Tag | Content |
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EnhancerAtlas ID | HS170-00063 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr1:31225840-31228650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:31227857-31227868 | TTTCTGGGAAG | + | 6.02 | TCF3 | MA0522.2 | chr1:31226894-31226904 | AGCAGGTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_09454 | chr1:31213287-31232169 | CD14 | SE_10168 | chr1:31213284-31236569 | CD19_Primary | SE_10991 | chr1:31200236-31237145 | CD20 | SE_12025 | chr1:31215434-31231414 | CD3 | SE_13126 | chr1:31225755-31231455 | CD34_Primary_RO01480 | SE_13496 | chr1:31223360-31227247 | CD34_Primary_RO01536 | SE_13496 | chr1:31227251-31231821 | CD34_Primary_RO01536 | SE_14586 | chr1:31213183-31237364 | CD4_Memory_Primary_7pool | SE_15642 | chr1:31225772-31231357 | CD4_Memory_Primary_8pool | SE_16057 | chr1:31225561-31231446 | CD4_Naive_Primary_7pool | SE_16511 | chr1:31225655-31231488 | CD4_Naive_Primary_8pool | SE_17022 | chr1:31225965-31231414 | CD4p_CD225int_CD127p_Tmem | SE_17372 | chr1:31209247-31236610 | CD4p_CD25-_CD45RAp_Naive | SE_17902 | chr1:31209743-31235259 | CD4p_CD25-_CD45ROp_Memory | SE_18435 | chr1:31206875-31235130 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19221 | chr1:31225835-31231719 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20090 | chr1:31213732-31235754 | CD56 | SE_20783 | chr1:31215526-31235927 | CD8_Memory_7pool | SE_21654 | chr1:31224788-31233416 | CD8_Naive_7pool | SE_22073 | chr1:31215463-31231671 | CD8_Naive_8pool | SE_22484 | chr1:31213283-31234726 | CD8_primiary | SE_31319 | chr1:31226089-31227234 | Fetal_Thymus | SE_31319 | chr1:31227389-31235046 | Fetal_Thymus | SE_32510 | chr1:31215436-31239752 | GM12878 | SE_43662 | chr1:31214270-31233570 | MM1S | SE_50449 | chr1:31215714-31235694 | Sigmoid_Colon | SE_53612 | chr1:31215423-31231885 | Spleen | SE_55204 | chr1:31226107-31231617 | Thymus | SE_59019 | chr1:31215557-31239184 | Ly3 | SE_60258 | chr1:31215621-31235310 | Ly4 | SE_60651 | chr1:31202709-31239413 | DHL6 | SE_61144 | chr1:31205054-31253025 | HBL1 | SE_62248 | chr1:31201545-31253778 | Tonsil | SE_67247 | chr1:31214270-31233570 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 31227443 | 31228328 | chr1 | 31228142 | 31228235 |
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Enhancer Sequence | GACAGGGTTT TGTCCTGACC TCAAGTGATC CACCCGCCTC AACCTCCCAA AATGCTGGGA 60 TTACAGGCAT GAGCCACCGC ACCTGGCCGT ACTTTTTTTT TTTTCCAATT TAAAAGTAGT 120 ATACTTGAGC CACAAAGTAA AGTACCATTG GATTATAACC CAAAGCATAC AGTAAAGATC 180 CCTGGGTCCC TGTAATATAA ATAAATCATT TATTTATATA ATAAACTGGG AGTACAGACA 240 AATCTCCTTG AGAAATTCCA AGTAATTTAT GTAGCTACTC TGCCCTCAAG GAGGTGGGGC 300 GGAACTCCCC ATTCATCAAA CTTGAGTTGC TTGGAGCAGC ATAGTGACTT CCTTCTAAAA 360 CATACAGCAT GGAAAGGAGA AAAAAAGAGT AACTTTACAA AGGAGTAACC TCAGCCGGGG 420 GCTCAAAGTC