Tag | Content |
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EnhancerAtlas ID | HS176-10995 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr13:33692770-33695030 |
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) |
FOXP2 | MA0593.1 | chr13:33694127-33694138 | TTTGTTTACAT | - | 6.14 | HOXA13 | MA0650.2 | chr13:33692924-33692935 | GTTTTATGGGG | - | 6.02 | IRF1 | MA0050.2 | chr13:33693903-33693924 | AGTTACTTTCTTTTTTATTCT | + | 6.2 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_45536 | chr13:33692809-33694613 | Osteoblasts |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I033119 | chr13 | 33693289 | 33695226 |
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Enhancer Sequence | AGCAGAACAG ATAAAATTCC CTGCCCTTTA GGGTTTACAT TGCCATGGGG ATTTTGAGAA 60 CGTCTGGTCA ATGGGAGGTT TGGTGAAAAC AATGTGGGTC GTGGATGAAA GAATCCCAGA 120 TAAACAGCCA TATCCAGTGC CCCTGCAGGG GAGAGTTTTA TGGGGAATAT GTTCATGAAA 180 CAGACTAATA TCATAAGTAC ATATTTTGAT TTAAGGAATT TATTTACTTT TTCTTCTTTG 240 GAATTCTTGG CACTTACTTT TCTACCTGTT TGTTTTTATG CAGTAAGCTA TGGCTCTAGT 300 GAGAATGATT CCTGGGTGGC TTTTTTTTCA GACCTCAAGA TATTGTCATA TCATGCCTTT 360 TTCATCTTAG AGTCTAGACT CCTCCCCTAC TTGATGAATA AATGGAGCAT TAAGGCATCA 420 AGGACAGAGT GGCCCTAATG AGAATGAGTG AGGCAGAGCA GAGCCCGGCA AGAATGAAGA 480 TCCTGCAATG GTGGGGCAGG TTAAGCTCTA GGCCCTCTAG AGGAACTTTC TGTGCTGGAC 540 TTACCCGCTA TTCAAAAAGG AACTGAACTT TCCTGGGCAC CCTGGCTTAT AGTGAAATAA 600 TATGTCTGCT ATTTTTTAAA TGCCTATAGG GAGTTGATTT GCTTCAACCC TCAATTTTCA 660 CAGCTCTCAT TCCCCAGTGG CTCATGGGTT GGCCCACTTC TGCAAAGCAA GGTAGAACCT 720 TCCTGAGTGG CTGGTCAGGT AGACAGTGGC CACTAGTGTC AGCCACTGCT CATCCCCCCT 780 ATACCTGGAG GAAAGCCTAA TACAGGTCGT CTTACTGATC ACTCTGTGTG CCAGGCCGGC 840 CTCCACCCAA GTTCGGGTAT GTGACAAAGG CTTTCCTGAT TGCTGCAACA AATGGAGAGC 900 AGTCCTCATT CTTTTAAATT GTGGTAACAG CAGGGGAAGG ATTCCAAGCC ATTAGAGCAT 960 ACTCAGGTTT TTGTATATGT CAGCCGAATG GATCACAGGG GAAATTATAC ACTGCTACTT 1020 TTTGTGGCCA TAAAAACAGA ATTCTTAGTA ATATTTCTTT GCATTCCAAG GTTTATCGCT 1080 CTAATCCCAC ACATCAGGAT ATTCAGGCTG ATAATATTGT CACTTAAAAT ATGAGTTACT 1140 TTCTTTTTTA TTCTTAAAGT TTGGAATGTC TAGAAAATGC ACAGTTTTGC CATACTTAGA 1200 TGATTCGCCA CAAAGAATCC AGACAATATT TATCTTCCTT CAACTGGCAA CAACTCCAAA 1260 TTTCATCAAA GGGCATGGAA AGAAAGCATG TACTGTCAAA AGAGAAAAAA ATTCAAGATG 1320 TCAGGTGAGT GATTATTGGG GTGAGATCCA TCTCCGATTT GTTTACATCT TCTGCTTTTC 1380 TGATTTTGGA AGGAGGCCCA GGACTGTGCA CACCACAGGG CTGGCTGTGC TGTACGAGAG 1440 TTCTCATAAT CGAGATGCCC TGAAGGTAAA TACTTCAGTG TGACTCACAA ATATTTATCC 1500 TCATATGAGC AGGTATTATT CCATTTGAGA AGAATTCCTA CTTTTTTAAC AGCAGAGAAA 1560 TGTTGATCAG GATCTACAAA AAGAATAAAG CAGACAGTGT TTCTGTTTAA ATTGTCGAGC 1620 ACGTTCCTCT TTTGTCCACC GTGTCTTGCG GGCTGTTTCT GGGCACACAG TCATGTGCGT 1680 GCACACACAC ATCCCAGAGA TGCTATCTTT GTATTGTTTG GTTTCCAAAT TTCTTTCTCG 1740 TTTCAGCAAA TATTGTTATT TTAATTATTT TAGACATGTC TGCAGCTCTC CAGCTGTGGG 1800 CTCTGAGCTG CTTTTTCTGA CTGAGATCTT AGGATGTCCA GAGGGTAGTC AGGGATTTAT 1860 TGTGCTGCCT CGAAGTCTGA CAATAACCTT CCTGCCCTGG CCTTGTCTTC TAGGGGACAT 1920 GGGAAATATA GACGTATATA TATATTTTGG TTTCTGTGGA TTTTTGTTGG AAGTACAGCA 1980 GGAAAATTTT CTTTCATAAA CCTAATAAAG AAAAGGTGGT CTCAAATCAG ATTCCAGTTA 2040 TAGTAGCTGA AGATGGCCAA AGGGAAAGAT GGAAAGAACC TCTCTTCAAA GCTATTGATG 2100 AGCTGATGAT TGAGCTAACC CTGGAACCGT TCTATTTCCT GACTTTTTTT TTTTTTGAGA 2160 CGGAGTCTTG CTCTGTCACC CAGGCTGGAG TGCAGTGGCG CATTCAAGTG ATTCTCCTGT 2220 CTCAGCCTAC TAAGTAGCTG GGATTACAGG CACCTGCCAC 2260
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