| Tag | Content |
|---|
EnhancerAtlas ID | HS182-07551 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr15:78569820-78571000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIC | MA0687.1 | chr15:78570366-78570380 | TTCTTCCTCTTTTC | - | 6.47 | | ZNF263 | MA0528.1 | chr15:78570352-78570373 | TTCTCTTCTCCCTCTTCTTCC | - | 6.05 | | ZNF263 | MA0528.1 | chr15:78570358-78570379 | TCTCCCTCTTCTTCCTCTTTT | - | 6.13 | | ZNF263 | MA0528.1 | chr15:78570355-78570376 | TCTTCTCCCTCTTCTTCCTCT | - | 7.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr15 | 78570794 | 78570890 | | chr15 | 78569905 | 78570023 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH15I078275 | chr15 | 78567772 | 78570087 | | GH15I078278 | chr15 | 78570821 | 78570970 |
|
Enhancer Sequence | AGACCTCCCA AGGCACCCAT TTCCTCCCTC AAGGAGGAGT TTGAGGATCA CAGTTTACAC 60
GAAGCTCCAG ACCACTGGTT GTGAGCTCAA CACCCTGGCA TTGTGTCCAA GATGCCCTTA 120
CGTGGTCACA GCCCAGATCC TAGCCCTCCT GAGCCGGGGC TGGGAAGCAT CTGTGTGTAA 180
CTTCTTTGGG AAAGCCTGTC CTGTCCAGGG GTGGACTATT TGAGGTCCTG GGCCCCACCA 240
AGAGCCAGCG TTCCTTGCTG TCTCAGCTGA CCCCAGCCTA GGGAGCCGGG AGCCAAATGG 300
AGTGAGGGTG GTGGAGAAAG AGCCCCAGAG GGAAGGAAGT GGCAAATCCC AAGAAATCCA 360
TTTCCTTCTT TATTATAAGG AAGGGTGGAG CATCCAGGAA ACCTGCCGTT GGAGAGTTCT 420
TTGGGGATTT GTTTGTCCTT TTTGTTTTGT TTTTGTTTTT ACTTTGTTCT CTTTTGCACC 480
CTCTCTTTTC TTCACCCCTC TTTTGTGTTG GCTTATTTCT TGTTTCTCCA TTTTCTCTTC 540
TCCCTCTTCT TCCTCTTTTC TGCTGTTGAA ATGCCTTCTT CCCCAGAGCC TTTTAGCCTG 600
TTATGAGCAT TGCTGAGGAT TGGATTAATT AAAAAAGTGA TTTTGGAGCC ACACAAGGGT 660
GTGATGGCCC TGCCTGCAGG CAGGTATTTA CCTGCCGGGA GAGCCTAACT CGTGGTCTTC 720
TTCTCTTACC TGTAGTTTTC CATGCTTGGT CAGTTTCCCA GCTCCCAGCA AGCTAGAAGC 780
AGAAGCATGG GGAGTAGGGC TTGAGAGCAG CAAGAAGCGA CACCTGATAG GAATGGGGAG 840
ACAGAAAAAC CAGTCATATG TAACTTAACG AAGGGGATAT GTTCTGAGAG ATGCATTGTT 900
TGGCGATGTC GTTGTGGTGT GAACACCATA GAATGTACTC ACACAGACCT AGATAGCATA 960
GCCTGCTACA CCCTAGGCTG TGTGGCATAG CCTGTTGCTC CTGGGCTAAA ACCTGCACAG 1020
CAGGTTGCTG TACTGAATAC TGTGGGCAGT TGTAGTACGA TGCTGAGTAT GTGAGTATCT 1080
GAACATAGGA AAGGTGCAGT AAAAGTTTGG TGTAATCTTT GCAACCATCT TCATAAATGT 1140
TGTTGACTGA AAGGTCACTA TGCTGTGCAT GACTGTATTT 1180
|
