Tag | Content |
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EnhancerAtlas ID | HS078-00465 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:22259210-22261000 |
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: 40 | 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 | chr1:22258943-22259419 | Bladder | 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 | chr1:22255389-22259487 | Fetal_Intestine | SE_28012 | chr1:22259788-22261138 | Fetal_Intestine | SE_28954 | chr1:22245252-22259468 | Fetal_Intestine_Large | 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 | chr1:22256470-22259564 | NHLF | 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 | chr1:22257119-22259542 | Psoas_Muscle | SE_48478 | chr1:22259611-22261201 | Psoas_Muscle | SE_48565 | chr1:22255431-22261202 | Right_Atrium | SE_49456 | chr1:22259694-22261125 | Right_Ventricle | SE_50206 | chr1:22256100-22259609 | Sigmoid_Colon | 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 | chr1:22256041-22259505 | HSMM | 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 | AGGAACAGCA GACGCAGAGA CCCTAAGGTG GGAGTGTGTT TCACATGCTC AAGAAACAAA 60 GCCTTGGTCA GGCGAGGTGG CCCATGCCTA TAATCCTAGC ACTTCAGAAG GCTGAGGTGG 120 GAGGATAGCT TGAGTTAAAG AGTTTGGGAC CAGCCTGGGC AATACAACAA GATCCCATCT 180 CTATTTGTTT TAAATTTTTA TATTCATTAG AAAAGAAAAG GCTGGGTGCA GTGGCTCACG 240 CCTATAATCC TAGCACTTTG GGAGGCCGAA GGGGGTGGAT CATTTGAGCC CAGGAGTTCG 300 AGACCTGCCT GGGGGAACAT GGCAAAACCC TGTCTCTATA AAAAATACAA AAATTAGCCA 360 GGTGTAGAGG AGGGTGTCTG TAGTCCCAGC TACTCAGGGG GCTGAGGTGG GAGGATCACC 420 TGAGCGTGGG AGGTTGAGGC AGCGGTGAGC TGTGATTGTG CCACTGCACT CCAGCCTGGG 480 TGACAGTGTG AGACCCTGTC TCAAAAAAAA AAAAAAGAAA AGAAAAAGAA ACAAAGACTG 540 GTATAGCTGG AGGAGTTTGA GAGGAGCAGG TGGCAGGAGG CCGGGTGTTG CAGGGCCTCG 600 TAGGCTATAT TAAGTCAGGG GCTGGGACCT AATTCTGAGC ACCGCAGGGA GGTGGTGAGC 660 AGGAAACACA GGTGAATGGG AGGATTCACT GAGAAACTCA GAGCAGACAG TGGGTACTGG 720 GTAAGTCTGA AGTACCCGTA TTACTGTGTC ATCATCCAGC CTGGCACCCC AAGAGCTCCT 780 TCCCCTCCAC TTTGCTCACC CGTCTTCCGG GCCCTGAACC CAGTCACCTC CTGCCACCTT 840 CTTTCCACCG TCTCCCGGGC AGGGCTTCAG ACCCACAGAT CCTAACTTGT CTGCGCTCAG 900 CCTGAGAGCA GGCCCGGGCC AAGCCAGGCA GGGGCCACAA CTCCCCAGAC AGGGGGAAAT 960 GGGCCTAAGG GATGGGGGGG TGGTCCATCT CTGCCCCTTC CAGCTTCTAC CCTGCAGACA 1020 GACCTGCAGC CTGCCCTCCT TCCCTCCGGG AATGTCCAGG GCACACTCAA AACCCCATCC 1080 TGTGCCGGCT GCAGGTACGG AACAAGTAGG CTAGTGTCAG GTGACAGAGC AGCTGGCTGC 1140 GTGGAGGAGG GCTGAGGGAC CGCCAGGAAG GGGAGGCTCC TGCAGTTCAG CTGGCAGCCT 1200 CCCCAGTGAG GAAATCCAGC TGAGGCAGGA AACAGGTATC TCAGCGACTT CCCTCCTAGG 1260 CCCTGGAAAA CACCTTAATC ACCACCGAGG CTCCCTCAAG ACGCCTGTCC CCTGCAGGGC 1320 CGCCCTAAAG GGGTCAGCAG GCCAAGGCCT GCCGAGTCAC CCAGGCCCAG CCCCCTCCTC 1380 CAGCAAGCCT CCTCACCTCC CAACAGCTGA AATTACACCC ACACTTAATC ACAGATCAGC 1440 TTCCTGTGGT CCTGTCCCCC GTCCCGGGGA AGCCTGGAGC TCCCTAAGGC CCATCTCACC 1500 CTGCTGCTGT GCCCAACCCT TCCCCATAAG CCACTGGCTC CGGACCAAAC TGAAGGGCAG 1560 ATGAGAGCAA GGGTAGCAGG CAAAGAGGGT CCAAGGTGTG CTGGGAGCCT GGGCTAGGAA 1620 TTGATCTCAT TTTTGACTTG CAACAAACTC CTCAACCCCA TTGTACAGAT TTGGAAACTA 1680 AGGCTCAGAG AGAGGAACTC GCCCCAGATC ACACAGCCAG AAACCGCAGC CCAGAGACTC 1740 ATACTTGGGT CTGTAAGACT TCAGAGACAG GCCAGGCATG ATGGCTTATG 1790
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