Tag | Content |
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EnhancerAtlas ID | HS038-21146 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr8:38793600-38796350 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF4G | MA0484.1 | chr8:38795601-38795616 | TGCACTTTGACCCCT | - | 6.21 | Hnf4a | MA0114.3 | chr8:38795599-38795615 | GCTGCACTTTGACCCC | - | 6.78 | NR2C2 | MA0504.1 | chr8:38795601-38795616 | TGCACTTTGACCCCT | - | 6.3 | PPARG | MA0066.1 | chr8:38795905-38795925 | GTGGGGCAAGGTCACCCCCA | + | 6.34 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_01112 | chr8:38793267-38796600 | Adrenal_Gland | SE_02046 | chr8:38792906-38797424 | Aorta | SE_02449 | chr8:38792819-38797453 | Astrocytes | SE_03039 | chr8:38792819-38796540 | Bladder | SE_09752 | chr8:38792854-38797628 | CD14 | SE_10253 | chr8:38792914-38797711 | CD19_Primary | SE_10916 | chr8:38778152-38824593 | CD20 | SE_20358 | chr8:38793003-38797733 | CD56 | SE_25987 | chr8:38789829-38797700 | Duodenum_Smooth_Muscle | SE_26945 | chr8:38792798-38796597 | Esophagus | SE_30474 | chr8:38792683-38797435 | Fetal_Muscle | SE_35181 | chr8:38791545-38797788 | HeLa | SE_37318 | chr8:38792814-38797748 | HSMMtube | SE_40765 | chr8:38788682-38797591 | Left_Ventricle | SE_42292 | chr8:38789499-38797614 | Lung | SE_43830 | chr8:38792904-38796597 | MM1S | SE_44905 | chr8:38792860-38797384 | NHLF | SE_45759 | chr8:38791665-38797652 | Osteoblasts | SE_48823 | chr8:38792663-38796524 | Right_Atrium | SE_49720 | chr8:38793346-38796420 | Right_Ventricle | SE_50238 | chr8:38792759-38796543 | Sigmoid_Colon | SE_51979 | chr8:38793035-38796553 | Skeletal_Muscle_Myoblast | SE_52798 | chr8:38792885-38797648 | Small_Intestine | SE_53542 | chr8:38792660-38797616 | Spleen | SE_54989 | chr8:38791683-38797578 | Stomach_Smooth_Muscle | SE_56232 | chr8:38793215-38796134 | u87 | SE_62854 | chr8:38792840-38824305 | Tonsil | SE_63754 | chr8:38793035-38797448 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr8 | 38794203 | 38794537 | chr8 | 38794582 | 38795442 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I038934 | chr8 | 38792014 | 38798166 |
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Enhancer Sequence | CTCTGTAAGT CGATCTGGTT TCTAAGCAAG GGGAAGTGTC CAGTCCTTTG GGCATTAGTA 60 TTTAGGGACG TTGCATGGTG TTGAAATGCT CCCCTGAACC CACACAATGC CTGTGGAGGC 120 TTAGCTGCTA ATGGGTGGCT GTAGAGGTAT GTGGTTCCAA GTTGTTGGAG GGTGGACCTA 180 CAGCCTCTTA CTCCTTGAAC ACATCAATCC ATAATGCTCC CAGCTCCTGC GCAGGAGGTG 240 TTATGTGGTG GTGGAGCTGG GGTAGGGGTA GTACATGATC CATGACCTTT TTTTGTAATT 300 GGGACGAAAG GGAACACGAA AACAATCACC AAAAATCCAG CAACTGTGAA GGATTCTCTC 360 AAAGGGTACA GTCAAACAAA AAATATTGGG GCTTCACTGG ATTTTTTACC AGTCACCTGG 420 ACAGGATTAC TGTGGAGGGA AGGCTAAGAA GGCCCTGAGA AGCCACTCAG