Tag | Content |
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EnhancerAtlas ID | HS191-26035 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr3:58053410-58054690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr3:58053949-58053964 | AGGGGACAAAGGCCA | + | 6.44 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_01957 | chr3:58053408-58054941 | Aorta | SE_23194 | chr3:58053617-58054189 | Colon_Crypt_1 | SE_27681 | chr3:58052157-58054828 | Fetal_Intestine | SE_29426 | chr3:58050504-58054962 | Fetal_Intestine_Large | SE_37989 | chr3:58050972-58053538 | HUVEC | SE_41579 | chr3:58053510-58054717 | LNCaP | SE_45969 | chr3:58051053-58053642 | Osteoblasts | SE_65730 | chr3:58053250-58054315 | Pancreatic_islets |
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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 |
GH03I058064 | chr3 | 58049836 | 58054833 |
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Enhancer Sequence | CCTCCCAGGT TCACGCCATT CTCCTGCCTC AGCCTCCTGA GTAGCTGGGG TTACAGGCGC 60 CCACCATCAC GCCCGGCTAA TTTTTTGCAT TTTTTAATAG AGACGGGGTG TCTGGATCTC 120 TGACCTCGTG ATCCGCCCAC CTCCGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC 180 CACGCCTGGC CAGAGGTTTT CTTAAAAACA ATAACAACAA AAACAGTTGT GGAAAGCATG 240 TAGAGTGTGG GTTTTTTCGG TCTTCAGGTT GGCAGGGCAT CTGATACTGG GACCCAGGTT 300 CCTTCCCTCA CCTTGCTGTG CCTCTCCTAG TGCAGGCCAA AGCCAGGTGA CTGCGCTGTC 360 TGGGCTCCTG GCTGGCAATC GGGGAAAGAG TGCATGGAGC AGGCATGCCC ACTGTTCAGG 420 TCCTGAAGCC GTGGCTCATT TCATATCATT TGTTGCTTAT TTGAAAGACA GGCACAGCAC 480 TGACTTCCAG GGGAGGCTGA CTGACCATCT AGGTGGAAGT TGCATGCCTG GGAGGGAGAA 540 GGGGACAAAG GCCACAGATA GGCATCAGTT ATCAGGGCCT TAAGTCTGCC TTGTTGGCAT 600 GCAGCCTTTT ATTGGATCAA GGCCCTGGAG AAAAGCCCTG AGCAGGAGGA GATAAGCCAG 660 CTTGGTCCCC TTCATCCTAC CCAGGGGCCT CTGGGGTACC TGAGCCAAAG TGCACAGTTC 720 ATTGGCTGTG TGGATGGAAG GGATATGGGA CTTGAAAATG GGACACTGGT CCTGGGCAGC 780 TGACCGACAT GGTCCTCCTT AACCTGCTGT CTGGGGAGAT GGGTTGCATC TGGCTAGGTT 840 TTGACTGAGG AACTGAGGAG AGCTGTCAGC TGTCCCCGCT TTGGTTCAGA ATGCCCTTTT 900 GTTTGGACAG CTGAAGCCTA CAATTCAGCC ATGGTTTGTT TGGGCTCAGA AAACAGGCAA 960 GGATGGAGAG AAACTGCAAA GCTGACCTGG GCTGTCAGTG GGCACCAGGT CCTGCTGGCC 1020 TGGGGTCTGG ATGCAGGAGA TCTGAGCTCT TCAATGTGGG GTGGTCTTGC AGCAGCTCTT 1080 CACAGGCTGC TGCTGCTGCT GCTGTAGGCT CACCCAAGCA GCCAAGACGG ACAGGATCTA 1140 TTCTAGTTTT GTGCAGAGTT GGATATAGAA GAGGCATTAG AGGGAGAGGG GATGGGGAAG 1200 GAGTTCCAGG CCAGGTGAGC ATGGGGCACA GTAAACTGGG ATGTTAAGGA GGGGCCAGTT 1260 TGTGACCAGC CTGGGCAACA 1280
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