Tag | Content |
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EnhancerAtlas ID | HS105-83156 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr9:127032870-127036120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr9:127034788-127034802 | AATCCCTGGGGATT | - | 6.11 | ESR2 | MA0258.2 | chr9:127035484-127035499 | AGGTCACACAGCCCC | + | 6.23 | Klf1 | MA0493.1 | chr9:127034226-127034237 | AGCCACACCCA | + | 6.14 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_01861 | chr9:127032779-127037444 | Aorta | SE_03002 | chr9:127034359-127035045 | Bladder | SE_03002 | chr9:127035339-127036740 | Bladder | SE_06625 | chr9:127032359-127035602 | Brain_Hippocampus_Middle | SE_09789 | chr9:127031721-127038557 | CD14 | SE_23712 | chr9:127031859-127034802 | Colon_Crypt_1 | SE_24006 | chr9:127032818-127034759 | Colon_Crypt_2 | SE_24006 | chr9:127034780-127035298 | Colon_Crypt_2 | SE_26169 | chr9:127033936-127036212 | Duodenum_Smooth_Muscle | SE_27460 | chr9:127032898-127037010 | Esophagus | SE_29975 | chr9:127032839-127034581 | Fetal_Muscle | SE_29975 | chr9:127035274-127036616 | Fetal_Muscle | SE_31765 | chr9:127032168-127034974 | Gastric | SE_36996 | chr9:127032676-127034888 | HSMMtube | SE_38009 | chr9:127032565-127034202 | HUVEC | SE_42506 | chr9:127032254-127035465 | Lung | SE_44809 | chr9:127033026-127033590 | NHLF | SE_45648 | chr9:127032140-127035240 | Osteoblasts | SE_47283 | chr9:127034164-127035001 | Panc1 | SE_47557 | chr9:127032888-127033741 | Pancreas | SE_47557 | chr9:127033756-127034318 | Pancreas | SE_49326 | chr9:127032861-127034327 | Right_Atrium | SE_50283 | chr9:127031869-127034925 | Sigmoid_Colon | SE_52726 | chr9:127032033-127035009 | Small_Intestine | SE_54297 | chr9:127032840-127034042 | Spleen | SE_60448 | chr9:127019058-127056389 | DHL6 | SE_63558 | chr9:127032863-127034220 | HSMM | SE_65907 | chr9:127032061-127034681 | Pancreatic_islets |
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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: 3 | ID | Chromosome | Start | End |
GH09I124270 | chr9 | 127032907 | 127034904 | GH09I124273 | chr9 | 127034923 | 127035012 | GH09I124272 | chr9 | 127035275 | 127038902 |
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Enhancer Sequence | TTGCTATTTA ATGTCTCACT CCCTGGACAC AAGATACTTT CAGGGTGAGT GCAGACCTCA 60 CAGGTGTGGG CACACCTGCC CCCGACCCTC CTGCCTGCAT CCGGGCCCCT GCTGCAGGTA 120 ACGGGTGGCA GAGGTTGCTG GGTGCGGGAG CAGGCAGCTG AATACCCGTC CTGGGGAGGC 180 AGCTGAGACT CTGTGCTGCC AGCATGTGCT CCATTATTCC ACCAGACTCC ACTTAACACA 240 GATTCAAAGA TGACATGAAG CATTTCAGGA CAGTGAAAGC ACAGCATGAA GCCCTACGCT 300 TGGGGCTCCC TTCTTAGGGC AGGGCCAGGT CACCTGGACA TGAAGCCAGC CTGATGGGAG 360 GGGCCATAGC ACCCACACAC ACATTTCACA CAGAGCAAGG GCCTTATGTT GGTTCTCTCC 420 ACAGAGCTGG GGCCAGATCT GATTTGAAGG GAAAGTTCTG TGTTAAGCAC TGTCTGCAGA 480 CTGCTGGCCC AGCAGGTTAG TCGGCCAGCC AGGGGCTCTC CCTCTTCATC CGGAGCCTCT 540 GGTGCCAAAG ACACACCATG GTCAGCCCTC CCTGACTTAA TCTCTCACAC CATTGCCAGA 600 GATTGTTGCA GTAACAAACC CAACCCCTCT GACTTCCGCT CCTTGAGTGA CAAGGGTCAG 660 AAATCGAGTG GCGCGGTTGC CAACCTTCTC ACTCAGGAAC AACGCCAAAC