| Tag | Content |
|---|
EnhancerAtlas ID | HS176-16093 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr17:25710930-25712450 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr17:25711261-25711282 | GCAGCTGTCCGAGGTGATGTG | - | 6.03 |
| | | 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 |
| GH17I027384 | chr17 | 25710687 | 25712468 |
| Enhancer Sequence | TGGGCTTTAC AGATCATTAT TACCATCATC ACCGTCATCA TCATCACCAT CAGACTACTG 60
ACAACTGCTG TGTTTGGCAC TTATTAGAGA CCCTTATGTT GTCTAGTTTA ACTTGATTCT 120
TAAATCCACC ATGTGAAGGA AGTATTCTTA CCCCATTTTG CAGATGAGGA AACTGAGGCA 180
CACAGAGGTT AAATGACTTG CCCAAAATCA TTTAACTTTG AATTCAGGTC TATGACTGCA 240
AAGCCTTAAC TCTTCCCACC ATATGTCCCT TCCTAAGGAA GCAGATGCTA AGGAATGTTC 300
ATTGGCTGAA TGAATGAACA AGCAAAGAAA CGCAGCTGTC CGAGGTGATG TGTGGAATTT 360
CCAAGCCCCA GGAGGTTAAG CGGGTTGTTG AAGGTCGCAG AGCCAGACAG CAGTGAGGTA 420
AGTAAGGAGT CCCGGCTCTG GTCTCAGTGC AGGCTTCCCT CACAAACCTC CTTGCTACTT 480
TGAGCAGAAG CAACCTTGTT TTGGCAGCTG TTTTGCCCTT ACTCATGCCT GGGATAACAG 540
TGGACTCCCG ATTTGCATGC CAACTCATTT CCTACCCTTC AGGGAGCTGG GCAGGAGGCC 600
CAGCACTGGG TCCTGCCAAT CCCCAGGCGA GCTATCAATG GCAACTGCCA GCTAGTCACG 660
GGAGAGTCAT TTCATTCTCT CTCCCTTTTT CTCTAAGTCC TTCCAGCAGG AGGACTCTCA 720
GAGTTCCTGC TGGATGAGTA GGTATCCCCT GGGGCCGCAA GGCTGGACAG GCACCTTGGA 780
CCTCCCTATC CAAGCCTCCT GGGGCTTCCA CCGAGGATCA ATATGAGGGT GTGGAGACAG 840
TTTTGTGGCC CTGGGCAAAT TGAAGTCCCT TCTCCAGGTC TCAGTTTTTA CGTATCTCCC 900
AAATGGGGGA TTGGGTGAGC TGGCCCTCCA GGTCTGCACT CTGTTTCCTG GGCTCTTCTC 960
TAATGAGCCT GCCTGTGACA TTGTGCAGTT CCCCCAGCCT CACTCTTGCT GGGAACAAGG 1020
CCCAATTTGG ACCTTCTACC AGGGTGGGAA ATGAGTCGAC TGGGAAATTA GAGACTGCTG 1080
TGAATCCAAT CATGAGTAAG GGTGAAATTG ATGCCAAAAG TTTCTGCTTG AAGCAGCAAG 1140
GGGTTTTGTG AGAGAAATCC TGAGCTGAAA GCCAGAGGAG GCAGGGGGGT CTCTGACATA 1200
GGTTATCTGC TGCTGATCAG GGGTTCCCTG GTGGCAGGTG ACAGAAACCC AATTCAAGCC 1260
AGCTTGAAAA AAGATGCATT TGTTGGCCCA CAGAACTATG CAGAATAGGC AAGATTTAAA 1320
CACCACCCAG CAAGCACTCT CCCCTTCCTC CTTAACAACA GAACCCCTCT ATTGTTAAGG 1380
GATGGTGAGG TGTGTTTCAC AGATTTCCCT GCACATGGGA ATGGCCAATG AGCTAGAAAT 1440
GGAAATCTTT GAGTGGGGCT TCTAGGATGC TCTTTAAAGG GCTGACCCCT GCCTCTTCCC 1500
TCATCTTTCT GCCTGGAAGG 1520
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