Tag | Content |
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EnhancerAtlas ID | HS145-12911 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr2:95999190-96000360 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RELA | MA0107.1 | chr2:95999761-95999771 | GGAAATTCCC | - | 6.02 |
| | 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 |
GH02I095333 | chr2 | 95998773 | 96002010 |
| Enhancer Sequence | GCCCTGGACC CTGACTCCTC TCCTGTGGTG GCCTCACCAG GGCCCGCCCT CGGTCAACCT 60 AGCCTCGAAG AAGGGAATGC TTGGGTGTTT CCAGAGACTC CTCAGAGCAC GTGCTCAGGA 120 TAGAGTCCTG ATGCTTCTAG AGACCGTATG GGCAAGTCCT GTAGCCTCTG TTGGTTGCAA 180 TTGTGACAGC TCGTAGGAGC ATGGTGAGGA TTCAATGATA CTATGTCAGT GAGTGCCTAG 240 GACAGTGCCT GGCACATGGT AAGCAGCAAT GAATGACACT GCTGCTATCC ATTATTATTA 300 CCCAATTCCC TCACTGAACG CAGAGGGCAT GATGGGTGGC TGAGTCCTCC CAGCTTCCTT 360 GAGGCAAAGG TGGGACTTGG ATAGGGGGCG TCTCACTCCT GCCCAGCACC CTGGCTGCTC 420 CCCTGCTGCT TTCTGACTCA GACCCCAAGG TTGTGATTCC CAAGTCATTC GTCTGCATTC 480 AGCTGACACA GGCCATCTGC AAGACACACA CCTCTCTGAG CTGTCAGAAG ACACTGCAGA 540 AGCTGAGATC CTGGCATCAA GCGTCCCAGA TGGAAATTCC CCAAGACACC CTTGGGCCCT 600 CGGCTCAAGT TCAAACAAAG AAATGCTTAT GTTCAGAGAT CTTCACAGAT CACCAGCGAG 660 GATGTGACTT GAGAACACTT TGCGTCAGCA TCATAAAACA TGAGGATTGA TGACCCGTGT 720 GAGTGGGGCG AGTGCCAGGG GAACACAGGC TCTGAGTTGG CCGGCCGTGC TTCCTGCATA 780 CACTCTGTGC AGAGGGTGCC AGCCTAGACT GGCGGGGGGG TTAGAATAGC ACCGCACTAG 840 TTAGCATGTC CCATAGGACC CTGTTTACAG CACACTTGCA TGGGCATGTG TGCACCTGGT 900 TCTCATGACA ATATGCAGGG TGGGCAGGGG TTAAGGAATG CTTCCCCACT TTGGGGATGA 960 AGGAAACTGA GGCTCAAGGA GGTGCGAAGC CAGGCAGCTG AGGTCACACA GCCTTGGATC 1020 TCCCTACCGT CACTATCCTC CCCTCTTGCC AGCAGAGAGA GGTGGGAAAG CCACGTTCAG 1080 CCAAAACCCA GAAATTTACC CAGAGAAACT CACAAACCAA CATGGTGGGC CTTGTACAAA 1140 CTCTAAGAGT ATGAAGAGAA GAGCTACAGC 1170
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