Tag | Content |
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EnhancerAtlas ID | HS089-06960 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr19:47600120-47600870 |
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: 35 | 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_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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I047093 | chr19 | 47596433 | 47604071 |
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Enhancer Sequence | GGGTCAGCTG AGCCGGAGTG GGTGGCAGCC TCAGCACGCC CTCCCTTATG TCCAACACCG 60 CGGCACAGCA GGCGACAGTC TTGCCCAGGG TCAGCTGAGG CCTCCTTCCC TGTCCTGATG 120 CCACTCGCTG GCTCGGACGA AGGTACAGGC TACTCTACAT CTAACACCTG CGGGCAGAGG 180 ACAAAAGACC ATTCAAGGAA CTCCAAGAGC CTTAACCATC ATCCAGAATG ATTCTAGAAA 240 GGAATCACCA AGGTAGAGAA GTGCAGCATT CAAATTCACC CTACAAAGAC CTGAGCCAAA 300 GAGGGATTCT GCACATTATC GATATTAACA GCTCCAGGCA CATCTGGGCT CAAAGAGAAT 360 CAACCATACA ACTTTTCACA AAACAGGCAG TGACTACTTG AAATTTTGTT TCCCTAAAGT 420 TGAGAGAGGC AGAGAAATAC ATAGGATTTT TTTGTTGTTG TTAAACTGCT GACGGTTGAT 480 AAAGGGGCAC TGAGACAGCA ACAATAAACA GATCACTGCA TTCTCAGGGC CCTCTGGCCA 540 TGTCAGGCCC TCAAGCCCCT CCGAGCCCTG GGCTAACTTC TGTCCACAGT CACCTCAAGG 600 GGTCCCCCCT CACGACACCC AAGATGCTCT CCTAGCTAAA CGTCCTGCGT GAACACGAGG 660 TCTTGACTAT ATTCTTCAGA CTCTGTTCAA CAGAAAGCAA AAAGAAAGGA AGTCGAGCCA 720 AATGGGAATC CCGTGGGCCA CCAGCGCGAC 750
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