| Tag | Content |
|---|
EnhancerAtlas ID | HS049-00443 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr1:110967480-110968930 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr1:110968286-110968297 | CTTGAGTGCTT | - | 6.02 |
| | | 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 |
| GH01I110425 | chr1 | 110968501 | 110968650 |
| Enhancer Sequence | ATGCTGTTCT CTCTTGGCCT TATTTCCAAG GTTTGGACTC AAAGTATTAT TTTTTAACAT 60
CACAGAAATT TTTTATGCCC TGGTCTCTTG AGGGTAGGGA CTGTGTCTTT TTCATCTTTG 120
CCCCTTTCCA CATGCTCTGG TTTGTAGAAC AGAATTGAAG AAGGAGCCAT GTGCTAGATA 180
GAGCGGGTTG GGAGCAGCAG ACCTGCCTGC TCATTGTTTC TGTGACCTTG ACCCATCCTG 240
TAGTCTCCCC ACGCCTTGCT ATTCTCATCC ATCAACGATG AGATTGCACC TAAATCCTGG 300
GTGCTGTGCT GGGCCTGGGG ATGCTGTCTA ATCCCTGGGT TTCCTTCTAG TTTGCTCTAA 360
TCACCCATAT GAAAAAGAAG CTACTCAAGG CAAACATATA AATGAAACGG ATAATGAATG 420
AATAGTATTT TTTCTTGCTT TCTTTGGAAG AGGCATCCTG GATTCTACTT GAAGCCTGCA 480
GCCCTGACTC CTGGGCTGGG AGGTGGGCGA GGACTTGTAT TTTGTAGCTC TGCTAGAGAG 540
GGAACAGCTG TCCACTGGTG GCAGGACTGA CGCCTCCCAG AATACAGGGG CTTTGGATCA 600
GCAGGCGTCA GAGGGAAAGG AAACTGGCAT CCGAGTCTGC CTTTGAGAAA GGAGTAAATT 660
ACTATCTTAT TATAAATTCA TGATCCACTC ATTGCTGTTT TCAATTAATT TCTTGACAAA 720
TCTGGCTGTT CCTTTTCTTA TTTTCCTTAG GACAGGAGGT GTCCTGGTGA TCAGCTGGAG 780
CTCGGGGGAG CTGTTGCTGA AATTAACTTG AGTGCTTTGG AGAGAGATTT ACATGGCAGA 840
GTGGAGCCAG GGCTGCTCCT TTGGCAGGCA CTGCTGTGCC ACTGTGGAGG CGCCCCTGCT 900
TTTCCCATGC TTTGCAGTGT CTTTAAAGGC CTTTGGAGCC ATGCCCAGGC TCAGCCCCAT 960
CCTGGTGTCC CCCTGTGTCC GTTTTGCCAC TGCCCGGCTA CTTCACTTGG CCATGGGCCT 1020
TACCAGCTTG CAGACAAACC CGTCCATCTA CGCCTCCCAG CGCAGCTTGG CCCACTTGCA 1080
AGCACTTACA GAGGGTTTCA GAAGGAACAT GTCTGCCATC TGTGTTTGGA GACTGTGTCC 1140
CAGACTTTTG AGCTCACATT AGTCATGGCC ACAGACGGGA CTGGAGTCCT GCCCACTGGA 1200
GTCCCAAAGG TCTCTGGTGT TTGTTTTCCA CTCTGCATGC CTGGGTTGGG GGATGGCAGG 1260
GGGATACAGG TTGTTGGAGT ACCTCCCAGC CGGGCCGTTT CCTTGGTTCC CTGGGGCTGC 1320
CTTGCTTCCT CTCTAGATCA TCAGTCTCAG CAGAGGAAAC CAAAAATCTC CTCCTCGCCC 1380
CGCAACCACC TTTTGCTGAC TGCTAAGCAT CCCTGCTCTG AAACCATAAC CACCATAAAA 1440
GCAATAGGCT 1450
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