Tag | Content |
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EnhancerAtlas ID | HS175-13363 |
Organism | Homo sapiens |
Tissue/cell | SK-N-MC |
Coordinate | chr19:41832750-41835090 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr19:41833281-41833292 | CCGAATCCACA | + | 6.02 | KLF4 | MA0039.3 | chr19:41834029-41834040 | GGAGGGTGTGG | - | 6.32 | KLF5 | MA0599.1 | chr19:41833549-41833559 | GGGGCGGGGC | - | 6.02 | SPIC | MA0687.1 | chr19:41834976-41834990 | AGAAAGAGGAAGCA | + | 6.04 | ZEB1 | MA0103.3 | chr19:41833774-41833785 | GGGCAGGTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 33 | ID | Coordinate | Tissue/cell |
SE_01266 | chr19:41832850-41835062 | Adrenal_Gland | SE_01941 | chr19:41826114-41834937 | Aorta | SE_02341 | chr19:41827299-41835217 | Astrocytes | SE_06609 | chr19:41827940-41835020 | Brain_Hippocampus_Middle | SE_10534 | chr19:41829088-41835289 | CD19_Primary | SE_10928 | chr19:41826548-41839191 | CD20 | SE_13335 | chr19:41832811-41834898 | CD34_Primary_RO01536 | SE_14053 | chr19:41832911-41833520 | CD34_Primary_RO01549 | SE_14717 | chr19:41828274-41835424 | CD4_Memory_Primary_7pool | SE_17526 | chr19:41828356-41835571 | CD4p_CD25-_CD45RAp_Naive | SE_18470 | chr19:41831462-41835430 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19170 | chr19:41831258-41835426 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20013 | chr19:41827344-41835576 | CD56 | SE_20919 | chr19:41832350-41835435 | CD8_Memory_7pool | SE_22408 | chr19:41828648-41835382 | CD8_primiary | SE_26210 | chr19:41832721-41833701 | Duodenum_Smooth_Muscle | SE_27131 | chr19:41832876-41835375 | Esophagus | SE_29782 | chr19:41832691-41835131 | Fetal_Muscle | SE_31885 | chr19:41832910-41835349 | Gastric | SE_37091 | chr19:41826651-41835398 | HSMMtube | SE_38093 | chr19:41826925-41835502 | HUVEC | SE_40475 | chr19:41833510-41834578 | K562 | SE_40475 | chr19:41834586-41835198 | K562 | SE_41125 | chr19:41824878-41835177 | Left_Ventricle | SE_44313 | chr19:41826974-41833634 | NHDF-Ad | SE_44313 | chr19:41833706-41835039 | NHDF-Ad | SE_44950 | chr19:41832756-41835161 | NHLF | SE_45824 | chr19:41826675-41835471 | Osteoblasts | SE_48776 | chr19:41832710-41835338 | Right_Atrium | SE_50262 | chr19:41826769-41835431 | Sigmoid_Colon | SE_52575 | chr19:41832732-41835420 | Small_Intestine | SE_62666 | chr19:41801738-41841748 | Tonsil | SE_65513 | chr19:41833044-41835376 | Pancreatic_islets |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I041321 | chr19 | 41827009 | 41835422 |
