| Tag | Content |
|---|
EnhancerAtlas ID | HS031-13782 |
Organism | Homo sapiens |
Tissue/cell | Denditric_cell |
Coordinate | chr20:16536390-16537440 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NEUROG2 | MA0669.1 | chr20:16537203-16537213 | AACATATGTC | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr20:16537191-16537206 | TGACCTTTTGACAAC | - | 6.06 | | SOX10 | MA0442.2 | chr20:16536888-16536899 | AAAACAAAGAA | + | 6.62 | | ZNF263 | MA0528.1 | chr20:16536680-16536701 | CCTCCTTTACCATCCTCCCCC | - | 6.28 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGGGAAGATG GCAAAAACAA AAACAACCAC AAAATTTTCT CATTCTTCAA AATCAAAACA 60
GAAAGGAATT CAAGCCAAGA TCAAATCAAA GACAATCAAA TCAGTTTCAT GAGCACTTAG 120
GCTCTAGAGA AGGAGGAATG GATTATTTCT ACTGACTCAT TAATTCATTT ATTAGTCATT 180
AGAAAGGGCA GAAAATCTGA AAACTATTTG TTGGTAGAAA ACATAGGCTA TGTTACCCTG 240
GAAACAAGGT TCCCTTGGGG AAAAGCTTGC CTTGGAGTAT TCCTAAATTC CCTCCTTTAC 300
CATCCTCCCC CTTCCAACAC TGGGCCACTC ATTAGACACT GATAACATCA GCCCCCACCT 360
CCCCAGCTCA TCTTCAGAGG TGGTCCAGTA CCAACAGAAT AAAGGCTGTT CATCTCAGCA 420
CTAGAAGAAA CTTACAGGTC ACTTGGGTGC AACTTCTTTA CATGACACTC TAGCTGGTGA 480
TCAGCCTCAC CAAAAACAAA AACAAAGAAA CAGCACAACC AGGTGGTATC ACACCTGTCT 540
CCTCAACAGA ATGGCTCTCC ACATTCTCAC ACCGCTCTGC CATGAACCAA CTGGTCACTA 600
ACTGGCTACC CGGAGACTCC AGAGAGCAAG GACTATGCCC ACTGTGGCCT CGATGCAAAA 660
CACGATGCTT TGCACTCTAT ATGTGGTCAG TAAATGCTTG CTGAGTGAAT AATCATGACT 720
GTATACATCC ATGCCTCTTG CGCAAATCAC TGTGTGTCTA TTCTTGCCCC CTGGGATTCT 780
GTTCTCCATT AGCAGCACAA GTGACCTTTT GACAACATAT GTCAGGCCAA CACATGTTCT 840
CACTCCTCCA ATGGCCCTAC CACACTTAAA ACCTAAGACT TTAGGTGGCT TAATAGGCCC 900
TATATGAGCC ACACTTCCCT ATTCTGGGCC CACAGACCTC CCTGCACCCA TTGCATGTTC 960
CAGGCATGCT CCTGACACAC AGCCTCTGCA CTGGCTGTTA CTTCTGCCTA GAATATTCTT 1020
CCCAGATATT CCCACGGTTC ATTACCTTAC 1050
|
