Tag | Content |
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EnhancerAtlas ID | HS129-23152 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr20:61064320-61065090 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr20:61064638-61064654 | TCTGGACTTTGAGCCT | - | 6.04 | TFAP2A | MA0003.3 | chr20:61064444-61064455 | TGCCTGAGGCA | - | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_12737 | chr20:61064488-61064634 | CD34_fetal | SE_27678 | chr20:61051059-61066009 | Fetal_Intestine | SE_28621 | chr20:61046610-61066140 | Fetal_Intestine_Large | SE_31818 | chr20:61064006-61065097 | Gastric | SE_53255 | chr20:61064064-61065589 | Small_Intestine |
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Enhancer Sequence | CAGATCCCCT TCCAGAAGTG AAGAACATCT CAGCCGTGCC CTGGCAGGCC TGGCTCCTCC 60 CCCTCCACAC CTGAAGTTTC TGTTTAAAAT GTTTGGCCAC TGGAGGGGTG AAGACACTCA 120 CCTGTGCCTG AGGCACTTTA TTATCCTGAC TGAGCGCGCC CTGCACCTCT CACTGTCCTG 180 AAGTGGCTCG GCCCTCGGGC TTCATCTGGG CCTTCTGTAC CTGAGCCTGG GCTTGGCCCA 240 GCGTGGCCAG TGGGCTCCGG GCCCCTCCTG CCAGCCTAGC ACTTCTGAGA CAGAAGCCTG 300 GCGCAGCAGG CAGGCACCTC TGGACTTTGA GCCTGGGCCC TTGACAGCCA GGGAGAGGGC 360 GACCCCCAGC ACACACTACC CTAACCTTTA GCAACGTCCC CACTGCAGAT GGGGGTGCTA 420 GCCTTGAAAG TTGGGTGCCC CAAGGGTTGG GGCAGGAGGG CAAGGGGCCG CCCCAGGGAG 480 GTGGTGCATG ACACAGCCTA TAACAGGCAG TGACTCACTG CTCATCCAGC CATAAAGTCA 540 GGGTGATAGG CTCAGTGTCC CAGCCGTGCT CCCTGGAGTC CCTGCCCCAA CGTCATTCCC 600 TTCTCTGCAG CCTGCGCTGG GCAGAGCTCC CTCCCCAGGG GGGCCGCCTG GGCCACTCTG 660 GGACCATCCA CCCATTCCAG ACCCACCCAT TCCAACTCAC TTGCTACTGC TGGGGAGACT 720 GAGTGCCAGG GAGGGGGAGC AAGGGTAGAT GGAGAACTAA CAGTGTCAGA 770
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