Tag | Content |
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EnhancerAtlas ID | HS006-10301 |
Organism | Homo sapiens |
Tissue/cell | Astrocyte |
Coordinate | chr12:122310080-122311590 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:122310355-122310370 | TGAACTACTGACCTC | - | 6.07 | RARA | MA0729.1 | chr12:122310352-122310370 | TCTTGAACTACTGACCTC | - | 6.1 | ZNF263 | MA0528.1 | chr12:122310490-122310511 | TCTCCATCCTTTCCCTGCTCC | - | 6.81 |
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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 |
GH12I121871 | chr12 | 122309456 | 122312164 |
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Enhancer Sequence | GTTGCAGTGA GCCAAGATCA CGCCACTACA CTCCAGCCTG GGCGACAGAG CGAGACTCCT 60 CTCAAAAAAA AAAAAGAGAT GGAGTCTTGC TCTGTCGCCC AGGCTGGAGT GCAATGGTGC 120 ACTCCCACTG CAACCTCCGC CTCCCAGCTT CAAGTGATTC TCCTGCCTCA GCCTCCTGAG 180 TAGCTGGGAC TAACAGGAGC CCGCCACCAG GACCAGTTAG TTTCTTTTGT ATTTTTAGTA 240 GAGACGGGGT TTCACCATGT TGGCCAGTCT AGTCTTGAAC TACTGACCTC AAGTGATCCA 300 CCTGCCTCAG CCTCCCAAAG CATTGGGATT GCAGGCATGA GCCACCGTGC CTGGCCTAAA 360 ATTTCTTGTC TCTCCAGCAT CCACTCCTGT TCTCATAACA GCGTCTCCCT TCTCCATCCT 420 TTCCCTGCTC CGTTCATGTC GTTTGGGTGG GGCATGTGAG CCAGGACTGG GCAGTGAGAA 480 TCCCTGTGAT TGGTTCAGGG CTGGGCACCT GGCCAGAACT GGCCATATGG ATTTGCTCTG 540 GATCTTCTGC TTGAGAAAAG AGGCTCACTC TGAGCTCTGA GTATGCTGCA CTGATCCAGT 600 GGTGCTGCGG GGGCCAACCC TGAGTCAGCT GAAGGAAAAC ATGCTTGTAT ATAAAGCCAG 660 AACAGAGAAA CCAGAGCTGA GAGAAGATAG GCTGATTCCT GATGTCTGAG CAACTTGTTC 720 CAGGCAGAAA CAAGCTCCTG GATGAGTCAA ACCTTTTTCC CTTTTGCTTA AGCTAGTTTG 780 AGTTGGGTTT CTGGCATTTA CAACCACTGG TGCTGACAAA CACAAAGAAA GAAACAATAA 840 CACCACCACC ATCTGTGAGC ATGTATTCAC TGTCAAGCAC CGAGGTAGGG ATCATGGGGA 900 TTGTCTGTTC CACAGGGAGG TAGTACTTGA TCATTTTGTT TGCATTTGCT GGCACACATA 960 AAATAAAGTT GACTGATTTT AGCAGTTTTT ATTATTATTT TAAAACTCTC TGCAGACATT 1020 GCATCCCTGT GGTAGATTCT ACTGTCCATA ACCCTTCAAG GAAGGCCTCA ATGCCCAGCT 1080 GTAGGGAGAC TGGTTGGCTG TCACCTCCTA TCGGATCTGC CTCAGCTGTA GAGACTTGGC 1140 CACAGCTTTC CCAGAGCAGC CCACTTTTTG TGATTGAGCA AGGGAGTAGA GAGGCTGGTC 1200 CCTTTCAGCC CAATGGGGGT GACTCTGACC AGTGAGTCTG TCTCCAGGGC CCCGGTAGGG 1260 CTGGCCAAGG CCTTGTGGAG TCTCCACCAC TGAGTTCTCC TTCTCCCCAG TCCAGCCTCC 1320 TCTGCTTCCT TTCACTGATG TGGATCCTTA AAATCATTTT ATGGCCGGGC GCGGTGGCTC 1380 ACGCCTGTAA TCCCAGCACT TTGGGAAGCT GAGGCGGGCG GATCACAAGG TCAGGAGATC 1440 GAGACCATCC TGGATAACAC CATGAAACCC CATCTCTACT AAAAAAATAC AAAAAATTAG 1500 CTGGGCGTGC 1510
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