Tag | Content |
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EnhancerAtlas ID | HS091-27985 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:166726350-166727300 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr2:166727267-166727282 | AAGGTCAAAAGTACA | + | 6.07 | RARA | MA0729.1 | chr2:166727267-166727285 | AAGGTCAAAAGTACATTA | + | 6.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AGACGGAATC TCACTGTTGC CCAGGCTGGA GTGCAGTGGC GTGATCTCGG TTCACTGCAA 60 CCTCCACCTG CCAGGTTCAA GCAATTCTCC TGCCTCAGCC TCCCGAGTAG CTGGCACTAC 120 AGGTGCACAC CACCATGTCC AGCTAATTTT TTGTATTTTA GTAGAGACGA GGATCCCCGT 180 GTTGCCCAGG CTGGTTGCGA ACTCCTGAGC TCAGGCAATC TGCCTGCCTC GGCCTCCCAA 240 AGTGTTGGGA TTATAGGCAT GAGCCAAAAA AATTAAATAC ATAAATAAAT CCTTGAAATA 300 GTTTTCAATT ACTACCTACT ACTATATTAT TGGTCAAATC TTACATATGT GACAACCTCA 360 TGTTGGATGT TTTGATAACC AAAAGCAGCA AAAAATTCAG TTACAATTTT TAAAATTGGA 420 AACCTTTGAG AAATTTCGGA ATATTTCCTG TGATAAATTT CTCTACGTGG GATCACTTGG 480 TTAAACGAGA GACTCTTATT TTGTGCTGTT TTTAGAGAAC AGCCTTCTCG AACTTGCTTT 540 TTGCTGTTTA TAAGTTATTC CCTTCAGGAA GGCTGTGCTA CACTTCGATG AGCAGCGGTC 600 TGAATGCGGT GGTTTCCTTG CACCTTTGCC AACCTTGCTT CTAAAAAAAT CTGTCAGCAT 660 GAACGCTGTT GTATGATCCT ATTTTAAAGC TATTCACTTG TCATCTCCAG TCGCAAACTA 720 GGATAGCTCC TGTCAGATTC TTAATTGGTC TTTTGGTTTC CATAGTGATT CCATTATCTA 780 CTTCTACTCT AGTGCAAAGT TCAACTTGCT TCCTCAGCTG TCCATGCATA AAAGCCTTCC 840 AGATTTGCTC TAGGTTCTTG ACTTCTGGGG AAGAAAGATA TTTCCTCTTG GACCCAGTTC 900 ACCATACTAG CTGAATTAAG GTCAAAAGTA CATTAAACTT ACAACTGTGT 950
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