Tag | Content |
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EnhancerAtlas ID | HS059-23713 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr19:47600150-47601080 |
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 | TCAGCACGCC CTCCCTTATG TCCAACACCG CGGCACAGCA GGCGACAGTC TTGCCCAGGG 60 TCAGCTGAGG CCTCCTTCCC TGTCCTGATG CCACTCGCTG GCTCGGACGA AGGTACAGGC 120 TACTCTACAT CTAACACCTG CGGGCAGAGG ACAAAAGACC ATTCAAGGAA CTCCAAGAGC 180 CTTAACCATC ATCCAGAATG ATTCTAGAAA GGAATCACCA AGGTAGAGAA GTGCAGCATT 240 CAAATTCACC CTACAAAGAC CTGAGCCAAA GAGGGATTCT GCACATTATC GATATTAACA 300 GCTCCAGGCA CATCTGGGCT CAAAGAGAAT CAACCATACA ACTTTTCACA AAACAGGCAG 360 TGACTACTTG AAATTTTGTT TCCCTAAAGT TGAGAGAGGC AGAGAAATAC ATAGGATTTT 420 TTTGTTGTTG TTAAACTGCT GACGGTTGAT AAAGGGGCAC TGAGACAGCA ACAATAAACA 480 GATCACTGCA TTCTCAGGGC CCTCTGGCCA TGTCAGGCCC TCAAGCCCCT CCGAGCCCTG 540 GGCTAACTTC TGTCCACAGT CACCTCAAGG GGTCCCCCCT CACGACACCC AAGATGCTCT 600 CCTAGCTAAA CGTCCTGCGT GAACACGAGG TCTTGACTAT ATTCTTCAGA CTCTGTTCAA 660 CAGAAAGCAA AAAGAAAGGA AGTCGAGCCA AATGGGAATC CCGTGGGCCA CCAGCGCGAC 720 GGCACAAAGG CGGTCTCAAC AAAACAGCAA CCAGGTTTCA GCGATGCCAC TTAACAGACT 780 GCCGGCAAAA TCCGTGTCAG AGTGGGATTA AATGCCAAGG GAACATGCTT AATAGACCTC 840 GACATAATCC CCCAAGAAAA GTGGGGGAAG CCCCACCGCG CTAATCATTT CAATCTAGAC 900 CTGCCAAACT CTCTTGAGAC AAGCAAGCAG 930
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