Tag | Content |
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EnhancerAtlas ID | HS047-30249 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:1505980-1507160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr7:1506478-1506499 | GAGCTGAAAATGAAACCCAGA | - | 6.05 | KLF5 | MA0599.1 | chr7:1506554-1506564 | GCCCCGCCCC | + | 6.02 | Zfx | MA0146.2 | chr7:1506266-1506280 | GAGGCCCAGGCCCC | - | 6.08 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_01174 | chr7:1505850-1507349 | Adrenal_Gland | SE_23483 | chr7:1505614-1507860 | Colon_Crypt_1 | SE_24254 | chr7:1505624-1507371 | Colon_Crypt_2 | SE_25042 | chr7:1505145-1509022 | Colon_Crypt_3 | SE_27601 | chr7:1505944-1507244 | Esophagus | SE_29524 | chr7:1505520-1507434 | Fetal_Intestine_Large | SE_31792 | chr7:1505917-1507287 | Gastric | SE_50602 | chr7:1505551-1507327 | Sigmoid_Colon | SE_54079 | chr7:1505779-1507516 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 1506357 | 1507000 | chr7 | 1506918 | 1507075 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I001465 | chr7 | 1505531 | 1507328 |
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Enhancer Sequence | CTGGGGTCCA ACCCTGAGTC CCCCGTGAGC CCAGCAGGGC CCGCCATGGG GTGTCCTTTT 60 GGGCCTGGCC CAGTGAGGGG GTTTGGAAAG AACTGGGACG TCCAGTTCTG CCTGCCCATG 120 CTCAGCTTCC TACAGGCCAC TTCCCAGGAC AGAGGGGCTG CTGTCCCCAG AGGAGGCTTC 180 AGCCATACCC TTCTCTTCAG AAGCACCTGG AATGACCCCA ACCGCTGGCT GGGCCTGGGC 240 CTAATTGGGT CAGGGGTCTG GGTTGCTCTG AGGAAGGGAG CTGGGGGAGG CCCAGGCCCC 300 CCAAGCAGCT CCTGCCCTGC ACCCTACCTG CCACATGACC TCGGGCCACT GTCTGGGCTT 360 CCCGGGGTGA ATGGGGGAGA CACCTCATGG GGAGACCTGC ACTCCTGCTG CCGAGGGCGC 420 TCAGGCCCCA GGTGCCCACA CTCAGCCTGT GGCTGCCACC GTCTGGCCTG TTTGAAGGTC 480 AGGGTCCATC CCCAGCCAGA GCTGAAAATG AAACCCAGAA GCACTTGTTT TGAGACTGAA 540 GCAGCAAGTG AGCTTGTCAC TATGGCATCC CCCGGCCCCG CCCCGTCCCC GCCTGGAGAA 600 GGCAGCCCGG GACTGCCGGG AACCACTGGG AGGGGCTGGG ACCCTGCCTG GCCTGGCTCA 660 GACATACTCC TGGGCCTCCC TCCACTCCTG AAAGGAAGGG AACTGTGGAG TCTGGGCTGG 720 ACCCTCTGAG TCCTGGGCTC TAGTGGTCAC CCTGGGCGAG GGGCTCACAG CCACAGCCAC 780 ACAGGAAGGT GCTGATCCCA GATCCTCCAC TGTTCCAGAA CAGACGGCCC GGGACCTGCC 840 AGCAGCCACC CAGTGGCACA GGGGTCCTGC TGGGTGCCCC ACACGGCTGG TTCCCAGGGT 900 CCCTGGGCCC AGTGGCCGTG GTGAGGAACT TGGGGAGCCG GAGGGAGGGA GAGGCCAGGC 960 GTGGATCGTG GCCTGACCCA GGGCTCCCTG GTCCATTTCG CAGCCCCCTG TCCAACCTGG 1020 GGTCGGCACC GTCATTCCAA CACCCACACT TCTGCTCACA CCGGCCCCTG CCAGGTGCCC 1080 GCCGCAGGCA CAGATTCCAG TCTACCCATT TCTCTGTCCA GGCGCAGTCA AGTTTCCCTC 1140 TCAGGCGTCT TCCCCATCTT TCCCAGCACA GATCGCAGAG 1180
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