Tag | Content |
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EnhancerAtlas ID | HS049-02315 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr14:69148810-69151780 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:69151674-69151692 | CTTTCCTTCCTTCCTTCC | - | 10.53 | EWSR1-FLI1 | MA0149.1 | chr14:69151678-69151696 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr14:69151682-69151700 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr14:69151686-69151704 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr14:69151690-69151708 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr14:69151694-69151712 | CCTTCCTTCCTTCCTTCC | - | 10.83 | EWSR1-FLI1 | MA0149.1 | chr14:69151654-69151672 | TTTCCCTTCCTTCCTTCC | - | 7.55 | EWSR1-FLI1 | MA0149.1 | chr14:69151702-69151720 | CCTTCCTTCCTTCTTTCT | - | 7.85 | EWSR1-FLI1 | MA0149.1 | chr14:69151658-69151676 | CCTTCCTTCCTTCCTTCT | - | 9.09 | EWSR1-FLI1 | MA0149.1 | chr14:69151670-69151688 | CCTTCTTTCCTTCCTTCC | - | 9.09 | EWSR1-FLI1 | MA0149.1 | chr14:69151698-69151716 | CCTTCCTTCCTTCCTTCT | - | 9.09 | EWSR1-FLI1 | MA0149.1 | chr14:69151666-69151684 | CCTTCCTTCTTTCCTTCC | - | 9.17 | EWSR1-FLI1 | MA0149.1 | chr14:69151662-69151680 | CCTTCCTTCCTTCTTTCC | - | 9.47 | NEUROG2 | MA0669.1 | chr14:69149432-69149442 | GACATATGTT | - | 6.02 | Stat6 | MA0520.1 | chr14:69149123-69149138 | AGTTCTCTGGAAAGC | - | 6.37 | ZNF263 | MA0528.1 | chr14:69149384-69149405 | CCATCCTGCTCCCCTTCCCCC | - | 6.03 | ZNF263 | MA0528.1 | chr14:69151654-69151675 | TTTCCCTTCCTTCCTTCCTTC | - | 6.39 | ZNF263 | MA0528.1 | chr14:69151670-69151691 | CCTTCTTTCCTTCCTTCCTTC | - | 6.45 | ZNF263 | MA0528.1 | chr14:69151674-69151695 | CTTTCCTTCCTTCCTTCCTTC | - | 6.48 | ZNF263 | MA0528.1 | chr14:69151666-69151687 | CCTTCCTTCTTTCCTTCCTTC | - | 6.93 | ZNF263 | MA0528.1 | chr14:69151678-69151699 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr14:69151682-69151703 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr14:69151686-69151707 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr14:69151690-69151711 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 | ZNF263 | MA0528.1 | chr14:69151694-69151715 | CCTTCCTTCCTTCCTTCCTTC | - | 6.94 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_03035 | chr14:69149829-69150429 | Bladder | SE_09837 | chr14:69145943-69153774 | CD14 | SE_10804 | chr14:69147805-69153516 | CD19_Primary | SE_11797 | chr14:69147184-69154238 | CD20 | SE_25846 | chr14:69147216-69151396 | Duodenum_Smooth_Muscle | SE_26618 | chr14:69147082-69150870 | Esophagus | SE_26618 | chr14:69150872-69151624 | Esophagus | SE_27779 | chr14:69147782-69150672 | Fetal_Intestine | SE_27779 | chr14:69150857-69154054 | Fetal_Intestine | SE_28733 | chr14:69142983-69154144 | Fetal_Intestine_Large | SE_29577 | chr14:69146058-69153767 | Fetal_Muscle | SE_31476 | chr14:69149177-69149668 | Gastric | SE_31476 | chr14:69149776-69150715 | Gastric | SE_36049 | chr14:69148571-69151003 | HMEC | SE_36049 | chr14:69151041-69156465 | HMEC | SE_36916 | chr14:69146511-69158224 | HSMMtube | SE_40886 | chr14:69147194-69149654 | Left_Ventricle | SE_40886 | chr14:69149746-69152857 | Left_Ventricle | SE_42158 | chr14:69147179-69151806 | Lung | SE_44336 | chr14:69146331-69154085 | NHDF-Ad | SE_46756 | chr14:69149870-69150688 | Ovary | SE_48603 | chr14:69147190-69151762 | Right_Atrium | SE_50095 | chr14:69147189-69153363 | Sigmoid_Colon | SE_51137 | chr14:69146762-69151267 | Skeletal_Muscle | SE_51770 | chr14:69147182-69154099 | Skeletal_Muscle_Myoblast | SE_52662 | chr14:69147197-69153302 | Small_Intestine | SE_54587 | chr14:69148740-69150722 | Stomach_Smooth_Muscle | SE_55866 | chr14:69148008-69153685 | u87 | SE_60240 | chr14:69134391-69156849 | Ly4 | SE_62911 | chr14:69129549-69162790 | Tonsil | SE_63560 | chr14:69147182-69157806 | HSMM | SE_65119 | chr14:69148699-69149696 | NHEK | SE_65119 | chr14:69149700-69150601 | NHEK | SE_65119 | chr14:69151208-69153616 | NHEK | SE_67722 | chr14:69148008-69153685 | u87 |
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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 |
GH14I068679 | chr14 | 69145901 | 69157990 |
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Enhancer Sequence | TCATCTCACT TTTTTTTTGT CAGCAGCCTA GAGGGAAGGG GACACAATCC CAATTTTAAC 60 ACCAAAGCAA CTGAGACCTA CAGATATTAA ATTACTTGCT CCAGATTACA ACTGAGACTC 120 AAACCCATCG CCTGGCCACA AGTCTGGTGC CCTATCTACA CCAATCTGTC TCCGGTAAAC 180 CTAACTAGCT AGTCAACTTT TCCCATCCAT AGGCCAGACA CCTTTTGAAA TAACAAACCA 240 TCTGATCTCT AGAAAAACTG AAAGGCCAGT TCCAGTTGTC AGACACACCA AGCTCGAGAG 300 AGTCTCTCCC AAAAGTTCTC TGGAAAGCCC AGGGATTCCG AATTCCAAAG CCAGCCAAAT 360 TTGAATTTCC TCTATAAAGA GATAGTCCCT CCTGGTTTAG AACATAACCT TCCTCATTAG 420 GCTGGTTCCA TGTTTTGTAA TAACTTTTGC TTACACCACA AAATTGTCAT AGATTACGAA 480 AACACAAAGG CCTTGGAAAA AAGGCCCAGA GCCCCCTGGA AGTCATTATT TCTTCCTTTA 540 GCAATTGCTG AGTTAAGCAC CATAAATATG GTTCCCATCC TGCTCCCCTT CCCCCGCCCT 600 CCCCGCCCCC CACGATCAGC TGGACATATG TTAGGAAGAA AGCAGGGACG TGGGGGTGGA 660 AGAAGATTCG CATGTCGTGA ATCTTGAGCA CTGAAAAGAA AAAGTGGGGA GAGGGCGGGG 720 AGTTTGCAGC CCTGGAAATG GAATCTCTGA AGGATTTATT GCCTTTGAGT ATCTCACAAG 780 GCTTTTTTTT TTTTAATAAA AATCTGTAGC TTATGGCTTT TTTTTTTTTT