Tag | Content |
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EnhancerAtlas ID | HS120-02576 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr17:1018150-1019090 |
Target genes | Number: 18 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr17:1018924-1018938 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 17 | ID | Coordinate | Tissue/cell |
SE_01841 | chr17:1017900-1019002 | Aorta | SE_09651 | chr17:1017785-1020412 | CD14 | SE_23220 | chr17:1017867-1018962 | Colon_Crypt_1 | SE_23794 | chr17:1017976-1018925 | Colon_Crypt_2 | SE_24832 | chr17:1017956-1018975 | Colon_Crypt_3 | SE_26634 | chr17:1017954-1019189 | Esophagus | SE_28034 | chr17:1017873-1019244 | Fetal_Intestine | SE_29195 | chr17:1017861-1019259 | Fetal_Intestine_Large | SE_31579 | chr17:1017933-1019161 | Gastric | SE_40640 | chr17:1017872-1019327 | Left_Ventricle | SE_42145 | chr17:1017886-1020432 | Lung | SE_49097 | chr17:1017909-1019004 | Right_Atrium | SE_49495 | chr17:1018072-1018468 | Right_Ventricle | SE_50313 | chr17:1017897-1019209 | Sigmoid_Colon | SE_52631 | chr17:1017926-1019209 | Small_Intestine | SE_54272 | chr17:1017918-1019108 | Spleen | SE_65254 | chr17:1017805-1020481 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I001114 | chr17 | 1017441 | 1020012 |
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Enhancer Sequence | TGTGCCAGGC ACAGTTCTCG GCACCAGAGA CTGCAATGAG CAAGTTTTGT TACAAAACCG 60 ACAAAATCTC TCTCTCGTGA GAGTTCACAA TTCTAGCACG GAGTTGGTCC TGAGGCCACA 120 GAGGTAGGCA GGGGGTCCAG GGGTCAGGTC ACACAAGGCC TTGACAGCTG TGCAAAGGGA 180 AGGGGGGCCC CATAGGCGAA GGGAAGGTGC TGGAGGATTT CAGGACAGGT GTGACAGGAC 240 ATTCATCCTG CATCCCTCCT GCTGACATCA GATGACTCTT TCTAAAACAC TGCTCACTCT 300 ATGCCCAGCA GGAAGCCACC AAGCCAGCCC AAACAAGAGC CGTGGGGCCC CAGCTGATGA 360 CTCACCCATC TCACTGTTGA CAGTAACCTC TCAAAGGGCC TGGCACGTTC TCACTTCCAG 420 GCCTTTAACA ACGGCAGGTC CTCGGCTTGA AGCACTTTCT CCCGCCTCTT GGCTTCTCCC 480 TGGCTCTCCC AGCTTTCCTG GCAGAAACTC AAGCCCCACC TCCAGACTGT ATGAAGCTCA 540 GTAGCTCTTC AGCCAATGGG AACTGACACC AAAGGGCAAG TGCCAGGGCA GTTGCAGCCA 600 CTAACTGCAG CCACAGATGG GACTGGATTC GTCACCTTCC AGATCACCTT GCTCCTCCCT 660 CTGCCTCCTC TCTGTTCTAG TACAGGTCAC TCCAAAATCA TATACATAGT TCAACTACAT 720 AAAGCTAATG TTGGCCAGAT GCAGTGGCTC ACGCCTGTAA TCCCAGCACT TTGGGAGGCC 780 GAGGCGGGCA GATCACCTGA GGTCAGGAGA TCAAGACCAG CCTGGCCAAC GTGGTGAAAC 840 CCCGTCTCTA CTAAAAATAC AAAAAATTAG CCAGGCGTAC TGGCGGGTGC CTGTAATCCC 900 CGCTACTAGG GAGGCTGAGG CAGAAGAATC ACTTGAACCC 940
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