Tag | Content |
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EnhancerAtlas ID | HS049-00711 | Organism | Homo sapiens | Tissue/cell | Fetal_spinal_cord | Coordinate | chr1:204775980-204776960 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:204776244-204776263 | TGCTGCCCCCTAATGGCAG | - | 6.11 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I204806 | chr1 | 204775721 | 204776774 |
| Enhancer Sequence | GAACTCAAAG AATTGTAAGT CTTAAACGAT GGCTTTAAAC AAATTTTGTG AAAATTTAAC 60 CATCAGGTCT GGTATAAGCC AGCTCCAGGA CACCACTGGA AGGGTTCCTG TTTTGGAAGC 120 TGGACTCTGT CCTCCTCTTG GAGCCCTCGG AGAGAGCAAG CGAGGCTGCT CTGTTCTGGA 180 GGCTCCGTGC CCCTGAGGCC TTTGACCCCG TTACCCGCGT TCCTCCCCTT GAAGCCCGGT 240 CCCGCTCTCC CAACACCAGT GTTCTGCTGC CCCCTAATGG CAGCTTCTGC CATCTGCGGC 300 TGTCCGGGAG CTAGATCCAC CGCAAAGTCC ACCAGCTCCG CTCCAGGATC AGAGACCCCT 360 GAGCAGGTTA AACAATCTTC CCCCTCCACT CCAGACTTTT GGAACCCAAG GACGGCCGGG 420 TCAGAGTACC CAGGACCTCA AGCCCCGCTG CCCCTTGTCC ATCCCAGAAT CGTGGTTTCC 480 CACTGCCCTC TGCAGTGCCG CGGCGAAGTG ATGAGCCCGG CACTGTGGCG CCACCTAGTG 540 CCTCTGCTGG GTCAGTGGCA CCTGCACCTG CACTGCCAGC CCCCTGCTGG GAGAATTCCG 600 ACTCAAGAAC TGTAGTTTGT TGTGTGTTGT TTTTGCTTTG GGGCTCACTG GGAAACTCTC 660 ACCAGTCACC TGCATTACAG CCTGGGGCTT CCTGTCACTG TAGAGCAGGT AAGAAGAGGA 720 GGGAAAGAAA AGACCTCAGC AGCACAGCAC CAGACCTTCC TCCACTTGGT GGGGCCTTCT 780 GACCACGAAT GGTGAATAGT CCAACTAACA ACTAAAAGCT CCAGCTGGGA GGACCCTGGA 840 GCTCCCCTGA GCCTGTGGCC TTCAAACGGT ACTGACCAAG CCCATCAGTA AGCAGTGCAT 900 TTTACAACGC AACAGTCCAG GACACCCCTG CGTTGAAAGA ACTCAGGAAG CAATACTTAC 960 CCTTAGTATG CATAGCGTAT 980
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