Tag | Content |
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EnhancerAtlas ID | HS042-39317 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr6:13762540-13763710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr6:13762846-13762856 | TTCAAGTGGT | - | 6.02 | Pou2f3 | MA0627.1 | chr6:13763524-13763540 | TATTATGCAAATTTGC | + | 6.62 |
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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 |
GH06I013760 | chr6 | 13760539 | 13763964 |
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Enhancer Sequence | GTCAGGCTGG TCTTGAACTC CTGACCCCAG GTGATCCGCC TGCCTCAGCC CCCCAAAGTG 60 CTGGGATTAC AGGCGTGAGC CACCACGCCT GGCCCAGTTT TCATTTTTAA AAAATCTATT 120 ACATGCTCAT GATAAAAAAA ATTAAGCAGT GCACAGTGAA GAGTATACCC CCCTCACAGC 180 ATTCCCCCCT GCAGTTCCCA TCCCCCCAGG CAACTACTGT TATGAATTTT TTTGTGTATC 240 CTTCCAGAAA GAGTCTATGC ATATAAGAGC AGCTTTGATT TTTGAGATGC ATTTTTGTAT 300 GTTCAGTTCA AGTGGTTCAC AAGATGCCTT TTCCAAATAA CTCCATGGCA ACGCAACTCT 360 GGAACTCACA CGCACATGGA TGTATACATG GACACACACA GTCGTTCTTT TGAGCATAAA 420 ATGGAGGGGA AATGATGCAA CAGAGAGTGA ATAGAAGGCA TATTCCAGTA AACCACAGTG 480 GTTAGTGGCT TCTCAGATGG TTCCAGACAG CTTTTTATAC AGAAATAGCT CAGTGAGAAC 540 ACCCCAGCCT ACTCAGACTG CAGAACAAAT CCCAGGAACT TGCTTTTGTG CAATCTCCCC 600 CTTGAAGCTC AAGTCTAAAC ACATCAGAGC TTGGCAGGGC TGCATGGGTA CATTAGCGAA 660 CAGACAGAAC ACCCTGGCTC CTCAGGCGCT CCTTGTTTTT TTCCCTCTGG ACCAGCAGAT 720 TTTTCTTACA GCTTACACCT GCTCCTCCCC GACCCCCAAC AACATGCAGA AAAGGAAAGC 780 CCCTCAAGTT TTCCTTGATC AAGAGGTTAA ATAAAAAAAC AACTCTCTTT CACACTCTAA 840 GGGAAAGGAA AATAAAAACC ACCAGTAGCT AAGACACACA CACACACACA CACACACACA 900 CAAACACACA CACACATTTG GCAGAAATAA ATTAAGAAAA ATCATTCTAT GTATGAGACC 960 ATTCTGAAAC TAAGTGATGC ATGATATTAT GCAAATTTGC AAGGTGTATT TGTCCTCAGA 1020 ATAGAGATGG CTGAATGGGA GTGATAGTGT CTTGATAAAT TGTTGTTCTA GAAATTTTCC 1080 AGAACTGAAA TGTGCAACAG GACATTTGAG AACTATCTTT TATCTAAATA CTGATGTATT 1140 AATAATATAG CAGTATTAAA AGCACTGTCA 1170
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