| Tag | Content |
|---|
EnhancerAtlas ID | HS101-22789 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr2:3359670-3361440 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:3360984-3361005 | GCGTACTTTCATTTTCAGTAA | + | 6.22 | | NFYA | MA0060.3 | chr2:3360730-3360741 | TCTGATTGGTT | - | 6.62 | | NFYA | MA0060.3 | chr2:3360801-3360812 | TCTGATTGGTT | - | 6.62 | | NFYA | MA0060.3 | chr2:3360814-3360825 | TCTGATTGGTT | - | 6.62 | | NFYB | MA0502.1 | chr2:3360731-3360746 | CTGATTGGTTGCTTT | - | 6.7 | | NFYB | MA0502.1 | chr2:3360815-3360830 | CTGATTGGTTGCTTT | - | 6.7 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH02I003357 | chr2 | 3359907 | 3360169 | | GH02I003356 | chr2 | 3360372 | 3361572 |
|
Enhancer Sequence | AAAAGAAACA ACAACCAACA GAAAAACGGC TACCGAGGAT TCAAACAGGG TCCCTGGGAA 60
GCAAGCTCTA AAGTTCTAAC GGTATCTAAA GGAGACTTAC TAGCGAGTGC TCTTGGGAAC 120
TATTCCATGT TGGGGTGAAG GAGGAAGGGC TGGGCTGAGG GAGAAGATGA AATGCATCAC 180
ATCTGCAATG GAGGTCTCAG CCAATCCAAT GGGGAGCTCT GGAGCCGGAC GGCCCTTCAG 240
AGTTAAGGCC AGATGGCCGG GGTTTTATAC CACCCAACCC CTACCCCCAT GGGTCAGTCA 300
CTGGATGCAG GCTTTTCCTG AGGAGGGGTG TGACCTTGCG CAAAGTGCCT CTGTTCAGCT 360
GAGGGCAATT CCTGGAGCAG GGCCCAGCTG AGAGCTATCA GCCCCCAGCA ATCTCAGAAG 420
TGGCTGGATT TCCTGAAAGA GAAACGTAGG CTGTATACAA CAGCCTGAAT TGCAATAGCT 480
ATGGTTAATA TGTTTAATAA TTAGAAGATA AAACTAAGAT CTCAGGTGAT GAATCTGAGG 540
CTTAGAGGAA AAAGTTGTAC AACTGGTTAC TAGAGCTGTG ACTAGCACTG CAGGCTTATA 600
AATTCAAATC CATCTGTTTT AGGACAAGCA TTAACTGCAC CTGGATCAAG TTCCCGTGGC 660
CAGCATAATA ATGGCCCTCC ATCCATATCC ACATTCTAAT CCCCAGAACC TGTGAATGTG 720
AACTTACGCG GTAAAGGGAC TCTGCTGATG TGCTTAGATT AAGGACCTTG AGATGAGGAG 780
GCTCTCCTGG ATTATTTAAT CGCATGGGTC ACTGAAATCA GAAAACCTTC CCTGGCTGTA 840
GCCCCAGAGA AATGTGACCA CAGAAAAGAG AATCAGAGAG GTGGTGAGGC AGGAGAACAG 900
GGTCTGGAGG CAGGGCCTAA GGCCAATTCA CCCTGACTTC CTAGAACTAA ACTGAAAGGA 960
AAACGCTAAT TTTCCCCACC CAAGTAACAA AAGGACCAGA GGCTACACCC TTTGCAAACC 1020
CTCACCTTTT CTGCATGGCA GTAGGGAAAT TGAAAGTACC TCTGATTGGT TGCTTTTTGC 1080
AACTAATCAG ATGTTTGCAT AAAGCTGTAA CTTTGTAACT TCACTGTAGC CTCTGATTGG 1140
TTGCTCTGAT TGGTTGCTTT CTACAACCAA TCACACTGAT TGTGGGCCAT CACTTCATTT 1200
ACATGGGGTA AACACCAAGT GGCCAATGGG AAACCTCCAG CAGGTATTTG GACCTGAGAA 1260
GATTCTGCAT TCAGGGCCCT TGAGCAGCTG CTCGGCCCAA TCCCACCCCA TGGAGCGTAC 1320
TTTCATTTTC AGTAACTCTC TGCATTTGTT GCTTCATTCT TTCCTCACTT TGTTTTGTCC 1380
AGTTCTTTGC TCAAGATGCC AAGAACCTGG ACACCCTCCA CCAGTAACAA TGGCAGCTGT 1440
GAGGAGGACC CAGTGGCTGT TGCTGGATTT AGAGATGAAT GAGAGTTGTT AAAGCAAACT 1500
AAATATGGCC TGAGAAGGAC TCCCTGCTTC TATATTTGAG TCCTTGTGGA TGAAACATAA 1560
CCTACCTTAA TATGCAGACA AGATTGAGAA CCTAACTTAG GAGTATGCAC CTGTAACAAC 1620
TGAGTCTTGG CCAATCCCAG CAGCCATACT TCAACCACTC ATACACTGCT GAGTGTTCAA 1680
ACTGTGTTCA AATAAGGCAA ATGCCAGCCT GTAACCCATC CAGCTGTTTC TGCACCTCAC 1740
TTCCCATTTC TGTATGTCAC TTCCCTTTAT 1770
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