Tag | Content |
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EnhancerAtlas ID | HS146-12536 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr6:33622090-33623540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr6:33622321-33622335 | GGTCCCTTGGGACT | - | 6.57 | HEY2 | MA0649.1 | chr6:33623291-33623301 | GGCACGTGTC | - | 6.02 | Npas2 | MA0626.1 | chr6:33623291-33623301 | GGCACGTGTC | + | 6.02 | RREB1 | MA0073.1 | chr6:33622640-33622660 | ACCCACACCAGCCCCTCACC | + | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 33622686 | 33623431 | chr6 | 33622967 | 33623098 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I033654 | chr6 | 33622494 | 33623710 |
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Enhancer Sequence | CAACAAACTG AGTGCTCTTT CGGAAGTGAT GTCCACTCAT GCTGGCAATG CTGAGGGGCC 60 TAGGTGGGGC AGCCCTTGGT GGCTCCATCT GCTTGTGGAA TTGCCATTTT TCCCTTTTCT 120 TTCTAGGAAG TTCTGTCTTC CTTGATCTTT GGTTCACTCT GTTTCTACTC CCGATGGTCC 180 CATGGAGCTT TTGCCTCCTT ATGAACTGGA TGGAAAATCT AATTTTTCTT TGGTCCCTTG 240 GGACTGGATG ACCAGCTTTG ACCAGAGAAA AGACACAGCT TTCTTAGAGG GAACAGGAAA 300 GGACCTGAAG AAGGGGTTTT GTTTCTGGGA CCCTCGAGTG GCTCTCTCCT CTCCAGTCTC 360 CCCACACAGC CATCTCCTTT CTGTTCCACA CTGCCAGAGC ATTGTACAAT CAGGGACTCA 420 CACAGCTGCA GCATGAGAGG GATCTCAGGG CCACTGAGTC CTGCTCCGTG CCCAGGCTGT 480 GGATCCCTCC TGTGATGGGG AGCTCACTGC TTCCCAGCCC AGCCCAGGCT ATTGTCACAC 540 AGGCCCAGTC ACCCACACCA GCCCCTCACC AGCACCCAGA ATCCTCCCTC CCCTCCTACC 600 AAGCTTTCGA ACAGGCTTTT CCAACTCCTG CCTCCTTTGG ATAAGCAGAA AAATTGGACA 660 CCCTTCCTGC AGCTTAGGCT TATGGGAATG ACACTTGTTT TATCTACTTG CCAAAATAAA 720 AATTGTACTA GAGAACATGT TTCTGGAATT TGGATTTGCC TTGTCTTAGG TCAGATTCCT 780 AGAAGCAGAG CCTAAGATGG GTGAATTCTT GAGGAAGTTC TCAGGAGAAC ACAGTGAGGG 840 AGCCTCTTCC TCTTTGTATA GGGCAGGAGA AGAAGCTGAG CAAGGGTGTG GTTTCAGTGG 900 AAGATGCGCC TCAGCCTGAC CCCTCGGGGA GCTCAGGATT GTGAGCTGTT CCTCGGACTG 960 TCCCCTCCAG AGGCTGGGCT GTTCTATGCC TGTGTCAGTC ACTGGATAGG GGCTGCCCCT 1020 GGGAAGAGGG GTATGTCATT TCCCAGGCAT CTGTGTGCAA GATGGTTTCC ATCAGCCAAG 1080 GCAATTAGCT AAAGAGGATG CAGATGTGAG CTGTTAGCTG CCAATACTCA CAAAAGCTGG 1140 GCACAGACAT GGCATAAGGG TGAGGCCCCA GCAGCCTCTG GTAAATCTCC TAGGGGAAGA 1200 GGGCACGTGT CCACCCCACC AAGTGAGATG CACTGCTCTC AAACCTGCCT CTGAGCCTCC 1260 CCATTCTACT CAGCATATTC CAGGATGCTC CAAATTCTGT GAGGTTCTTC CAACCGCTTC 1320 CTCTCTACCT GCAGCGGGGA ACGGGGGTGG GGAAGGGTTG GGAGAGAAGA GCTGCAGGCT 1380 GGGGTTTTCT CCAGGGAGGG CCCTGAGCCC CAGATGAATC ATTCCCCTCA CCCCCAACCT 1440 GCCCCACCAC 1450
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