TTTTTTTGTA 840 TAGGGCAGTA AACAAGAGCT CTGAAAGGGG AAGGAAGCCA GGAGAAAGCC AGCTCCATTA 900 GTCACGCAGC AGCATATCCT GTCACAAAGG ACCCCAGTTG AGTAATCGCC CAAAATATGC 960 CTGTTATTTT TTTCTGTCAG AAAAAAAATG GGGCCTGCCA AAACGTACTG TAAAAAAAAA 1020 AAAAATCTGG TGTCTTAGGC CCAGAGAGGG AAAAGAAAAT AAAGAAGAAA GAGTCATAAT 1080 TTCACAGTGC TCTTCAAACC CTCTCCCCAG CTTACCTGGA AAAGAAAAAG CCTTCAGACT 1140 CTTCACCACG ACAGAGCCTG CCAGGCTTGA AGAAAGCTAC AGCCTTGGGA TGGTCCAGTT 1200 CTCAGAGTCT TCATAGTTAC TTGGTGCCAA GAGCTTAAAA AGAGGAGGGG TGGTCGGGGA 1260 AAGTTGAAGG AGGACAGCAC GGGGGGAGAG AAAAAATGAA CAGAAAGGGA CCCAGGATAT 1320 TGAACAAGTC CTTTGACGAG CTTTAAATGG GTGAGGCATT GCTCATAGGG AACCCGCAGG 1380 AGCCCACACC AGTTCCATGA GTATTGCATG AGCCCAGCAG GGGCTAGTGA CTTCCAGCCA 1440 ATGGCCGAGC CTGCTTCGTA AGCTTTTCTG ATGGCCCCAG CAAAACCAGC ACTGTCTCAG 1500 GCCTCCACCA TGCCCTGTGG GTGTTTGGGC CACAGACTGG ACAACAAGGA CTTGTGCAGA 1560 AGGACATCGG ACTCTGGAGA GGTCTGAAAC AAGGGGTGGG GAGAGACAGG CTGGTCAGAG 1620 CTGCCTGCAA CCTCCCGTAT TCTCCTGGAT TGGCCTTCCA AAACCCGGGC TGACAGGCTC 1680 TTGGTAGGAA AACAGGCCCA GCAAACAAAG GTGTTCTCAA GCCCAGTTCA GTCACTGCCT 1740 CTGTCCCATG CTCTTAGTCT CATGGCTCTC AGGAGCAGGA CACAAGAGAC GGTTATGCCC 1800 AAGCACAGAA CACTCTTGGA AAGCCATCCT TTCCCTTCTG CTGACATTCT GACCCCCTCA 1860 AGGGTTGTCC ATGGGGAACA GGCTTTCTGC ACCCAATTGA CCAAAAAATA ACAGAAGCCT 1920 TCTCCTTAAG AAAGAGAGCA GGCCAGACAC AGTGGCTCAC GCCTATAATC CCAGTGCTTT 1980 GGGAGGCTGA GGTGGGAGAA TTGCTTGAGC CCAGGAGTTC AAGACCAGCC TGGGCAACAC 2040 AATGAGACCT CGTCTCTACA AAAAAACTTA AAAATTAGCC AGGCATGGTC TCAGCTACTC 2100 AGGAAGCTGA GGTGGGAGGA TTGCTTGAGC CCAGGAGGCT GAGGCTGCAG TGAGCCGTGA 2160 TCATGCCACT GCACTCCAAC CTGGACAATA AAGCAAAAGA TCCTGCCTCA AAAAAGAAGA 2220 AAGAGAACAG AGCCCTACAG AGAAGGAAGA AGGCAGGCAC ATTGTCACTT TTGCTCTCAA 2280 GCTCCCTGGA TCTCTCCTAG AGGAGAGACC CCCAAACCTG CCTGCACTCC GCAGGAGCTG 2340 ACTGGGGGAG GACCCTTTCC AGGGACACCT CCCTGGAGGT GCTCTAATAT TTGGCTGCTT 2400 GGCCATTCTG GGCCAAGAAG ACTCCTTCCC TAGCCCAGGA CCATTAGTCT CCCTGATGAT 2460 TGCTGCAGAA AGGCCCAATT TTCAGGGCCC TACCTAGCCC TTCAATACCT TTGAGCCACC 2520 CATCTTGTCT GAGCCAGAGT CCTAAAGCCA GTCCTGAGCT TCAAGACCCA TGCTTGCCCT 2580 GGCCACTGCT TCCCCTGGGA GAGCTGCCTG GCTTCCTGCA GAGAGCTGGC CTGCAAGTTG 2640 GAAGGGCATA TTCTCCTCCC GGCTCCCTGG CTAAATTGCT ATAGAATTTC AGGTCACTCA 2700 AGTGAACTTT CTGTGACTAT TTTTTCCTCC CTTCAAGATT TATCAACTAT TAATTGGAGC 2760 CTCTAGATGC CTGCAATGTG GAGGTCCTGA GAATTCAATA CAGAATAATA CAAATGCAGT 2820 TCTTCCTGTG AAGCCTGGAC AACCTTTCCC TTCCTTCCTT CCTTCTTTCC TTCCTTCCTT 2880 CCTTCCTTCC TTCCTTCCTT CCTTCTTTCT TGAGTTTCCT GATGCCAGCT CCTCAGATGG 2940 TGAGCCAGCG GTGGGAAGGT AGTGGTGGGG 2970
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