| Tag | Content |
|---|
EnhancerAtlas ID | HS053-02295 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:114656200-114657610 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:114656375-114656393 | TCTGCCTTCCCTGCTTCC | - | 6.38 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 114656359 | 114657416 | | chr1 | 114656563 | 114656717 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I114112 | chr1 | 114655186 | 114657830 |
| Enhancer Sequence | AGCCAGAAAT GAGACATCTT TGTGGACATC TGCCTTCCTC TTTTGGATTT AGATCATCAT 60
CAAGCCCTGA TAATTCTAAC TCCAAATTCC ATCTCAAGTC CACCCACCTC TCTCCATCTC 120
CAGTGCCACA CGGAGGCCAA AGCCTACCCC CCTGCCAGCA TACAGCCGCC TCCTATCTGC 180
CTTCCCTGCT TCCCTTGCTC TCCCGCCCCA TTCTCCACAC AGCAGCCAGA GTGCTCTTCC 240
CCAGATGGAA AATGGATTGT ACCACTCCTT GTTTAAAACC TCCAATGGCA TCCCCTTTCA 300
CTAGGAATAA AAACAAAAGC ACTTATCAAG ATCTACAGGG CCCTCCACGA ACGGGGCTGA 360
CTCTTCAGCC TCCCCCCGTG CCAGGGCTCT CCTCACAGGC TTCCTCAAAT GCCCCAGGCT 420
CTTCCTGCCC CATGACTTTG CACTTTCTCT TCCTCTGATT GACCGTTCTT TCCCCAGCTC 480
TTCACATGGC AGAGACCCAC TCATCTCAGG CCACTTCCTC CAGCGCCTCC CTCTGCTGCC 540
AACTGTGTTC CCGAAGGACA GATCTGGGTC TGTTTTGCCA GGGCCAGGAC AAGGGTGAGG 600
CAAAGCAGGT GCCCAGGTAC AAAAGTGAAG GAAGTGCTCA CTGTCAGGTT CATGCATGTA 660
TCCAAGAGTG AGTGTCCCCT TCCATTCTGC CCCCTGGGTA CTTCACTCGC CTCACCCTAA 720
TCTCAACCTC ATATTTTACT CACCACTGTA TTCTCAGTAC TGAGCACGGT GCCTGGTGTA 780
TAACAGATGC TGACAAGTAT TTGTTGAATT AATGAGCAAC TCAGCTTTGT GGGGCTCACC 840
TGGTTAAGGT GGCAAAATGA ATGGGTGACA AGAGTAGGCC CTTGCTTAAC CTCAGCCTCA 900
GCCTCTGGTC TCCCCAGGAG GGTTGCTGTG GTTATTGAGA TGGTGTCAGG GTGGAGCCTC 960
ATAGGTGTTC CTCAGCGGGT GGGCTGAATA TTCCCTGCAT TAGAAGCTTG GGAGGTGGAG 1020
ACTTGATTCC TGAGCTGCGC CCAAGATCTA CTGAGTCATC ATCTCTGGAG GCGGGGCCTG 1080
GATGTTTGCA TTATTGACAG GCTTCCCAGA TGAGTGTTAC ATAGCCTCAG TTCGTGATAT 1140
AAGGCGAGAG ATTCTGAGGT TGCCCCAGGT CAGACCCTAT TAGAATCTCT GTGACATGGA 1200
ACATGTCCTA ATGCAACTGA AGTCATTAAA TATCAGAGCT GCCAAGCAAA AGTTAAGGCA 1260
TAAAAGGCCT CTTCTCTTTT TTTAGGCACA AGCAAGGGTT CTGAAGGATC GAAGCCATGT 1320
GGGCTGCTGG ACTGGTCCTG GCCCTCACCA CTTACTTCCC TTTGCCTTTT TCCTGTGCAC 1380
CACATGGCAC ACTGGGTATA TTTTAGAAAG 1410
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