| Tag | Content |
|---|
EnhancerAtlas ID | HS180-00804 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:23710010-23710830 |
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 | ATTATTACTC TTTTGCTCAA TGAGGTGAGT AACATGCTCA GCATGAGTAG GGCAGAATGG 60
GACCTGAAAC CAGGGATCCT GACTTATCTT GTACTTCTTG CTAAGTACCT TAGAACTTTT 120
GGAGCACCTG CAGCCTGCCT GGTGGCCCAG ACATCACATG GTGCACATGC AAGTCAGAGA 180
GCAGTTGGAA ACTGACAATA GGCACGTGAC CACACTCTGT TCCTTCAGGA GACTTGGCAG 240
GAAGGAGCAC TCTGGGAGGA GTCTTTGTTT GGCTCCCATG CGTGAAAACA AAACTTCTGC 300
CTTTGCAGGA GCTGGGGCAG TCTGAGTTAC AGACTTGGGT AAGACTTTCA GAGCTTCCTT 360
AGGAGGGAAG GATGGCCTGG TGGCATTTAG GTTCAACTCC TTTCTGACAG GGCTCAGCCT 420
TCCTGTTTCC CATCCTTGGC TGTGGCCAGG TTCAAAGGAA ATACCATCTG TGGAAGCACT 480
TTCCAAAGAG GCGTGGTCCA AGTGCAGAAT GTTTTTCCTC TCCTCTGTGG ATCTCAGGAA 540
GCCGATTCCA TCTGTGCTCA AATGACAGAC TTGCTCATCC TGTGATAAAA TGTGGGCTGC 600
TGCCCCCACC CCAGCTTGGT GCCCTTCTAA AATGAAAACA TGCATGTGTG TTCTCTCCCC 660
ACCTCCCCAA CAGCAATCCG CCACTATCTC TGGCTCTGCA GACCTACTCT GTGCAGGCTG 720
GCAAGTGCTG CCATGCACAA GGCCCCTTCT GGGTTGTGGG TACACTACGC CTTATGCGGG 780
CGAGGTATGT GGATAACAGG GAAGGGGGAA ATACATAAAC 820
|
