Tag | Content |
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EnhancerAtlas ID | HS051-20110 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr3:134944460-134945610 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
INSM1 | MA0155.1 | chr3:134945348-134945360 | TGCCCCCAGGCA | - | 6.04 | NFIC | MA0161.2 | chr3:134944481-134944492 | TTCTTGGCAGA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCTGGAACTG AAGCCCCACA GTTCTTGGCA GAGCTTTCAG ACTGTGGCAA GTTTAGGAAG 60 GCCACACCTC AGGTGAGTGG GGATGATGAT AGTGGCCACC AAGAGCCACA GGGAAAGGGT 120 CCAGTCCCAG GTTGGAGGAG GGGAAACTGA GGTGACTCTG CCTCCCACTC TGACAAGCCC 180 AGCTGCCCTT GGGACAGCCA TACTGTAAAC CGTAGGCCCA AGCAGGACAG GCAGGGAAGC 240 AAAGACCAGG GTTCTAGACC CACCAGGCTG GGTGAAAGTT AGGTCTGGGA ATGTGGGAGC 300 AACTCCAAGG GCTGGTTTTC TAAGGAATGG GAAAATGGAA AGTAAATCTT AAAGTAGATC 360 AAACAATAAA GAGATTAGTC AGTGGGGAAA GAACAGGTAA GATGCAAGCA GCATTTGCTA 420 AAGCCTAAAT CTAGCTGGGG AACCCCAGCT TACCCCCAAG TGGGGTTTCT GTAGTGCAGG 480 CCTAGGCAGG CCAACGGCAT CAGTGGCCTC AAGAATGAGG ATTGGGGACA GCTGTGGGCA 540 GCTTGGCCCA TGGTCCAGCC TACACTACGG CTTGCATGCT GCTCTTGCAA CCTGTGCCCT 600 GTCTCATGGC AGTTTCCTCC CACATCCTGC TCAGTAGCTC TTCAAAGCCT TTGCCACACT 660 CCTTATGTCC CTGCCCTACC GCGGCACTCT TCTGTCCCAG CAGCTGGCCT GGCTTCCTCT 720 TTTATCACAG TACCTCTGAG CTTTCATGTG CTGCTCAGTA ACAGTTTGTG GAATGAATTA 780 AGAAATTCAC GAACGAGTGA CAGACATGCC CCTGGAGATC TGAGATATCA AGGAGAATGG 840 TCAGTGTAGA ATGGGGCAGG AGCCCGAGTA CTCAGGGAGC AGTATGGCTG CCCCCAGGCA 900 GCTGGGTTCT TCACAGTAGG AAGAGACCTT TCAGTTTCTG CTCTTCCAAC CCTGAATTCG 960 ACTCTTTCCC TGTGGCTCTG CACGGCTGTG ATAACCAGCC CCATTCACCT ACTTTTGGCC 1020 TTCAAAACCT TCTACTTTCT TCCCCTACAC CTGGGGGAGG AATAATCCCA GAACATGCAG 1080 GAGAAGGGGC TTATTGGTCC AACTTGGAAG GTTGTTGGCC TATCTGAAGA AAGAAATCTC 1140 TAGAATGCCA 1150
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