Tag | Content |
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EnhancerAtlas ID | HS010-02642 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr2:197047270-197048130 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr2:197047784-197047799 | AGAGGTCAGGGTTCA | + | 6.14 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_10521 | chr2:197046244-197048452 | CD19_Primary | SE_11003 | chr2:197004269-197049818 | CD20 | SE_12009 | chr2:197046196-197049793 | CD3 | SE_14450 | chr2:197046438-197049882 | CD4_Memory_Primary_7pool | SE_15449 | chr2:197046745-197050335 | CD4_Memory_Primary_8pool | SE_15831 | chr2:197046909-197050257 | CD4_Naive_Primary_7pool | SE_16343 | chr2:197045987-197049903 | CD4_Naive_Primary_8pool | SE_16923 | chr2:197046189-197049558 | CD4p_CD225int_CD127p_Tmem | SE_17371 | chr2:197017698-197050924 | CD4p_CD25-_CD45RAp_Naive | SE_17889 | chr2:197045960-197050955 | CD4p_CD25-_CD45ROp_Memory | SE_18248 | chr2:197044767-197051808 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19479 | chr2:197045981-197049709 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20298 | chr2:197046090-197049810 | CD56 | SE_20837 | chr2:197046143-197049744 | CD8_Memory_7pool | SE_21479 | chr2:197046142-197049990 | CD8_Naive_7pool | SE_21958 | chr2:197046061-197049938 | CD8_Naive_8pool | SE_22412 | chr2:197045968-197050576 | CD8_primiary | SE_25485 | chr2:197028707-197051784 | DND41 | SE_31361 | chr2:197045969-197049538 | Fetal_Thymus | SE_39688 | chr2:197046058-197049512 | Jurkat | SE_43658 | chr2:197046505-197048761 | MM1S | SE_50957 | chr2:197047280-197048445 | Sigmoid_Colon | SE_55307 | chr2:197047378-197048251 | Thymus | SE_58309 | chr2:197014096-197142249 | Ly1 | SE_59970 | chr2:197014195-197079563 | Ly4 | SE_60673 | chr2:197014298-197048781 | DHL6 | SE_62197 | chr2:197014112-197048492 | Toledo | SE_62200 | chr2:197013935-197160826 | Tonsil | SE_66583 | chr2:197046058-197049512 | Jurkat |
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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 |
GH02I196181 | chr2 | 197046000 | 197050220 |
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Enhancer Sequence | AACAGGAAAT TGCAGAAATA AAGATTTGAT CAGTCGCCAT TAATTCAGTA AGCTTTGTTT 60 AGTTTAACCT AAGCTAACAG CACATTTATA ATTTGCCCAA ATAAATCACA CAAATTATCA 120 GAATAGGCTA GTTTTGTATA TAATTATCTC TTAATCACCA GTCCTTGCGT TCTTCTTCTC 180 ATTAAGCCTG TCTCTGAGGA GGTTGTCCTT TCACAGTAAA AATAGGCAAT ACCTTTGAGA 240 CACTTTCTGT TACTCATTGA CCTAGAAAAA TCCCCTCTAG TAGCTCAGTC CTGAGTAGGT 300 CTGAAAGCTT CTGGGTCAAT CACACATGCT GAATGTGGCA CAGGATATAT TAATATTAAT 360 AACACTTGAT GTCTGTACAG CATTTTAGTC AATATAGAGC TTTCACATGC AATGACTTAT 420 CTGAGCCTCA ACAGTCTGGG GATTACTGTT AGCAAAGCTA GTGTTATCCC ATTTTACAGA 480 TGAGAACAGA GGTCGTGAGA GTGACTTGTC CATCAGAGGT CAGGGTTCAG TCTAGGGCTG 540 AAGACTGTGG GCTCTTTCGA GTGACCCCTA ACAGAGAAGA CTCTCCAGAG AGCACACTTA 600 CCTGAGACAT GCTTTCTCTT TTCTCTCACC CCACCCCTTG CCTGAAGCAT TATAGGAGCC 660 CTATGACAGA TCAGCTGCGA ACAATGCAGA AGAAAGGGAA ACATAATTTT TCTGGAGGAC 720 CCAAAGTCCA GATGGCAAGC CAGACCAAGC CCCACGGCTG TCTTACCTGC AGGTGTGTGC 780 AGCACCAGAA GCCCCAAAAC AGTGTTCACA TCTCCCCATC TGGCCGGGCC ACACTCACTC 840 CCTGCTGTGG CCCAGATTGC 860
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