Tag | Content |
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EnhancerAtlas ID | HS003-23950 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr19:46791910-46794290 |
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) |
EWSR1-FLI1 | MA0149.1 | chr19:46792155-46792173 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr19:46792159-46792177 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr19:46792081-46792099 | GAAATGAAGGAAGGAGGA | + | 6.21 | EWSR1-FLI1 | MA0149.1 | chr19:46792150-46792168 | GGAAGGGAGGGAGGGAGG | + | 7.08 | EWSR1-FLI1 | MA0149.1 | chr19:46792092-46792110 | AGGAGGAAGGAAGGAAGG | + | 7.85 | EWSR1-FLI1 | MA0149.1 | chr19:46792096-46792114 | GGAAGGAAGGAAGGGAAG | + | 8.57 | Foxd3 | MA0041.1 | chr19:46794102-46794114 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr19:46794106-46794118 | AAACAAACAAAC | - | 6.32 | MITF | MA0620.2 | chr19:46792767-46792785 | GTTGGTCATGTGACTTCC | + | 6.18 | MITF | MA0620.2 | chr19:46792767-46792785 | GTTGGTCATGTGACTTCC | - | 6.18 | RARA | MA0729.1 | chr19:46794258-46794276 | CATTGACTCTCTGACCTC | - | 6.01 | STAT1 | MA0137.3 | chr19:46793185-46793196 | TTTCCTGGAAA | - | 6.62 | Stat4 | MA0518.1 | chr19:46793182-46793196 | ACATTTCCTGGAAA | - | 6.41 | ZNF263 | MA0528.1 | chr19:46793447-46793468 | CCCTCTCCCTACCCCTTCCCC | - | 6.17 | ZNF263 | MA0528.1 | chr19:46792094-46792115 | GAGGAAGGAAGGAAGGGAAGG | + | 6.1 | ZNF263 | MA0528.1 | chr19:46792142-46792163 | GAAGGAGAGGAAGGGAGGGAG | + | 6.39 | ZNF263 | MA0528.1 | chr19:46792139-46792160 | AGAGAAGGAGAGGAAGGGAGG | + | 6.49 | ZNF263 | MA0528.1 | chr19:46792148-46792169 | GAGGAAGGGAGGGAGGGAGGG | + | 6.54 | ZNF263 | MA0528.1 | chr19:46792086-46792107 | GAAGGAAGGAGGAAGGAAGGA | + | 6.55 | ZNF263 | MA0528.1 | chr19:46792093-46792114 | GGAGGAAGGAAGGAAGGGAAG | + | 6.74 | ZNF263 | MA0528.1 | chr19:46792101-46792122 | GAAGGAAGGGAAGGGGAAGGG | + | 6.86 | ZNF263 | MA0528.1 | chr19:46792147-46792168 | AGAGGAAGGGAGGGAGGGAGG | + | 6.99 | ZNF263 | MA0528.1 | chr19:46792160-46792181 | GAGGGAGGGAGGGAGGGACGG | + | 6 | ZNF263 | MA0528.1 | chr19:46793416-46793437 | TTCCCTTCCCTTCCCTTCTCT | - | 6 | ZNF263 | MA0528.1 | chr19:46792152-46792173 | AAGGGAGGGAGGGAGGGAGGG | + | 7.05 | ZNF263 | MA0528.1 | chr19:46792097-46792118 | GAAGGAAGGAAGGGAAGGGGA | + | 7.07 | ZNF263 | MA0528.1 | chr19:46792090-46792111 | GAAGGAGGAAGGAAGGAAGGG | + | 7.79 | ZNF263 | MA0528.1 | chr19:46792156-46792177 | GAGGGAGGGAGGGAGGGAGGG | + | 7.97 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_27946 | chr19:46792069-46793558 | Fetal_Intestine | SE_28936 | chr19:46791917-46793672 | Fetal_Intestine_Large | SE_30198 | chr19:46791978-46793929 | Fetal_Muscle | SE_40980 | chr19:46791479-46793912 | Left_Ventricle | SE_42682 | chr19:46791903-46793939 | Lung | SE_49076 | chr19:46792088-46793432 | Right_Atrium | SE_49717 | chr19:46792161-46792660 | Right_Ventricle | SE_54344 | chr19:46791375-46794680 | Spleen | SE_54901 | chr19:46792014-46793795 | Stomach_Smooth_Muscle |
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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 |
