Tag | Content |
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EnhancerAtlas ID | HS044-09566 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr4:6931130-6932300 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr4:6931335-6931356 | GGGGCAGGGGTAGGAGGGGAG | + | 6.54 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_01116 | chr4:6930704-6931597 | Adrenal_Gland | SE_23500 | chr4:6930367-6932400 | Colon_Crypt_1 | SE_24085 | chr4:6930758-6931713 | Colon_Crypt_2 | SE_24085 | chr4:6931755-6932301 | Colon_Crypt_2 | SE_26379 | chr4:6930398-6932259 | Duodenum_Smooth_Muscle | SE_27664 | chr4:6927858-6933966 | Fetal_Intestine | SE_28549 | chr4:6927396-6934981 | Fetal_Intestine_Large | SE_50164 | chr4:6925918-6932478 | Sigmoid_Colon | SE_52623 | chr4:6930358-6932359 | Small_Intestine | SE_54195 | chr4:6930997-6932354 | Spleen |
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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 |
GH04I006924 | chr4 | 6926250 | 6933811 |
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Enhancer Sequence | GGATCTGGAG AGAGATGTGA ACAAAGCAGC AAAGCCCGTT GACAGCTCAG AAAGAAGTAA 60 CAGGGCTGAG ATGCCAGCTG GCCTTCGAAA GTGCTGTCCA CCCGCCTGAG GGTGGAGGTG 120 GTGAGGGATC AGCTTGTGCA AAGTCATGGG GGCAGGAGAG AGCCCAGCCT TCCTGGGAAG 180 GTGCCGTAGC ATGAGGCGCT CAGGAGGGGC AGGGGTAGGA GGGGAGACCA CAGAGATGGT 240 AGACGCCCAG ATGGGGCAGG ACTTTGAGGA CGACATTTAG TCTCAAGACT CAAAGCCTGT 300 CACAGCCAGA CTGCATAAGA TGAAAGTCTG CACAGGAGCG GATGGGCTGC CTTGATGAGA 360 ATGAGTTAAA CTGTTAGCTG GATAGAGTTG AGATGAGCAG CTCCCTTTGG AGAATGCAGT 420 TGCCCTGTTC TGAGCTCAGC TTCTGGGCCA GGCACTTCTG TCGCTTTCTA AAGCATTTCA 480 CAGCTCACTG GAGACAGACT CAGAAAGGCT AACTGCACAG ACTGCAGAGC TGCGATTTGA 540 ACATTCACTT GTTAACTCCA AAGTCCATGC TGTTTCTAAA AAAGACAACA CCCTGTCTCT 600 TGTAACATGT GTAACGTGAT CAGAAAGGGG GAAGTGCGGG GCTGGGAGAG CAAAAGGAGA 660 TGAATGAGAA ATCAGAGGTG CAATGGTGAT TTTGCAGGGC GGTGTTGGAA CTGTGATGCT 720 CTGCAAAAGG GAGGAAGCGA GCAGAGCTCT AAGCCGGGTC AGGGTCTAGC TGGGTGGCGT 780 CTGTCCGGGC ACTGAAGCTC CTTGGTGGGA AGACGGTTGG AGAATTGCTT CTTGAGCCAT 840 CGCGGGCCAG CAGGATGAGA ATGCCTTTTC CTCCTCCAGT TACTCCAGGC ATTTGAAAGT 900 GTGGGAGTGA GGCTGGAGTC AGCCGTTTGT CACGGGGCCT GCTGCTGGGT TGGTGGCCTT 960 TGTGGGCTGG CCATCGACAG GGGAGGGAGA TACAGTAGAA TCACTGCAGG TGCCTCCTGG 1020 AGGCCTTGAG CCAGAGAGAA GCAGAAAGGA CTTTAGCAAG CAAGGAACTC GTAGGATGGT 1080 TCCCATTATT CCTCACTAAA AGTCTATGAG GGGGCCAGGC GCAGTGGCTC ACGCCTGTAA 1140 TCCCAGCACT TTGGGAGGCT GAGGCGGGTA 1170
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