Tag | Content |
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EnhancerAtlas ID | HS020-42263 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr7:151519800-151521240 |
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 | TTAGTGCAAT GGCCTTGGCT GTGTGGAGCC AGGGTCAGGG GTGCAGACCC ATGTGGACGC 60 CACCTGCACC CTGGGTCAGG TGACAGGGAC CTGCCTCCAC ACCTCCACGT CACACTCCCT 120 CCCTCCCCAC AAAAGGTTGC CCAATGAATC CACAACACAG AATGTTCAGC CCTGATTCAA 180 AAATGAAACA AACAAGAAAA CAACCTCCAG CGACTAATCA GCCTGGGGAA GCTGAGTGGC 240 CGCCAAGCCC GGCTCTATCA CTTGAAAATC TAGGGCTCCT AGAATTCCTC CCAGCGACCT 300 GGTTTTCAGA CCCCACCCCA CCCCACCCCA CAGCGGAAAA CGCAAGCTCA ACTGCAGAAC 360 CTGCTCCCTG ACCCCTGGCT TGTCACAGCA GCAGGGGCCA GGCCACAGCC GGACTCTGCC 420 AGGCGTGGCC CCTCTCAGCA CAGCCGCCTG GGGACACTCT CTATGAAGCT CAGGAAGAAC 480 AGGAAAAATG TGTATCCAGT TTTGTTGGCT ACAGGGATTT TGTATCAACA TTTTTTTTTC 540 CAAAAATTGA ATAAACACTA AAACTTAAGC TGAAACTTCT TAAATGTTTT AATGATTTTA 600 AAAGAAATAT CTCAGAATGC ATTATACTCT GCTGTTATGG GTTAAAGTGC TTGCACCCGC 660 AAAAAAGACA TTGGAGTCTT CACTCCCAGA ACCTCAGAAT GTGACCTTAT TTGGAAATAG 720 GGGCTGTTGA ATTTGGCCCC ATTTGTGAGT GGTCACATGG GCCAGGCACC GTGGTGGGTG 780 CAGACCCCTC TCCTAAGTCA GTCCAGGGAC AAGAGAGTAG ATCCCAAGGA GATGGAACCT 840 CACTCACCCT CTGCCTAACC AGTCCTGGCC TACTGGGCCA TCTGGGGGCC TCATCTCTGA 900 TTAAAATGTC AAACTCCACA TCAGAGGCTA GGGAGAGACG TGGGAAGAGA TGACACCCTC 960 CATCTGTTTC TGGAAACTTC CACAGCCTGA TCCTATGATC CTTTACCAGG GCTGGGCCCA 1020 GGGATGTGGG GCCCAGAGTC ATTCCTGGTG GATGGGGGCT GGAAAGGAGG TAAAGTCCAC 1080 CCCTGGCTAA ATCATTCGTC TACCTGGAGA GAAAATTAGA ACCTCTGGGG AGTTTTCAAA 1140 AACTAGATCC CAATTAAGAA CTACTGAATC AAAATTGCTG GGGCTGAGAA CTGGGTGATT 1200 GAAATATTCT GCTAAGTAAG AACCACTGAT AGCACCCACC CACCTCACTG TAAAGACGGG 1260 GAAACAGGCA TAGAGAGAAA ATGGTGTGTG GGAGGCCCCC AGTTATTCTT GGTATAACTT 1320 ATGGAGGCAG AACCCAAGGA ACCTCTGAGA AGGGAACTGT GAAGTCGGAA ATCTGAGCTT 1380 TCCCTTTAAG AAGGAATCAG CTTTTGATTT AAAGTAAACT GAGAGGCAAT TCCTTGGACT 1440
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