Tag | Content |
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EnhancerAtlas ID | HS047-03156 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:226288040-226289130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr1:226288394-226288409 | CTCGGTGGGTGGGCG | - | 6.05 | IRF1 | MA0050.2 | chr1:226288606-226288627 | AAAAGAAAAAAGAAAGCACAA | - | 6.26 | NRF1 | MA0506.1 | chr1:226288406-226288417 | GCGCATGCGCA | + | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_23364 | chr1:226288328-226288640 | Colon_Crypt_1 | SE_23849 | chr1:226288300-226288591 | Colon_Crypt_2 | SE_65669 | chr1:226287955-226288637 | Pancreatic_islets |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I226100 | chr1 | 226287902 | 226289101 |
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Enhancer Sequence | GTTTTGTTTG TTTTTTGTTT TTGTTTTTGT TTTTGTTTTC AGAGGGAGTC TCGCTCTGTC 60 GCCCAGGCTA GAGTGCAGTG GCACCATTTC GGCTCATTGC AACCTCCACC TCCCGGGTTC 120 AAGCGACCCC AGACTCCCGA GTGGCTGCGA TTACAAGCAC CCGCCACCGC GCCCGGCTGC 180 ACTCTAGCCT GGGCAACAGT GCAAGAGTCC GTCTCAAAAA AAAAAAAAAA AGAGTAATAG 240 ACTGTATTTC CCGAAGTATA TTCATGGCCT TGGATGTTGT TAACAAGCAT TAAGATTTTA 300 AAAGGGCCCG AGGTCAAACC ATTTAGGAAG AATGCCTAAT TCCCACAGTT AAGGCTCGGT 360 GGGTGGGCGC ATGCGCACAG GATCCTCGCC GTCAGGCACC TGCGGAACAC ACTTGGAAAT 420 CGCTTTTTCC GGAGGCCCAA TTTCATTTCA TTATACACCA CACCACACTG TGCTGGGCTG 480 TGGAGGAAGA ACGGGAAGCA GTTTTGGTCC AGTCCTCCAG GACCTAGTTT TAGGAAGAGG 540 GTGGCAAGGC AAAAAAAAAA AAGAAAAAAA GAAAAAAGAA AGCACAAATC CAATTACAGT 600 TATGAGTTTA TGACAAAGTT TCTATAAATG ACGGACCGCA TACAGACAGG GCCCCATAAG 660 ATTATGATGG AGCTGAAAAA TTCCTATGGC CTAGTGATGT CATAGCCTTC TTAAGTCTTA 720 GCGCAACCAA TGCATTACTC ACGTGTTTAT GGTGACGCTG GTGTAAACAA ACCTACTGCA 780 CTGCCAGTCA TATAAAAGTA TAGCAGAGGG GTCCCCAACC CGTGGATCAG TACTGGTCCA 840 TGGTCTGTTA GGAACCGGGC GGCACAGCAG GAGTTGAGCG GCGGGCCAGC CCCCAAAGAA 900 AGCTTCATCA GTACTTACAG CCACTCCCCA ACACTGGTTT TGCTGCCTGA GCTCCGCCTC 960 CTGTCAGATC AGCAGAAGCA TTAGATTTTC CTAGAATCGG AAACCTATTG TGAACTGCAT 1020 ATGCCAGGGA TCTAGGTTGT GCACTCCTAA TGAGAATCTA ATGCCTCATC TGTCACTGTC 1080 TCCCATCACC 1090
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