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Enhancer Sequence | CTTGAGCCTG GGAGGCGGAG CTTGCAGTGA GACAAGATCG CGCCATTGCA CTCCAGCCCA 60 GGCGACAGAG CAAGACCCCG TCTTACACAT ATACACACAC ACTCACTCCC CTCTCCTGGA 120 GAAACACCAT TCCCACAGAT GATTAACATA TGCAGAAAAC ACCACATTTC AAGTCAAACT 180 TACACTTAAA AATGCACAAA TTTACACTCA GAAGAACAGT GAAGATGTTG AGAAAAATAT 240 CAGACACACA ATATGCCCCA GATACATGGC CGACTTGCAG AATCAAACAG TGCCAGAGCA 300 TAAAACCCAC AGAAAATACA ACAGCTTGCC CAGCAGAAAT ACAAAATGCA GACGCACACC 360 CCAGAAATGC AGCGCAGCCA CAAACACACG GAGCTAACAC GTGCTGGGGA CACACATAGA 420 CAAGACCATC CATACCAAAC AGCACACAGG CCCCCAGAAC ACCCATGCCA GACGCAGCTC 480 ACGCCACAAA GCTTGGAATC ACGCACACAA TAAGTTCCTG AACACACAAA TCCGAATCCA 540 CACTGGAACC TCAAATACTC TGCATGTCCA GAGACTAAGG GGGAAGGGGC TTTCTCTCAC 600 CCACCAATCT CCCCACTCCC CCTTGCTGAC CCGGGTCCCA GGCCCGTCTT GGGGGCGGGG 660 GAGGGGGCAG GAAGGCCTGA GCTGGCCTCC CCCAGCAGCT TCCTGCCCCA CGGGGGCTGG 720 ACAGGAAGCT GGGGCTCCAG CCGGAACCCA GGCTCCCCCC ACGACTTCCC TCTGTGGCCC 780 CGGGCCGCCT GCAGAGGCAG GGGCGGGGCA GGGGGAGGAA GCGGGGAGCC CCAAACCCCC 840 TGCCCTGCCC CTGCGGTCGG CCACAGGCGG GGGCAGACTT GTCCCGACGG GGCTGAGCCA 900 CCCATCGGGC CTGGGTGCCA GGGTGGCAGG GCAGGGGCAG TGCGCACGCG GCCAGAGGAA 960 GGTGCTGAGC CCACAGTTTC CCCTCCCCGC CCTGTGGGGC TGTGCCAGCT CAGCCGGCAG 1020 CCCTGGGCAG GTGGGCGGGG TGTGTCATGA GGGCGTGTTG GGCAGGCCGA CCACACCGCG 1080 AATGTGCAGC CAGCACTTGT CCTCAGGCCG AGGCACGAGC TGGGGCTGGG CATGTGAGGG 1140 CCGCGTCTGC CACCCTGGGG GTGTGTCTGC TCCGTCTGGG ACCCTGGGTG TGACAGTGTG 1200 TCTGGGCGTG ACGTGACGGG GTCGCTGCAA TCTGTGGGGC CCTGTGGGAC TCCCCAGGCT 1260 GGAATTGTGC GTGTGTGGCG GAGGGTGTGG GATGTCAGAC TGAGTGGGTA AGACCGACCT 1320 GCTGTCTGTG AGGTTGTGAC GTGTCAGACC TCTGTGTGGG GTGTGTCTGG TGGGACTGTG 1380 ACAGGTCCGA CTGTGGACAT GCACCCTGGA CCTGTTTGTG ACTGTGAACC CATGGAGGAG 1440 GAGGTGGCTG TTGAGGGATC CATTTCCTGT CCGGGCTCTG ATGCCGTGAT GCGTGTGCGT 1500 GCATGACACT GTTTGAATCA GTGTCTGGTG TGCGGTGGTT GCGACCATGA CCCTGTGGAA 1560 TATATTTGTA TATGACTGTG TTGTGCCAGG TCCCTATTGA AGTCTCTGCT CGTGTTGTGT 1620 CCCAGTGAGG CTCCGAGGCT GGGTGGTGTT TACGTGATGG GCTGACACTT TCTCTATTTG 1680 TATCTGTGTA TATGTGGGCT GCAGCTGCTG CCAAATGACA CAGCCCATGT GTTACGGGCC 1740 CTGCAGGAAT CTCTGTGTGT CCACGGCGGC TCTGAGAGGT GAATATTTGT GTAGTGTGGG 1800 GCACCGTCCG TGTTTCCCGC CGTGTGAGTG TGTCTGCATG TGTACACGCA CCACATCCTC 1860 ATAGGGCTGC AGCGATTACA GCCGAGTCAC TGTGTCCTAG CTTGTGACTC TGCCTCTTGG 1920 GGCCAGACCT CAGCATCTCT ATACCTATCC ATTTGTTGGC ATGTCCTTGC ATAGTGAACT 1980 CCTGCCTCCC CACTCCTCCC TCAGCCCTGT GTGCTTTGGG ACCTGAGGCC AGAGGAGTAA 2040 CCACATTTCT ACCCCTATGC TGAGCTGGGA GGGCCCCAGG TCCCTGGCAC CCAGACCCAG 2100 TGCTGCCAAC AGCTCTCATG CCCACAGGCA AAGGAACCGC AGCACTCATA CTGTCCTTCC 2160 TCCCAGGACA ATCACTGGGT GTGGGGAAGT GAAACCTAGG AGAAAGAGCA GAAACTGAGA 2220 GGCAGGAGAA AGAGGAAGCA GGAGAGAATT CACAAGCAGG ACCATAGCAG ATGGGAAGAA 2280 ATGGAGACAG CAGAGGGAGA CCCACCTGTG GCTGCTGCCA TTTCTTGCCT GGACAGCTGG 2340
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