Tag | Content |
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EnhancerAtlas ID | HS104-00005 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:958720-959500 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:959249-959260 | TGGGTGTGGCT | - | 6.14 | NR2C2 | MA0504.1 | chr1:959093-959108 | TAGGGTCAGAGGGCA | + | 6.37 | SP1 | MA0079.4 | chr1:959247-959262 | GGTGGGTGTGGCTTA | - | 6.01 | ZNF263 | MA0528.1 | chr1:958958-958979 | TGAGGAGGGGCTGGAGAAGGG | + | 6.18 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_57930 | chr1:958868-959111 | VACO_9m | SE_57930 | chr1:959358-960218 | VACO_9m | SE_69072 | chr1:955444-963640 | H9 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 959012 | 959267 | chr1 | 958905 | 958959 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I001023 | chr1 | 958815 | 961479 |
|
Enhancer Sequence | CCTGGGGGCT ATGCAGGGGG AGGGGCAGCA CCCAAAATAA GGAACGCTGC GGCCTTTTCC 60 CCAGCCTGTG GTCAGTGGTC CCCAAGCTGC CTTCAGGGTC CAGGGCCTCA GTGCAGCACA 120 GAGGAGGGTC CCCTGGGTCC CCCACTGGGA GGACATGATA ACCTTGGTCC TCTTCTGGGC 180 ACTCATGGTC TGGGGAAAAG ATGGGGGCAT CGTGGACTCA GGATAGGCTG TCAGGAGCTG 240 AGGAGGGGCT GGAGAAGGGG GTTAGGGCGA GGAGAGGTTC CTGTCCCTGC AAGATCAGGA 300 GAGGGGGTCA CTAACCCCAC AGCCAGGTGG GTCCAGCCCG AGAGTCCGTG ACTTAGTAGC 360 TGAGGACTTG CTCTAGGGTC AGAGGGCACA TGGCAGGAGA GTCACCCCGG CTGAACGAGG 420 CTCTGCATCT TACCGAAGCC GCTCTACGGG TGCCAGGCAC TGGCTCTGGA GCGAGTGCCC 480 AGGCGGAGCA GAGCGCTGGG AGGAGGGTCC GTGGGGAGCC CCTGCCAGGT GGGTGTGGCT 540 TAGCCCAGCT GTGGGCAGTC GCACTCAGGG ACGAGCTCCA GGTGGGGAGC CTGGGACCCA 600 CAGCCAGTAT GCAGCTTGGG GAGCACCCGG GAGGGGCTGT GGCCACCGGA CCCCCTGGGG 660 TGGGGCTGGC CAGGGGAGGG TTAGCCAGGG AGGACTGTCA TGGGAGGGGC CTTGCAGGTG 720 AGCCAGGGGC CAAGGGGAGC CTCAGGAGGG AAACAGCATG AGGAGTGGGG GAGCCCAGGA 780
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