Tag | Content |
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EnhancerAtlas ID | HS078-12005 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr3:46458550-46460000 |
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) |
RREB1 | MA0073.1 | chr3:46459080-46459100 | AGTTGGTGGGTGGGTGAGGG | - | 6.02 | ZIC4 | MA0751.1 | chr3:46459562-46459577 | TCTCTGCAGGGGGTC | - | 6.24 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_29537 | chr3:46457237-46458989 | Fetal_Intestine_Large | SE_62170 | chr3:46419501-46460269 | Toledo |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr3 | 46459057 | 46459612 | chr3 | 46458763 | 46458990 | chr3 | 46459822 | 46459994 |
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Enhancer Sequence | TTTTTGCTTT TTACCGCAGG TACCCATAAG CAAAACATGG CATTGTTCAC CATGCTTTTA 60 CATTATTCAC ATAATTTTAA GTTATTTACA CAACAATGTA AAACCATGGT GAACCATGCC 120 ACATGTTGCT TATGGGTACC TGTGGTAAAA ATCCTGCTAC TAGCTCATTT TGCAGTGTCT 180 ATAATGACAG GTAATGCTCC ATTCACTCCT TTATGACACT TGCAAAAACT GAGAACATAA 240 CGCCTCCCAG TTAAGCAGGC ATCTGGGCAA TGTGAGGAGA ACAGAAATAG ACCACGCTGC 300 ATTTATCTCT CTTGATGACA GGCATTGAGA TTTCCACTTT TTCTGGTTTC TTATTATGTC 360 TCTACTGGGC ATTCTTACAT ACATCTTGCA CGCCATGGAA AGTTTCTCTA GGGCAGTGGT 420 TCACAAACTT TTTGGATACA GAATACTTTT ATGTGCTTGA AAACTGAGGA CCCCATACAG 480 CTTTAGTTTA TGTGGGTGTA AGGTTCTAGC CCAAACTGAA GTCCGAAGGG AGTTGGTGGG 540 TGGGTGAGGG GTAGCTGAAA AAACACCCGA GGAATCATAG GCAGTTTGAA CATGGCCTTA 600 TCCTCTCTCT GGGCACGAGC CATATGTCCA GTGTCAGCAG GGTAATTATA CCTTTTACAG 660 ACAATAGAGG CTCTGAAGCA ATCACGAGCT CACGTGAGTG GTCACCTAAT GCACCTCAAG 720 TGGCATGGTT CATAATGTGC GGAGTCGTGT GCCTACGCTC CAAACCCACT GAGTCATGGT 780 GCACCAAAAA GTGGCCTCAG CCTGCTCCTG ACTAAAGCGC AGCCATCTTC CTTACACTCC 840 ACCCCTAGGC CAGGGGCATC CTCCAGGTAG GGACATGTGC CCGTAGGGTG GAGCCCTGAA 900 TCCATAATCC ACAGCAACAA TACGGAGAGC AACAGCTCAC GACTAGGATT CCAGCTATGC 960 TACTTATGAC TATCAGGGCC CAGCGTAGGC CAGAGCCCAG GGATGTCTAC CATCTCTGCA 1020 GGGGGTCATC AGTAAGGCTC TTGACTACCT TAATCTCCTG TGAGACCCCT TGCAGGGCTG 1080 CTGTTATGTT CTGCCAATTG TCAGGGATAA AGGTACAACA TTGTGTTCCT AAAAGGGCAC 1140 AGGTGCCTCC TTAGGCAGCA GTTACTATGT CTAAGACCAT TCGGTTTCGC AACACCACCT 1200 TTCTGATCTG ATCAACCTCA TCCATTAATG GGAAGAGGGC CACTCAGGTG TAATTCAGAG 1260 CCTGAGCAGC ATGCTCTGCA AGAGCAGTAA CTTGGCTTCT ACAGTTGTGA CACACACTCC 1320 AGGGCTAGTG CCTGTCAAGG GGTAAAACCA CCAGGGTGCT CATTACACTT GCAAAAACCG 1380 AGAGTGTAGC ACCTCCCAGT TATGCAGGCA TCTGGGCAAT GTGAGAACAG TGGCAGGTAC 1440 ATGAGGCCAC 1450
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