Tag | Content |
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EnhancerAtlas ID | HS095-20335 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr3:37010760-37011970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr3:37011156-37011174 | GGAAGAGAGGGAGGGAGG | + | 6.14 | EWSR1-FLI1 | MA0149.1 | chr3:37011152-37011170 | GGAAGGAAGAGAGGGAGG | + | 6.73 | EWSR1-FLI1 | MA0149.1 | chr3:37011148-37011166 | GGAAGGAAGGAAGAGAGG | + | 7.82 | EWSR1-FLI1 | MA0149.1 | chr3:37011144-37011162 | AGAAGGAAGGAAGGAAGA | + | 8.2 | RFX5 | MA0510.2 | chr3:37011491-37011507 | TGTTGCCAAGGAAACC | + | 6.1 | RFX5 | MA0510.2 | chr3:37011491-37011507 | TGTTGCCAAGGAAACC | - | 6.23 | ZNF263 | MA0528.1 | chr3:37011145-37011166 | GAAGGAAGGAAGGAAGAGAGG | + | 6.11 | ZNF263 | MA0528.1 | chr3:37011201-37011222 | GGAGGAGGAGAGAAGGAGTGG | + | 6.35 | ZNF263 | MA0528.1 | chr3:37011149-37011170 | GAAGGAAGGAAGAGAGGGAGG | + | 6.78 | ZNF263 | MA0528.1 | chr3:37011235-37011256 | GGAGGGGGAGGAGGAGAAGGA | + | 6.7 | ZNF263 | MA0528.1 | chr3:37011226-37011247 | AGTGGAGAAGGAGGGGGAGGA | + | 6.92 | ZNF263 | MA0528.1 | chr3:37011221-37011242 | GGAGGAGTGGAGAAGGAGGGG | + | 6 | ZNF263 | MA0528.1 | chr3:37011241-37011262 | GGAGGAGGAGAAGGATAAAAG | + | 7.18 | ZNF263 | MA0528.1 | chr3:37011192-37011213 | GGGGGTGGAGGAGGAGGAGAG | + | 7.37 | ZNF263 | MA0528.1 | chr3:37011238-37011259 | GGGGGAGGAGGAGAAGGATAA | + | 7.37 | ZNF263 | MA0528.1 | chr3:37011195-37011216 | GGTGGAGGAGGAGGAGAGAAG | + | 7.38 | ZNF263 | MA0528.1 | chr3:37011153-37011174 | GAAGGAAGAGAGGGAGGGAGG | + | 7.61 | ZNF263 | MA0528.1 | chr3:37011198-37011219 | GGAGGAGGAGGAGAGAAGGAG | + | 7.64 | ZNF263 | MA0528.1 | chr3:37011229-37011250 | GGAGAAGGAGGGGGAGGAGGA | + | 9.38 | ZNF263 | MA0528.1 | chr3:37011232-37011253 | GAAGGAGGGGGAGGAGGAGAA | + | 9.68 | ZNF740 | MA0753.2 | chr3:37011184-37011197 | GGGGGGGGGGGGG | - | 6.03 | ZNF740 | MA0753.2 | chr3:37011187-37011200 | GGGGGGGGGGTGG | - | 6.44 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 37010977 | 37011113 | chr3 | 37011163 | 37011850 | chr3 | 37011455 | 37011827 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I036968 | chr3 | 37010223 | 37012549 |
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Enhancer Sequence | AAATCCTTAT TAATCATAAG CAATAAGTAG ACAATGCCTA CAGTTGATAA ATTAAGAATT 60 AGCAATATAC AGAAATATAT ATGAAACCAA AATAACTAAT GAAAGAAAAG GAGGCTGGGC 120 ACGGTGGCTC AGGCCTGTAA TCCCAGCACT TTGGGAGGCA GAGGCAGGCA GATCATTTGA 180 GTCCCGGAGT TTGAGACCAG CCTAAGCAAC GTAGTGAGAC CTCATCGCTA CAAAAAAACA 240 GAAAAATTAG CTGGGTGTGG TGGTGTATGC CTGTATTCCC AGCTACTTCA GAGGCTGAGG 300 CAGGAGAATC AGTTGAGCCC AGAAGGTGGA AGCTACAGTG AGCCAACAGA GTGAGACCAT 360 CTCAAAAAAA ATTTAAAAAA ATGAAGAAGG AAGGAAGGAA GAGAGGGAGG GAGGGAGCGT 420 GGGCGGGGGG GGGGGGGTGG AGGAGGAGGA GAGAAGGAGT GGGAGGAGTG GAGAAGGAGG 480 GGGAGGAGGA GAAGGATAAA AGGTTACAAG TGGTTGTTAC TAGGAATGGG GGAGAAGAGA 540 AGTGGGTAAT GGCACTGAAG CTTTTTATTA TGTCTTTCAG CATTCTCTGA TTGTTCTTAA 600 ACCATCAACA GATCTCAGTA TGTAGACTAA AAGGGAATAT TTGGTGAAGA GATCTTCTTT 660 CACTATTGTA CACTTGCTAT GGACATGTCC ATGCCTGCTG CCTGGCAGGC ACCATTCATT 720 AAGTAGGCCC CTGTTGCCAA GGAAACCAGC TCTTCACTGA TACCAAAGAT AATGCAGAGG 780 CCTGCCGCTC ACCAAGCAAC CTTCCTCATG AGCTATGCCC CCACCTTCCT GAACTGTCTC 840 TTGCTCCTGT TTGATACTGT CATGCTGCAC GAAGCTTACA CTTGCTATCT CTCACTTCCC 900 TCTTAGTCAT CTGTGATGCT GGCTAAGGGA GCTAGGCCAG TCAGCAGTGA CCTGTTGCCC 960 TTGGTTTATT ATAAGCAAAC TGTTCACAAG AAATGAACTT CTGTTGTTTT ATAAATGATA 1020 TGCATCACAG AACACAGAAT AATATCAAAA CCACATTAGT TTTTTCATAC TTGCTTCATT 1080 GACCCCAGGG GAAGAGGGGA GAGCAGGGAG AGGACTTTCT CTTTTTTTAA ATACTAATTA 1140 TATTGAGGTA TAAAGAACAT ATAGTAAGTT CACAGACCTT AAGTATACAG TTTGATGAGT 1200 TTTGGCAAAT 1210
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