Tag | Content |
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EnhancerAtlas ID | HS050-67385 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr8:129566950-129568380 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr8:129567806-129567817 | ATATTTACTTA | - | 6.14 | IRF2 | MA0051.1 | chr8:129567561-129567579 | AATTGACTTTCATTTTCG | - | 6.07 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_18498 | chr8:129564151-129570821 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19394 | chr8:129564209-129569930 | CD4p_CD25-_Il17p_PMAstim_Th17 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I128551 | chr8 | 129563997 | 129570009 |
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Enhancer Sequence | CAATAAATGA TAAAGCTTAT AATTATAGAT GAGAGCAATT GCTTCTTTTT TTGTTCTTAC 60 CTTCATTTCA GTTTATCTTC CTGAGCTATA GCTACCTCTG TAAGGGTTAG GAAAACATTT 120 AAAATATCTA AACAGTGATT CCTTTCTCAA GCGTTCGGAA ATTGATGAAT CATCTTACTC 180 TGCAGCATTC AAAGTAACTG TGTGCTTGAC ACATAGGAGG AAAAGTGGGC TCTTTGAAAT 240 GTGAGCAGAG CACCGATCGT GTCACCTGCC CGGCGCGTGA CCTGTTCACT TTCCACCTGA 300 CCCTCTGTGC CCAATGTCAC CTGGAGCCTG AAACCTGGAA GGGAAAAGTC CTTGACTGGA 360 GTCAGTGGAG AGAAAATCAT CACCTGCTTG GGCACAAACA TGCCTGGTGA CTGCGTCACT 420 GTCTGTTAAG TGGGATCAGC TAATAGTTGC ACAGCGGGCC TTCAAAGCAT CACGGCAGAA 480 CTGATGAAGT TCCTGTAATG CATTCCCTGT GTGAAGGCCT TGGACTTTAG AGCTCAAGTG 540 CGCCAGGAGC ATTTTGAGCT TGCCGACAGG CTCTCCCATG GATTCTATTT GGTTATACGG 600 CAGTGGAAAA GAATTGACTT TCATTTTCGT CACTCTCTGC CTGAGTCTCT CGACTGCAGC 660 CACACTTCTG TTTCCCGTAT ATTGCATAGG CTATTCCCTC TACCTGGGAC ACCCTCCCCT 720 CTGGATTGCA GCAAGATTTG CTTCTATGTT TCACTCAGTT ATCTACTTAC AAATCACCTC 780 CTTAGGGACC TTGCAGGCTG CTCTCTTTCT CCTTACCTGG CTTCATTTTC CTTCACAGCA 840 CCTGATACTA TTACACATAT TTACTTAGTT AGTAGTCCAT GCTTTTTCTT CCCCACTGGA 900 CCATAAGTTC TCTGAAGGCA AGAGCCACAT TTGTGTTTTT CCACTGATCT GTCCTCAGTG 960 TCTACAATAG TACTCAACCC ACAATATAAC CTTGAGAAAC ATTTCTTAAA GAAGTGAATA 1020 AATGAACGAG TGAAGGAGTG ATTTTTTTCT CATTTTACAA ATGAAACAAG TCAAAAACAA 1080 AGAGGGGAAG TAAGCTAGTC CAGCTCTACA ACCATTTAGT GGCACAGCTA GTATTAACAT 1140 TTTGATTTCC TAACTCACAA TCTAGGATTT TATTTTCGTT TTATTCCATA CAACACTGTT 1200 CTCCAGAAAT TTGGCAACTC AGACGGCACT TGACTTTTCA CAAACACATT TCTTGCTGTC 1260 TTTAACCTGT TCATGTCAAT GAGAATGACT ATAACCTCAT GAGAGACAAG TGTTTACTAG 1320 TTAAGTTCTT ACTGAAGTGA TTGGTCTTAG AACTCCCTTT CAAGGGCAAA GACGATTGAA 1380 AATTAGTTAT ACAATTACAT TTTTAAAACA TTTTTGAGTA TAATGATTTT 1430
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