Tag | Content |
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EnhancerAtlas ID | HS048-30219 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:139069060-139070800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr5:139070043-139070061 | CCCTCCTTCCTGCCTCCC | - | 6.86 |
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| Number of super-enhancer constituents: 35 | ID | Coordinate | Tissue/cell |
SE_03140 | chr5:139069067-139071158 | Brain_Angular_Gyrus | SE_03865 | chr5:139061968-139071368 | Brain_Anterior_Caudate | SE_04768 | chr5:139026027-139072090 | Brain_Cingulate_Gyrus | SE_05771 | chr5:139026065-139074431 | Brain_Hippocampus_Middle | SE_06683 | chr5:139027027-139071104 | Brain_Hippocampus_Middle_150 | SE_07722 | chr5:139028082-139075240 | Brain_Inferior_Temporal_Lobe | SE_08785 | chr5:139069309-139069575 | Brain_Mid_Frontal_Lobe | SE_08785 | chr5:139069627-139069864 | Brain_Mid_Frontal_Lobe | SE_11063 | chr5:139062370-139071009 | CD20 | SE_13414 | chr5:139069366-139070204 | CD34_Primary_RO01536 | SE_20188 | chr5:139068775-139070160 | CD56 | SE_25255 | chr5:139069064-139069746 | Colon_Crypt_3 | SE_27739 | chr5:139069095-139070045 | Fetal_Intestine | SE_28684 | chr5:139069137-139070268 | Fetal_Intestine_Large | SE_29581 | chr5:139069017-139070747 | Fetal_Muscle | SE_30930 | chr5:139062746-139070067 | Fetal_Thymus | SE_31417 | chr5:139069048-139069898 | Gastric | SE_34346 | chr5:139069079-139069805 | HCT-116 | SE_36941 | chr5:139068133-139079024 | HSMMtube | SE_40547 | chr5:139069055-139070220 | K562 | SE_40649 | chr5:139063240-139070837 | Left_Ventricle | SE_45813 | chr5:139068478-139071914 | Osteoblasts | SE_47460 | chr5:139069058-139070040 | Pancreas | SE_47460 | chr5:139070142-139070393 | Pancreas | SE_48579 | chr5:139069052-139070779 | Right_Atrium | SE_51090 | chr5:139069051-139070668 | Skeletal_Muscle | SE_53351 | chr5:139068907-139071015 | Spleen | SE_55117 | chr5:139069131-139069747 | Thymus | SE_55730 | chr5:139068898-139071496 | u87 | SE_58504 | chr5:139012442-139092243 | Ly1 | SE_59951 | chr5:139067745-139092302 | Ly4 | SE_63555 | chr5:139069256-139070924 | HSMM | SE_65250 | chr5:139062919-139071491 | Pancreatic_islets | SE_67548 | chr5:139068898-139071496 | u87 | SE_68692 | chr5:139069080-139070081 | H9 |
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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: 1 | ID | Chromosome | Start | End |
GH05I139683 | chr5 | 139062979 | 139081910 |
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Enhancer Sequence | CAAGCCCAGA AAGGTCTGGA AACAAAGGGC ACAGTATGGA GCGAGGATAG GGGATTAGGG 60 GGTAACCTAG GATCACCGCC CCCTCCCCTG CAATGACAGG GCGTGGGTAT TTCGGGGGCC 120 CGAAGTGGGT ACAGCCTGAA TCCACAAAGG CTCCTGCCCA CCGCTCCCCC TGGTGTCTTC 180 CCACCAGGCT CCCAGCCCCT CTTCCAGCTT TGAGGCCTGC CCGGGAGGGG CACCCCCTGT 240 GGCTGTTTTG GCTCTGCAGC AGTGGGTCCA CAGGCAGCTG CTGGGAGTCT TGGGGAGCGG 300 CTGCAAGGGT GAGGGCGAGC AGTGGCCGCT GCCGTTGATA AGGCGACGGA AGCCTCAGGA 360 GCGAGGACGC AGTGAAGCCA TGGAAACACG GCTGAGGTGT GAGGCTGGCT CAGCCGCTTC 420 CCCCAGGTGG CCACCTCCCA GGCCTGGCGG GGCCCCGCGA GACAGGTCCT GCCACTGGCT 480 GCCTCGCTCC CTGCCCTCCT GGGGGCCAGG TCTGGGCTGC TGACTGGGCT AGCTTGGTGT 540 CACCCAGCCA TCTCCCCAGG GCCAGGCTGG GGTCAACCCT GGGTCTGAGT AGGGAGGGCT 600 GAGGACAGTG GCAGGGGCCT TCTGAGTTCT CAGGCCCCAA AGCCCCCTTA GCCTGGTCAA 660 TCCCTCCCCT TCTACCACCT ACTCCTTTCC TATAAATATG TGTGCATTAT TTACCTTAAG 720 CATTTTGATA AATCATAATA GCAGAGACAT CTGCTGTCAA AACTGCAAAC TGCATTTGGG 780 GCTCAGCTGG TGAACGATGA GGGCTAGAGG CCAGGGATAT AAGGGCTCTG ATGGCCTGGG 840 GGAAAAAATA GGGATGACCC CACCCCTCAT CCAGGGCTGG GCCTTGAAGG GGACCCAGGC 900 CCCATCCTTT GGGACCCCTC CTCACCAGCC ACTTAATCAC AAAACCCTCC CAAGGAAGCT 960 ATCCACCACG CCCCAACTGT GTTCCCTCCT TCCTGCCTCC CTCTGCCTCA GAATTAATGC 1020 AGCAGTGACA GCGGCTGAGA AGTCCCCCAG AGCGGAGATT AACTCCCAGG GCAGCGCGGG 1080 CGGGGTTGGC CATGGGAGGC TTGGGGGTGG GGGGTCTGAC GCACAGGCCT GGCAAGATTA 1140 ATCACCCTGC AGCCGGCCTC ATCACGAGGG CGCCCAGAGC TCCGGGCCCC CACCTCGAGG 1200 AGGGGTGCTG GGTCGAATGT CAGGAGTCTG CTCTGCCTCC CGCAGCCCTC ATGGCCCCCA 1260 GTCCAACTCG TGGGAGGATT CTGGGAGCTG AGTTTCCTTC TCTTCCATTT TGCTGGCCCT 1320 CAGGGACCCT AAGGACCGAG CAGCAATCCC GTGGTCTCAT TCCCTCCCCC AGTTTCTGGC 1380 CTGGCTCAGC AGCCCTGCAA TGGGGGAGGC TCTGACCCTT GCCTCCCTGC CTACTTCTTG 1440 CTGTCCCCAC TGGCCCCGCT CCCATGGCTC CCCGAGACTG CCAGTTCCCT AACATAGAGC 1500 TAGAGGTGGG GGCCACTGAA AGAGGTCCCT GGACCTGCTG TATTTATTTG GGGGACTCAA 1560 AGAGATGTGT GATGGATCCG ATGGCTCTGG ACCTGCTATC CAGCCAGCCC TCTTGAACTG 1620 TCCTGGGGGG CTTGTGGAGA TGGTGGAGAG AGATACAGAG TGAGTGGGCA GATACAGATG 1680 AGGCTACTGG GTGATAAAGC ACTGGGGTCA GTACCTGGGA ACTGGCCTTT GTCAGCCAGT 1740
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