Tag | Content |
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EnhancerAtlas ID | HS177-19834 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr6:116550320-116551120 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 7.21 | RFX1 | MA0509.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 7.24 | RFX2 | MA0600.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 6.93 | RFX2 | MA0600.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 7 | RFX5 | MA0510.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | + | 6.55 | RFX5 | MA0510.2 | chr6:116550613-116550629 | GGTTGTCATGGTAACA | - | 6.82 |
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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 |
GH06I116228 | chr6 | 116550108 | 116551187 |
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Enhancer Sequence | TTAACCAAGC TAGTAAGCAA AAACCACAAT TACTTTTGCA CTAACCTAAA AAATCAGTCA 60 TCCTCATTTC TTCCCTCCCT TTTAAGTTGT CCTTCTGTTT TCTCAGGTTT GTCCTCACTA 120 CATTCCCACC ACTGCCCGCA TCATCCCTTG TGTGAAATGG CACAATATTT AAGTCATTGC 180 TCCAAATGGT TAAAGTAAAG TTAATGCAAC TGAGCTGGCT GGGATGGAAG GCACAGCGAG 240 CCAATCACGA AACACAGCAT GGCCTTAGCG AGTCGCACAG GTTTGACGTC AGCGGTTGTC 300 ATGGTAACAG GGGCAAAGAT GCTGATGCCA GTGTCAGTCA GGACTGAGCT CCTCCCTCCA 360 GTCTGATTCC TGCCAGTGCT TAAGGATGTA TGGAGGGGAG AAGCGTCTTC CAAGCAAAAT 420 CTTCATCCTC TGTTCTCTAT CACGTGCAGT GCGTCACCAG ATCCTCGCCA GTGCTGAGGG 480 TGGGGATACG GGGGAATCTC TGACTTGCAA GATTAAATTA TCATTGGAGA GGGAACGTGT 540 CAGCCTTGTT CACCGCAGTG TCGCCAATGC TGCTAGCTCA GTTCCTGCCC CTGCCCACCA 600 TTGGGAGAAT CATGAGCCAA CTCTCTCTGT CTCTCCTCTC TCTCTCTCTG TCTCGTCCCT 660 TGGCCTTAGC TGTCACCAAT ACACTGACTC TGACTCCCAA ATCTTTCCCT GAGACCTGTT 720 TTCCTGAGTC TCATACGCAG TTCCTCCTCC ACACTAGGCA GCTCCACTCA GTGTTCTGAT 780 ATCAAGCTTG AGATTCTCCT 800
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