Tag | Content |
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EnhancerAtlas ID | HS108-30284 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr4:48730740-48731800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr4:48731225-48731241 | CACAGTGTAAACAAAG | + | 6 | NFKB1 | MA0105.4 | chr4:48730963-48730976 | AGGGGATTTCCCT | + | 6.15 | NFKB1 | MA0105.4 | chr4:48730963-48730976 | AGGGGATTTCCCT | - | 6.1 | REL | MA0101.1 | chr4:48730964-48730974 | GGGGATTTCC | + | 6.02 |
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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 |
GH04I048728 | chr4 | 48730801 | 48731901 |
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Enhancer Sequence | AAACCATGAA AGTAAGAAGA GAGGGTTGCT TCCAAGATGG ACGAATAGTA ACAGCTCTGG 60 TCTGCAGCTC CCAGCAAGAT CAACGCAGAA GATGGTGATT TCTGCATTTC CAACTGAGGT 120 ACCTGGTACA TCTCACTGGG ACTGGTTGGA CAGTGGGTGC AGCCCACGGA GGGCAAGCCG 180 AAGCAGGGCA GGTCGTCACC TCACCTGGGA AATGCAAGCG GTCAGGGGAT TTCCCTTTCC 240 TAGCCAAGGG AAGCCGTGAG TGACTGTACC TGGAGGCGCA GTACACTCTT GCCTAAATAC 300 TGTGCTTTTC CCACGGTCTT CGCAACTGGC AGACCAGGAG ATCCCCTCCC GTGCCTGGCT 360 CAGCAGGTCC CATGCCCACG GAGCCTTGCT CACTGCTAGC GCAGCAGTCT GAGATTGACC 420 TGGGACGTGG GAGTTTGCTG AGGTGCATCT GCCACTGCTG ACACTTGAGT AGGTGGTTCT 480 ATGCTCACAG TGTAAACAAA GTGGCAAGGA AGCTCCAACT GGGCGGAGCC CACCACAGCT 540 CAGCAAGGCC TACTGCCTCT CTAGATTCCA CATCTGGGGA CAGGCCACGT CTGAATAAAA 600 GGCAGCAGAC AGCTTCTCCA GACTTAAATG TCCCTGTCTG ACAGCTCTGA AGAGAGCAGC 660 TGTTCTCCCA GCACGGTGTT CGAGCTCTGA TAACGGACAG ACTGCCTCCT CAAATGGGTC 720 TCTGACCCCT GTGTAGCCTG ACTGGAAGAC ACCTCTCAGT AGGGACTGAC AGACACCTCA 780 TACAGGCGGG TGCCTCTCTG GGACGAAGCT TCTAGAGGAA GGATCAGGCA GCAATATTTG 840 CTGTTCTACA GCCACCGCTG GTGAAACCCA GGCAAACAGG GTCTGGAGTG GACCTCCAGC 900 AAACTCCAAC ACATCTGCAG CTGAGGGGCC TATTAGAAGG AAAACTAATA AACAGAAAGG 960 AAGAGCATCA ACATCAACAA AAAAGACATA CCCACCAAAA CCCCATCCGT AGGTCACCAA 1020 CATCAAAGAC CAAAGGTAGA TAAAACCACA AAGATGGAGA 1060
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