Tag | Content |
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EnhancerAtlas ID | HS017-30456 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr7:75961460-75964140 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr7:75964044-75964065 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | KLF16 | MA0741.1 | chr7:75963884-75963895 | ACCACGCCCCC | + | 6.14 | Nr5a2 | MA0505.1 | chr7:75962497-75962512 | GCTGGCCTTGAACTC | - | 8.25 | SP3 | MA0746.2 | chr7:75963883-75963896 | CACCACGCCCCCT | + | 6.29 | SP8 | MA0747.1 | chr7:75963884-75963896 | ACCACGCCCCCT | + | 6.52 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_00055 | chr7:75946036-75989884 | Adipose_Nuclei | SE_00909 | chr7:75962142-75963519 | Adrenal_Gland | SE_00909 | chr7:75963702-75964165 | Adrenal_Gland | SE_01790 | chr7:75962397-75963521 | Aorta | SE_08490 | chr7:75962682-75963609 | Brain_Inferior_Temporal_Lobe | SE_09722 | chr7:75962354-75963963 | CD14 | SE_13415 | chr7:75962552-75963741 | CD34_Primary_RO01536 | SE_25131 | chr7:75962781-75963333 | Colon_Crypt_3 | SE_26581 | chr7:75962698-75963371 | Esophagus | SE_29613 | chr7:75962490-75963805 | Fetal_Muscle | SE_40697 | chr7:75961252-75961976 | Left_Ventricle | SE_40697 | chr7:75962024-75963509 | Left_Ventricle | SE_42246 | chr7:75962032-75963487 | Lung | SE_42246 | chr7:75963684-75964262 | Lung | SE_46372 | chr7:75962418-75963811 | Osteoblasts | SE_48077 | chr7:75961308-75963569 | Psoas_Muscle | SE_48077 | chr7:75963608-75964222 | Psoas_Muscle | SE_48614 | chr7:75961309-75962009 | Right_Atrium | SE_48614 | chr7:75962032-75963562 | Right_Atrium | SE_51109 | chr7:75958937-75964445 | Skeletal_Muscle | SE_52964 | chr7:75962870-75963504 | Small_Intestine | SE_65008 | chr7:75962598-75963596 | NHEK | SE_65376 | chr7:75962902-75963289 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr7 | 75961529 | 75961688 | chr7 | 75963669 | 75963722 | chr7 | 75962812 | 75963444 |
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| Number: 2 | ID | Chromosome | Start | End |
GH07I076331 | chr7 | 75961253 | 75962009 | GH07I076332 | chr7 | 75962248 | 75964021 |
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Enhancer Sequence | ACTCAAAAGA GGGGAAGAAT AGGGGGTGGG TACTACTTGA GTTCAGAGCA GAAGGAAACC 60 AGGAAAGAGA TGCTTTGCTC CACCACCTCT TGTTCCCGGC ACTTCTGCAA ACACTCCTCC 120 TGCATGAATA AACACAGGCA CCTCGTGTCT CATTCTGCAC TGACGATCTG TCATCCAGCA 180 GACCGCTGTC ACTCATGCTG AATTCTGATG TGTCCACAAA TAACGGAAGA TTGGGCTTTT 240 CCCAGCTCCA TCATTCGCTA AGCAATCTTG GGGACAAGCC GCTTCATTTC TCTGGGCTTT 300 GGTTTTCTTA TCTGCAAAAT GGGGATTTCT GCTTCTTTCA TAAGGTAATA TACAGGTATA 360 TCAGACAAAT AAGAAAGTCT TTTTTTGTTC TTTTTGAGAC ATGGTCTTAC TCTGTTTCCC 420 AAGCTGAAGT GCAGAGGCAT GATCACACCT