Tag | Content |
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EnhancerAtlas ID | HS187-14757 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:231557950-231559260 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr2:231558608-231558620 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr2:231558612-231558624 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr2:231558616-231558628 | GTTTGTTTGTTT | + | 6.32 | MITF | MA0620.2 | chr2:231558347-231558365 | TTTTGTCACATGACCTTG | + | 6.06 | MITF | MA0620.2 | chr2:231558347-231558365 | TTTTGTCACATGACCTTG | - | 6.06 | TCF7L2 | MA0523.1 | chr2:231558253-231558267 | ACACATCAAAGGAA | + | 6.91 | TFAP2A | MA0003.3 | chr2:231558286-231558297 | AGCCTCAGGCA | + | 6.32 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_64777 | chr2:231557370-231559718 | NHEK |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I230692 | chr2 | 231557328 | 231559770 |
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Enhancer Sequence | TGAACTCCTG GCCTCAAGTG CTGTGCCCAC CTCGGCCTCC CAAAGTGCTG GTATTACAGG 60 TGTGAGCCAC CATGCCCGGC TTACTTTGTT ATTCTTTATA TGACCCAGAA CACACTTTCT 120 GCAGTAAGTA CAGATTCTCA AGCACCATGA ATTGCCTCCT CTGTACAGGC ACTGGGCAAG 180 GCCTGGGAAC ATCACAGAGA ATACCCAAAG TCCCTAAGAA TTCTCAGGGG TTCCCCGGTT 240 ATCACTAGCC CGCGGGACCT CGCCACCGAC ATGCTTGTTT TATCAAGCTG AAGCAGGTAT 300 CTGACACATC AAAGGAAAAT CAACTATGGA TGGTGGAGCC TCAGGCAGCC AAAGAGATGA 360 TTACAGAATG GAGACATCAT CTGGGTCTCC TCACCCTTTT TGTCACATGA CCTTGCTGAA 420 ATCAGGAAGA GCACCTTTCG ATTCCTGTGA AGTTGCAGAG ATGGCAAGTC CTGTTGCTTG 480 CTGCCTTCAA ACACCCCTGA CTACACACTC AACCCAGTGG AGCCATCACT GCCTGTCCTG 540 TGCCCCCACC AAGAAGGGGA ATGAGATGAG GTCAGATTGA TTAAAAATGT GCATGCCTTT 600 TATTTTTTTG GCCTCCCCCT CCCCAGATTG TAGGGCTTCC CCTTGGCAGT TTTTTTTTGT 660 TTGTTTGTTT GTTTGTTTTG TTTTGTTTTG TTTTTTGAGA CAGAATTTCG CTCCTGTTGC 720 CCAGGCTGGA GTACAATGGC GTGATCTTGG CTCACTGCAA CCTCCACCTC CCAGGTTCAA 780 GTGATTCTCC TGCCTCAGCC TCCCAAGTAG TGGAGATTAC AGGTGTGCAC CACCATGCCT 840 GGCTAATTTT GTATTTTTAG TAGAGACCAG GTTTCACCAT GTTGGTCAGG CTGGTCTCAA 900 ACTTCTGACC TCAGGTGATC CACCCTTCTC AATCTCCCAA AATGCTGGGA TTACAGGCGT 960 GAGCCACCAC GCCCAGCCTC CCCTTGGCAC TTTTAACTTC CAGGCTTACC CTTGGCCTTC 1020 ATACTGGTCA CTAAGCCAGC TCCAAGACCT GAGTGGCACC TGCTCCAGTC CAGTTCTGCC 1080 TTGGCCTGGC TTCTGCCCAA TGCCTGTCCA GGGTGGGACC TAAGCTGCCT GGATATTATT 1140 TCCTCCTTCC GATAAAGGCA TACCTGGGTG TGTTTACCAC TGTCTCAGCT CAGAAGCATC 1200 TCAGACCAAT TCCTTTCTAT TTCACTCAAG ACAGAATGTG GGAGTTTCCC CTCCACAACT 1260 GCACCACTGC CTGAGGTGTC TAGGGCCACA CTTCCTTCTC TGAACTTGCT 1310
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