| Tag | Content |
|---|
EnhancerAtlas ID | HS181-14260 |
Organism | Homo sapiens |
Tissue/cell | Sperm |
Coordinate | chr6:155469470-155470660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr6:155469867-155469877 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr6:155469867-155469877 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr6:155469867-155469877 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr6:155469867-155469877 | AACAGCTGTT | - | 6.02 | | RUNX1 | MA0002.2 | chr6:155469602-155469613 | TTCTGTGGTTT | + | 6.32 | | ZNF263 | MA0528.1 | chr6:155470500-155470521 | GAATGAGGAATGGGATGAAGA | + | 6.09 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 155469804 | 155470181 | | chr6 | 155470200 | 155470600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I155148 | chr6 | 155469641 | 155471202 |
|
Enhancer Sequence | ACTGTTTGTC TACACCTGAG TTTTCTTCCA TTGCTCATGT CACTTGTGCA GTGACTGAAC 60
GCATGCTGTC ATCTTGGTGG TATTTCTTGG CTCACATCTT GGTGGTATTT CTTACACCCT 120
GGGGGAAATA ATTTCTGTGG TTTTTCATTT TAGGTACCTA ATGTTTGCCA TTTTGTGACA 180
TGGGTGATAT GATATGCTTT ATGACCTTTG GCGGCTCTAT GTATATACTG AAATATTTTG 240
TGACCCAAAC TTAATTCCTA ATTTGAATAG TGCCTTCTGG CCTTGATGAT TCACTCATAT 300
ATTGTCATTT TCTGAACAAA ATCCATACAA TAAAACCACT AGAAGATTAG ACAGGTAAGA 360
TTCTAATACA ATAGCTTTGG AAAACGTGGT TTGGTGTAAC AGCTGTTTCT GTGTCTATGG 420
ATTGCAAAAA AACAGTAATT TTTCTGGTTA TAACAGAGAA GCACGTAACG AAATGCTTTC 480
TTTTCTCTGC TGCGGTTCCA TATTCATATA ATAAATGGCT GCTTCCTATG GCATTTGCAT 540
TTTAGAGAAG GGAAAACAGT TTGAAAATTT TTATTTCCCT TTGCTCAGAC AACCTAAACA 600
CTTAGACAAG TGTTAGTGGA ATTTCGAGCA TCCCTATCTT AGTCAGGTTT CCTAGGAGAC 660
AGACTTTGAT AGTGATTTAG ATGTAAAAAG TTTTACTGGG AATGCTCTCA GGGACAACGC 720
CAGCCTGGAG TGAGGGAGCA GGATCTGGGA GGGACAAGTT GCATTGTGAT GCAGCTTGTC 780
CCACAGCGAG CTGTGGAGCT GGGAGGGCCA TTCAGAGCTC TGCATGGAGG CAGGGTGGCC 840
GGCCTTCGTC CCCTCAGGCC AGCAGGGCAA GGCAGCTCCC CTCAATAGAG GTGAGTTACC 900
ACGAGGGGAT CTGTGTGTGA GCTGGGAAAA GGAAAGCAAT GCCTCTGTCT TGAAGGGGGA 960
ATCCGGGTGA TTCACTATAG AATCCACTAC AGCCCCCTCC AAAACCAGTT GTCAAATGAC 1020
CTGGGAACTT GAATGAGGAA TGGGATGAAG ATAGATAGTG AGCAGGTTCT TGCATTTTTC 1080
TTCCTTTAGT TACTTGTTAA GTTATTACAG AGAAACCAGT TTCTTTAGGA AAAAAAATTT 1140
CATGGTAACA CAACAATTTA GACATAGTGT GACTTATTAG AAAGGAATTT 1190
|
