Tag | Content |
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EnhancerAtlas ID | HS073-04257 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr14:93130630-93131840 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr14:93130699-93130720 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | Zfx | MA0146.2 | chr14:93130958-93130972 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_09231 | chr14:93110445-93138700 | CD14 | SE_11367 | chr14:93112295-93138546 | CD20 | SE_12927 | chr14:93130916-93133657 | CD34_Primary_RO01480 | SE_13454 | chr14:93129453-93130860 | CD34_Primary_RO01536 | SE_13454 | chr14:93130913-93138291 | CD34_Primary_RO01536 | SE_14116 | chr14:93130840-93134030 | CD34_Primary_RO01549 | SE_17647 | chr14:93129342-93130827 | CD4p_CD25-_CD45RAp_Naive | SE_18942 | chr14:93130970-93138607 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20176 | chr14:93130875-93133565 | CD56 | SE_53660 | chr14:93131064-93133120 | Spleen |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I092663 | chr14 | 93129604 | 93133487 |
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Enhancer Sequence | GGAAACAGGA CACCTGCAGA CCCTTTGTGA ATTGTTAACA TTCAACCCCC TCCGCTTCAT 60 CATTTTCTTT CTTTCTTTCT TTTTTTTTTT TTTTTTTTTT GAGATGGAGT CTCACTCTGT 120 CGCCCAGGCT GGAGTGCAGT GGCGCGATCT CGGCTCACTG CAAACTCCGC CTCCCGGGTT 180 CACGCCATTC TCCTGCCCCA GCCTCCCAAG TAGCTGGGAC TACAGGTGGC TGCCACCATG 240 CCCAGCTATT TTTTTTTTGT ATTTTTAGTA GAAACGGGGT TTCACCGTGT TGCCCAGGAT 300 GGTCTCGATC TCCTGACCTC GTGTTCTGCC CGCCTCGGCC TCCCAAAGTG CTGGGATTAC 360 AGCAGTGAGC CACTGAGCCC GGCCATTCAT CATTTTCTTT CTCTCTCTGC ATACATAATG 420 TTTTGTCTGA ATAGCGTAAG GGTAACTTAC ATACACCTGT GTCCTTTACC CCAAACGCTT 480 TCCTAGGTAT TTTGTGGCAT GTATGTATGT AACATTACAT AACTCTTACA TAGCCACGGT 540 GGAGTTGTCC GTTGCATAAA TTTATGTTAA TACAGCATTT TTGTCTAAAC TTTCAGGTTG 600 TCACTTGACC TAATAAGGTC CTTTTTAGAA TTTCCCCCTC ATGTTCAGGA TCTGATGAAG 660 GGTTAGATAT TCCGTGTGCT TGTCATATGT TTTTAACCTC CTTTAATTTG GAATATCTCA 720 TATCTGTGGC TGAATGATGG AAATAGAATC TGAGGAGTGC GTCATTAGAC AATTTCATTG 780 TTGTGCAAAC ATTTTAGAGT GTACTCACAC AAACCTAGAT GGCACAGCCT ACTATACACC 840 TGAGCTGTAT GGTATGGTCC ATTGCCCCCA GGCTACCACC CTGTACAGCA TGTGACTATA 900 CTGAAAACTG TAGGCAGTTG TAGCTCAGTG GCAACTATTT GTGTATCTGA ACATATCTAA 960 ATGTAGAAAA GGTGCAGTAA AAGTCTGGCA TTATGATCTC ATGGAACCAC CGTCATATAC 1020 GTGGTCCATC ATTGACCAAA AGTTCATTAT GCGTTGCGTG ACTGTATTTC CACAGCCTTT 1080 GTCTCTTTTT TTTTTTTTTT TTTTTTTTTT TGAGACAGAG TCTCGCTCTA TCGCCCAGGC 1140 TGGAGTGCAG TGGCGCAATC TCGGCTCACT GCAAGCTCCT CCTCCCGGGG TCACGTTATT 1200 CTCTTGCCTC 1210
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