Tag | Content |
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EnhancerAtlas ID | HS170-02575 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr22:37638220-37639320 |
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 | CTGATGCATG GCAGCAGCCG ATGGCTGCTA GGGAAGACCT GACCCTGCTC TTCCCTCTCA 60 CCTCCCCCGT GGAGCAGAGC AGTTACCAGG TCAGGGTTTG AGTCAGAGTG GTCTGGGTTC 120 AAATCCTGTG AGGCTTTGGG CAAATTACTT AGCTTCCCTG AACTTTCATT TTCCCACCTG 180 TAAAATGGAC CTATTAGGTT TGGTGAGAGG ATAAATAGAG AAGGCTAGAT TAACCCCAGA 240 GCTGGTACAT AGGAAGGAAG TGATAACGCG CGCCTCCTCC ACCCTCAGCA TGCGAGGCTG 300 GGAGCGGGTG CAGGTAGCTC AGCCGAAGCC CAGAGGCCAA GGGACAGCTC TGGGCCTTCC 360 CCTGCCCTGC GTGGTTTTGT CACTTCCTGC TCAGAGAAGA CAGCTCATCC TCTCCTCCTA 420 CCATCGCCCT CCCCTGGGCC TGCCACCGAG GTAATTTTGA ATGACTGGAA CGTTAACCCT 480 TGACTTCCGC CCGCCCCTCC TCCGATCAGA TACAAAGCAG AAGTGAACAG GGCTGGGGCA 540 GGCGAGGGCA GATAAGGAGC CATGCATCAG AATCAGCTGA GGCTGGTGGA CAAATGGGCC 600 CGCCCCCACC TAGATGGGTC ACAGCCAAAG TCGGGGCCAC AGGGCCCAGG CCAGGAGAGC 660 TGAGTCTCTC AAAGCCTTGG GCTGCTCCTC TGTAGAATGG GAAGGCTGGA CAGGAGGCCC 720 CCTTCCAGCT AGAACATGCT CCAGGGTGAG CCTGTAGGCT GGACCCTAAG ATGTGGCTGC 780 TGGCAGGCAT GACAGATTGA CAAATTGGAC CTGTCCTTTT ATTTTGTGTT TTTTTAAGAG 840 ACAGCGTCTT GCTCTGTCAC CCAGGCTGAC TGCAGTGGCA CCATTATAGC TCACTGCAGC 900 CTCAAACTCC CGGGCTCAGG CGATTCTCCC ACCTCAGCCT CCCCAGTAGC TGGGACTGCA 960 GGCGCATATG CCACCACTCC TGGCTTAAAA AAATTTTTTT ATAGACATAG GTTCTCGCTA 1020 TGATGCTTAG GCTGGTCTCA AGCTCCTGGC CTCAAGCAAT CCTCCCATCT TGGCCTCTCA 1080 AAATGCTAGG ACTACAGGCA 1100
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