Tag | Content |
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EnhancerAtlas ID | HS176-19784 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:20564850-20566100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr2:20564964-20564976 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr2:20564968-20564980 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr2:20564972-20564984 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr2:20564976-20564988 | AAACAAACAAAC | - | 6.32 | NFYA | MA0060.3 | chr2:20565956-20565967 | TCTGATTGGCT | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 20565226 | 20565440 | chr2 | 20565144 | 20565451 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I020365 | chr2 | 20564898 | 20567277 |
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Enhancer Sequence | CTCAGAAGGC TGAAGTGGGA GGATTGCTTG AACCCAAGAG GTTGAGGCTG CAATGATCTG 60 AGATGGCACC ACTGCAATCC AACCTGGGTG ATGGAGTGAG AACTTGTCTG ATTAAAACAA 120 ACAAACAAAC AAACAAACAA AAAAACAAGG TAACAAGACT TCACCTGAGT GTACCGTGCA 180 GTACATGCAT GTTCTAACAC ACACGTGAAG TGGCACCCTA CCTGTACAAT GCACTCATCT 240 GCATTTGCAC CCACATGCCT GCCATCAGCG TCATGGTCCT CACTGTGCCC CTTTCGTATC 300 TACGTGCCCA TCAGCATGCA CATTTGCAGG GTCAGCAACT TCAGTCAACC ATGATCCCTG 360 TACCCTGGTC CTTAGCATGT CCTTTTCTTG GTTCCTGATT TTCGTTTTCT TTTCAGAGAA 420 ATGCAAGATG CTGAGTTGAA AGCATTTCCC CATAGTAGCT GCATTCTTCC TATTTGCTCA 480 GCTCTGAGTC ATTTCAGGAG TCATCTTTGA CTTTCATCTG TCTCTAAAGC CTTACATATA 540 AGTCATCAGA AAATCTGCCT TTGAGATATA TCTCCAGATT CTGTGAATTT CCAGGTACTT 600 CCACCACAAC TGTGGTCCAC GCTACCATCA TCTCTCAGCT GGGTTACTGC AAAGCCTCCT 660 GTCTCCCTGC TCCCACACTT GGCCAAATCT AGTTTAGTTT GTAGCCAGCC AGTGTGTTCC 720 TTTTATAACT CAAATTGGAT CATGTCACTT CTCTGCTAAG AACCCTTTAA TTGATCCTCG 780 TGCTACTTGG GAAAAATCCA AAATCTCTAC CATATCTTCA TGACCTGGCT CCATGCTGCC 840 TCTCAAATCG CCTACCCCTC TCACCCTCAC TTGAGCCACA CTGGATGCTT TGCTGTTCCT 900 CAAACACACC AGACACACTT ACTTCAGGGT CTTTGTGTTT TTAATTCCTC TGCCTGGACC 960 ATTTTCTCCC AGATACACAC AGACATCACT TCCTCACTTC CTTCAGGTTT CTGCTCAAAT 1020 TCATTGTATC AGGAACCCCT CCTCTAAAAA CTCTTTCTTG GATAACACAC ATTCATATTC 1080 TTCCTAGCCA TTCTGTGCCT CCTTACTCTG ATTGGCTTTT CTTCAGAGCA CTTATCACTG 1140 CCTGAAATAT TATTTGTTTA TTGTCTGTCT TCCTGCACTA GAGTGTAAGC TCCCTGAGAC 1200 CAGGGAGTTT GTTCTGTTCA TGGCTTACCT CAGCTTCTAG AACAGTGCCT 1250
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