Tag | Content |
---|
EnhancerAtlas ID | HS080-00492 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:22259720-22261400 |
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 | Nr2f6(var.2) | MA0728.1 | chr1:22261308-22261323 | TGAACTCCTGACCTC | - | 6.22 |
|
| 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 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAAAAAGAAA AGAAAAAGAA ACAAAGACTG GTATAGCTGG AGGAGTTTGA GAGGAGCAGG 60 TGGCAGGAGG CCGGGTGTTG CAGGGCCTCG TAGGCTATAT TAAGTCAGGG GCTGGGACCT 120 AATTCTGAGC ACCGCAGGGA GGTGGTGAGC AGGAAACACA GGTGAATGGG AGGATTCACT 180 GAGAAACTCA GAGCAGACAG TGGGTACTGG GTAAGTCTGA AGTACCCGTA TTACTGTGTC 240 ATCATCCAGC CTGGCACCCC AAGAGCTCCT TCCCCTCCAC TTTGCTCACC CGTCTTCCGG 300 GCCCTGAACC CAGTCACCTC CTGCCACCTT CTTTCCACCG TCTCCCGGGC AGGGCTTCAG 360 ACCCACAGAT CCTAACTTGT CTGCGCTCAG CCTGAGAGCA GGCCCGGGCC AAGCCAGGCA 420 GGGGCCACAA CTCCCCAGAC AGGGGGAAAT GGGCCTAAGG GATGGGGGGG TGGTCCATCT 480 CTGCCCCTTC CAGCTTCTAC CCTGCAGACA GACCTGCAGC CTGCCCTCCT TCCCTCCGGG 540 AATGTCCAGG GCACACTCAA AACCCCATCC TGTGCCGGCT GCAGGTACGG AACAAGTAGG 600 CTAGTGTCAG GTGACAGAGC AGCTGGCTGC GTGGAGGAGG GCTGAGGGAC CGCCAGGAAG 660 GGGAGGCTCC TGCAGTTCAG CTGGCAGCCT CCCCAGTGAG GAAATCCAGC TGAGGCAGGA 720 AACAGGTATC TCAGCGACTT CCCTCCTAGG CCCTGGAAAA CACCTTAATC ACCACCGAGG 780 CTCCCTCAAG ACGCCTGTCC CCTGCAGGGC CGCCCTAAAG GGGTCAGCAG GCCAAGGCCT 840 GCCGAGTCAC CCAGGCCCAG CCCCCTCCTC CAGCAAGCCT CCTCACCTCC CAACAGCTGA 900 AATTACACCC ACACTTAATC ACAGATCAGC TTCCTGTGGT CCTGTCCCCC GTCCCGGGGA 960 AGCCTGGAGC TCCCTAAGGC CCATCTCACC CTGCTGCTGT GCCCAACCCT TCCCCATAAG 1020 CCACTGGCTC CGGACCAAAC TGAAGGGCAG ATGAGAGCAA GGGTAGCAGG CAAAGAGGGT 1080 CCAAGGTGTG CTGGGAGCCT GGGCTAGGAA TTGATCTCAT TTTTGACTTG CAACAAACTC 1140 CTCAACCCCA TTGTACAGAT TTGGAAACTA AGGCTCAGAG AGAGGAACTC GCCCCAGATC 1200 ACACAGCCAG AAACCGCAGC CCAGAGACTC ATACTTGGGT CTGTAAGACT TCAGAGACAG 1260 GCCAGGCATG ATGGCTTATG CCTGTCATCC CAACACTTTA GGAGACCGAG GCGAGAGGAT 1320 CGCTTGAGGC CAGGAGTTTG AGACCAGCCT GGGCAACAAA GTGTGATGCC CTCTTTTTTT 1380 TTTTTTGAGA CAGAGTCTTG CTCTGTCGCC CAGGCTGGAG TGCAGTGGCG CGATCTCGGC 1440 TCACTGCAAG CTCCGCCTCC CGGGTTAACG CCATTCTCCT GCCTCAGCCT CCGGAGTAGC 1500 TGGGACTACA GGTACGTGCC ACCATGCCTG GCTAACTTTT TGCATTTTTA GTAGAGACAG 1560 GGTTTCACTA TGCTGGCCAG GCTGATCTTG AACTCCTGAC CTCATGATCC GCTCGCCTCG 1620 GCCTCCCAAA GTCCTGGGAT TACTGGCGTG TGCCACCGCG CCTGGCCCCG AAAAACTTTT 1680
|