Tag | Content |
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EnhancerAtlas ID | HS044-10728 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr5:139620290-139621780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr5:139620878-139620899 | GGAGGCTGGGGAGAAGGGGAA | + | 6.19 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23431 | chr5:139619202-139622461 | Colon_Crypt_1 | SE_24605 | chr5:139619874-139621889 | Colon_Crypt_2 | SE_28509 | chr5:139619582-139623682 | Fetal_Intestine | SE_31400 | chr5:139615731-139623973 | Gastric | SE_41163 | chr5:139618857-139623978 | Left_Ventricle | SE_43055 | chr5:139619856-139623214 | Lung | SE_48219 | chr5:139618750-139623208 | Psoas_Muscle | SE_51117 | chr5:139619841-139627183 | Skeletal_Muscle | SE_53259 | chr5:139619243-139622195 | Small_Intestine | SE_64598 | chr5:139620246-139621701 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr5 | 139621472 | 139621707 | chr5 | 139620295 | 139620494 | chr5 | 139620603 | 139621406 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I140239 | chr5 | 139619055 | 139627656 |
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Enhancer Sequence | CACCTAGAAG ATGCAGTTGT AAAATTTCTG GGCCCCACCG CAGGTGCTCT GAAGAACTGT 60 GAGGGCTGCC TTGGGGGTTT CTCCTGCGCT AGTCATCCCT GCTTTGGGCG ACTGAAGCAA 120 GGAAAACGCA GGTCACTCCC ACCTCCAGAC CCACGCTACT CCCCATTGCC CATCCTCCCA 180 ACAGCCCAGG AGCAGAGATT CTGTCCTCAG CTAAAGGTGA AAAGGTCCTA AGGCTTTTGG 240 GAAACTTGGT GCTCCAGGAA ATAAGTGACT CGGGTTTCTA AGTTATGTGT GGGCACTCAA 300 CGCCCCTGTC ATGGCTGTCA CAGCCCTCTG GTTTGAAGTC CTCCATTTTG TAGCTGCTGT 360 TTCTAACCTC TGTCAGCACT GCCTGGGAGT AATGAGTTCA AAGTCCCTAG TTCCCCACGT 420 TTCCAAGTAT GTTATGTGAA AGCCCTGGCA AGAACGAACC TGATTAAACT GGAGGAAAAA 480 GGTGGAGCAA GCAAGACTAG GACGTTTTTG TTTCCCCAGT TAAGCTGCCT GAGGTTCAGG 540 GGCTCTGACA GGTGAGAAAG GCATGGCCAC CGCCTCAGCC CTGTCTCTGG AGGCTGGGGA 600 GAAGGGGAAG CAGTGAGGAG ACTGACTGAT GTCCTGATGC CCATGCCCCA CACGGCGGTC 660 ATGAAGACTG AGTGGCCCCA TGTCCAGAAA GCCCTCAGCA CAGGGCCTGG CACTTGTGAA 720 TACCTCAATA AATGGTAACT TAAGAGAGCC TGTGAGGCCC CTCCCACTGC AGCCAGCCTC 780 CAGCTGAGTC TCTGGCCTGA AGCCCAGGGA TGGCCTGCAC ATGAATCAAG CAGGCTATTT 840 CCAGAGCTGG CAGGGGAGGG GCTTTCTGTC CCAGGGGCAG GCGAGCCAAT CCTGTGACAG 900 GGAGAGCACA GGGAAGGGGT TATTCAAGGG GATCTGCATG CCATTGTATT CTGGTTTCCC 960 TGTCCAGAGC TGCCCATGCA GGATCCCGGG GTGGGCAGGC CATCCAGGCA GATGGAAGGG 1020 ACACTCTGCC TGGGGCTTTC CTGCTGCAGT GACCCCAGGG CCTGGGGTGG CCAGGCTTCA 1080 GTGGGTAGGG TAGGCTCTGG CTGGATGTGA GAGATGACTT TGCTGTAGCC CCAGTCACCT 1140 CTGTTCTCTT TCTGATCCCT TTTCTATCCC AGTTGGGTAT GAGCAAGCCT GGCTTGCCAG 1200 AGGCTTTAGA GCCATAAAGG CCTGGGTTCG GATTCTGCCC TTGCCTCTGC CTCGTCACAT 1260 GTGCTTGAAC GAGAGACTTG AGCTCTCTAA GCCTCGAATT CCTTGCCTGT GAAGTGGGAA 1320 TGATGGTAGT ATCTACCTCA GGGTTGCTGT GAAGACGAAA TCAGGTACTT GACCTTAGGA 1380 GGCCTCAGAA TAAATGAGCC ATTCATCCTC TCCCTCTGAG CAGGCTTTCC TGGTGAAGGG 1440 CATCTAGACC CAGACCTGTG CTGCTGAGTG GAGCCAAATG CAAGTGGACT 1490
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