Tag | Content |
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EnhancerAtlas ID | HS093-14608 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr18:74920290-74921560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr18:74921026-74921047 | TTTCACTTTCTCTTTCCTCTG | + | 6.67 | IRF1 | MA0050.2 | chr18:74921020-74921041 | TTCCAGTTTCACTTTCTCTTT | + | 9.66 | IRF2 | MA0051.1 | chr18:74921025-74921043 | GTTTCACTTTCTCTTTCC | - | 6.79 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I077206 | chr18 | 74918749 | 74922095 |
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Enhancer Sequence | ATGGTCTAGT GGTGCTAGAT TTTGTTAGTT CTAATACAAT ATGGTCACCT AAACTCTCGT 60 TTCATACTTT CCCTCCCCCA TATTATATTA TAGTTTACAA TATTATGTTA TAGTTTATAA 120 TATGACTATC ATCTTTAATA CTTTCTTTAC ATACATTGAG AACATCAGAC AGCATTATCA 180 TTTTTGCTTC CAACCATGGA ACATAATTTA GAAAACTCAA GAGGAGAAGG AGTCTATTTA 240 TTTACCCATA TTTTTTACTT TTGCTGTTGT TCTCACTTTC TTCCCAATAT TCCAATATTG 300 CTTCTTTTAT AATTTCCCTT CTGTTTAGGA AACTTCCTCG AGCCATGCTT TGAGTAACCC 360 TGCTGATGGC AGATTCTCTT AGTGCTCCTT CACTGGAGAA TATCTCTATT TATACCCGTC 420 CATGAGGGAC ATTTTCCCTG CCATAGACTT TTGGTTGACT GGCCTTTTCT CTTGGTATTT 480 GAGACGCTTG CTACTTCCTT TTGGGTTCCA TGGTTTCAAA CGGAAAATTT GCACGTCCTA 540 CAAGCAATGT GTTTCTCTCT GGCTACTTTG CAGCTATTTT TCTTTGTCTT TAGTTTTTCA 600 GACCTTTGAT TATGATGTAT CTTGGTATAA ATTTCTTTGG GTTTACCACA TTTGGAATTT 660 TCTCAGATCC TTGAATCTTT AGTATATTTC ACTAAACTTG GGAAGTTTAC AGCCATTTAA 720 AAAATATACC TTCCAGTTTC ACTTTCTCTT TCCTCTGAGG ATGACACAGG CTCCTGAGAG 780 TCTGTTCTTT CTCCTCAGCC CACTTCCTCA ATGCTGCTCT GAGTTGGTGA CTTCTGGCCC 840 TCGTCCAGTC TTTTGTCCTC TCGCTGTCCT GGTTGAGTCC ACGCATTGAG GTTTTAGGTT 900 TGTTTGTCTT TTGGTTATTG TGTTTTCTTG CTTTATAATT TCTTTTTTTT TTTTTCAGAC 960 CGAGTCTCAC TCTGTCACCC AGCTGGAGTG AGGTGGCATG ATCTCTGCTC ACTGCAACCT 1020 CTGGCTCCTG GGTTCAAGTG ATTCTCCTCT CTCAGCCTCT CGAGTAGCTG GGACTACAAG 1080 TGCCCACCAT CGTGCCAGGC TAATTTTTGT ATTTTTAGTT GAGGTGGGGT TTCACCATGT 1140 TGGTCAGGCT GGTCTCGACC TCCTGACCTC AGGTGATCCA CCTGCCTTGG CCTCCCAAAG 1200 TGCTGGGATT ACAGGCGTAA GCCACCATGC CCGGCCTCCT TTGGTTCTTC TTTATTCTTT 1260 TGCTAAAATT 1270
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