Tag | Content |
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EnhancerAtlas ID | HS060-22865 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr22:21102350-21104190 |
Target genes | Number: 12 | Name | Ensembl ID |
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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 | AAACTTTATA AATTAAGGTG TGGGCAAATG GACCAAACAC TGGGTTTCTG TCCTGGGTCT 60 GCCCCTCCCT AACTAGCTGT GGGACTGTCA GTAAGTCAAA GCCCCTCTAT GACCAGCTAC 120 TGCTCATTTG ACTGAGGACA AGGCCAATTC CCCGAGCGGC TGTCATGCAG TCACTGCGGT 180 GTTGCACCGT CAATGGGAGA GGGCCATTTA TTCTTTCAGC ACATCCTTGC TGAGCATCTG 240 CTGTGGTAGC CACCAGGCAA ATAAGCTACA AAGCCTTGGC CTTGCGGTCA ACAGGCAGGC 300 TGTGTGGTGT GGAGCCTCGG TTCTCTACTG CAGCATACCA GCAGCCTGGT GTGGGTGAAC 360 TGGACAGCAG GAACGAAGAA CAACACCTGT GTCCACCTGG CCACCCAGTG GGAGAAGGGT 420 GCTGGGCAAT GGGATACCTG GCAGAGCCCA GGGGTGTGAG GGAGGCCTCC TGCTCTGGGG 480 ACCACAGGGG GCTCAGCCTG CAGGAGTACC AAGGACAAGG GTCTCGAGGG TGGGGGCAAG 540 CCTGGAACAG ATGCAGGCCC TGTTTACAGG CGTGAACCAA CTAATTCCCT TAAGAAGAAA 600 TGTACAGGAG TATATACATG CAGAATTGTC TCAATGGTTT TGGGGGACTC CTGGAGCTCC 660 AGAAACCCAT CCTTGGACAC TATGACGATG AAGAGTGACT AATAATCAAG TTTAAAAGGG 720 AAGTACACTG ACCAGATACC CTATTAAAAC CAGACTACTC TGGTGGGTGG AGGAGAGGGC 780 AGATTCGGGG AAGGCTGAGG CTGGGCACGG AGGGTGGGGA ATAAGCACAC TGCAGGGGAA 840 GTGAAAGGGC AGGCCTGGGG CACGCCAAGG GGACACCTGG TGGAAAAATC AAGACCGCTT 900 CAAGCCTTTT CATTTTCCAT TTCCTTCTTA GGCCAGACCT GCGTGAGAAA GTAAAAAGCT 960 CTATCAGCTG CTTTTTTTGT CCACTTAAAC TTTCTAGGCA TTAGAGGGGG CCTCCCCTCT 1020 TCAGACGACA GACAGCCTTG GGACCTGAGG CCCTTTTGCT GTAAATGAAC AAAGGGAAAT 1080 AGTTTCTTGC CACTGCGTTT CCACACAGCT CTCAGGGCTC TTGGAGCTGG CTGCTCTATC 1140 CTTCCTGGAC TCCACAACCA GAAACACTTT TGAGCCTGTT TCATCTTTAA AGTGCTGCCA 1200 GGGTAAACCT CACAAGAGTT CCTCTCAGCA CACCCACTCT CTGCTAACAC AGATTCCTTC 1260 CAGAGGTATT TTTCTCATCT TTGATTCCTT TTAAGGCAAT TCTTTCCTCT CACACCCTGT 1320 GGCATTACAT GGTTTACTTC GTGGCCATCT GAGTTTCCAA ACCAGTGTTT TTGTCTGAAA 1380 GACTCCCATG CACCTACATG TGCAGCTTAT GTGGAGCTTT AATGGGACAC AAGTCCCCAA 1440 CTCTGCCTCT GCTCCACCAG CCTTGGTCAG GCCCCTGCCT TTGGGCACAG GTGCCAGCAA 1500 TGCACTTGGC ACTTAGAGAT GCTGCCATCT GGCAGCCTCC CACATCCACC ACACAAGCCC 1560 TTCCTCTCGT GAGCAGCCCC CAAGTCTTGC CACAGACCTG GCACCTCACC TGGTGTGAGC 1620 CGTCAGATGC CCTCCTTGTG CCCTGGCCAG CACTGGCCCC ACAGGCGCTC CTAACACACA 1680 GAGCAGCCTC TGAGGCATCT ATTATTCTCA GGCCCTAGAC TGATGCTTCC AGTCTCCATT 1740 CACACTAGTG CTATTTGGAT TTTGAGTTCT TCATGTCTCT GTAAAGCTTT TTTGGGAGTT 1800 TGAAGGAGCT TATGGCAATT GCCTTTTGAT GGTTTCAAGT 1840
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