Tag | Content |
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EnhancerAtlas ID | HS138-07210 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr11:57559150-57561480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr11:57559558-57559575 | GGGAACAGTCTGTACCC | - | 6.39 | Ar | MA0007.3 | chr11:57559558-57559575 | GGGAACAGTCTGTACCC | + | 6.45 | CDX2 | MA0465.1 | chr11:57561086-57561097 | TTTTATGGCTT | - | 6.62 | LMX1B | MA0703.2 | chr11:57560919-57560930 | TTAATTAAATT | - | 6.32 | NR3C1 | MA0113.3 | chr11:57559558-57559575 | GGGAACAGTCTGTACCC | - | 6 | NR3C2 | MA0727.1 | chr11:57559558-57559575 | GGGAACAGTCTGTACCC | - | 6.05 | Nr2f6(var.2) | MA0728.1 | chr11:57560221-57560236 | CGATCTCTTGACCTC | - | 6 | SPIC | MA0687.1 | chr11:57559363-57559377 | GACTTCCTGTTTTG | - | 6.22 |
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| Number of super-enhancer constituents: 20 | ID | Coordinate | Tissue/cell |
SE_00588 | chr11:57558300-57562425 | Adipose_Nuclei | SE_23577 | chr11:57558515-57560185 | Colon_Crypt_1 | SE_23577 | chr11:57560202-57560743 | Colon_Crypt_1 | SE_23577 | chr11:57560966-57561475 | Colon_Crypt_1 | SE_25895 | chr11:57558911-57561838 | Duodenum_Smooth_Muscle | SE_27154 | chr11:57558231-57560871 | Esophagus | SE_27154 | chr11:57560929-57561764 | Esophagus | SE_27712 | chr11:57559033-57561746 | Fetal_Intestine | SE_28738 | chr11:57559389-57561702 | Fetal_Intestine_Large | SE_29910 | chr11:57559119-57561749 | Fetal_Muscle | SE_32413 | chr11:57558490-57560154 | Gastric | SE_32413 | chr11:57560171-57560725 | Gastric | SE_33882 | chr11:57558280-57561381 | HCC1954 | SE_36122 | chr11:57558194-57561787 | HMEC | SE_38452 | chr11:57558479-57561109 | HUVEC | SE_43078 | chr11:57558461-57562087 | Lung | SE_46534 | chr11:57558931-57561650 | Osteoblasts | SE_50561 | chr11:57558359-57561685 | Sigmoid_Colon | SE_52712 | chr11:57558457-57561603 | Small_Intestine | SE_64417 | chr11:57559081-57561186 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr11 | 57560800 | 57561400 | chr11 | 57559600 | 57560800 | chr11 | 57559748 | 57559971 | chr11 | 57559200 | 57559449 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I057790 | chr11 | 57558407 | 57561702 |
