Tag | Content |
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EnhancerAtlas ID | HS098-53736 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr7:151519770-151521020 |
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) |
RREB1 | MA0073.1 | chr7:151520109-151520129 | ACCCCACCCCACCCCACCCC | + | 6.22 | RREB1 | MA0073.1 | chr7:151520110-151520130 | CCCCACCCCACCCCACCCCA | + | 7.67 | Rhox11 | MA0629.1 | chr7:151520425-151520442 | ACTCTGCTGTTATGGGT | + | 6.01 | SRF | MA0083.3 | chr7:151520501-151520517 | TGACCTTATTTGGAAA | - | 6.01 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_27759 | chr7:151515467-151522964 | Fetal_Intestine | SE_28667 | chr7:151515549-151522536 | Fetal_Intestine_Large | SE_31948 | chr7:151518883-151520398 | Gastric | SE_31948 | chr7:151520420-151522146 | Gastric | SE_52790 | chr7:151515699-151522164 | Small_Intestine | SE_65519 | chr7:151519099-151520356 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I151818 | chr7 | 151515801 | 151522380 |
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Enhancer Sequence | CAGCGTCTTC CCAAGCTCTG ACAGACACGC TTAGTGCAAT GGCCTTGGCT GTGTGGAGCC 60 AGGGTCAGGG GTGCAGACCC ATGTGGACGC CACCTGCACC CTGGGTCAGG TGACAGGGAC 120 CTGCCTCCAC ACCTCCACGT CACACTCCCT CCCTCCCCAC AAAAGGTTGC CCAATGAATC 180 CACAACACAG AATGTTCAGC CCTGATTCAA AAATGAAACA AACAAGAAAA CAACCTCCAG 240 CGACTAATCA GCCTGGGGAA GCTGAGTGGC CGCCAAGCCC GGCTCTATCA CTTGAAAATC 300 TAGGGCTCCT AGAATTCCTC CCAGCGACCT GGTTTTCAGA CCCCACCCCA CCCCACCCCA 360 CAGCGGAAAA CGCAAGCTCA ACTGCAGAAC CTGCTCCCTG ACCCCTGGCT TGTCACAGCA 420 GCAGGGGCCA GGCCACAGCC GGACTCTGCC AGGCGTGGCC CCTCTCAGCA CAGCCGCCTG 480 GGGACACTCT CTATGAAGCT CAGGAAGAAC AGGAAAAATG TGTATCCAGT TTTGTTGGCT 540 ACAGGGATTT TGTATCAACA TTTTTTTTTC CAAAAATTGA ATAAACACTA AAACTTAAGC 600 TGAAACTTCT TAAATGTTTT AATGATTTTA AAAGAAATAT CTCAGAATGC ATTATACTCT 660 GCTGTTATGG GTTAAAGTGC TTGCACCCGC AAAAAAGACA TTGGAGTCTT CACTCCCAGA 720 ACCTCAGAAT GTGACCTTAT TTGGAAATAG GGGCTGTTGA ATTTGGCCCC ATTTGTGAGT 780 GGTCACATGG GCCAGGCACC GTGGTGGGTG CAGACCCCTC TCCTAAGTCA GTCCAGGGAC 840 AAGAGAGTAG ATCCCAAGGA GATGGAACCT CACTCACCCT CTGCCTAACC AGTCCTGGCC 900 TACTGGGCCA TCTGGGGGCC TCATCTCTGA TTAAAATGTC AAACTCCACA TCAGAGGCTA 960 GGGAGAGACG TGGGAAGAGA TGACACCCTC CATCTGTTTC TGGAAACTTC CACAGCCTGA 1020 TCCTATGATC CTTTACCAGG GCTGGGCCCA GGGATGTGGG GCCCAGAGTC ATTCCTGGTG 1080 GATGGGGGCT GGAAAGGAGG TAAAGTCCAC CCCTGGCTAA ATCATTCGTC TACCTGGAGA 1140 GAAAATTAGA ACCTCTGGGG AGTTTTCAAA AACTAGATCC CAATTAAGAA CTACTGAATC 1200 AAAATTGCTG GGGCTGAGAA CTGGGTGATT GAAATATTCT GCTAAGTAAG 1250
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