Tag | Content |
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EnhancerAtlas ID | HS044-09694 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr4:40674420-40675700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr4:40675086-40675097 | CTGAGTCATCC | - | 6.32 | JUNB | MA0490.1 | chr4:40675086-40675097 | CTGAGTCATCC | - | 6.14 | NFE2L1 | MA0089.2 | chr4:40675082-40675097 | AAAGCTGAGTCATCC | - | 6.45 | Nfe2l2 | MA0150.2 | chr4:40675084-40675099 | AGCTGAGTCATCCTT | - | 6.06 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33946 | chr4:40673626-40676306 | HCC1954 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 40674578 | 40674731 | chr4 | 40674929 | 40675349 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I040670 | chr4 | 40672919 | 40676225 |
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Enhancer Sequence | AGGATAAGGA GACAGTGACG GGCAGGGAAC AGCGCTGCTT TAAATAAGTT GGTCAGGGAA 60 AGACACTCCA GTCAGATGCC ACTTGAGCAG AGATCTGAGT GAATTAACGA CATGAACTAG 120 AGAAAGAATA TTCCACGCCA AAGAGAACAG AGGCACAGTG GCCCAAGGCA GGCAGGAGTT 180 TAGCATAACT CAAGGGAGGG TCCAGAGGTC CTGCGGCTGG AGTGGAGTGA GCCGGAAAGA 240 GGAAGGAAAG GTCACATGAA GAGCTGGGGC CAGGTCCTGA TGGTAAGTGC TCTTTGGAAC 300 TCCTCCTTTT AAAACTGGCG TGTCTTCAGG AAGCTGAATA TCTACAAAGC TAGGCCTCGG 360 AGAGAAGGCT TTTCCTGAGT ATGTTTGTGT GAGTGATTCC GTGTGTTAAC AAAGCGCCCC 420 AGGATTTGCC TTTTCTTCCC CTGTTTCTTG CTGTTAGAAT GTTAATCTGG CTAAATCCAT 480 TCAGCTTCAC TCGTTTGGAA ATCAGTCATC TAATGCTTGT AGCGAAAAAA GGAGACAAGC 540 TAATACATCT CAACAGAGCA GATACGTGGG AGCCACTCCC ACAGATCAAG ATCCTTGCAG 600 AAACCCAAGC CATTGTTCAG CCAATAGTAA ATAAGAATCC GAGTCATTCT AAAACTGAGT 660 AGAAAGCTGA GTCATCCTTC CCTCTATCAA GAGCTTTATT CCTTTTGCAT CCTGTGGATC 720 TTGGTTGGTT AACACATTAC TGAATGGTGA CGTGGGTAGG TCTGTCTGCC TGCATCAAAT 780 CCTGCCCTAA CCACATTCTC AAGATAGTTT TCACCACATT TACTAAACTT CCTTGAACCT 840 CAGTTTCCTC CTCTGCAGGA GGAGGGTATG AATGCTTTAT TAGTTTTCTA CTGCTGTGTA 900 ATAAATTAGC ACAGATCTAG AGGGTAAGAG CTACTCCCAC TCATCATTTC ACAGTGCTGT 960 AGGCCAGAGG CCCCAGATGG CGTAACCAGG TTTTCTGCTA AGAGCCTTGA AACGCTGAAA 1020 TCAAGATGTT GGTTGTCCGT GTCCTCACCT AGAGCTCAGG GTCTTCCTCC AAGCTCATCC 1080 CTGTTGTCAG CAGAATGTAG GTTCCTGCAG TTGTGGGACC GAGGCCTTGT TTCCTCACTG 1140 GCTGTCAGCA GAGGCCATTT CTCAGCTCCT TAAGCCTGCC CCCTTCCTCC ACAGTGACCC 1200 TCTATTCCAA AGCAGCAACT ACACACCTAA CCCTTCTGAC ACTTGGAAAA CATCTGACTT 1260 CTGCTCTCAG CCAGAGAAAG 1280
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