Tag | Content |
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EnhancerAtlas ID | HS131-00122 |
Organism | Homo sapiens |
Tissue/cell | ME-1 |
Coordinate | chr1:17608230-17609140 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYA | MA0060.3 | chr1:17608991-17609002 | TCTGATTGGTC | - | 6.14 | NFYB | MA0502.1 | chr1:17608992-17609007 | CTGATTGGTCCATCT | - | 7.16 | ZNF263 | MA0528.1 | chr1:17608821-17608842 | TCTCTCACCCTCTCCACCTCC | - | 6.08 | ZNF263 | MA0528.1 | chr1:17608433-17608454 | TCCCCTCTCCACTCCTCCCCA | - | 6.14 |
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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 |
GH01I017281 | chr1 | 17608096 | 17609295 |
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Enhancer Sequence | AGCCACCGTG CTTGGCCTGC TTCTAAATCT TGAGCTTGCC TTTGAAACAC CTGGACAGGT 60 GGGGCCCCAC CCCAGCGGTC CTGATTCAGC AGGTCTAAAG CACGGCCCGA GGCACTGCTG 120 CCGCGCTAAC AAACACCCAG GTGGTGCTGA TGCTGCCTTT TAGAGGAACA CAGTTTGAGT 180 AGCACTGCTA TAGGTCACCC AGCTCCCCTC TCCACTCCTC CCCACCTCAT CCCCTAAAAG 240 AACTCAATTT GCCCATTGTC AGAGCCTTGT GGGGAACCTG TCCACACCAC CATTGCTTCA 300 TGCCCCGCTT TTTCCTTCCT CTTTTCAGGC AACATTTTGC CCTCCGCTTG CAAAGCCTCT 360 TTTCACTCCC CTTCCTTCCT GTTCGAGGCT ATCTTGTAAT TATATATGTG CCCCAAGAAG 420 TTTGTGCAAT GATTCAGGTT CTTGTGTTCG CAAGAGACAG AGTCCTACTG AAGCCAGCTT 480 CAGCCAGAGG GAGTCTTAAT ATAAGGACAC CAGAAACCTG AGGGCAGGAT AGCTGCAGCA 540 GAGCCTGGAA CCCTCTCTGT TTCTGTGTCT ACATCATTCA TTCTCTCTCT TTCTCTCACC 600 CTCTCCACCT CCTACTTCTT CTCCCTCTTC TTCCAGCTTG GCTTCCTTTG CTTCTCTGTT 660 CCTGGGGACA AAGATGAGTA TGGCCATGCA CAGAGACACT GACACGGGCA GAGACCAACT 720 AGACGCTCCC ATTGTCAGTT TCAAATTCCT GGGAGAGGGA CTCTGATTGG TCCATCTTGG 780 ACCAGCTGTT CTCCCTGGCC CAATCAGTTA TGGCCTAGAA GGTTGGGATT CTGCAGCACA 840 AACATGGCAG CTGCCACAAT CCACAATTCC AAATTCACAT TAGGGCAGTT TCCAGAGCAC 900 GTTGCCAGAG 910
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