Tag | Content |
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EnhancerAtlas ID | HS116-06811 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr11:75179260-75180730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TFAP2C | MA0524.2 | chr11:75179349-75179361 | TGCCCTGAGGCA | - | 6.18 | ZNF740 | MA0753.2 | chr11:75179721-75179734 | ACGCCCCCCCCCC | + | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr11 | 75179587 | 75180265 | chr11 | 75179265 | 75179578 | chr11 | 75180501 | 75180727 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I075468 | chr11 | 75179064 | 75181265 |
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Enhancer Sequence | CCTTAACAGA ACATGGGGTC TGAAGTCTGC ACACATCACT CTGAATGTTA CAGAATTTCA 60 GAATCGCAGA GCTCCCCTGC CTGTCCCCTT GCCCTGAGGC AGCGAGCGTG TCTGCAGCCT 120 CCAGGACACG AGCTCACCCT ACTCTACTCC ACTGGCTCCT GGGAAGGGGC TTCTCCTTCC 180 AGATGCTGCC TAGTCCTTCT GTGGACTCAA AATTCTTCCT TCCAAGACAT GGAGCCTGAC 240 AACGGAAGGC TGGGTTGAGG GAGTCTGGCA ATACTGGGTT TGAATCCCAG ACTGGCCACG 300 ACTGAGTGAC CTTGGGGAAG ACATTTACCT TCTCTGTGCC CCAGCTTCCT GCTCTGTAAA 360 ATGGGGACAG TATCGGCATG CTGCCCAGAC CACTAAAACC TCCCATGCAC GGCATCTGGT 420 GAGGCTGACC TTCCAGGCAG GGGAGTTACT GCCCTCCCCC GACGCCCCCC CCCCGGGAGG 480 TGGAGCTGAA ATCTGCCTCC TCCACTGCTC CCCTGCAGCT GGTTCTCTGA TACCACACAG 540 AACAAGGCCA GCCAAAGGGT AAGAAATATT GGGGTCAAAT GACCACAGAG TGGAGAATAC 600 ACAAAAGAGC TGGATTTTCA CCCAGGCCCT TTTCCCACCG GCTGTGTGGC TGTAGGCCAA 660 TCGCTCAGGA CCTCTGACCT CAGCTTCCTC CTCTGTTCAC AGAATGACAT CACCACCACC 720 TCACAGGAGG ACTGCCAGGC CCCAGCACGA TTACAGATGT AAGCTGTAAG TCGCCAAATC 780 CAGGATCGTT CCTGTAATTA TCATTTCGCG TCTGACAGCC CTTTAATTAT GTGAAGACAG 840 TGATCAAACC TTTCCTCCCT GCTCTACACC ACATCTCTCC AGCTGCTGAG GACAGCCAGG 900 TTGATTGCCT TCCCCCAACC CAGGGCGGGT GCCATGGTCA GCCAGATGCA GAGGCCAGGC 960 CTGGCTCTGT AGGCTGTGGC CCTGGGAACC AGCACCAATA GAGGAAGAAG ACCCTGGCAT 1020 GGTAGCTGCC CAATCTCACT CACAGGCTGC ATCCCGGGCT GTGGGGAACA GAGTCCTGTG 1080 TGAGCTCACC ATGGCATTGG GGGTGGGTGG GGATGGTAAT CCTAAGAGCC CTTTACTTGC 1140 TCCATCTCAT CATCCCCACA GTTCTGCAAA GCAGAGGAGA CCAAGTCACA GAGGAAGGAA 1200 GGGACTTGCC CAAAGTCACA AAGGGCACAC ATAATGGTGG AACCACAATT CACAACCAGG 1260 TCTGTGTACC TCCAGTGTCC CCAGCTGTCT CGGGGCAACA AGGAGCAGGA AATGTAAATT 1320 ATCCTTGTCT GACCAAGGTG GAAACAGGCT CAGAGGGACA GGGCCTTGCC CAAGGTCACA 1380 CTTTGAGTCA CAGGCTGCGC CAGAGCAGGG ACCCTGGGAT TTCAGAGTTA ACTAAGATGC 1440 CAGAGATTAT CTCGCCTCAT CTCCTAAAGA 1470
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