GH19I046287 | chr19 | 46790798 | 46793790 |
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Enhancer Sequence | CAAAAATTAG CCGGACATAG TGGCGCACAC CTGTAATCCC GGCTACTCGG GAGGCTGAGG 60 CACGAGAATT ACTTGAATAT GGGAGGCAGA GGTTGTAGTG AGCTGAGATT GCCATTGCAC 120 TCCAGACTGG GCAACAGAGT GAGACTCCAT CTCAAAAAAA AAAAAAAAAA AGAAATGAAG 180 GAAGGAGGAA GGAAGGAAGG GAAGGGGAAG GGAAGGAAGA GAGACAGAGA GAGAAGGAGA 240 GGAAGGGAGG GAGGGAGGGA GGGAGGGACG GACAGACGGA CGGACGGAAC TAACTCTATG 300 AGTCACAGAG AGGTTAAGTA ATTTGTTCAA GGTTCTGCAG CTGGTAAATG ATGGGATTAG 360 AATGCAGGCA GCCTGGCTCC AGAGTCCACT ATAGGAAAAC ATTGGAGCCC ACTTAATGGG 420 GCTGCTGTGA CATTCCAATG TGAACAGGAA TGCCAAGGGC TCAGGACAGC GCTTGGCACA 480 GGATCTGTGC ATCATGCTTG GAACTGGTGC TGTTTATTTC CATCACCTGA TTCTGGGTTG 540 GCCTTGGCTT GGGTTTGGAG GGATTTTCTG CCCCTGGCAG TGTTCCAGGG GTGGCAGCTG 600 GACTTTTTAA ATCCAAGGAC CTTGTTAGGA GTCAGAGTTG GGCAAGGGGA GACTGGAGAT 660 AAAATCCGAT CACAAGAGGT AGCTATGAAT AGGTCAGGAG CAATTCTCCC CAGCCTTGAG 720 CAGTAGGGAG GATGAGTCAA CAGAAGTGAA CTCACCCTTC CTACTTGTTA TAGAATTATA 780 CATCCATGAC TGTACCATGT GACTTTACAT GTCTTCTTGA GTATGTCAAA TACATTCCCT 840 GACCCACTGA GGTCAGGGTT GGTCATGTGA CTTCCTGTGG CCAATAGGAT GTGAGTCATA 900 CCCAATAAAG ATAACCAGAC CTGATGGTAA GTAGAATATC CATGAAGATG TGCAGGAGAC 960 CATGGCCAGC AACACTGGCT TATCAGAACT GGGTTCATGC ACAGGTCTGA GTTTTTGTTG 1020 CTGAACCCTC TTTCCCTGTC AATAAGACAA GCATTTATTC CCCAGTATCC CAAGGCCTAT 1080 GACTCCACCT CCAGGCTGCC ACTCATAGGT GGAGCTCACC TGGCACCTGC GGCTGGAACA 1140 TCTACTTATC ACCTTTCCAT GTGGCTCCTT GGGCTTCCTC ACATCATGGC AGCTAGGTCC 1200 CAGGGGCTAT GGGACCTAGC TAGATATTGT GCTTCATAGC TAGATACGGT GCTATGAAGA 1260 GTGTGGCAGT TGACATTTCC TGGAAATGGT CACAGTAATA TTTTGAGTCT CACATGCTCT 1320 CCCTTGTGGT AGCTTGCCCC TCCCATCAAA AGGCAGAGTA TTTTCCTTTT CTTGAAGCTG 1380 GGCAGAACTT TGTGATTGCC TTGACAGAGG GGAAAAAAAG GGTTGGGGGG GTGCAGAAGT 1440 GACACTATAT GCCTGTGTGA CTTCCAAGGC TAAGTCATAA AAGCAGACAC GGCTTTTTCT 1500 TGTCCTTTCC CTTCCCTTCC CTTCTCTCTC TCAGCCTCCC TCTCCCTACC CCTTCCCCAC 1560 CACTGGCCTC TGGGACCTAG CTGCCATGAT ATGAGGAAGC CCAAGCAGCC ACAGGGAAAG 1620 GTCACAAGTA GAAGTTCCAG CCACAGGGCC CAGGTGAGGT CCCAGCTGAT AGGCAGCATC 1680 AACTGCCAGA CAGGTGAGTG AGAAAGCTTC AGATCATTCC AGTCCACAGC CTTTTAAGCC 1740 ACCCCAAGGG GTGTCAAGTG CAGCAAAGAT GAGCCATACC TGCTGAGCCC TGCCCAGATT 1800 GCAGATCTGT AAGCAAAGCA AATCTTTTCA CTGGGGTGGT TTGTAAACTA GGGAAGTTCC 1860 AGCTCTTTCC TAGTTGAAGA CTTTTCCCTT CTTTAAAACC TAACTCAGGC CGGGCACAGT 1920 GGCTCATGCC TGTAATCCCA GCACTTTGCA AGGCCAAGGC AGTTGGATCA CTTGAGGTCA 1980 GGAGTTTGAG ACCAGCCTGG CCAACATGGC AAAACCCCAT CTCTATAAAA AATACAAAAA 2040 AATTAGCTGG GTGTGATGGT GCACACCTGT AGTCCCAGCT ACTCGAGAGG CTGAGACAGG 2100 AGAATTGCTT GAACCGGGGA GGTGGAAGTT GCAGTGAGCC AAGATTGAAC CACAGCACTC 2160 CAGCCTGGGC AACAGAGTGA GACTCTGTCA GAAAACAAAC AAACAAACAA AAAACACCTA 2220 ACTCAGATGT TGCTTTCCTG CTTAAAAGCC TCCCATGTTC CCATCTCCTT CAGAGTAAAA 2280 GCCGAAGTCT ATACTTAATC TAAAAGATCC TTCCTACATG ATCTGCCAAT ACCACGGTTT 2340 CCTGTCAACA TTGACTCTCT GACCTCTTAT CCCACTCTCC 2380
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