ACGTGGTGCC 720 CCAGAGATCA GAGAGGGTGA GGAGCTTGGA TTCCACCAGC TGTCACGCTG TTCCCAGCCC 780 CAAAATGGGG AGGCTCAGCA CCCACAGGGA GTGACGTCTG GTTACTCTGA AAACATGGAC 840 AAGGAGGCTC AGGTGAGGGG TACTTACTTA GTACCCACTG TGCACCGGAG ACCCGGCCAA 900 GTACTTTCCG TGTGTTGCCT TCGTTAATCC TCGTGACAAC TTTGAGCTGA TCCTGTTTTT 960 CAGATGAAGT TAACTGAGGC TCAGAGAATG AAGCTGCCAG TCCAAAGCCA TAAACCACAC 1020 ACTTTGGAAA CTGAGATTTG AACCCAGGCC CGGCTGGCCC CAGAGTTAGT GCTCTTTGCA 1080 CACGAATCCC AGGCACACTG GCTGGCTGAG GTCCCTCCCT GGCTGGGCCT CTTGCCCCCA 1140 CCGTCTGCTG CATCTGCATC TGCAGGACAG GGGCCAGACC TCAGCGCTGC TGCCTGTCCA 1200 CTCCTGCCCC TGAGCAGTCC ATCCTTGTTC TTGGCAGGGA GCAGATCTCA GGGCCACAGC 1260 TCCAGCTTTT CTCCTGCAAG GCCTGGCCAG CTCTGTGGCT GTACTTGTGC CCAGAGAGAC 1320 AGGTGGCAGC GGCAGAGTTA GGCACACCTG GCCGTGAGCC ACACCCACCT TGTGCTCCCC 1380 GTGTCTCCTG GGCTTGTTAC CGCCCACTCA GGCCTCTGTT TTCCCATTTG TGGAGCAAGG 1440 GGTAATAGCA GATCCTGTCT CTGGGGCAGT TTTCCCAATC TATTGTGGTA AGGGTGTATA 1500 GTCCTCAGTT CCACGCCAGG CCCAGAAGAG GCCTTTGATA CTCTGTGTTG ATGGTAAACG 1560 ACATGGTATG GGGTGAGCTC GGAGCTTGGT GGCCCCTGTG ACGCTCTGGG GAGCGCTTCC 1620 CCAGGCCACA GGGCAGGCTC TCAGTCCAGA GCTGCCCTCC CTAAGGAATT CATCCCTTCC 1680 TTGTTTTCTT TGTTCATTCA TTTCATCCCA CAGATCCAGG CGCTCTGCTG AGATACAGTA 1740 ATGAGCCCCA GGCATGAAGT CCCTGCCTGC ACAGGGCTGG TGCTGTGGTT CCTAAACAAG 1800 AAACCGGTGC AGGGTTCCTG GCCAGGCAGT GCTGGGGAGA GGTAGCTGGG ACAGCGTGGT 1860 GGCCCATGGC TGCCACAAAG AATGGAGTTC CTTCAATCTC TTTCTTCCAT TAAAGGGCAA 1920 TCCCTGGGGA TTTAACATGC TGCCTTTCGT GTGAGGTCCC AGCACTCCCA GCGTCCTGGG 1980 AAGGCCTCAT CGGGCTTTGC TTTGCTTCAA GGTGTCTTTG AGAAATCAGT TTTTCCAGTT 2040 GCAATGTGGG AGTTTTCCCC AGGCTCTCCT GAGACTCACA ACCGCTCCCC CTAACGCTGC 2100 TGGTCATGGA GACCCACCTG GGCCAGGCCC TGGTCACATG TGATCGCATC GACCTCTCTT 2160 GGTGACCTTG AGAGTCAGGT CCTATTAATT CATTTTACAG ATGAGGAAAG GGAGGCTGAG 2220 TGAGGCTGCA TCATTTGCTG AGGAGCACAG TGTGCCCACT GCCAAGTCAG GATTTGAACC 2280 CACGCCCGTG GCTTCCAGAC CACACTATCG GAACCACTCT GCCCTAGTGT GAATGGATGT 2340 TTTTTTAATT CTTGGCAGCA GAAAAACCAA AGATTCTGCT CAAAGCAGTA GACTCTCAGC 2400 GGCCCATGTG TCAGGGCTGT GCTGGGTGCT GCAGGAGAGC TCTGCAGAGA AGAATAGAGA 2460 CAGACTGTTG GTGCTAAAAT TGGCCTGAAA AATGACCATT TCCGCGTGAG CCAGGATTGC 2520 GTTGACTCCT TGCTCCAAGG CTGTGAGGTG TGTGGGGTTA GGTTCATGTG ACAGATGAGG 2580 AAGTGGAGGC TCAGAGAGGC TGTGTGGCTT GCCAAGGTCA CACAGCCCCG GGCGGCCTTA 2640 TTCCACATCC ACCTGCTCTG TCTGCCATCA TCCATGGTGG TCTCCGGACT AGCTTTGGCC 2700 TCCCCAACAT CCTGCATTTG GATAAACTGA GGCCTAAAGA ACAATTCAGG GCTTGATCCC 2760 GAATGGGGGA GGGGACGGAA CCCTTTGCAT GCTTGTGGAA ATGGACACTC ATTCCACAGC 2820 GAAACTGCCT TCAAAATGCC ACTGATTCTC AGGGCAGGAG AAGACTTAAG AAATGACAGC 2880 GGGCAGTCAG GGCACGTGTG TCTGTGACAG CAGAGGGGCC CGTATCCACC CTTCCTGGGA 2940 CCGACAGCCA GGGTGATGGG GTTTTATAGC ATCTGGAACA GGCAAGCCTT TTATAAGAAA 3000 ATGTTTCCAA AGTTGTCCCG TCCCACCGTT GGCAAGCAGT CCTTAAACGG CAAAGAAACA 3060 GCCGTGCTCT GCATTCACGA AATGGTGAGC TGGCATTTAG GCCATTTATT TAAAGCGGGA 3120 GTTGAGGAGG CTAAAGACTT CAGTTCTGAG TGGCGGCTCG CAGCCTCACT GCAGCAGGGG 3180 AGCGTAATCT TCAGGGTTTT CTTCCCATTT ACGGGTTTTT TTGTTGTTGT TGTATATTTG 3240 TAAAATGAGG 3250
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