Tag | Content |
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EnhancerAtlas ID | HS098-10030 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:57565870-57569200 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr11:57566650-57566661 | TGTGACTCATT | + | 6.62 | Gata4 | MA0482.1 | chr11:57569079-57569090 | GAGAGATAAGA | - | 6.32 | LMX1B | MA0703.2 | chr11:57568986-57568997 | GTTTTAATTAA | + | 6.14 | LMX1B | MA0703.2 | chr11:57568989-57569000 | TTAATTAAATT | - | 6.32 | Myod1 | MA0499.1 | chr11:57566460-57566473 | AGCAGCTGTTGCT | + | 6.59 | SOX10 | MA0442.2 | chr11:57567120-57567131 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr11:57567120-57567130 | AAAACAAAGG | - | 6.02 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_00588 | chr11:57565379-57570901 | Adipose_Nuclei | SE_04676 | chr11:57566140-57567276 | Brain_Anterior_Caudate | SE_04676 | chr11:57567708-57569592 | Brain_Anterior_Caudate | SE_23577 | chr11:57565909-57567459 | Colon_Crypt_1 | SE_23577 | chr11:57567961-57568304 | Colon_Crypt_1 | SE_25895 | chr11:57565428-57569258 | Duodenum_Smooth_Muscle | SE_27154 | chr11:57565241-57568721 | Esophagus | SE_27712 | chr11:57565226-57568638 | Fetal_Intestine | SE_28738 | chr11:57565180-57568913 | Fetal_Intestine_Large | SE_29910 | chr11:57567795-57569018 | Fetal_Muscle | SE_32413 | chr11:57565760-57566307 | Gastric | SE_32413 | chr11:57566321-57567360 | Gastric | SE_32413 | chr11:57567749-57568390 | Gastric | SE_33882 | chr11:57565732-57568771 | HCC1954 | SE_36122 | chr11:57565689-57568939 | HMEC | SE_37202 | chr11:57565740-57571962 | HSMMtube | SE_38452 | chr11:57566280-57567445 | HUVEC | SE_38452 | chr11:57567506-57570056 | HUVEC | SE_43078 | chr11:57565820-57567203 | Lung | SE_43078 | chr11:57567731-57568490 | Lung | SE_46534 | chr11:57565737-57567485 | Osteoblasts | SE_46534 | chr11:57567788-57568983 | Osteoblasts | SE_50561 | chr11:57565736-57567409 | Sigmoid_Colon | SE_50561 | chr11:57567725-57568508 | Sigmoid_Colon | SE_52712 | chr11:57565239-57567309 | Small_Intestine | SE_52712 | chr11:57567688-57568504 | Small_Intestine | SE_64417 | chr11:57565688-57567762 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 57567716 | 57569000 | chr11 | 57566316 | 57567172 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I057797 | chr11 | 57565307 | 57570910 |
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Enhancer Sequence | TTTAGGAATT CAGAACCAAA AGAGACAGTT GAGGACGTGT ATAAGAACTT TCTTGTGTTT 60 TTAATCCCAA AGTTAAAAAC AAACTTTGAC CTCACAAGGG CCTTGACATT CTATGCTTAG 120 GGTCTTATTA TTTGATTGTA AAGTGAAATT GTGGTGGCAT CCTTGGGTGG GGGTCGGGGG 180 ATACATTAGC AACACTCTGA AAGGTCACTA AGCAGCTGCC TACTCTGACT TTACTACTTG 240 TTCCTGGAGA TTCTTTGGTG ATGTGAAAAA AGGAGTGATT GATGTTTGGA CTGGTACATG 300 GTTTGCCTTG TTGCATTGAG AGAATGCTTT AGAATGGGGT CGACAGACCC CTGAAAATGA 360 CCACGTAGAA CTATTTTAGG CTTTGCAGGC CATGTATCAT CTTTGTCGTA TGTTGTTCTT 420 TTTTTCAAAC AATCTTTTAA AAATAGCATT ATGGGGATGT ACAAAAACAG GTTTGGCCCA 480 TGGGCTGCCA ATGCTGCTTC AGAATAAATT AGAAACAGTG TTTTCCAGGT AAAGAGAAAT 540 GATAAGAAAC AAGGGATGAT TTATGGTTGT CTTGATGGTA AGGATATCCT AGCAGCTGTT 600 GCTGAATTTC TCTATATGGG GTCATGACCT TTTAAAGCAA ATGCCTTGGT GCTCATTTTC 660 CTCATATATT AGGTAGCTTT