Tag | Content |
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EnhancerAtlas ID | HS133-09416 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr14:69148220-69151550 |
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) |
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 |
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| Number of super-enhancer constituents: 36 | 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 | chr14:69148029-69148688 | Ovary | 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 | TAAGATGATT TAGTTACAGA AGAAAAGGCA GGCAAGATGG AGCAGGCAGG TGCCTTTTGT 60 CTGGGTTTGA CAAGAGAGTT TCCTGGGTAG GGAAGGAATG TGATCAAAGT TATGATTCTA 120 AGACCTGCCT GGAAGATGAC CAGGGAGTGG GCAAACTTGG AAGCAAAACC AGCCTCCCAA 180 ACACCTGTGT AATATCGTGT CCTGGGCCAC TGTATAAATA ACCTCCCTCC TGTTCATCAG 240 TAGGCTTTGT AGTTCTCAGC CTCTCTCCTC TGTTGAAAGT GTGAGCCAGC CCTTTGCATG 300 AAGAAGCATT AGAAGGGATC ACTGCATACT TCTTTAATTG TCAAGAATGC ATACATGCCA 360 TGCATATGAA AGATATAGTG GACTTTGGGG ACTGGGGAGT GGAGCAGGTT GGGAGTGGGG 420 TGAGGGATAA AAGATTACAC CTTGGGCACC GTGTACACTG CTTGGGTGAT GGGAGCATCA 480 AAATCGCAGA AATCACCACT GAAGAACTTA TCCATGTAAC CAAAAACCAC TCGTACCCCC 540 AAAAATATTA ACATTAAAAA AAAGAATTCC CACCGTGCCT TAAACTTATG TCATCTCACT 600 TTTTTTTTGT CAGCAGCCTA GAGGGAAGGG GACACAATCC CAATTTTAAC ACCAAAGCAA 660 CTGAGACCTA CAGATATTAA ATTACTTGCT CCAGATTACA ACTGAGACTC AAACCCATCG 720 CCTGGCCACA AGTCTGGTGC CCTATCTACA CCAATCTGTC TCCGGTAAAC CTAACTAGCT 780 AGTCAACTTT TCCCATCCAT AGGCCAGACA CCTTTTGAAA TAACAAACCA TCTGATCTCT 840 AGAAAAACTG AAAGGCCAGT TCCAGTTGTC AGACACACCA AGCTCGAGAG AGTCTCTCCC 900 AAAAGTTCTC TGGAAAGCCC AGGGATTCCG AATTCCAAAG CCAGCCAAAT TTGAATTTCC 960 TCTATAAAGA GATAGTCCCT CCTGGTTTAG AACATAACCT TCCTCATTAG GCTGGTTCCA 1020 TGTTTTGTAA TAACTTTTGC TTACACCACA AAATTGTCAT AGATTACGAA AACACAAAGG 1080 CCTTGGAAAA AAGGCCCAGA GCCCCCTGGA AGTCATTATT TCTTCCTTTA GCAATTGCTG 1140 AGTTAAGCAC CATAAATATG GTTCCCATCC TGCTCCCCTT CCCCCGCCCT CCCCGCCCCC 1200 CACGATCAGC TGGACATATG TTAGGAAGAA AGCAGGGACG TGGGGGTGGA AGAAGATTCG 1260 CATGTCGTGA ATCTTGAGCA CTGAAAAGAA AAAGTGGGGA GAGGGCGGGG AGTTTGCAGC 1320 CCTGGAAATG GAATCTCTGA AGGATTTATT GCCTTTGAGT ATCTCACAAG GCTTTTTTTT 1380 TTTTAATAAA AATCTGTAGC TTATGGCTTT TTTTTTTTTT TTTTTTTGTA TAGGGCAGTA 1440 AACAAGAGCT CTGAAAGGGG AAGGAAGCCA