Tag | Content |
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EnhancerAtlas ID | HS176-25188 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr22:37638190-37639100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr22:37638702-37638723 | ACTTCCGCCCGCCCCTCCTCC | - | 6.37 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_09557 | chr22:37634437-37642109 | CD14 | SE_10320 | chr22:37636792-37642449 | CD19_Primary | SE_11141 | chr22:37613444-37642817 | CD20 | SE_11906 | chr22:37636463-37641591 | CD3 | SE_14617 | chr22:37636675-37641576 | CD4_Memory_Primary_7pool | SE_15501 | chr22:37636980-37641397 | CD4_Memory_Primary_8pool | SE_15906 | chr22:37636629-37641711 | CD4_Naive_Primary_7pool | SE_16510 | chr22:37636656-37641486 | CD4_Naive_Primary_8pool | SE_16969 | chr22:37636687-37641807 | CD4p_CD225int_CD127p_Tmem | SE_17369 | chr22:37612712-37642072 | CD4p_CD25-_CD45RAp_Naive | SE_17862 | chr22:37613647-37642207 | CD4p_CD25-_CD45ROp_Memory | SE_18463 | chr22:37621942-37642050 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19164 | chr22:37629500-37641686 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20119 | chr22:37629579-37642292 | CD56 | SE_21034 | chr22:37636787-37641122 | CD8_Memory_7pool | SE_21592 | chr22:37636905-37641494 | CD8_Naive_7pool | SE_22062 | chr22:37636322-37641634 | CD8_Naive_8pool | SE_32637 | chr22:37636891-37642045 | GM12878 | SE_39809 | chr22:37637346-37640136 | Jurkat | SE_43640 | chr22:37637121-37642434 | MM1S | SE_50312 | chr22:37634450-37642011 | Sigmoid_Colon | SE_53490 | chr22:37634390-37642107 | Spleen | SE_55137 | chr22:37636700-37641817 | Thymus | SE_55695 | chr22:37636956-37641542 | u87 | SE_58850 | chr22:37613664-37681838 | Ly3 | SE_60812 | chr22:37614284-37642429 | DHL6 | SE_61227 | chr22:37613918-37681610 | HBL1 | SE_62378 | chr22:37613614-37642624 | Tonsil | SE_66668 | chr22:37637346-37640136 | Jurkat | SE_67282 | chr22:37637121-37642434 | MM1S |
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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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Enhancer Sequence | CGAGGCCTAT CAAAGCACTG AGCACAGGGC CTGATGCATG GCAGCAGCCG ATGGCTGCTA 60 GGGAAGACCT GACCCTGCTC TTCCCTCTCA CCTCCCCCGT GGAGCAGAGC AGTTACCAGG 120 TCAGGGTTTG AGTCAGAGTG GTCTGGGTTC AAATCCTGTG AGGCTTTGGG CAAATTACTT 180 AGCTTCCCTG AACTTTCATT TTCCCACCTG TAAAATGGAC CTATTAGGTT TGGTGAGAGG 240 ATAAATAGAG AAGGCTAGAT TAACCCCAGA GCTGGTACAT AGGAAGGAAG TGATAACGCG 300 CGCCTCCTCC ACCCTCAGCA TGCGAGGCTG GGAGCGGGTG CAGGTAGCTC AGCCGAAGCC 360 CAGAGGCCAA GGGACAGCTC TGGGCCTTCC CCTGCCCTGC GTGGTTTTGT CACTTCCTGC 420 TCAGAGAAGA CAGCTCATCC TCTCCTCCTA CCATCGCCCT CCCCTGGGCC TGCCACCGAG 480 GTAATTTTGA ATGACTGGAA CGTTAACCCT TGACTTCCGC CCGCCCCTCC TCCGATCAGA 540 TACAAAGCAG AAGTGAACAG GGCTGGGGCA GGCGAGGGCA GATAAGGAGC CATGCATCAG 600 AATCAGCTGA GGCTGGTGGA CAAATGGGCC CGCCCCCACC TAGATGGGTC ACAGCCAAAG 660 TCGGGGCCAC AGGGCCCAGG CCAGGAGAGC TGAGTCTCTC AAAGCCTTGG GCTGCTCCTC 720 TGTAGAATGG GAAGGCTGGA CAGGAGGCCC CCTTCCAGCT AGAACATGCT CCAGGGTGAG 780 CCTGTAGGCT GGACCCTAAG ATGTGGCTGC TGGCAGGCAT GACAGATTGA CAAATTGGAC 840 CTGTCCTTTT ATTTTGTGTT TTTTTAAGAG ACAGCGTCTT GCTCTGTCAC CCAGGCTGAC 900 TGCAGTGGCA 910
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