CACTGCAGCC TCAAACTACT GGGCTCAAGC 480 AATCCTCCCA CCTCAATCTC CAGAGTACCT GGGACTACAG GTGTGCACCA CCATGCATGG 540 CTGATTTCTT TTTTTTTTTT TTTTGGAGAC AGAGTTTCAA AAAGACCTGG TCTCACTCTG 600 TTGCCCAGGC TGGAGTGCAA TGGCATGATG TCGGCTCACT GCAACCTCCC CCCAAGTTCA 660 AGCGATTCTC CTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGGCGTGTG CCACCATGCC 720 TGGCTAGTTT TTGTATTTTT AGTAGAGACA GCGTTTTGCC ATGTTGGCCA GGATGGTCTC 780 AAACTCCTGG CCTCAAGTGA TCCACCCGCC TCAGTCTATG GCTGATTTAT TTATTTCTTT 840 ATTTAGAGAT GGGGTCTCAC TATATCAATC CGCTGGAAGT GCAGTGGCAC TATCTTGGCT 900 CACTGCAACC TCAGCCTCCC AGGGCTTCAA GCAATCCTAC CTTAGCCTCC TGAGTGGCTG 960 GGACTAAGGC ACATGCCACC ACACCCAGCT AATTTTTGTA TTTTTCTGTA GAGACAAGGT 1020 CTTGCCATGT TGCCCAGGCT GGCCTTGAAC TCCTGGCCTC AAGTGATCCA CCCACCTTAG 1080 CCTCCCAAAG TGTTAGGATT ACAGGTGTGA GCCACTGCAT CCAGCCATTT AAAAATTTTT 1140 AGTAGAGACA AGGTCTCACT ATGTTGCCCA GGCTGGTCTT GAACCCTTAG TTCAAGTGAT 1200 CCTCCCACCT TGGCCGCTCA GAGTGCTGGG ATTACAGGTG ACAGCCATTG TGCCCAGCAA 1260 AGTCTTCTTG AAAAAGTAAA ATGCTACAGA AACATGAGGA ACTACTTTTA AGAATACCCT 1320 GAATAATTTT CCTTCATTTT AGTTCTCACC ACAGGGGATG TCTACATTTC CTAACGATCT 1380 CCCAGCTCAT CTTCCTGTAT CGAGTGTCTC TTCTCCGTTT CATCCTCTTC TCTATATTAA 1440 GCGGAAACTG CCTTAGCTGC CTCACATCGC TTCCTTTCCA TAAACCCTAG TTCCATACAG 1500 CCTGAAAAAA AACTGCCCAG ACTTGGCTTT GGAAGGAGCT GAGCCCTTGG GCGCTGCTGC 1560 CACCCATCTC TGGCATACTT TACTGAGTGT GCGAATGCTG AAGACAAACC GCCCCGCGGT 1620 GCAGCCCTCA TGACTGCCTC CAGTGCAAGG AGAGGCCAGC GTGCCGAAGG CCACAAAGAT 1680 CAAGTTCTGG CCTTTCCCCT AAATCATGTT GTCCTTATTT CAAGGGCCAG GAGCTATTTA 1740 AAGCTCAAAT TATCTCACCA GTCCTGGGGG CACTCCTCCT GCCACAAATG AAGTCTCCCA 1800 GCAGTGCCCA GAGAGGCAAT CTGTACTTAT GTAAAGTCTG CCTAGCTGTC CCCAGACACA 1860 TTGGAACAAG GAGATTATGA AATGCCAGGA TCACCTTTGG ATACAGTAGC TCGACCACAT 1920 TTGGAACACG CCCAGATGTT CCCTGCCAGT GAAAAACTAA GTTAGAGGGG AAACCCTTCA 1980 GCTCTAAAAA GTCTAAAGAA AAGTTGTTCT GAACACCTTA AATCAAAATT TTTAAAAATC 2040 CTTTATCCTT TAGATCATAA TTACTTGCAT AAGAATCTGT TATTTTTAAA TTAAAATAAG 2100 AGATCCCCAC CATATTAGTT TTAAAGGTCA ACAGATAACC TCTTAAAAGA ACAAGTTATT 2160 CTAATAGTGT CTAAAATGAT TTAATCAAGA CAGAATGACA GAATGACTAT TCAATGTGGG 2220 AAGATACGGG ATCTTGTATC ATTTGGGAAG GGAGGTAACA TTTTTCAAAA CAGTCATTAA 2280 ATTTGTTGTT GTTGTTTAAA CAGAGACAGG GTCTCACTCT GTTGCCCTGG CTGGAGTACA 2340 GTGGTGCAAT CACAGCTCAC TGCAGCCACG CCACAAACTC CTCTGCCTCA GCCTCCAGAG 2400 AAGCTGGGAC TACAGGCATC TACCACCACG CCCCCTAATT TTTGTATTTT TTGTAGGGAC 2460 CAGGGTCACC CTATGTTGTC CAGGCTGGTT TCGAACTCCT GAGCACAAGT GATCCTCCAG 2520 CCTTGGCCTC CTAAAGTTCT GGGATTACAA ACATGAGCCA TTCTGCCTAA CCTTCTTCTT 2580 CTTTAAAAAA AAAAAGAAAG AAAGAAAGAA AAGAAAAGAA ATGGGGTCTC ACTCTGTTGC 2640 CCAGGCTGGA GAGAAATGGC GTGATCACAG CTCACTGCAG 2680
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