Tag | Content |
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EnhancerAtlas ID | HS133-03729 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:227061560-227063060 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SRF | MA0083.3 | chr1:227061689-227061705 | TGCCCATATGTGGGCA | - | 6.5 | SRF | MA0083.3 | chr1:227061689-227061705 | TGCCCATATGTGGGCA | + | 6.61 | ZNF263 | MA0528.1 | chr1:227062988-227063009 | GGAGGAAGGTGAGCAGGGAAG | + | 6.22 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr1 | 227061913 | 227061971 | chr1 | 227062015 | 227062087 | chr1 | 227062156 | 227062342 | chr1 | 227062384 | 227062434 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I226873 | chr1 | 227061434 | 227064266 |
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Enhancer Sequence | AGTACTCATG GAAAAGCAGA TTTGATGGCT GTGTAGAGCA TTTGAATTAT TTATCCTACC 60 AGTCCCACAG CAGGACACTT TCCCACCCTC CCTTTTGCCC CAGAGAAGCA GTGCCCTCTG 120 TCCTCCCCAT GCCCATATGT GGGCACTCCC CACCATGGAG CCAAACCTAC CTGGGCAAGT 180 AGCAGAGGGA GAGCAGAGTG AGCCCTGGGG GCAGGAGAGA GACTTGAGAG TTTTGAGGTG 240 ACAGATGAGC TGGTGAGTGA GTGATTAGGG AGCATTTCTT GACACATACC TGCCCGTGGT 300 GAAGGCATGT GTCTTGTGAG TGTGCTCCCA GAAAGCCTGT GTAGTGTGTG GTGGGCCTGC 360 CTGTGTGACC AAACCCTGGC CACTGGGTAC GTGACCCTCA CAAGTGCTGA CTGGGCTGAG 420 AAGAGCTCCT TGATGGGCAG TTTGGAGACT TGAGTTGTAA CTGTGGCTTT TGGCCATGGG 480 ACATTAACTG ATTACTTTTG CCCCTCTAGG CTTCAGTTGT CCTTAATTAT AATACAGGGA 540 GCTGACTAGG TGGCGTTGAT GGCCTTTACG GTCCTTGCCA GCTCTGACAT TGTCCTATGG 600 ATATGTCCTT TCATTTGATA ATATGTTTAC GTGGCCATAG TGCCTGGGGC TGGGCCGGGA 660 ATGGAAACTT GATCTCTGGG GCCTGGCCTT TGAAGCCAGT TCATGTGTCT GGTGGTTCAG 720 CAGATCCGTA ACTTTCCAAG AGGCACATCC ATAGGCTACC GTGTCCTTTC TCACTGTGTC 780 CCTCCTCCAT TTCATCTTCT TTATAACTAC GACTTATTGA ACATCTACTG TGTGCTGGAC 840 ACTTTACAGG TTATCTCTAG GTTTTACGAT AATCTTGCAA GGTATGCCTG TTCTGCTTTT 900 TACAGCAGAG GAAATGAGCT GTGTCAGATT AGACTGTCTG AGGCCTCTTG GCCAGGGAGT 960 ATGTGGTTCA AATCACATAG GCAGGCGATC TGAACCCTGT CAGTCTCCAA AGCCTCTGCT 1020 TTTGACCGCT GACTTGCTGC TGCTTGTTTA AAAATAAATG TGTTTCTGGA GCCTACTCCA 1080 GAGGGGCGTG CTAGGGGCTC CCTCTCCCAC TTCCCCACAA ACCACCCTTT TCCCTGGCTG 1140 CTTCAGGAAA TGAGAGAACT CTGCCTGGGC CCCAGGCACT TCTGAGTGGG ACAGGGCTGT 1200 TAGAGGTAAG TCTAGAGCCT GGCCCAAAAT TCAGGAGGCC CCATCAGAGG GCCCCTGGGG 1260 CCTGTGGTCC GGGAGGGTGG TAGGGCAGTA CCTCACTTCC CTTTGAGACT CAGGCCCCAG 1320 CTCTGGCTTA GGCCAGGGAG AACCATCCCC AAGTGGTATG TGTTACTATA TGAGCTGAGA 1380 TGGATGGTCA GCTGGACCAA ATACATAGTC GGGTACCCAG GGCCAGGGGG AGGAAGGTGA 1440 GCAGGGAAGC TGTGGGCAAT TGTCTGGGTA TCACCTGACC TTAGCAAACT CTTCCTTGTT 1500
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