Tag | Content |
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EnhancerAtlas ID | HS118-10208 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr2:102246600-102247440 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPIB | MA0081.2 | chr2:102246897-102246909 | CACTTCCCCTTT | - | 6.07 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 102246696 | 102247032 | chr2 | 102246727 | 102247245 |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I101630 | chr2 | 102246727 | 102247245 |
| Enhancer Sequence | GGCAGATTTT GAATGAAATT GTCTTACCTT TTAAAAGTGT ATTTTAATAA TTTTTTTTTT 60 TTTACCGTTA AGGTGTATCT CTCAGGGACC TGTGCACAAG CTCTGTGCTG AGTTGTAAGC 120 TAAGAGACAA ATCTGCACGT GGCCTGTTGG CCTCCTGATC TGGCACCTGC CTCTATACCT 180 TGCACAATCC GCACCCTGGC AGCTGCCGGG AGGAACAATA TGCCACCAAA GGCCCTTCAC 240 CTGCGGTCTG CAGGCATGTG AGCGCCTTTG CCAGCAGGAA CTTGGTCAGG AGTGTACCAC 300 TTCCCCTTTG TTGGGAATTC CAGGCTGACG TGGGGATGTG ATTTGAGGGT GTGACCAACC 360 TGGAGGAAAA CAGGGAGTTG GGCCGCGTTA TCCTGACTCA CCGTCTTGTG TTTGCGCCAC 420 ACTGCCTGTG AGGTTGGAAC AGGGGACAAT GGCTCACAGG GGTCTTTCCA CCCTGCCAGC 480 CAATGCCTCC TTCTCTGCCT AGCTTGTCCT CACCCCGAAA GTGCCTGCTT CTGACCTCTT 540 CTTGGTCCAC CCGGGCTGGC CCGTGATTGG CATTCTAGAA ATGCTGCTCG AGGGACCGGG 600 CCTCCATGCT CTGCCTACTT CACTCTGACT CCACATTCCC TGTCACATCT CTGCTTAGAC 660 AGAAACCCCT TAACAGCTCC AGCTCTCTCC CACCCCATGC TGGAAATCCA ACTTGCTATG 720 GGAAAGGTCT CGCTGAAAAG AACACCACAT TCCTGCCCCT CCACACTCGC CAGCTTCAGA 780 TAAATGGAAG GGTGAGAAAA AAAGCACGAG CACATGGAAC GAGCCAGGAA GAAGCAGACG 840
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