Tag | Content |
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EnhancerAtlas ID | HS182-04468 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:122610480-122611800 |
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) |
ALX3 | MA0634.1 | chr11:122611666-122611676 | TCTAATTAAA | + | 6.02 | PHOX2A | MA0713.1 | chr11:122611663-122611674 | TAATCTAATTA | + | 6.32 | PROP1 | MA0715.1 | chr11:122611663-122611674 | TAATCTAATTA | + | 6.14 | Phox2b | MA0681.1 | chr11:122611663-122611674 | TAATCTAATTA | + | 6.32 | Tcf12 | MA0521.1 | chr11:122611158-122611169 | CAGCAGCTGTT | - | 6.32 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_25355 | chr11:122610121-122611826 | DND41 | SE_59613 | chr11:122525607-122628654 | Ly4 | SE_61505 | chr11:122561031-122628026 | Toledo |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I122740 | chr11 | 122611325 | 122620507 |
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Enhancer Sequence | ACATTTGGGG CTGGGCAGTG GTTCAAAAGT ATCACTTTCC CATTAAGCTT TATGGGATTT 60 ACCTACAAGA TGGATAACAC ATCCTTCAGA CAGATGGCAC AGCCCTGAAG CCATTGCCTA 120 ATTTCTTCTT CAGTGTTCTC CTTTTATCCT GTCTTCTATG ATAGCTGATT TCCTTACATT 180 CATGTCCACC CAGAAATAAC TAGTTTCTAG AAAAGCTGTA ATATGGATTG TATTTCTGTA 240 AAGCCATATG TTCCATACGT CCTGACATCC TCGCAGATGC CATTTGATTC CATTTTGTCA 300 TATTCATTTA ATAAATATTG AGTGTCTGCT TGGTGCCTGG CATCTGCAGT GCAAAGAGGA 360 ATAATATTCA GTTCTACACG CTGAAGGATC CCATATTTTG TGGCAAAGCA AGATCTAAAG 420 ACATAATTTA AGTAGACTGT GAATAGGTTA ATTTGGAGCT ACTAACTGGC TATCATGCAG 480 GTGGGAATTG GGAGGTCACA AGAAACTTTC AGCAAATCTG GCATTTGAAC TGCACCTTGA 540 ATTGTGAACT GAATCTTCCC AGGTGAAGAA AAGGGGATGG GCTTTCCTGA CATGTTTCCT 600 GATGAAAGAG CATGTACTTG AAAGAGAATG GCTGGCTCTG TAAAGGGTGA ACCGTGTGTT 660 GTCCCAGGAT TAGGATGCCA GCAGCTGTTT ACTGAAAGCA CAATATGTGT TGTGTGCATG 720 GTGCTAAGTA CTTGTTTTAT TTCACTTGAT GCACACGGCA ACCATATGAG GCAGTCCTAT 780 TATTATTCCC ATTGTACATG GGATATCACT GATGCTTAGA GAGGTTGGAT AACTTGCCCA 840 TAACAGAGTG ATAAGCTATA ATTTGAATAT AAACCATCCT GTACACTCCT GAGTCTGTAC 900 TTGCAAGCGA CCCTGCCATA CCAGATGTGT GCAGGCCATC TGTGTACATG TGTGTGGGGC 960 AAGGGGGCAA GCTGAAGGCA GAAAGGTCAG TTGAGGCCAG CTTTGAGATA CTGAACACCA 1020 AGATAGAGGT TGTTGTAGAC AAACATCTCT GCATGTTCAT TTTTTATAAA AATTCACTAT 1080 ATTACTTTTA AAGTGAAACA GAACCCACTC TTTAGAGCAT TTTTTAGCAA AAGTCCTGCT 1140 TTAGTGGGAC ATAATGTGTA CATAAAATGG GGACTGAGGT TAGTAATCTA ATTAAAAACA 1200 AATCGTTCGC AGGGATTTTG ATTCCTTCTT ACTTCAAAGC GCATATTAAC ATATAAATGA 1260 ATTCTGTCCT CAAGGTAAGC CCCAATTACG TAAAAGTATT TCCAGGTTAT TCGCTCTTTT 1320
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