Tag | Content |
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EnhancerAtlas ID | HS182-05867 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr13:47179950-47182790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr13:47181591-47181602 | AAAACAAAGAC | + | 6.14 | ZNF263 | MA0528.1 | chr13:47181734-47181755 | TTCTCCTTCTCCTTCTCTTTC | - | 6.04 | ZNF263 | MA0528.1 | chr13:47181740-47181761 | TTCTCCTTCTCTTTCTCCCCT | - | 6.53 | ZNF263 | MA0528.1 | chr13:47181737-47181758 | TCCTTCTCCTTCTCTTTCTCC | - | 6.55 | ZNF263 | MA0528.1 | chr13:47181731-47181752 | TCCTTCTCCTTCTCCTTCTCT | - | 6.77 | ZNF263 | MA0528.1 | chr13:47181725-47181746 | TTTTTCTCCTTCTCCTTCTCC | - | 6.84 | ZNF263 | MA0528.1 | chr13:47181761-47181782 | TCCTCCTCTTCCTTCTTCTTC | - | 6.96 | ZNF263 | MA0528.1 | chr13:47181719-47181740 | TTCTCCTTTTTCTCCTTCTCC | - | 6.98 | ZNF263 | MA0528.1 | chr13:47181722-47181743 | TCCTTTTTCTCCTTCTCCTTC | - | 7.09 | ZNF263 | MA0528.1 | chr13:47181716-47181737 | TCCTTCTCCTTTTTCTCCTTC | - | 7.25 | ZNF263 | MA0528.1 | chr13:47181752-47181773 | TTCTCCCCTTCCTCCTCTTCC | - | 7.27 | ZNF263 | MA0528.1 | chr13:47181746-47181767 | TTCTCTTTCTCCCCTTCCTCC | - | 7.61 | ZNF263 | MA0528.1 | chr13:47181728-47181749 | TTCTCCTTCTCCTTCTCCTTC | - | 7.89 | ZNF263 | MA0528.1 | chr13:47181758-47181779 | CCTTCCTCCTCTTCCTTCTTC | - | 7.98 | ZNF263 | MA0528.1 | chr13:47181755-47181776 | TCCCCTTCCTCCTCTTCCTTC | - | 8.17 | ZNF263 | MA0528.1 | chr13:47181749-47181770 | TCTTTCTCCCCTTCCTCCTCT | - | 8.46 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_11526 | chr13:47178229-47184294 | CD20 | SE_32604 | chr13:47179224-47182784 | GM12878 | SE_54689 | chr13:47178235-47180271 | Stomach_Smooth_Muscle | SE_54689 | chr13:47180338-47181814 | Stomach_Smooth_Muscle | SE_60060 | chr13:47158419-47187371 | Ly4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 47180727 | 47180924 | chr13 | 47181871 | 47182248 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I046604 | chr13 | 47178302 | 47184488 |
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Enhancer Sequence | TTTGTGATAA TGGGTGAAAA TGTGATTAGA ATTCACATTC TAGGTTTAAT AATGACAGAC 60 TACTTATGAA AGATAAGATG TCAGAGCTGG AAGGCTTCTT AGATATTGTC GGGTTCAATA 120 TTCTTTTCTC ATTAGAGGAA ATGGAGACTC AGAGACATGA AGTGACTTCT CCAAGGTCAC 180 ACAGTAAGTG AGTGATGAAG CTGGGAGTAG GACCTCTTTT GCCTGACTCC AAACACAGCT 240 TTCCCCAACT ATTGAGGAAA AGGACTCAGG ACAATTTAAC ATTTCAAGTC ATTGAAATAT 300 CCTTTAAATG CTCAAACTCT AATTTTAACC TTATGTGTGT GTGTGTGTGT GTGTGTGTGT 360 GTGTATAAGT CGTTCTAAAG TACTTAACCT TCTGAAATCT TATTTTGACC ATGTAGAACA 420 CAGTTCGACC TTTTTTCAAT CTCATCATTA TCAACACTGT TTTGTGAACA TGGGTCATTG 480 TGGTTTTAAT TCATGGGTGC CCTTGGGCTA TTCTGAGTCT ATAGGACTTG CCCTTAGTTA 540 CATTAACACT CCCACATGAC AAAACTCATG AGTGCATGGG