Tag | Content |
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EnhancerAtlas ID | HS104-28606 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr19:4368140-4370640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr19:4368796-4368807 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr19:4368796-4368807 | GGTGACTCATG | + | 6.02 | STAT3 | MA0144.2 | chr19:4369359-4369370 | CTTCTGGGAAG | + | 6.14 | ZEB1 | MA0103.3 | chr19:4369634-4369645 | CCCACCTGCCC | + | 6.14 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_00671 | chr19:4367358-4370687 | Adipose_Nuclei | SE_00953 | chr19:4367901-4368893 | Adrenal_Gland | SE_00953 | chr19:4369010-4378529 | Adrenal_Gland | SE_03081 | chr19:4369074-4370040 | Bladder | SE_05654 | chr19:4367191-4368894 | Brain_Cingulate_Gyrus | SE_05654 | chr19:4369240-4377898 | Brain_Cingulate_Gyrus | SE_06216 | chr19:4367183-4378196 | Brain_Hippocampus_Middle | SE_08374 | chr19:4367491-4368908 | Brain_Inferior_Temporal_Lobe | SE_08374 | chr19:4369264-4378128 | Brain_Inferior_Temporal_Lobe | SE_14750 | chr19:4367713-4381827 | CD4_Memory_Primary_7pool | SE_26598 | chr19:4366396-4381720 | Esophagus | SE_27964 | chr19:4368934-4370626 | Fetal_Intestine | SE_28734 | chr19:4368689-4371124 | Fetal_Intestine_Large | SE_30332 | chr19:4367899-4377712 | Fetal_Muscle | SE_31749 | chr19:4367970-4370977 | Gastric | SE_37296 | chr19:4367503-4381769 | HSMMtube | SE_38442 | chr19:4367780-4370501 | HUVEC | SE_40064 | chr19:4369030-4370537 | K562 | SE_41739 | chr19:4367436-4368814 | LNCaP | SE_41739 | chr19:4369076-4370863 | LNCaP | SE_42702 | chr19:4367366-4368910 | Lung | SE_42702 | chr19:4368985-4371398 | Lung | SE_44622 | chr19:4367416-4368934 | NHDF-Ad | SE_44622 | chr19:4368946-4371782 | NHDF-Ad | SE_45249 | chr19:4368856-4370426 | NHLF | SE_47754 | chr19:4369028-4369583 | Pancreas | SE_48336 | chr19:4367194-4378514 | Psoas_Muscle | SE_49011 | chr19:4367383-4368893 | Right_Atrium | SE_53019 | chr19:4368963-4371180 | Small_Intestine | SE_53804 | chr19:4367718-4371316 | Spleen | SE_65589 | chr19:4367712-4380728 | Pancreatic_islets | SE_69091 | chr19:4368091-4368910 | H9 | SE_69091 | chr19:4369037-4370799 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr19 | 4370446 | 4370604 | chr19 | 4368982 | 4370436 | chr19 | 4369210 | 4369467 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I004367 | chr19 | 4367437 | 4382197 |
