Tag | Content |
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EnhancerAtlas ID | HS187-12788 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:8450130-8451880 |
SNPs | Number: 2 | 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 | chr2:8450888-8450906 | GGGAGGAGGGGAGGAAGT | + | 6.36 | FOXP1 | MA0481.2 | chr2:8450733-8450745 | AAGTAAACAGGA | + | 6.07 | Foxo1 | MA0480.1 | chr2:8450734-8450745 | AGTAAACAGGA | - | 6.32 | NR2F1 | MA0017.2 | chr2:8450657-8450670 | CTCTTGACCTCTG | - | 7.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_20349 | chr2:8448174-8458311 | CD56 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I008309 | chr2 | 8449764 | 8451750 |
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Enhancer Sequence | CCTGGTTAAC ATGGCTATGT TAAAAGAGGG GGACTTTTAC TCCATCTGAA ACCAAGTGGC 60 AGAGAGCGTG TGGTGGCAAT GGGGTGGGGG TGGCTGGGTA TGTCTGCATT CCCTGGATAG 120 AAATTTATAG CGAAATGGGT GGCAATCATT TCTGGTTGTT AGATTACTTA TCTGACACAG 180 GGCTAACAAC TAAGAGTTGC TGAGAAAGGC AGATGTAGTT TAGAGCAGAA GGGCACGGGA 240 TCCCACTCCT GAGTCCTGCA GTAAAGTGGC TGTGTGTGGC CTGGTCAAGC TGCCCACTGT 300 GGCTGGGACT AGGGTTCCTC CTTTAAAATA CAAGGGGACT TAAACTAGAA GCGGCGTGGA 360 GAATGACTAG CACCCCAGCT CAGCACCCTG GTGGCTTCCC ATAATTTACT CCTCCAACTT 420 CTCGGCAGCT CCGAGACACA GGCAAGTGGA CTGAGCAGCT TAACTTTACA GATGGCGGCA 480 AAAGCGTGGC TCTCATGGGA GGGGGTGACC TATCCTTGAG CTCAGATCTC TTGACCTCTG 540 GGGTCTAAAA AATTACCAAG ACAAGCCTGG GGGAGTGGGC CCCAGAGAAG GAGGGTGACC 600 CACAAGTAAA CAGGAGAAGT GGGGTGTCTT TCTAACTAAC CCTCTTATCA ACGTTCCGAG 660 TATTTGCCCT CAAATGGTTA ACCAAAGTGA CACCCAAGGC AGAAACGGGC CTGGAAAGGT 720 CCCTGATGCA CAGAGGCTGG TGTGGCGGGA GGGTGTGTGG GAGGAGGGGA GGAAGTGGCA 780 CTCTGGTGGC TTTGTGCAAT TATTTTCCAA GACTAACAGG ATGCTGTTTT CTTCAAACAA 840 ATCTGATGTC CTTGTGCCCT ATTGCCCTTG ATTTAGATCA GTTTCAAAGA CAACTTCCCC 900 CAAGGTGATC CAGGCACGTG ATGCTCCTTT TAAATTGTCC TTCAGAATGC GTTTGAAGTA 960 TTGGTCCTTG CTAGTGGGTA CATTTTCCTT GGCCCAGCTA ACTATCAGGT CGTTTTCAAA 1020 GTAGTTTCTT TCAAAAGTAG CCCCTTTGAA GTAGTTTCTC AGTAGACATT TTGGCATCAA 1080 ACTGTACAGA CATTTATGTA AAACATCACA TCAGCCACCA GGCTGCTTCA GAGGCCGAAA 1140 GCAGCTCAGG GTTTATCATG ATCTAAGTGT CCTAGCCAGT AAGTGAGAGA GGGCTCCCAA 1200 AAAGGCAGAA CAGAGACAAA GGTCGAAAAG CAAAGCCATC TCACTCCCTC GGTCACTTGC 1260 CCACTCATTT CAAAGAGGCA TAAGGAGCCC CAAATCCACG CTACCTCTAT TCTAGAGATG 1320 AATGAGGCAC AGTTCCTGCC ATCAAGAACT CTGCAGAAGG AAAGGAAAGG CTGACACCAG 1380 CCACAGTGTT GAGAGGGAAG TGCAGGACAG GTTAGGAGGC TCCGGAGGGC AGAGAGGCTA 1440 TTGGCTGAGG CTAGAGGAGG CTTCTGGGAT GGATCCTGGA AGGATAAATG GGGTTCCTCC 1500 ATGTGCTCTA TCTCTAGAAT GCAGTGGCTT ATCCAGAGGT GTGCTCAGTT GAAAAAAATA 1560 AAACTTGATT TTCAATGTTT GCCAATTTCC TTGTTGTAAA CACTCCCACC TAAGAATAGC 1620 AAATTTTAAG TTACCAATGG AGACCAACGT GACTTCACTG AACGCAGAGT TGGGAAGAGA 1680 CAGGCAGTGG CCACCGTGAT ATAGTATGTC ACCCTACAGA CAGGAGGGGC ATAGAATACC 1740 TTCAGGAAAA 1750
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