Tag | Content |
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EnhancerAtlas ID | HS177-22511 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr8:38794020-38796370 |
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 | ACAGGATTAC TGTGGAGGGA AGGCTAAGAA GGCCCTGAGA AGCCACTCAG ATTACCAAGA 60 AGACATTCAG CAGCCAGATA ACTGCTGGGG GTTGGGGCAG GTGGCTGCGA GGCCACCCCC 120 GTCCCATTTG TACAGAAGGG GCCGGAGCAG GCCCTCTCTT GTGCTGAGAG CTGGGGTGGG 180 GACTGGTTAA CGGTGCCCAC ATGTAACTGC TGAATTCAGC TTCTATTAGC AGCCGCTCCC 240 TGGAGCAGGC ACCACTGCTG ACCCGTGATG CAGCGGTGAT AAAAAGGCCG GGAGATTTAG 300 AGCCTCCCCA GGAAGAGGAA CTCTTTGTAC AGTGAGGAGA GCCAGGTGGC ACCCCGCCAG 360 CACTGAGGTT TCGGAAGTCC TGTGCTCCCC ACACACCCTC ACTGCAGGCC TCTTGGGAGC 420 CTCTTCTGCC CTGCACATCC CCTTTCATCC TCAGGGGCTG GAGGCCTGGG GGCCCCTGAG 480 CCAAGGGTCT ATCGGCTCCA TCTTGTAACA AGCTTTGGGA GTCTTGTACC CTGGCTGGTC 540 AGGAGATGAA CCTGAAGGGG ACTGGGGGAC TCTGGAGGAG AGGCCACCCT TGGCTGGAGG 600 GGCAGCCCGC CCCTGTGCCT GTGGTATGCA GGCAGAGTCT GGCAGACACA GCCCAGTACA 660 AAGGCACAAG ATGCAGGGCA GCGTCAGGGC GGATTAAAGA GGGAGAGAAT GACCTCAGGG 720 AAGGAGGAAG GGCCTTTTCA AGTCCAGCCT TGCTAGCACA GCTGCCGGCA ATTTGTGCAT 780 GCCTTGTGGT GAGAAATGTG GCTGCCTCCC CGGGCCAGAG CAGCCAGAGG CCCAGGCCTG 840 CCCGCCCTCC CTGGCTTGTC CTCATCTTGC TGAGAGCTCC TGAGGTCGTT TCTCCAGGAG 900 GGTCGGAGAT GGAGAATTGA GAGCAGAGGA GCAGAGAACC TCGCAGTAAT AAAGGAAAAC 960 TGAAACCCTC TCCTGTGTGA GAGGGTTTGG GAAGCCTTTT TTTTTTATTT TTGGTTGGGG 1020 AAGAATGAAT TCAGTCTCCT GCTGAATCAT GATTTATAAA TGCAGCTCAG ATGAGGGTTT 1080 TAGAGTTCTC AGCCTTGGAG GCTGCGTCAT TTAGAAAGGG TGACCTGCCG TTTAGCCCCT 1140 TCCCGAGAAA GGCAGGGCTG GATGGGCATT TTGCAAAACC CACAGCTGCC ACTGGGTCGG 1200 GTTACACAGA GCTCAGAGCC TTTAACTCCT GCCTGACTCC CTGCCAGAAA GCAGGGGTTT 1260 TTCCCAGAAT GACATTTAGC CTCAGAGGCG CTGGACTCCA GCTCAGCATT CCAGGTCATT 1320 ATTTGTTAAC TCTTAGGTAT TCCTTCTTGG AGGAGAGCGC TTGCCACCGT GTCAGGTGGC 1380 CTGGCCAGAG GGCTGCGTGT GGGCTGGCTG TTCAGGGTGT GTGCTTCTCT GCTGTCTGCT 1440 GAGGGCCAGT GATGGGAAGA TGAGGACGGG CGTGTGGCCC TGGCCCTTTG GAGAGACAGA 1500 GATGAAAGTG ATGATTGGAT GTCATCCAGA GCATCAATGG CAACAGAACC AGTTCTTAGC 1560 AAACTAGAAA ATAATTAAAG CTGCACTTTG ACCCCTGCCT CCACCCGCCG ACTGCACAGC 1620 CAACCCCGCT GTCCCACCCC CAGCTGTGTC CCAGTTGTCA GGGCCTTGCT TTCAGCCACC 1680 TCTCAGAAAG AACTTGTAGG GGCTCATGGA TCCTTTTTTG AGACTGATGA AATGCATGGA 1740 TGCCTTCTCC AGGTAAATGC ATAGGTGTAC AGACACACCC TGCTTTTGCC TATAATTTCA 1800 GGGAGCCCAT TGACCTCCTG AAGCTGGTCC AGAGACCCCC ATCCCATGTA GGTGGCTGCT 1860 ATTCCCCTGA TCCTGATGCC ACCTTGTGGG GCAAGGTCAC CCCCAGATAC CAGGGCAGAG 1920 GCCGCAGCAG AGCTAGGAGA CCTTGTTTTG CTGCCACTGC TTCTGCCAGA GGGGCCCCAG 1980 CTCCTCTTCC GGCCATGGGC AGACAGGGTG GGGCTGGCCC TAGCCGTGCC TGGCCGCTGA 2040 CGAGCTTGCA GCTCCTGTGG TCTGTGTTTG ATCTGATAAG CGCAAGTTCC TGAGAGTCTG 2100 TTGAGCTGTG GAGCAGCCCT GTCTGCGTCA CTCTACGGGG GACCTGTGCC CACTCCCTGC 2160 TCACATCCCT GACCTCTGCT CGCTGCTGGG GTGTTCACAG GACCCACCAG TCAACCACTG 2220 CTGGGTAGCG CCTCTGCTGT GGCCACCTCG GCTGTGTGGA TGGCTGCACT TTGGTGGCCT 2280 CACTGGAGTC AGACGGTCGG GTGACCTCAC CCGCCTGCAG CCACGCCTCT TCATGAGAGG 2340 AGGTGAAGCC 2350
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