Tag | Content |
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EnhancerAtlas ID | HS050-30071 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:74476360-74477450 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr17:74476412-74476426 | GCCGCCTCGGCCTC | + | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_06656 | chr17:74476486-74477911 | Brain_Hippocampus_Middle | SE_09479 | chr17:74476548-74482651 | CD14 | SE_10700 | chr17:74476430-74481233 | CD19_Primary | SE_11207 | chr17:74472779-74482731 | CD20 | SE_20219 | chr17:74476551-74480225 | CD56 | SE_53021 | chr17:74476710-74477980 | Small_Intestine | SE_60182 | chr17:74474557-74499337 | Ly4 | SE_60872 | chr17:74475283-74503238 | DHL6 | SE_62418 | chr17:74475150-74527312 | Tonsil | SE_65717 | chr17:74476867-74477584 | Pancreatic_islets |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I076480 | chr17 | 74476361 | 74482481 |
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Enhancer Sequence | CACCATGTTG GCCAGGCTGG TCTCGAACTC CTGCCTGACC TCAAGTGATC TGGCCGCCTC 60 GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCTACCAT GCCCGGCCTA TATATATATT 120 TTTTGGGACA GAGTCTTGCT CTGTTGCCCA GGTTGGAGGG CAGTGGCACC ATCATAGCTC 180 ACTGGAGCCT CGACCTCCCA GGCTCAAGCA AGCCTTCTAC CTCAGTGTCC TAAGTAGCTG 240 GGATTACAGG CATGTGCCAC CACACCCAGC TCTTTTTTAA TTTTTTTTGC AGAGACAGAG 300 TCTTGCTATG TTGTCTAGTC TGGTCTCGAA CTCCTGGGCT CAAGTGATCT GGCTGCCTCA 360 GCCTCCCAAA GTGATGAGAT TACAGGCATG AGGCGACCTC GCCCAGCCTC ATTCTGAATT 420 TAAAATCGCC ATTGTCTAAC TTTTCTCCGT CAAGGCCAGC GTGTGTTTTC CTAACTCCTC 480 ATCCAGTCCC TCCCCTCTGC ACCATGACGC TCCTGCCTGC TGCTGTGTCT TCTGCAGAGC 540 TCTCGGGTGA ACGGGGGGCG TTAACATCGC TTCCCTTTAT ACTCCAGACT GTGCAGGAAG 600 CCCACGCTGC CACAAGCCGG TTTTCAATGA GCTCTTTATG GGGCACTAGA CCAGACTGTC 660 AGAAACACTG ATCTGTTCTC GTCCTCCCAA AGGAAGCGGA CACTGCCTAG GCGGGCTGCT 720 GATGCCAGGG AGACACTGTC CCCTGCTCAC CCATGTCAAA GAAAGCCCCC AGCCCTCAGA 780 AGAGAGACTG AGAGTCCAGG CCTAGGGGGT GAAATGAGAA CAGCCAGGGC CCCAGGGTTA 840 CCAGCAAGCA CTTTCTTGGG GCTGGCCCTT CCTGTGTGCC CCTGACCACG ATGAGAGTGA 900 GCCCGGTTCC TGGCTTTACT CCCTGTGATA TTTCGGGCCC AGGAAGGAGG GGGTAGGGCC 960 CGAGTCAAGG GCTGCACAGA CAGCAGCTGT GGCTCAGGAA GGAGCCCCTC TGGGAAGTGA 1020 AACTGACCAG AAAGTGTCAC GTGGGTACAT CTGTTACCTA CGGCAGAACA GTGAGCCCCC 1080 AGGCCAGCCC 1090
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