Tag | Content |
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EnhancerAtlas ID | HS187-13243 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:54220970-54222540 |
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) |
HES2 | MA0616.2 | chr2:54221521-54221531 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:54221521-54221531 | GGCACGTGCC | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 54221629 | 54221800 | chr2 | 54221958 | 54222266 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I053993 | chr2 | 54220370 | 54223125 |
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Enhancer Sequence | AGAAAGTTGA GAATTTGTAA AGTAAGGAAG AAAATAATTT GGGAAAGAGG ATGTATAATA 60 TAGGAAACTG GGCCAGGCAC GGTGGTTCAC GCCTGTAATC CCAGCGCTTT GGGAGGCCGA 120 GGAGGGTGGA TCACCAGGTC AAGAAGTTGA GACCATCCTG GCTAACACAG TGAAACCCCG 180 TCTCTACTAA AAATCGTACA AAATATTAGC CAGGCGGCTG GGCGTAGTGG CTCACGCCTG 240 TAATCCCAGC ACTTTGGGAG TCCAAGGCGG GCGGATCCCG AGGTCAGGAG ATCGAGACCA 300 TCCTGGCTAA CACGGTGAAA ACCCTTCTCT ACTAAAAATA CAAAAAATTA GCTGGGCGTG 360 GTGGCAGGCG CCTGTAGCCC CAGCTACTCG GAAGGCTGAG GCAGGAGAAT GGCCTGAACC 420 CAGGAGGCGG AGCTTGCAGT GAGCAGAGAT CGCGCCCCTG CACTCTAGCC TGGGTAACAG 480 AGCAAGACTC CGTCTCAAAA AAAAAAAAAA AAAAAAAAAC GAAAAAAAAC AAAATATTAG 540 CCAGGCATGG TGGCACGTGC CTGTAGTCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC 600 ACTTGAACCC AGGAGGTGGA GGTTGCAGAG AACCAAGATT GCACCACTGC CCTCCAGCCT 660 GGGTGACAGA GTAAGACTCA GAAAAAAAAA AAAAAAAAAG AGGAAACTGG CAGGAAAGAG 720 GTCATGCTGG GGTGGACTAT GAGAGGCAAT AATTCGAAAT TATATCGTGG AAATGCTTCA 780 ACCTCTACCA AGACCTACTT CAAAAGGAAA ATCTTGTGTT GAGTAGCAGT TAAAAATGGA 840 ATAAGATATC AGACCTTCAA CCAAATAGTT CTTAATAGCT CAAAACTACT ATAGGATAGC 900 AATTTTATTC CCAAATTATT CTAGAACTGA ATATCTGAAA CTCAGTGACC AAAAGCCAGT 960 CAACCAATCT TCCACAGCCT AATACACACA CATAAAATAT ACCTCTGGCA TTACATTATA 1020 ACTTCCCCCA TCAAACAAAA CAGGAAGAGT GGTTATGTTG GGCTGATAGT GTAAGATGGT 1080 CTGTCATGTA GCGTTTCCGT TATATTCTGA ATTTGAGTTG GTATACCATG TGACAGTTCT 1140 TTATATATAT GTTTTCAACA CCGCTATGAC AAGAGTGTCT TTCTGTTTTT GCGTCAGTGT 1200 CTCATGAAAA GAAGACATAA AGAATATTCA AAAGAAATTT TAAGAATCTT TGTTATCTGA 1260 AGGTCGTATC TTTAGTGCAT GTTCTGTCTC TCATAGTTGC TAAACTCTAG CTGCAGCTCT 1320 TCTCTCAGAG AACTGCTCTG TCCTGCCCAT CTATCCCATT ATGACTTTCA GTTGTGAGAT 1380 GAAGATATCT GTTTGAGAAA AAAAATTGGT TCCTCTAAAT AGAGAAATGT CCAAATAGCT 1440 ACTTTAGTCT CTTCTTTAAT CTCAAGTTAC ATCAGAGAAA AGATTTCAGC ATGTATAAAA 1500 CATCCATATC TACAGTGACC TTGGTGTTTT TCTCAATGCA TAAATCATCA CATTTCTTCA 1560 TTTTCTAGTG 1570
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