Tag | Content |
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EnhancerAtlas ID | HS012-07416 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr12:6650810-6652530 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr12:6652396-6652411 | AGGTCAGCAAGTCCT | + | 6.11 | FOXH1 | MA0479.1 | chr12:6651713-6651724 | TGTGGATTGGA | - | 6.62 | HNF4G | MA0484.1 | chr12:6652352-6652367 | AGAGATCAAAGGTCA | + | 6.56 | NR2C2 | MA0504.1 | chr12:6652352-6652367 | AGAGATCAAAGGTCA | + | 6.16 | Nr2f6 | MA0677.1 | chr12:6652353-6652367 | GAGATCAAAGGTCA | + | 6.72 | Rxra | MA0512.2 | chr12:6652353-6652367 | GAGATCAAAGGTCA | + | 6.45 | STAT1 | MA0137.3 | chr12:6651001-6651012 | TTTCCTGGAAA | - | 6.62 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_01052 | chr12:6648769-6651707 | Adrenal_Gland | SE_01797 | chr12:6648556-6652067 | Aorta | SE_04287 | chr12:6650237-6652427 | Brain_Anterior_Caudate | SE_05332 | chr12:6650294-6652367 | Brain_Cingulate_Gyrus | SE_06104 | chr12:6634289-6652782 | Brain_Hippocampus_Middle | SE_07088 | chr12:6650102-6652376 | Brain_Hippocampus_Middle_150 | SE_08199 | chr12:6650221-6652656 | Brain_Inferior_Temporal_Lobe | SE_09914 | chr12:6648851-6652443 | CD14 | SE_23524 | chr12:6648638-6652692 | Colon_Crypt_1 | SE_24159 | chr12:6650074-6652530 | Colon_Crypt_2 | SE_25120 | chr12:6650103-6652651 | Colon_Crypt_3 | SE_26082 | chr12:6649010-6652690 | Duodenum_Smooth_Muscle | SE_28112 | chr12:6648696-6652782 | Fetal_Intestine | SE_29041 | chr12:6648677-6652857 | Fetal_Intestine_Large | SE_29717 | chr12:6649024-6652370 | Fetal_Muscle | SE_31984 | chr12:6648714-6652101 | Gastric | SE_34479 | chr12:6647137-6651052 | HCT-116 | SE_35085 | chr12:6639660-6651120 | HeLa | SE_37055 | chr12:6640622-6655597 | HSMMtube | SE_40788 | chr12:6640835-6651077 | Left_Ventricle | SE_42446 | chr12:6648625-6652260 | Lung | SE_44234 | chr12:6648752-6651902 | NHDF-Ad | SE_46050 | chr12:6648598-6652144 | Osteoblasts | SE_48132 | chr12:6639708-6652567 | Psoas_Muscle | SE_48689 | chr12:6648529-6651388 | Right_Atrium | SE_50270 | chr12:6640944-6652634 | Sigmoid_Colon | SE_51214 | chr12:6648847-6652632 | Skeletal_Muscle | SE_52680 | chr12:6640930-6652710 | Small_Intestine | SE_53477 | chr12:6648698-6652636 | Spleen | SE_54922 | chr12:6648452-6651132 | Stomach_Smooth_Muscle | SE_63832 | chr12:6650104-6652225 | HSMM | SE_68771 | chr12:6648788-6651019 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr12 | 6652108 | 6652298 | chr12 | 6652334 | 6652508 | chr12 | 6651340 | 6652107 |