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Enhancer Sequence | CCCTCTCTCC ATCAGACGTG CAGGTAGGAC TTTGGCATGG TCACAGAGAG GCTATGATCC 60 TTTTTGGGAA GCTACTCTCC TTTTGGTGAT GGGCTGTCCA GTGCCCGTTC TTCCAGGGAT 120 TTTTTTCCAG GGGTGTTAAA TGCTGATAAG AGACAAGGAA TATTGCTGCT GGACTGAGCT 180 GGGTGCAGTT ACTATCTCTA GAAGCATCCA TCTGACTTCC TGTTTTGCTG GAGTAGGTTT 240 TTTGGGGTGG GCTACAATTC TAGTAATGGT AGATAGTTTA GTTTGCAGCT GTACTCAAGT 300 TACTTTTCTT TTCTGATTTT TTTTTCTTGG TATCAAAAAA TCAGGAAAGT AAATGCCCAC 360 TTAATGGTTG GGCATCTTGT GCTCTCAGCC CTAGTTCAGT CTCCCTGAGG GAACAGTCTG 420 TACCCAGGTG TGGCAGTATC CATAAATTGT GTACTCCTGC TCCATATTGT CCTTGTGTGC 480 TCTTTTTGTT GGCTGTGTAA ATCATGTGTT GGAGGAAGGG GTCATTGTTA ATTCTGTTGG 540 TTAGAGTTGG AGAGGGAGCA TCATGCTGCT GTTTAACCCA AATAACCACA GGAGCCAGTG 600 GTCTCTGGGT TGGCTGACTC TGTGATGTGA CTTGGGAGAG TTGGTGTTAG AAATGAGAAG 660 TATCTTGTGT TTCCTCTGGT TTTTCTAGTC TGACTTTGCT GTGATGTAAT CTGTCTGAGG 720 TTTTGTCTGT CTTCCTCTGT GTGTGTGTGC GTGTGTGCGC GCGCACTCGC GCATGTGTGT 780 GTGTGGTAGA CATTGCCTGA TAGATTGCAT CTTACGAGAG ATCTCTGAGT GGGAACCAGA 840 ACAGTACTCA TGCCCTGATA GTCCTTTTCA TTGAGTAATT TTTATTTATT TATTTAAATA 900 GGAGTGCAGT GGTGCAATCT TGGCTCACTG CAACGTTCGC CTCCCGGGTT CAAGCAATTC 960 TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC TACAGGCGTG TGCCACCACA CCCAGCCAAT 1020 TTTTGTAGTT TTAGTAGAAA TGGGGTTTCA CCATGTTGGC CAGGATGGTC TCGATCTCTT 1080 GACCTCGTGA TCCACCTGCC TCGGCCTCCC AAAGTACTGG GATTACGCGT GAGCTACTGC 1140 ACCCGGCTGA GTGATTTTTT TTTTTTTTTT TTTAAGATAG AGAAAGTCCC TCATACTGAG 1200 GAGCCTTGCA GTTGAGAGAG AACAGAATTC CAGTTGGAGG ATCAAGGAAT TTGAGGGAGG 1260 CAGCATGCTT GCAGTGTTCC TAGGATTTTT ACAGGAACTA CAATAGAAAG TTAGGGATGA 1320 AATTATATTG AAAGGAGAAA GCTGGACTGC TCAGGTTTGG AGGTCATGGG GAATTCCAGG 1380 ATTCAGTATG TGGTTGCTCT CTTATTTTTA ACTTCTGCTT AGCAGTAAAA CCACACCCTT 1440 CCTTCTTCCT GAAAGTAATG TTTAACTTCC TCTCCCTGCA GCATTACACT CTATGTAATG 1500 GGAGTGGGGT GGAGGAAGAG TCTCCCAAGG TGGTTGGATC TCACTATTCT ACTGGAAGAG 1560 GAGCAGGCAA ATATATTTTT ATGTGGTATA ATGTCATTAG ATTATTTCCT GCTGCTTAAG 1620 ACAGAGCAAC TTCTGGATGA CATTTTGGAA TGTATTCTGT GGCTCTAATA ATTGTTGGTA 1680 AAGATATTGA GCCTTCTGTT TTCTTGAGGG GAGTTGGGGT GCTTGTTTTT GTACTTGGAA 1740 AGGGAGACTC GTATCTCTTG CTTTTTTCTT TAATTAAATT TCTGTTTTTT ACATTAGGAC 1800 ATGATAGCCA TCTTGCTTCT TTCTTTAAAA AGCTGCCTGG AATGGGAGTT TCCAGTGGTA 1860 GTACTGCATG AAGATTCATG AGACTATAAA GCTCTTTGGA AACCCCCCAA CTTAGCCCTT 1920 CCAACTTTCC TTACATTTTT ATGGCTTTCC AAAAAGGTTG CATGTAAGGG AAATTATCTA 1980 GGTCTGTGCT GTTTATTCAG CAAATAGTTT TTGAGCACCT GTTATGTGCC AGGCACTGTT 2040 CAAGGCACTA GACTAAACTA AACTTATCCC AAAAAACCCT CTGCCCTCGT GGAGTTTACG 2100 TTCTTATGTT CCAGAGACCC TGTCTGCCAG AGTTCCAGGC CTGATTTTCA ATTTTGAGGA 2160 AAGTGCTAAG ACTAAAGAGT GAATGGTTCT TTTATGAGTA CTGACACAAG GACTCCAGGC 2220 CACACATATC TTCTTGAAAG CCCTTTTCCT GTTTGAAAAA AAGATCGTTT GTATTTGATA 2280 GAGCAAAAGA AGGCCACAAA ATGAATTGTC TTCTTGTGGG CTGTGTTTCA 2330
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