| Tag | Content |
|---|
EnhancerAtlas ID | HS150-09831 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr7:33744280-33745440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:33745229-33745241 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr7:33745233-33745245 | GTTTGTTTGTTT | + | 6.32 |
|
| | 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 |
| GH07I033705 | chr7 | 33744627 | 33747536 |
|
Enhancer Sequence | CATCAGTGGT CAGTTTAGCT GCAATATTCA CAGCACATTT GCTGGGGTTC AATTGATCAC 60
TGCACACAAG AGATAGAGTC AGCAAGGATG TGGTGCGGAG AGGCCAGGGG CTTGGGGGCT 120
TCCGCTCTCA CACATCTTCA AGCCCCATTT TGAAATGGTT TGAATTAATG ACACTTATTC 180
AGACAGACAA AGGAGGTAAA TGGAAATATT AGACAAGGCT TTGCACCTAC TTTGCTCAAC 240
ATTTCCCGTC ACCTTGAGTG CTGGAAACAC TCCACAGTCT TGCTCAGCCT GACCCAGGAG 300
CCGCATGAGC TCACATGCTG CTCGCAGACT AAAGCCAAGG ACCCTATTAG CGGAGGTTCA 360
CTAGACCAGT CTCAGGGACC TGAGCCCCTG TCCTCCAGCA TCAGGGCTGC CCTCTTTGGG 420
GGTGCCAATC CTCTCACCGA TTTTATCATT TTTGTGCTAT TTTGCTGGCA GTGCATGGAG 480
TAAGGGCACC ATTGAAAAAC TCATACCAAG TCGCATTTGA GTTTGCTGGC TGGGCTGCCA 540
AGCATCACCA AGCCAACAAA GTGAGGGCTA GGAGTCAGAG CTCGGCTTGA ATCCTCACTT 600
TGCCATTCAC TATGCGTGTG ACTTTCATCA AGCCACTTAC ACACTCTGAA TTCATCAGCC 660
ACACAGGATC CTGTGAGGCT TCACCGAGAC AAGCTGCGTC AAATGCGTGT AGGAGCATGT 720
GCTCCCGAGT CCTTCTGCCT TTGTCTTCCT GGTCCACCTC TGCTTCCTTA CCAGATAAGC 780
TGGAGCACAG GTCGTGGGAC CCTACAGGGA AGCAGAATCT CTAGAGCTAC TTGATCTGGC 840
AGGATATGCT CATTTGCAGA GTTTGAACTT GACATTGATG GCCTGCAAAG CCATTCTTTA 900
GCCAAGCCTA GGAATTTGTT CCCAGGGAAG CAGCTGGCTT TGTTTTTTTG TTTGTTTGTT 960
TGTTTTTCCC TGCTGGGCTG TGAAAAGCTA TCCCATTTCA CCCTCCTTCC ACAGGTAAGG 1020
GGCAAGAGTC CCCAGGGTAG GCAGGTGGGG AACAAAGGAT TGCAGTACAG ATTGAGTGGA 1080
TGCAGGGCCC CTTTGTTTCA TGGCCTACTG TGTGAAGGGA GTGAATGGGA GGCAAAGGCC 1140
TGCCAATGAG TAGATTAATT 1160
|
