Tag | Content |
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EnhancerAtlas ID | HS104-59426 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr8:130603990-130605420 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr8:130604652-130604673 | GGGGGAGGGGAGGGGAGGATG | + | 6.01 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_13667 | chr8:130602888-130606982 | CD34_Primary_RO01536 | SE_25360 | chr8:130593661-130609405 | DND41 | SE_39973 | chr8:130603631-130604313 | K562 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr8 | 130604348 | 130604400 | chr8 | 130604361 | 130604767 | chr8 | 130604400 | 130604585 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I129591 | chr8 | 130603341 | 130606133 |
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Enhancer Sequence | CTGTTACCCA TTTTAGAGAA GGCACATGGG GACAGGAAGT GACTGTCCCA GGTTGCCTCT 60 TAAGAGATTA AGTGCAAGAG GCTCCAAGCT GAAATGGAGG CATCAGGACA GGGTCCTGAC 120 CCCCTTCCAG GCCCCCTTAC TGACCAGCCC CTGAGAGCAG GGCTACACTT CTGTCTGGTG 180 ACCTCTGCTA GTGTTAAGGG GCCCACTCTT TGCTCCATCT CTCTTGGCCC AGAGCCAGGG 240 GTGGGCTGTG GAAAGACACA AGGGTGGATA AGTCTGAATG GACCCCCCCT CCAATGGTCA 300 CACCCCCCCC AGCCCCAATT CAGTTAAAGA TTGCAGGAAG TGGTTTGTCC GTTTAGAAGT 360 CTTCACAGCT CTGAGGCCCT TCTGAGAAAT TAACTTGCAG TTCTCTAAAG ATAGATTGCG 420 CAAAATGGGA GGGGGCAGCC CCCAAGGACC CTCCAACAGC AATTCTCCTG AGGACTTCCA 480 GAGACCTCTG CCAGTGCCCC CACCCCCACC CCGCCCCCTT GAGCAGCTGC CTGTCCTTGG 540 ATGGACCAAA TCAACACCCG ACTCTTGTGC AAGGCTCGGG TTTCATGTCC CCAGTGAACA 600 AATTCTGTTC TGAAGAGGCA GTGGGGTGGG GAGGCTGAGG CGGGGAGGGG ACATCAAAAA 660 CAGGGGGAGG GGAGGGGAGG ATGGTGGGGG TGGGGTTTTC AGCTGCTCAT GTCATTTATT 720 TTCCACGGAA TCTTAACTGT AATTTCAAAC TGCATCTGGG TTTTCTGAAA CTATGTGATT 780 TGCCATGAGG TTCACAGAGA GTTTAGGCCT TGCTCCAAAC TTCAGCGCTT TCACGCCTAG 840 AAAAACAGGA TCCAGGAAGG CAAAGTGATG TGAAGAAGGG GATACTGCTG TCCCCTGATG 900 GAGGGACATG TAAAGAAATA AATAAGCAAT TGGTTTAGCC AGGGTAGAGG GTAGGGACAT 960 GGGTGCCACT CAAACATTGA AATTTCCTAG CAATCAGACA GAGCAGAGCT GGCCTTGGGA 1020 GGAACAAGTC TGTAATTTTT TTTTTTTTTT TTTTTACTTT GGACAGAGTT TTTAAGCAAC 1080 TGGTTTTGGA AAAAGAAGGT GGTTCTACCA AGAAAGGCTA AGATGGGCTT GAAGCTTACA 1140 TATGCCGCCA ACCCATATCC CCAACCAGCA CCCTGATCAG AATTGCTCCT TCGCTTACAC 1200 AATCCTTAAG ATTTACTCCA GTTTGTTTGC AGATCTCCTG TCTGGAGTAT TGGGGATATA 1260 GAGACTGAGA CACAGTGAGC TTGGGATCTA GTGAGAGAGG CGGAAAAGAC ATAGACGAAG 1320 AGGACCCTGT GGTTCCATAC AACAGCATGA GTATTGCAAA GCGTAGCTGT GCAGAGAAGG 1380 GAGCGACACC CTGAGGGCGA TGGGAGCTGC AGGCAGAGAC CATCAGAGGA 1430
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