Tag | Content |
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EnhancerAtlas ID | HS065-02668 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr19:36488900-36490330 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:36490093-36490112 | CAGCCTGTAGGGGGCAGCA | + | 6.48 | Foxq1 | MA0040.1 | chr19:36489049-36489060 | TATTGTTTATT | + | 6.62 | Nr2f6(var.2) | MA0728.1 | chr19:36489666-36489681 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr19:36489281-36489296 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH19I035998 | chr19 | 36489853 | 36490896 |
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Enhancer Sequence | TTTTGAGACA GGGTCTCTGT CACCCAGGCT GGAGTACAGT GGCACAGCTC ACTGCAGCCT 60 CGACTTCCCG GGCTCAAGTG ATCCTTCCAC TTCAGCCTTC TGAGTAGCTG GGACTACAGG 120 CGTGCACCAC CACACCCAGA TAATATTTTT ATTGTTTATT TTATTTTATT TATTTATTTT 180 TGAGACAGAG TTTTGCTCTT GTTGCCCAGG CTGGAGTGCA ATGGTGCGCT CAGCTCACCA 240 CAACCTCCGC TTCCCAGGTT CAAGCCATTC TCCTGCCTCA GCCTCCTGAT TACCTGGGAT 300 TACAGGCATA TGCCACCATG CCTGGCTAAT TTTTGTATTT TTAGTTAAGA TGGGGTTTCA 360 CCATGTTGAC CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCTGTCCA CCTCGGCTTC 420 CCAGAGTGCT GGGATTACAG GTGTGAGCCA GCGTGCCTGG CCTATTCTTT ATTTTTCGGA 480 GACAGGGTCT CACTGTGTTG CCCAGGCTGG TCTCAAACTC TTGAGCTGAA GCGGTCCTCC 540 CACCTCAGCC TCCCAAAGTG CTGAGATCAC AGTCATGAGC CACCATGCCC AGCCTGATTT 600 AACCTTTTTG CCTGAATGCC CTTATCAGTG AAATGGGCTT AATAAGAGCC TCCCTGATGT 660 GGCCATTATG ATGGTACAGT GAATTAAATG CCTGTTGTGA GGCCAGGCGC AGTGGCTCAC 720 GCCTATAATC CCAGCACTTT GGGAGGCTGA GGTGGGCAGA TCACCTGAGG TCAGGAGTTC 780 AAGACCAGCC TGACCAGCAT GGAGAAACCC TGTCTCTACT AAAAAATATA AAATTAGCCA 840 GGCATAGTGG TACATGCCTG TAAGCCCAGC TACTCAGGAG GCTGAGGCAG GAGAATTGCT 900 TGAACCCGGG AGGCAGAGGT TGCGGTGAGC CAAGATCGTG CCATTGTACT CCAGTCTGGG 960 CAACGAGAGT GAGACTCCAT CTCAAAAAAA AAAACAAACC CTGTTGTGAC AGCAGATGAT 1020 GAGGCCTGAC CCCCACCCAT GGCCCTCCTG CCCTCTTGGG TTGACTTGCA ACTGTAGAAG 1080 CAGGTTCTCA GGAGGCTGCA GCCTCCTCCC CTGAGCCCCT GCATCTCTGT TGCTCTGCCT 1140 GAGGGCTTCC TGGGAGTCCT GGAAGGTGGG TTAATGTGCT CAGAGGCAAC CCTCAGCCTG 1200 TAGGGGGCAG CAGTCACTGG ATGAGCGCCC TGGCCCACCT CTCATCTGGT GGGACAACAT 1260 GTGTTCTGCA GGGTTCCTCA GGGGCACCCA TGGAATGGAG CCCCAGTTGC CCACAGTGGT 1320 GTCCACTCCA TGAGCACCTT TTTTGGCTTT TCCCCTGCCC TGTCTCTTCC CCACTCCCGC 1380 TTCCTGGGAT CACATCCCAG ATAAATCATC ACCCGAGTCC TTGGCTCCAA 1430
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