Tag | Content |
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EnhancerAtlas ID | HS141-10695 | Organism | Homo sapiens | Tissue/cell | NB4 | Coordinate | chr2:127588260-127589940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:127588943-127588962 | TAGCTCCACCTGGTGACCA | - | 6.4 |
| | 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 |
GH02I126831 | chr2 | 127589301 | 127589450 |
| Enhancer Sequence | GAAGCAAGAC CCTGGGAGGG ATATGAGGGT CTAACATATT TTTCAGTCTT GCGGTGGATA 60 AACGATGCTC ACAAATTCTT TGACACACCT TTGGTGAAGA GATGCAATAT TTATTCCCTC 120 TCCTTGAATC TGGGCAGGCT CTGCATTTGC TTTCATCCAT TAAATGTGTC AGAAGTCATG 180 CTACGCCAGT AACCAGGCCC AGGCTTTGAG ACTAGCAACC TCCACATCTC ATCTCTGGGC 240 ACACCTGTTT TTGGAGCCCT GAGTTGCTGT GTAAGAAGTC CTGCTAGCCT GCTAGAAAGA 300 CAACCTGGAG AAACTCTGAC TCCACAGAGA GGAAGTGGGG TCCCACTGAG CCCAACCACT 360 CCCTTCTCCA CCCTTTGCCC CTTTTAGGCA TGAGTGAAGC CTTTTTAGAA CCTCCAGCTG 420 CCTAAAGTCT TCATAGAATA GCCAGTCAAT GCTGCATGGA GCAAAAGAGT CACTCCAGTG 480 AGCCCTATCC AAATTCCTGA CCCTCAGATA ATGAGCATAA TACAATGAGT AGTTTTAAGG 540 CACTAACTTG GGGTAGTTTC TCATGTAACA CTGGATAATT GGAACGCGTG ATGTTCTCTA 600 TTAACGTGAC GCAGATATAG TAGTCCCTGC TCAAGTCCAT GTAGAATGAG GCTGGGTGCA 660 CACAGCCAGC TTTGTTTCCT GCCTAGCTCC ACCTGGTGAC CAGGTGGCTG GACCAGAGGA 720 GGGGATACAG GGACAGGAAC CAGGGCAAGG ACAACAAGAC CATTTGGCTA CTGAACCAGG 780 GTCCTGGTCT CCTCGGCACT GTGTCCTGAG CCCTGATGCG AGAGGCCACA GAGGTCAGGT 840 AGGGTCTCTG TCATTCACCT TTTCGACAGG AGACAAAGGA AAACTCCAAA CAAGCGAAAA 900 CAGAGAAAAG AACAATGGGC TTGGAGACAG CCCCACTAGG TGACCTGGAG CAGAGTGAGC 960 CAACTTTCTC CTTCCTGAGA ATAACAATGG CTGCTATTAT TGAGCTCTGA CTCTACACAA 1020 AACCCACACA AGCACTAATG TGAGTCACAC ATCCTCACGG CAACCCTAAG ACACAGAAGC 1080 TCCTACTTCC ACCATACACA GCTGGTGGAG CCATGGGCTG CCCTCTGGGA GCAGCACAAC 1140 AGAGAGAAAG GAACACACAG GCTCTGTAAT CATAGCAGCC GGATTGAAAG CCCACCCCAC 1200 TGCTGGCCAC ACCTTCCCCA ACCGCAGTCT ACTCATCTGA CGACAGGATA AGAAGGCTGG 1260 CCCCACTTGA GCTTGACGTG AGGATGACAT GTCATGGCAT ATGAAAAGTG ACGGGCACAA 1320 TAGAGGCTCT TGGTAAATGT TGGTCTCTTC CCTTAAACCC TCAGACAAAA ATTCCCAAAC 1380 ATTTCCAGGT TGAACTTTAT AATTTAGAAA AAAGTGAAAT ATTTGGTGTG TTGTTTTCAT 1440 TTTGTTTTTA ATCCAGAAAA TCCTAAAGGA GACAGTAAAA ATCAGATTGC TTTAAGCAAT 1500 CCTTCCCCAC TAGTGCATGA ACTTGGCAGA GCAGATGTGC AGAGCTCAGG CTGCTGAGGT 1560 CATGGGAGTG AAGGGCCAGC AGGGCTCCAG ACTTGGAGAG GGCTGGTTTG GAAACCTGGT 1620 TTTACTGCTT ATTCAGTGTG AGACTATGGC AACTCCCTGC ATCTCCCTGG TCCTCAGTTT 1680
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