| Tag | Content |
|---|
EnhancerAtlas ID | HS177-18702 | Organism | Homo sapiens | Tissue/cell | SK-N-SH_RA | Coordinate | chr5:153897420-153898620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr5:153898324-153898335 | AGAGATAAGGA | - | 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 |
| GH05I154516 | chr5 | 153896208 | 153898222 |
| Enhancer Sequence | ATTCTTTGGG CCTTAGTTTC TTCACCTCTC AAGCAGAGAT AAAAGTGGGT GACAGGGAGG 60
AGCCTGTCCT TAGCTCCAGA AGGCCAGGGA AGCAGCAGGC AGAGTCGGGC AGGGCGTGAA 120
GCACGTGGGG CTCTGGGCTC ACCCTGCTGG GGCTCAAGTC CCACTTTCCC CGCTTATCTC 180
AGTGTGACTT TGAGCAATCA CTTGACCTCC CTCTCTGTGC ATTGGTTTCC CCATATGAAA 240
AAAACAGGGG AAGAACAACA CGAGTCAACC TCCATGAAGT GCATAGCACG TAATGAGTGC 300
TCATAAGTGT GAGTTACTGT TGTTTTTGTT CGCAGGAGAA TATGGCGTAG TAATTACAGT 360
ATTGGGGTTG ACGAACTGGC TGTGCTGTGT GACCTTGGGC AACTGACTTA ACATCTCTGA 420
GCCTCTGTTT TCTCATCTGT AAAACAGGGG CAGTGTGTCT TTGAGGCTCT AGTGAGGGTC 480
TTGGCACAGA TTGTGGCCCC ATTGGCTGGG GTGAAGCTGG GAGCTGCCAG TGACCTGCAG 540
GGAGGGGTGC CTGCCTGAAA GATGGAGACA GCCTGCAGGC CTTTGTTTAC AGAGCCCATC 600
TCTCCTCTGA TGGATGCGGC CAGCAGAAGT CTGTTTGCAA GTTTCTCCTG GAAACATGAA 660
TCAAGGTCTG TTTGGAGAAC ACGTGCGCTC CTCTGTCAAA CATTCCACCC GTGCTGGGGC 720
CACAGAGCCT TGAGAGCAGA GTGGGTCCCA GATTGTCCCC AGAGATAGGG GATAGGCCAG 780
GATACCCAGC CCCTCCGGCC AGGCTTCAGA GGGGACAGCC TGGGCTCCGA GACAGATGCC 840
CTCCCTGGCC TCAAGGAGCT CTCTAGAAAG CAAGATAAGA CCCGGACTCG ACCAGAAAAC 900
AGGGAGAGAT AAGGACCCAT CTGCTTCCAC TCTTGTCCCC TCTGATCCTC CACAGCAGCC 960
CTGAGTGATC TTTTTAAAAT GTAAATTTCA TGGCTCACTC CTGCTCACAA CCCTCTGTGA 1020
CTTCTTTAGT AGTTGAATCA AAATCTGATT CCAGGCCGGG CTTGGTGGCT CACACCTGTT 1080
TAATACCAGC ACTTTTGGAG GCTGAGGTGA GCTGATCACT TGAGGTCAGG AGTTCGAGAC 1140
CTGCCTGGCC AACATGGGGA AACTCTGTCT CCACTGAAAA TATAAAAATT AGCCAGGCAT 1200
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