Tag | Content |
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EnhancerAtlas ID | HS098-18493 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr14:101364210-101365290 |
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) |
LMX1B | MA0703.2 | chr14:101364595-101364606 | GTTTTAATTAA | + | 6.14 | RARA | MA0729.1 | chr14:101364810-101364828 | AAATGGCATTTTGACCTT | - | 6.16 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I100898 | chr14 | 101364368 | 101370395 |
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Enhancer Sequence | ATGAATATAT GAGTGCATAA ATTAGCAAAA TAAAAGGGGG CTTTTCTGGA CCAATGATGA 60 GACAGTGTTT ATGAACAAAA GATCATGATT AATCCAGTTC TGCACAAAAC ACTGAGGTCC 120 ATTAGAAGAC AATAGGTCTT GGCTGTTTCA TTCCTTTTAA GAGCTGTTTA ATATTCCACG 180 GTATGTATGC ACCATTGTTG ATTACACTCT TCTACTGTTG AAAATCCCAG CTGAAAGTGC 240 TCTGGGGGAG GAGAAGCTTT GGTCACAGTC CTAGCCGTCA GGGTGGGTCA CAGATTCATA 300 GGTGTTCATT AAATTATTTT TTAAAAAAGA ATACATAAAA ATGGTGCTTA ATGCAGATCA 360 GTGAGGAAGC GTGTCACAAA TCGAGGTTTT AATTAATACG ATTCTGCTCA ACTAATGCCC 420 GATAAAAAAG ATCTAAGCTG TTTCCATTTT TTGTTGCTGT TACCAACGAC ACTGCAGTGA 480 GCATTCTTGC AGCTAAATCT GTAAACACAT CCTCGACTGT TCCTTTACCC CAGCTTCTTA 540 GAGATGGGGT GGTGGGTTAA ATTGTTTGCA AAAGTTTATT TTCATTGAGT GATCTTTCTA 600 AAATGGCATT TTGACCTTGT TACTGTCTTG CTTTAAAGCC TCCATCTGAC TTCCTGGAGC 660 TTCCGGGACG GGGTCCAAAA AATAAGGCCT TATCCTGGCA TGGAAGACCC TTTAGGGTCT 720 GTCTTGGAAC TTGCCAGCCT CAGCCCCTCC CCACTGGTGT TTACCTGCTA GGCGCACCTC 780 ACCCCCACGG GGCTACCTGT TTCTCTCAGC GGGCTCCCTA CTTCTTAGGC TTTGCGCGGC 840 CGTGCCTTTT CAGCCAGTTT CTCCCCGGCC TTAAAGAGCA GGCTTGAAAT ATCCCTGTTG 900 GGGAGCCCAA AGTTAGATGG GCCCCACGAA ACACTGTGTT CAGAAGCCCA CCGAAGCCCT 960 GACCCTGGAA GTGGGATGCC TCATTGACAT TTTTTTCCCA ATTAAAGGGA ATGTTTTGCA 1020 TTTTTCTAGA ATTGATGAAA CTGGTCAACT GTTACTCACC CTCCTTCCTT TGTCCCTTTC 1080
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