| Tag | Content |
|---|
EnhancerAtlas ID | HS007-08134 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr19:17817120-17818250 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU4F2 | MA0683.1 | chr19:17818123-17818139 | TGGAATAATTAATGAA | + | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH19I017706 | chr19 | 17817641 | 17817790 |
| Enhancer Sequence | TCACTATCCC TAGGAAGACC TCAGGCAGAT TGCTACCAGC TGCCAGAGAG CTACTTGTAG 60
CCAGTAGATT TCCAAAATAA AATGATAAAT TACAAGAATT AAGTAATACC AGGTGAGCGC 120
TTAGCATATG CAGGGTTACA CCCTCGGGCT GTTTTAACTC TTTTAATCCC CACAGCGACC 180
CTACCAGTTC AATTGATGGC GAAACCAAGG CCCAGGGAGG TCGCACCTCT GGGGAGAGAC 240
AGAGCTGAGA TTTGAACCCC ACCAAGCTTG GTGTCTGTGC CCTTGACTCC TCAACCTCAC 300
GTTTTACAAT AGGGTCATTA GTAGAAAGGG AGGTGCGGGG ACGTTGGTGA CCGTTAGACT 360
TGCTGCGGGT CTGGATGTCG ACACATGGTG CTGCTTGGGG GCCCAGACGT GAGCAGGAAT 420
TGGAAACTGG GTCTGGACCC AGGTTGGTCA CCTCCGCCGG GGTAACAACA CTGCGCGCCA 480
CTTTGGTAGG TCGCATCCAG CTCGGGATCT GGACCACGTG GCTGGGATGC AGCACAGCCC 540
CTGACCACGC CCCTGTGACT GCCGCTGCCT GGACCACGGC TGGCGACCAA TGAGAAGGCG 600
CACATCAAAA GCTCCGCCTA CAAGGCCGTT CTTGCTTGCT GATTGGCCAT TTCAGCTTCC 660
CATCACCTCT CCCATCCTCT GGCCTACAGC CTCCCTGGAA TTTTTCCCAC ACATCTCCCC 720
CGCAGGCCTT TGCACACGCT GTTCCCACAG CCAGAGATAC CTTTTCCCCT CTTCTCCGGG 780
ATAAACTGCT TTATCCCCCC TTCTCTGCTA AGATGGCCCC TCCTCCAGGA AGCCTTCCCT 840
GACTCCCAAA AGTGAGTGGA GGAGGTCAGC TGCTCTCATC ACATTAGTTT TCTTATTTGC 900
CTCCCAAGCA GGCTATAAGC TTCTTAGAAG CCAGGACTGG GTCTCAGATA GCTTTGTCTC 960
TCCATTGCCT CACATAGTAG GTACTCAAGA AACGTATGTC AAATGGAATA ATTAATGAAT 1020
TAATCTGGTC TCAAAGATTG AGGAGCACTG AGCTAGCAGT TAGGAGCTAG GAAATCCTGA 1080
AGGCAGGGCT GGGACACCCG CTGCTGGCTT GGCACAGAGT CTAACACACA 1130
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