Tag | Content |
---|
EnhancerAtlas ID | HS197-08614 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr17:4386150-4387600 |
Target genes | Number: 21 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr17:4386443-4386457 | GGGGGCGAGGCCTG | + | 6.69 |
|
| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_23583 | chr17:4385402-4387697 | Colon_Crypt_1 | SE_24329 | chr17:4385419-4387592 | Colon_Crypt_2 | SE_26970 | chr17:4386118-4387624 | Esophagus | SE_28097 | chr17:4378603-4387608 | Fetal_Intestine | SE_29102 | chr17:4378472-4387704 | Fetal_Intestine_Large | SE_31567 | chr17:4385380-4387675 | Gastric | SE_42277 | chr17:4385387-4387616 | Lung | SE_53037 | chr17:4385363-4387724 | Small_Intestine | SE_57545 | chr17:4385406-4386959 | VACO_503 | SE_57545 | chr17:4387038-4387669 | VACO_503 | SE_65581 | chr17:4383216-4387811 | Pancreatic_islets |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I004475 | chr17 | 4378469 | 4387600 |
|
Enhancer Sequence | GTAAGCAAAG GTGTGGAGGG AGGATCCCAG GGGCACGATC TCTGGATCCC AACCAGTTGG 60 GGGGCTAGAG CAGAAGGGGA GCTCATTCCC TCTTTCTCAG CCCTGTCCTC TGGGGTCCTG 120 GAATCCAGCC ACAGGCTCAT CTCCCACCCC TCAGCAGACG TCCCCACAGT TCCCCGGAGA 180 GTTGTCACCT CTGCGTTCTC CCCCTGCCCC AGGTCTCCAT GCTTCCCTGC TCAGCCTCTG 240 CCCCCCAGGT AGCTGTCTGC TCACTGGCCT GTCTCACCCT CTCAGGGGCG TCTGGGGGCG 300 AGGCCTGGGT GGGGGTGCAG GAGGCAGGCT GCCTGGTGGC TGCTGCTCCG ACTTGCTGCA 360 AGCCCTTGGG TGGCCCTGGT TTCGCCCTCG GCTATAAAGG GAACGGCCCT TCTAAGAAGG 420 GAGAGCCAGA AACAGAGGTG TTTTTGTCTC AGAATAGAGT GAGCCTGGAT TTTTGGGAAC 480 CCAAAGCCTC TTATTTCTGA AATTACCCCC TGGGCTCTCC AGCTTCTGTG GGCCCAGCCT 540 TGGCTGCTGG CTGCACGGAG ACAATGAGGA CTTGGAACAG GCTGGGGGAG ACCCACCTCT 600 CTCGCCACTG GCAGCAGTGA CTGAGCTGGG CCCAGCAGGT TGGGGTTCCT GGGAGAGGAG 660 GAAGGGGCCA GCCTACCTGG ACCTAACTGT GGGGGTCCCA GCAGCCCCAG CCTCCATGTG 720 GACCTTTCTG AACATTCAGG TTCCTCCCTC CAGGAAGCCT CACCTGCCTT CCCAGAGCCA 780 CCAGTGAGTA ATCACATAAT TATGGGGTGA GAAGGAAGTC CTTGGGGAAG GTGCAAAGCT 840 GTTGGTCAGT TCCTTCTCAG GCCTGTTGAC AGATCCTGGT GATGGCAAGA GGCCCGGTTT 900 CTCTTGCCAC CTGTACATGG TGGCTCAGTC CCAGTGACCC TGGGACCAGC GAGTCACTAC 960 AGTGCCTCCT GCCACTCTGC CCTGCCCACC ACCAAACCCC CTGCATCTGT CCCCTGGGAT 1020 TCTGGAATCC AGAGATCGTG TCCCTGGGAT CCTCCCTCCA CACCGTCGCT TACACTGTCC 1080 CCTGCCTGGA ATGCCTTTCC CCGTCTCTTT GCCAGTTACT CTGCCATCCG TTTACAGGGC 1140 TAGTGATGAA CTTGTCCTCC TCATCTTTCT CAGATTTCTG AATGTTCTAT TACAAATGCA 1200 TAAATATTGC TAGAAACACC GGCTCCTCCT TGCCCATCAC AGCAGAGTGG TCAAAAGGCC 1260 AGATCCTAGA GGGAGAAGGC CTGCAATCCT CTCTCAGCCC TGTTATTTCA GGCTGGGTGA 1320 TGTTGGGCAA GTCACTTGCC CTCCCTGTGG AGGTTTTCCT CATCTGTAAA AATGCAGGTG 1380 ATCATCATCT CCCTCTCATG GGTTGTTCAA GTTGATATAT AAAATGTATA CAGCAAGCAT 1440 TCAATAAATG 1450
|