Tag | Content |
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EnhancerAtlas ID | HS059-03833 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:204421370-204422920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr1:204421660-204421674 | AATCCCAAGGGAAT | - | 6.57 | EBF1 | MA0154.3 | chr1:204421660-204421674 | AATCCCAAGGGAAT | + | 7.04 | ZNF263 | MA0528.1 | chr1:204422805-204422826 | GAAGAAGGGAGAGGATGAGAA | + | 6.66 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00064 | chr1:204417530-204422553 | Adipose_Nuclei | SE_03975 | chr1:204421893-204422820 | Brain_Anterior_Caudate | SE_04850 | chr1:204421758-204422908 | Brain_Cingulate_Gyrus | SE_05834 | chr1:204414554-204422838 | Brain_Hippocampus_Middle | SE_06778 | chr1:204419046-204422484 | Brain_Hippocampus_Middle_150 | SE_07775 | chr1:204421681-204422937 | Brain_Inferior_Temporal_Lobe | SE_10255 | chr1:204419836-204423398 | CD19_Primary | SE_10905 | chr1:204414650-204438582 | CD20 | SE_25125 | chr1:204417816-204422942 | Colon_Crypt_3 | SE_26688 | chr1:204416875-204421560 | Esophagus | SE_28866 | chr1:204417158-204423024 | Fetal_Intestine_Large | SE_30246 | chr1:204418561-204421552 | Fetal_Muscle | SE_31610 | chr1:204417780-204422694 | Gastric | SE_34711 | chr1:204415846-204421729 | HeLa | SE_37407 | chr1:204418938-204421997 | HSMMtube | SE_40776 | chr1:204417564-204421617 | Left_Ventricle | SE_40776 | chr1:204421796-204423031 | Left_Ventricle | SE_42225 | chr1:204417746-204421550 | Lung | SE_42225 | chr1:204421747-204422546 | Lung | SE_48201 | chr1:204414946-204421702 | Psoas_Muscle | SE_49909 | chr1:204419158-204422984 | RPMI-8402 | SE_50149 | chr1:204415315-204422829 | Sigmoid_Colon | SE_51536 | chr1:204417745-204423045 | Skeletal_Muscle | SE_52421 | chr1:204416678-204422949 | Small_Intestine | SE_58430 | chr1:204415099-204506026 | Ly1 | SE_59794 | chr1:204415680-204491493 | Ly4 | SE_62377 | chr1:204415291-204492168 | Tonsil |
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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 |
GH01I204445 | chr1 | 204415101 | 204423341 |
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Enhancer Sequence | CCAATTTTTT AAAGTTCCTC CTGGGCCAGA ACACTGTGCA GCACCCTTTT TTTTTTTTTT 60 TTTTTTTTTT TGAGACAGGG TCTCGCTCTG TTGCCGAGGC TGGATACTCA CTGCAGCCTT 120 GACCTCCCAG GCTCAAGTGA TTCTCCCACC TCAGCCTCCT AAGTAGCTGG AACCACAGGT 180 GTATGCCACC ACACTTGGCT AATTTTTTGT ATTTTTTGTA GAGATTGGGT CTCCCTTGTT 240 GCCCAGGCTG GCACCCCTTC TCTTGACAGC AGCAGTAATT GTGACCAAAA AATCCCAAGG 300 GAATGGTGGA ACTCAAGGGC CATTTAATGC AGCTATCCTC TGCCTGCAAG GAGTTTCTCC 360 TGTCCTGGCA GTTGTTTGCT TGAGGACCTT TAATGCACAC CCCATGTCCT TTTTTTTTTT 420 TTTTTTTTTT AAGATAGGGT CTCACTCTGT TGCCCAGGCT ATAGTGCAGT GGTGTGATCA 480 TGGCTCACTG CAGCCTCGAC CTCCCAGGCT CAAGTGACTC TCCCACCTCA GCCTCTTAAG 540 TAGCTAGGAC TACAGATGCA CGCCACCACA CTCAGCTCAT TTAAAATAAT TTTTTAGTAG 600 AGATAAGGCC TCTTTGTGTT GCCCAGGCTG GTCTCAAATT CCTGATCTCA AGTGATTATC 660 CCGCCTTGTC CTCCCAAAGT ACGGTGAGAC TACAGGTGTG AGCCATCGTG CCCAGCCATA 720 TACACCTTTA TTGCTCTAAG AATTACCTAA GTGTGAAGGG CATGAGAAAG GGTCCATTTT 780 CCCAGTTGTC CATCTGTAAA AGGACCCACC TCTTCCAGCA TCTCCAGATT CTTCATCTAC 840 CTATTTTGCA TCCTCGGCCT CCCCAGGACC CTCCTCAGTC TCTTTAATCT GTGCTACAAA 900 TACTTAGCTT GCAGTGCTGC TCTGCAAATG AGGACTCTAA TATAGTCAGT GTGGGGAAGC 960 AAAGCCGGGG GCAGCAAACA GGGGATTTTC TGACTGACTG GAAGGAAGGT AGAGCATAGC 1020 ACAGATGAAG CACAGGGCAG GAAAACCCCT GCGGTGCCCC CATTCAAGCA AGGCACCCTC 1080 TCCTCCGTTT CCTTCCTGCT TTGCTTGGCT GACGCCTACC TTCCCGACAC CAAATTATTG 1140 TTTACATGTG GTGATTAATA TTACCTTGTG CTTTTGGTTT CATATTTATA TTTATAACCC 1200 ACCTATCTCA TCTCGACGCC ATAACTGCCT CTGAGTGAAA CCAATGTCCC CATTTCTCAG 1260 TTTGAAAAAA TGAGGCACAG AAAGAATAGA GAGAAAGTAG TATTCGAGAC AGAGCTAGAA 1320 ATAGAGGCTC ACTCCTGGGA ATCCAAGCTC AATATTCTTT CTCTAGACAA CCCTCCCTTC 1380 TCTATATATA AAGGGAAAAG CACAGTCTCC TCTCCATAGT CTACAGGAAC TGAGGGAAGA 1440 AGGGAGAGGA TGAGAAGCCC TCCAACTAGT TAAACTCTTT AAGGGAGACA AGATCAAAAA 1500 ATAAAGTATT ATTAAAATTA ACAACTAACA TTTAATTTTT TTTTTTTTGA 1550
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