Tag | Content |
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EnhancerAtlas ID | HS103-11462 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr19:12681930-12683310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN | MA0488.1 | chr19:12682936-12682949 | ATGACCTCATTTT | - | 6.2 | JUND(var.2) | MA0492.1 | chr19:12682935-12682950 | TATGACCTCATTTTT | - | 7.08 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 12682326 | 12682767 | chr19 | 12683142 | 12683251 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I012571 | chr19 | 12682361 | 12682510 |
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Enhancer Sequence | TGAAGCCATG AGAAGCAAAT AAGTAACTTG TTAAACAAGA AGGTAATAGA TCTAAAACAA 60 TAGCTCAGGA AGTTAGAGGC CCAGATATGT TTGCTTTCCC CATATAAACT AAGGGTAAGA 120 TCTTTTTTTT TTTTGAAAGG GAGTCTTGCT CTTTCACCCA GGCCAGAGTG CAGTGGCGCT 180 ATCTCGGCTC ACTGCAAGCT CTGCCTCCTG GGTTCACGCC ATTCTCCTGC CTCAGCCTCC 240 TGAGTAGCTG GGACTACAGG CGCCCGCCAC CGCGCCTGGC TAATTTTTTG TATTTTTAGT 300 AGAGACGGGG TTTCACCGTG TTCGCCAGGA TGGTCTCGAT CTCCTGACCT CGTGATCTGC 360 CCGCCTCAGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCACGCC CGGCAGGATA 420 ACATCTTAAC ATACATCCCG GAGTTGTCTT TCAGAGGCTT GGAACCCCAC TGAGGACCCC 480 CGCTGAACAG ATCCATTCAC TGGCACAGAC TCCTAGATAA GGAAGAAGTG AAGACTAAAC 540 TTGACCTTTG TTCTGTTTCT TCCTTGGGGG ATTAGAGAAA GTCACTCCCT GTAACCAGTT 600 ATTTTTCTAC TGACCCCTGT CAGGCCTCTG AGCCCAAGCC TGCACGAATA CATCCAGATG 660 GCCTGAAGCA AGTGAAGAAT CACAAAAGAA GTGAAAATAG CTGGTTCCTG CCTTAACTGA 720 CATTACCTTG TGAAATTCCT TTTCTTGGCT CAGAAGCTCC TCCACTGAGC ACCTTATGAC 780 CCCCACTCCT GCCCGCGAGA AAACAACCCC CTTTGACTGT AATTTTCCAC TACCTACCCA 840 AATCCTATAA AACAGCCCCA CCCCTATCTC CCTTCACTGA CTCTTTCTGG ACTCAGCCTG 900 CCTGCACCCA GGTGAAATAA ACAGCTTTAC TGCTCACACA AAGCCTGTTT GGTGGTCTCT 960 TCACACGGAC ACGCGTGACA ACCCGATTTT TCTTTTTTTT AATCTTATGA CCTCATTTTT 1020 CTCAGAGATG AAGTCTTGTT ATGTTGCCTA GGCTGGTCTT GAAATCCTGG CCTCAAATGA 1080 TCCTCTTGCC TAGGCCTCGC AAAGTGCTGG CATTACAGGC ATGAGCCACC GCACCTAACT 1140 TAAAGTTTTT TTTTTTTTTT TGAAACGGAG ATTCACTCTT GTTGCCCAGG CTGGAGTGCA 1200 ATGGCGTGAT CTCAACTCAC TGCAACCTCT ACCTCCCGAG TTCAAGCGAT TCGCCTGCCT 1260 CAGTCTCCCA AGTAGCTGGG ATTACAGGTG TGAGCCATTT GCCCAGCCTA GCTTAAATTT 1320 TTAAACAAAA CTTCTCTCTT CCTTTTTTTT TTGTTTGTTT TTGAGATGGA GTCTCGCTCT 1380
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