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Enhancer Sequence | CCGTGGGCCA TGGCCTGTGC CCCTGGTGCT CCCCAGGTCT GATTGGTGCT TGCCTGCCCC 60 GAGCTGTCAC AAGACGTGGC CAAGGGATGC CATGAGGGTC CGTGTGGTGC CACACTGCGT 120 TGGCTGTGTG GGGCTGGGGG GTGTCCAGCA GGGCAGTCAG GAGTTTAGGA CCCAGCCTGG 180 GAGGAAGTGA CCCAAGAGCA GGAAGTGCGG GGGCAGGAGA AGCTTGAGCC TGGGGCTCTG 240 CCCACGCCAG GCACCTGGTG TACCCTCTAG CCCATGCCTG GAGGTCACAG CCCAAGGCAC 300 CATGAGTGCA AATGCCCCCA ACCCCAAGTT CTGCAAAAGG TAGCCTGCCC GGAGTACACG 360 GCTGGTCTTG TGTCCTGGCA ACCTGCCCAA AAAGACACCA GCCCCTTTGC CAAGGAATTC 420 CTGGCCCTCC TCCAAGGCTT GGCTCTGGAA GCCCCCACAC CACGGGACTG TCCTCACCCA 480 CGCATCGGGA CCCTTTCTGT CCACCTGCCT TCATGTGCGG GGTGTGCCGG GCATTCAGTG 540 AGCACAGGCC CCATGCCTCT GACCCCTGTC CCTTTCCTGC CTGTGGGTTG GTGGCTCTCA 600 ACTCAGCCAC ACAGCACCTT GGAAGCTTCT TAAAAATCCC CTCGTTGGCC GGGCGCGGTG 660 ACTCATGCCT GTAATCCCAG CACTTTGGGA GGCTGAGGCA GGCGGATCAT GAGGTCAGGA 720 GATCGAGACC ATCCTGGCTA ACACAGTGAA ACCCCGTCTC TACTAAAAAT ACAAAAAAAT 780 TAGCCGGGCC TGATGGCGGG TGCCTGTAGT CCCAGCTACT CGGGAGGCTG AGGTAGGAGA 840 ATGGTGTGAA CCCGGGAGGT GGAGCTTGCA GTCAGCAGAG ATCCAGCCAC TGCACTCCAG 900 CCTAGGCGAC AGAGCAAGAC TCCATCTCAA AAGAAAGAAG AAAGAAAAAA AAAATCACCT 960 CGTCACACCC ACCGCGGGAG GGCTGACTCT GGCACAGGTG AGAAGCAGGA ACTGTCCCTT 1020 GCGGGGCAGG AGAGTGGGGC TGCCCTCCAT TTCTGCTGAA GGCATTAGGA GGAAGGAGCC 1080 CCCCCTCCCT AGGTGTTTTT GGGGCGTTCC ACTCTATTTC CTGGGACAGT TTCACTTCTT 1140 TTGATTGTGG CGAGAGAGGG CGTGCTCAGA GCCAGCGGCT GCCGGAGAGG GAAATGAGTG 1200 GCTGATGTGA GACTGGACTC TTCTGGGAAG CCGGGAGGAG AACTGAAGCC AGCGGGCTGC 1260 GAAACCACAC CTTCTGGGCG GAGGCCACCC CGGCCCCACG ACCTGCCCAG GCAGGACCCA 1320 GTGTGCAGGC TGGCAGGAGT GGCTCCGTCA GGGCCCTTCC CCAGCCCCCT GCCTCTCACA 1380 GGGCAGGAGG AGAGGCCCTA CCGGCGAGGA CCACATCCTG CCTCTGAGGG GAGGGGCTGG 1440 GGACCCGCCA CGGTACCAAA GACCCACCTG GTGGCCTCTG GCTCTGGCCC TGGCCCCACC 1500 TGCCCATCTC ACCTGGGAAT CCAGGACCCT GCCTTCCTGA GCCCCAGGAC GACTTCCTGA 1560 ACCCCCACAA CCGCCTGACT CCTCGCACCC CTGACACCCG GGAGGCTGTG CCCTAACTAC 1620 CCGGGTCCCT CTGCTCAGCT CCAGCCAAGT CCCTTGTGGT GACTGATGGT CCCCCACGGG 1680 CCAGGCACTG GGCAGGGGAC ACAACCCTGT AAGGCCCCTT CTCTCCAAGG CTTATGGGCT 1740 AGAAACCAGC ACAGATGGAC ACAGGGATGA GCAGCCACAA GGGAAACACG GGAAAAGCAA 1800 GGCAGCCGGG CCACGTGCAG CGCCGGCCGC AAGCGCGGAA ACCAAGCGTG GGCTCCTGCC 1860 CGCTGGGGCC CTACTCACTG CGGTCTCCAC ACCAGCACAC TGCTGAGCAC GGAGGGGACC 1920 GAGAGTCTGC GGCAGAGCTG GGCGCCACGG GGAGGCTCAC CAGAGGGCGC CTCTGGGCTC 1980 GCTGTCAGGA GCGAGTGTTC CTAACCCTGG TGCCATCTGC CAGGCAAGAG CTGCCTGTTG 2040 TGGGGCAGCC AGCCCCAATG CCCCCGCATC AGAGACCCTA CCGGTGGGGA GGGAGGACTG 2100 AGGCCATGGT CCCAGCAGTC CATTCCTGCC GAGGGAGACT CTGCAGGCTG GCTGTAGCCC 2160 TGACTAGTGC AGCGGACTCA GCAGTGGCAA TGACAGCTCC GCACTCGAGT CCATCCCATA 2220 CCCACAAGGC TCGCCTCCTG TTCCCACCCC GCATGGCAGG AAACGGAGGA AAATAATGGG 2280 GCCACTCAGT AGCCAGGGAC CCAACAGGGC TCAGGGGTGA GACCACCCTC CGCTGACTGA 2340 ACCTGCATCA GGGTGGCAGG GTGGGTGGGG GCCCCCTCCC CACTCTCCCA CAGGGCCCCA 2400 CCTGGACGGG GTCAGAGTAC CAGCTGCAAA CCCCGAGTGA CCAACCGCAG GCCCCACAAG 2460 GGCTGCCATC CTGAGAGCAA CACCAGCGCC TTCTCTCCCC 2500
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