Tag | Content |
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EnhancerAtlas ID | HS024-01222 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr1:183296440-183297880 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr1:183297670-183297685 | CCCCATGAGTCAGCA | + | 6.3 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_01962 | chr1:183296374-183297932 | Aorta | SE_48814 | chr1:183296370-183298137 | Right_Atrium | SE_55065 | chr1:183296123-183298752 | Stomach_Smooth_Muscle |
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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 |
GH01I183326 | chr1 | 183296124 | 183298752 |
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Enhancer Sequence | TCGGCCTTCC AAAGTGCTGG GATTACAGGC ATGAGCCACT GTGCCTGGCC CTAATTATAC 60 ATTTTTTAAA TAACAAAGTG GAGACAGACA TTTAAGATAA CTTCTCTCAG TTCACACAGC 120 GAATTATGAA GATGTGTTGG CTCAAGCATC ACCAATCCAG TACGCCAAAA GGGCCATATT 180 TGCAGGCATT CCTTCTTGCT ACCTCGACAG CTCATGTATA CCAGTGCTTC TTACTGTTTG 240 CCAGCAACTC TTCTCAAATT CAGACATCTG TACACTGCAC AGACATCAGT ATGTCCCAGA 300 ATCGTTTCCA ACGGAGTGGT GGGTAGGGGT GAGTGGTTGA AGAAGAGCAG GGATGTTTAT 360 TCGCCAGCAC TGAGTTCTCT GTACTCACAA ACTAGGCAAT TTCTCAGTGC CACAAGGACA 420 TTTCTGAGTC ACTTGGACAG ATCTCTTGGG AGTGATGCCT GGAGAATTAG AAATAAAAAT 480 AGTCTTCTTA GCTGCTGTTT TTTGTGTGTG TATGTGTGTT TTTCCCCTTT TGCCCTGGGA 540 AGCTACTGCT TTCCCTCCCT GTCCTCGCTG GCCCTGTCTA CTCCCTGGCT CCCCTGGGTT 600 TCAGAGGAGC TGGCACTGAA CACTGCTCTT TCTCACTTGA CATCCTCTCT CCAACTTAGC 660 AAGCAGGTCT TCTGCCAAAT CTCCAGGTCG GTGGCTCATC AACGTCAGCT GCCCCCACAG 720 CTTCTAGGGC AGGCGGAGAG GTTGTTCCCT CCAGGACTTG GGCCAGAGAG GGGAGAATAG 780 GGGTCATGGG AGGGAACCAT CACCTGGTCT CGGACCACAC AGTATTGCAG CTGGACTCCA 840 GCCACTCAAA CACACTGAGT TGGCAGGTCC CTGAAAACTG AAAAGGGAGA GGGATCAGAT 900 GCCGCAGGCC AGGACCCTGG CTTCCTGGCT CCCTGGCTTC CTCCCCACCC ATCTGCTCTA 960 CCCCCTCTCA CCTCCAGAAG CCTTGGAGGG GCTATGATTG TTTTGGACAG TCTGAAGCTG 1020 AGATCAGCAA AATACGGACC CTCAGAGAGC ATTTTGAAAA GAGCCTCTCT GGTGCTACAT 1080 GTTAATAAGC CCTTCTAGGA GAATGCTCTT CTAGAATTTG CCATTTCTGC CTCCCTACCA 1140 TTCCTCCTTG GGCAATGCCC TTGGGCAATG AAACCTCTGC TCTCTAGTCC TTTCTGAGGG 1200 AGATGGTGAT CAGGACAAAG CCCTAGCCAG CCCCATGAGT CAGCATGGTC ACTGCTGATC 1260 TGACCATCAG GCTTGGTGTC AGGAGCTAGC AATCCTCCTG GCTCTAGTTA GGTGACTTGT 1320 CTCTAGGAGC CCTGCCTACT GTCCTCCCAA CCTCAACACC TAGTGCCATG GGAATGATGT 1380 TCTGCACCAA CAAACCTTTG CCTCCTGTGA GGAAGATCTT GTGGAATGTC TGCCGCAATC 1440
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