Tag | Content |
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EnhancerAtlas ID | HS060-25027 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr3:125770880-125771950 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:125771647-125771665 | CCTTCCTGCTTTCTTTTC | - | 6.15 | KLF4 | MA0039.3 | chr3:125771201-125771212 | CCACACCCTCC | + | 6.32 | RREB1 | MA0073.1 | chr3:125771194-125771214 | CCACCACCCACACCCTCCCT | + | 6.14 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTCCTTTCTG CTCTCAGACC AAGGAAGATG AGCACTGTTT AGTTTCTTCC TGTACCTTAT 60 CTACCAGGCT GTGGAATTCA GAATCCAGTT CCAGCTCTGA TGGAGTTCTG AGTTTGCCCT 120 CTCTTAAAAC TTGAGAAGAA AACAATGCCA CCAGGCAGGG TGTCCTCCCA CACCTCACAG 180 TCTCCTGGTG GCATCTGGCC ACAGCTCTGT GCAGCTGTCC TCTCAGCCTG CACACCCTCC 240 ACATAGGGTG GGCCTCCGTC CTCAGCAGGG GAACCAAGGC CATCATCAAG TACTCCCCAG 300 CTGGCCTTTG GGCACCACCA CCCACACCCT CCCTAACGTC CTGTGGAGCC CAGCGTGCTC 360 ATGGGCACTC TCTCTGTCTA TACCCAAGAC CCGGCACCTA CCAACCCCAA AGTCACAGCA 420 AACTCCTCCT TTCAGCCTGC GCCACCCAGC AGCCTTCCTC CTGCTCTCTG AGCACTACTA 480 CCTCTGAACA AGTGCCTGTT CTCACCCATC ACCCTCAGTG CTGCAACTCT ATGGCTCTCA 540 CCGTCTCCCT AAAGGAAGTG GTGGCCTCCT GATGGGTAAG CCCCATCTGC TGCTCTCCCT 600 GCAGGGTGGC ACTGTCCTCC CCTCCACGGA TAAAGCACCT GCTGACAGGC ACAGCTCTGT 660 ACCCTCTCCC CTGGCCTCTG GGCCTCCACC CCCAGTCCTT TGCCAACCTC ACTATCCACC 720 CCATCTCGGC CCCTCTTCTT CCTCCTGACC ATGTTAATAC CGATCTTCCT TCCTGCTTTC 780 TTTTCAGTTC TCCTTTCTCC TCACACCCTC TCCCTTCCGC AGCTCGAGTA CCCTTCCACT 840 GTGCACACAG CACTATCTTC CAGCAGACAC CCCACCTGCT CCATGCTCCC GGGGCTTTCA 900 GCAGGAAGCC TGGGCGGAAG ACGGCGGGGG AAGCTGAATC CTGATGCATA GTGGTCCCAT 960 CCTCCTTGCC AGACGTTGCT ATGACTGGTC AGTGAGACCT GAGAAGTCCT GTCTGGTCAC 1020 ATCGGGTATC ACACAACCGT GACGGGACTA AAGTCTATGG ACACTGGCTG 1070
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