ACCAGCAACA GTGGTAAGTC AAGTTGGCAG AACCTTTTCT TAGTACGATG 480 TTCTGAGACT GGCACATCAT CTCTGTGGTC TTCCTCCCAA AAGCACATTC CCAGACTAAT 540 CATGAGAAAA CCACCAGAGA CCCCAGTTGA AGAACATTTG ACAAAATGCC TGACAAATAC 600 TCCTCGAACT GTCAAGATTA TCAAAAACAA GAAAAATCTG AGAAACCATC ATACCAAGAG 660 GAACCTAAGG AAGTGTGAAG ACTAAATGTA ACGCGGCATC CTGGATGCAA TCTTGGAACA 720 GAAAAAGGAT GTAAGAGGAA AGCTGGGGAA ATAGGGGTGA AGCACTGACT TTAATAACAG 780 CCCACGAATA TTCATTCACC CATTGCAACA AACGCACCAC ACTAACGTTG AGACGTTAGC 840 AATAGAGGAA CTAGGCATGG GGGACGCAAG AACTATCTGT ACTGTGTTTG CAATATTTTC 900 GTAAATCTAA AACCGTTCTA AGTACGTGCT CATTGTACCA AATATGGAAA ATACAGAAAA 960 GTAGAAAAAA TAGAGCTTTC ACTATCCTAG AACCCAAATA CATTTCCTCC TCGCCCAGTT 1020 TTGACGTATC CTGTTTTGAC ACTGTTGAAA TCATAGCAGG TGTTAAGTTT TTTAACCCAG 1080 ACAATGCATT TCTGACAGTG GAATTCCGGG CACTCTGGGG AAGAGGGGTC AGGAAGAAAG 1140 AGATTTCTGG GCAAAAGTGT CTTCTGGGGG TGTCCACTTT CTACCATCGA CTTAGAACGT 1200 GCTTCAGGTT GACAAAAAGC CAGGACCCAA GAGACCCAAT TTAAGAAATT TCTCTAGACT 1260 GGGCTCGGTG GCTCATGCCT GTAATCCCAG CGCGTTGGGA GGCCAAGGCA GGAGAATCAC 1320 TTGAGGCCAA GGGTTTGAGA CCAGCCTGGG CAACATAGTG GGACCCTGTC TCTACAAAAA 1380 AAAATATTTA AAATTAGCTG GCCATGGTGG CATGCGCCTG TGATCCTAGC TACTCAGGAA 1440 GCTGAGGTGG GAGGATCTCT TGAACCCAGG AGTTCAAGGC TGCAGTGAGC TGTGATGGCA 1500 CCACTGCATT CCAGCCTGGG TGACAGAGCA AGACCCCATC TCTTAAAAAC AAAAACAAAA 1560 CAAAACAAAT CAAACCACAA AAGATGGGCA AGTTACTGAA CTTTGAAAAA AAGAATAGAT 1620 TTTTTAAAAA AAGAAAGAAA GTTTGCTGGG TTCCCAAAGT GTGCAAGTTT GGGTGACCCA 1680 GAGAATCCTC TACACAAACC CACTGACATC CTGAGGAAGA TGCCCGAGCC CAAAGCTACG 1740 GACCAGGCTT CCCTCATGTA ATAACGCCCT CATGACTCAA TAGAGCGTGG CACTGTCTCA 1800 GGATGGCAAG GTCTCAATTT AACCCTCCCT AGAGGGGCCA AGTCCACAAA TAGCTCATGA 1860 TGTGCAGAGT CGTCACCCAT GGCTGGGTCC AGATGACAGC CAGCATGGGC TATTGACACA 1920 TCTGGACCAC AGCTTCTCTT TTTCCATCCA GATGCTCAAG GTCCTATCAG CACACCTGTT 1980 GCCAGCTAGC CTATGGGAAA GCCCCCAGGC CCTGCCCTTT CTGGGAAGGA GAGAGGACTC 2040 TTTCGGGGTG CAGGAAGATA ACCCCCCACT GGAGTCAACT GAGGACCACA GCCTGGAGAC 2100 AACCTGGGCC GAGCGCACAG CTTCCAGGAC ACCCCTCTGC TCTTTTGCTT GCTCCTGCTC 2160 TAGAACGTCT CATCACTCAT AGGCATTGGT TCTCAACTGG GAGAGATTGG GCCCCATAAC 2220 TAGAGACATT TTTGGTTATC ACAAGTGGCA GGGTAGGGAG ATGGGCAGTG CTGCTAGTAT 2280 CTAGTAGGTA GAGACCATGG ATGCTGCTGA ACTTCCTCTA ACGCACAATT CACTCCCCCA 2340 AGATGAAGAA TTATCCAGCC CAAAATATCA ATGGTGCACT GCAGAGAAGA TCCAACTTCT 2400 TAGCTTGTCA CTCAAAACCT TTATCACCTC CTCCCCAAAC TCCAGGTTTG TCTCTATTGT 2460 GTCCCTGTAG AAGCCGAACA CATACGCCAT TGCTCACCTG TTTCTCCTCA CCTTCCATAC 2520 TGCCCACAAC CAAACTCTCC CTCCTGCCAA TGGCACCACC TCCAAGAAGT CTTCCATGAT 2580 TGCTAGGGCC CACACATTCT TCAGCTCTGT GAGCAGGGAC CGTATATCAC ACCACCATTT 2640 ACAGGTGAGG ACATCGGATG GCACGATCAA CAAGAAACCT TAACAGCCCC ACAGTCCCGG 2700 GTTTGCAGGG CAGCCTCTGG GCCCACACAA CCTGCAAATG GATTTGACTT GGCCTGCACT 2760 GAGATTTTTT TCTACCATGC ATCAATCACT AGCATTGAAA CATCAGAAGA 2810
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