| Tag | Content |
|---|
EnhancerAtlas ID | HS102-00394 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr1:23709960-23710830 |
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 | CCCTCATATC AAAATGATCC TCACATCATC AAACCTGGGA GAAAGGCATT ATTATTACTC 60
TTTTGCTCAA TGAGGTGAGT AACATGCTCA GCATGAGTAG GGCAGAATGG GACCTGAAAC 120
CAGGGATCCT GACTTATCTT GTACTTCTTG CTAAGTACCT TAGAACTTTT GGAGCACCTG 180
CAGCCTGCCT GGTGGCCCAG ACATCACATG GTGCACATGC AAGTCAGAGA GCAGTTGGAA 240
ACTGACAATA GGCACGTGAC CACACTCTGT TCCTTCAGGA GACTTGGCAG GAAGGAGCAC 300
TCTGGGAGGA GTCTTTGTTT GGCTCCCATG CGTGAAAACA AAACTTCTGC CTTTGCAGGA 360
GCTGGGGCAG TCTGAGTTAC AGACTTGGGT AAGACTTTCA GAGCTTCCTT AGGAGGGAAG 420
GATGGCCTGG TGGCATTTAG GTTCAACTCC TTTCTGACAG GGCTCAGCCT TCCTGTTTCC 480
CATCCTTGGC TGTGGCCAGG TTCAAAGGAA ATACCATCTG TGGAAGCACT TTCCAAAGAG 540
GCGTGGTCCA AGTGCAGAAT GTTTTTCCTC TCCTCTGTGG ATCTCAGGAA GCCGATTCCA 600
TCTGTGCTCA AATGACAGAC TTGCTCATCC TGTGATAAAA TGTGGGCTGC TGCCCCCACC 660
CCAGCTTGGT GCCCTTCTAA AATGAAAACA TGCATGTGTG TTCTCTCCCC ACCTCCCCAA 720
CAGCAATCCG CCACTATCTC TGGCTCTGCA GACCTACTCT GTGCAGGCTG GCAAGTGCTG 780
CCATGCACAA GGCCCCTTCT GGGTTGTGGG TACACTACGC CTTATGCGGG CGAGGTATGT 840
GGATAACAGG GAAGGGGGAA ATACATAAAC 870
|
