Tag | Content |
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EnhancerAtlas ID | HS045-09548 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr10:107711660-107712920 |
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) |
FOXP2 | MA0593.1 | chr10:107711971-107711982 | ATGTAAACAAA | + | 6.14 | Foxd3 | MA0041.1 | chr10:107712823-107712835 | AAACAAACAAAC | - | 6.32 |
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| Number: 1 | ID | Chromosome | Start | End |
GH10I105952 | chr10 | 107711776 | 107712630 |
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Enhancer Sequence | ATAGTGATGA TGGTTGTACA ACACTGTGAA TATATTTAAT GGCAGTGAAT TTTATACTTT 60 AAAATGATTA CCATGGTAAA AGTTATGTAT TTTACTACAA GCCTTTAAAA AATGATATCA 120 ATAGAGGGGT CATTTGCATT CTGGCCACAG AAGGGACTAA AGAAATGGAA GGCTACATGT 180 AAACTGGCAG TGTCTGTAAA GAGGATTCCA ACTTTAAACA ATGAGTTAGA GTATTCACGG 240 TTCCTTCTGC TGAATTAAAT TGTTTGACCA AAAGCTGCCT CCATACCTAG CAAATGGTAA 300 CCTAGGGTAA CATGTAAACA AATTGCAAAC TAACTTGAGA GTACATTCTT GTAGAAAATA 360 ACAGAGCCTC AGTCAATCTC AGCAGCCGAA CTTTCAGGCA GTCACGGGCT GCAAACTGCT 420 CAGGCATGTC TGAACAAGGC AAATGCTAAG CTGCAACCAA TCAAGCTGTT TCTACGTTAT 480 CACTTCCTTT TTCAGTCAGT AAATACTGCC TGCTCACATT GCTGGGTGAA GCTCTCTGAA 540 CCTCTCTTGG TTCTGAGTGC TGCTGAATTC ATGAATCTTC TTTGCTCAAA TAAACTCTGC 600 TAAATTTAGT TTGTCTAAAA TCTTTCTTTA AACACTTGCA AAGCTTCAAT TCGATACTTC 660 TGTTATTCCA ATTCATCAGC ATGTTGGCTT GGGATTACAC CCCTTCTGAG AGGAAATTTA 720 TTTTAATTTT ACTCAAGCAA TTTTCATCAC AAAAACGATT AAAACATGGA TTTAGTTTTC 780 AAACAGGTCT TAGTCCTTTG GGACAGAAGA TGTAGTTTTA CATAATAAAT GTTTAAGTAA 840 AAACAAAAAC GGAACCCATG AGAAGTGAAG CACCAGTTCA GTACAGACTT TGAGTTATTT 900 CTAAGCTTTG GTGAGAGAAG CGTTGCCTGC CCCTATTTGG CCCCAAACAC TCCTGACAAC 960 CATATCCGAG GTCACCGCGT GTATGTTGAC AGAATCTTCA TTCAGATGTT GAAAACATTT 1020 TGAAAATTTC TCTACAGCCA GCTAGGGAAC ACAGTTTCTT TTTCCCCATT ATGGCTTAAT 1080 CATCAGCTTT CTTCTGCTTT CTTTTACCTT CATGTGGGGA AGGCCACCTA GTTCCCAGCC 1140 TGAAATCCGA GGAAAACAAA ACAAAACAAA CAAACAAAAA CAATATTCAT GCCACAAGGT 1200 AAGGAATTAG TCATTTGATG TTTATTTAAT TTTCTTCCTG ACTGGTGAGA TTTCCTACTT 1260
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