ATTACCAAGA 480 AGACATTCAG CAGCCAGATA ACTGCTGGGG GTTGGGGCAG GTGGCTGCGA GGCCACCCCC 540 GTCCCATTTG TACAGAAGGG GCCGGAGCAG GCCCTCTCTT GTGCTGAGAG CTGGGGTGGG 600 GACTGGTTAA CGGTGCCCAC ATGTAACTGC TGAATTCAGC TTCTATTAGC AGCCGCTCCC 660 TGGAGCAGGC ACCACTGCTG ACCCGTGATG CAGCGGTGAT AAAAAGGCCG GGAGATTTAG 720 AGCCTCCCCA GGAAGAGGAA CTCTTTGTAC AGTGAGGAGA GCCAGGTGGC ACCCCGCCAG 780 CACTGAGGTT TCGGAAGTCC TGTGCTCCCC ACACACCCTC ACTGCAGGCC TCTTGGGAGC 840 CTCTTCTGCC CTGCACATCC CCTTTCATCC TCAGGGGCTG GAGGCCTGGG GGCCCCTGAG 900 CCAAGGGTCT ATCGGCTCCA TCTTGTAACA AGCTTTGGGA GTCTTGTACC CTGGCTGGTC 960 AGGAGATGAA CCTGAAGGGG ACTGGGGGAC TCTGGAGGAG AGGCCACCCT TGGCTGGAGG 1020 GGCAGCCCGC CCCTGTGCCT GTGGTATGCA GGCAGAGTCT GGCAGACACA GCCCAGTACA 1080 AAGGCACAAG ATGCAGGGCA GCGTCAGGGC GGATTAAAGA GGGAGAGAAT GACCTCAGGG 1140 AAGGAGGAAG GGCCTTTTCA AGTCCAGCCT TGCTAGCACA GCTGCCGGCA ATTTGTGCAT 1200 GCCTTGTGGT GAGAAATGTG GCTGCCTCCC CGGGCCAGAG CAGCCAGAGG CCCAGGCCTG 1260 CCCGCCCTCC CTGGCTTGTC CTCATCTTGC TGAGAGCTCC TGAGGTCGTT TCTCCAGGAG 1320 GGTCGGAGAT GGAGAATTGA GAGCAGAGGA GCAGAGAACC TCGCAGTAAT AAAGGAAAAC 1380 TGAAACCCTC TCCTGTGTGA GAGGGTTTGG GAAGCCTTTT TTTTTTATTT TTGGTTGGGG 1440 AAGAATGAAT TCAGTCTCCT GCTGAATCAT GATTTATAAA TGCAGCTCAG ATGAGGGTTT 1500 TAGAGTTCTC AGCCTTGGAG GCTGCGTCAT TTAGAAAGGG TGACCTGCCG TTTAGCCCCT 1560 TCCCGAGAAA GGCAGGGCTG GATGGGCATT TTGCAAAACC CACAGCTGCC ACTGGGTCGG 1620 GTTACACAGA GCTCAGAGCC TTTAACTCCT GCCTGACTCC CTGCCAGAAA GCAGGGGTTT 1680 TTCCCAGAAT GACATTTAGC CTCAGAGGCG CTGGACTCCA GCTCAGCATT CCAGGTCATT 1740 ATTTGTTAAC TCTTAGGTAT TCCTTCTTGG AGGAGAGCGC TTGCCACCGT GTCAGGTGGC 1800 CTGGCCAGAG GGCTGCGTGT GGGCTGGCTG TTCAGGGTGT GTGCTTCTCT GCTGTCTGCT 1860 GAGGGCCAGT GATGGGAAGA TGAGGACGGG CGTGTGGCCC TGGCCCTTTG GAGAGACAGA 1920 GATGAAAGTG ATGATTGGAT GTCATCCAGA GCATCAATGG CAACAGAACC AGTTCTTAGC 1980 AAACTAGAAA ATAATTAAAG CTGCACTTTG ACCCCTGCCT CCACCCGCCG ACTGCACAGC 2040 CAACCCCGCT GTCCCACCCC CAGCTGTGTC CCAGTTGTCA GGGCCTTGCT TTCAGCCACC 2100 TCTCAGAAAG AACTTGTAGG GGCTCATGGA TCCTTTTTTG AGACTGATGA AATGCATGGA 2160 TGCCTTCTCC AGGTAAATGC ATAGGTGTAC AGACACACCC TGCTTTTGCC TATAATTTCA 2220 GGGAGCCCAT TGACCTCCTG AAGCTGGTCC AGAGACCCCC ATCCCATGTA GGTGGCTGCT 2280 ATTCCCCTGA TCCTGATGCC ACCTTGTGGG GCAAGGTCAC CCCCAGATAC CAGGGCAGAG 2340 GCCGCAGCAG AGCTAGGAGA CCTTGTTTTG CTGCCACTGC TTCTGCCAGA GGGGCCCCAG 2400 CTCCTCTTCC GGCCATGGGC AGACAGGGTG GGGCTGGCCC TAGCCGTGCC TGGCCGCTGA 2460 CGAGCTTGCA GCTCCTGTGG TCTGTGTTTG ATCTGATAAG CGCAAGTTCC TGAGAGTCTG 2520 TTGAGCTGTG GAGCAGCCCT GTCTGCGTCA CTCTACGGGG GACCTGTGCC CACTCCCTGC 2580 TCACATCCCT GACCTCTGCT CGCTGCTGGG GTGTTCACAG GACCCACCAG TCAACCACTG 2640 CTGGGTAGCG CCTCTGCTGT GGCCACCTCG GCTGTGTGGA TGGCTGCACT TTGGTGGCCT 2700 CACTGGAGTC AGACGGTCGG GTGACCTCAC CCGCCTGCAG CCACGCCTCT 2750
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