GAACTTTTTG ATATCCTTCC 600 TCATTGTCAG TTGTCACTTT TTGCTACTTT CAGAGGTGAT ATTTATAGCA TTTCCCCCCT 660 TCTGTGTTGT TCCTACCCAC AGGATTTTAA CTTACAGAGA TGACTGAATG ATGACACAGA 720 GGGGACAAGT CCATTGAAAT AAGTCTTGTT TTGTTTTGTT TTGTTTTGTT TTTTGGGACA 780 GGGTCTCACT CTGTCGCCCA TGCTGGAGTA CAGTGGCACA ATCTCAGCTC ACTGTAGCCT 840 TTGTCTCCCA GGTTCAAGCT ATTCTCCCGC CTCAGCCTCC TGAGTAGTTG GACTTACAGG 900 CGTGGGCCAC TACGCTCGGC CAATTTTTGT ATTTTTAGTA GAGATGGGGT TTCACCATGT 960 TGGCCAGGCT GGTCTCGAAC TCCTGACCTC AAGTGATCCT CCTGCCTCGG CTGGTGTGCT 1020 AGGATTACAG GTGTGAGCCA CAGCACCTGG CAGAAAGAAA TTTTTTTTTA TTACTCACAT 1080 TTCCTAAGAG AAGAGGGCAT TCCATGCCAC ACAGGGCCAG GAGGAGAAGC ACCTATTTGG 1140 GTGAAGAGGA AGAGATGGGA GTCAGGGGAA AGCCGAGGCC AGAGCCTTTA CTGGGTTTTT 1200 ATGGAAAAGG CAAGGCAGAC TGGAGGAATC AGCTTGGGGT TGGCTAGGCG CTGGGATGGT 1260 CTTTAGTTGT CAGTTCCTGG CCCTGAGAGA TTTAGGGCAG GGGAAATGTG GGCTGGGTAA 1320 CTGAGAGTTA GATAAGGAGG TGGCTCAGCT AGATCACAGA GGAGATGGAA ACTACTTGGC 1380 TGTTAACTTG CCCTGTAATT GATGGATACC AAATAGCCAA ATACAGATTC GGAGAAAATG 1440 CAGGACAACT TCCCAGGCTT ACTTTGCTGC CATTCATTTT GTGGTGAACC AAAAAACCAC 1500 TTACACAAAC CTGTTGGAAG GGGTCTCTTT TGTGAGTACT GTCAAAGAGA GCTATCTAGA 1560 AGAGACCTTT TTTTGTGAGT GGTGAGGTTT AGGCTGAATT TTTATTTTGT TTTGGTGCTT 1620 TTCTGTAATT TGGGATTATT AAAAACAAAG ACTAGACCTT TTTATAGATA GAAACAAGGC 1680 TCTTTTATTT GGAAATACCA TGTGCATAAA TGATGAATAA ATAGAGTCAG TGAGGACCTT 1740 CTTGCCCTCA TGATTCATTG TTCTTCTCCT TCTCCTTTTT CTCCTTCTCC TTCTCCTTCT 1800 CTTTCTCCCC TTCCTCCTCT TCCTTCTTCT TCTTTTTTTT TTTTTAATAT GAGACACAGT 1860 CTCGCTCTGT TAAACACTTG TATTAGTTTC ATTGAAAGTG TAATATAAAA TCTGAGGATC 1920 TCAGACATCT TAGGAAGATG ACTGTCATTT ATTATCTATT AACCAGGTGA GCAACTTCCT 1980 GGCGAGTGAG GGGTGCGGCA GGGAAGGGTG GAGACGCAAA GGCACAGTTC CCTTTGTAAT 2040 GGAGAGCTTC AGCTCCTGGG AAGGATCTGC AATGCTTAGT GGGGCTGTTC ATCTCTAATA 2100 TAGTTAATAA TTACTGATTT GTATGAAGCA GAACTGAGGG CAGGGAGGGA TGTGGGAAGG 2160 CCACAGGAGA TATGAGTTTG CAGCCAGAGT TTACCGGTGA TGAATCACCT TCTGATCAAA 2220 GCAGGAGGCT GGGACCTGTG GGGGATGCAC TTCGACCCTG GGGTGTGACC CAGGAAGTCA 2280 GTGATTTGTG AAGGGCATCA TAGGTCACAG ATGCCTTTCC AAAGTTACCA GAACTTGGGA 2340 TCCAATTTAT TTCTCTTAGT CCAGGCTCAG GTTTGATTCC CAATCCCTTG CATTCACACG 2400 AGTCACAGGG CAGAAAAGTG CAGACGTGTT CTTGTGCGAC CTCCAGATGT GGTGTGGAGA 2460 TGGAAGATGG TACTCTCATC ATTAGAGCTG ATTTGCTTTG GAATTAAAGA GAGACATACG 2520 CACTGTGTTT CTGTGGCCCA TCATAGTTTC CACTGATGGT GCCATGTGTC ATTTGGGGTA 2580 ACATTGACTT GTATTTCCAC TCAGTGTGAG GAAAGGACCA TAAGACAGAA TTGGAGTAAT 2640 TTCTGGAAAA AAGAAGTAAA TGCTTAGTAG AGTGTCATAC AGTCTTTTAA TAACAAGTAT 2700 TTGATAAACA TGATTTTGTT ATCCATCCTT CTGCAGGAAA AGAAGCCAAG TTAATTTTCC 2760 TGAGTTTACA GATTGGAGGG TTTTTAGTAT AACCTGTGCC TTTTTCCTTC ACCCTGTTTC 2820 CTCTTTTACT ACTACAGTAA 2840
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