Tag | Content |
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EnhancerAtlas ID | HS053-09085 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr12:31398700-31400300 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX3 | MA0684.1 | chr12:31399705-31399715 | AAACCGCAAA | + | 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 |
GH12I031245 | chr12 | 31398791 | 31400190 |
| Enhancer Sequence | AAGCTTCACT GAGGCAATGT GGTATGATTC TGGAGTGGAG TGAAAGCCTT TTCTGACCCA 60 GATATCCTGT CATTAGTGTT CACAGCCAAC ACGGTCTCAG TTGTGCCTAC CTGGCTTGCA 120 GCATTGGGCT CTGCCCCCCG GCCTCTGTTA TTTCGGGACC CTATCATCCC CATTGCTGGC 180 AGCAAGCCCA GCGCTGTAAC AGCATCTCCT GCCATCAGCC TGCCCTTTGG AATGCTGGGC 240 GGCAACTCCA GGGCTTCTCT GTGATGCTGG TGCCCTCCTC ACCAGGCCAT GACTTAGCAC 300 GCCGGTAAAC GGAGTATGCT CTGGGCCCTC CTAGGGAACA CTGTGGGGGG TGGATTTTCT 360 GGCCTCTATA GTCTAACCAG TTTGGCATGC CCACTGCTCT GGACATCCTG ATTCCTTCCT 420 TCACCATTTG CTGTGGCAGT TCTTCCAATT CTACCTCACT TAACGTGGGT CAATACTTTT 480 CCAGGCCTCT AAGAGGCAAC CTCTTAGAGG TTGTGATGTA GTAGTATGTT GGCGCCATCT 540 CCCGGGGTCC TCGTCAGGGT GTAAATTCCG TACCGTAAAA GAAAGTTCTC CCTTTTCCAA 600 TTTGTATTTT GTTTCCTTTG GTTCAGCACC CTCAAGATCC AGTCCCGTAC ATATTCCCCC 660 AGTTCCTGAT GGTTCACATT GACCAGGCCT ACAACTACTT TTTTTTCTTA GCAGGTTTGT 720 TTTCTTAGCG GGCCCAGCAC TTCTGTGGCT GGGTTATGTT CTAACTTGCC CTTAGCTTCG 780 GGTCTGATGG CCAAGAGAGG AGGCAGAGCT GAATCCTGAG CAGAGCACGA GTTTTCTTGC 840 AAGACACGAT CCTCCACATG ATCTTCAAAT AAGCCGGAGG CTCTAGCCTC TAACAGAGAG 900 GAGTGGATCA CTTCTGCAGG CCCTCTTCCC CACTTATTAC CGGCAGCCTT GCACTCACAG 960 GAATGCCTTT CTTCACAGGC TTCCATTCCA AAGATCTTAT TATCGAAACC GCAAATATGT 1020 CGCATACCAA CGTCTGAGCC CTTTTAATTA CTGTCATTGC CTCCTCCCTG ACAGCTGTCT 1080 ACAGCACCCG AATTATTTTC TTTGCACTGT TAGGACAACC TCACTTCACG GCTGTAATTG 1140 TCATCAACAA AAACAACCCC TTCCTAATCA ATTCAATCAA ATGCCTAACA ATTGGTAGTA 1200 TTTTTGCTGG ATTTTTAATC TCCAACAATA TTATTCCAAT ATCAGTTCCC CAAATGACTA 1260 TGCTCCTTCA CCTAAAACTC ACAACCCTCA GCGTAACTAT TTTAGGCTTC TCACTAGCAA 1320 TAGAACTTAA CCTTGTAACT AACAACCTCA AACTCAAGCA CCCATCACAA ATATTTAATT 1380 TCTCCAATAT ATTAGGATTT TACCCAATCA CAATACACCA CACAACACCA CACTCAAATT 1440 TCCATGCAAG ACAAAACCTA ACCTCTCTTC TACTAGAACT GATTTGATTA GAAAAATCAA 1500 CACCAAAAAA TACTGCCCAG GTTCAAATGA TAGCCTCCAC CATTGTATCT AACCAGAAAG 1560 ATCTAATTAT GCTCTACTTT TTCTCCTTCC TTATCCCATC 1600
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