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Enhancer Sequence | GTGGTGGGGC AGGCAGGGCC ATCGGGGTTA ACAGGTGGCG TTCACAGCGC CTCTGTTGCC 60 CCCGCCAGGA GGCCAACACG CCAAGAGCAG TGGCTGGGCC GGGGGCCCAG GCAGCCATTA 120 CTGAAGGCTC AGATTTTAAA ATAAACCAGA CCAAGGCAGA AGGCAGCGAA TACACCATTG 180 TTTCCTCTGC TTTTCCTGGA AATCTTTGCC TATGGAGGAA TGCAAAGGTA CTGCTGCAGG 240 CTGTGTTCTT TTAAGACTGA TAAGAGTGGT GAGGAAAGTC AGTGTGGGCG GGATGGAGCA 300 GATCCACAGG CTCCCAGGGC CACACAGGTT CCTATGGGGC CCGGCTCACC CCTCATCCCC 360 TGTACTGCGC TGGTCCTGGG CTGTCCCCTC ACTGCACTGT GAGCTCCCGT AAGGGTTAGC 420 GACAGGTTTT CCTCATCCTG GCAGACCCAG ACCTCGAAGG GAATTAACTC TCTCTGTGAC 480 CCGTGGCATA CAAGCCTGGC TAACTGCTGA AAGGGGCCCA ATCCTCTTAC CATTCTCTCC 540 TTATCACTTT ATTTTCTCAC CTAAAAGCCA TTTTCAGACA CTAAAAGGAA GACTCCCATA 600 TTGGAGGTGC CATTGATTCT GAGACCTGTC CTGATTTCAG AAATGTCACA CGTGGAAAAC 660 ACGGGGCTCA GAATCAAAGA AATCCGGTCT CCCTCCCCGG GCCCATTCTG CAGCCCACAC 720 TCTGAGGCAG GCGGAGAGGC AGGGCCCAGG CAGCACAAAC TCAGTGCCAG GGACAGTCGA 780 CTGCCTCTCT TTGTTTTGGG TACAAAGGGC AGGGGCCGCA AGGGGAAGCA AAATGAAACT 840 TCCTGGAGAT GACGTTCGTG ACTGCCTGAG TGAAGAGAAC GGGGAGGATA CCAGCTGCCA 900 TAATGTGGAT TGGACAGAGA GGGTGGGAAC TTAGAGAAAG AAGGAAACAG GTTACAGGGC 960 CAGACAGCAG AGATGGTCAG GACAGTGACA TTTGGGGTGA GATGGCGGCT GGCTGGGTGA 1020 GAAGCCCTAG TGGGGACAGC TTCCCTGGCA GGCTTGGATC CACAGCTGGG GCCCCACAGT 1080 AGTGGGAGGA GCAGGACACG GTGACTGTTC AACCCAGGGG GAAAATACAG TGCCACCAGC 1140 CCTTGTTCAG ATCAGCTGCC TACACCCCAA TTTCTCCACC TTGGAAGAAC CGGAGTGCAG 1200 GGAGCTGGGT TCTGGAACCA TCACTCAGGG AGACTGGGAA GAAGGAAATG AACCAAATAT 1260 ATTCTACTGA AATACAAGGC TAGTACTGCC ACCAGTAGTC TCTGCATATG TCTATGTCCC 1320 CACTTAATTC ACAAATTTAC AGCAGGAACA AGGTCAGGAG GTGAACGTGC ATGTCAGGAG 1380 ATGTCCTTGA CAAGCCACCT TGAAAACTGC AGGCTCGCTG TGTGAACAGA CTTGGGGGTG 1440 GGACGGGAGG AGACAGAGAG AGGTGAGGAG CGGTGGGGAA GAACTGCCTC CCGCCCACCA 1500 CTCTGGGCCT TGGCTTTACC TTGCTCCATC TTAGTGACCC TGAGAGATCA AAGGTCACAA 1560 AGATAAAGGC ACCTTGGGTA CTCCTGAGGT CAGCAAGTCC TCCTAACGGT TCCCCTAATG 1620 CAGAAGTCCC CAAACCCCAG GCCACGGACC AGTACCTGTC TGTGGCCTGT TAGGAACCAG 1680 GCCAAATAGC AGGAGGTGAG CAGTGGGCAA GTGAGTGAAG 1720
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