GGTTAAGAGT GAACAGGGCT GGGCCCAGGG GTAGAGGCCC 720 CATTATCTAA GACTGAGTCA CTCACCTTTC AGGTGTCTTG GATAGCTAAT CCAACTCCCA 780 TGTGACTCAT TTTTATTCCT ACAGGAGCAC CAGACCTCGG CTGGTGCAAC CTAGAGCAGT 840 GGTAGATAAC AGCCTTCATT GAAGCAGTCT GTCCAGGGTG TTGGCTCTAC TGCAAGTCTG 900 CTTTTTCTGA CTTCCTCATT AGTAAAGAGT GATTGGACCC AGATGGGTGT GGGTGGCCAG 960 GTCATTCTCT GCCATCCCTA GTTGTGCTAG TTCACATAGA GTTTTGGGCC TGGTTCTTGG 1020 GTTTGTTCCA GGGTAGCACT GGACTTGGAA ACCTGCTTGA CTAGCAAGCA TATTTGCTGC 1080 TTCCTGTTCC AGGCTAGAAG AGTAATACAA GGTCAAACTT AAACAGTGAG GCAGTGATTA 1140 GTGGAAAAAG CACTGAACCC TGAGACCTTG GTTCTAGTTG TGCCTTTGCC ACTAGCTAAG 1200 TAGCCTCAAG CAAGTCATTT GGTCTTCCCA GGCACAGCTT TGTTTCTTGT AAAACAAAGG 1260 AAAGAATGTC CAATCCACTG CCTTTGTATA GAAAAGGATA TAGGATAGAG TTATCTGGAA 1320 ATTTTGGTTA TGGTAATTGT TCTTATAATT TTGTATATTA ATAATAGAGG TTAAACATGT 1380 TCAATACAGA GCCTGAAAAA CCCAGAAAAG CATTACCATC TATTGATAAA GAACCACTGT 1440 TAACATTTTG GTGCATATCC TTTGAGTTTT TTTAATTATA CATGTAACTA TATCCTATTT 1500 TCCCTCTACT AAAATGGAAT CTTAACATAC TGCTTAATAG CCTACTTTTA AGCTATCTAA 1560 GCTATTCATT TTGTTTCCGT GTTTTTTTTT TTTTTTTTTT TTTTTTTGAG ATGGAGTCTT 1620 GCTCTGTCAC CCAGGCTGGA GAGCAGTGGT GCGATCTGGT ATTATACCCA GGAGGCTTTT 1680 TGTTCCATGC ATGGTATTTT ATAATGTTAG TAAATACTTT TCCTTAATTT TATAGTAAGC 1740 AGAAAATTTT TATGGTTGGG GTGGATGCAA AAGTGATACA TAATAGTTTA GAAGACAACC 1800 AATTTTGTTT TACCAGCTGT TTGGGCATTT TTAGTACCCC CTTCTTGATT TGAAGGGTTT 1860 AATCTTGACC TTTTTTTTTT TTTCTTCGAA ATAGAGTCTC GCTCTGTCAC TTAGGCTGGA 1920 GTGCAGTGGC ACAATCTCAG TTCACTGCAA CCTCCACCTC TTGGGTTCAA GCGATTCTCT 1980 TGCCTCCGCC TCCCAAGTAG CTGGGATTAC AGGTGCCCAC CACCATGCCC AGCTAATTTT 2040 TGTATTTTTA GTAGAGATGG TGTTTTTCCA TGTTGGCCAT GCTGGTCTCG AACTTCTGAC 2100 CTCAGGTAAT CCGCCCACTG CAGCCTCCCA AAGTGCTGGG ATTACAGATG TGAGCCACCA 2160 TGCCTGGTCC TGTTTCCGTG TTATTTTAAG ACCATCTTGG TCATGGTTTA CTAAATGCTT 2220 TGTCCATCTG AATCACTGTT GCATAGTTGA TGTTGATACC TGTGAGGCAG GCCTTCTGCT 2280 CAGGGCAACC TTGAGTATTT GTTGACAGTG GGAGTGGTTT TGTAGAACAA ACAATGGCTT 2340 ATTTGGAGAG CTCCACACAA TAGATTATCC TCTCCTGTGG GAGCCAGAAA GAGATGAGCT 2400 CACAGATAAT GGGTTTCTTC CTTCCTGGTA GTTACGAATA AATAATAGTG TGACAGACTC 2460 ACCCTCTAGT GGTTGTTGGT AGTACTGAAA CAGGAAGAAT TGTCTCCTGG TTTGATTTTT 2520 CTTACTTTCA ATTGCTTTCT CTGTTCCTAG TGGCTGGGCT TCCCAAATGT GATGTTGGTG 2580 AATAGGCTTC ATTTTGAAAG AGCTGGAGGT ATTGTCTTTA GAAATTGGAG GATGGAATCT 2640 TACCTCTTAA CACATTTGTT GAGTAGCAGA CATGACCTTG GAATGACTGT GAAAATTACT 2700 TTTCAAGTTT ATACCTCATC AGTACCAAAG CCAGATCCTC CTGTGATGTA GCAGGAAGCC 2760 CTTTATTAGT TTTTCTCTAT CAATCCATCT TTTATAATTT CCAAAATAGG ATAAGGAGAA 2820 GCTTAAATAT GAAATGTATT TAAAGGTCTT ATCCTACCAG TTGTTTCCTG TGTGTAAATG 2880 CCTAATTTCC TGTTTGGTTA AGGAACTGTT CTCAGACTTC TGTGGCATTG AGTCAGTTGC 2940 TTTGGTTAAT TCTGTTCTCT GAGAGTTTAT CCTGATCTCT ACCTAGACAA GTTAATAACT 3000 GTCAGATATC ATTCAAATAA ATGATAAGTA GTAAGGATTT GGTTCTTTCT TTTTGATTAG 3060 CCTTTCCTGA ATGCTTGTTA CTTTCTAAGC CTGCAGACTT CAAAGAAAAA AATGTAGTTT 3120 TAATTAAATT GCAGGTGTTT TTAAAATTAT TACCTTTTAT TTTTACTAAC CCATTGAGGA 3180 AAATTGATCA GTATATTATT CATGCAAAGG AGAGATAAGA TGAGCACACT GAAACTCCAG 3240 TTAATCCTCC TTTGCAGATG AGGGTAATGG GAATGTCCAG GAAGCTAGCC ATAATGACTT 3300 GATGTATTCT CTTGGTTCTT CCAAAACTTC 3330
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