTGT TCCTTCAGGA GACTTGGCAG GAAGGAGCAC 240
TCTGGGAGGA GTCTTTGTTT GGCTCCCATG CGTGAAAACA AAACTTCTGC CTTTGCAGGA 300
GCTGGGGCAG TCTGAGTTAC AGACTTGGGT AAGACTTTCA GAGCTTCCTT AGGAGGGAAG 360
GATGGCCTGG TGGCATTTAG GTTCAACTCC TTTCTGACAG GGCTCAGCCT TCCTGTTTCC 420
CATCCTTGGC TGTGGCCAGG TTCAAAGGAA ATACCATCTG TGGAAGCACT TTCCAAAGAG 480
GCGTGGTCCA AGTGCAGAAT GTTTTTCCTC TCCTCTGTGG ATCTCAGGAA GCCGATTCCA 540
TCTGTGCTCA AATGACAGAC TTGCTCATCC TGTGATAAAA TGTGGGCTGC TGCCCCCACC 600
CCAGCTTGGT GCCCTTCTAA AATGAAAACA TGCATGTGTG TTCTCTCCCC ACCTCCCCAA 660
CAGCAATCCG CCACTATCTC TGGCTCTGCA GACCTACTCT GTGCAGGCTG GCAAGTGCTG 720
CCATGCACAA GGCCCCTTCT GGGTTGTGGG TACACTACGC CTTATGCGGG CGAGGTATGT 780
|
