Tag | Content |
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EnhancerAtlas ID | HS092-04404 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:204026140-204027290 |
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) |
Foxd3 | MA0041.1 | chr1:204026222-204026234 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:204026226-204026238 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:204026230-204026242 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr1:204026234-204026246 | AAACAAACAAAC | - | 6.32 | Zfx | MA0146.2 | chr1:204026735-204026749 | GAGGCCTAGGCGGG | - | 6.24 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I204056 | chr1 | 204026117 | 204027458 |
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Enhancer Sequence | TTGAACCCAG AGGCAGAGGT TGCAGTGAGC CTAGATTGCG CCACTGCACT CCAGCCTGGA 60 TGACAGAGCA AGACTCCGTC TCAAACAAAC AAACAAACAA ACAAACAAGA ACCTGTAGAG 120 TTATCTTAGC GATATTGACA TCCTTTTCTA TTATCTCCTT ATCTATTGCT GCATAACAAA 180 TTACCCCAAA ACTTAGTGAC TTAAATAATA AATATTTTTC ATCTTACACA GTTTCTGTGG 240 GTCAGGAATT TGGGAGTGGC TTAGTTGAGT GATTCTGGTT CAGGGTCTCT CATGAGGTTT 300 TTCATGAAAC TATTGGCTGG GGTTGCAGTC TCTAAAGACT TGTCTGGGAC TAGAGGATCT 360 TATTCCAAGC TCACTCACCT GGCTGTGGGC AGGAGGCCTC AGTTCCTTGC CATGTGGGTC 420 TTTCTACAGA GCTGCTTGAT ATGGTGGGCG GCTTACCCCA CAGCAAGTGA TTGAAATGCC 480 ACTCTGCATT TCATGACCTG ATTCATCCCG CATTGTAACT TCTGCCTTAT TCTATTCATT 540 AGAAGTGAGT CATAGCTGGG CACAGTGGCT CACTCCTGTA ATCCCAGCAC TTTAGGAGGC 600 CTAGGCGGGT GGATCACTTG AGATCAGGAG TTTGGGACCA GCCTGACCAA CATGGTGAAA 660 CCCCGTCTCT ACTAAAAATA CAAAAATTAG ATGGACGTGG TGGCAGGCAC CTGTAATCCC 720 AGCTAATCGG GAGGCTGAGG CAGGAGAATT GCTTGAACCC GGCAGGCGGA GGTTGCAGTG 780 AGCCGAGATC TTGCCATTGC ACTCCAGGCT GGGCAACAAA GCAAAAAAAA AACAAAAAAC 840 AAAAAAGTGA GTCACAAAGT CTCAAAAAGA AAAAAGAAAA AAGAAGTGAG TCACAAACCA 900 CAAAGTCCAG CCCAAACTCA ATGAAAAGGG ATTACTCAAG GGTAAGGACA TGAACACCAA 960 GAGGGGGATT ACTGGGGGAC ATCCTGGAGA TTTACTACCA CAGATATCTT TATGGGCTGA 1020 CTACAATTTT AATAATCTGG AAGTTTAGTG ACATTGAGAT TTAAATGGTC AATCCATCTT 1080 TGCCTCATTT TCCACACAGC ACTGTAAGGA AAAAGTCCTA ATTCTTAGAA ATGAAATTAT 1140 TTCCTAGAAT 1150
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