Tag | Content |
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EnhancerAtlas ID | HS108-27214 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:46994280-46995340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr22:46994451-46994463 | TGCTGTGATTTG | - | 6.52 | Gfi1b | MA0483.1 | chr22:46994451-46994462 | TGCTGTGATTT | - | 6.62 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_09872 | chr22:46993763-46999311 | CD14 | SE_24734 | chr22:46994618-46995112 | Colon_Crypt_3 | SE_25451 | chr22:46994081-46997407 | DND41 | SE_26636 | chr22:46993579-46995336 | Esophagus | SE_28479 | chr22:46994266-46995298 | Fetal_Intestine | SE_29306 | chr22:46994169-46995396 | Fetal_Intestine_Large | SE_31503 | chr22:46994006-46994998 | Gastric | SE_40615 | chr22:46994039-46996733 | Left_Ventricle | SE_42318 | chr22:46993552-46996694 | Lung | SE_61894 | chr22:46957289-46995869 | Toledo | SE_65649 | chr22:46994399-46995375 | 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 |
GH22I046596 | chr22 | 46991897 | 46996570 |
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Enhancer Sequence | AGCGGGAGGG AGGGGTGGAT GGACTGGTTA TTTGCACCTC GGTGTTTGTT GCCAGAGGAT 60 TCTAATTGAG CAAGCTGTAA GACCTTGTCT AGGATGAGTC CTGGCCTGAA CGCCTCTAAG 120 TTGCTTTCTC TCCCACTTTG GAGAAAAGCA GTTCTGGTTA CCGGCTTGAT TTGCTGTGAT 180 TTGCTGACTG CCGGCTCCTG GCTCACCTGT GGGTCTAGGT GGTAGCTTCT GGTTAGTTGA 240 GGTATATGGG GGTCTGCTTG GGGGAAGGAG CTTGTTTAGA ATGTGGGGAG ACCCTGAGGT 300 CAGACAGGGC CTGTGGTGCA GCTCCGAGCT CCTTGAGGGC CAAGTATACC CGAAATTGGA 360 ACTAGGAGCT GACACTGAAA GCCAAGTCCT CAAAATCCGT GCGGGCCAGC GGGGAAGGAT 420 GGAGCTGGCC TTGTCTGGAG AGCACGCTTA GCAGCTACAT GGTGGGTTTC AGGCTGGGAC 480 TGAAAGAAGG GGAACCAGGA GGGGACATGC ATGGGAAGAG GGTAACACAG GAGACAGGAG 540 CCGCCCTGCA CCCAGAGGGC TAGGGTTGGG GGTGGTGGGA CTGTGAGCTC CTCTGGTGGC 600 CTCCGGTGCC CACCAGCTCA GTGCCCTGCA GCACCCCCGG AGGAGGATGG GGGTCCCAGG 660 GAACTGTGTG ACACAGAGGC CGTGACAGAG ATGGAGGATC AGATCAGGAC ATCCCAAGTC 720 CTTGACAGAA CCCCTAGCAC ACAAGAAGTA GATTTTTGGA GCCTTTGTTA ACAGATGGGA 780 CCACTGGGGG TCAGATATTT CTGCTGTTGA GCCACCCTGG GCGCAGACAG GGCCTGTGTG 840 TGAGAGTGCT TGCGTTGTCA GTTACGCAAT TTGCAGATGG CTCGTGATTT TTCAGACGTT 900 GAGCTGGTCG TTTCATAGTT GTGCTTTTAG ATACTAAGTT GTTTTTTTTT TTGAGACGGA 960 GTCTTGCTCT TGTTCCCCGG GCTAGAGTGC AGTGTCACGA TCTTGGCTCA CTGCAACCTC 1020 TACCTCCCGG GTTCAAGTGA TTCTCCTGCC TCAGCCTCGC 1060
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