Tag | Content |
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EnhancerAtlas ID | HS046-19829 |
Organism | Homo sapiens |
Tissue/cell | Fetal_muscle_leg |
Coordinate | chr2:99081000-99083290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr2:99082903-99082914 | AATGAGTCACC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr2:99082727-99082742 | TGAACTCTTGACCTC | - | 7.64 | RARA | MA0729.1 | chr2:99082724-99082742 | TCTTGAACTCTTGACCTC | - | 6.45 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_09236 | chr2:99079158-99084603 | CD14 | SE_12066 | chr2:99079319-99084532 | CD3 | SE_14904 | chr2:99079467-99083737 | CD4_Memory_Primary_7pool | SE_15794 | chr2:99079364-99083484 | CD4_Memory_Primary_8pool | SE_16648 | chr2:99079378-99084411 | CD4_Naive_Primary_8pool | SE_17250 | chr2:99079662-99084190 | CD4p_CD225int_CD127p_Tmem | SE_17594 | chr2:99079277-99085843 | CD4p_CD25-_CD45RAp_Naive | SE_18010 | chr2:99079280-99085912 | CD4p_CD25-_CD45ROp_Memory | SE_18598 | chr2:99079254-99085535 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19649 | chr2:99079438-99084324 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20144 | chr2:99079165-99092088 | CD56 | SE_21398 | chr2:99079564-99083893 | CD8_Memory_7pool | SE_22521 | chr2:99078980-99086005 | CD8_primiary | SE_32475 | chr2:99078939-99094101 | GM12878 | SE_39553 | chr2:99079503-99082482 | Jurkat | SE_39553 | chr2:99082746-99084676 | Jurkat | SE_43508 | chr2:99078937-99085664 | MM1S | SE_50377 | chr2:99079480-99084237 | Sigmoid_Colon | SE_52736 | chr2:99079487-99082603 | Small_Intestine | SE_52736 | chr2:99082704-99084118 | Small_Intestine | SE_55432 | chr2:99079621-99082544 | Thymus | SE_55432 | chr2:99082626-99083275 | Thymus | SE_63026 | chr2:99060396-99125684 | Tonsil | SE_66467 | chr2:99079503-99082482 | Jurkat | SE_66467 | chr2:99082746-99084676 | Jurkat | SE_67159 | chr2:99078937-99085664 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 99081402 | 99081780 | chr2 | 99082804 | 99083102 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I098462 | chr2 | 99079012 | 99091939 |
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Enhancer Sequence | CTGCCCAGCC TCTTCTTCTG CCATGTCTGC CCTGACAGGG GCAGAGTTCT CAGTTCCCAT 60 GTCAGAACTC GGCACCAGCT TCTCTGTTGA CAGTTGCAAG GCCTGTGGCT GAGAGAAGTA 120 CTTGTGCTGT GTTTCTGCAA GGTAAGATGG CCCTGATCAC AGCTCATGAT GCCTGAGATC 180 AGGAGGGTCT GCTCCATGAG ATATCAGCAG AGGCCATCCT GTGAAATATT TTAACTAATT 240 GAACTGAATG TTGAAGACAA