Tag | Content |
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EnhancerAtlas ID | HS182-09469 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr17:42312300-42313630 |
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) |
EWSR1-FLI1 | MA0149.1 | chr17:42312386-42312404 | CCTTCCTTCCTTACCTCC | - | 8.14 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_34401 | chr17:42312220-42313452 | HCT-116 | SE_53422 | chr17:42312193-42313009 | Spleen |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I044234 | chr17 | 42311806 | 42314313 |
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Enhancer Sequence | TCCATCTTGG GAAAAAGTCA GCTGAGCACT CCTGCTGGGC CCTCAGGCCA TAACCCACAC 60 CTCCTGCTTC TGCTTCCTCA CCCAGCCCTT CCTTCCTTAC CTCCTGTCAG CTGGCTCTGG 120 GCCCAGGTAC ATGGGAAAGA AAACCTTCTG AGGTCACCAT GTGGTCTGCC AACCCAGCAG 180 GCTTTCCATG ATGTCACTTC ACTTTGCTGA GCAAATTTCA CCCATTTCTC TTCAGGCTAC 240 TTCTCAGATA TATTCCATTT CATAGACTCT ATTCCTTCAA GATATTCCAC CTCTCTCATC 300 ACTGGGACAG TTACTGCTTG TCCCTCAGGA GTCAGATCAA ATGTCTCTCC CTCCAAGAAG 360 CCCTGCCTTA CTCCAGCTCC CTCTGCTCCT GCCACTCCCT GCACAATACT AGTGTTTTCT 420 TTTGTTTTGT TTTTGAGACA AGGTCTCACT CTGTCACCCA GGCTGGAGTG CAGTGGCGCG 480 ATCACGGCTC ACTGAAGCCT TGACCTCCTG GGCTCAAGTG ATCCTCCCAC TGCAGCCTCT 540 GGAATACTGA GACTATAGGC GCTTGCCACC ACGCCTGGCC ACAATTTTTT TTTTTTTTTG 600 AGACAGGGTT TTGCCACATT GCCCAGGCTG GTCTCAAACT CCTGGGCTCA AGGCATCTGC 660 CCACCTCAGC CCCTCCCAAG GTGCTGGGAT TACAGGCGTG AGCACCATGG CCAGCCAGTG 720 CTCACTCTTG CTGAACGTCG GGCCCCATGC TGACTGCAGG TCCTATGATA GCATGGGCTA 780 TGTCAGCCCG CCTCTGCTAC TGACTCACTG ACATGCACAG ATTCCCAGTT TGCCTCCTTA 840 CAGCGAATTC CTCCTGTATG AATTCACTTC CAGGTGAATC ACTTTAATCA TGTCACTTCC 900 CAGCCCAAGA ACCTGCAAGA CTCCCTAATG CCTCCTGAAT CAAGTCCAAA CCCTTCTGGG 960 CAGTTAGGGT TCTTCAAACT TGACCTTGCT TTTTCCATCT TATATGAACC TCTTCTAGAA 1020 GGACTCACCT CTGCAGTCAA GACTTCCCTG TGCTGTCGAT ACACCATTCC CACCTCCCTG 1080 CCCTTGGCCA AACCACTCCC CTACCTACCT GGAAGGTACC CCACCCTCCA TTCTCCCTGA 1140 CCCTTGAGAA CAAATTGAAT TCCTTTCTTT TTGAGACGGA GTTTTGCTCT TGTCGCCCAG 1200 GCTGGAGCGC ACTGGCACCA TCTCATCTCG GCTCACTGCA ACCTCCACCT CCCGGGTTCA 1260 AGCAATTGTC CTGCCTCAGC CTCCCAAGTA GCTGGGATTA CAGGTGCACG CCCCCACACC 1320 CGGCTATTTT 1330
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