Tag | Content |
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EnhancerAtlas ID | HS184-05303 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:34675150-34676220 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr11:34675662-34675675 | ATATGCAAATGCT | - | 6.33 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_23244 | chr11:34674252-34676211 | Colon_Crypt_1 | SE_26655 | chr11:34673708-34677938 | Esophagus | SE_31738 | chr11:34673765-34676924 | Gastric | SE_33847 | chr11:34673660-34677748 | HCC1954 | SE_34914 | chr11:34672715-34678354 | HeLa | SE_35339 | chr11:34673649-34679228 | HepG2 | SE_41618 | chr11:34675235-34676052 | LNCaP | SE_50680 | chr11:34674352-34676099 | Sigmoid_Colon | SE_52951 | chr11:34673750-34676443 | Small_Intestine | SE_56256 | chr11:34671428-34679748 | u87 | SE_57552 | chr11:34675295-34676229 | VACO_503 | SE_64547 | chr11:34674107-34677482 | 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 |
GH11I034652 | chr11 | 34673801 | 34678102 |
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Enhancer Sequence | GCCCTAAAGA ATCAATGCAG TCTCTGGGGT TGGTGTATTC ATTGGGGTAA TAGCCCTTCA 60 GTAGGATAGT TAATTACAGC CTTATATGGG TCAGTTTCTT TCAGAATAGT TTATAGTCTC 120 TACTGCATGG AAGCAGAACC CCGGAAAAAC CTTGGTCATT TGCCTGAGTC TTTATTTTTC 180 GAGCTCCCAT GTAATTGAAT GCAGTGAAAT ATCTTTCTAT GTTTTAATGC TAGTTACCAG 240 CTGAGCTAAG GCGAGGCCCA GCGTAAACTG ATGCCCTCTG TGATAAACGC AGGTGGGGAA 300 ATAGGCTTTG TTTTGATTTC TCTGTCATCT GCCCATTTCA TAAAATGCCC GCTGCCGGTG 360 TCCTGTTCTG CTCGACAGTC CTCCAGCCTG TCATGCCAGC TCGGGCTTGA TGTGTTTATC 420 CACTGACTTG TTGAGCCTAA AGCTAGGGTG GCACGGTCTA TTAGAACACT GAAATTTGTA 480 TATCCCGTAA AGAAATGGCT CACAGCTGAA TCATATGCAA ATGCTTCTAA TCTTTGCTTC 540 TTGCGAAGCA GCTTAGCTGA AGTCACGCTC TCTCACTTGC ATCACAAACC TGTGGCTTGT 600 TGCTGCCCCT GCCTGGACTG GATAGGACCT TGGCCTGGAG TGCCTGGGAG CCAAGCAAGA 660 GAAAGCCAGG CTGGACAACT TCTCCAGGGC AAGCCATTAT TTTATAAGAA TGAATCACTT 720 AACCACATGG CTAACTTCAA AGGTCTTGAC TTTTATCCTA GGGCAGAAGA AGGACACATA 780 TTAAAGAGAG GTTAAAGATC AAAAGATATC AGTGGTAAAG CAGGCCAGTG ATTCCACGGC 840 TTACCCCTGC ACACTGCAAC AGGCAGAGAG GTCTGGAAGA AATTAGGTTC TTCTTTTGCC 900 TTTGACTGCT TATTCCCCTT TATGATGATG GAAAGATTTT TATTTGGGGA TTAAAAAAAG 960 AACGTTCCTA GCTGGGTGGA GCCTAGCTTG GGTAAACGGC TGACAACTCA AAGAATATTT 1020 CCTCATGGTT TATCTAGTGT AGAGGTTTTA GAGTCCATGG ACTGCTGCAT 1070
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