Tag | Content |
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EnhancerAtlas ID | HS085-02159 |
Organism | Homo sapiens |
Tissue/cell | Heart |
Coordinate | chr22:36857100-36858790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr22:36857358-36857375 | TGAACTCCTGGAAGGCA | - | 6.09 | Klf1 | MA0493.1 | chr22:36857967-36857978 | AGGGTGTGGCC | - | 6.32 | RREB1 | MA0073.1 | chr22:36857523-36857543 | TGTGGGGTGGGGGTTGGGGG | - | 6.95 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_01080 | chr22:36857974-36858779 | Adrenal_Gland | SE_01722 | chr22:36857091-36857655 | Aorta | SE_01722 | chr22:36857721-36859098 | Aorta | SE_02575 | chr22:36857704-36858950 | Astrocytes | SE_23071 | chr22:36857089-36857632 | Colon_Crypt_1 | SE_23071 | chr22:36857824-36858668 | Colon_Crypt_1 | SE_23740 | chr22:36857838-36858703 | Colon_Crypt_2 | SE_24731 | chr22:36857036-36857656 | Colon_Crypt_3 | SE_24731 | chr22:36857819-36858753 | Colon_Crypt_3 | SE_26443 | chr22:36857449-36859078 | Duodenum_Smooth_Muscle | SE_27096 | chr22:36857754-36858952 | Esophagus | SE_27650 | chr22:36857704-36858960 | Fetal_Intestine | SE_31378 | chr22:36857774-36858914 | Gastric | SE_37504 | chr22:36857328-36859186 | HSMMtube | SE_38695 | chr22:36857456-36865052 | HUVEC | SE_41064 | chr22:36857713-36859089 | Left_Ventricle | SE_42094 | chr22:36856361-36864828 | Lung | SE_46578 | chr22:36857697-36859010 | Osteoblasts | SE_47671 | chr22:36857292-36857617 | Pancreas | SE_47671 | chr22:36857763-36858820 | Pancreas | SE_49127 | chr22:36857795-36858927 | Right_Atrium | SE_49784 | chr22:36857822-36858751 | Right_Ventricle | SE_51467 | chr22:36856823-36865059 | Skeletal_Muscle | SE_52340 | chr22:36857786-36858905 | Small_Intestine | SE_53283 | chr22:36857017-36864617 | Spleen | SE_54687 | chr22:36857443-36859071 | Stomach_Smooth_Muscle | SE_57815 | chr22:36857833-36858755 | VACO_503 | SE_63127 | chr22:36801020-36866853 | Tonsil | SE_64152 | chr22:36857664-36859071 | HSMM | SE_65459 | chr22:36857151-36859090 | Pancreatic_islets |
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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 |
GH22I036457 | chr22 | 36853475 | 36869221 |
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Enhancer Sequence | CCTGGGAGGT GGAGGTTGCA GTGAGCCAAG ATCACACCAC TGCACTCCAG CCTGTGCAAC 60 AGAGTTAGAC TGTCTCAAAA CAAAAACAAA AAACAACTTT TCTCAAGCAT CACCTCCTTC 120 CCATGCTTTA CCCGACAATC TCCTTTTGCA GATGTGCTGC TTTTCAGGGC TTGCGGCCAG 180 TCTGTACTCT GTCACCATGG TGGTAAATGT CATCTCTCCT GTAGCATTTA GACTTTAGAT 240 GTGTCCATGT GTTTGCTGTG AACTCCTGGA AGGCAGGGGC TGTGTCTTGC TCTAGTTCCT 300 ATCACCCAGC AGGCCCAGAG GGGCTCCGCA CAGACGCTTG CTGGCTGAGG TAGCCAGTTT 360 GGCCTGGAGA GAGTATTCCC GCCTCAGGAG TGGATCATGA GGAAATGGAA TCTCCTGCCT 420 CCTTGTGGGG TGGGGGTTGG GGGAGGTGGA TAAAAGAGAG GCTCCACCTG GCACGGTGGC 480 TCGTGCCCAT AATCCCAGCA CTTTGGGAGG CCGAGGTGGG TAGATCACCT GAGGTCAGGA 540 TTTTGAGACC AGCCTGGCCA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAATTA 600 GCTGGGCACC TGTAATCCCA GCTACTCGGG AGGCTGAGGC TGGACAATCG CTTGAATCCA 660 GGAGGTGGAG CTTGCAGTGA GCCAAGATTG TGCCACTGCA CTCCAGCCTG GGGGAAAAGA 720 GCAAAATTCC ATCTAAAAAA AAAAAAAAGC GGATCAAGGT CCCTACTCTG GGCATGAGAG 780 GAGGGATCCT TTGACACTCC TGGGAGCAGC AGTGTGGCAG AGGAGGAGGA GCAGGGCATG 840 GGGTCAGCCA CCCTCAGTCC ATTTCCCAGG GTGTGGCCTT AGGCACGGTC ACTACCTCTC 900 TGGGCTTCTG TCTCCACATG TATGAAATGG AATCAGTCCC TCCTTCCACA GGTGTTAGGT 960 CGAAGAAGGC ACCTCTGGTG GTATCGGCAC AGAGGCTGGA CACTGGATGA CTTCTTTGCT 1020 GGGACACTGA GGTAGGGGGC AGACCAGAGA CAGACAGCTA CTTGCCTAAG CTCACCCAGC 1080 AAGCTGGCTG AAGGTGGAGA ACTGGCTTGT CCTCCAGTTG GTAGTTAACA GCTGTCTAGC 1140 AGGAGTGTTC TTGCTCCCAG GAGACGCTCC GTTGGCTGCC ACAGAGGTAA GCGTGAGAGT 1200 GCGCTCAGAA GTGGCTGGGA GGCATGGAGA ACAGAGGAGC AGGTTCAGGG TGAATTCCAG 1260 TGGGCATTCT CCAAGGGTGA GGTCACTGCC TCCAACTCCC TAGGGCTGCC TGAGACACAG 1320 GCACCACCAA GCCAGCTCCA GAGCAGGAGG AGGTGGTGGC AGGGACCAGG GCCAGGTCAC 1380 AGGGCTGAAT GTAAGGCCCT CAGCCTGGTA CAGCGACGGG CCCCTCCCAT GGTGCTGGGG 1440 TCCTTACCTT GGGAAGCCCG GTGTTTCCTG TTTAAGATGT GGCTGGGGGT AGGGGAAAGG 1500 AGAAAGCCAC ACAGATAACA CTTCTGGAAC TTCCAATCGG TGCCAGCGTG CTTCCACCTG 1560 CTGAGCCGTG ACCTCATTTG CAGGGACTGT CATGAGCCCC AACTTGGAGA TGGTGCAACT 1620 GGGGCTCAAA ATGGTGAAAA CCTTGTCCCA AAAGGAAAGC AGTATAGCTA ATGAGCAAGA 1680 ACAAAGAGAA 1690
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