Tag | Content |
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EnhancerAtlas ID | HS133-00609 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:22259470-22261150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:22260239-22260257 | CCTGCCCTCCTTCCCTCC | - | 6.94 | IRF1 | MA0050.2 | chr1:22259726-22259747 | GAAAAGAAAAAGAAACAAAGA | - | 6.27 | PLAG1 | MA0163.1 | chr1:22259471-22259485 | GAGGCCGAAGGGGG | + | 6.33 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00032 | chr1:22219419-22267496 | Adipose_Nuclei | SE_00908 | chr1:22257227-22261178 | Adrenal_Gland | SE_01556 | chr1:22255302-22261200 | Aorta | SE_02999 | chr1:22259717-22261042 | Bladder | SE_06476 | chr1:22259338-22261230 | Brain_Hippocampus_Middle | SE_23160 | chr1:22259914-22261112 | Colon_Crypt_1 | SE_23793 | chr1:22259948-22260936 | Colon_Crypt_2 | SE_24796 | chr1:22259841-22260926 | Colon_Crypt_3 | SE_25801 | chr1:22255322-22261322 | Duodenum_Smooth_Muscle | SE_26605 | chr1:22257148-22267389 | Esophagus | SE_28012 | chr1:22259788-22261138 | Fetal_Intestine | SE_28954 | chr1:22259743-22261125 | Fetal_Intestine_Large | SE_29681 | chr1:22259549-22261125 | Fetal_Muscle | SE_36920 | chr1:22219607-22267740 | HSMMtube | SE_37945 | chr1:22255424-22263634 | HUVEC | SE_39947 | chr1:22259818-22261137 | K562 | SE_40620 | chr1:22245016-22267401 | Left_Ventricle | SE_42167 | chr1:22255391-22261338 | Lung | SE_44366 | chr1:22256010-22261093 | NHDF-Ad | SE_45173 | chr1:22259606-22261097 | NHLF | SE_45699 | chr1:22255392-22261252 | Osteoblasts | SE_46764 | chr1:22259750-22260910 | Ovary | SE_47433 | chr1:22256278-22263564 | Panc1 | SE_48478 | chr1:22259611-22261201 | Psoas_Muscle | SE_48565 | chr1:22255431-22261202 | Right_Atrium | SE_49456 | chr1:22259694-22261125 | Right_Ventricle | SE_50206 | chr1:22259642-22261140 | Sigmoid_Colon | SE_51733 | chr1:22256087-22261431 | Skeletal_Muscle_Myoblast | SE_52462 | chr1:22249821-22261125 | Small_Intestine | SE_53700 | chr1:22257155-22261200 | Spleen | SE_54522 | chr1:22243934-22263810 | Stomach_Smooth_Muscle | SE_63519 | chr1:22259557-22261240 | HSMM | SE_68865 | chr1:22259621-22261105 | H9 |
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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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Enhancer Sequence | GGAGGCCGAA GGGGGTGGAT CATTTGAGCC CAGGAGTTCG AGACCTGCCT GGGGGAACAT 60 GGCAAAACCC TGTCTCTATA AAAAATACAA AAATTAGCCA GGTGTAGAGG AGGGTGTCTG 120 TAGTCCCAGC TACTCAGGGG GCTGAGGTGG GAGGATCACC TGAGCGTGGG AGGTTGAGGC 180 AGCGGTGAGC TGTGATTGTG CCACTGCACT CCAGCCTGGG TGACAGTGTG AGACCCTGTC 240 TCAAAAAAAA AAAAAAGAAA AGAAAAAGAA ACAAAGACTG GTATAGCTGG AGGAGTTTGA 300 GAGGAGCAGG TGGCAGGAGG CCGGGTGTTG CAGGGCCTCG TAGGCTATAT TAAGTCAGGG 360 GCTGGGACCT AATTCTGAGC ACCGCAGGGA GGTGGTGAGC AGGAAACACA GGTGAATGGG 420 AGGATTCACT GAGAAACTCA GAGCAGACAG TGGGTACTGG GTAAGTCTGA AGTACCCGTA 480 TTACTGTGTC ATCATCCAGC CTGGCACCCC AAGAGCTCCT TCCCCTCCAC TTTGCTCACC 540 CGTCTTCCGG GCCCTGAACC CAGTCACCTC CTGCCACCTT CTTTCCACCG TCTCCCGGGC 600 AGGGCTTCAG ACCCACAGAT CCTAACTTGT CTGCGCTCAG CCTGAGAGCA GGCCCGGGCC 660 AAGCCAGGCA GGGGCCACAA CTCCCCAGAC AGGGGGAAAT GGGCCTAAGG GATGGGGGGG 720 TGGTCCATCT CTGCCCCTTC CAGCTTCTAC CCTGCAGACA GACCTGCAGC CTGCCCTCCT 780 TCCCTCCGGG AATGTCCAGG GCACACTCAA AACCCCATCC TGTGCCGGCT GCAGGTACGG 840 AACAAGTAGG CTAGTGTCAG GTGACAGAGC AGCTGGCTGC GTGGAGGAGG GCTGAGGGAC 900 CGCCAGGAAG GGGAGGCTCC TGCAGTTCAG CTGGCAGCCT CCCCAGTGAG GAAATCCAGC 960 TGAGGCAGGA AACAGGTATC TCAGCGACTT CCCTCCTAGG CCCTGGAAAA CACCTTAATC 1020 ACCACCGAGG CTCCCTCAAG ACGCCTGTCC CCTGCAGGGC CGCCCTAAAG GGGTCAGCAG 1080 GCCAAGGCCT GCCGAGTCAC CCAGGCCCAG CCCCCTCCTC CAGCAAGCCT CCTCACCTCC 1140 CAACAGCTGA AATTACACCC ACACTTAATC ACAGATCAGC TTCCTGTGGT CCTGTCCCCC 1200 GTCCCGGGGA AGCCTGGAGC TCCCTAAGGC CCATCTCACC CTGCTGCTGT GCCCAACCCT 1260 TCCCCATAAG CCACTGGCTC CGGACCAAAC TGAAGGGCAG ATGAGAGCAA GGGTAGCAGG 1320 CAAAGAGGGT CCAAGGTGTG CTGGGAGCCT GGGCTAGGAA TTGATCTCAT TTTTGACTTG 1380 CAACAAACTC CTCAACCCCA TTGTACAGAT TTGGAAACTA AGGCTCAGAG AGAGGAACTC 1440 GCCCCAGATC ACACAGCCAG AAACCGCAGC CCAGAGACTC ATACTTGGGT CTGTAAGACT 1500 TCAGAGACAG GCCAGGCATG ATGGCTTATG CCTGTCATCC CAACACTTTA GGAGACCGAG 1560 GCGAGAGGAT CGCTTGAGGC CAGGAGTTTG AGACCAGCCT GGGCAACAAA GTGTGATGCC 1620 CTCTTTTTTT TTTTTTGAGA CAGAGTCTTG CTCTGTCGCC CAGGCTGGAG TGCAGTGGCG 1680
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