Tag | Content |
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EnhancerAtlas ID | HS073-03444 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr12:112214800-112216010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr12:112215354-112215372 | GGAAGGAGAGAAGGATGC | + | 6.18 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_00590 | chr12:112208849-112216385 | Adipose_Nuclei | SE_09863 | chr12:112208638-112219903 | CD14 | SE_23600 | chr12:112214606-112216143 | Colon_Crypt_1 | SE_24557 | chr12:112214736-112216115 | Colon_Crypt_2 | SE_27423 | chr12:112214605-112216165 | Esophagus | SE_28501 | chr12:112210440-112216206 | Fetal_Intestine | SE_29428 | chr12:112210430-112216401 | Fetal_Intestine_Large | SE_31648 | chr12:112210406-112216470 | Gastric | SE_42456 | chr12:112210459-112216201 | Lung | SE_50330 | chr12:112214664-112216375 | Sigmoid_Colon | SE_52697 | chr12:112210388-112216342 | Small_Intestine |
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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 |
GH12I111772 | chr12 | 112210428 | 112216668 |
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Enhancer Sequence | GTGAAATCAA CGTGTGTTGA GTCAGTAAGT AAACCATAAA GATGGAGATT TGGGAATCAG 60 AATTCCAACC TCCTTGAAGG CAGACCTGGG CTATGGCTGG AGGTTGGAGT TGGGAAAAAC 120 ACAGGCCTTG GAGTCCCAAA GACCTGGCTT CAAAGCCTGG CTCTGCCTTT GCTGCTGTGT 180 GACCTAGAGC CAAGTGGCTG GACTCTTCTG TGCCCAGCAT CCTCTGCTGT GAAGTGGAGA 240 GGATGAAGTT CACCTCCTAG GTTTGCTATG AGGTTTAAAT GGGAACAATC CAAGTACACA 300 GAACCGCTGG TGTGGGGCTG GTTCTTGAGG GGTAGCTAGT GAATGTTAGC CATGTCCATG 360 ACACGCAGAG GGCTGAGTGG ACTTCCTCCC TGGGTGGGGG AGGAAGAAGC TTGGGGATAG 420 TACAAGGCCA ACCAGACCTA CTTCCACCCA GCCCAGCCTA GTGCTTCTCT GTACTCTCCT 480 AACCCTGCTG ACCCAAGTGC TTTGCTGTGA GGCAGTTGTG TGTGAGGCGT GAACCCTGAG 540 CCTGTGCTAC AGGGGGAAGG AGAGAAGGAT GCCTACTCAA TGGCTGCAAG CTGCCTGCCC 600 GCCCCCCACG CCCGTGAGCC CCCATCTTCC AGCAGGCAGA CCCGGGAACT CCCTTCTCCT 660 CCACGGGCAC CCCGAGGAGG AGCTGACTTT CAGAGTCGGG GAGTAAACAC CCAGGACCTG 720 CTGCCCAGGC ACGGCATAGT CCAACTTGAA CTTAGGTCTG GCAGTTTCCT GGCTTTGAAC 780 CTGAGCTCTT TATTGCCACA CCTGTCCCCA CACTGGAAAT GACCCAGCCC TCCCGTGGAA 840 AGAAAGAAGG GTGCCATTTC CCTAAAAATT AACGATTGAC TAACTAATAT GAAACCACAC 900 AAGCACGCCT CCAGAACCCC AGTTAATGTT TACCCATGTT CTTCTCCGGT GCCAAGAGCC 960 TTTCCTGTGG GTGCACAACT GCGGGTTCCA CCATAGAGAT TATGCGGAAC AAATTTCAGC 1020 CTGGGAATAT GATTCCTGCT AGGCCCTTAC CTGAACGACT CCTTCCTGGG GCACTCTGTT 1080 TCCACCCTGC CATCGTCATG GCGTTGGGCA TTCACTCCAT GCTTGGCGCA GAGACTGCAG 1140 ACCCTCACAT GGCTTTATAA AAAGGGGGCT CTAGGGTGAT TCCCACCCTA CAGATGAGGA 1200 AACAAAGACA 1210
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