Tag | Content |
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EnhancerAtlas ID | HS104-29265 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr19:18514560-18516020 |
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) |
Nr2f6(var.2) | MA0728.1 | chr19:18515187-18515202 | GAGGTCAGGAGTTCA | + | 6.22 | STAT1 | MA0137.3 | chr19:18514640-18514651 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr19:18514640-18514651 | TTTCTGGGAAA | + | 6.32 | Stat4 | MA0518.1 | chr19:18514640-18514654 | TTTCTGGGAAAGGG | + | 6.56 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_24446 | chr19:18514232-18514828 | Colon_Crypt_2 |
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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 |
GH19I018401 | chr19 | 18512101 | 18514911 |
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Enhancer Sequence | CCAGAGGTCT GGGAGTCTTG GGGTCTGGGG CCCCTGGGGT CTGGGCCTTC CTGACACAGC 60 CCCAGCTGGC TACTCCCAGG TTTCTGGGAA AGGGGACAGC TCAAGGCTCC ACTGGCCTCA 120 TCCCTGGCTG AAGGGAGCCT GGAACTTTCA GAGGCCACCT CCCTGGGGTC CCTCTGCTGC 180 CCCCTGATGT ACCTGAAGCC GTCCCAGGCT TGAGTCCCAG GCAGGGCCAG CCAGTCTGCA 240 CAAAAACCTC CAGGCAGCCG CCAGAGATGG CCCCAGACAG AGAGACACCA GCCCGCCCCC 300 CAGCTATACT CAGAGATGCC AAGAGACCCT CAGAAACACT TGGGGGCCAC CATAGGCATG 360 CAGAGACACC TAGGGACACT CAGAAACGCC CAGGGATGCC CAGAAAACCT CAGAGACCCC 420 CAAGATCCTC AGAGACATTT AGAGACCTTC AGAGACTCCC AAAGACCCTC AGAGACCCTC 480 AGAGACCCTC AGAGATCCCC AGAGACCCTC AGAGACCCTC AGAGATCCCC AGAGACTTTC 540 AGAGACATTC AGAGACATCC AGGCTGGGCA TGGTGGCTGA CGCCTGTAAT CCTAGCACTT 600 TAGGAGGCTG AGGCAGGTGG ATCACCTGAG GTCAGGAGTT CACGACCAGC CTGGCCAACA 660 TGGTGAAACC CCGCCTCTAC TAAAAATACA AAAATTAGCC AGGAATGATA GTGCACGCCT 720 GTAATTCCAG CTACTCGGGA GGCTGAGGCA GGAGAATCAC TTGAACCCAA GAGGCAGAGG 780 TTGTAGTGAG CTGAGATTGT GCCACTGCAC TCCAGCCTGG GTGACAGAGC GAGACTCTGT 840 CTCAAAAAAA AAAAAAAAAA GGCTGGGCGG GGTGGCTCAC GCCTGTAATC CCAGCACTTA 900 GGGAGGCTGA GGTGGGTGGA TCACAAGGTC AGGAGATTGA GACCATCCTG GCTAACACGG 960 TGAAACCCCG TCTCTACTAA AAATACAAAA AATTAGCTGG GCGTGGTGGT GGGTGTCTGT 1020 AGTCCCAGCT ACCGGGGAGG CTGAGGCAGG AGAATAGCGT GAACCTGGGA GGCAGAGCTT 1080 GCAGTGAGCC AAGACCACGC CACTGCACTC CAGCGCAGGT AACAGAGCGA GACTCCATCT 1140 CAAAAAAAAA AAAAAAAAAA AGATAAATAT TCAGAGACAT TGAGACCACC CAGAGATCCT 1200 CACAGACCCT AGAGATGCCC TGGAAAGCCC AGAGGCCCCC CCCCCCGCGA AAGAAAAAAA 1260 CATGGAGAGC CAGGCAAGAA GCTCCCTGGG GTGGCCCCGC CTCAATTCAA CCCCATCACC 1320 ACATTCACCC AACACCCTCA GGTCCTCAGA GCCCACCCTG AGGTGGGTGA TGCCAGAGTC 1380 CCTCCAGGCC TCAGCCTGGG TGCTGCCCCA AGAACCCTCA GTCTAGGCAG TGGGGCAACC 1440 ATGGATGCCT GGCCCTGTGG 1460
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