Tag | Content |
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EnhancerAtlas ID | HS047-08775 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:121437950-121438860 |
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) |
GRHL1 | MA0647.1 | chr12:121438425-121438437 | GAAACCGGTTTT | + | 6.04 | GRHL1 | MA0647.1 | chr12:121438425-121438437 | GAAACCGGTTTT | - | 6.52 | TFCP2 | MA0145.3 | chr12:121438426-121438436 | AAACCGGTTT | + | 6.02 | TFCP2 | MA0145.3 | chr12:121438426-121438436 | AAACCGGTTT | - | 6.02 |
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| Number: 2 | ID | Chromosome | Start | End |
GH12I121000 | chr12 | 121438321 | 121438470 | GH12I121001 | chr12 | 121438477 | 121439944 |
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Enhancer Sequence | CCTGAGTTTG TAATCTATGA TGCCATTGTC AGGAGTGGGC ACTTTGGAGT CAGGTGGGTG 60 GGCTTTGCAG CCTGCCTTTT TGCAAGCTGC CCCCTTTCTA TAAGGTTCCT GGACCCGGCC 120 CTGGCAGCTG TCATGACAGC CACTGAGGCC ATTCTGTGTC CTGGCATTCA CCCCATGAGG 180 CGTGTCCATG ACCACCCCCA TTTTACAGAT GAGAAAGTGG ACACTCAAGG AGGGGAGGGA 240 CTTGCCTCAT CTCCCACAGC TACCAGATGG CAGGGCCAGG ACTCGAACCC AGGTCCCACC 300 TCAAAGCCCA TTCTCTTAAC CATTGCCATC AGTCAGGGTT CTCCAGGAAC ACAGAACCAA 360 CAGATTTATT TGAAGGACTT GGCCCGTGTC TGCGGGGGGC TGGCAGGCCT GAAATCTGTT 420 GCTGGCAGCT CTGGGGAGTG AATTCTGCAG CCTTGAGGCA GAATTCCTTC TCTGGGAAAC 480 CGGTTTTTGC TCTTACGGCC TTCCACTGAT GTAGGAGGCC CACCCATATT TTCAGGGTAA 540 TCTCCTTCAC TCAAAGCCAA CTGATTGTGG CATTAACCAC ATCTACAAAG CACCTGCATT 600 CACAGCAGCG CCTAGATTAG TGTTTGACTC AGCCTAGCCA AGCCAACACG TACAACTACC 660 TACCTCGGCA TCTCACCGGG GCTTCTCCAG TGTTCACACT AAGATGTACT CAGGCCACTC 720 CATGGGCGGC CGTGGACCCT GGCTGGGAGG CTCCCTTTGA AGAACCGAGG GTAGAGGTGT 780 GACTTTGGGG TTCCTGTTAT CTGCTGTGAT CCAGGAGGTG TGGCCCTGCC TCCCCATCCT 840 GAGTACCCCT AGGGACAGGC AGGTGGGGTG GGTGTGGGTG CCTGGTGGGT GGCTAGCAGC 900 CTTGTTTGCC 910
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