GGCCTGTGGC AGTGTTGTAT TTATATGTGA CAAGCCGAGA 300 GTCCTTGGAC AACCTTGGAA ACTCCTTTTT AGGACAGAAT CAACTGAGAC GATACACACG 360 AAGGAGCTTT TGTGAGCAGA GTACAGAGCT CGTTATTGCA GTACAAGGTT GTAGGTTTTC 420 ACACAGCTTT TGAGGATGGG TTGGTGGCCC AGGGAGGATG TCAGGAACTG TCCTTCACTA 480 ATGGGGATTC TCGAGTTCCT ACCACGTGCC AGATAGCGTG CTGATTGCTT TGTATCCACT 540 TCCCTTTTAA TCCCTTGTAT TAGCTTCCTG TGGTTGCTGT AACAAACTCG GTGGCTTAAA 600 GCGAAAGGAA CTTATTCTCT CACTGTTCTG GCCTCCAGAA TCACTGGGCT GAATCAAGCT 660 GTGGGCAAGG CCATGTTCCC TCCAGTAGCT TAGGGCGGAA TCCATTCTGT GGCTGCTGGC 720 TTGCCTCGGC TGCCGGCCCC TTCCTCATCT TCACACCAGC AGGGTAACAT CTTCTCTCCG 780 TGACTCCGCT TCTCTCTGCT TCTGTCACAC GGCCCTCTCT TCTCTCCGAA ATCTCCTGCC 840 TTCATATAAG GACATTTGTG ATGGCATTTG GGGCCTACCA GTGTAATCTA GGATAATCTC 900 ATCTCAAGAT TCGAAACTTA ATTGAGTCTG CAAATCCTTT GCTGTATAAG GTAACATTAA 960 TAGGTTCCAA GGATTTGAAC GTGAACCTCT TTTGCAGGGG GCATTATTTG ACCTGCCATA 1020 CCTCACAGCA GCCTGATGAG GACCATACTG TCCCACATAC AGTGGGCTTA ATGAGGAAGC 1080 TGAGGCTTGG GGAGGCCTAG GGGTGGCCAT GGTCCTTTCC TCTCCCAGAC TCTGGGGTAG 1140 CTGACTCTGG GGTCATTTTG TCATGTTGCT GGGCACTCAC TTGGTGAACA GATAATCCCC 1200 TGTCATTTTA CTATGTTGTT ACATGGGTTT GAAAAAAGAG TTTTTCAACT CTCTGGCTGA 1260 GCCCCTGTTC CTGTGAGGGC CTGTGGTTTT TCCTCCCGGC TCCACCCTGG TTTCGGCGCA 1320 GTACTTGAGC AGACGGTGGC TTGGGTCTCA CTCTAGCGCC CTCCCCCTTC CTCTCTGGCT 1380 GTGTGCCCAG GCTGGCCCTG CCCACCTTGC TCAGTCTCTG CTCCATCTGC CACAAGTCTC 1440 ACTCCAGCCC TCCCCCCAGT AGCTTAGGAA GGGACCTTCT TGTTACGTTT TTTGTTTTGT 1500 TTTGTTTTTT GTTTTTTTGT TTTTTTGAGA TGGAGTCTCA CTCTGTTGCC CAGGCTGGAA 1560 TGCAGTGGCG TGATCTCTGC TCACTGCAAC CTCTGTCTCC TGGATTCAAG CGATTCTCCT 1620 GCCTCAGCCT CTTGAGTAGC TGGGACTACA GGCGTACGCC ACCATGCACA GCTAATTTTT 1680 GTATTTTTAA TAGAGATGGG GTTTCACCAT GTTGGCCAGG TTGGTCTTGA ACTCTTGACC 1740 TCAAGCAATC TGCCCGCCTT GGCCTTCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGT 1800 GCCCGGCCTT GTTATGTTTT TTAAGCTAAC CCTGTAGAGC ACTCACTGTG CACCAGCACC 1860 TGTTGGCTCA AGGGGGTGAC AGACATTCCC TATCACAGAT TACAATGAGT CACCGGCATT 1920 TTTGGAATTT CACTAAGCGT CGTTGCTGTG CTGTGCCTCA GCATGCAGCA CTTCATTTAA 1980 TCCTCTGGAC ACCTTGAATG ATAAGTGTCT GTCATCCCAT TTTACCCGTG AGAGAATTGC 2040 GGCTCAGAGA AGTTGTCACC CAGCTGGTTG GTGGCAGAGG TTTCAGAGGT CTTTCTGTGC 2100 ATAAAACCCT CACTTATGGT TATGCCAGGT AGGCCTTGGA GGGGATAGAC CCATCGCCAA 2160 ACTCACAGGA GAGAGAGGAG GGCACTCACA GGTGATGATG TCTATCTGTC TTCTTTCTGG 2220 TGGGGACCCA GAGTTTTATT TCCATCTCGT TTTCTTTATG AATGCTTGTC TCACACTTAT 2280 GTATTTTTTG 2290
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