Tag | Content |
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EnhancerAtlas ID | HS074-00092 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:10570520-10572130 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:10571394-10571412 | CCTCCCTTCCTTCCTGCC | - | 7.82 | EWSR1-FLI1 | MA0149.1 | chr1:10571398-10571416 | CCTTCCTTCCTGCCTCCC | - | 7.88 | ZNF263 | MA0528.1 | chr1:10571397-10571418 | CCCTTCCTTCCTGCCTCCCCC | - | 6.33 | ZNF263 | MA0528.1 | chr1:10571393-10571414 | CCCTCCCTTCCTTCCTGCCTC | - | 6.63 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_20679 | chr1:10569696-10574662 | CD56 | SE_33671 | chr1:10568472-10571497 | H2171 | SE_36701 | chr1:10569594-10572189 | HMEC | SE_47404 | chr1:10566553-10580264 | Panc1 |
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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 |
GH01I010507 | chr1 | 10567258 | 10578342 |
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Enhancer Sequence | AGCTTATCTA CTTTGCTCTG GCATGGAGAA GGAAAAGTCC CATTTCCTGC TAGGCTGCCA 60 GGCACTTATG TAAGACTTTT AGGTGCCAAA GTAGGAAAGG AGTCCCTGTG TTGTATGGCC 120 GTATATATTT TGCATGTGTG TTTCCTGGCT GTTTGGCACC TAGGCACTTT GCTAAGCCCT 180 GTATGGGTTG GGCATATACC GTATTGCTCA GCTCCTGGCA GAAAATAGGC ACTCATACAT 240 ATTTGTGGAA TGAGTGAGTG TGTGTGCTCA CTTATGTGCG ATGGAGATGA TGAGCCAAGG 300 AGTTGGATTG CACAGTTGCT GCCTGGCGTC CTGCTAGGAA CTTAGGGTGC AACATTCCCA 360 CTGGGCCACA CATATGCCGA TGTTCAGTGG ATGACTGCTA CGCAAGCAAC ATAAAGAGGC 420 CATTTTATGA AAGGGAACAT CAGAGGAAAC ATTATAACTG AGACCTTTAT AGCCTTTCCA 480 TTATTATGGT TTAAATCTTG ACAGTCTTTA TTTGCAATGA CACTGGGACC AGTAAAGACA 540 ATGCTCACTC CCACCTCCTC GTTCTCCACA TCCTGTTCCG TAGCTGTGGT GCACCGATAG 600 GCATCGTTAA ATGTGCAGGC AGCAGAGCTG CTGGTTTGTC TAGAAACAGC CCCTTTTGAC 660 TCAGAAGTTG GAACCCAGAT GACTCACCAT TCTATTTGTT TTATTGCAAC TGTCATTTCA 720 TAAAATGCCC TGACAGCTTT AAACTGTAAA TGCCAAAGTG AGGTTTTTGT CTTTTTTATT 780 TTGTTATCTC CTGTTTTTTC TAATCTTTTA TATTTCTATT TTCTCCTTTC TTTTCAGACT 840 TATTTTCTCT TTCATTACTG TCTCTTTCTC TGTCCCTCCC TTCCTTCCTG CCTCCCCCCT 900 TTGATGACTC TAATGGCATG AGTAGTTGAA GTGGTTTTTG CTAACATCAT GGTGCGTTCT 960 TTCCAGCTTT AATGCTATCT GATTGAGCGT GTCTCCCCTC AGATTTTTGT GTAGGGTTTA 1020 GAAATGGAAA TGACCATGCA CATCAGAGTT TAAATTTTCC TAGGAAAGTC TGCCATGAAC 1080 TGTAGGACCT ATAACTTCTA GAGATGGAGG GACCCCTGAC ATCTGTGGAC TATGGACTCC 1140 TGACTTCTGT GGACTCTAGA ATTTATGACT TCTGTGGATT GTGGGGCCTC TGACTTCCAT 1200 AGACCGTGGG ACTGTGACTT CTGTGGACCC AGGGACCTCT GAATTCCATG GACTGTGAGA 1260 CCTCTGACTT CTGTGGCCTG TGAGATCTCT GACCTCTGTG GCCCGTGGGA CCTCTGACTT 1320 CTGTGGTCTC TGGGACCTGT GACCTCTTTG ACTTCCAAGT CTTCTGTGGA CTGCAGGACC 1380 TCATCAACAC GTGTATTGCC AGAAGAGAGG CTTGATTGTG TTAACCTGTT TCTCTCCAGA 1440 GGTGTCACAT ACTAGAATTT CTGCTCAGTC TTATGGCTTA GGTGGGGTGT TGAGTCTAAA 1500 TATATATATT TTTTGAGACG GAGTCTTGCT CTGTCACCCA GGCTGGAGTG CAGTGGCATA 1560 ATCTTGGCTC ACTGCACGCT CCGCCTCCCG GGTTTACGCC ATTCTCCTGC 1610
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