Tag | Content |
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EnhancerAtlas ID | HS073-08511 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr2:110271110-110272600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr2:110272469-110272490 | CCTCCCTCCCTCTCATCTTCC | - | 6.24 | ZNF263 | MA0528.1 | chr2:110272472-110272493 | CCCTCCCTCTCATCTTCCCCC | - | 6.82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 110271634 | 110272105 | chr2 | 110272143 | 110272349 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I109513 | chr2 | 110271162 | 110272526 |
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Enhancer Sequence | TATATGCACA TACACACACA CTGCATGCAC ACACCACACA AGCCACGTGC ATGCACAAAC 60 ACACGTCCAC ACACTATATG CACATGCGCA CACATCACTT GCACATTTGC ACACACACCC 120 TTCTCCCAGT TCTAGGACAC CTGCGTAGAT GAGGCTTTGC AGGAGGAGTG CCACAAGGGA 180 AGGAGGGAGG TGGGTGCCCA TGGAGGCTGT AGTCTGTGCT GCCTCACCTC CCCAGAGCCA 240 GCCTGTGGCT ACAGAGGATG TGGCCAGGGG TGTAGGGGAT TGGGTATCAC CAGCAAACCA 300 AGCCCTCACC CACAGCCACA TTCTAACTTC AGCATCCAAC AAAGCACTTC AGCTACCCCA 360 GGGGGACCAC CGTGATGGTG GCCGATGAGC AAATCCTAGA AGAGCAAGCA GCCGGGTGGA 420 GCCCAGGCAG CCTCCTGGGC CTGGGGGCCT TCTGGTCCCC AGTGAGTCTG CGGCTCCATG 480 TCAGAGTTCT CCTCACCACT CAAAGCTAGA ACGGAGAAGG GCCTTAATGT GGGCATGTTC 540 CCACGGTCCT TAGAAAGGCA GTAAGCCTGG TTTATGTTGC TCCATCAAGT GCTCTTGCAG 600 CTCTGAGGTT TGGTTGAAAC TTAAACTCAG CATCAAGCTA GCCGGGCCAG ATTCTGAGCT 660 TATGTAACGC CCTGGAAACT CCCATGTGCT GGACTGGCTG TTTCTGGAAT CTTATTATGA 720 TTCATAACTT GGTTACGGCT CTGAGCTGGT AAATACGGAG TTTCTGCTGT GGACTCAGAA 780 AACCACGTTA TAAAACACAG ACCAGGGCTG TTAGGAAAAC GCAGCCCCGG GTGTGCGAGT 840 GCCCACAGCT GCAGCCCATC CGCCCACCGC CCCCAGGGCT AGTGAATTAT GACTGTGCAC 900 AGCTCAGACC TCCATGGATG AAAGGCAGAC TCACAGGGCC CTGTACGAGT TCAGTGTGGG 960 GCACTTGGCT GTGTGTTGGA ACCAGCCTGT GTGCAGGCCA GGCGGGATGC CGCAGGGAAG 1020 CCCTGGTGTG GGACCAGGGC CGTCCCTAGA GTTGGGCTCT TTCCCCTGTG TACAGACCCC 1080 CACGCAGGGA CCTTGAGCCT GCAGTGCTCT GCCAGAGTGG CCTCAGGTGT GGCTACAGCC 1140 TGGACTGGAG TTTTCCTTCC CCTCATTTTT CACTTTCAGT CGCTGTGGGA CCGATTGGTC 1200 TCTGGACTCT TCTTGCAGCT TTATTCCATG GTTCGAGGTC CACAGCTTGA CTCCCTTGGG 1260 GGTTTGGGTG CCAGGGGAGA GGGCTGCCCC CCAGGCCCTG GGCACGGCGG TCACTTTCTC 1320 ACTGCCTCCT CCTTTCCCTG GTCAGGTGGT GCTTCCCACC CTCCCTCCCT CTCATCTTCC 1380 CCCATGCCCC TCACACACTT CCCTCTCCTC AAGCCTCTGA CTTCCATTAG CCAGAGATGC 1440 CTGGGACATG GAGCCAACCA CATCTGCCAA CTCTCATGCC CAGAGCCCTG 1490
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