Tag | Content |
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EnhancerAtlas ID | HS065-02766 |
Organism | Homo sapiens |
Tissue/cell | GM18508 |
Coordinate | chr19:47599990-47601020 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr19:47600582-47600594 | AAACTGCTGACG | + | 6.02 |
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| Number of super-enhancer constituents: 36 | ID | Coordinate | Tissue/cell |
SE_03022 | chr19:47598055-47600395 | Bladder | SE_04522 | chr19:47597859-47601876 | Brain_Anterior_Caudate | SE_06463 | chr19:47596498-47603370 | Brain_Hippocampus_Middle | SE_07150 | chr19:47598244-47601908 | Brain_Hippocampus_Middle_150 | SE_08585 | chr19:47597109-47601648 | Brain_Inferior_Temporal_Lobe | SE_11185 | chr19:47596089-47600251 | CD20 | SE_13373 | chr19:47600379-47601265 | CD34_Primary_RO01536 | SE_17540 | chr19:47596774-47600508 | CD4p_CD25-_CD45RAp_Naive | SE_17955 | chr19:47596306-47600458 | CD4p_CD25-_CD45ROp_Memory | SE_19321 | chr19:47596321-47600144 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22411 | chr19:47596363-47600199 | CD8_primiary | SE_23136 | chr19:47596536-47601740 | Colon_Crypt_1 | SE_23866 | chr19:47597093-47601786 | Colon_Crypt_2 | SE_24862 | chr19:47596917-47601736 | Colon_Crypt_3 | SE_25954 | chr19:47596517-47601744 | Duodenum_Smooth_Muscle | SE_26646 | chr19:47596502-47602696 | Esophagus | SE_27626 | chr19:47596238-47604236 | Fetal_Intestine | SE_28544 | chr19:47596123-47604268 | Fetal_Intestine_Large | SE_31552 | chr19:47596626-47601943 | Gastric | SE_34095 | chr19:47597597-47601630 | HCC1954 | SE_36699 | chr19:47598365-47600618 | HMEC | SE_41315 | chr19:47598005-47601805 | Left_Ventricle | SE_42396 | chr19:47596544-47602441 | Lung | SE_47643 | chr19:47597827-47600486 | Pancreas | SE_47643 | chr19:47600602-47600920 | Pancreas | SE_48411 | chr19:47596498-47602335 | Psoas_Muscle | SE_49033 | chr19:47598058-47600543 | Right_Atrium | SE_49033 | chr19:47600551-47601779 | Right_Atrium | SE_50229 | chr19:47596382-47603151 | Sigmoid_Colon | SE_51583 | chr19:47596585-47601903 | Skeletal_Muscle | SE_52381 | chr19:47596493-47602514 | Small_Intestine | SE_56677 | chr19:47600272-47601347 | u87 | SE_57563 | chr19:47599728-47600528 | VACO_503 | SE_58017 | chr19:47599738-47600436 | VACO_9m | SE_62357 | chr19:47596302-47618092 | Tonsil | SE_65381 | chr19:47596646-47601723 | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I047093 | chr19 | 47596433 | 47604071 |
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Enhancer Sequence | AGAGGGACAT GATCACCACC CAGGCCACTA ATATTTTAAA TGCCATATCT GTGCCAGGTT 60 GCTTGACTAC CTCCTTTTCT GCACTGACAA GAAACTTGGT CCACAAGGCA GGTGCCTGAT 120 CATCAGGGCT GGGTCAGCTG AGCCGGAGTG GGTGGCAGCC TCAGCACGCC CTCCCTTATG 180 TCCAACACCG CGGCACAGCA GGCGACAGTC TTGCCCAGGG TCAGCTGAGG CCTCCTTCCC 240 TGTCCTGATG CCACTCGCTG GCTCGGACGA AGGTACAGGC TACTCTACAT CTAACACCTG 300 CGGGCAGAGG ACAAAAGACC ATTCAAGGAA CTCCAAGAGC CTTAACCATC ATCCAGAATG 360 ATTCTAGAAA GGAATCACCA AGGTAGAGAA GTGCAGCATT CAAATTCACC CTACAAAGAC 420 CTGAGCCAAA GAGGGATTCT GCACATTATC GATATTAACA GCTCCAGGCA CATCTGGGCT 480 CAAAGAGAAT CAACCATACA ACTTTTCACA AAACAGGCAG TGACTACTTG AAATTTTGTT 540 TCCCTAAAGT TGAGAGAGGC AGAGAAATAC ATAGGATTTT TTTGTTGTTG TTAAACTGCT 600 GACGGTTGAT AAAGGGGCAC TGAGACAGCA ACAATAAACA GATCACTGCA TTCTCAGGGC 660 CCTCTGGCCA TGTCAGGCCC TCAAGCCCCT CCGAGCCCTG GGCTAACTTC TGTCCACAGT 720 CACCTCAAGG GGTCCCCCCT CACGACACCC AAGATGCTCT CCTAGCTAAA CGTCCTGCGT 780 GAACACGAGG TCTTGACTAT ATTCTTCAGA CTCTGTTCAA CAGAAAGCAA AAAGAAAGGA 840 AGTCGAGCCA AATGGGAATC CCGTGGGCCA CCAGCGCGAC GGCACAAAGG CGGTCTCAAC 900 AAAACAGCAA CCAGGTTTCA GCGATGCCAC TTAACAGACT GCCGGCAAAA TCCGTGTCAG 960 AGTGGGATTA AATGCCAAGG GAACATGCTT AATAGACCTC GACATAATCC CCCAAGAAAA 1020 GTGGGGGAAG 1030
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