Tag | Content |
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EnhancerAtlas ID | HS095-12765 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr17:43653740-43654950 |
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) |
EWSR1-FLI1 | MA0149.1 | chr17:43654277-43654295 | TCCTCCTTCCTTTGTTCC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr17:43654748-43654763 | GAGGTCAGAAGTTCA | + | 6.38 | RARA | MA0729.1 | chr17:43654748-43654766 | GAGGTCAGAAGTTCAAGA | + | 6.88 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_24643 | chr17:43654536-43654924 | Colon_Crypt_2 | SE_64997 | chr17:43652951-43655118 | NHEK |
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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 |
GH17I045576 | chr17 | 43653767 | 43655170 |
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Enhancer Sequence | AAATCCCCAA ATATTTGGCT AAAACAATTA ATGCACGAGG TCCTGGAGGT TAAGGGGGTG 60 GGAAACAAAG GAACTCAGCC CCAACTGGGG GTAAAGGGAA TGGTGATCAG AGAAGGCAGG 120 CTGGAGAGGG TGATGGATGG GTGACTAGGA GGTGGGTCTG TGAGAACTAC GAAGAAATAA 180 GTATTACTAG ATCAATTTGA GATGAAGAGA AGAAATAAGG AGTGAACAAG GAAAAGAGAA 240 ATAAGGGGGA TGTAAAAAGT AAAGTAGAGG TTCCTCTTCA AGACTTTCCT CTCTAATTAA 300 GAATAAATAG TAACTTCTCT TAGAAGCAAA ATTTATTCAA AGACCTGTGC TAACATTCTT 360 AAATATCTGC TAGCCATAAT AAAGAAATCA ATGTACTTTA TGTTCTTAGC TCCCACAATT 420 TAGCCTAAAT ATTTGCCCTG GCACGCTTAG GCTGGTCCAA GCAAGCATTA GGTCATAGCC 480 TGTTCCTCTT CCTTATTTAA AAGTGTTTTT ACCTTTCTCA ACATTCCACA AGTTACTTCC 540 TCCTTCCTTT GTTCCCCTCT ACCTTTGCCT CTTTTAAAAA GTTCTAAGTT ACTAACCAAT 600 CGGGACAAAT ACAGAATGTG AGGTCCCGTT CCAGCCAAAG GAAACCGGAA ACAGCAGTAA 660 GGTAGATGCG TCAGGTTATA AATGACCCTA TCTCCTTTGT TGGGTGTACT CTCATGGCAA 720 AACTGCCCGT GAGTGTACCC TTTCTGCAGG AAGTAAAAAT GGCCTTACTA AGTAAACTAA 780 ATTTATGTTC AAGTGCTGTT TCTTCACGGC ACCGGGGAAC AAGCATTTCA AACAGGAGAT 840 TTAGAAGTCA GTTCATCCTT GACTCCTTTC CTCCCGCTCA CCACATCCCA GCCTAACCAA 900 TCTATCTCAT TCAGGATTCA TTCTAATGCC TGAATTATTT TCTGCCAGGT GCTGTGGCTC 960 ACACCTGTAA TCCCAGCACT TTGGGAGGCC AAGGCGGGTG GATCACTTGA GGTCAGAAGT 1020 TCAAGACCAG CCTGGCCACT TGAACCGAGG AAGAGGTTGC AGTGAGCCAA GGTCATGCCA 1080 CTGTACTCCA GCCTGGGCGA CAGAGTGAGA CTCTGTGTCA AAAAAAAAAA GAAAAGAAAA 1140 GAAATTAAAA TTGAATTTGC AATAATCCAG CAAATAATCC TATTTATATA CCTAAGAGAA 1200 ATGAAAATAT 1210
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