Tag | Content |
---|
EnhancerAtlas ID | HS019-08621 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr19:47599900-47601140 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Mafb | MA0117.2 | chr19:47600582-47600594 | AAACTGCTGACG | + | 6.02 |
|
| 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 |
|
| 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 |
|
Enhancer Sequence | ACAGACTGGA GGTATACATG CTGGGGTTCC ATAAAGAAAA GCTAAGAACA ACATTACTCT 60 CGACACTTAA GTCTAGAAGG GATAAAGCTG AGAGGGACAT GATCACCACC CAGGCCACTA 120 ATATTTTAAA TGCCATATCT GTGCCAGGTT GCTTGACTAC CTCCTTTTCT GCACTGACAA 180 GAAACTTGGT CCACAAGGCA GGTGCCTGAT CATCAGGGCT GGGTCAGCTG AGCCGGAGTG 240 GGTGGCAGCC TCAGCACGCC CTCCCTTATG TCCAACACCG CGGCACAGCA GGCGACAGTC 300 TTGCCCAGGG TCAGCTGAGG CCTCCTTCCC TGTCCTGATG CCACTCGCTG GCTCGGACGA 360 AGGTACAGGC TACTCTACAT CTAACACCTG CGGGCAGAGG ACAAAAGACC ATTCAAGGAA 420 CTCCAAGAGC CTTAACCATC ATCCAGAATG ATTCTAGAAA GGAATCACCA AGGTAGAGAA 480 GTGCAGCATT CAAATTCACC CTACAAAGAC CTGAGCCAAA GAGGGATTCT GCACATTATC 540 GATATTAACA GCTCCAGGCA CATCTGGGCT CAAAGAGAAT CAACCATACA ACTTTTCACA 600 AAACAGGCAG TGACTACTTG AAATTTTGTT TCCCTAAAGT TGAGAGAGGC AGAGAAATAC 660 ATAGGATTTT TTTGTTGTTG TTAAACTGCT GACGGTTGAT AAAGGGGCAC TGAGACAGCA 720 ACAATAAACA GATCACTGCA TTCTCAGGGC CCTCTGGCCA TGTCAGGCCC TCAAGCCCCT 780 CCGAGCCCTG GGCTAACTTC TGTCCACAGT CACCTCAAGG GGTCCCCCCT CACGACACCC 840 AAGATGCTCT CCTAGCTAAA CGTCCTGCGT GAACACGAGG TCTTGACTAT ATTCTTCAGA 900 CTCTGTTCAA CAGAAAGCAA AAAGAAAGGA AGTCGAGCCA AATGGGAATC CCGTGGGCCA 960 CCAGCGCGAC GGCACAAAGG CGGTCTCAAC AAAACAGCAA CCAGGTTTCA GCGATGCCAC 1020 TTAACAGACT GCCGGCAAAA TCCGTGTCAG AGTGGGATTA AATGCCAAGG GAACATGCTT 1080 AATAGACCTC GACATAATCC CCCAAGAAAA GTGGGGGAAG CCCCACCGCG CTAATCATTT 1140 CAATCTAGAC CTGCCAAACT CTCTTGAGAC AAGCAAGCAG GAGAAAAGCC TGCCGTGGCG 1200 GCCTGTGCAG GGAGCACTCT ATTCCCAGAG CCTGGATTGG 1240
|