Tag | Content |
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EnhancerAtlas ID | HS043-23114 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr2:99081880-99083240 |
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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I098462 | chr2 | 99079012 | 99091939 |
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Enhancer Sequence | GTGTAATCTA GGATAATCTC ATCTCAAGAT TCGAAACTTA ATTGAGTCTG CAAATCCTTT 60 GCTGTATAAG GTAACATTAA TAGGTTCCAA GGATTTGAAC GTGAACCTCT TTTGCAGGGG 120 GCATTATTTG ACCTGCCATA CCTCACAGCA GCCTGATGAG GACCATACTG TCCCACATAC 180 AGTGGGCTTA ATGAGGAAGC TGAGGCTTGG GGAGGCCTAG GGGTGGCCAT GGTCCTTTCC 240 TCTCCCAGAC TCTGGGGTAG CTGACTCTGG GGTCATTTTG TCATGTTGCT GGGCACTCAC 300 TTGGTGAACA GATAATCCCC TGTCATTTTA CTATGTTGTT ACATGGGTTT GAAAAAAGAG 360 TTTTTCAACT CTCTGGCTGA GCCCCTGTTC CTGTGAGGGC CTGTGGTTTT TCCTCCCGGC 420 TCCACCCTGG TTTCGGCGCA GTACTTGAGC AGACGGTGGC TTGGGTCTCA CTCTAGCGCC 480 CTCCCCCTTC CTCTCTGGCT GTGTGCCCAG GCTGGCCCTG CCCACCTTGC TCAGTCTCTG 540 CTCCATCTGC CACAAGTCTC ACTCCAGCCC TCCCCCCAGT AGCTTAGGAA GGGACCTTCT 600 TGTTACGTTT TTTGTTTTGT TTTGTTTTTT GTTTTTTTGT TTTTTTGAGA TGGAGTCTCA 660 CTCTGTTGCC CAGGCTGGAA TGCAGTGGCG TGATCTCTGC TCACTGCAAC CTCTGTCTCC 720 TGGATTCAAG CGATTCTCCT GCCTCAGCCT CTTGAGTAGC TGGGACTACA GGCGTACGCC 780 ACCATGCACA GCTAATTTTT GTATTTTTAA TAGAGATGGG GTTTCACCAT GTTGGCCAGG 840 TTGGTCTTGA ACTCTTGACC TCAAGCAATC TGCCCGCCTT GGCCTTCCAA AGTGCTGGGA 900 TTACAGGCGT GAGCCACCGT GCCCGGCCTT GTTATGTTTT TTAAGCTAAC CCTGTAGAGC 960 ACTCACTGTG CACCAGCACC TGTTGGCTCA AGGGGGTGAC AGACATTCCC TATCACAGAT 1020 TACAATGAGT CACCGGCATT TTTGGAATTT CACTAAGCGT CGTTGCTGTG CTGTGCCTCA 1080 GCATGCAGCA CTTCATTTAA TCCTCTGGAC ACCTTGAATG ATAAGTGTCT GTCATCCCAT 1140 TTTACCCGTG AGAGAATTGC GGCTCAGAGA AGTTGTCACC CAGCTGGTTG GTGGCAGAGG 1200 TTTCAGAGGT CTTTCTGTGC ATAAAACCCT CACTTATGGT TATGCCAGGT AGGCCTTGGA 1260 GGGGATAGAC CCATCGCCAA ACTCACAGGA GAGAGAGGAG GGCACTCACA GGTGATGATG 1320 TCTATCTGTC TTCTTTCTGG TGGGGACCCA GAGTTTTATT 1360
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