Tag | Content |
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EnhancerAtlas ID | HS089-06769 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr19:36488840-36490300 |
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 | CAGCTCCCAT ACTTACTGAT TATGTGATCA CAGGCGAGTG ATTTAACTTT TTTTTTTTTT 60 TTTTGAGACA GGGTCTCTGT CACCCAGGCT GGAGTACAGT GGCACAGCTC ACTGCAGCCT 120 CGACTTCCCG GGCTCAAGTG ATCCTTCCAC TTCAGCCTTC TGAGTAGCTG GGACTACAGG 180 CGTGCACCAC CACACCCAGA TAATATTTTT ATTGTTTATT TTATTTTATT TATTTATTTT 240 TGAGACAGAG TTTTGCTCTT GTTGCCCAGG CTGGAGTGCA ATGGTGCGCT CAGCTCACCA 300 CAACCTCCGC TTCCCAGGTT CAAGCCATTC TCCTGCCTCA GCCTCCTGAT TACCTGGGAT 360 TACAGGCATA TGCCACCATG CCTGGCTAAT TTTTGTATTT TTAGTTAAGA TGGGGTTTCA 420 CCATGTTGAC CAGGCTGGTC TTGAACTCCT GACCTCAGGT GATCTGTCCA CCTCGGCTTC 480 CCAGAGTGCT GGGATTACAG GTGTGAGCCA GCGTGCCTGG CCTATTCTTT ATTTTTCGGA 540 GACAGGGTCT CACTGTGTTG CCCAGGCTGG TCTCAAACTC TTGAGCTGAA GCGGTCCTCC 600 CACCTCAGCC TCCCAAAGTG CTGAGATCAC AGTCATGAGC CACCATGCCC AGCCTGATTT 660 AACCTTTTTG CCTGAATGCC CTTATCAGTG AAATGGGCTT AATAAGAGCC TCCCTGATGT 720 GGCCATTATG ATGGTACAGT GAATTAAATG CCTGTTGTGA GGCCAGGCGC AGTGGCTCAC 780 GCCTATAATC CCAGCACTTT GGGAGGCTGA GGTGGGCAGA TCACCTGAGG TCAGGAGTTC 840 AAGACCAGCC TGACCAGCAT GGAGAAACCC TGTCTCTACT AAAAAATATA AAATTAGCCA 900 GGCATAGTGG TACATGCCTG TAAGCCCAGC TACTCAGGAG GCTGAGGCAG GAGAATTGCT 960 TGAACCCGGG AGGCAGAGGT TGCGGTGAGC CAAGATCGTG CCATTGTACT CCAGTCTGGG 1020 CAACGAGAGT GAGACTCCAT CTCAAAAAAA AAAACAAACC CTGTTGTGAC AGCAGATGAT 1080 GAGGCCTGAC CCCCACCCAT GGCCCTCCTG CCCTCTTGGG TTGACTTGCA ACTGTAGAAG 1140 CAGGTTCTCA GGAGGCTGCA GCCTCCTCCC CTGAGCCCCT GCATCTCTGT TGCTCTGCCT 1200 GAGGGCTTCC TGGGAGTCCT GGAAGGTGGG TTAATGTGCT CAGAGGCAAC CCTCAGCCTG 1260 TAGGGGGCAG CAGTCACTGG ATGAGCGCCC TGGCCCACCT CTCATCTGGT GGGACAACAT 1320 GTGTTCTGCA GGGTTCCTCA GGGGCACCCA TGGAATGGAG CCCCAGTTGC CCACAGTGGT 1380 GTCCACTCCA TGAGCACCTT TTTTGGCTTT TCCCCTGCCC TGTCTCTTCC CCACTCCCGC 1440 TTCCTGGGAT CACATCCCAG 1460
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