| Tag | Content |
|---|
EnhancerAtlas ID | HS048-23734 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr21:38160090-38160930 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr21:38160518-38160528 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr21:38160518-38160528 | GGCACGTGCC | - | 6.02 | | NFE2L1 | MA0089.2 | chr21:38160578-38160593 | TCATGACTCAGCTGT | + | 6.11 |
|
| | 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 |
| GH21I036787 | chr21 | 38160210 | 38161040 |
|
Enhancer Sequence | AAAAGACCTG TGAAGATGCC TGATCAGCTG TCAGGGTTAC GTAGACACTG GCTGCTGTTA 60
TTTACTGTTC CCTGGCTGAT AAAATAGCCA GGTCACCTGT GCCGATGACC AGACCCACCC 120
CCTACCCACC AGCAGGGCTG CCAGGGCTTT CTGGGGAGAC GCTGCAGCTT GGTTCTTATT 180
TCCTTTGCTC TGCATCCCTC TGGGTTGACT TGAGTCTGAT CATGGGTTTA TTCCATTTCC 240
ATTTTGCTAG ATTCCCTCCA CTCCCTCAAG CTTCTACAAA ACTGTGGGGC CACCACTCCC 300
CACAAAAGAT TAAAACCAAG ATGTTTCCTA GAGGTGGCAT TTTGTCTTCC TGAAGCTGTT 360
CTGTGCACAG GTCCTCTCCA CACTCATGCC AAATGCTCGG TGAAGCGTCT TCCTGAATGT 420
CCCTAAGGGG CACGTGCCAC TGGCAGAGCT GATGGGCACA CCTCACTCCC ACACATGCTG 480
TGCCGAGCTC ATGACTCAGC TGTGCAGGGC CCGCCCAAGA GTGAGGCAAA CACCAACACC 540
GCACAGCGAC CCTTTGTCAA TGGTGGGGAC CTCAGTGGCT TCTCCATCGG AACTTAGGGC 600
TGACGGGCCT CCAGACCTAC TGTTACACAC TGGCCCACGG AATGACCCTC ATAAACCCAA 660
GAACAGTAAA CAGAGCTTAA CATTCTAACG AAATCAAGAT TGCTGTGTGT GCTTTCACAA 720
AATGAAACTG CCTGGAACTT CTCATAACGT TTTTTATGAT AAGCATTAAA ATGCAAAGAG 780
GAAGATTAAA GTTCCTGCTA CAGACCAGAG CAGTAATGAG TGTGGGAGGA GGAGCTCTGG 840
|
