Tag | Content |
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EnhancerAtlas ID | HS182-20134 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr7:104993560-104995230 |
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 | chr7:104993977-104993997 | TTGTTGTTGTTGTTTGGTGG | - | 6.42 | Tcf12 | MA0521.1 | chr7:104994500-104994511 | AACAGCTGCTG | + | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_25374 | chr7:104991033-104995488 | DND41 | SE_66307 | chr7:104994292-104995451 | Jurkat |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I105350 | chr7 | 104990788 | 104996910 |
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Enhancer Sequence | AGTAATTGCT AAGGAACTCC CAACTCCAAA GTTCCATAAG GATGACTCTT AATTGAAAAA 60 AGTAAGATAG CACAGTTGTA AGCTTCGACT TGGTAGTTTT AAATCTCAGC TCTACAACCT 120 ATCAGCTCTA AACAATGGGC CTGCTGCTGA ACATTTCTGT GCCTCAGTTC CTCATCTGTA 180 AAATGAGAAT AATAGTGCTG TTAGAATTCT TCCAGGTAAT GGTTTTGTTT TTTTGTGTTT 240 TTTTTTGAAA CAGTCTCCCT CTGTCACCCA GGCTGGAATG CAGTGGTGCA ATCATGGCTC 300 ACTGCAGCCT TGACCTCCTG GGCTCAAGCA ATCCTCCCAT CTCAGCCTCC CAAGTAGCTG 360 GGATTACAGG AGCGTGCCAT CCAGCCCAGT TTGTTGTTGT TGTTGTTGTT GTTGTTGTTG 420 TTGTTGTTGT TTGGTGGAGA CAGGGTTTTG TCACGTTGCT CAGGCTGGTC TCAAACTCCT 480 GAGCTCAAAT GATCCGCCTT CTTTGGCCTC CCAAAGTGAT GGGATTACAG ACTGCCTTCA 540 AGCAAATTCA TCAGGCCCAT GTTCCTGAAT GCCCCAAGGT GAGCAGTAAG GAACAGAAAA 600 ACACTTTCCT TCTCCAGAAA ATCCCACTCC TGAGCTGATA GGAGGGGATC TCAGAAAGAA 660 TCATCACAAA AGACAGGACA AACTAAAGAA GCTGGCAGAC TTTTTTAATT CTTCCCAGTA 720 CAAACTGGAA CTAGACATGC AGAGAGCCTT CCTAAAGGCA ACGCCCAAAT CCCACGTGAG 780 GCCAAACTTC TCCCCAGGGA GACTGAGAGC CAATGTTCTT ATCATAACAC TCCTCCCCAC 840 AGTGCACCCA CAGACAAGGA AGCCTGAGCA GTTGTGGCTG TCACACAACA GATGCAGCGT 900 TCAGGCCAGA ACCTTCCAGG ACCTTCCTCT TTGCTGGCCC AACAGCTGCT GCATCTGCCT 960 GGCCTTCGAG GAGCAGCCAG TATGTATGTG GCTGTGTGGA GCAAGAATGT GCCAAAATAA 1020 GCAACCAAGT CAATCAGAGA TGGGTTTGGG GCTAAGTTGA CATGGTAACA GGACCAGTCA 1080 CAGGTCTCCC CATGTATGGT GGGACCACAG AGCCCTATGT CCTCCATTCA TTCTTCTCTG 1140 GGCAGTTTCT GTCCAGGACA GCTATGGGGC AAATTCCACC TTATCCTTAA GACTCACCAC 1200 CTGGGTGTGC GTGGCTCTTG CCCGGCAGCT CATCCAGCTC ATCCACCCTG TACTCAGAGA 1260 TGCTTTTTTC CTCCTGCACA GGCTGTGGGT CCTTTCCCCT AACGAATCAC TCCAGGTAGT 1320 AGCCCACAGT CCTGGCCACA AAGGCCACAG GGTATGTAAC TTAAGTAGCA TAGGTAAGCA 1380 TTACGATCCA AAGCACAAGC CACACATCAT CAGGCAGCCT GGCACAATTT ACTGGGAATC 1440 CACTCATGCA TAGCAATGCA AGAGATCACA CCCTGTTTTA TGCAACAGTT GGGTACCACA 1500 AATAATCTGC AGCACAGCCC ATACTCCTCT GTCCAGCCCT GGTCTCTACC TGCTGGCTGG 1560 GAACAGACAT TGCTACTCCT AGCAGCCCAC ATGGCCTCCT GTTGTTTTTT AATAACAACT 1620 ACAGTCAGAT ATATAACTCA CATGTACAAT TCACCCAATT AAAGTGCACA 1670
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