Tag | Content |
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EnhancerAtlas ID | HS054-00380 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr1:96880950-96883190 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:96881353-96881365 | ACTAAAAATAGA | + | 6.27 | MEF2B | MA0660.1 | chr1:96881353-96881365 | ACTAAAAATAGA | + | 6.32 | MEF2C | MA0497.1 | chr1:96881351-96881366 | CTACTAAAAATAGAA | + | 6.57 | REL | MA0101.1 | chr1:96882812-96882822 | GGAAATCCCC | - | 6.02 | USF1 | MA0093.2 | chr1:96881296-96881307 | GGTCACGTGGT | - | 6.32 | USF2 | MA0526.2 | chr1:96881293-96881309 | GCGGGTCACGTGGTCA | + | 7.37 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I096415 | chr1 | 96881221 | 96882960 |
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Enhancer Sequence | CACTTTGGGA GGCCAAGGTG GGCGGATCAC GAGGTCAGGA GATCCAGACC ATCCTGGCTA 60 ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAAATT AGCCAGGCAT GGTGGTAGGC 120 ACCTGTAGTC CCAGCTACTC TGGAGGCTGA GGCAGGAGAA TGGCCTGAAC CCAGGAGGTG 180 GAGCTTGCAG TGAGCCGAGA TCGCACCACT GCACTCCAGC CTGGGCAACA GAGCGAAACT 240 CTGTCTCAAA AAAAAAAAAA ATAGAAGAAG AAGAAGAAGT AAGGTCATGG CCGGGCGCGG 300 TGGCTCACAG CTGTAATCCC AGCACTTTGG GAGGCCAGGG CGGGCGGGTC ACGTGGTCAG 360 CAGTTCAAGA CCAGCCTGAC CAACATGGTG AAACCCTGTC TCTACTAAAA ATAGAAAAAT 420 TAGCTGGGCT TAGTGGCGGG TGCCCGTAAT CCCAGCTACT CGGGAGGCTG AGGCAGAAGA 480 GTCGCTTGAA CCCAGGAGGC GGAGGCTACA GTGAGCTGAG ATCTTGCCAT TGCACTCTAG 540 CCTGGGTGAC AAGAGCAAGA CTCCGGGAAA AAAAAAAAAA GAAAAAAAGA AAAAAAAGAA 600 GTAAGGTCAC CAAAGCCAAT AGGCCTAAAG GCAGACCTAA AACTAGCTGC CTCAATCAAA 660 GTAAAGTTAG ATGCCACAAC AAATAAACCC CTAATTCTCA GTGGTGTAAC GTGAGAACTA 720 TTTCTCCTTC ATGTAAAATC CACTACTCTT CCCACATATG ACTCATGTTC CTTCTGTCTG 780 TGGCTTCATC ACTTACAAGT GGCTTGGATC TGCTGGATCC TCTAATTCTG GCTGACAGAT 840 CGGAAAAATA GAGGGTGAAA GACTAAGTGT GAAAGTATTA CATGACAGGT CTGGAAATGG 900 CACGCATTTC TTTGGCCTGG AAACCACTGG CAACAACTTA GTCACACTTC CCTCACGTAA 960 ATGCAGGGGG ACTGGGAAAC ATAGATCCTG ATTTAGAAGG AACTTCCTAG GAAAATCTCT 1020 GTACTGCGGA AGGGGAGCAT GCTCTGGTAG AGAGTTAGTC ATCTCTACCG CACAAGCCAA 1080 ATCTAAACAG CTCAATAAGA CAGGCATTAC TGGAAGTGGA GCTCAGCAAG CTTGGACAAA 1140 ATAAACCATG TGCCAATTCT TAAGCCAGCC AGAGACCAGA TGCCTCTGGC ATAGACATCC 1200 CTGCCAGTTA GGGCAAGATC CAGTTGATTA AGATACCGGA GTGGAATGAG CAATATGGGA 1260 AAACTGATCA ATCAGAGAAA AAAAATCCCA GCATGAAAGC CACGATTTTT CCCCCTCCAT 1320 TCCTCTCATC CAGAGATGGG CTGCCTGGCA CAAAATTCAA TCCGAATTTG AATTCTACTT 1380 AATATCAGCA ATAGAATTTT TCATTGGCCT TGTTCTGCAT TCAGTGATAA AAGCAGCACA 1440 CAATTATTTT CGATTGGACC AATGAGATTG TGCTGAGAAG TCTCTGAAGA CTGTCTGCTG 1500 AGTGCCAGTT GTTAATGAAT CCCATTTGTC TTTCTTGATT AAGTCTGCTA TTACCCCCGT 1560 TTAGTCCTGT CACCAACCCT TTAGCAAGAA TTTTCATATC ACTGTTTAGA TGAGAAATTA 1620 GCCTATAAGA GCAGCACTCA TCAATCAGGA GACAGTTTAT TTAATACAGT TTACAGTTTA 1680 TGAGTTCAAA AACTGTAGCC TCATACATTA GAAATGGATC CCTGTCCTAG ACAGACAATC 1740 AGGGGGTTCA GTTCACTTGA CAGGCATGGA GAAATGACTT TGAATGTGAG ATATGCACTT 1800 AGAGAAGGGC TGCAGTATCA CACGCCTGCA GCAGAGTATC AGGAGGCTTT CACTTCTGAT 1860 TAGGAAATCC CCTTTGGTTT AAGCAAGTGC TTCATTTTAA TACTTAACCA TGCCTCCCTA 1920 CAACACTGTG ACCAGAAAAT TCAAAATGAA ATTTTAGAAT AGAATCACTT CTTTGTGATA 1980 CCAAATCTTT ATTCTGGATT GCTATATCAT TAAAACAGTT CGTGAAGAAT ATTTATCTGC 2040 TTCTTGAAAT CATAAAGAGC AAGATATCCA TGAAAATCTT CCTTTTGCAA AGAGTAGTGA 2100 GTGGCATTTC CTTTCAGTCA CCAAAAGTAA AAAATTGCAG GAAAAAAGCC CCAGATCTTT 2160 GGCATTAACT GTATAGCTAC ATGACCATAC AAAATGGATG ATTTTGGCCC CCAGGAGAAT 2220 TTTAGGAAGC CCAAATTGGC 2240
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