| Tag | Content |
|---|
EnhancerAtlas ID | HS141-01488 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr1:186587060-186588240 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:186587382-186587393 | TGGGTGTGGCC | - | 6.62 | | NFIA | MA0670.1 | chr1:186587613-186587623 | GGTGCCAAGT | + | 6.02 | | POU4F2 | MA0683.1 | chr1:186588106-186588122 | CTAATTAATGATTCAC | - | 6.13 | | SPI1 | MA0080.4 | chr1:186587939-186587953 | ACAAAGAGGAAGTA | + | 6.18 | | SPIC | MA0687.1 | chr1:186587939-186587953 | ACAAAGAGGAAGTA | + | 6.89 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 186587154 | 186587268 | | chr1 | 186587444 | 186588060 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I186617 | chr1 | 186586933 | 186588332 |
|
Enhancer Sequence | CTAAAGCATA CTCTGGGAGA ATGGAGAGAA AAACAACTGT GTGATGGAGT CAGGAAAGGA 60
CTTCGTTTGA GCTGATCACT ATTCCCCTCA GACTAAAACA AAGTGTTTGT CCATCTGAAA 120
GTGCTGATCT ACAGTTTTGA GACAGAGGGC AGTGGATGGA CAGTGGATGG GTCGGGTTTT 180
GGCAATGAGA GGGAGCTGAT TTGAATTAGA GGAAGTAAAA AAGTATGGGA GAGTTCTGTG 240
GGGAATCATT AGGACTCCTT AGGAGATAAC AGACGATTCC AAGCAGCAGA TGAGGTGAAG 300
TCGAACTCCA CTGGACCTGT GGTGGGTGTG GCCAGCGTCA TCCATCCAGA GTGAACCCCA 360
ACAGGAGCCA CTCCGGGGCT GGGGCAGGCG GATGATCTGC AGACAAGGCT TTTAATGGGC 420
TATGTTTGGG AAAAATATAT TTTATATATA ATAGATTATA TTTGTAAAGA CTTGTAGTTT 480
CAGGATTTCA TACAAATTAG CTTTCCAGTA TTGAGCCACT GCAGTTAGGG CCCGGTCTCT 540
GTCCAGCAGG CTGGGTGCCA AGTTCAGTGT CACAGCGTTC AGCAGGTGAG ACACTCTTAA 600
TAGGCAGACA CGGTGCCTCT GAACGCACAA CGTGCAGTAA AGGAAATGCA GGCAATCCCT 660
GTAAGGAGGA AGTGGTTAAG GGATCGAAAG CAGCTTGAGA CTTGTGCAAT GCAGTCATTG 720
TCACCGAAAA CTCCAAATGC GTTTTCATTT TCAAATGCTG AATTACACAC AGGATTGCAC 780
AAGGAAAGTC TCAGAAGACT TCCAACCAGA GAGCCTTGAT TCCAACTGGC TTTGCTTCCA 840
AGAGCACATT CGGGACATTT TGAAAACCTG CCCCCAAAGA CAAAGAGGAA GTATTTTGTT 900
GTGGAAATCT GGTGGGTGTT TTTTGTGTGT GAATGGATGA GGAAAACTGC ACGCTCGTTT 960
AATTCAATAA GTTAATATCA TCTGGCAAAA GCATCTCTCA TACAGGAGGG ATTGAGGGTT 1020
TTTAACAAAA CATTTTCCCT ATGGACCTAA TTAATGATTC ACTCATTTAG TGTTAATGCA 1080
CTTACTCATC CTTTAATTTA TTACTCAGAT ATGTTGGCCC CTCACATCCC ATTTATCTGT 1140
TAGAAACAGT CAAGCTTGCC CAAATATGAA TAAAGCTGTT 1180
|
