Tag | Content |
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EnhancerAtlas ID | HS038-10199 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr19:19772390-19773960 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr19:19772816-19772837 | AGGGGGAAACTGAAACTCAGA | - | 6.12 |
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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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Enhancer Sequence | TGAGTTCTCC CTCCCAGTAA CACCACAAAG GCAGGGGGAT TTGCCTGTTT TGTTCACTGC 60 TGTTTCCCCA GCACCTAAGA CACAGAAATG TTGAATGGAA CTCGTTCAGT GCTCCCTGGA 120 CCCCGTGAAC CGCCATCCAT TCCTCTGCTG CTCTGCTAGA CCGAGCTGCA TGGAGACGAG 180 CTGCATGGAG ATGGGGGGAG CACAATGATG ACCCGCAGAA ACAAAGCGCC ACCGCACGGG 240 TGGTTCATGG GCCTCCAAAG CAGGCAGCAA ATAACAACAA TCACATAACT ACAAACGTGA 300 CGTCACGGAA GAAAGGTACA AGAGGCTATA CGCTGTGATG GCCCCAGGGC GGGCACTCTG 360 CAGATATCAT CTCCGCTTCT CAAGATGGCA CCCAGTAGTT GTTAGTTACG GTTCTCAGTT 420 TACAGAAGGG GGAAACTGAA ACTCAGAGAG CAGAAGCGGC CCTTTCTGAG ATCTGAATCA 480 AACCCAGATC CACCTCTCCT GGCTGATGGC TGTTCAGCTC CTCCCACTTC TCCATCCCTG 540 GAGAGGAAGT TAAGAGCTAA GCTGCTTAGC TGCAGGTCAA AAGGCAGCTG AAGTTTGAGC 600 GGTGCCACAG TCCCCTTAAC CCCTCCTTTA TTTTGTCCCT CATTGGTGTC TTTCATTGTA 660 CTACCTCAAA GCTACCACGT TGAGCTCCTC CCCTGGGATA GATAAGTCTT TTTGAAGGAC 720 AGAACAGGTT GTCTCTCAGG AGAGGAGAAT GAGGATTCTA CCCACATTCA GAGCCAGCCA 780 GGGTGGGGGG CTTCTGTCTT TCTGTAGCCC TTGATGCTGT TCCCTTTTCC TCTTCTTGAG 840 GCAAACACAC TCCTGGAATC AGAGGGGAAG CTTCCTGATA TACCTCAGTG TCCATGGCTC 900 CAAACCTGCT GGTGTCACCT GAGGCAGGCC CAGAGAGAGA CGACACAGTC ACTGCTTCAG 960 GCCCAGGGAA GCTCACAGTC ACCAACTCCT CCGACGACAC TTGGTCACTC AGAACTCTAA 1020 ACTGTGGGTC AGGAGCGCGA CCTTGCTTGC TGTTGTATCC CCGACAGAAC TCAGTATCAC 1080 CACCCTCATT TTGCGGAAAG ACATCATGTA AATGACTCGC TCATAAACAC CTCTGCCTCT 1140 CTTCAACACT GTAATTAACT GCATTTCATG CTCCTTTCCA TCACAGTATG GAAGACCACT 1200 AAGCACTGGA CAGCAAGACT TGGTTCAGTC TAAGAACCAA CTAAGCTTCA TAGATGGGGG 1260 AAACCTATCC CAGTGATCTC GCCTTACACT TTGAAAACCA AGGTAGGAGA CAGATGAGAT 1320 GGAAGGTAGG GCCGTTTCCA GAACAAGAGT AGTCGCTAAT ATGGGAACTA GTATAAACAA 1380 CTCCTACCTG ACCTGGGCGA CGTATGCTGG GCCCTGCGCT AAGCCTTTTA CAAGTATTAC 1440 ATCACTGAAT CTAAATGACC ATAACAGGGA GGACTTCAGA AAAAGGAAAT AACCCGCACC 1500 AGGCATGCAC AGCAAGTCAG CAGTGGGGTC ATGATTAAGC CTGCGCCAAA GTGTAGAGGG 1560 TGCCCCTGGG 1570
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