Tag | Content |
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EnhancerAtlas ID | HS017-03071 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:226287840-226289070 |
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 | TTTATGAATA TTAATGATGA CTTTTATATT CAGCGTTCAC TTCGTGGTGA CACCTAGCTA 60 GTGTTTAGTT TTTCAAAAAT TTCACTCCTT GGACCATTGG GTAATAACCA GCAAACAACA 120 GGTAAGAGTC CCAAACTGCT GCTTGAAAGA GAAAAATCCC TTTGGAAGAC CACGGTAATA 180 ACTACTACTA ATGTGTGGGG GTTTTGTTTG TTTTTTGTTT TTGTTTTTGT TTTTGTTTTC 240 AGAGGGAGTC TCGCTCTGTC GCCCAGGCTA GAGTGCAGTG GCACCATTTC GGCTCATTGC 300 AACCTCCACC TCCCGGGTTC AAGCGACCCC AGACTCCCGA GTGGCTGCGA TTACAAGCAC 360 CCGCCACCGC GCCCGGCTGC ACTCTAGCCT GGGCAACAGT GCAAGAGTCC GTCTCAAAAA 420 AAAAAAAAAA AGAGTAATAG ACTGTATTTC CCGAAGTATA TTCATGGCCT TGGATGTTGT 480 TAACAAGCAT TAAGATTTTA AAAGGGCCCG AGGTCAAACC ATTTAGGAAG AATGCCTAAT 540 TCCCACAGTT AAGGCTCGGT GGGTGGGCGC ATGCGCACAG GATCCTCGCC GTCAGGCACC 600 TGCGGAACAC ACTTGGAAAT CGCTTTTTCC GGAGGCCCAA TTTCATTTCA TTATACACCA 660 CACCACACTG TGCTGGGCTG TGGAGGAAGA ACGGGAAGCA GTTTTGGTCC AGTCCTCCAG 720 GACCTAGTTT TAGGAAGAGG GTGGCAAGGC AAAAAAAAAA AAGAAAAAAA GAAAAAAGAA 780 AGCACAAATC CAATTACAGT TATGAGTTTA TGACAAAGTT TCTATAAATG ACGGACCGCA 840 TACAGACAGG GCCCCATAAG ATTATGATGG AGCTGAAAAA TTCCTATGGC CTAGTGATGT 900 CATAGCCTTC TTAAGTCTTA GCGCAACCAA TGCATTACTC ACGTGTTTAT GGTGACGCTG 960 GTGTAAACAA ACCTACTGCA CTGCCAGTCA TATAAAAGTA TAGCAGAGGG GTCCCCAACC 1020 CGTGGATCAG TACTGGTCCA TGGTCTGTTA GGAACCGGGC GGCACAGCAG GAGTTGAGCG 1080 GCGGGCCAGC CCCCAAAGAA AGCTTCATCA GTACTTACAG CCACTCCCCA ACACTGGTTT 1140 TGCTGCCTGA GCTCCGCCTC CTGTCAGATC AGCAGAAGCA TTAGATTTTC CTAGAATCGG 1200 AAACCTATTG TGAACTGCAT ATGCCAGGGA 1230
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