GGAGAAAGCC AGCTCCATTA GTCACGCAGC 1500 AGCATATCCT GTCACAAAGG ACCCCAGTTG AGTAATCGCC CAAAATATGC CTGTTATTTT 1560 TTTCTGTCAG AAAAAAAATG GGGCCTGCCA AAACGTACTG TAAAAAAAAA AAAAATCTGG 1620 TGTCTTAGGC CCAGAGAGGG AAAAGAAAAT AAAGAAGAAA GAGTCATAAT TTCACAGTGC 1680 TCTTCAAACC CTCTCCCCAG CTTACCTGGA AAAGAAAAAG CCTTCAGACT CTTCACCACG 1740 ACAGAGCCTG CCAGGCTTGA AGAAAGCTAC AGCCTTGGGA TGGTCCAGTT CTCAGAGTCT 1800 TCATAGTTAC TTGGTGCCAA GAGCTTAAAA AGAGGAGGGG TGGTCGGGGA AAGTTGAAGG 1860 AGGACAGCAC GGGGGGAGAG AAAAAATGAA CAGAAAGGGA CCCAGGATAT TGAACAAGTC 1920 CTTTGACGAG CTTTAAATGG GTGAGGCATT GCTCATAGGG AACCCGCAGG AGCCCACACC 1980 AGTTCCATGA GTATTGCATG AGCCCAGCAG GGGCTAGTGA CTTCCAGCCA ATGGCCGAGC 2040 CTGCTTCGTA AGCTTTTCTG ATGGCCCCAG CAAAACCAGC ACTGTCTCAG GCCTCCACCA 2100 TGCCCTGTGG GTGTTTGGGC CACAGACTGG ACAACAAGGA CTTGTGCAGA AGGACATCGG 2160 ACTCTGGAGA GGTCTGAAAC AAGGGGTGGG GAGAGACAGG CTGGTCAGAG CTGCCTGCAA 2220 CCTCCCGTAT TCTCCTGGAT TGGCCTTCCA AAACCCGGGC TGACAGGCTC TTGGTAGGAA 2280 AACAGGCCCA GCAAACAAAG GTGTTCTCAA GCCCAGTTCA GTCACTGCCT CTGTCCCATG 2340 CTCTTAGTCT CATGGCTCTC AGGAGCAGGA CACAAGAGAC GGTTATGCCC AAGCACAGAA 2400 CACTCTTGGA AAGCCATCCT TTCCCTTCTG CTGACATTCT GACCCCCTCA AGGGTTGTCC 2460 ATGGGGAACA GGCTTTCTGC ACCCAATTGA CCAAAAAATA ACAGAAGCCT TCTCCTTAAG 2520 AAAGAGAGCA GGCCAGACAC AGTGGCTCAC GCCTATAATC CCAGTGCTTT GGGAGGCTGA 2580 GGTGGGAGAA TTGCTTGAGC CCAGGAGTTC AAGACCAGCC TGGGCAACAC AATGAGACCT 2640 CGTCTCTACA AAAAAACTTA AAAATTAGCC AGGCATGGTC TCAGCTACTC AGGAAGCTGA 2700 GGTGGGAGGA TTGCTTGAGC CCAGGAGGCT GAGGCTGCAG TGAGCCGTGA TCATGCCACT 2760 GCACTCCAAC CTGGACAATA AAGCAAAAGA TCCTGCCTCA AAAAAGAAGA AAGAGAACAG 2820 AGCCCTACAG AGAAGGAAGA AGGCAGGCAC ATTGTCACTT TTGCTCTCAA GCTCCCTGGA 2880 TCTCTCCTAG AGGAGAGACC CCCAAACCTG CCTGCACTCC GCAGGAGCTG ACTGGGGGAG 2940 GACCCTTTCC AGGGACACCT CCCTGGAGGT GCTCTAATAT TTGGCTGCTT GGCCATTCTG 3000 GGCCAAGAAG ACTCCTTCCC TAGCCCAGGA CCATTAGTCT CCCTGATGAT TGCTGCAGAA 3060 AGGCCCAATT TTCAGGGCCC TACCTAGCCC TTCAATACCT TTGAGCCACC CATCTTGTCT 3120 GAGCCAGAGT CCTAAAGCCA GTCCTGAGCT TCAAGACCCA TGCTTGCCCT GGCCACTGCT 3180 TCCCCTGGGA GAGCTGCCTG GCTTCCTGCA GAGAGCTGGC CTGCAAGTTG GAAGGGCATA 3240 TTCTCCTCCC GGCTCCCTGG CTAAATTGCT ATAGAATTTC AGGTCACTCA AGTGAACTTT 3300 CTGTGACTAT TTTTTCCTCC CTTCAAGATT 3330
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