Tag | Content |
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EnhancerAtlas ID | HS066-02916 |
Organism | Homo sapiens |
Tissue/cell | GM18516 |
Coordinate | chr19:47600160-47601060 |
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: 34 | 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_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 | CTCCCTTATG TCCAACACCG CGGCACAGCA GGCGACAGTC TTGCCCAGGG TCAGCTGAGG 60 CCTCCTTCCC TGTCCTGATG CCACTCGCTG GCTCGGACGA AGGTACAGGC TACTCTACAT 120 CTAACACCTG CGGGCAGAGG ACAAAAGACC ATTCAAGGAA CTCCAAGAGC CTTAACCATC 180 ATCCAGAATG ATTCTAGAAA GGAATCACCA AGGTAGAGAA GTGCAGCATT CAAATTCACC 240 CTACAAAGAC CTGAGCCAAA GAGGGATTCT GCACATTATC GATATTAACA GCTCCAGGCA 300 CATCTGGGCT CAAAGAGAAT CAACCATACA ACTTTTCACA AAACAGGCAG TGACTACTTG 360 AAATTTTGTT TCCCTAAAGT TGAGAGAGGC AGAGAAATAC ATAGGATTTT TTTGTTGTTG 420 TTAAACTGCT GACGGTTGAT AAAGGGGCAC TGAGACAGCA ACAATAAACA GATCACTGCA 480 TTCTCAGGGC CCTCTGGCCA TGTCAGGCCC TCAAGCCCCT CCGAGCCCTG GGCTAACTTC 540 TGTCCACAGT CACCTCAAGG GGTCCCCCCT CACGACACCC AAGATGCTCT CCTAGCTAAA 600 CGTCCTGCGT GAACACGAGG TCTTGACTAT ATTCTTCAGA CTCTGTTCAA CAGAAAGCAA 660 AAAGAAAGGA AGTCGAGCCA AATGGGAATC CCGTGGGCCA CCAGCGCGAC GGCACAAAGG 720 CGGTCTCAAC AAAACAGCAA CCAGGTTTCA GCGATGCCAC TTAACAGACT GCCGGCAAAA 780 TCCGTGTCAG AGTGGGATTA AATGCCAAGG GAACATGCTT AATAGACCTC GACATAATCC 840 CCCAAGAAAA GTGGGGGAAG CCCCACCGCG CTAATCATTT CAATCTAGAC CTGCCAAACT 900
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