Tag | Content |
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EnhancerAtlas ID | HS038-20892 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr8:11843630-11844610 |
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) |
KLF13 | MA0657.1 | chr8:11843949-11843967 | CAGGGAGGGGCGTGGCCT | - | 6.51 | KLF14 | MA0740.1 | chr8:11843952-11843966 | GGAGGGGCGTGGCC | - | 6.25 | SP1 | MA0079.4 | chr8:11843953-11843968 | GAGGGGCGTGGCCTG | - | 6.62 | SP3 | MA0746.2 | chr8:11843953-11843966 | GAGGGGCGTGGCC | - | 6.18 | SP4 | MA0685.1 | chr8:11843951-11843968 | GGGAGGGGCGTGGCCTG | - | 6.64 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I011986 | chr8 | 11843710 | 11844709 |
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Enhancer Sequence | CTATAAACTA TTCCATACTT TTAGGGGGAG ACCCTTGCAT GCACTTCCAG ATCCCAGCGT 60 AGATTAAGTG CAGCCATTCC TTACTGTTCC TCACAGGAGG CCTTGCGGCC AGCTACAAAG 120 TTCAGGCGCT GGTTGCAGTT TGAAAGAATC TCCCAACGGG GTTCACAGTA CAACCTCGGT 180 GGGGACGAAC TTCCTTGGCC AGGGCCGGGG CGGGGAGGGT GAAAAGCGGG CTGCAAGTGC 240 AGGAGCCGTA GGTGCAGAAG TCGTGGGTGC AGAAACTGCA AGTGCAGGAG CCACGGGAAC 300 ACGCCGGCTT TGCAGCGGAC AGGGAGGGGC GTGGCCTGAA CGCCTGGACT GCAATCTCTG 360 CGGGGAAAGC TTATGACTCC CGGCAGCCGC GAGTTCTGAT TACAGGCTGA CAGGAACTCA 420 GCTCGCTGCT TCCAGTGGAA CACCGTGGGA GTGGATCTGC CTTGTCAAGT GGGTAGGAAC 480 TGTGGAGCTT ACCACCGCCT GCTACTCCCT ACTTCTTGCA CAGACTCTTC TGTGCAGCAG 540 GGGCAGCAAC GCTGCCCTCT GAAACATTAA CCTAGTGGCC TGAGACCCGC TCCCATCCCC 600 CAATACCCAT AGAAGCTCCT TCTTTCTCTG CACACGGAGA CCAGTGTGCA GGCCCTCCCG 660 ACCCAGCCCC TACCTGGCTT TGCCCGGCCA CCCGCCCTGG TAACTCAACG CAAAGGACAG 720 AGTCTCCTGG GAGCGACATG GCCCCGCCCA TGTCCGGAGA AACCAGAGTA TCCCCCTCTG 780 GGCAACATCA GGCAAGCAAA AATCCCAGGG CTACTACCGC AGCTGCTGCT CTTTTGCAAG 840 CGCCACCTCC TAGCTGGAGG CCAACCCACA CAGTCCTTGA CAGTATCTCC TGGTAGATTA 900 ACATTGCACC CAGGAAGGAG AAAACCGCTA TGGGATCTCA GCTATCACTG CTGCCTGCAC 960 CACTCTGGCT GAACAGGAGG 980
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