Tag | Content |
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EnhancerAtlas ID | HS176-18832 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr19:19080080-19081240 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr19:19080467-19080480 | GAAAATTCCAGAA | - | 6.17 | IRF1 | MA0050.2 | chr19:19080083-19080104 | CGGAGGTTTCACTTTCTTTCT | + | 6.21 | IRF1 | MA0050.2 | chr19:19080101-19080122 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | Nr2f6(var.2) | MA0728.1 | chr19:19080323-19080338 | TGAACTCATGACCTC | - | 6.26 | RARA | MA0729.1 | chr19:19080320-19080338 | TCTTGAACTCATGACCTC | - | 6.12 | RREB1 | MA0073.1 | chr19:19080534-19080554 | CCCCACCCCGCCCCCTCCCA | + | 6.24 |
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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 |
GH19I018966 | chr19 | 19077181 | 19084286 |
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Enhancer Sequence | TATCGGAGGT TTCACTTTCT TTCTTTCTTT CTTTTTTTTT TTGAGATGGA GGCTTGCTCT 60 GTCTCCCAGG CTGGAGTGCA GTGCTACGAT CTCGGCTCAC TGCAACCTCC ACCTCCCAGG 120 TTCAAGTGAT TCTCCTGCCT CAGCCTCTGG AGTAGCTGGG ATTACAGGCA CGCACCACCA 180 CACCCAGCTA ATTTTTGTAT TTTTAGTACA GATGCAGTCT CGCCATACTG GTCAGGCTGG 240 TCTTGAACTC ATGACCTCAG GTGATCCACC TGCCTGGGCC TCCCAAAGTG CTGGGATTAC 300 AGGCGTGAGC CACCGCACCC GGCCTGAGGT TTCATTTTCT GTGGTGTTGG CTACCTTCCA 360 TCAACCTCAA TCCAAACATA TTAAGTGGAA AATTCCAGAA ATAATTCGTA AGTTTTCAGT 420 TGCCTGCCGT TATGAGTAGT GTGATGAAAT CAGTCCCCAC CCCGCCCCCT CCCACCCTGG 480 ATATGAATCA TCCCTTTGTT AAGGGTGCCC ACGCCATAGA CACTACCAGC CGGCTAGTCA 540 CTTAGTAATC TTCTGGGTGA TCAGATCAAC CGTGTCAGTA TTACAGTGCT TATGTTCCAG 600 AAATCCAAAT TTTATTAATT TTCTATTTTA TTATGTTATT GTTGTTAATC TTTTACTGTG 660 TCTCACTGAT AAATTAAACT TTATCATAGG TATGTATGTA TGCATAGGAA AAAAACAGTG 720 CATACACGTT TGGTATTTTC TGAAGTTTCA GGAATTTACT GGCAATCTTG GAACATATTC 780 CCCACAGGCA AGGGGGAACT ATTGTATTAT TTTGGTATTC AAAATAAAAG AGGCTGGGCA 840 TGGTGGCTCA TGCCTGTAAT CCCAGCACTT CGGGAGGCCA AGGCAGGAGC AATCGATCCC 900 TTGAGCCCAG GAGTTCGAGA CCAGCCTGGG TAACATAGTG ACAGCCCGCC TTTACAAAAA 960 CTTTGAAAAG TAGCCGGGTG TGGTAGCTCG TGCCTGTAGT ATCAGCTACT CTGGAGGCTG 1020 AGGTAGAATT GTCTTGGGCC CAGGAGGCTG CAGTGAGTTA TGATCACGCC ACTGCACTCC 1080 AGCCTGGGGG ACAGCATGAG AGCCTGTCTC AAAAAATTAA AACAAAATAG CACACAGAAA 1140 AAAGTTTTTG AAATTAGCCT 1160
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