Tag | Content |
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EnhancerAtlas ID | HS073-09664 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr22:21102460-21104190 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr22:21103261-21103271 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr22:21103261-21103271 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr22:21103261-21103271 | ATTTTCCATT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 6 | Chromosome | Start | End |
chr22 | 21103813 | 21103939 | chr22 | 21102814 | 21102884 | chr22 | 21103174 | 21103455 | chr22 | 21102482 | 21102632 | chr22 | 21103106 | 21103771 | chr22 | 21102960 | 21103031 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I020748 | chr22 | 21102832 | 21106225 |
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Enhancer Sequence | GACCAGCTAC TGCTCATTTG ACTGAGGACA AGGCCAATTC CCCGAGCGGC TGTCATGCAG 60 TCACTGCGGT GTTGCACCGT CAATGGGAGA GGGCCATTTA TTCTTTCAGC ACATCCTTGC 120 TGAGCATCTG CTGTGGTAGC CACCAGGCAA ATAAGCTACA AAGCCTTGGC CTTGCGGTCA 180 ACAGGCAGGC TGTGTGGTGT GGAGCCTCGG TTCTCTACTG CAGCATACCA GCAGCCTGGT 240 GTGGGTGAAC TGGACAGCAG GAACGAAGAA CAACACCTGT GTCCACCTGG CCACCCAGTG 300 GGAGAAGGGT GCTGGGCAAT GGGATACCTG GCAGAGCCCA GGGGTGTGAG GGAGGCCTCC 360 TGCTCTGGGG ACCACAGGGG GCTCAGCCTG CAGGAGTACC AAGGACAAGG GTCTCGAGGG 420 TGGGGGCAAG CCTGGAACAG ATGCAGGCCC TGTTTACAGG CGTGAACCAA CTAATTCCCT 480 TAAGAAGAAA TGTACAGGAG TATATACATG CAGAATTGTC TCAATGGTTT TGGGGGACTC 540 CTGGAGCTCC AGAAACCCAT CCTTGGACAC TATGACGATG AAGAGTGACT AATAATCAAG 600 TTTAAAAGGG AAGTACACTG ACCAGATACC CTATTAAAAC CAGACTACTC TGGTGGGTGG 660 AGGAGAGGGC AGATTCGGGG AAGGCTGAGG CTGGGCACGG AGGGTGGGGA ATAAGCACAC 720 TGCAGGGGAA GTGAAAGGGC AGGCCTGGGG CACGCCAAGG GGACACCTGG TGGAAAAATC 780 AAGACCGCTT CAAGCCTTTT CATTTTCCAT TTCCTTCTTA GGCCAGACCT GCGTGAGAAA 840 GTAAAAAGCT CTATCAGCTG CTTTTTTTGT CCACTTAAAC TTTCTAGGCA TTAGAGGGGG 900 CCTCCCCTCT TCAGACGACA GACAGCCTTG GGACCTGAGG CCCTTTTGCT GTAAATGAAC 960 AAAGGGAAAT AGTTTCTTGC CACTGCGTTT CCACACAGCT CTCAGGGCTC TTGGAGCTGG 1020 CTGCTCTATC CTTCCTGGAC TCCACAACCA GAAACACTTT TGAGCCTGTT TCATCTTTAA 1080 AGTGCTGCCA GGGTAAACCT CACAAGAGTT CCTCTCAGCA CACCCACTCT CTGCTAACAC 1140 AGATTCCTTC CAGAGGTATT TTTCTCATCT TTGATTCCTT TTAAGGCAAT TCTTTCCTCT 1200 CACACCCTGT GGCATTACAT GGTTTACTTC GTGGCCATCT GAGTTTCCAA ACCAGTGTTT 1260 TTGTCTGAAA GACTCCCATG CACCTACATG TGCAGCTTAT GTGGAGCTTT AATGGGACAC 1320 AAGTCCCCAA CTCTGCCTCT GCTCCACCAG CCTTGGTCAG GCCCCTGCCT TTGGGCACAG 1380 GTGCCAGCAA TGCACTTGGC ACTTAGAGAT GCTGCCATCT GGCAGCCTCC CACATCCACC 1440 ACACAAGCCC TTCCTCTCGT GAGCAGCCCC CAAGTCTTGC CACAGACCTG GCACCTCACC 1500 TGGTGTGAGC CGTCAGATGC CCTCCTTGTG CCCTGGCCAG CACTGGCCCC ACAGGCGCTC 1560 CTAACACACA GAGCAGCCTC TGAGGCATCT ATTATTCTCA GGCCCTAGAC TGATGCTTCC 1620 AGTCTCCATT CACACTAGTG CTATTTGGAT TTTGAGTTCT TCATGTCTCT GTAAAGCTTT 1680 TTTGGGAGTT TGAAGGAGCT TATGGCAATT GCCTTTTGAT GGTTTCAAGT 1730
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