Tag | Content |
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EnhancerAtlas ID | HS047-17475 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr19:39193470-39195120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr19:39194987-39194998 | GGGCGGGAAGG | + | 6.62 | Foxd3 | MA0041.1 | chr19:39194183-39194195 | AAATGTTTGTTT | + | 6.27 | Foxq1 | MA0040.1 | chr19:39195091-39195102 | AATAAACAATA | - | 6.62 | TFAP2C | MA0524.2 | chr19:39194391-39194403 | TGCCTTGGGGCA | - | 6.62 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_00865 | chr19:39188085-39193891 | Adrenal_Gland | SE_00865 | chr19:39194025-39194834 | Adrenal_Gland | SE_01543 | chr19:39190294-39194051 | Aorta | SE_01543 | chr19:39194086-39205969 | Aorta | SE_04868 | chr19:39190349-39193915 | Brain_Cingulate_Gyrus | SE_05805 | chr19:39182078-39206004 | Brain_Hippocampus_Middle | SE_06803 | chr19:39191797-39193818 | Brain_Hippocampus_Middle_150 | SE_07777 | chr19:39185584-39193917 | Brain_Inferior_Temporal_Lobe | SE_07777 | chr19:39194039-39206085 | Brain_Inferior_Temporal_Lobe | SE_23062 | chr19:39190396-39193754 | Colon_Crypt_1 | SE_26525 | chr19:39180697-39193852 | Esophagus | SE_26525 | chr19:39194058-39205949 | Esophagus | SE_27614 | chr19:39180632-39201469 | Fetal_Intestine | SE_28533 | chr19:39164445-39201888 | Fetal_Intestine_Large | SE_29583 | chr19:39191405-39193843 | Fetal_Muscle | SE_31384 | chr19:39190375-39193912 | Gastric | SE_31384 | chr19:39194037-39199678 | Gastric | SE_35430 | chr19:39190316-39193869 | HepG2 | SE_36926 | chr19:39191350-39194830 | HSMMtube | SE_40594 | chr19:39180727-39193965 | Left_Ventricle | SE_40594 | chr19:39194015-39206697 | Left_Ventricle | SE_42097 | chr19:39180674-39193834 | Lung | SE_42097 | chr19:39194095-39205995 | Lung | SE_47114 | chr19:39164477-39226374 | Panc1 | SE_47461 | chr19:39194099-39194556 | Pancreas | SE_48555 | chr19:39190300-39193928 | Right_Atrium | SE_50056 | chr19:39182445-39193963 | Sigmoid_Colon | SE_50056 | chr19:39194910-39205530 | Sigmoid_Colon | SE_52339 | chr19:39180899-39193971 | Small_Intestine | SE_52339 | chr19:39194079-39204831 | Small_Intestine | SE_53291 | chr19:39194893-39205783 | Spleen | SE_54534 | chr19:39190299-39193637 | Stomach_Smooth_Muscle | SE_56725 | chr19:39194131-39194749 | VACO_400 | SE_65266 | chr19:39190217-39194643 | 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: 1 | ID | Chromosome | Start | End |
GH19I038673 | chr19 | 39164536 | 39206516 |
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Enhancer Sequence | ATCTTCTCTG TGACCTCTCC ACCTGCTTCC AAGCAAGCCT GCCCTGGAGT ATTCTGCTCA 60 GAGGTCAGTG AGCAGGGTCT CCTGTGGTGT CCTGGGCCTC CAGCTCTGCA GTTAGCTTTG 120 GAACTCACCC CTGTGCCCAG CCCTTCCCCG AGAGTGCTTG CAGCAGTGGC GCCCCTCTGT 180 CTTCTTTGGA AGCCACTCCA TCATGCCCCT TGCATATGGC GTGTTGACAA GTTGGGAGGA 240 CTGCCCTAGG CACGGCTGGC TGATGGACTC TGGGATGAGG CACTGCCTTC TCTCACCCAG 300 CCGCAGACAC ACAGCTGTCC TGGGCCTTGC AGAGATGATT TTTCTCTTAA GTTACTGAGG 360 CTGAAGAAGG TGTGGTCCAA GCCCTTCTTT TGAGAAGTTT CAGCAATTTT TTTTTTTTTT 420 TTTTTGAGAT GGAATCTCAC TCTTGTCACC TAGGCTGGAG TGCAATGGTG CAATCTCAGC 480 TCACTGCAAC CTCTGCCTCC CGGGCTCAAG CAATTCTCCT GCCTCAGCCT CCAGAGTAGC 540 TGGGATTACA AGCACCCGCC ACCACGCCAG GCTAATTTTG TGTTTTTAGT AGAGACGGGG 600 CTTCACCATC TTGGCCGGGC TGGTCTCGAA CTCCTGACCT CAGGCGATCC ACACCTGCCT 660 CAGCCTCCCA AATTGCTGGG ACTAAACAGG CGTGAGCCAC CACAGCCGGC CGCAAATGTT 720 TGTTTTTAGG TTAGTTCAGA AAGCGTGCAG TCTGGCCTCA GGCCCGTGCT CTCCCCTTCC 780 TGACAACACA GCAGCCATGC TTGTTCCTCA CTGGCCTTCC AGGCACTGGA TCCAGTGGTG 840 GTCAGAGCAG CCCCGCCCTC ACGAGGGCAG GCAGACAGTG AACAAGTAAA CAGCCCGACC 900 AACATGTGAT TTCACTAGTG ATGCCTTGGG GCAGCACAGG GGCCAGGGAG AGGAACTGGG 960 TGGCGGGTTG GGGAGCTCCT TGGGACGGGC AGTCAGGGAA GCCACCACGA GAGGTGACAC 1020 AAGCAGAAGC TTACACGATG AGAAGGACCA GCCAGTTGAG GGTCGCAGGC TAGGGGCGTG 1080 CTTTGTGAGT GGACAGAGCG TATCAAAGCA AGAAAGAGCC TGGCTTGCCC AGAGGATGCA 1140 GCTAGAGAAT TCCAGCAGGA TGGCAGGGCC TGGGCCTTCA GGGCAAGCCC TTTCCCTGTG 1200 GGCCAGGCAT GGTGGCTCAC ACCTGCAATC CCAGCACTTT GGGAGGCCAA GGCAGGAAGA 1260 TCACTTGAGC AGGAGTTTGA GACCAGCTTG GGTAACATAA TAAGACCCAG CCTCTACAAA 1320 AAGTTTAAAA ACTAGCAAGA TGTTGTGGCA TGCGTCTGTG GTCCCAGCTA CTCGGGAGAC 1380 TGAGGCAGAA GGATTGCTTG AGCCCAGGCA GTCAAGGCTG CAGTGAGCTA TGACTACACC 1440 ATTGCACTCC AGCCAGCCAG ACCCTGTCTC AAAAGAAGGA AACCAACCAT GCTCGCTGCT 1500 GTGTCGATGT GGATTATGGG CGGGAAGGGT ACATAGGAGG CAGCCGCATT GAGCTCTGGA 1560 GATGACAGTG GCTTGGTGGA GAGTGTCGGC AGTAGGATTG GAAGGAAGTG GACAGATTCA 1620 CAATAAACAA TAATGTAGTG CACATTTGCT 1650
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